National Vaccine
Information Center

Your Health. Your Family. Your Choice.

MedAlerts Home
Search Results

From the 7/23/2021 release of VAERS data:

Found 506,830 cases where Vaccine is COVID19 and Patient Did Not Die



Case Details (Reverse Sorted by Onset Date)

This is page 274 out of 5,069

Result pages: prev   175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 239 240 241 242 243 244 245 246 247 248 249 250 251 252 253 254 255 256 257 258 259 260 261 262 263 264 265 266 267 268 269 270 271 272 273 274 275 276 277 278 279 280 281 282 283 284 285 286 287 288 289 290 291 292 293 294 295 296 297 298 299 300 301 302 303 304 305 306 307 308 309 310 311 312 313 314 315 316 317 318 319 320 321 322 323 324 325 326 327 328 329 330 331 332 333 334 335 336 337 338 339 340 341 342 343 344 345 346 347 348 349 350 351 352 353 354 355 356 357 358 359 360 361 362 363 364 365 366 367 368 369 370 371 372 373   next


VAERS ID: 1442352 (history)  
Form: Version 2.0  
Age: 40.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 1805022 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Electrocardiogram, Loss of consciousness, Palpitations, Sensory disturbance
SMQs:, Torsade de pointes/QT prolongation (broad), Peripheral neuropathy (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: The patient was not pregnant at the time of reporting. The patient does not have diabetes.
Allergies:
Diagnostic Lab Data: Test Date: 202106; Test Name: Electrocardiogram; Result Unstructured Data: Abnormal
CDC Split Type: USJNJFOC20210666494

Write-up: PASSED OUT; HEART PALPITATION; SENSATION ON HEAD LIKE FLASH OF LIGHT; This spontaneous report received from a patient concerned a 40 year old female. The patient''s height, weight and medical history were not reported. The patient was not pregnant at the time of reporting. The patient does not have diabetes. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 1805022, and expiry: 25-MAY-2021) dose was not reported, 1 total, administered on 19-MAR-2021 for prophylactic vaccination. No concomitant medications were reported. On an unspecified date in JUN-2021, the patient experienced heart palpitation and passed out. It was reported that the patient heard her heart beat very fast. The patient went to emergency room (ER) and they sent her home. The patient had couple more episodes. The patient also reported that while sleeping she felt the sensation on head like flash of light. The patient''s palpitation comes and goes, she feels palpitation then sensation of passing out. The patient went to ER again and she mentioned that they said nothing was wrong. In JUN-2021, electrocardiogram (EKG) performed was not normal. ER recommended the patient to go to heart doctor once she has insurance. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from passed out, and heart palpitation, and the outcome of sensation on head like flash of light was not reported. This report was serious (Other Medically Important Condition).; Sender''s Comments: V0: 20210666494-covid-19 vaccine ad26.cov2.s-passed out. This event(s) is considered unassessable. The event(s) has an unknown/unclear temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).


VAERS ID: 1442367 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Male  
Location: Ohio  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Confusional state, Dreamy state, Fear, Hyperhidrosis, Loss of consciousness, Posture abnormal, Seizure
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Convulsions (narrow), Dystonia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Abstains from alcohol; Seasonal allergy
Preexisting Conditions: Medical History/Concurrent Conditions: Chest burning; Comments: no previous medical history or conditions, no Family history of seizures/epilepsy, no Illness at the time of vaccination, no Past history of similar event, no History of allergy to vaccine, drug, or food, no Family history of any disease (relevant to vaccination) or allergy, no Other Suspected causes including co-administered vaccine(s)/risk factors. The patient had no drug abuse or brain surgery.
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20210667371

Write-up: SEIZURE; PASSED OUT; POSTURE CONTRACTED; DIAPHORETIC/ SUPER SWEATY; CONFUSED; AFRAID; IT WAS LIKE A DREAM; This spontaneous report received from a pharmacist concerned a 27 year old male. The patient''s height, and weight were not reported. The patient''s past medical history included chest burning, and concurrent conditions included seasonal allergy and non-alcoholic user and other pre-existing medical conditions included no previous medical history or conditions, no family history of seizures/epilepsy, no illness at the time of vaccination, no past history of similar event, no history of allergy to vaccine, drug, or food, no family history of any disease (relevant to vaccination) or allergy, no other suspected causes including co-administered vaccine(s)/risk factors. The patient had no drug abuse or brain surgery. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular and batch number: 1808609 expiry: unknown) dose was not reported, 1 total administered on JUN-2021 for prophylactic vaccination. No concomitant medications were reported. On unspecified date in JUN-2021, Reporter stated that the patient had his head backwards, the patient posture contracted, passed out in the observe area, which was tight and small area. Reported did not see that patient fall to ground. Reporter assumes that patient must have had a fall to get from the chair to the ground when she was able to see. Reporter stated that the seizure was about 15 seconds, eyes rolled back, blank stare, eyeballs twitching, full blown seizure. Reporter stated that when patient came back, he was super sweaty, diaphoretic, and only remembers that his chest was burning prior to vaccine. Reporter mentioned that patient did not know that he passed out. Reporter stated that patient said it was like a dream and do not know how long he was out and stated that he just said his chest was burning. Reporter mentioned that the guy was afraid and did not know what happened. Patient was confused upon waking up. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from seizure, passed out and it was like a dream and the outcome of posture contracted, diaphoretic/super sweaty, confused and afraid was not reported. This report was serious (Other Medically Important Condition).; Sender''s Comments: V0- 20210667371-Covid 19 vaccine-Seizure, Passed out. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).


VAERS ID: 1442368 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Unknown  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Feeling abnormal, Headache, Nausea
SMQs:, Acute pancreatitis (broad), Dementia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20210667604

Write-up: FEELING AWFUL; EXTREME HEADACHE; NAUSEA; This spontaneous report received from a parent concerned a male of unspecified age. The patient''s height, and weight were not reported. No past medical history or concurrent conditions were reported.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose was not reported, administered on 22-JUN-2021 for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On JUN-2021, the subject experienced feeling awful. On JUN-2021, the subject experienced extreme headache. On JUN-2021, the subject experienced nausea. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the extreme headache, nausea and feeling awful was not reported. This report was non-serious.


VAERS ID: 1442370 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Male  
Location: Nevada  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 203A21A / UNK - / -

Administered by: Military       Purchased by: ?
Symptoms: Abdominal distension, Abdominal pain upper, Chills, Colonoscopy, Injection site pain
SMQs:, Acute pancreatitis (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: TESTOSTERONE
Current Illness: Hypotestosteronism (Patient had on Testosterone injections for Low T (but had not in the past month).); Non-smoker; Social alcohol drinker (occasional social consumer.)
Preexisting Conditions: Comments: Patient had no known allergies.
Allergies:
Diagnostic Lab Data: Test Name: Colonoscopy; Result Unstructured Data: colon twisted
CDC Split Type: USJNJFOC20210667910

Write-up: STOMACH PAINS; CHILLS WITH FREEZING SHIVERS; PAIN WHERE VACCINE WAS INJECTED; ENTIRE STOMACH FEELS BLOATED AND GASSY; This spontaneous report received from a patient concerned a 55 year old male. The patient''s height, and weight were not reported. The patient''s concurrent conditions included low testosterone, alcohol use, and non smoker, and other pre-existing medical conditions included patient had no known allergies. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 203A21A, and expiry: 07-AUG-2021) dose was not reported, administered on 23-JUN-2021 for prophylactic vaccination. Concomitant medications included testosterone for low testosterone. On JUN-2021, the subject experienced entire stomach feels bloated and gassy. On 23-JUN-2021, the subject experienced pain where vaccine was injected. On 25-JUN-2021, the subject experienced stomach pains. On 25-JUN-2021, the subject experienced chills with freezing shivers. Laboratory data (dates unspecified) included: Colonoscopy (NR: not provided) colon twisted. Treatment medications (dates unspecified) included: simeticone. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from chills with freezing shivers, and had not recovered from stomach pains, pain where vaccine was injected, and entire stomach feels bloated and gassy. This report was non-serious.


VAERS ID: 1442386 (history)  
Form: Version 2.0  
Age: 68.0  
Sex: Female  
Location: Florida  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 043A71A / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Headache, Heart rate, Heart rate decreased, Pain in extremity, Therapeutic response unexpected
SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Feeling abnormal; Hepatitis C; Neuropathy (Patient took treatment in 2018 which increased neuropathy); Postural orthostatic tachycardia syndrome
Preexisting Conditions: Comments: Patient wore a heart monitor and normally heart rate was in 150 - 160s when play ball. Patient can not take certain medications because liver enzymes.
Allergies:
Diagnostic Lab Data: Test Date: 202106; Test Name: Heart rate; Result Unstructured Data: 10 beats lower per minute; Comments: Instead of playing in 160s patient was playing in 150s.; Test Date: 202106; Test Name: Heart rate; Result Unstructured Data: 140s; Test Date: 202106; Test Name: Heart rate; Result Unstructured Data: 130s; Test Date: 202106; Test Name: Heart rate; Result Unstructured Data: Low 140s; Test Date: 202106; Test Name: Heart rate; Result Unstructured Data: 156; Test Name: Heart rate; Result Unstructured Data: 150s
CDC Split Type: USJNJFOC20210700524

Write-up: LOWER HEART RATE; LITTLE HEADACHE; SORE ARM; POTENTIALLY HELPED SYMPTOMS OF POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME/LESS ADRENALINE RUSH/ LESS NEUROPATHY; This spontaneous report received from a patient concerned a 68 year old female. The patient''s height, and weight were not reported. The patient''s concurrent conditions included postural orthostatic tachycardia syndrome, neuropathy, hepatitis c, and adrenaline rush, and other pre-existing medical conditions included patient wore a heart monitor and normally heart rate was in 150 - 160s when play ball. patient can not take certain medications because liver enzymes. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 043a71a, and expiry: UNKNOWN) dose was not reported, administered on 02-JUN-2021 for prophylactic vaccination. No concomitant medications were reported. On JUN-2021, the subject experienced potentially helped symptoms of postural orthostatic tachycardia syndrome/less adrenaline rush/ less neuropathy. Laboratory data included: Heart rate (NR: not provided) 10 beats lower per minute, 140s, 130s, Low 140s, 156. On 02-JUN-2021, the subject experienced sore arm. On 03-JUN-2021, the subject experienced little headache. On 05-JUN-2021, the subject experienced lower heart rate. Laboratory data (dates unspecified) included: Heart rate (NR: not provided) 150s. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the little headache, sore arm, lower heart rate and potentially helped symptoms of postural orthostatic tachycardia syndrome/less adrenaline rush/ less neuropathy was not reported. This report was non-serious.


VAERS ID: 1442614 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-06-02
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0191 / 1 LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Blood test, Blood triglycerides, Body temperature, Body temperature abnormal, Erythema, Fatigue, Feeling hot, Pruritus, Rash, Scratch, Somnolence, Urticaria, X-ray
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: AMOXICILLIN; CIPROFLOXACIN
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19; Infection; Pneumonia; Shingles; Tooth disorder (Verbatim: Bad tooth); UTI (Verbatim: UTI)
Allergies:
Diagnostic Lab Data: Test Date: 202012; Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Test Date: 202012; Test Name: Triglycerides; Result Unstructured Data: Test Result:High; Test Date: 202011; Test Name: Body temperature; Result Unstructured Data: Test Result:97.1; Test Date: 202011; Test Name: X-ray; Result Unstructured Data: Test Result:pneumonia
CDC Split Type: USPFIZER INC2021664845

Write-up: Broke out in a rash on my face and it was very itchy, it was all in the lower area, it was pretty heavy and it itched/I woke up itching my face; scratching; Broke out in a rash on my face and it was very itchy, it was all in the lower area, it was pretty heavy and it itched/ like a red rash and it was all below my eyes going from ear and behind my ear; is that shingles because I had shingles before but very mild (not clarified further) but this is pretty red.; I was like tired; I was sleepy; I do not feel like I have a fever but my face is very warm; I checked the temperature, it was 97.1 and normally, my temperature runs lower than 97, usually my temperature runs 96.1; was broken out and it is almost like welt; This is a spontaneous report from a contactable consumer. A 75-year-old female patient received first dose of BNT162B2 (BNT162B2), via an unspecified route of administration, administered in Arm Left on 02Jun2021 at 12:05 (Batch/Lot Number: EW0191; Expiration Date: 02Jun2021) as DOSE 1, SINGLE for covid-19 immunization. Medical history included bad tooth, urinary tract infection and shingles from unknown dates and covid-19 and pneumonia from Nov2020. Concomitant medications included amoxicillin (AMOXICILLIN) taken for bad tooth, start and stop date were not reported and ciprofloxacin (CIPROFLOXACIN) taken for urinary tract infection, start and stop date were not reported. Consumer stated, "I got my COVID shot on 02June2021, Wednesday and my shoulder didn''t even hurt it didn''t get red, nothing, I felt great and then the next day Thursday I felt fine. And then yesterday morning I broke out in a rash on my face and it was very itchy, it was all in the lower area, it was pretty heavy and it itched. And then this morning it''s still, I put Aloe Vera on it yesterday and it calmed it down and it felt better, it wasn''t itching anymore but this morning I woke up and it''s still there and it''s ''welt'' looking today. For her Medical Condition, Consumer stated, "Yes, I am, I have bad tooth in my mouth and I have to have it pulled and I have been on antibiotics for a week I guess. I might also mention that I had COVID in November last year and my doctor asked me to wait for 6 months before I got the shot. I had my blood work in December and everything is good. Ya everything is normal except my triglycerides are too high." Consumer stated, "I was sleepy when I got my home from getting shot, I was like tired, so I laid down on couch and rested and I have been fine and started talking. I had no side effects, no side effects, I talked about it too much. This Saturday, I woke up itching my face, scratching and I looked in mirror and I was broken out like a red rash and it was all below my eyes going from ear and behind my ear and it itches all across my face. I broke out in a rash and today, it is worse. Today, I put some aloevera on it and it helped and it saved it otherwise I just keep scratching my face of. I didn''t have fever, I checked the temperature, it was 97.1 and normally, my temperature runs lower than 97, usually my temperature runs 96.1 or something like that, I do not feel like I have a fever but my face is very warm and was broken out and it is almost like welt. I did had Covid back in November and I was very sick then, I was in the hospital, they did take me to the hospital to get an X-ray and I did have spotted pneumonia but I don''t even remember that week, I was ill. So, before I got my shot, I told them that I had urinary tract infection and I also have bad tooth and it has to be pulled (Consumer had urinary tract infection and bad tooth before getting the vaccine)and I have been on strong antibiotics (Unspecified Medications) for the whole week until I got my shot, I still was taking like 25mg of antibiotics per day for two different infections but the antibiotics works with each other and they said, I can go ahead and take my shot, it would be fine. The only thing that I am wondering is that, if it could have triggered this, I do not know. Also, I am wondering, is that shingles because I had shingles before but very mild (not clarified further) but this is pretty red. Could it be possibly be a reaction to the vaccine?" The patient underwent lab tests and procedures which included blood test: normal on Dec2020, blood triglycerides: high on Dec2020, body temperature: 97.1 on Nov2020 and x-ray: pneumonia on Nov2020. Therapeutic measures were taken as a result of broke out in a rash on my face and it was very itchy, it was all in the lower area, it was pretty heavy and it itched/ like a red rash and it was all below my eyes going from ear and behind my ear/i woke up itching my face. The outcome of the events was unknown. Information on Lot/Batch number was available. Additional information has been requested.


VAERS ID: 1442615 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Male  
Location: Pennsylvania  
Vaccinated:2021-05-27
Onset:2021-06-01
   Days after vaccination:5
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0178 / 1 LA / OT

Administered by: Pharmacy       Purchased by: ?
Symptoms: Blood test, Body temperature, Chest X-ray, Computerised tomogram, Fatigue, Headache, Pyrexia, SARS-CoV-2 test
SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: GABAPENTIN; SEROQUEL; CHLOROQUINE
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: None
Allergies:
Diagnostic Lab Data: Test Date: 20210607; Test Name: Blood work; Result Unstructured Data: Test Result:normal; Test Date: 20210601; Test Name: Fever; Result Unstructured Data: Test Result:102; Test Date: 20210608; Test Name: Fever; Result Unstructured Data: Test Result:102.6; Test Date: 20210607; Test Name: chest X-ray; Result Unstructured Data: Test Result:normal; Test Date: 20210607; Test Name: CT Scan; Result Unstructured Data: Test Result:normal; Test Date: 20210605; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210607; Test Name: Covid test; Test Result: Negative ; Comments: Nasal Swab
CDC Split Type: USPFIZER INC2021665116

Write-up: fever of 102, fever was getting higher as 102.6; fatigue; headaches; This is a spontaneous report from a contactable consumer (patient) from Pfizer sponsored program COVAX US Support. This 42-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via intramuscular in left arm on 27May2021 at 14:00, at patient age of 46-year-old, as single dose (Lot number EW0178, Expiry Date: Aug 2021) for COVID-19 immunization. The patient was not diagnosed with COVID-19 prior to vaccination. The patient had no other medical history and no known allergies. The patient''s concomitant medications included gabapentin, quetiapine fumarate (SEROQUEL), chloroquine. The patient had no past drug reaction. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced the adverse events from 01Jun2021. The patient got a high fever of 102 which had lasted a week and it was not getting any better. The patient also experienced headache and fatigue. The patient went to the emergency room on 07Jun2021, where they did blood work and a chest X-ray and a CT scan. Everything came back normal and they can not figure out why he had this persistent high fever. The patient wanted to know how long this is going to last or what was going on. On 08Jun2021, the patient reported fever was getting higher as 102.6. It was going up little more everyday. The events resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Covid test post vaccination included Rapid test on 05Jun2021 showed negative (Nasal Swab); Non rapid test on 07Jun2021 showed negative (Nasal Swab). The patient received treatment including paracetamol (ACETAMINOPHEN), ibuprofen (MOTRIN), Ibuprofen. The outcome of the events was not resolved.


VAERS ID: 1442640 (history)  
Form: Version 2.0  
Age: 52.0  
Sex: Female  
Location: Tennessee  
Vaccinated:2021-06-09
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0171 / 2 LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Burning sensation, Condition aggravated, Eye irritation, Eyelid skin dryness
SMQs:, Peripheral neuropathy (broad), Corneal disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021684035

Write-up: Burning in toes and feet; eyelids were dry.; burning in my eyes and feet/felt both eyes started to burn.; burning in my eyes and feet; it is persisting and worsened.; This is Spontaneous report received from a contactable consumer (patient). A 52-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0171), via an unspecified route of administration, administered in Arm Left on 09Jun2021 between 14:00 and 15:00 (at the age of 52-years-old), as 2nd dose, single for COVID-19 immunization. Medical history and concomitant medications were not reported. Prior Vaccinations within 4 weeks was None. Historical vaccination included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/lot number: EW0185) via unspecified route of administration in the left arm, on 19May2021 in a daytime 15:00 or 16:00, as 1st dose, single for COVID-19 Immunization and experienced little weak. On 09Jun2021 (day of vaccination), after the needle was out of her arm, the patient experienced burning in her both eyes and feet, especially her left foot and it was still present. On 10Jun2021, the patient experienced burning in toes and feet, eyelids were dry. Caller stated that she did not even feel the needle go in her arm. It was reported that the patient took Pfizer BioNTech Covid-19 Vaccine because lots of people died without it and she figured that she needed to get it. Caller stated that she hadn''t weighed herself in a while but she thought she would be about 230 pounds. Caller thought this would last only a little while. She got afraid since it kept going. She read up that toxins can cause burning like that. She wasn''t sure what was in the syringe and had her questioning what was in the syringe. It started right after the shot. It burned the rest of the day and into the night. Caller said she woke up last night and it was still burning. This morning it felt like her eyelids were dry. She didn''t feel burning as much. They were just dry. It improved but her eyelids were dry. She said the burning in her eyes was a 10 yesterday but a 1 now. Caller stated that her toes were burning especially the left. It moved down from the top to the bottom of the foot. It started this morning. Caller looked on the website for side effects and this was not on the list for side effects. The burning started with the toes and spread to the middle of feet, especially left foot. She was drinking water to try and get the toxins that were in there out. She did not know what would cause this as it was not on the list of side effects. It spread form the toes to the foot. Caller said the right toes were burning but not as bad as the left. Caller stated that she did not do anything but drink water to try and get the toxins out. She went online and say there were toxins in the vaccine and she was wondering about the toxins and what was in the syringe, or if it was outdated. The outcome of the events burning in my eyes and feet/felt both eyes started to burn, burning in toes and feet were not recovered. The outcome of the events eyelid skin dryness and condition aggravated was unknown. Information on Lot/Batch number was available. Additional information has been requested. Follow-up (11Jun2021): This is a follow up spontaneous report from a PPD Pfizer. This PPD Pfizer reported in response via mail follow-up activity which included that: After listening to the call recording associated with the caller confirmed the spelling of her first name. Additional information has been requested; Sender''s Comments: Linked Report(s) : US-PFIZER INC-2021683896 same patient/drug, different dose/event


VAERS ID: 1442649 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0183 / 1 LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Aphonia, Chest discomfort, Chills, Coagulation test, Cough, Feeling cold, Feeling hot, Hyperhidrosis, Oropharyngeal pain, Rhinorrhoea, SARS-CoV-2 test, Thrombosis, White blood cell count
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Thrombophlebitis (broad), Hypoglycaemia (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FENOFIBRATE; VITAMIN D 2000; IRON; LOSARTAN; HYDROCHLOROTHIAZIDE
Current Illness: WBC increased (she has a high white blood cell count and is anemic.)
Preexisting Conditions: Medical History/Concurrent Conditions: Anemic (she has a high white blood cell count and is anemic.); Overweight (She is overweight)
Allergies:
Diagnostic Lab Data: Test Date: 2021; Test Name: Blood clot; Result Unstructured Data: Test Result:High; Comments: her blood clot was already high.; Test Date: 20210530; Test Name: COVID-19; Test Result: Negative ; Test Date: 2021; Test Name: WBC; Result Unstructured Data: Test Result:High; Comments: high white blood cell count
CDC Split Type: USPFIZER INC2021715089

Write-up: Her body produces mucous/blowing her nose; She had a horrible cough she couldn''t get out; her blood clot was already high; lose her voice; She had chills; rattle in her chest; She was cold ,and it was hot (88 degrees); She was sweating, and was warm all over her body.; She was sweating, and was warm all over her body.; Her throat seemed sore after.; She had dry cough. It felt dry; This is a spontaneous report from a contactable consumer (Patient) via Medical Information Team. A 48-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EW0183, NDC number and Expiry date: Unknown), via an unspecified route of administration, administered in left arm on 01Jun2021 (at the age of 48-years-old) as dose 1, single for COVID-19 immunisation. Medical history included ongoing high WBC/white blood cell count increased and anaemic. Patient was overweight. Patient said that before the shot, she as been exposed to COVID-19 and never caught the virus. She has taken a COVID-19 test and it was negative two days ago and does not have COVID. Concomitant medication(s) included fenofibrate taken for blood cholesterol, colecalciferol (VITAMIN D 2000), iron, losartan and hydrochlorothiazide taken for blood pressure, from an unspecified start date and ongoing. It was reported that, two days after getting vaccinated, the patient got sick, and she feels like she has pneumonia. She was overweight. On an unspecified date in Jun2021, her body produces mucous/blowing her nose, and she had chills on 03Jun2021. Patient said that it all started a little after the shot. She felt like she had sand in her throat and she woke up feeling bad. She had a horrible cough on an unspecified date she could not get out. She still has a rattling in her chest. She wants to know if it is possible for this to stay in her chest and form a blood clot. Patient said that after vaccination, she had her nephew graduation, and she screamed at it. Then her throat seemed sore after and she would lose her voice, but it would come back. Her throat started hurting. As the days went on, she felt like there was dust in her throat. She had dry cough and it felt dry. It was like more dust had collected in her throat. Patient felt real sick, but she never had a fever. She was cold and it was hot (88 degrees) in and was sweating and was warm all over her body. Patient has a higher than normal WBC/ and that was one of her main concerns about getting the vaccine. Since her blood clot was already high and she was scared it would put her WBC in maximum overdrive. There was no investigation assessment. The patient underwent lab tests and procedures which included coagulation test: high on unspecified date in 2021 her blood clot was already high, SARS-CoV-2 test: Negative on 30May2021 and white blood cell count: high on unspecified date in 2021 (high white blood cell count). Patient wanted to know if there is any chance of getting pneumonia with the vaccine for which patient received response as "a review of the Prescribing Information for Pfizer COVID-19 vaccine failed to find any information regarding pneumonia being an adverse event with the vaccine". Patient was wondering if Pfizer is getting reports of side effects being full on pneumonia like symptoms that last. Patient asked if there was any chance that of blood clots after vaccination, and would like to know if anemic people who had the vaccine had adverse events and if there had been reports of cytokine storm and received response which says, failed to find any information regarding cytokine storm being an adverse event with the vaccine and was asked patient to consult with her doctor or health care provider for further guidance. The outcome of the events rattle in her chest, her throat seemed sore after, she had dry cough and her blood clot was already high was not recovered, and the outcome of chills, she got sick, her body produces mucous/blowing her nose, she had a horrible cough she couldn''t get out, she was cold, and it was hot (88 degrees), she was sweating, and was warm all over her body and lose her voice was unknown. Information on Lot/Batch number was available. Additional information has been requested.


VAERS ID: 1442675 (history)  
Form: Version 2.0  
Age: 75.0  
Sex: Female  
Location: Louisiana  
Vaccinated:2021-06-11
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8733 / 1 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Circumstance or information capable of leading to medication error, Oropharyngeal pain, Rash, Tongue blistering, Tongue discomfort
SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Heart disorder (Heart problems); Multiple allergies (Allergic to everything)
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021734353

Write-up: This is a spontaneous report from a contactable consumer or other non hcp. A 75-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Solution for injection (Batch/Lot Number: ER8733), dose 1 via an unspecified route of administration, administered in Arm Right on 11Jun2021 as dose 1, single for covid-19 immunisation. Medical history included cardiac disorder ongoing Heart problems; multiple allergies Allergic to everything. The patient''s concomitant medications were not reported. consumer stated received her first dose of the Pfizer-BioNTech covid19 vaccine last Friday. She has since been experiencing a rash which she has been treating with Benadryl (Lot 1795513, Expiry Jul2022, UPC 125471702) every 4 hours. She went back to her doctor who stated they would normally give a steroid shot in this situation but didn''t want to affect the efficacy of the dose she received. Caller is a consumer who took her first dose of the Pfizer COVID shot last Friday, and she had a terrible rash reaction to it all over her body. Caller states that she has been taking Benadryl all week and she is still broken out. Patient saw her doctor this morning and her doctor said that she normally would give the caller a steroid shot, but the doctor decided not to give the steroid to the caller because the doctor was afraid the steroid would deplete the care that the one COVID shot had given to the caller. Patient is wondering about if a steroid injection could affect the effectiveness of the COVID vaccine. Patient reports that the same day as her shot, her tongue had a strange feeling and her throat is sore and she has blisters on her tongue, and these are ongoing. Patient woke up the next morning with the rash, which is also still ongoing, but improved. Patient states that she was holding off on getting the vaccine because she is allergic to everything, so she was afraid, but she ended up taking it and now she wishes she hadn''t. Therapeutic measures were taken as a result of rash/ terrible rash reaction to it all over her body (rash). The outcome of the events was recovered and Indicated she would not be receiving her second dose was unknown. Follow-up (PRD 18Jun2021): This is a follow up spontaneous report from a contactable consumer. This consumer 75-year-old female consumer(patient) reported information included. Description of complaint: PC for non-suspect product. While completing a safety report for the suspect product, caller mentioned she has been taking Benadryl all week for a rash, and she is still broken out.


VAERS ID: 1442678 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0177 / 1 LA / OT

Administered by: Pharmacy       Purchased by: ?
Symptoms: Arthralgia, Arthritis, Back pain, Bone pain, Fatigue, Gait disturbance, Migraine, Pain, Pain in extremity, Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Peripheral neuropathy (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Osteonecrosis (broad), Arthritis (narrow), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: COMBIPATCH
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021735619

Write-up: Major pain in her joints/bones, in her hands and in her knees, her back, lower back; Major pain in her joints/bones, in her hands and in her knees, her back, lower back; Arthritis; Tiredness; Joint pain in hands and knees (throbbing and stabbing pain; throbbing and stabbing pain; Hands and knees have the most severe pain; Swelling of hands; Harder and harder to walk; Migraine/migraine headache; This is a spontaneous report from a contactable pharmacist. This pharmacist reported for a 62-year-old female patient that received bnt162b2 (BNT162B2 Formulation: Solution for injecction), dose 1 intramuscular, administered in Arm Left on 01Jun2021 13:00 (Batch/Lot Number: EW0177) as DOSE 1, SINGLE for covid-19 immunisation. Medical history was not reported. concomitant medication(s) included estradiol, norethisterone acetate (COMBIPATCH) taken for an unspecified indication, start and stop date were not reported. Patient not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, was the patient diagnosed with COVID-19 was no and Since the vaccination, has the patient been tested for COVID-19 was no.The patient experienced joint pain in hands and knees (throbbing and stabbing pain), throbbing and stabbing pain , hands and knees have the most severe pain , swelling of hands, harder and harder to walk, migraine/migraine headache on Jun2021 (Unspecified day) major pain in her joints/bones, in her hands and in her knees, her back, lower back, major pain in her joints/bones, in her hands and in her knees, her back, lower back, arthritis, tiredness on an unspecified date. Caller states she had almost immediately after the shot came a major migraine headache, it didn''t last very long, it went away, and since then it comes and goes, but not an every day occurrence. Caller states what is an every day, constant occurrence, which had her concerned, which has been affecting her work, she works on a computer with a keyboard and mouse is there''s major pain in her joints/bones, in her hands and in her knees, her back, lower back. Caller states she has arthritis in lower back and have had injections done there so that''s no surprise. Caller states she has had some tiredness. Caller states she''s constantly working with her hands etc. so her hands get tired. Caller states what she''s never had before is this constant throbbing pain, pain in her joints that are in her hands, knees, and she has a constant pain across her back, is that her clavicle the back part? Caller states the upper part of her back where her shoulders connect together, that whole section is a throbbing pain. Caller states her hands and knees are throbbing and in pain constantly, it keeps her up some nights. Caller states she is right now rubbing her knuckles and hands. Caller states she does have a high pain tolerance and she pushes through it until she clocks out. The patient not received treatment for the events. The outcome of the events Major pain in her joints/bones, in her hands and in her knees, her back, lower back, Arthritis and Tiredness was unknown and other events was not resolved.


VAERS ID: 1442689 (history)  
Form: Version 2.0  
Age: 58.0  
Sex: Female  
Location: California  
Vaccinated:2021-06-14
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0164 / 2 LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Chills, Cough, Headache, Migraine, Myalgia, Rhinorrhoea, Routine health maintenance, Urinary tract infection
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Blood pressure high; Breast cancer; Cancer; Heart attack; Kidney cancer
Allergies:
Diagnostic Lab Data: Test Date: 20210616; Test Name: annual visit; Result Unstructured Data: Test Result:Normal; Comments: Everything as far as her other results were normal; Test Date: 20210616; Test Name: annual visit; Result Unstructured Data: Test Result:UTI; Comments: She found out she had a UTI when she had her wellness visit and they gave her blood test results
CDC Split Type: USPFIZER INC2021749119

Write-up: runny nose; migraine headache; Slight headache; Muscles hurt; Little bit of chills; UTI; cough; This is a spontaneous report from a contactable consumer reporting for herself. A 58-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EW0164; Expiration date was not reported), via an unspecified route of administration, administered in Arm Left on 14Jun2021 11:00 (at the age of 58-years-old) as single dose for COVID-19 immunisation. Medical history and concomitant medications were reported as none. The patient did not have prior Vaccinations (within 4 weeks). Family Medical History included cancer, high blood pressure, heart attack, kidney cancer, breast cancer. The patient previously took first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EW0186) in left arm on 24May2021 13:00. The patient experienced cough on Jun2021, runny nose on an unspecified date, UTI (urinary tract infection) on 16Jun2021, slight headache on 17Jun2021, muscles hurt on 17Jun2021, little bit of chills on 17Jun2021, migraine headache on an unspecified date. Caller wanted to know if the adverse events that she is experiencing are included among the commonly reported adverse events from getting the Pfizer Biontech covid-19 vaccine. She was mostly concerned about the cough and runny nose. In response, patient was given overall safety summary that in clinical studies, adverse reactions in participants 16 years of age and older included fatigue (62.9%), and chills (31.9%). No specific information for coughs and runny nose being a effect, patient was referred to HCP. Caller stated that she was unsure if the cough and runny nose that she was experiencing were the signs of covid-19 or an AE of the Pfizer BioNTech Covid-19. The vaccine was at 95% efficacy 7 days after the 2nd dose of the Pfizer Biontech covid-19 vaccine. It may not protect everyone from covid-19. Patient was requested to speak to her doctor/hcp for some guidance as the cough/runny nose she was experiencing may require extensive evaluation to assess if it was an AE of the vaccine or a symptom of covid-19. Upon follow-up on 21Jun2021, patient reported additional events she experienced which included UTI, slight headache, muscles hurt, little bit of chills. Reason for the patient taking Covid Vaccine was that she was hearing a lot of announcements that Covid has been reported as decreasing. Patient had the second shot of the Covid vaccine on 14Jun2021. Her doctor prescribed her medication two days later for a UTI. She was just calling about this cough too and asked if that is normal after the Covid vaccine. She had a cough off and on and sometimes gets sniffles. She was going back to work the day later this report. She asked if that was okay since she had the shot last week. The medication the doctor gave her for the UTI was Nitrofurantoin and the next day to this report was her last day on it. She was taking 1 tablet twice a day. The cough started Saturday and it was off and on. She called Doctor''s office, then she guessed her assistant called back and said she should call Pfizer and where she went to get the vaccine. She should ask them if it was normal to cough this way after the vaccine. Cough started the past Saturday or Sunday, 19Jun2021 or 20Jun2021. Thursday, she had a slight headache, her muscles hurt, and a little bit of chills. She slept all day. She still had a slight headache, but she was thinking that was because of the UTI medicine which can cause some headaches. She was trying not to take Tylenol or anything because she didn''t want to kill the vaccine in her. It was not like a migraine headache, and she only feel it when she was sleeping. The muscle pain and chills went away on Friday, and she had recovered completely from both. She found out she had a UTI when she had her wellness visit and they gave her blood test results. She found out on Wednesday 16Jun2021. She didn''t have any symptoms, they just found it during her annual visit. Everything as far as her other results were normal. That was the only thing they found. She was hearing a lot of announcements that Covid has been reported as decreasing and how it is safe to go back to work and those who are vaccinated can have no mask. It was reported that history included that the only medicine she was taking is the one for her UTI. She wanted to call because her boss said it was worse, she would have to call her primary physician, and he said to call administration site. When she had her lab results from her annual wellness visit, they found the UTI, she had no symptoms. Event onset time (24-hour clock) for slight headache, muscles hurt, chills was reported as 1500 or 1600 and for cough was towards the evening. AE(s) did not require a visit to emergency room or physician office. Patient was not hospitalized. Relevant tests included none. Clinical outcome of the events muscles hurt, little bit of chills recovered on 18Jun2021, events of cough, slight headache were not recovered and for the other events was unknown.


VAERS ID: 1442700 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Mississippi  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Asthenia, Chills, Decreased appetite, Dehydration, Fatigue, Feeding disorder, Feeling abnormal, Gingival pain, Illness, Influenza like illness, Pain
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Dementia (broad), Gingival disorders (narrow), Guillain-Barre syndrome (broad), Dehydration (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021756085

Write-up: She is drinking juices and sprite to keep from getting dehydrated; she has been feeling horrible; Has been sick; Chills; Can''t eat; No appetite; Tired; No energy; Body aches; When she tries to eat her gums are sore; The physician she works for says flu like symptoms; This is a spontaneous report received from a contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONECH COVID-19 VACCINE, Batch/Lot number was not reported), Solution for injection, via an unspecified route of administration on Jun2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date in Jun2021, the patient had been sick, chills, can''t eat, no appetite, tired, no energy, body aches, when she tried to eat her gums are sore, the physician she worked for said flu like symptoms, she was drinking juices and sprite to keep from getting dehydrated, she had been feeling horrible. Got first dose of vaccine on Thursday and had been sick, chills, can''t eat, no appetite, tired and no energy. Patient wanted to know, if this was normal. Patient also reported body aches, when she tried to eat her gums were sore, and no appetite. She was drinking juices and sprite to keep from getting dehydrated. The physician she worked for said flu like symptoms. She asked, should it be going on this long? She stated she will have to ask about the second dose because she may not take it if she was still sick then. The outcome of events was unknown. Information on batch/lot number has been requested.


VAERS ID: 1442702 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-06-15
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Diarrhoea, Dyspnoea, Headache, Pain
SMQs:, Anaphylactic reaction (broad), Pseudomembranous colitis (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Noninfectious diarrhoea (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021756167

Write-up: Pain; Diarrhea; difficulty breathing; headache; This is a spontaneous report from a contactable consumer or other non hcp (patient boyfriend). A 47-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number and Expiration Date not reported), via an unspecified route of administration on 15Jun2021 (at the age of 47-years-old) as dose number unknown, single for COVID-19 immunisation. The medical history and concomitant medications of the patient were not reported. The investigation assessment was not provided. The patient experienced pain, diarrhea, difficulty breathing and headache on an unspecified date in Jun2021. Reporter stated that he does not know if these are typical side effects, but the patient got the Covid-19 shot last Tuesday, 15Jun2021, and started getting side effects 3 days ago. The seriousness of the events was reported as non-serious. Reporter questioned if these are common side effects and was it normal for side effects to start up to 7 days after the vaccine and how long would they last. The report was not related to a study or program. The outcome of all the events was reported as unknown. Information on the lot/batch number has been requested.


VAERS ID: 1442709 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Female  
Location: Maine  
Vaccinated:2021-06-22
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Pain in extremity, Pallor
SMQs:, Hypotonic-hyporesponsive episode (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021770402

Write-up: whiteness on both hands, specifically on the fingers.; a sore arm down to her hand; This is a report from a Pfizer sponsored program received via a contactable consumer (patient''s mother). A 15-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number and expiration date: not reported), via an unspecified route of administration, on 22Jun2021 (at the age of 15-year-old), as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunization .The patient''s medical history and concomitant medications were not reported. After the vaccination, the patient experienced sore arm down to her hand and whiteness on both hands, specifically on the fingers on Jun2021. Reporter would like to know, what that is. The outcome of the events was unknown. Information on the lot/batch number has been requested


VAERS ID: 1442713 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: New York  
Vaccinated:2021-06-10
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0186 / 1 RA / -

Administered by: Private       Purchased by: ?
Symptoms: Diarrhoea
SMQs:, Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021783113

Write-up: Diarrhea; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in right arm on 10Jun2021 10:30 (Lot Number: EW0186; Expiration Date: Aug2021) as dose 1, single for COVID-19 immunization at the age of 65-year-old. The patient received the COVID-19 vaccine in hospital. Medical history and concomitant medications were none. No family history. The patient did not receive any vaccinations prior to COVID vaccine. The patient did not undergo any relevant tests. The patient experienced diarrhea and stated that its looks like it is water on an unspecified date of Jun2021 (reported as about 4 days ago). The event did not result in any emergency room or physician office visit. It was reported the event was persisting (not recovered). She is scheduled for the second dose on 01Jul2021.


VAERS ID: 1442716 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:2021-06-14
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Burning sensation, Expired product administered, Pain in extremity
SMQs:, Peripheral neuropathy (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021787833

Write-up: Mentioned that they may have lock the vaccine in freezer for too long and might have expired and the caller was advised to take three doses; Ache in the arm and burning; Ache and burning in her arm; Ache in the arm and burning; Ache and burning in her arm; This is a spontaneous report from a non-contactable consumer (patient) received via Pfizer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, lot number and expiry date not reported) via an unspecified route of administration, on 14Jun2021, as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced ache in the arm and burning; ache and burning in her arm on an unspecified date in Jun2021. The patient took her first dose of vaccine on 14un2021 and it was mentioned that they might have lock the vaccine in freezer for too long and might have expired and the patient was advised to take three doses (two more doses). The reporter was asking how effective the vaccine was in three doses and how safe was that for her body and heart since she experienced ache and burning in her arm after the first dose. The outcome for the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.


VAERS ID: 1442778 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Fatigue
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20210666567

Write-up: EXTREME FATIGUE; This spontaneous report received from a patient concerned a female of unspecified age. The patient''s height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose was not reported, administered on 23-JUN-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On JUN-2021, the subject experienced extreme fatigue. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from extreme fatigue. This report was non-serious.


VAERS ID: 1442779 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Texas  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: SARS-CoV-2 test, Suspected COVID-19
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202106; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Test Date: 202106; Test Name: COVID-19 virus test; Result Unstructured Data: Positive
CDC Split Type: USJNJFOC20210666578

Write-up: SUSPECTED COVID-19 INFECTION; This spontaneous report received from a patient concerned a female of unspecified age. The patient''s height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported) dose was not reported, administered on JUN-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On JUN-2021, the subject experienced suspected covid-19 infection. Laboratory data included: COVID-19 virus test (NR: not provided) Positive, Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of suspected covid-19 infection was not reported. This report was non-serious. This case, from the same reporter is linked to 20210700575.; Sender''s Comments: V0: Medical Assessment comment not required as per standard procedure as the case assessed as non-serious.


VAERS ID: 1442811 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Texas  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: SARS-CoV-2 test, Suspected COVID-19
SMQs:, Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202106; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Comments: home COVID-19 testing kit
CDC Split Type: USJNJFOC20210700575

Write-up: SUSPECTED COVID-19 INFECTION (TESTED POSITIVE FOR CORONA VIRUS BY USING COVID-19 TESTING KIT AT HOME); This spontaneous report received from a consumer concerned a male of unspecified age. The patient''s height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unk) dose was not reported, administered on JUN-2021 for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On JUN-2021, the subject experienced suspected covid-19 infection (tested positive for corona virus by using covid-19 testing kit at home). Laboratory data included: COVID-19 virus test (NR: not provided) Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of suspected covid-19 infection (tested positive for corona virus by using covid-19 testing kit at home) was not reported. This report was non-serious. This case, from the same reporter is linked to 20210666578.; Sender''s Comments: V0: Medical Assessment comment not required as per standard procedure as the case assessed as non-serious.


VAERS ID: 1443255 (history)  
Form: Version 2.0  
Age: 55.0  
Sex: Male  
Location: California  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Bell's palsy, Computerised tomogram
SMQs:, Hearing impairment (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: insulin
Current Illness: diabetes
Preexisting Conditions: diabetes
Allergies: no
Diagnostic Lab Data: Ct Scan administered at ER
CDC Split Type: unknown call kaiser

Write-up: I contracted Bell''s Palsy from my second dose of the Moderna Covid 19 vaccine administered in June 2021.


VAERS ID: 1443307 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Female  
Location: Utah  
Vaccinated:2021-05-24
Onset:2021-06-01
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8736 / 2 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Arrhythmia, Ascites, Atrial fibrillation, Blood test, Chest discomfort, Computerised tomogram abnormal, Dyspnoea, Electrocardiogram abnormal, Pericardial effusion, Pleural effusion
SMQs:, Liver related investigations, signs and symptoms (narrow), Hepatic failure, fibrosis and cirrhosis and other liver damage-related conditions (narrow), Anaphylactic reaction (broad), Acute pancreatitis (broad), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Supraventricular tachyarrhythmias (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Metoprolol, Vitamin D, Calcium, Magnesium, Lutein,
Current Illness: none
Preexisting Conditions: none
Allergies: opiates drugs
Diagnostic Lab Data: EKG-positive for a-fib CAT scan
CDC Split Type: vsafe

Write-up: About a week after the vaccine, I started to notice a subtle difference in my heart beat. At night, I could feel my heart beat was a little off. I went to the doctor for something unrelated and was place on EKG that''s how the doctor detected my arrythmia. He said I had A-fib and sent me to the ER. The ER confirmed my A-fib with an EKG and prescribed Eliquis, furosemide and potassium. A few days after discharge, I had chest heaviness and couldn''t breath. I went to the ER. They did an EKG, CAT scan, blood work which also confirmed A-fib and build up of fluid around my heart, lungs and abdomen. I followed up with a cardiologist office and was to continue with the medications at discharge. I am being followed with a cardiolgist. Since then, my heart rythm is back to normal from what I can tell.


VAERS ID: 1443368 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Throat irritation
SMQs:, Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient left the clinic and developed itching in throat with in four hours post vaccine, was taken to the emergency room for treatment, given benadryl.


VAERS ID: 1443502 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: California  
Vaccinated:2021-05-14
Onset:2021-06-01
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 016C21A / 2 RA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Ear disorder, Vertigo
SMQs:, Vestibular disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Synthroid, Generic Cytomel
Current Illness: None
Preexisting Conditions: Sinusitis
Allergies: None
Diagnostic Lab Data: Vestibular Therapy on 6/25 and 6/29 and continuing.
CDC Split Type:

Write-up: Vertigo. I have had vertigo before, so it may be unrelated, but I have debris in both ears this time and it?s been a different experience.


VAERS ID: 1443617 (history)  
Form: Version 2.0  
Age: 49.0  
Sex: Female  
Location: Washington  
Vaccinated:2021-05-10
Onset:2021-06-01
   Days after vaccination:22
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 203A21A / 1 RA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Alopecia, Thyroid function test normal, Vitamin D
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Vitamins
Current Illness: N/A
Preexisting Conditions:
Allergies: Sulpha
Diagnostic Lab Data: Checked thyroid and vitamin D levels. Both were normal.
CDC Split Type:

Write-up: My hair started falling out. As much as you might see with a chemo patient. I went to the doctor and she ran labs and found nothing and has referred me to dermatology. She doesn''t think it''s vaccine-related, but I was told to report it anyway, just in case. I can''t get in to see the dermatologist until August.


VAERS ID: 1444586 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: California  
Vaccinated:2021-05-15
Onset:2021-06-01
   Days after vaccination:17
Submitted: 0000-00-00
Entered: 2021-07-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0185 / 2 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Angiogram, Blood test, Ear discomfort, Fatigue, Head discomfort, Headache, Illness, Lethargy, Magnetic resonance imaging, Migraine, Muscle tightness, Musculoskeletal stiffness, Oral discomfort, Pain in jaw, Pruritus, Swelling, Tension headache, Toothache
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Dystonia (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Osteonecrosis (broad), Hypersensitivity (broad), Arthritis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Acyclovir 400mg daily
Current Illness: None
Preexisting Conditions: None
Allergies: Sulfa group
Diagnostic Lab Data: MRI/MRA on 6/29/21 at Medical Center Blood tests on 6/28/21 at Medical Center I was on steroid pack medicine twice; 6/12/21 and 6/25/21 (MethylPrednisolone)
CDC Split Type:

Write-up: severe burnt sensation on ceiling of mouth, indescribable entire jaws/teeth pain, itchiness, the most severe migraine pain reaching level 100, intense severe tight neck, stiff neck, brain pressure, back of the head tightness, uncontrollable fatigue, lethargy, temple headache, ear clogging, severe inflammation type of swelling on right neck from 6/1/21 to present and ongoing, still sick as of 7/2/21.


VAERS ID: 1446002 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Female  
Location: New York  
Vaccinated:2021-06-10
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Computerised tomogram, Dizziness, Gait disturbance, Headache, Lumbar puncture, Nausea, Photophobia, Vomiting
SMQs:, Acute pancreatitis (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious meningitis (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Corneal disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202106; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown; Test Date: 202106; Test Name: lumbar puncture or a spinal patch; Result Unstructured Data: Test Result:Unknown
CDC Split Type: USPFIZER INC2021725496

Write-up: Nausea; She was very limp, she was throwing up and very dizzy; She was very limp, she was throwing up and very dizzy; She was very limp, she was throwing up and very dizzy; Severe Headache; Light sensitivity; This is a spontaneous report from a contactable consumer (patient''s mother). A 16-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: Unknown) via an unspecified route of administration on 10Jun2021 (at the age of 16-year-old) as single dose for Covid-19 immunization at a Hospital. The patient''s medical history and concomitant medications were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. The reporter stated that patient was very limp, she was throwing up and very dizzy and with a very severe headache and light sensitivity. Patient never had any of those type symptoms before and happened four days after she got the COVID shot. Reporter stated that, the evening of the 13Jun2021. It was headache and the headache got very severe through the next day. Reporter stated that, she had no idea and do not think it was anaphylactic reactions. She thought it was a severe headache which been reported and the MRI they were looking for blood clot as patient was experiencing severe headache that need her throw up, she did not know 100 times, and that end up in the hospital. There was light sensitivity when the CT scan and lumbar puncture was done to see if there was meningitis. CT-scan and spinal patch were done and patient was given nausea and dizzy medications and reporter and patient were waiting for the MRI. The events were serious (hospitalization) on 16Jun2021. The patient underwent lab tests and procedures which included computerised tomogram: unknown and lumbar puncture: unknown on an unspecified date in Jun2021. Therapeutic measures were taken as a result of events dizzy and nausea. Outcome of the events was unknown. Information about lot batch number has been requested.


VAERS ID: 1446003 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: New Jersey  
Vaccinated:2021-06-04
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Leukopenia, White blood cell count
SMQs:, Haematopoietic leukopenia (narrow), Systemic lupus erythematosus (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Neoplasm
Allergies:
Diagnostic Lab Data: Test Date: 202106; Test Name: white blood cells; Result Unstructured Data: Test Result:low
CDC Split Type: USPFIZER INC2021726556

Write-up: he got the first dose on 04 Jun 2021, he was told that today he''s scheduled for the second dose, but the doctor told him on Monday that he had low white blood cells; This is a spontaneous report from a contactable consumer (patient himself). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number was not reported), via an unspecified route of administration on 04Jun2021 as dose 1, single for covid-19 immunisation in front of a hospital emergency department. Medical history included he had cancer. The patient concomitant medications were not reported. The patient stated that he got the first dose on 04Jun2021, he was told that today he was scheduled for the second dose, but the doctor told him on monday that he had low white blood cells on an unspecified date in Jun2021. The patient lab test included white blood cell count was low on an unspecified date in Jun2021. The outcome of the event was unknown. Follow-up attempts are needed; information about lot/batch number has been requested.


VAERS ID: 1446011 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Male  
Location: New York  
Vaccinated:2021-05-31
Onset:2021-06-01
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0178 / 2 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Asthenia, Chills, Hypotension, Lethargy, Pain, Syncope, Vaccination site pain
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: CABG; Coronary artery disease; Hypertension
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021749128

Write-up: faint; Soreness at injection site; chills; lethargy; body aches; weakness; Hypotension; This is a spontaneous report from a contactable consumer (patient reported himself). A 62-year-old male patient received his second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EW0178), via an unspecified route of administration, administered in Arm Left on 31May2021 at 10:15 AM (at the age of 62-year-old), as a single for covid-19 immunisation. The patient medical history included Coronary artery disease, CABG (Coronary artery bypass) surgery and hypertension. The patient had no known allergies. The patient received an unspecified concomitant medication within two weeks of vaccination. The patient previously received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EW0179), via an unspecified route of administration, administered in Arm Left on 10May2021at 10:00 AM, as a single for covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 Prior to vaccination. The patient did not have covid prior vaccination. The patient was not tested for covid-19 Since the vaccination. On 01Jun2021 at 09:00 AM, the patient experienced faint, soreness at injection site, chills, lethargy, body aches, weakness, and hypotension. Hypotension was continued to till the date. The patient visited physician office for the events. The treatment received for the adverse events was none. The patient was not resolved from all the events at the time of this report. Information on Lot/Batch number was available. Additional information has been requested.


VAERS ID: 1446015 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Florida  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0171 / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Dyspnoea, Erythema, Fear, Feeling abnormal, Feeling hot, Heart rate decreased, Movement disorder, Swollen tongue
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Akathisia (broad), Dyskinesia (broad), Dystonia (broad), Parkinson-like events (broad), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Drug allergy (I am highly allergic to a lot of medications)
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021751209

Write-up: Not being able to breathe/Could not catch my breath at all because of the fear; Tongue was swollen; Face was red; Feeling real hot; Pulse was slow; It is horrible; It scared me to death; Could not catch my breath at all because of the fear; I just could not move that much; This is a spontaneous report from a contactable female consumer (patient) via Pfizer sponsored program. An unspecified age female patient received first dose of BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number EW0171), via an unspecified route of administration in Jun2021 as a single dose for COVID-19 immunization. Medical history included allergic to a lot of medications from an unknown date and unknown if ongoing. The patient''s concomitant medications were not reported. The patient previously took flu shot in 1991 and got deathly sick. Patient stated that, she received the first dose of her Pfizer Covid-19 vaccine about a week or two ago and she was calling because she experienced that night (Jun2021), not being able to breathe, her tongue was swollen, and her face was red, and she was enquiring if she should receive the second dose. She was feeling real hot, her pulse was slow, it is horrible and she still get by herself and it scared her to death. She was highly allergic to a lot of medications (Unspecified Medications), She haven''t taken the flu shot (Unspecified Flu Shot) for probably 30 years because she got deathly sick when she got it but now, she decided to ahead and get it (Covid Vaccine) and she was scared to death and she could not catch her breath at all because of the fear. She just does not think she should take the second shot. No treatment was given for the events, because she lives by herself and the neighborhood she lives in, she did not want to call any of them and plus she did not have the money to go to the hospital, since she was not on the insurance. She just could not move that much; she just could not move. She was so sick of not getting to catch her breath (not clear, hence not captured as event). The outcome of the events was unknown. Information on Lot/Batch number was available. Additional information has been requested.


VAERS ID: 1446022 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Maryland  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EWO180 / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Asthenia, Back pain, Head discomfort, Headache, Ocular discomfort, Oropharyngeal pain
SMQs:, Retroperitoneal fibrosis (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021764882

Write-up: headache; painful throat; back pain; weak eyes; At times I feel so weak and my head seem heavy on me; head seem heavy on me; This is a spontaneous report from a contactable consumer or other non hcp. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EWO180), via an unspecified route of administration on 01Jun2021, as dose 2, single for covid-19 immunisation. The patient medical history was not reported. The patient''s concomitant medications were not reported. The patient had received the first doses of the vaccine (batch number: EWO163) in 16May2021. In Jun2021, the patient stated that, took 2 doses of the covid-19 vaccine 1st dose on 16May2021 Pfitzer EWO163 2nd dose 01Jun2021 Pfitzer EWO180. Since I took 2nd dose I had been having headache, painful throat, back pain & weak eyes. At times I feel so weak and my head seem heavy on me. These were symptoms and issues I never had before now. I visited my primary care doctor and he gave medication which I took for four days and there was no change, I just came back from the Emergency room and have been sent to the withheld for more. Treatment was given for the events. Outcome of the events were not recovered. Additional information has been requested.


VAERS ID: 1446060 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Male  
Location: Virginia  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0178 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Hypoaesthesia
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Systemic: Numbness (specify: facial area, extremities)-Severe, Additional Details: NUMBNESS IN LEFT ARM


VAERS ID: 1446085 (history)  
Form: Version 2.0  
Age: 27.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-06-17
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Alopecia
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Sertraline 50mg
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Hair loss


VAERS ID: 1446104 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: Georgia  
Vaccinated:2021-03-30
Onset:2021-06-01
   Days after vaccination:63
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8734 / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Anaemia, Antimitochondrial antibody positive, Blood test abnormal, Fatigue, Pyrexia
SMQs:, Haematopoietic erythropenia (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pertussis vaccination as a baby, had a fever and other than that nothing, 1990 ish would''ve been the time frame
Other Medications: Perphenazine, Pramipexol, Adderall, Klonopin, Clonidine, Wellbutrin, Doxepin, Gabapentin, Melatonin
Current Illness: N/a
Preexisting Conditions: Bipolar disorder
Allergies: Benadryl, Phenergan, Ambien, Flexural
Diagnostic Lab Data: Blood work - unknown date - results showed anemia and positive for AMA
CDC Split Type: vsafe

Write-up: So I had started getting fevers every once in a while and became very fatigued so I went to my PCD and they did bloodwork and found I am anemic. Then I went to the rheumatologist and I was studied because I tested positive for an AMA. They didn''t find anything further so I am back to seeing my PCD for the fatigue and anemia. I don''t remember when I saw those DRs but it was post vaccination some time.


VAERS ID: 1446148 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2021-06-26
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0196 / 1 RA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Axillary pain, Breast pain, Pain in extremity, Peripheral swelling
SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Lipodystrophy (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt called on 07/03/2021 to report pain/swelling in the right arm. No rashes or discoloration and no restriction on the movement. Pt described pain going through right armpit to right breast Pt will observe for few more days and seek doctor''s advise if needed.


VAERS ID: 1446166 (history)  
Form: Version 2.0  
Age: 16.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2021-05-01
Onset:2021-06-01
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Autoimmune disorder, Psoriasis
SMQs:, Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Normal one a day vitamin
Current Illness: Teenage acne
Preexisting Conditions: N/a
Allergies: N/A
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pt began to have symptoms which were thought to be dandruff but after going to dermatologist on 7/2, she has been diagnosed with psoriasis. I am reporting as this is an autoimmune disease with no genetic history. This is the second of three children who have been diagnosed with an autoimmune disorder either during pandemic/vaccination; the other being type 1 diabetes with no genetic history. Confirmed through multiple tests. Other child age was 13 at time of diagnosis . Maybe unrelated but I did believe that any autoimmune diseases diagnosed after a vaccination that is to provide an autoimmune response to a disease should be reported. Will also report to WHO


VAERS ID: 1446218 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-05-19
Onset:2021-06-01
   Days after vaccination:13
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0185 / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Depressive symptom, Mood altered
SMQs:, Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Depression (excl suicide and self injury) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: tree nuts
Diagnostic Lab Data: Visit to the primary care physician 6/2021 Psychiatry evaluation
CDC Split Type:

Write-up: Marked mood changes including lability and depressive symptoms. Should the two doses of the vaccine have the same lot number?


VAERS ID: 1446281 (history)  
Form: Version 2.0  
Age: 59.0  
Sex: Male  
Location: California  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Condition aggravated, Lung cancer metastatic
SMQs:, Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Metastatic lung cancer, smoking, COPD, peripheral vascular disease
Preexisting Conditions: Metastatic lung cancer, smoking, COPD, peripheral vascular disease
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Hospitalization 6/1/21-6/24-21; repeat hospitalization on 7/2/21. All from prior metastatic lung cancer.


VAERS ID: 1446289 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Male  
Location: Texas  
Vaccinated:2021-04-12
Onset:2021-06-01
   Days after vaccination:50
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 031A21A / 2 AR / SYR

Administered by: Public       Purchased by: ?
Symptoms: Guillain-Barre syndrome, Immunoglobulin therapy, Lumbar puncture, Magnetic resonance imaging
SMQs:, Peripheral neuropathy (narrow), Guillain-Barre syndrome (narrow), Demyelination (narrow), Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 4 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Atenolol, vitamin D3 50,000 IU, flonase
Current Illness: None
Preexisting Conditions: High blood pressure.
Allergies: None
Diagnostic Lab Data: MRI and Spinal tap on 6/30/2021
CDC Split Type:

Write-up: Diagnosed with Gillain Barr? syndrome and I would to be involved with a case study to determine if the vaccine caused the development of my condition and would like to know if similar reports have been made to help the community. Still undergoing treatment IVIG.


VAERS ID: 1446291 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Male  
Location: Arizona  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0181 / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Hypoaesthesia, Pain in extremity
SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer covid # 1 ..Got Shingles from it he believes
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: nka
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient said his arm has been sore since he received the second dose and the pain has now moved down his arm and his thumb has become numb.. travels a lot so couldn''t let us know til now.. Did not consult a md yet


VAERS ID: 1446355 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Male  
Location: Oregon  
Vaccinated:2021-05-24
Onset:2021-06-01
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0187 / 2 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Arthralgia, Muscular weakness, Oral herpes
SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Oropharyngeal infections (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Arthritis (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: Pain like arthritis in left arm, mainly in left forearm but the whole arm just feels weaker, especially when grabbing and lifting things. Does not seem to be getting any better and not sure if it is getting worse started a week or so after last shot and has been consistent for the past month. Plus I have had two episodes of cold sores on my lips within a month which is very unusual because I haven''t had a cold sore in more than 5 years before I had this vaccine, so I was thinking my immune system might be weaker or something because of the vaccine allowing the cold sore virus to appear twice on my lips within a month. Hopefully my arm gets better and I quit getting cold sores ASAP.


VAERS ID: 1446376 (history)  
Form: Version 2.0  
Age: 73.0  
Sex: Female  
Location: Texas  
Vaccinated:2021-06-29
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 009D21A / 1 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Contusion
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Accidents and injuries (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none that we are aware of (patient''s son stated that he was going to try arnica for the bruise on his mother''s arm)
Current Illness: according to consent form, none
Preexisting Conditions: according to consent form, none
Allergies: penicillin
Diagnostic Lab Data: none that we are aware of
CDC Split Type:

Write-up: Patient came to pharmacy to show us her bruised arm, 5 days after her first Moderna dose. I assured her that it was a common side effect and she acknowledged that she had also been told beforehand.


VAERS ID: 1446462 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Male  
Location: D.C.  
Vaccinated:2021-05-01
Onset:2021-06-01
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-07-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 036C21A / UNK LA / -
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 045B21A / UNK LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Alopecia areata, Influenza like illness
SMQs:, Immune-mediated/autoimmune disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies: Penicillin
Diagnostic Lab Data: None (yet)
CDC Split Type:

Write-up: Alopecia areata just after second Covid Moderna shot, which caused severe flu-like symptoms for 48 hours after the shot was administered.


VAERS ID: 1446476 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Florida  
Vaccinated:2021-05-01
Onset:2021-06-01
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-07-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Pruritus
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None
Current Illness: None
Preexisting Conditions: Ulcerative Colitis
Allergies: Amoxicillin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Skin it extremely itchy and no amount of scratching satisfies it. Each itchy episode begins with 1 itch, and lasts 10-15 minutes. Scratching it causes the itch to travel all over the body. There is no rash, just itchiness. This happens 3-5 times a day, every day. I first noticed about 1 week after receiving my 2nd dose.


VAERS ID: 1446628 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Male  
Location: Washington  
Vaccinated:2021-04-21
Onset:2021-06-01
   Days after vaccination:41
Submitted: 0000-00-00
Entered: 2021-07-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA O31B21A / 2 - / SYR

Administered by: Other       Purchased by: ?
Symptoms: Computerised tomogram, Pulmonary thrombosis, Ultrasound scan
SMQs:, Embolic and thrombotic events, venous (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: Nuvidual
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data: CT scan ultrasound
CDC Split Type:

Write-up: Blood clot in my Lung


VAERS ID: 1446713 (history)  
Form: Version 2.0  
Age: 34.0  
Sex: Female  
Location: California  
Vaccinated:2021-05-03
Onset:2021-06-01
   Days after vaccination:29
Submitted: 0000-00-00
Entered: 2021-07-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8734 / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8736 / 2 LA / SYR

Administered by: Pharmacy       Purchased by: ?
Symptoms: Palpitations
SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Blood pressure medication
Current Illness: none
Preexisting Conditions: high blood pressure
Allergies: various fruits
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Palpitations, sense of danger


VAERS ID: 1446717 (history)  
Form: Version 2.0  
Age: 37.0  
Sex: Female  
Location: Unknown  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Urinary tract infection
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Infected tooth nerve 12 days after first pfizer vaccine. No history of tooth issues. UTI 14 days after 2nd pfizer vaccine. No history of UTI or infection.


VAERS ID: 1446760 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Male  
Location: Texas  
Vaccinated:2021-05-24
Onset:2021-06-01
   Days after vaccination:8
Submitted: 0000-00-00
Entered: 2021-07-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Angina pectoris, Bedridden, Dyspnoea, Fatigue, Loss of consciousness, Palpitations
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Other ischaemic heart disease (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: unable to breathe, bed ridden with bouts of unconsciousness and severe chronic fatigue for over two weeks along with heart pains and heart palpitations. The inability to breathe and bouts of unconsciousness have subsided with chronic fatigue and heart palpitations still present. I haven''t sought medical treatment because I have no insurance and I can''t afford it.


VAERS ID: 1446853 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Male  
Location: Alaska  
Vaccinated:2021-05-28
Onset:2021-06-01
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-07-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 042A21A / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Asthenia, Contusion, Diarrhoea, Dizziness, Drug hypersensitivity, Fatigue, Feeling abnormal, Feeling cold, Flatulence, Hypoaesthesia oral, Irritability, Joint stiffness, Muscular weakness, Musculoskeletal stiffness, Myalgia, Paraesthesia, Pruritus, Respiratory tract congestion, Seasonal allergy
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Angioedema (broad), Peripheral neuropathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Dementia (broad), Pseudomembranous colitis (broad), Dystonia (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Conjunctival disorders (narrow), Hypersensitivity (narrow), Arthritis (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: allergic rhinitis
Allergies: none known and confirmed at time of vaccination
Diagnostic Lab Data: None yet. I''ve scheduled an appointment to visit with my PCM later this month.
CDC Split Type:

Write-up: Within two weeks of vaccination: energy level down, muscle ache, diarrhea, congestion, extra gas (intestinal). Ongoing: extra gas (intestinal); cold flashes that course quickly through body; tingling in arms, hands (like a buzz or very fine pins and needles); irritability; itchiness (upper body, face and head); numbness on front of tongue; stiff finger joints; brain fog; quick onset of fatigue; sudden faint feeling; feeling of weakness in muscles; bruise on right upper arm which remained for a couple weeks; apparent reduced allergen/pollen resistance. Also, it seems I may now be having novel allergic reactions to peanuts. I had long consumed peanuts and peanut butter without incident before taking the vaccine.


VAERS ID: 1446888 (history)  
Form: Version 2.0  
Age: 48.0  
Sex: Female  
Location: California  
Vaccinated:2021-05-04
Onset:2021-06-01
   Days after vaccination:28
Submitted: 0000-00-00
Entered: 2021-07-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0151 / 2 RA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Blister, Rash pruritic
SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications: N/A
Current Illness: N/A
Preexisting Conditions: just allergy
Allergies: food, dust and pollen in general
Diagnostic Lab Data:
CDC Split Type:

Write-up: From June 1 midnight, got itchy rashes around my waist mostly, a few of them on arm and right thigh, mid to late June, rashes move to both feet and left leg, July 4th, move to right leg. late June, there are 31 rashes on right leg. Some of the rashes become blisters. The rashes/blisters heal themselves in 2 weeks mostly, but it reoccurs at different place of the body till now, and so sign of stopping. Took Zyrtec or Claritin can ease the itches, touching by hands or clothes made them more itchy. My daughter (12 years old) has similar symptom two weeks after her first dose, (June 18 first dose of Pfrizer, July 1st rashes started from feet, then to legs.)


VAERS ID: 1447032 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: Kansas  
Vaccinated:2021-04-01
Onset:2021-06-01
   Days after vaccination:61
Submitted: 0000-00-00
Entered: 2021-07-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Parosmia
SMQs:, Taste and smell disorders (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft, Xanax
Current Illness: None
Preexisting Conditions: None
Allergies: None
Diagnostic Lab Data:
CDC Split Type:

Write-up: I lost my smell and taste while I had covid. I regained both after about 5 weeks. Just recently, I have no been able to stand the smell of body odor, my breath, taco meat, pickles, they all smell the same to me, kind of like a rotting onion/sour type smell.


VAERS ID: 1447036 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Male  
Location: Kansas  
Vaccinated:2021-05-31
Onset:2021-06-01
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-07-05
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 038C21A / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Angioedema, Mouth swelling, Oral herpes
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Oropharyngeal infections (narrow), Oropharyngeal allergic conditions (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient presented with angioedema. He stated the day after his second shot, he had what appeared to be 2 cold sores, one on each corner of his mouth. He says each day the swelling has gotten worse. (Presenting from vaccine almost 6 weeks ago) He was advised to seek medical advice, to which he declined. He was then advised that if he would not do that, he should take benadryl and ibuprofen.


VAERS ID: 1449424 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Body temperature, Bronchitis, Chest X-ray, Cough, Culture, Dyspnoea, Headache, Pain, Pyrexia
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: HUMIRA; LISINOPRIL; TRAMADOL; METFORMIN; GLIMEPIRIDE
Current Illness: Abstains from alcohol; Back pain; Blood pressure high; Diabetes; Heart murmur; Non-smoker; Penicillin allergy (PENICILLIN ALLERGY MANIFESTED BY SORE THROAT/CANNOT BREATH.); Rheumatoid arthritis
Preexisting Conditions: Medical History/Concurrent Conditions: COVID-19 (The patient was hospitalized for five days and under home health care for two months.); COVID-19 pneumonia; Cyst breast (The patient had an outpatient surgery done to remove a cyst on the middle of her breast.); Difficulty in walking; Ear infection; Incisional drainage; Slurred speech; Comments: The patient had sulpha drugs allergy manifested by difficulty of breathing.
Allergies:
Diagnostic Lab Data: Test Date: 20200722; Test Name: Chest X-ray; Result Unstructured Data: Pneumonia; Test Date: 20200722; Test Name: Body temperature; Result Unstructured Data: 104 F; Test Date: 20200722; Test Name: Culture nose; Result Unstructured Data: Positive for covid-19
CDC Split Type: USJNJFOC20210702976

Write-up: BRONCHITIS; SHORTNESS OF BREATH; BODY ACHES; COUGHING; HEADACHE; FEVER; This spontaneous report received from a patient by a Business partner on 24-JUN-2021 was received on 24-JUN-2021 and concerned a 67 year old female. The patient''s height, and weight were not reported. The patient''s past medical history included incision and drainage, covid-19, covid-19 pneumonia, cyst on middle of breast, slurred speech, difficulty in walking, and several ear infection, and concurrent conditions included penicillin allergy, moderate to severe rheumatoid arthritis, heart murmur, no tobacco use, abstains from alcohol, high blood pressure, back pain, and diabetes, and other pre-existing medical conditions included the patient had sulpha drugs allergy manifested by difficulty of breathing. The patient experienced drug allergy (cannot breathe/chest pain, bronchitis) when treated with infliximab. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: UNKNOWN) dose was not reported, administered on JUN-2021 for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. Concomitant medications included tramadol for back pain, glimepiride for diabetes, metformin for diabetes, lisinopril for high blood pressure, and adalimumab for moderate to severe rheumatoid arthritis. On 22-JUL-2020, Laboratory data included: Body temperature (NR: not provided) 104 F, Chest X-ray (NR: not provided) Pneumonia, and Culture nose (NR: not provided) Positive for covid-19. On JUN-2021, the subject experienced bronchitis. On JUN-2021, the subject experienced shortness of breath. On JUN-2021, the subject experienced body aches. On JUN-2021, the subject experienced coughing. On JUN-2021, the subject experienced headache. On JUN-2021, the subject experienced fever. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the shortness of breath, bronchitis, headache, coughing, fever and body aches was not reported. This report was non-serious.; Sender''s Comments: V0: Medical assessment comment not required as per standard procedure as the case is assessed as non serious.


VAERS ID: 1449425 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Male  
Location: North Carolina  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 202A21A / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Arthropathy, Cough, Musculoskeletal discomfort, Nasopharyngitis, Pain in extremity, Pyrexia
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20210702990

Write-up: COLD; COUGH; FEVERISH; FEELING LIKE KNEES BENDING WHEN STANDS UP; CAN NOT SIT TOO LONG IN TOILET AND CHAIR; SEVERE PAIN IN LEGS BEHIND THE KNEES; This spontaneous report received from a patient concerned a 43 year old male. The patient''s height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 202A21A, and expiry: UNKNOWN) dose was not reported, administered on 16-JUN-2021 for prophylactic vaccination. No concomitant medications were reported. On JUN-2021, the subject experienced feeling like knees bending when stands up. On JUN-2021, the subject experienced can not sit too long in toilet and chair. On JUN-2021, the subject experienced severe pain in legs behind the knees. Treatment medications included: paracetamol. On 16-JUN-2021, the subject experienced feverish. On 17-JUN-2021, the subject experienced cough. On 18-JUN-2021, the subject experienced cold. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from cold, and feverish on JUN-2021, had not recovered from cough, feeling like knees bending when stands up, and severe pain in legs behind the knees, and the outcome of can not sit too long in toilet and chair was not reported. This report was non-serious.


VAERS ID: 1449451 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-06-09
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 022B21A / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Asthenia, Fatigue, Vaginal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Guillain-Barre syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 3 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Anaemia
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20212

Write-up: Very heavy vaginal bleeding, it was a whole lot of blood; Very Tired; weak; This spontaneous case was reported by a consumer and describes the occurrence of VAGINAL HAEMORRHAGE (Very heavy vaginal bleeding, it was a whole lot of blood) in a 42-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 022B21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient''s past medical history included Anaemia. On 09-Jun-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In June 2021, the patient experienced ASTHENIA (weak). On 17-Jun-2021, the patient experienced VAGINAL HAEMORRHAGE (Very heavy vaginal bleeding, it was a whole lot of blood) (seriousness criteria hospitalization and medically significant) and FATIGUE (Very Tired). The patient was hospitalized from 24-Jun-2021 to 26-Jun-2021 due to VAGINAL HAEMORRHAGE. The patient was treated with TRANEXAMIC ACID on 23-Jun-2021 for Vaginal bleeding, at a dose of 1 dosage form and Surgery (hysterectomy) for Vaginal haemorrhage. At the time of the report, VAGINAL HAEMORRHAGE (Very heavy vaginal bleeding, it was a whole lot of blood), ASTHENIA (weak) and FATIGUE (Very Tired) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. The patient''s concomitant medications were not reported. On 02-Jun-2021, the patient had her normal period and was not pregnant at the time of the report. On 17-Jun-2021, the patient called her gynecologist and made an appointment for 06-Jul-2021 to do an ultrasound. On 23-Jun-2021, Wednesday, the patient stated that she could not wait to see the doctor and went to the emergency room at night. It was reported that the patient was discharged at 2 am, as the bleeding stopped for a little bit. On 24-Jun-2021, Thursday morning, the patient woke up with whole lot of blood and went to her obstetrician/ gynecologist (OBGYN). The patient''s OBGYN could not believe the amount of blood patient had lost and stated that if the patient had lost any more blood, she could possibly have died as the patient''s blood was so low. The patient was hospitalized, and an emergency hysterectomy was performed. On 26-Jun-2021, the patent was discharged from the hospital. It was reported that the patient''s second shot was due on 30-Jun-2021. Company comment: This case concerns a 42-year-old female hospitalized with a serious unexpected event of vaginal hemorrhage, and nonserious asthenia and fatigue. Event latency 9 days after first dose mRNA-1273. Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Most recent FOLLOW-UP information incorporated above includes: On 28-Jun-2021: Follow-up information received on 28-jun-2021 contains significant information regarding seriousness and surgery, medical history and event details.; Sender''s Comments: This case concerns a 42-year-old female hospitalized with a serious unexpected event of vaginal haemorrhage, and nonserious asthenia and fatigue. Event latency 9 days after first dose mRNA-1273. Based on current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.


VAERS ID: 1449453 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated:2021-04-09
Onset:2021-06-01
   Days after vaccination:53
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA UNKNOWN / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Deep vein thrombosis, Pulmonary embolism
SMQs:, Embolic and thrombotic events, venous (narrow), Thrombophlebitis (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20212

Write-up: developed DVT with PE; developed DVT with PE; This spontaneous case was reported by a consumer and describes the occurrence of DEEP VEIN THROMBOSIS (developed DVT with PE) and PULMONARY EMBOLISM (developed DVT with PE) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Unknown) for COVID-19 vaccination. No Medical History information was reported. On 09-Apr-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In June 2021, the patient experienced DEEP VEIN THROMBOSIS (developed DVT with PE) (seriousness criterion medically significant) and PULMONARY EMBOLISM (developed DVT with PE) (seriousness criterion medically significant). At the time of the report, DEEP VEIN THROMBOSIS (developed DVT with PE) and PULMONARY EMBOLISM (developed DVT with PE) outcome was unknown. The patient had no history of DVT or clotting issues. No concomitants medicines were reported. No treatment information was provided. Action taken with mRNA-1273 in response to the event was not applicable. Very limited information regarding these events has been provided at this time. Further information has been requested.; Sender''s Comments: Very limited information regarding these events has been provided at this time. Further information has been requested.


VAERS ID: 1449460 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:2021-03-01
Onset:2021-06-01
   Days after vaccination:92
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA UNKNOWN / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Pancreatic carcinoma
SMQs:, Non-haematological malignant tumours (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20212

Write-up: Suddenly diagnosed with pancreatic cancer; This spontaneous case was reported by a consumer and describes the occurrence of PANCREATIC CARCINOMA (Suddenly diagnosed with pancreatic cancer) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Unknown) for COVID-19 vaccination. No Medical History information was reported. In March 2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In June 2021, the patient experienced PANCREATIC CARCINOMA (Suddenly diagnosed with pancreatic cancer) (seriousness criterion medically significant). At the time of the report, PANCREATIC CARCINOMA (Suddenly diagnosed with pancreatic cancer) outcome was unknown. Concomitant product use was not provided by the reporter. It was reported that 2 weeks ago, she was suddenly diagnosed with pancreatic cancer. She was on hospice.Treatment information was unknown.The patient received both scheduled doses of mRNA-1273 prior to the event; therefore, action taken with the drug in response to the event was not applicable. Company Comment: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. Unlikely, that the event is related to the vaccine.; Sender''s Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.Unlikely, that the event is related to the vaccine.


VAERS ID: 1449495 (history)  
Form: Version 2.0  
Age: 57.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-06-02
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Arthralgia, Lymphoedema, White blood cell count, White blood cell count abnormal
SMQs:, Haematopoietic leukopenia (broad), Neuroleptic malignant syndrome (broad), Retroperitoneal fibrosis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: VITAMIN E [TOCOPHEROL]; ALEVE; FASLODEX; LEVOTHYROXINE; VITAMIN D NOS
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Adhesive tape allergy (Verbatim: Adhesive tape allergy); Iodine allergy (verbatim: Iodine Tincture Allergy); Lymphedema (verbatim: Worsening lymphedema since Jan2021 or Feb2021).
Allergies:
Diagnostic Lab Data: Test Date: 202106; Test Name: White Blood Cells; Result Unstructured Data: Test Result:Below 1; Comments: White Blood cells were below 1 on Monday; Test Date: 202106; Test Name: White Blood Cells; Result Unstructured Data: Test Result:Above 1; Comments: White Blood cells were above 1 on Wednesday
CDC Split Type: USPFIZER INC2021742485

Write-up: White blood cells were below 1 on Monday, repeat labs Wednesday they were above 1; Worsening lymphedema since Jan2021 or Feb2021; Joints hurt; This is a spontaneous report from a contactable nurse. A 57-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; lot number: unknown) via an unspecified route of administration on 02Jun2021 (age at vaccination: 57-year-old) as dose number unknown, single for COVID-19 immunization. Medical history of the patient included adhesive tape allergy, iodine tincture allergy, lymphedema (worsening lymphedema since Jan2021 or Feb2021). Concomitant medications included Tocopherol (Vitamin E), naproxen sodium (Aleve), fulvestrant (Faslodex), Levothyroxine, Multivitamin capsule, Vitamin D for unspecified indication, started and stopped on an unspecified date. Patient previously took Macrobid on an unspecified date for an unspecified indication and experienced allergy. On an unspecified date in Jun2021, patient white blood cells were below 1 on Monday and her white blood cells were above 1 on Wednesday, worsening lymphedema since Jan2021 or Feb2021, joints hurt. MD is aware. Outcome of the events were unknown. Information about lot/batch number has been requested.; Sender''s Comments: Limited information of white blood cell count prior to vaccine preclude a comprehensive causality assessment, underlying medical conditons of lymphedema and allergy may be contributory to events. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate


VAERS ID: 1449498 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Male  
Location: Georgia  
Vaccinated:2021-05-28
Onset:2021-06-01
   Days after vaccination:4
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0186 / 1 LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Haematuria, Headache
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Tubulointerstitial diseases (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021747446

Write-up: He is seeing his urine color as red after the vaccine. He is having the problem still today. Every time when he passes urine he sees the color red.; Dose 1: headache; This is a spontaneous report from a contactable consumer (patient, self-reported). A 35-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0186 and expiry date was not reported), via an unspecified route of administration, in Arm Left, on 28May2021 at 6:45 pm -7 pm (age at vaccination: 35 years), as a single dose for COVID-19 immunization. The patient took covid 19 vaccine because everybody was getting the vaccine and he might go back to the office. The patient''s medical history and concomitant medications were not reported. The patient reported that on an unspecified date in Jun2021, he was seeing his urine color as red after the vaccine. He was having the problem still today. Every time when he passes urine he sees the color red. The patient was not sure if what he was experiencing was a normal side effect of the vaccine. He hasn''t seen his experience listed on the list, so he just wanted to check. The patient also stated that he has seen this before when he has had a beet root, but for the past two days he has never had a beet root. He had a headache 3 or 4 days before he received the second vaccine (Dose 1: headache). He took Tylenol for the headache. Headache occurred in the evening on Monday or Tuesday before the vaccine, he was not really sure. He stated maybe 6:14-6:15 pm for onset. Complete recovery the same day. Outcome of the events was recovered on an unspecified date in Jun2021. Information on the lot/batch number has been requested.


VAERS ID: 1449508 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Tennessee  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021748887

Write-up: A patient had a second trimester fetal loss right after getting the Covid vaccine.; A patient had a second trimester fetal loss right after getting the Covid vaccine.; This is a spontaneous report from a contactable physician. An adult female patient of an unknown age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at an unknown dose on an unknown date via an unknown route for Covid-19 immunization. Medical history and concomitant drug were not provided. Medical history and concomitant drug were not provided. It was unknown if the patient received any other vaccines within 4 weeks prior to the COVID vaccine. Patient had 32 weeks gestation period. Patient had a "second trimester" (as reported) fetal loss right after getting the Covid vaccine. The event onset date was Jun2021. Treatment received for the event. It was unknown if the patient diagnosed with COVID-19 prior to vaccination, and unknown if the patient been tested for COVID-19 since the vaccination. The report was assessed as serious with seriousness criteria of hospitalization. Information on lot/batch number has been requested.; Sender''s Comments: Based on available information, a possible contributory role of bnt162b2 cannot be excluded for the reported events miscarriage. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1449524 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: California  
Vaccinated:2021-06-12
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0171 / 2 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Insomnia, Rash, Rash pruritic, Vaccination site rash
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021750645

Write-up: It''s so itchy; I had some rash underneath the vaccinated area and on my lower thigh which got worse; I had some rash underneath the vaccinated area and on my lower thigh which got worse; sleepless nights; This is a spontaneous report from a contactable consumer (patient). A non-pregnant 50-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0171), via an unspecified route of administration, administered in Arm Left on 12Jun2021 13:30 (at age of 50 years old) as single dose for COVID-19 immunisation. Medical history was none. The patient''s concomitant medications were none. The patient didn''t receive any other vaccines within 4 weeks prior to the COVID vaccine. No other vaccine in four weeks. No other medications in two weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0180), administered in Arm Left at 50 years old for COVID-19 immunisation with no reaction. Got 2nd dose on the 12Jun2021 and 2 days after (14Jun2021) patient had some rash underneath the vaccinated area and on lower thigh which got worse until few days later. It''s so itchy, though patient has been taking anti-allergy (Allegra) and tried over the counter anti-itch lotion, the itch didn''t go away. Until today, it''s still itchy and it reached down legs now which caused sleepless nights (Jun2021). AE resulted in: Doctor or other healthcare professional office/clinic visit. Treatment received (still have to visit clinic for the itch). The outcome of the events was Not recovered.


VAERS ID: 1449527 (history)  
Form: Version 2.0  
Age: 53.0  
Sex: Female  
Location: Kentucky  
Vaccinated:2021-06-12
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0177 / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Body temperature, Confusional state, Dysphonia, Fatigue, Feeling abnormal, Hot flush, Hypersensitivity, Influenza, Mood swings, Nasal congestion, Oropharyngeal pain, Pyrexia, Sinusitis, Vaccination site bruising
SMQs:, Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210614; Test Name: body temperature; Result Unstructured Data: Test Result:Fever
CDC Split Type: USPFIZER INC2021750905

Write-up: Fever; Allergy; Tiredness; brain fog; Flu symptoms; mood swings; confusion; Hot flash; congestion; sound little bit crackly; sore throat; allergy sinus; bruising at the site of the injection; This is a spontaneous report from a contactable consumer (patient). A 53-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EW0177) via an unspecified route of administration on 12Jun2021 (at the age of 53 years old) as dose 2, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Historical vaccine included the patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0168) via an unspecified route of administration on 22May2021 (at the age of 53 years old) as dose 1, single for COVID-19 immunisation and no reaction experienced. On 14Jun2021, the patient had Fever, allergy, and tiredness. About three or four days after the vaccination, on an unknown date in Jun2021, after the vaccine she developed bruising at the site of the injection which remained for a week, after she was fed that injection and the bruise that a long to show up, she would have expected the bruising next day or two day but it took 3 or 4 days for the bruise to show up to feel it was there she just took a picture of it, She want to say on day 4 was when she got this brain fog, very big brain fog and came down flu symptoms, where appeared or very big allergy sinus symptoms and the brain fog sort of made her feel how can she say this mood swings, she had mood swings with the brain fog, it was sort of confusion and with allergy sinus, She felt lots of tiredness and did have fever that would come and go, she was going to say it happen it would appear and then stay about 5 or 2 minutes, then they then may be one or two hours it appeared again almost like a hot flash kind of thing, fever thing had subsided and the allergy sinus had subsided, she want to say because she was in a desert planet that had help to dry it up but she feel like was still left with brain fog. She still had sort of feel like a little congestion or sore throat but sort of affecting like a little bit of her airway she wanted say, it made her sound little bit crackly, she did not know how to describe that. Patient stated, the symptoms seems to had subsided but as she mentioned the bruise was still on her arm she had concern about blood clotting so was taking low dose aspirin because that bruise appear, that bruise appeared 3 or 4 days later so the symptoms had 70% had resolved and 30% remained within the next day, she think was going to emergency room. Treatment, Benadryl over the counter medicine for sinus symptoms, she low dose aspirin a 81 milligram because she was concern about blood clotting incident and because she was at the bruise and she was also using a chest rub in cold and flu over the counter. There was one more thing she did use, she had can of oxygen, which athletes use, high altitude Travelers use oxygen to help them, she did use that, it helped her somewhat. Reporter seriousness for events was unspecified. The outcome of the events was unknown. Follow-up attempts are needed; Further information are requested.


VAERS ID: 1449536 (history)  
Form: Version 2.0  
Age: 51.0  
Sex: Male  
Location: Illinois  
Vaccinated:2021-06-20
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0187 / 1 RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Anxiety, Hallucination
SMQs:, Anticholinergic syndrome (broad), Dementia (broad), Psychosis and psychotic disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: CITALOPRAM; TRIFLUOPERAZINE; CLONAZEPAM; LISINOPRIL
Current Illness: Anxiety (Verbatim: Anxiety); Blood pressure high (Started about 20 years ago.); Depression (Verbatim: Depression); Obsessive-compulsive disorder (Verbatim: Obsessive-compulsive disorder)
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021757029

Write-up: Hallucinations: they happen sometimes, not all the time, and only when he is anxious, after first vaccine.; when his anxiety is high; This is a spontaneous report from a contactable consumer (patient himself). A 51-year-old male patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EW0187) via an unspecified route of administration in right upper arm (as reported) on 20Jun2021 10:35 as dose 1, single (at the age of 51-years-old) for COVID-19 immunization. Vaccination Facility Type was reported as pharmacy. Vaccine was not administered at Military Facility. Patient medical history included ongoing high blood pressure from about 20 years ago, ongoing depression from 1996, ongoing anxiety from 1996, ongoing obsessive-compulsive disorder from about 3.5 years ago. The concomitant medications included ongoing citalopram oral tablet at a dose of 40 mg from 1996 taken for antidepressant therapy, ongoing trifluoperazine oral tablet at a dose of 5 mg from 1996 taken for antipsychotic therapy, ongoing clonezapan oral tablet at a dose of 0.5 mg taken for anxiety, started about 5 years ago, ongoing lisinopril oral tablet taken for high blood pressure started about 15 years ago. On an unspecified date in Jun2021, patient stated his hallucinations began after the vaccine, stated they happened sometimes, not all the time, and only when he was anxious after 1st vaccine. Patient stated the hallucinations were somewhat better. The adverse events did not result in physician office visit or emergency room visit. The outcome of the events was recovering.


VAERS ID: 1450015 (history)  
Form: Version 2.0  
Age: 29.0  
Sex: Male  
Location: New Jersey  
Vaccinated:2021-05-01
Onset:2021-06-01
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 RA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Blood pressure increased, Electrocardiogram normal, Heart rate increased
SMQs:, Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Hypertension (narrow), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: NONE
Current Illness: None
Preexisting Conditions: None
Allergies: Very moderate to cold temperatures. (Not the intensity which needs to be specified)
Diagnostic Lab Data: Opted for EKG at a urgent care, it turned out to be normal.
CDC Split Type:

Write-up: Increased heart rate, Never observed such intensity of heart rate. Sudden increase happens even while siiting and working in office without any stress or anything. BP upper limit increased upto 223 mmhg ( measured using friends equipment tie on wrist type). Please if you can email me in a reply is there a chance it might cause me stroke?


VAERS ID: 1450069 (history)  
Form: Version 2.0  
Age: 15.0  
Sex: Male  
Location: Oklahoma  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 038B21A / 1 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Product administered to patient of inappropriate age
SMQs:, Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: 15 y/o inadvertently given Moderna.


VAERS ID: 1450280 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-04-01
Onset:2021-06-01
   Days after vaccination:61
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH LOT: ER8733 / 1 RA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH LOT: EW0162 / 2 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Immunoglobulin therapy, Platelet count decreased, Thrombocytopenia
SMQs:, Haematopoietic thrombocytopenia (narrow), Systemic lupus erythematosus (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: adapalene-benzoyl peroxide (EPIDUO) 0.1-2.5 % GlwP Apply 1 Pump topically nightly 45 g 11 ? albuterol (PROAIR HFA) 90 mcg/actuation inhaler Inhale 2 inhalations into the lungs every 4 (four) hours as needed for Wheezing or Shortness of Bre
Current Illness: none
Preexisting Conditions: Contraceptive use ? Asthma, exercise induced ? Allergic rhinitis ? Seborrheic dermatitis of scalp ? Acne vulgaris ? Gastroesophageal reflux disease with hiatal hernia ? Mild intermittent asthma without complication
Allergies: none
Diagnostic Lab Data: ER visit at Wake Med Hospitalization from 6/2/2021 - 6/4/2021 (2 days) HOSPITAL patient received IVIG/dex and prednisone
CDC Split Type:

Write-up: patient developed severe thrombocytopenia (platelet count =10K)


VAERS ID: 1450441 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: Colorado  
Vaccinated:2021-04-01
Onset:2021-06-01
   Days after vaccination:61
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8734 / 2 - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abdominal pain upper, Diarrhoea, Fatigue
SMQs:, Acute pancreatitis (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: None.
Current Illness: None.
Preexisting Conditions: None.
Allergies: None.
Diagnostic Lab Data: None.
CDC Split Type: vsafe

Write-up: I had experienced extreme fatigue. minor diarrhea, and stomach cramps.


VAERS ID: 1450675 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Male  
Location: California  
Vaccinated:2021-02-02
Onset:2021-06-01
   Days after vaccination:119
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Heart rate irregular, Palpitations
SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Loratidine (allergy)
Current Illness: none
Preexisting Conditions: Hepatitis B
Allergies: none
Diagnostic Lab Data:
CDC Split Type:

Write-up: irregular heart beat, faster heart beats/palpitations; this occurs randomly.


VAERS ID: 1450679 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-05-31
Onset:2021-06-01
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0178 / 1 - / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Heavy menstrual bleeding
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Patient had her period for 1 month
Other Medications: Sertraline 100mg 1.5 pills a day
Current Illness: N/A
Preexisting Conditions: N/A
Allergies: N/A
Diagnostic Lab Data: N/A
CDC Split Type:

Write-up: Patient has had her period for over a month


VAERS ID: 1450692 (history)  
Form: Version 2.0  
Age: 45.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-05-06
Onset:2021-06-01
   Days after vaccination:26
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0173 / 2 LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Blood test, Deep vein thrombosis, Fibrin D dimer increased, Joint range of motion decreased, Thrombosis, Ultrasound Doppler abnormal, Vaccination site pain
SMQs:, Haemorrhage laboratory terms (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Embolic and thrombotic events, venous (narrow), Thrombophlebitis (broad), Cardiomyopathy (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: none
Preexisting Conditions: Celiac Disease and Psoriatic Arthritis
Allergies: none
Diagnostic Lab Data: Blood work and Doppler scan
CDC Split Type:

Write-up: About three weeks after I received my second Pfizer vaccine, I noticed pain in my upper left arm, right at the vaccination site. Over the course of two weeks the pain intensified and got to the point that I was not able to use my left arm at all. The pain was debilitating. I contacted my primary care physician on June 17th 2021 who sent me for a D-diamer test. On Friday, June 18th, the D-diamer test was elevated so I went to the ER where they were able to do a doppler scan of my left arm. This confirmed the DVT (blood clot) in my upper left arm.


VAERS ID: 1452202 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2021-05-05
Onset:2021-06-01
   Days after vaccination:27
Submitted: 0000-00-00
Entered: 2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 001C21A / 2 LA / IM

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cerebrovascular accident, Dry eye, Seizure
SMQs:, Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Convulsions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Corneal disorders (broad), Conjunctival disorders (narrow), Lacrimal disorders (narrow), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: dose 1 4/4/21, dose 2 5/5/21, had a stroke on 6/1/21, no underlying conditions known, suspects possibly from vaccine, since then has relly ry eyes and is still in therapy from post- seizure


VAERS ID: 1453598 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: New Jersey  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Chest discomfort, Chest pain, Dyspnoea, Hypoaesthesia, Hypokinesia, Mobility decreased, Pain
SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Parkinson-like events (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: Patient had no medical history, no known allergies to medications and not taking any medications regularly.
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20210703857

Write-up: NUMBNESS IN THE ARM AND WHOLE BODY; DIFFICULTY IN BREATHING; CHEST PAIN; FELT LIKE COULDN''T MOVE BODY; COULDN''T MOVE HAND; PRESSURE IN CHEST; SHARP PAIN; This spontaneous report received from a patient via a company representative concerned an 18 year old male. The patient''s height, and weight were not reported. The patient''s pre-existing medical conditions included patient had no medical history, no known allergies to medications and not taking any medications regularly. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: not reported, expiry date: unknown) dose was not reported,1 total, administered in on an unspecified date in JUN-2021 for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date in JUN-2021, after 20-25 minutes of vaccination, the patient experienced difficulty in breathing, numbness, chest pain and felt like he could not move his body. All these events were subsided within 15-20 minutes. On 29-Jun-2021, patient experienced the events again. The patient experienced the numbness in whole body then numbness subsided to the arm. The patient was not able to move his hand and experienced the numbness in his hand. The patient experienced sharp pain. On 29-Jun-2021, the patient was admitted to the hospital. It was reported that by the time of patient admitted to the hospital, sharp pain was slightly improved but still felt numbness. The patient also experienced the pressure on chest and the numbness was improved. The number of days of hospitalization were not reported. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from sharp pain and numbness in the arm and whole body, and the outcome of felt like could not move body, difficulty in breathing, chest pain, pressure in chest and could not move hand was not reported. This report was serious (Hospitalization Caused / Prolonged).; Sender''s Comments: V0-20210703857-Covid-19 vaccine ad26.cov2.s- Numbness in the arm and whole body, difficulty in breathing, chest pain, felt like couldn''t move body, couldn''t move hand, pressure in chest, sharp pain. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).


VAERS ID: 1453603 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: New Mexico  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 042A21A / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Injection site swelling, Nasopharyngitis, Productive cough
SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Infective pneumonia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20210708303

Write-up: COUGHING UP PHLEGM; GENERAL COLD-LIKE SYMPTOMS; SWELLING AT INJECTION SITE; This spontaneous report received from a patient concerned a male of unspecified age. The patient''s height, and weight were not reported. No past medical history or concurrent conditions were reported.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: 042A21A, expiry: UNKNOWN) dose was not reported, administered on 22-JUN-2021 for prophylactic vaccination. No concomitant medications were reported. On JUN-2021, the subject experienced swelling at injection site. On 02-JUL-2021, the subject experienced coughing up phlegm. On 02-JUL-2021, the subject experienced general cold-like symptoms. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from swelling at injection site, and had not recovered from coughing up phlegm, and general cold-like symptoms. This report was non-serious.


VAERS ID: 1453607 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: New York  
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Injection site pain, Pain in extremity
SMQs:, Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Seasonal allergy
Preexisting Conditions: Comments: Unknown
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20210708457

Write-up: PAIN IN THE THIGHS BOTH SIDES; PAIN IN THE ARM AT THE SITE OF INJECTION; This spontaneous report received from a patient concerned an 80 year old female. The patient''s height, and weight were not reported. The patient''s concurrent conditions included seasonal allergies.The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: Unknown) dose was not reported, administered on 09-JUN-2021 for prophylactic vaccination. The batch number was not reported. The company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On JUN-2021, the subject experienced pain in the arm at the site of injection. On 13-JUN-2021, the subject experienced pain in the thighs both sides. Treatment medications (dates unspecified) included: acetylsalicylic acid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient recovered from pain in the arm at the site of injection on 13-JUN-2021, and had not recovered from pain in the thighs both sides. This report was non-serious.


VAERS ID: 1453707 (history)  
Form: Version 2.0  
Age: 17.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-04-11
Onset:2021-06-01
   Days after vaccination:51
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 RA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Blister, Condition aggravated, Pruritus
SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Immunocompromised (borderline immunocompromised); Rheumatoid arthritis (Strong Family History of Rheumatoid Arthritis)
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021689848

Write-up: itching on the hands; blister going in between the fingers; reaction had worsen; This is a spontaneous report from a contactable consumer or other non-health care professional. A 17-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration, in right arm, on 11Apr2021 at 16:30 (at the age of 17 years), as single dose for COVID-19 immunization. The patient medical history included Strong Family History of Rheumatoid Arthritis, states her mother is crippled, immunodeficiency and borderline immunocompromised. Historical vaccine included cervical cancer vaccine. The patient didn''t have any history of all previous immunization with the Pfizer vaccine considered as suspect and no additional Vaccines administered on Same Date of the Pfizer Suspect. The patient didn''t receive any vaccines prior 4 weeks. The patient concomitant medications were not reported. The patient previously took cancer vaccines and experienced eczema, cancer vaccines and experienced pyrexia, lo loestrin fe for contraception and experienced heavy menstrual bleeding. She has not taken the second dose yet which is more than 21 days. On 1Jun2021, the patient had experienced Itching and blistering on her hands and between her fingers and it mostly started at the palm and she can''t stop itching reported as worsened. Reporter wanted to know if anyone else had the same reaction. patient also started on birth control. She had prior reaction from cervical vaccine at 12 years of age, also had eczema at the top of feet and fever. Reporter wanted to know if her daughter can still take the second dose because her high school clinic has schedule for second doses on 24Jun2021. Reporter tried to ask if she could also take the second dose of the vaccine because she is "borderline immunocompromised", but she already had HCP appointments set for her and her daughter and decided shell ask the doctor as well. The events didn''t lead to emergency room or physician office visit. No investigation assessment performed. Patient received treatment with Zyrtec, reporter states her daughter called from school and she forgot to take it today at school, it does help somewhat. UPC, Lot, Expiration Unknown. Caller states they tried an itching cream, but it was not the proper one, she thinks it did work but it had an extra ingredient for a feminine product. She wants to note her daughter started on Birth Control, Lo Lo Estrogen, Dosage unknown. Caller states it was strange because she had heavy periods and they are trying to find out if she has fibroids or endometriosis, and the doctor gave her a packet of birth control and when they tried to refill it 3 weeks ago, their insurance didn''t cover it so it might be a combination of her stopping that. Caller states she thought maybe if someone else and reported it. Outcome of the events was reported as not recovered. Communication: Caller provided with Report Reference. The caller was provided with the phone number, hours of operation 8am-8pm EST Mon-Fri and 9am-3pm Sat-Sun


VAERS ID: 1453712 (history)  
Form: Version 2.0  
Age: 12.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-06-08
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0178 / 2 RA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Asthenia, Blood pressure measurement, Body temperature, Chest discomfort, Chills, Electrocardiogram, Eye pain, Feeling abnormal, Gait disturbance, Headache, Hypoaesthesia oral, Inflammation, Insomnia, Intraocular pressure test abnormal, Lip swelling, Meningitis, Myalgia, Nausea, Oropharyngeal pain, Oxygen saturation, Pain, Peripheral swelling, Pruritus, Pyrexia, Scratch, Urticaria, Vital signs measurement
SMQs:, Rhabdomyolysis/myopathy (broad), Cardiac failure (broad), Anaphylactic reaction (narrow), Acute pancreatitis (broad), Angioedema (narrow), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious meningitis (narrow), Accidents and injuries (narrow), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Glaucoma (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Meningitis (at 7 years old)
Allergies:
Diagnostic Lab Data: Test Name: oxygen and blood pressure; Result Unstructured Data: Test Result:unknown; Test Name: fever of 102; Result Unstructured Data: Test Result:102 Fahrenheit; Test Name: EKG; Result Unstructured Data: Test Result:unknown; Test Name: oxygen and blood pressure; Result Unstructured Data: Test Result:unknown; Test Name: took her vitals; Result Unstructured Data: Test Result:unknown
CDC Split Type: USPFIZER INC2021690635

Write-up: Meningitis pain; she woke up and said her face felt funny; pressure on her chest; pressure behind her eyes; muscle pain; she had not slept,; fever; headache; the chills; sore throat; nauseous; Caller states she was assuming hives; inflammation stayed around awhile; body aches / pain through her head and back down her neck; trying to push her eyeballs out and it is really painful; she was slumpy; swelling from the digging and scratching; her hands began to swell yesterday; she was just not feeling right; couldn''t walk by herself; lip swelling and numbness; lip swelling and numbness; itching on face, hands and feet / Caller states then her daughters hands and feet began to itch; This is a spontaneous report from a contactable consumer or other non health care professional. A 12-years-old female patient received bnt162b2 (PFIZER-BIONTECH mRNA COVID-19 VACCINE, solution for injection, Lot Number: EW0178; Expiration Date: 31Aug2021), dose 2 via an unspecified route of administration, administered in Arm Right on 08Jun2021 16:00 (age at vaccination: 12 years) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included, meningitis from an unknown date and unknown if ongoing at 7 years old. The patient''s concomitant medications were not reported. The historical vaccine include COVID-19 Vaccine on 18May2021 for COVID-19 Immunization (1st dose Expiry Date of Covid 19 vaccine: 31Aug2021, lot EW0168 ,anatomical location: Right arm) and had she had itching on the hands. And other vaccine includes flu shots (she does the flu shot every year) for immunization. The patient experienced Meningitis pain on unspecified date, lip swelling and numbness, itching on face, hands and feet / caller states then her daughters hands and feet began to itch in Jun2021. She has pressure on her chest on 09Jun2021. She had pressure behind her eyes, muscle pain,she had not slept, fever, headache, the chills , sore throat, nauseous, caller states she was assuming hives, inflammation stayed around awhile , body aches / pain through her head and back down her neck, trying to push her eyeballs out and it is really painful , she was slumpy, swelling from the digging and scratching, her hands began to swell yesterday in Jun2021. she woke up and said her face felt funny on 09Jun202. she was just not feeling right and couldn''t walk by herself on Jun2021, Caller relays her daughter will be (withheld) . HCP: Caller states she called the pediatrician office and 1 was by phone and she was seen by this provider yesterday and she encouraged her to reach out to us as well. Mom states she was aware of the possible symptoms to occur and her daughter came home Tuesday perfectly fine and went to bed and woke up with the typical symptoms, she had not slept, fever, headache, the chills, sore throat, nauseous and had all the symptoms pretty much. States she didn''t have anything weird going on during the observation time the day of the vaccine. Caller relays her daughter didn''t have anything weird after her 1st dose. Caller states she took a nap Wednesday about 24 hours after her 2nd dose and she woke up and her lips had begun to swell and she woke up and said her face felt funny and it was itchy. Caller states she was assuming hives. Caller states that there was nothing concerning as it wasn''t in that initial 15minutes to 4 hour and that this occurs 24 hours after and that was a concern. Caller states then her daughters hands and feet began to itch and that was kind of along the same lines and said hives and she would itch itch itch and there was swelling from the digging and scratching. Caller states she has numbness in her lip with the swelling. Caller states the other symptoms that are bizarre is more yesterday and it started some on Wednesday she had a pressure in her chest and this was a child, her daughter was very strong, she got up yesterday and tried to do school and had a fever of 102 and Wednesday evening was so sick with symptoms and she still tried. Caller states the pressure in her chest is concerning and told them yesterday and she needed to be seen. States her daughter described it to the doctor that it felt like someone was sitting on her chest sort of pressure and on a scale of 1-10 she was a 7. Caller provides that not at any time did she experience trouble breathing and she never saw her lose or get weird coloring. Caller states she called her doctor Wednesday afternoon and talked to another doctor, that she called the help line after hours as they close 4:30 or 5pm. States she was told it was good news that she did not have trouble breathing but to have it at this point was weird and no one knows what to expect and everyone is different. States she was told to do Benadryl and continue with pain medication for fever and discomfort. Caller states her daughter was miserable the rest of the evening. Caller relays that the swelling subsided and the inflammation stayed around awhile and yesterday she woke up better with no nausea and the common symptoms are better and she still had the fever. Caller relays that at about 9:00 she began to have a problem where she said that behind her eyes she had significant pressure and that scared the caller what with the brain and swelling. Caller states her hands began to swell yesterday, like her lip and her fingers are itchy and swelling and it''s constant itching and the pressure on her chest yesterday, that those 3 things freaked the caller out and she called the pediatrician and they said to have her checked out to make sure as nobody wanted to rush her to the ER as she was not struggling to breathe she was just not feeling right. Caller states the pediatrician did her research about heart inflammation and listened to her heart a couple of times and said her best observation for rubbing sounds was she did not hear any. Caller states when her daughter was younger she had meningitis and went through a whole lot with that and caller states she does not immediately rush to the hospital as that brings back emotions with that. Caller states the doctor said she didn''t see any immediate distress and would do an EKG or they could wait and see, that she thought the pressure might be like body aches and her daughter had laid in bed all day the day before and had a time with it. Caller states she couldn''t walk by herself and she was out of it. Caller states she could do the EKG or wait until today and they chose to wait. States that today she seems better and the only thing today is the continuing pressure behind her eyes that her daughter described as it felt like someone had 2 spoons and was trying to push her eyeballs out and it is really painful. Caller relays her daughter has been through meningitis pain and has pain through her head and back down her neck and the concern is swelling. Caller states it could be a weird reaction and the doctor thinks it is a weird headache she is having and is still doing ibuprofen. Caller relays that her chest is not nearly as heavy today and she has taken Benadryl again for itching and swelling. States the doctor says they don''t know what did it because the risk was there and the benefit and don''t want to get reactions. Caller states she had no problem with getting the shot, that weird things happen and the pediatrician is saying it can happen but doesn''t know. States it is kind of scary. Caller states they checked her out and they checked her oxygen and blood pressure and that made the caller feel better. States that 9:30-10 last night after she got home she was slumpy and her head was hurting and she had chest pressure. Caller states with the hand swelling, that the caller herself went through reaction and hives and the doctor had asked if her daughter had anything new introduced and no nothing was and her daughter didn''t seem concerned to share this but after her 1st dose her hands itched and she didn''t pay it any mind. States she had no face swelling. Caller states she is wondering if those little hand itches after the 1st dose she didn''t tell about till now was that a little bit of a sign that something else was there. States she didn''t mention it after the 1st dose and was good to go. States after the 2nd dose she said mommy my hands itched after the 1st dose, her lip didn''t swell and she told the doctor it''s not conditions on the list of symptoms and she didn''t have breathing issues. Caller states it''s a non severe reaction and is assuming to dose and said yesterday if she gets a booster what does Pfizer advise. Caller states they have all intention of getting what she needs in the future. Caller states she wants to make sure she doesn''t have worse and the lip swelling was freaky. Caller states she thought her daughter was out of the woods after the 20 minutes waiting and was home and then turned. Caller states it was pretty straight forward and knew what the expected symptoms were and they were fine and knew she was having the exact ones on the list and was not feeling well and had a fever. States she was thrown for a loop when others came up and the fact that they were 24 hours out, that she got the 2nd dose 4-4:15 on Tuesday and these evolved well after that time. Caller said they said to report this and her hope is that they can help if someone else has this issue. States when she said she was laying there my hands did itch after the 1st but not like this to this degree. States she never said anything and caller didn''t know. States she knows as a parent there are certain questions to ask and warning signs of potential allergic reactions. Caller states she is assuming this is some sort of allergic reaction, not the worst kind but pressure in the chest and other concerns about her heart having some sort of issue she knows have been reported.Caller states that today she could have done the EKG for more information but based on her listening and what she wanted to thinking the body aches and extensive issues with that she is glad she waited. States she was laying in bed at 6:30 and asked her if she wanted to get the EKG and she said she was afraid of going to the hospital and it''s not fun but would give answers if there is something else and she laid in bed until 9:30-10 and gave her more Benadryl and Ibuprofen and continued with that for the discomfort behind her eyes and the doctor is thinking it''s body aches. States the fever subsided yesterday.Caller states she would like to share that her daughter is a tough kid and tough kids can be taken down too and may not pay attention. Caller states she doesn''t over react but she is aware and if she had told her about her hands she would have thought allergic reaction, mild one and brought her to the doctor or at the 2nd vaccine and she didn''t say anything until after the fact. Caller relays her daughter has never been through hives and the caller has and has a lot of seasonal and environmental allergies and the caller was that kid. Caller states with her daughter not having seen her lip swell and her eyes started hurting and she started thinking the worst. States the doctor pushed on her and checked her lymph nodes and did a thorough exam that lasted about 30 minutes and nobody knows. States she appreciates all that Pfizer and the other companies have done, that we need this.Caller states her daughter goes to the pediatrician in 2 weeks for her annual check up. States the doctor yesterday said her body responded and had a hard time with it. States she does the flu shot every year and this was weird and she wanted us to know and hopes this report can help. Caller states her daughter is a tough kid nobody knows and today she is better, she has a headache behind her eyes still there.Caller relays that Friday she had her annual eye check up and it''s not a vision thing, that was fine until Wednesday and other other stuff and yesterday with pressure and she is sure it''s residual and her body adjusting and if she can help with letting other people know.Caller relays if it comes back she is going to do the EKG, that she is not the parent to say it is nothing and will follow through with Pfizer also. Caller states she didn''t have anything weird for heart beat and no rubbing sound and no signs and she thinks it was issues from body aches and hopefully she is on the up and up and nobody will have to leave and go to the doctor today. And didn''t think because it was not an immediate issue with her breathing and nothing like that and didn''t think it would be an issue with a booster. Caller states it could be that instead of sitting for 20 minutes they keep her longer and that when she fills out the sheet if was not an option, she knows there is severe reaction listed, she will make notes and make the person giving the dose aware that she had the delayed what they are believing to be allergic reaction and make sure, that she may never have it again and it could have been her system was so under attack. Caller states she doesn''t understand vaccines and knows it''s the body''s job to do something and she is not reluctant helping her be immune and she understands what to do in the event and doesn''t have an epi pen and her daughter has no allergies and no reactions to anything. Caller states she didn''t have the worry, that there is always a chance and you worry when something foreign goes in the body that there is a chance to react. Investigations: Caller states they listened to her heart and took her vitals and tests with her fingers checking her eyes to make sure her pupils were dilating correctly and move her eyes with a moving finger. Caller states she doesn''t know the medical term but the basics and let them know she was not in dire straights to rush to the hospital immediately. The patient underwent lab tests and procedures which included blood pressure measurement, body temperature: 102 fahrenheit, electrocardiogram, oxygen saturation, vital signs measurement was unknown and unspecified date. Therapeutic measures were taken as a result of lip swelling and numbness, itching on face, hands and feet / caller states then her daughters hands and feet began to itch, pressure on her chest , fever, swelling from the digging and scratching. The outcome of the events was unknown.


VAERS ID: 1453721 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Female  
Location: Missouri  
Vaccinated:2021-06-07
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0217 / 2 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Body temperature, Fatigue, Herpes zoster, Illness, Influenza like illness, Malaise, Pain in extremity, Pyrexia, Somnolence, Weight increased
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Opportunistic infections (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: LEVOTHYROXINE; MIRENA; DEXTROAMPHETAMINE HYDROCHLORIDE; WELLBUTRIN; PANTOPRAZOLE; CLONAZEPAM; LAMOTRIGINE; OXCARBAZEPINE; PROPRANOLOL; MECLOPRAM [METOCLOPRAMIDE]; OXYCODONE; TIZANIDINE; MULTIVITAMINS [VITAMINS NOS]; VITAMIN D3; FOLIC ACID
Current Illness: Anxiety (Verbatim: Anxiety); Back pain (Verbatim: Back pain); Bipolar depression (Verbatim: Bipolar Depression); Hiatal hernia (Verbatim: Hiatal Hernia); Jitteriness (Verbatim: Jitteriness); Nausea (Verbatim: Nausea); Shaking of hands (Verbatim: Hand shaking); Thyroiditis, unspecified (Verbatim: Thyroid); Ulcer (Verbatim: Ulcer); Vitamin D low (Verbatim: Vitamin D low)
Preexisting Conditions: Medical History/Concurrent Conditions: Acute back pain
Allergies:
Diagnostic Lab Data: Test Name: Fever; Result Unstructured Data: Test Result:101 to 101 plus; Test Name: Fever; Result Unstructured Data: Test Result:99-100; Test Name: Fever; Result Unstructured Data: Test Result:99.2-99.8; Test Name: Fever; Result Unstructured Data: Test Result:101
CDC Split Type: USPFIZER INC2021738743

Write-up: Shingles; Fever; Slept for 18 hours; Was a little sick with both vaccines; Tired and exhausted; Entire arm hurt so much; Didn''t feel well; she has just gained 100 pounds and was normally about 160 pounds.; it was flu-like symptoms; This is a spontaneous report from a contactable consumer (patient). A 46-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0217, Expiration date: Unknown) via an unspecified route, administered in Left Arm on 07Jun2021 at 10:00 (46-year-old at vaccination) as a dose 2, single for COVID-19 immunization. The patient''s medical history included ongoing thyroiditis, ongoing bipolar depression, ongoing anxiety, ongoing ulcer, ongoing hiatal hernia, ongoing jitteriness, ongoing hand shaking, ongoing nausea, ongoing back pain, ongoing vitamin d decreased and threw back out (back pain). The patient''s family history relevant was reported as none. The patient''s past medications included Flu shot which made patient sick for 24 hours, Benadryl which caused allergic reaction. The patient''s concomitant medication(s) included ongoing levothyroxine 0.125 mg taken for thyroiditis probably from 2009 or 2010, ongoing levonorgestrel (MIRENA) taken for birth control and regulate her menstrual from 3 years ago, her first one was about 2010 or 20211, dextroamphetamine hydrochloride 100 mg daily, taken for bipolar depression from 2003 and ongoing, bupropion hydrochloride (WELLBUTRIN) 600 mg taken for bipolar disorder from 2003 and ongoing; ongoing pantoprazole 80 mg taken for ulcer, hiatal hernia probably from 2016, took 80mg for 7 or 8 months. Before that she took 40mg, ongoing clonazepam 1-3 mg per day taken for anxiety bipolar depression and sleep from about 20 years, ongoing Lamotrigine 400 mg taken for bipolar depression, switched to 400mg about 4 months ago. 300mg before that. Been on it for about 20 years, taken as off-label use drug, ongoing oxcarbazepine 600 mg taken for bipolar depression been on it for about 20 years. About 3 or 4 months ago, it dropped from 900mg to 600mg, propranolol 80 mg, 3 per day as needed taken for Jitteriness from about ago and ongoing, she said there had never been a period when she has been on it consistently, her hand was shaking, metoclopramide (MECLOPRAM) 10mg, 1 or 2 tablets taken for nausea from 2000 and ongoing; ongoing oxycodone 7.5mg -325mg , 1 every 6 hours taken for threw her back out (back pain), Oxycodone: Has Acetaminophen in it. It was first prescribed about 1 1/2 years ago, taken as needed for back every 6 hour, tizanidine 6 mg capsule once or twice per day, taken for back injury from about 25 years ongoing now, ongoing (MULTIVITAMINS [VITAMINS NOS]) took as healthy nutrients, colecalciferol (VITAMIN D3) 50mcg, 2000 IU taken for vitamin D low and tiredness from 7 or 8 year and ongoing folic acid taken to help her regulate menstrual cycle from 20 or 25 years and Benadryl or Tylenol taken for fever within 2 weeks of her covid vaccine shots. No additional vaccines administered on same date of the Pfizer suspect and was not on any other vaccine Prior Vaccinations (within 4 weeks). The patient was not related to any study or programme. The patient was a really healthy person, at least she was before COVID. She worked out. She used to weigh 160 pounds. She had a good BMI and weight before. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0177) via an unspecified route, administered in upper Left Arm on 15May2021 at 15:00 or 15:30 (46-year-old at vaccination) as a Dose 2, single for COVID-19 immunization. The patient was sick, tired and had fever after first dose of vaccination. The patient stated that she had no idea if this was really her vaccine or not. They said that if anything weird happened, she should report it because the data was being tracked. On 07Jun2021, she was a little sick with both vaccines, fever for 24 hours and slept for about 18 hours. Her fever broke. She slept and was tired for a day and then she was fine. She said that it was a little bit better. She was taking pain medicine less, maybe every 8 hours during the day. She was taking it every 6 hours at night. She stated that it hurt so much. The patient stated that it was the second part where it got weird. She got the second dose of the injection. People kept telling her they reacted within 12 hours. The patient said that she was down in 3 hours. She had fever and was exhausted. She said this was not shocking for her. Her body tended to do that. She ran a fever of 101. She got it on Monday. She tried to work on Monday. About 2 hours after her shot, her boss kicked her off of her computer and she was sleeping. She was running fever then. On Monday, Tuesday and Wednesday, she did not go to work. Her fever was 101 to 101 plus. Thursday she woke up and felt a little better. Her fever dropped to the higher 99''s and lower 100''s. It did not go higher than 100.2. The patient said that she took Tylenol and it went down for the most part. She was exhausted and didn''t feel well. She said still was not feeling well. It was a different kind of not feeling well. After her shot, it was flu-like symptoms. It was different now that she was having pain. She dragged herself to her desk and worked Thursday and Friday. She functioned on Saturday. She slept during the weekend but she was functioning. Saturday her fever broke completely. On 12Jun2021 (Sunday) she woke up with what she thought was 3 bug bites on her arm. The patient stated that she flipped out. She thought it was 3 bug bites. Her entire arm hurt so much. The patient described it as it felt like a little person was under the skin poking her with needles. The patient stated that she sucked it up until Wednesday morning because she tended to do stuff like that. Then she started running a fever again. It started about 99.2 and jumped to 99.8. The bites were still there and she didn''t feel well. She stated that her fever was still in the 99''s. She normally ran low at 97.2 or 97.4. It was definitely better. It was down in the 99''s. The patient stated that he doctor on 16Jun2021 took one look at what the patient thought was bug bites and she said she had shingles. She was put on antibiotic and pain medicine. On Wednesday afternoon she was exhausted and didn''t feel well. She took a 2-hour nap. She was busy at work and forced herself to keep working. The patient reported that she was on day 3 of the antibiotic. It definitely still hurts if she doesn''t take the pain medicine. She was still running a fever under 101 but over 100. The patient was still working because she doesn''t have a choice. She stated that she has just gained 100 pounds and was normally about 160 pounds. Her body was not use to this, she doesn''t know if that was flipping her body out or not, it was flipping her out though. The patient consulted her primary HCP to know if there was a possible connection with the shingles and vaccine. But HCP didn''t really tell her about it. She was totally shocked. She thought she could only have shingles if she didn''t have the chicken pox as a kid. wanted to know if shingles was an unusual or common side effect. She stated that bumps from the shingles started 12Jun2021 or 13Jun2021. She thought she had banged her arm on something when she was working on her apartment. She still had the bumps. They were getting slightly bigger, and she still had pain. They were a little redder around the edges. She stated that the little dude under the skin was still poking. She said the pain medicine was working. She barely had pain with the pain killers. She stated that she got the second dose 07Jun2021. She was supposed to get it on 06Jun2021, but she had to push it off a day. She did not have any tests for the shingles. She said that both the doctor and a nurse practitioner looked and diagnosed her with shingles. The patient received antibiotics and pain medication as treatment medication for Shingles. The patient had not visited emergency room. She visited physician office for 3 bus bites on her arm, shingles. On an unknown date, the patient underwent lab test and procedure which included Body temperature: 101 to 101 plus, 99-100, 99.2-99.8, and 101 (units unspecified). The outcome of the events fever, Slept for 18 hours, tired and exhausted was recovering and the outcome of other events was unknown.


VAERS ID: 1453746 (history)  
Form: Version 2.0  
Age: 20.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0176 / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Diabetes mellitus, Drug level, Headache, Magnetic resonance imaging, Seizure, Thyroid function test
SMQs:, Hyperglycaemia/new onset diabetes mellitus (narrow), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: Test for diabetes; Result Unstructured Data: Test Result:Unspecified; Test Name: Drug panel test; Result Unstructured Data: Test Result:Unspecified; Test Name: MRI; Result Unstructured Data: Test Result:Unspecified; Test Name: thyroid; Result Unstructured Data: Test Result:Unspecified
CDC Split Type: USPFIZER INC2021756343

Write-up: seizure/she passed out convulsing; headache; This is a spontaneous report from a contactable consumer (patient). A 20-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EW0176 and Expiration date: unknown), via an unknown route of administration, in left arm on 01Jun2021 at 12:25 (at the age of 20-years-old) as dose 1, single for covid-19 immunisation. The patient has no medical history. The patient''s concomitant medications were not reported. She did various lab tests included drug panel test, test for diabetes, thyroid and MRI: results were not specified. On 01Jun2021, 2 minutes after receiving the vaccine, she got a bad reaction, so she mentioned that she got a seizure and she passed out convulsing and she would like to report this. She also had headache that lasted a while but when she woke up that was gone (improved). She had doctor visit afterwards, doctor recommended not to get the 2nd dose of the vaccine. She received treatment for events no other than Ibuprofen then no the dosage 2 of the 200 mg so 400 2 of them so 400. She wanted to know if the vaccination card needs to be signed off for the 2nd dose even if she is not eligible for it. Outcome of event seizure was unknown, and outcome of event headache was resolved on an unknown date in Jun2021. Follow up (22Jun2021): This is a Follow up spontaneous report from a Pfizer sponsored program COVAX US support. A contactable 20-year-old female consumer (patient) reported events information.


VAERS ID: 1453762 (history)  
Form: Version 2.0  
Age: 31.0  
Sex: Male  
Location: Texas  
Vaccinated:2021-06-19
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0178 / 2 RA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Abdominal pain upper, Ageusia, Chills, Cold-stimulus headache, Discomfort, Hypoaesthesia, Limb discomfort, Musculoskeletal chest pain, Near death experience, Pain, Pyrexia, Shock
SMQs:, Anaphylactic reaction (narrow), Acute pancreatitis (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Taste and smell disorders (narrow), Anticholinergic syndrome (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Hypovolaemic shock conditions (narrow), Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypoglycaemic and neurogenic shock conditions (narrow), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: HYDROCODONE
Current Illness: Marijuana use
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021758058

Write-up: uncomfortable; Extreme pain; Couldn''t taste cheetos; Pulp in his arm; Worst fever he can imagine; Chills all over; Brain stating out/ his brain goes fuzzy; gutting his stomach; ribs were sore; Almost died; He thought his body went into shock; Numbness; This is a spontaneous report received from a contactable consumer or other non hcp. A 31-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number: EW0178) via an unspecified route of administration in Arm Right on 19Jun2021 15:00 as single dose for covid-19 immunisation. Medical history included ongoing substance use. Concomitant medication(s) included hydrocodone and unspecified antibiotics taken for an unspecified indication, start and stop date were not reported. The patient received first dose of BNT162B2 (Batch/lot number: EN5318) via an unspecified route of administration in Arm Right on 20May2021 as single dose for covid-19 immunisation. The patient experienced worst fever he can imagine, pulp in his arm, chills all over on 19Jun2021, extreme pain on 20Jun2021, couldn''t taste cheetos on 22Jun2021, numbness, he thought his body went into shock, almost died, brain stating out/ his brain goes fuzzy, gutting his stomach, ribs were sore on Jun2021. Caller reported as he got the second Covid Vaccine in his arm. He literally almost died. He went to (withheld), and they said it is normal and he should take some Tylenol. If he can die it is not normal. The hospital didn''t want to do anything because they were afraid people would use him as a scapegoat and say if he is incapacitated, they will never take it. He had a bad dose or just had a severe adverse reaction. He had his vaccination card on him. It didn''t happen until he had his second dose. He had been shot in the face with a 357 Magnum at point blank range, and this is more painful than that. It is legit more painful. He has never felt worse pain in his entire life. His card says Pfizer Vaccine EW0178. Maybe he got a bad dose. Right now, he has to be careful to not sit in one position because he was very uncomfortable. Further reporter stated briefly extreme pain: They gave him the shot and he went to sleep, and his body was immediately super tender and painful. He thought his body went into shock. He was shot in the face by a 357 Magnum so he knows the feeling. It started at 0000. In the morning he woke up and tried to eat food and couldn''t taste Cheetos. He tried to go to the bathroom and peed on his leg twice, he was that kind of numb. The real pain came from trying to just exist. He was so tender that breathing was an obstacle and touching a pillow against his skin felt like getting hit by a bus for the next couple days. He still doesn''t feel all that great. He needs antibiotics and a painkiller. He was smoking marijuana because everyone left him in the cold. Pulp in his arm: He could feel like a pulp in his arm where it was worse. It felt like a bullet was put into his arm. It was all pulpy and feels nasty. It was dispersants of coagulation and blood or the medicine and blood or something else. Either way it is gross. He put his hand against it and massaged it and it hurt like hell. The pain subsided. It was like he has PTSD. He had to get that out of his arm. When he gets the pulpy stuff out of his arm the dispersing pain was less and less, but it was still super painful. That was how he woke up initially. It was there only slightly now. Brain stat icing out: He also keeps having his brain static-ing out which was not a good thing. His brain goes fuzzy. He has had no medical tests. The clinical outcome of the events Numbness, worst fever he can imagine, pulp in his arm, brain stating out/ his brain goes fuzzy was recovering and other were not recovered. Information on Lot/Batch number was available. Additional information has been requested.


VAERS ID: 1453779 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Unknown  
Vaccinated:2021-06-11
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Condition aggravated, Erection increased, Priapism
SMQs:

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Priapism (Verbatim:I have a pre existing condition called Low Flow Priapism.")
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021785272

Write-up: this condition causes him to have erections that last for long periods of time/preexisting condition has seemed to flare since having the dose; Low Flow Priapism/this condition causes him to have erections that last for long periods of time/preexisting condition has seemed to flare since having the dose; Low Flow Priapism; This is a spontaneous report from a contactable consumer (patient, self-reported). A male patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on 11Jun2021, as a single dose for COVID-19 immunization. The patient''s medical history included low flow priapism (I have a pre-existing condition called Low Flow Priapism). Concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0183 and expiry date was not reported), via an unspecified route of administration, on an unspecified date, as a single dose for COVID-19 immunization and no events reported. The patient reported that he received the 2nd dose of the Pfizer COVID19 vaccination on 11Jun2021. Since having the 2nd dose his "pre-existing condition has seemed to flare since having the dose." The patient reported having been previously diagnosed with "Low Flow Priapism." He states that on an unspecified date in Jun2021, this condition causes him to have erections that last for long periods of time, "generally speaking they can go anywhere to a day and sometimes become medical emergencies." Since having the 2nd dose of the vaccine, he stated that he has been having these concerns "quite often" which has not been the case in "some time." The patient advised after review of the prescribing information for Pfizer COVID19 vaccine he did not find information regarding prolonged erections or any data related to his diagnosis of Low Flow Priapism. Encouraged the patient to follow up with HCP to aid in medical decision making at this time based upon his condition and worsening symptoms also advised that all reported AEs were followed up on after being reported and studies remain ongoing. He was wondering, if you guys have heard of anything, anybody having the same issue flaring up after the COVID vaccine. Outcome of the events was unknown. Information on Lot/Batch number has been requested.


VAERS ID: 1454184 (history)  
Form: Version 2.0  
Age: 77.0  
Sex: Female  
Location: Illinois  
Vaccinated:2021-04-03
Onset:2021-06-01
   Days after vaccination:59
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / 2 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Pain in extremity
SMQs:, Tendinopathies and ligament disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Sandostatin, eliquis, B12
Current Illness: None
Preexisting Conditions: None
Allergies: Sulfa
Diagnostic Lab Data: None
CDC Split Type: vsafe

Write-up: I had a regular appointment with my doctor and that?s when I told him that my arm was hurting, and he said that I had to go to physical therapy. He did not prescribed any medications or do any tests


VAERS ID: 1454204 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-04-06
Onset:2021-06-01
   Days after vaccination:56
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6199 / 2 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Cardiac assistance device user, Echocardiogram, Ejection fraction decreased
SMQs:, Cardiac failure (narrow), Cardiomyopathy (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lisinipril 20mg ad Corey 25mg bid Omeprazole 29mg qd
Current Illness:
Preexisting Conditions: Cardiomyopathy Depression An3 Arthritis
Allergies:
Diagnostic Lab Data: Had a heart echocardiogram. Will be having a stress sonogram. Wearing a life vest.
CDC Split Type:

Write-up: My EF went from 45 to 30. Two months after vaccination.


VAERS ID: 1454291 (history)  
Form: Version 2.0  
Age: 22.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-02-27
Onset:2021-06-01
   Days after vaccination:94
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ENG202 / 1 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ENG204 / 2 LA / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Chest discomfort, Dizziness, Electrocardiogram, Heart rate increased, Sinus arrhythmia
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Disorders of sinus node function (narrow), Vestibular disorders (broad), Dehydration (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: effexor xr, hydroxyzine, aleve, mirena, zofran, magnesium, ocuvite eye performance, alburteral
Current Illness:
Preexisting Conditions: chronic migraine with brainstem aura generalized anxiety disorder cough variant asthma grass pollen allergy
Allergies: amoxacillin tetracycline
Diagnostic Lab Data: At Dr. appointment in March 2021 for separate condition, provider noticed rapid change in heartrate and performed EKG resulted with sinus arrhythmia and right axis deviation. Follow up EKG 1 month later showed only sinus arrhythmia. Note that sinus arrhythmia on EKG was first-ever noted in July 2020 during ED visit for acute migraine with stroke presentation.
CDC Split Type:

Write-up: New onset of rapid change in heart rate (accompanied by dizziness/lightheadedness) upon standing noticed in May 2021. The sensation in the chest feels like heart burn but appears upon standing. Routinely heart rate will change from 66-75 BPM to 104+ BPM following a change of position from reclined to standing and only 3-5 steps.


VAERS ID: 1454292 (history)  
Form: Version 2.0  
Age: 60.0  
Sex: Male  
Location: Florida  
Vaccinated:2021-04-07
Onset:2021-06-01
   Days after vaccination:55
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0151 / 2 LA / IM
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6208 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Ear pain, Erythema, Skin lesion, Subcutaneous abscess
SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Lithium and Lamictal
Current Illness: Bipolar Disorder. Hypercholesterolemia, BPH
Preexisting Conditions: Bipolar Disorder, Hypercholesterolemia, BPH
Allergies: None
Diagnostic Lab Data: none
CDC Split Type:

Write-up: June 2021- painful left ear lobe, erythema and abscess, treated at home with warm compresses, lanced small abscess, topical triple antibiotic ointment resolved in 1 week June 2021 - 1 week later - painful right ear lobe, erythema and abscess, treated at home with compresses, lanced small abscess, topical triple antibiotic ointment resolved in 1 week. June 2021 - 3 weeks later - redness on right side of neck at the collar line extending from the angle of the mandible to chin associated with a large grape-sized lesion. Treated with warm compresses, 2 weeks of Keflex, currently on Bactrim


VAERS ID: 1454402 (history)  
Form: Version 2.0  
Age: 65.0  
Sex: Female  
Location: California  
Vaccinated:2021-05-01
Onset:2021-06-01
   Days after vaccination:31
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN 0201A21A / UNK LA / IM

Administered by: Public       Purchased by: ?
Symptoms: Decreased appetite, Irritability, Memory impairment, Taste disorder
SMQs:, Taste and smell disorders (narrow), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Depression (excl suicide and self injury) (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: none
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: none
CDC Split Type:

Write-up: increased irritability I have an exceptionally good memory, and post-vaccine began to struggle a bit with it (memoryissues) impaired appetite/food tastes different


VAERS ID: 1454483 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Male  
Location: California  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 004C21A / 2 LA / SYR

Administered by: Other       Purchased by: ?
Symptoms: Aphasia, Asthenia, Bell's palsy, Blood test, Computerised tomogram, Disorganised speech, Facial paralysis, Hypoaesthesia, Lymphadenopathy, Pain in extremity, Peripheral swelling, Vision blurred
SMQs:, Cardiac failure (broad), Angioedema (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Dementia (broad), Psychosis and psychotic disorders (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Hearing impairment (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: antiacid - 48 hours before the vaccine - Zegerid; Omeprazole 20 mg
Current Illness: no
Preexisting Conditions: no
Allergies: Codeine - bad rash
Diagnostic Lab Data: 23rd - CT Scan and Bloodwork - immunologist on the 23rd - She said I wasn''t having a stroke. She said I was having a light case of Bells Palsy.
CDC Split Type: vsafe

Write-up: Had a really swollen, sore arm - and under arm pits it was really swollen too. I toughed it out for a couple of weeks. I called the clinic when it was still sore. I was not able to lift weights when I exercise - I was dropping them. I called the clinic and talked to a nurse. On June 22nd, around 1:00 or 2:00 - my whole left side went numb. I couldn''t speak. Left side of face was drooping. I had blurred vision. But then it got a little better within an hour or two ( I could communicate) and I called the clinic said to come in on 23rd - doctor thought I was still having a stroke due to symptoms observed. I have an optometrist is going to check my eyes. I am going to get a physical done next month (August 9th) at the clinic. I work out and tried to do some neck exercises - and dr noticed a past injury of left side of face -that happened 45 years ago - on the CT. Dr wonders if it''s related to that . I decided to do some neck exercises on Monday and yesterday I was bedridden after doing those exercises - lymph nodes swelled up. I still have some blurry vision; my face is still drooping but just a little bit. I do jumble my words.


VAERS ID: 1454558 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Michigan  
Vaccinated:2021-03-17
Onset:2021-06-01
   Days after vaccination:76
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / IM
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER - / 2 RA / IM

Administered by: Public       Purchased by: ?
Symptoms: C-reactive protein increased, Chest pain
SMQs:, Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Wellbutrin XL, Ability, Lexapro, Famotidine
Current Illness: None
Preexisting Conditions: None
Allergies: NKA
Diagnostic Lab Data: Elevated CRP levels in blood in April
CDC Split Type:

Write-up: No treatment. Frequent chest pain on left side of chest.


VAERS ID: 1454872 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: Oregon  
Vaccinated:2021-06-06
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 LA / SYR
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Intermenstrual bleeding, Menstruation delayed
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Fertility disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Zoloft 100mg
Current Illness: None
Preexisting Conditions: None
Allergies: Tree pollen allergy (birch) Oral allergy syndrome
Diagnostic Lab Data:
CDC Split Type:

Write-up: Delay in otherwise regular menstrual cycle. Breakthrough bleeding/unusual spotting in between periods


VAERS ID: 1456652 (history)  
Form: Version 2.0  
Age: 35.0  
Sex: Female  
Location: Arizona  
Vaccinated:2021-06-15
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0181 / 2 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Amnesia, Bipolar I disorder, Crying, Depressed mood, Fear, Hallucination, visual, Impulse-control disorder, Pain, Retching, Suicidal ideation, Vomiting
SMQs:, Acute pancreatitis (broad), Suicide/self-injury (narrow), Anticholinergic syndrome (broad), Dementia (broad), Psychosis and psychotic disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Depression (excl suicide and self injury) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: SERTRALINE; DIGESTIVE ENZYMES; IRON
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Celiac disease
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021766211

Write-up: The night of my vaccine I shot straight up in bed filled with fear and screamed out my husbands name. Then I proceeded to violently throw up all over myself and my bedroom on the way into the bathroom; The night of my vaccine I shot straight up in bed filled with fear and screamed out my husbands name. Then I proceeded to violently throw up all over myself and my bedroom on the way into the bathroom; I had nothing left to throw up but the violent retching wouldn''t stop for another 7 minutes or so; It was so loud and painful; After that I felt immense sadness; I was crying uncontrollably bc I felt so much pain and sadness; I was seeing black shadow spirits and lying pigs along with visions of China./ it sounded like a devil was coming out of me; Manic depression; Suicidal thoughts; Memory loss; Loss of impluse control.; This is a spontaneous report from a contactable consumer. A 35-years-old non-pregnant female patient received second dose of BNT162B2 (Formulation: Solution for injection; Batch/Lot Number: EW0181), via an unspecified route of administration, administered in Arm Left on 15Jun2021 at 09:00 AM at the age of 35 years as dose 2, single for covid-19 immunization.Medical history included coeliac disease. The patient had allergy to codine. Concomitant medications received within 2 weeks of vaccination included sertraline (SERTRALINE)100 mg, betaine hydrochloride, bromelains, cellulase, pancreatin, papain (DIGESTIVE ENZYMES) and iron (IRON). The patient previously received first dose of BNT162B2 (Formulation: Solution for injection; Batch/Lot Number: EWO161), administered in Arm Left on 18May2021 at 10:00AM as dose 1, single for covid-19 immunization. The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with covid-19 prior vaccination. Since the vaccination, the patient has not been tested for covid-19. On 15Jun2021, at night of vaccine the patient shot straight up in bed filled with fear and screamed out her husband''s name. Then she proceeded to violently throw up all over myself and my bedroom on the way into the bathroom. Once in the bathroom she continued to retch, and she was seeing black shadow spirits and flying pigs along with visions of China. she prayed to God that she wouldn''t die, the patient then took a shower and went back to bed. Around 2 hours later it happened again, this time she was retching so hard it sounded like a devil was coming out of me. She had nothing left to throw up, but the violent retching wouldn''t stop for another 7 minutes or so. She though her neighborhood could have heard me it was so loud and painful. After that she felt immense sadness as she cleaned up her vomit again. She was crying uncontrollably, she felt so much pain and sadness and she could hear sobbing from COVID victims. The days after she suffered from manic depression, suicidal thoughts, and memory loss as well as loss of impulse control. Therapeutic measures were not taken for the events. Adverse event resulted in Doctor or other healthcare professional office/clinic visit. The patient was recovering from events.


VAERS ID: 1456656 (history)  
Form: Version 2.0  
Age: 39.0  
Sex: Male  
Location: Arkansas  
Vaccinated:2021-06-19
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Cardiac disorder, Chest discomfort, Circumstance or information capable of leading to medication error, Dyspnoea, Feeling abnormal, Palpitations
SMQs:, Anaphylactic reaction (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Medication errors (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: PROPRANOLOL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Anxiety (Never been diagnosed with anxiety. He does not have anxiety.); Cardiac arrest (His father did pass away at 48 of cardiac arrest); Lung cancer
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021766700

Write-up: received the first dose of the Pfizer Covid-19 vaccine on 19Jun2021 and by 21Jun2021 he was in the heart hospital; he is trying to go back to how he was feeling before and has regrets about taking it now; when he walks from the truck to the office he gets short of breath.; He does not know if it is the rhythm of his heart or palpitations; Caller states the people he got the shot from didn''t follow procedure, they don''t need to be giving anybody a shot.; He reports he laid down and woke up and his chest was going something funny; This is a spontaneous report from a contactable consumer or other non-healthcare professional. A 39-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, in left arm on 19Jun2021 11:00 as dose 1, single for covid-19 immunization. Medical history included anxiety. Caller has never been diagnosed with anxiety. He does not have anxiety. Sometimes he gets nervous, he will take it to keep the jitters away and patient had family history of cardiac arrest as his father did pass away at 48 of cardiac arrest and his brother has lung cancer at 37 and is sick, from an unknown date and unknown if ongoing. Caller states his brother who is 37 has lung cancer and he is very sick. He had heard you can be asymptomatic with COVID. He goes to visit his brother, and he did not want to visit him and get make him sicker than he was right now, even though he wears his mask. Concomitant medication included propranolol (PROPRANOLOL) taken for anxiety, start and stop date were not reported. Started taking medication about 5 years ago He does not take it daily. He takes it if he has a major meeting. Caller states he received the first dose of the Pfizer Covid-19 vaccine on 19Jun2021 and by 21Jun2021 he was in the heart hospital (24-hour clock). Caller is wondering if there was anything he can do to reverse the vaccine in his body. Caller states he was trying to go back to how he was feeling before and has regrets about taking it now. Caller states, he want to let you know not really a question but a statement, you all doing very important work he know you all employed by Pfizer, but you all doing important work by taking these reports because if he had not seen some of this stuff, he would have asked the question before hand all he heard was it was safe and effective he did not know all of the other things that happen, thank you. On 21Jun2021 patient went to the heart hospital and on unspecified date rhythm of his heart or palpitations, on 21Jun2021 patient it made his chest do something funny, on 22Jun2021 patient experienced for walks from truck to office and has shortness of breath. Caller states he was calling about the vaccine, COVID-19. He states they said it was safe. He was reporting an adverse event. He would like this to be reported. He states he took the 19Jun2021 at 11am, by 21Jun2021 he was in the heart hospital. He states he was 39 years old and about as healthy as he can get. he works out 4 days a week. He was in exceptional shape. He is trying to get this off of the market. He does not want anyone else to experience this. He wants this reported all over the world. Caller states he has been getting a little better. He does not know if he can work out. He was going to the doctor to see. Caller clarifies that he went to ER and was not admitted to the hospital. He will also see the cardiologist. He does not know if it was the rhythm of his heart or palpitations, it made his chest do something funny. He reports he laid down and woke up and his chest was going something funny. He states he works out, and now when he walks from the truck to the office, he gets short of breath. He states it was not persisting, he feels a lot better. He states the shortness of breath started on 22Jun2021, when he went to work. He reports it was new so he will see how he was going to do. Patient had not received any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. Caller states he has not received a vaccination since his mama took him in elementary school. Patient had attended emergency Room and physician Office after experiencing events. Outcome of event received the first dose of the Pfizer Covid-19 vaccine on 19Jun2021 and by 21Jun2021 he was in the heart hospital, when he walks from the truck to the office he gets short of breath, He does not know if it is the rhythm of his heart or palpitations was recovering, he is trying to go back to how he was feeling before and has regrets about taking it now, Caller states the people he got the shot from didn''t follow procedure, they don''t need to be giving anybody a shot, He reports he laid down and woke up and his chest was going something funny was unknown. No follow-up attempts are possible. No further information is expected.


VAERS ID: 1456659 (history)  
Form: Version 2.0  
Age: 50.0  
Sex: Female  
Location: Virginia  
Vaccinated:2021-06-22
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Private       Purchased by: ?
Symptoms: Fatigue, Lethargy, Off label use, Overdose, Wrong product administered
SMQs:, Drug abuse and dependence (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Medication errors (narrow), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Atopic dermatitis (Existing Ectopic dermatitis due to poison ivy exposure); Rheumatoid arthritis (has long-standing rheumatoid arthritis (longstanding stable condition))
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021766735

Write-up: administered 1.0 mL of the Pfizer Covid-19 vaccine. He reports the vaccine was diluted, but received more than the recommended 0.3mL of vaccine; administration error/inadvertently received the Pfizer COVID 19 vaccine; administration error/inadvertently received the Pfizer COVID 19 vaccine; feeling more lethargic and fatigued; feeling more lethargic and fatigued; This is a spontaneous report from a contactable pharmacist reported for a patient. A 50-years-old female patient received an unknown dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number: unknown, Expiration date: unknown) via an unspecified route of administration, administered in unknown arm on 22Jun2021 at 14:50 pm (age at vaccination was 50 years) as unknown, single for COVID-19 immunization. The patient received second dose of COVID-19 vaccine MRNA (MRNA 1273) (MODERNA COVID-19 VACCINE, Batch/Lot number: unknown, Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on 02Jun2021 (age at vaccination was 50 years) as 2nd dose, single for COVID-19 immunization. Medical history included existing ectopic dermatitis due to poison ivy exposure and had long-standing rheumatoid arthritis (longstanding stable condition). The patient had no known vaccine allergies. The patient''s concomitant medications were not reported. The patient previously received first dose of COVID-19 vaccine MRNA (MRNA 1273) (MODERNA COVID-19 VACCINE, Batch/Lot number: unknown, Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on 30Jan2021 (age at vaccination was 50 years) as 1st dose, single for COVID-19 immunization and no reaction was reported. The patient previously received Adacel administered on an unknown date in Jan2020. There was no history of all previous immunization with the Pfizer vaccine considered as suspect. No additional vaccines were administered on same date of the Pfizer suspect. The caller was a Pharmacist and Medication Safety Officer inquiring about additional information regarding inadvertent administration of the Pfizer COVID-19 vaccine. Called in regard to a patient who inadvertently received the Pfizer COVID 19 vaccine on 22Jun2021 and already received both doses of the Moderna COVID 19 vaccine, first dose 30Jan2021 and second dose 2Jun2021. Caller reported that a patient was being seen yesterday (22Jun2021) in the ambulatory clinic for another condition and was supposed to receive a steroid, but there was an administration error and the nurse administered 1.0 mL of the Pfizer COVID-19 vaccine. He reported that the vaccine was diluted, but received more than the recommended 0.3mL of vaccine. Caller stated "roughly 3 doses of the vaccine". Caller reported that the patient had previously received both doses of the Moderna COVID-19 vaccine (first dose 30Jan2021, second dose 02Jun2021). This patient was being seen for something else. Patient was given one ml instead of 0.3ml of product which was diluted correctly. Caller corrected information provided by the agent stating the notes said that the patient received 0.9ml but that was close to one CC. Clarified the patient received the Pfizer COVID 19 vaccine 22Jun2021 at about 14:50 pm in unknown arm. When ask to provide information for the Moderna COVID 19 vaccine caller stated he did not have any information and cannot provide NDC, lot or expiration date. Caller reported that the patient was seen in the emergency room last night, but was having no apparent side effects. Caller reported the patient was feeling more lethargic and fatigued today. Mentioned the usual dose was 0.3ml but the patient was not even supposed to get that. That was a medication error. His question was regarding advice to give to the provider and patient and asked whether there would be additional side effects and what were the main side effects to advise. He received the response which confirmed Pfizer Covid-19 vaccine. Provided disclaimers and spoke from the attached document from page 3 and 4 under Inadvertent administration of the whole multi-dose vial of vaccine instead of the recommended Dose. Stated they are considering this an event with harm. Stated it was medically significant. Adds the only side effect the patient has had is fatigue and lethargy which was persisting. Patient was being seen for Ectopic dermatitis due to poison ivy exposure. The event inadvertently administered the Pfizer COVID 19 vaccine required a visit to emergency room. Caller reported that the patient was just observed in the emergency room and not admitted to the hospital. No relevant tests were done. The events were reported as medically significant. The causality was reported as unrelated to the product. The outcome of the event feeling more lethargic and fatigued was not resolved. Follow-up#01 (23Jun2021): New information received from a contactable consumer reported for a patient included: Updated the relevant medical history, historical vaccine, seriousness criteria and causality of the events and details of the medication error. Follow-up attempts are needed. Information on Lot/Batch number can be requested.; Sender''s Comments: Considering a plausible temporal relationship, a possible contributory role of suspect product bnt162b2 to the reported event of Lethargy ,Fatigue and AT risk events cannot be excluded cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1456660 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: California  
Vaccinated:2021-06-10
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: School       Purchased by: ?
Symptoms: Chills, Dizziness, Electrocardiogram, Fatigue, Headache, Heart rate irregular, Left atrial enlargement, Palpitations
SMQs:, Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow), Vestibular disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202106; Test Name: EKG/ECG; Result Unstructured Data: Test Result:Borderline left atrial enlargement
CDC Split Type: USPFIZER INC2021766770

Write-up: Strong beating heart, irregular heartbeat; Palpitations and lightheadedness.; Palpitations and lightheadedness.; Body chills; Throbbing headache; Fatigue; Borderline left atrial enlargement; This is a spontaneous report from a contactable consumer.A 33-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Batch/Lot number was not reported), via an unspecified route of administration on 10Jun2021 at 12:15 (33 years age at the vaccination) as dose 2, single for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The other medications patient received within 2 weeks of vaccination included Tylenol after the second shot. Patient had no known allergies. Prior to vaccination, the patient not diagnosed with COVID-19. Since the vaccination, the patient not been tested for COVID-19. It was reported that the patient was overall a healthy athlete. On 16Jun2021 at 08:00 AM, after second shot, after body chills, throbbing headache and fatigue passed (2-3 days), the patient started to have strong beating heart, irregular heartbeat, palpitations and lightheadedness. Patient went to urgent care on his 5th day of having this with a very irregular heartbeat, so they took him in right away. All tests clear but EKG/ECG shown borderline left atrial enlargement. Still watching and keeping record today. Adverse event resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. No therapeutic measures were taken for the events. The patient recovered from body chills, throbbing headache and fatigue in Jun2021, and patient had not yet recovered from rest of the events. Information on the lot/batch number has been requested.


VAERS ID: 1456701 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Unknown  
Vaccinated:2021-06-15
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Asthenia, Blood test, Computerised tomogram, Dyspnoea, Fibrin D dimer, Fibrin D dimer increased, Headache, Hyperhidrosis, Laboratory test abnormal, Pyrexia, Rash erythematous, X-ray
SMQs:, Anaphylactic reaction (narrow), Haemorrhage laboratory terms (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210623; Test Name: blood levels; Result Unstructured Data: Test Result:Normal; Test Date: 20210623; Test Name: CT SCAN OF LUNGS; Result Unstructured Data: Test Result:NEGATIVE; Test Date: 20210623; Test Name: D dimer; Result Unstructured Data: Test Result:not normal; Test Date: 20210623; Test Name: X- RAYS; Result Unstructured Data: Test Result:fever
CDC Split Type: USPFIZER INC2021787557

Write-up: D dimer that was not normal; shortness of breath; fever; Blood levels were not normal; headache persisted for 6-8 days; sweats; red circles over body that initially looked like rashes. The circles (dots, bumps) persist about long contact. They disappear and look like bruises.; loss of energy; This is a spontaneous report from a contactable consumer or other non-health care professional. A 50-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 15Jun2021 as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On 23Jun2021, the patient experienced went to urgent care on 23Jun2021 having some symptoms, shortness of breath.They did x-rays was also having a fever. Blood levels were not normal. D dimer that was not normal. States headache persisted for 6-8 days and included sweats. Following the visit to the Urgent Care he was given antibiotics and the shortness of breath improved on 24Jun2021. States he still has a little bit of headache and still has sweats. Also red circles over body that initially looked like rashes. The circles (dots, bumps) persist about long contact.They disappear and look like bruises. She indicates it was not hives. Since Wednesday. Also, indicates loss of energy.Stated odd adverse events. Called yesterday and reported to clinic. She is asking if he should receive second dose? Potential duplicate AE. Sent to emergency room for CT scan of the lungs, which was negative. Therapeutic measures were taken as a result of shortness of breath, headache persisted for 6-8 days and sweats. The adverse events shortness of breath, D dimer that was not normal and fever resulted in emergency room visit. The patient underwent lab tests and procedures which included blood test: normal, computerised tomogram: negative, fibrin d dimer: not normal on 23Jun2021 and x-ray: fever on 23Jun2021. Caller asked that if her partner is fully inoculated should he not receive second dose. The clinical outcome of the events D dimer that was not normal, fever, Blood levels were not normal , red circles over body that initially looked like rashes. The circles (dots, bumps) persist about long contact. They disappear and look like bruises and loss of energy was reported as unknown while for event shortness of breath reported as recovering and for headache persisted for 6-8 day and sweats reported as not recovered. Information about Lot/batch number has been requested


VAERS ID: 1456704 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Louisiana  
Vaccinated:2021-05-20
Onset:2021-06-01
   Days after vaccination:12
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Circumstance or information capable of leading to medication error, Haemorrhage subcutaneous, Rash macular
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Hypersensitivity (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021797379

Write-up: Gets black spots and it gets better. He states it is kind of bloody under there; broke out with red spots on quite a bit of his body; Did not take the follow up vaccination; This is a spontaneous report received from a contactable consumer or other non hcp. A male patient of an unspecified age received bnt162b2 (Pfizer vaccine, Formulation: solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 20May2021 as dose 1, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. On Unspecified date of Jun2021, the patient experienced that he gets black spots and it gets better. he states it is kind of bloody under there, broke out with red spots on quite a bit of his body, did not take the follow up vaccination. Patient did not received treatment for adverse events. Caller didn''t provide his mail address and doesn''t know whether his condition is serious or not. The outcome of the events was unknown. Additional Context: Caller states he is calling about the vaccine, the COVID vaccine. Caller took the first dose of the vaccine on 20May, he states 2 weeks after he broke out with red spots on quite a bit of his body. His doctor said he should come in to let him look at it. He didn''t know the regimen to do anything about it. He still has it though, it gets black spots and it gets better. He states it is kind of bloody under there. Caller states he did not take the follow up vaccination because his doctor recommended him not to. Caller is wondering if he should still have it. He is wondering if he should be able to take the other part of the vaccine. He does not know if he should do something about the spots. Caller states they have not really worsened. He states he does not have too much time, he could could call back at a different time to complete a safety report. The main question he is interested in is to know if doing nothing about these spots, is that alright. Are they going to go away, are they going to cause any damage. Rather than trying to figure out if he can receive the second shot or not. He guesses he has to do what the doctor says, he is seeing him again on the 7th. He didn''t suggest putting anything on them and was not concerned what so ever. He does not know if it is ok for us to contact him should we have further questions about this report. He does go to a doctor and if its a controversy and this is something else. He doesn''t want to be in a situation. Information on the lot/batch, further information has been requested.


VAERS ID: 1456709 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Male  
Location: New York  
Vaccinated:2021-06-19
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0180 / 2 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Inflammation, Myocarditis
SMQs:, Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021807456

Write-up: Myocarditis; Her son still has some inflammation; This is a spontaneous report from a contactable other hcp (Patients mother). A 14-years-old male patient received bnt162b2 (BNT162B2, Batch/Lot Number: EW0180 and Expiry Date: 19Jun2021), dose 2 via an unspecified route of administration, administered in Arm Left on 19Jun2021 as single dose for covid-19 immunisation. Patient previously received dose 1 of bnt162b2 (BNT162B2, Lot number: EW0178 and Expiration Date : Unknown to caller ) via an unspecified route of administration on 29May2021 as single dose for covid-19 immunization. The patient''s medical history was not reported. There were no concomitant medications. On 21Jun2021, The patient experienced myocarditis, About 2 days later, he was taken by ambulance to the ER, diagnosed with Myocarditis and admitted to the hospital, discharged on 23Jun2021. Caller states that she believes her son still has some inflammation, it is better but still ongoing, as he is still unable to exert himself at all. The claims are not in yet but it looks like they will be spending 5000 to 6000 dollar out of pocket. She is looking for some type of compensation for their expenses. Patient had no other vaccines on the same day as the suspect product. Myocarditis lead to Emergency Room. The outcome of the event myocarditis was recovering and inflammation was not recovered.; Sender''s Comments: As per the information provided in the narrative, the causal association between the suspect drug and the event cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.


VAERS ID: 1456759 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: California  
Vaccinated:2021-06-11
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 037CZ1A / 1 LA / SYR

Administered by: Private       Purchased by: ?
Symptoms: Discomfort, Limb discomfort, Lymphadenopathy, Pain, Pain in extremity, Sleep disorder, Swelling
SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: H1N1 vaccine years ago, worst body aches of my life. Lasted 24 hours.
Other Medications: None
Current Illness: none
Preexisting Conditions: asthma, chronic anemia, low vitamin D
Allergies: Allergies to shellfish, sensitivity to English walnuts family of nuts, roaches, pollen, gardenia flowers, sensitivity to latex.
Diagnostic Lab Data: None
CDC Split Type:

Write-up: About a week after the injection I started to feel a discomfort on my left side in the arm pit area. Felt like it was swollen and it felt uncomfortable to lie down on my right side because my left arm was causing pressure on my arm pit area. I felt minor pain/discomfort on left hand as well, the discomfort would radiate from my arm pit to my pinky finger and back. By the second week the pain/discomfort was more noticeable during the day and night time. It was not constant, but it would appear during the day. The third week I had one day (6/9/21) were the pain/discomfort caused me to not be able to sleep. I looked at my arm pits, they did not look swollen, but they felt swollen. By then both of my arm pits were now feeling discomfort but the left was more intense then the right side. I feel like the left side has swollen lymph nodes. I did not do anything but report. Did not take tylenol or anything medications for the discomfort.


VAERS ID: 1456977 (history)  
Form: Version 2.0  
Age: 14.0  
Sex: Female  
Location: Maryland  
Vaccinated:2021-06-11
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EW0186 / 2 LA / SYR

Administered by: Public       Purchased by: ?
Symptoms: Dysmenorrhoea, Heavy menstrual bleeding, Menstruation irregular
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Fertility disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Amtrytilline 40mg, Multi vitamin w/iron, Naproxen (PRN), Mili, Meclazine (PRN)
Current Illness: None
Preexisting Conditions: Migraines, low platelets
Allergies: Aloe, Prochlorperazine, Adhesive
Diagnostic Lab Data: None
CDC Split Type:

Write-up: Regular period started on June 8th. Period lasted for 3 weeks after receiving vaccine. She then started her period again June 28th. Periods have been heavier than normal with increased cramping.


VAERS ID: 1457016 (history)  
Form: Version 2.0  
Age: 74.0  
Sex: Female  
Location: Pennsylvania  
Vaccinated:2021-06-01
Onset:2021-06-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Pharmacy       Purchased by: ?
Symptoms: Lip swelling, Pruritus, Swelling face
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Propranolol, biotin, fluoxetine, Valisone, Premarin, Synthroid, Zyrtec
Current Illness:
Preexisting Conditions: Hypothroidism, hyperlipidemia, ostepenia, anxiety, GERD
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up: Itching, face swelling , lips swelling


VAERS ID: 1457028 (history)  
Form: Version 2.0  
Age: 71.0  
Sex: Male  
Location: California  
Vaccinated:2021-03-28
Onset:2021-06-01
   Days after vaccination:65
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8732 / 2 RA / IM

Administered by: Other       Purchased by: ?
Symptoms: Aphasia, Bell's palsy, Dizziness, Facial asymmetry, Hypoaesthesia, Vision blurred, Visual impairment
SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Hearing impairment (broad), Vestibular disorders (broad), Hypoglycaemia (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Prostate cancer (CMS/HCC) 2005 s/p prostatectomy ? Right inguinal hernia ? Urinary incontinence mild
Allergies: Scallops
Diagnostic Lab Data: Seen in Emergency Department on 07/02/21 07/07/21 Seen by Nurse practioner in a neurology clinic
CDC Split Type:

Write-up: Left sided Bell''s palsy Eyes: Positive for visual disturbance ( Blurred vision in the right eye Neurological: Positive for dizziness ( When he closes eyes.), facial asymmetry ( Left-sided facial droop), speech difficulty and numbness ( To the right side of the face). Negative for weakness and headaches.


VAERS ID: 1457116 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Alabama  
Vaccinated:2021-01-14
Onset:2021-06-01
   Days after vaccination:138
Submitted: 0000-00-00
Entered: 2021-07-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 041L20A / 1 LA / SYR
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 004M20A / 2 LA / SYR

Administered by: Work       Purchased by: ?
Symptoms: Antinuclear antibody positive, Arthralgia, Blood uric acid increased, Inflammation, Red blood cell sedimentation rate increased
SMQs:, Systemic lupus erythematosus (narrow), Arthritis (broad), Tumour lysis syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Pantoprazole, Metoprolol, Trazodone, Venlaxafine, Vitamin D, Probiotic, Losartan HCTZ, motrin
Current Illness: NA
Preexisting Conditions: Hypertension, high cholesterol, obesity
Allergies: NA
Diagnostic Lab Data: Positive ANA 6/29/2021, high sed rate and uric acid. Not sure if it is related but I have never had these inflammatory markers prior to vaccine.
CDC Split Type:

Write-up: Joint pain started a couple of months after the second dose. Inflammation increases


Result pages: prev   175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 239 240 241 242 243 244 245 246 247 248 249 250 251 252 253 254 255 256 257 258 259 260 261 262 263 264 265 266 267 268 269 270 271 272 273 274 275 276 277 278 279 280 281 282 283 284 285 286 287 288 289 290 291 292 293 294 295 296 297 298 299 300 301 302 303 304 305 306 307 308 309 310 311 312 313 314 315 316 317 318 319 320 321 322 323 324 325 326 327 328 329 330 331 332 333 334 335 336 337 338 339 340 341 342 343 344 345 346 347 348 349 350 351 352 353 354 355 356 357 358 359 360 361 362 363 364 365 366 367 368 369 370 371 372 373   next

New Search

Link To This Search Result:

https://medalerts.org/vaersdb/findfield.php?EVENTS=ON&PAGENO=274&PERPAGE=100&ESORT=ONSET-DATE&REVERSESORT=ON&VAX=COVID19&DIED=No


Copyright © 2021 National Vaccine Information Center. All rights reserved.
21525 Ridgetop Circle, Suite 100, Sterling, VA 20166