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From the 1/14/2022 release of VAERS data:

Found 8,620 cases where Age is Unknown and Vaccine targets COVID-19 (COVID19) and Symptom is Acute endocarditis or Atypical mycobacterium pericarditis or Autoimmune myocarditis or Bacterial pericarditis or Carditis or Endocarditis or Endocarditis bacterial or Endocarditis enterococcal or Endocarditis noninfective or Endocarditis staphylococcal or Endocarditis viral or Eosinophilic myocarditis or Fungal endocarditis or Giant cell myocarditis or Immune-mediated myocarditis or Lupus endocarditis or Lyme carditis or Meningococcal carditis or Myocarditis or Myocarditis bacterial or Myocarditis infectious or Myocarditis septic or Myopericarditis or Pericarditis or Pericarditis constrictive or Pericarditis infective or Pericarditis lupus or Pericarditis meningococcal or Pericarditis rheumatic or Pericarditis tuberculous or Pleuropericarditis or Purulent pericarditis or Streptococcal endocarditis or Subacute endocarditis or Viral myocarditis or Viral pericarditis

Government Disclaimer on use of this data



Case Details

This is page 22 out of 862

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VAERS ID: 1908592 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: California  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-11-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: 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? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101617599

Write-up: myocarditis; This is a spontaneous report from a Pfizer-sponsored program. No patient identifiers were provided but the reporter has firsthand knowledge of the patient and was reporting on a specific patient. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiration date were not reported) via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunization. Medical history and concomitant medications were not reported. On an unspecified date, the patient experienced myocarditis. Reporter called in regards to CEO withheld and spreading misinformation on the covid-19 vaccine, and they are criminals. Also paid 2.3 billion in fraudulent marketing in 2009. Complaints of kids being killed from having the covid-19 vaccine and will not inject his children with chemicals. Also stated that we should be killed for doing that. States that he knows people that have died from the Pfizer covid-19 vaccine and has a friend that was treated for myocarditis after the vaccine. The outcome of the event was unknown. This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts completed. No further information is expected.


VAERS ID: 1919533 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / 1 - / -

Administered by: Other       Purchased by: ?
Symptoms: 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? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USJNJFOC20211203875

Write-up: MYOCARDITIS; This spontaneous report received from a consumer via a company representative via social media post concerned a female of unspecified age, race and ethnic origin. 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 (series 1) (suspension for injection, route of admin not reported, batch number: Unknown and expiry: unknown) dose, start therapy date were not reported. 1 total, administered for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot number. No concomitant medications were reported. On an unspecified date, the patient experienced myocarditis. The action taken with Covid-19 vaccine ad26.cov2.s was not applicable. The outcome of myocarditis was not reported. This report was serious (Other Medically Important Condition).; Sender''s Comments: V0: 20211203875 -JANSSEN COVID-19 VACCINE Ad26.COV2.S- Myocarditis. 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: 1919654 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Maine  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Cardiac telemetry, Echocardiogram, Ejection fraction, Electrocardiogram, Investigation, Magnetic resonance imaging heart, Myocarditis, SARS-CoV-2 test, Troponin T
SMQs:, Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Crohn''s disease (well-controlled, not prescribed any medications)
Allergies:
Diagnostic Lab Data: Test Name: telemetry; Result Unstructured Data: Test Result:without any arrhythmias observed; Test Name: Echo; Result Unstructured Data: Test Result:significant for low normal left ventricular ejecti; Comments: significant for low normal left ventricular ejection fraction (LVEF) of 50%; Test Name: left ventricular ejection fraction; Test Result: 50 %; Comments: low normal; Test Name: left ventricular ejection fraction; Test Result: 56 %; Test Name: EKG; Result Unstructured Data: Test Result:no ischemic changes; Comments: did not show any ischemic changes; Test Name: EKG; Result Unstructured Data: Test Result:lateral ST elevation; Comments: lateral ST elevation myocardial infarction; Test Name: Tick panel (for Lyme, anaplasmosis, babesiosis, and ehrlichiosis); Test Result: Negative ; Test Name: Cardiac MRI; Result Unstructured Data: Test Result:LVEF = 56%, consistent with myocardial edema (T2 m; Comments: LVEF = 56%, consistent with myocardial edema (T2 mapping) and myocardial injury (focal late gadolinium enhancement (LGE)) with multiple foci in the midwall; Test Name: COVID-19 polymerase chain reaction (PCR); Test Result: Negative ; Test Name: Troponin T; Result Unstructured Data: Test Result:0.74 ng/ml; Comments: peaked
CDC Split Type: USPFIZER INC202101619992

Write-up: Myocarditis; This is a literature report. A 25-year-old male with well-controlled Crohn''s disease (not prescribed any medications) presented to the emergency department with chest pain. The chest pain began the day prior to presentation, worse with inspiration and with associated jaw pain. He reported that he received his second dose of the COVID-19 vaccine (BNT162b2 Pfizer/BioNTech) four days prior to presentation. He experienced malaise and myalgias that resolved within twenty-four hours after receiving the vaccine. Labs were significant for a Troponin T that peaked at 0.74 ng/ml (reference < 0:2 ng/ml). Tick panel (for Lyme, anaplasmosis, babesiosis, and ehrlichiosis) was negative since these are part of the differential work-up of myocarditis. His electrocardiogram did not show any ischemic changes, and echocardiogram was significant for low normal left ventricular ejection fraction (LVEF) of 50%. He was admitted for further work-up and started on colchicine and ibuprofen for presumed myopericarditis. He underwent cardiac MRI which showed a left ventricular fraction of 56% and findings consistent with myocarditis with myocardial edema seen by T2 mapping and myocardial injury with focal late gadolinium enhancement (LGE) with multiple foci in the midwall. He did not have evidence of pericardial inflammation. He did not undergo endomyocardial biopsy. COVID-19 polymerase chain reaction (PCR) was negative. During his hospital stay, he was monitored on telemetry without any arrhythmias observed. He was discharged on low-dose beta-blocker with plans for repeat outpatient echocardiogram and cardiac monitor to screen for any arrhythmias as well as activity restriction. Authors describe three cases of myocarditis in young, healthy patients following COVID-19 vaccine administration. The temporal timing of the cases correlates with similar reports in literature of myocarditis occurring 12-96 hours following immunization with an mRNA COVID-19 vaccine. These cases demonstrate a similar temporal relationship, increasing the likelihood of causality. This safety signal was not clinically apparent in the early vaccine experience, raising the possibility that the association is purely coincidental as viruses responsible for myocarditis follow a seasonal distribution. All three patients were ruled out for COVID-19 infection using the Centers for Disease Control and Prevention- (CDC-) approved gold standard test: polymerase chain reaction (PCR). Previous reports had demonstrated an association between COVID-19 infection and myocarditis. Routine antigen or antibody testing is not part of the clinical work flow, and some have questioned the utility of antibody testing in the post vaccination cohort. Conclusion: There have been early reports of a presumed link between COVID-19 vaccination and subsequent development of myocarditis, but no causative link has been established. The cases add to others where a temporal relationship between vaccination and myocarditis has been described. Ultimately, further exploration of this clinical phenomenon is warranted. Clinical course: EKG: lateral ST elevation myocardial infarction. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Sender''s Comments: As there is limited information in the case provided, the causal association between the event myocarditis and the suspect drug BNT162N2 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.,Linked Report(s) : US-PFIZER INC-202101620016 Same article/ drug/event and different patient


VAERS ID: 1919655 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Maine  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Angiocardiogram, C-reactive protein, Ejection fraction, Electrocardiogram, Investigation, Laboratory test, Magnetic resonance imaging heart, Myocarditis, Red blood cell sedimentation rate, SARS-CoV-2 test, Troponin T
SMQs:, Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (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:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Hospitalization; Obesity
Allergies:
Diagnostic Lab Data: Test Name: coronary angiogram; Result Unstructured Data: Test Result:showed no luminal irregularities; Test Name: C-reactive protein (CRP); Result Unstructured Data: Test Result:68.6 mg/l; Comments: peak; Test Name: ejection fraction; Test Result: 56 %; Comments: left ventricular ejection fraction of 56%; Test Name: electrocardiogram; Result Unstructured Data: Test Result:lateral ST elevation myocardial infarction; Test Name: telemetry; Result Unstructured Data: Test Result:he was monitored on telemetry without any; Comments: arrhythmias observed; Test Name: catheterization laboratory; Result Unstructured Data: Test Result:showed no luminal irregularities; Test Name: cardiac MRI; Result Unstructured Data: Test Result:showed a left ventricular ejection fraction of; Comments: 56% and evidence of myocarditis with myocardial edema demonstrated on T2 mapping and myocardial injury with focal LGE in the basal inferior, mid to distal lateral/inferolateral walls; Test Name: Erythrocyte Sedimentation Rate (ESR); Result Unstructured Data: Test Result:19; Comments: mm/h; Test Name: COVID-19 PCR; Test Result: Negative ; Test Name: Troponin T peak; Result Unstructured Data: Test Result:1.42 ng/ml
CDC Split Type: USPFIZER INC202101620016

Write-up: Myocarditis; This is a literature report. A 28-year-old male with a medical history significant for obesity presented with chest pain and lateral ST elevation myocardial infarction by electrocardiogram. He was taken to the catheterization laboratory, and coronary angiogram showed no luminal irregularities. On interview, he reported receiving his second dose of COVID-19 vaccine (NT162b2 Pfizer/BioNTech) three days prior to presentation. After receiving the vaccine, he experienced fatigue, chills, and myalgias that resolved the day before presentation. Labs were significant for Troponin T peak of 1.42 ng/ml, C-reactive protein (CRP) peak of 68.6mg/l (reference < 8:0mg/l), and Erythrocyte Sedimentation Rate (ESR) of 19mm/h (reference < 15 mm/h). He underwent cardiac MRI which showed a left ventricular ejection fraction of 56% and evidence of myocarditis with myocardial edema demonstrated on T2 mapping and myocardial injury with focal LGE in the basal inferior, mid to distal lateral/inferolateral walls. He also did not undergo endomyocardial biopsy, and COVID-19 PCR was negative. During his hospital stay, he was monitored on telemetry without any arrhythmias observed. He was discharged on low-dose beta blocker and activity restriction with plan for continued outpatient follow-up. Authors describe three cases of myocarditis in young, healthy patients following COVID-19 vaccine administration. The temporal timing of the cases correlates with similar reports in literature of myocarditis occurring 12-96 hours following immunization with an mRNA COVID-19 vaccine. These cases demonstrate a similar temporal relationship, increasing the likelihood of causality. This safety signal was not clinically apparent in the early vaccine experience, raising the possibility that the association is purely coincidental as viruses responsible for myocarditis follow a seasonal distribution. All three patients were ruled out for COVID-19 infection using the Centers for Disease Control and Prevention- (CDC-) approved gold standard test: polymerase chain reaction (PCR). Previous reports had demonstrated an association between COVID-19 infection and myocarditis. Routine antigen or antibody testing is not part of the clinical work flow, and some have questioned the utility of antibody testing in the post vaccination cohort. Conclusion: There have been early reports of a presumed link between COVID-19 vaccination and subsequent development of myocarditis, but no causative link has been established. The cases add to others where a temporal relationship between vaccination and myocarditis has been described. Ultimately, further exploration of this clinical phenomenon is warranted. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Sender''s Comments: Based on the information provided in the narrative, a causal association between the suspect drug and the event cannot be completely 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.,Linked Report(s) : US-PFIZER INC-202101619992 Same article/ drug/event and different patient


VAERS ID: 1922982 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Myocarditis, Ventricular extrasystoles
SMQs:, Ventricular tachyarrhythmias (narrow), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypokalaemia (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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101631177

Write-up: myocarditis; PVC (premature ventricular contraction); This is a spontaneous report received from a contactable reporter (Other HCP) from medical information team. A 6 year-old female patient received bnt162b2 (COMIRNATY) (Batch/Lot number: unknown) as dose number unknown, single for covid-19 immunisation. The patient''s relevant medical history and concomitant medications were not reported. The following information was reported: MYOCARDITIS (medically significant), outcome "unknown", described as "myocarditis"; VENTRICULAR EXTRASYSTOLES (medically significant), outcome "unknown", described as "PVC (premature ventricular contraction)". Child that was sent to hospital on Saturday, crushing chest pain, diagnosed with myocarditis and PVC. The lot number for bnt162b2 was not provided and will be requested during follow up.; Sender''s Comments: A causal association between BNT162B2 and the reported events cannot be excluded based on temporal relationship. 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 RAs, Ethics Committees, and Investigators, as appropriate., Linked Report(s) : US-PFIZER INC-202101626263 same reporter and vaccine, different patient and AE


VAERS ID: 1923506 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER8727 / 3 LA / IM

Administered by: Unknown       Purchased by: ?
Symptoms: Catheterisation cardiac, Magnetic resonance imaging heart, 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? 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: Heart Cath and heart MRI
CDC Split Type:

Write-up: Mtocarditis


VAERS ID: 1938546 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Atrioventricular block, Blood test, Cardiac stress test, Chest pain, Chills, Crying, Decreased appetite, Dehydration, Drug ineffective, Dry mouth, Dry skin, Echocardiogram, Electrocardiogram, Fatigue, Feeling abnormal, Feeling hot, Fungal infection, Heart rate increased, Hyperhidrosis, Immobilisation syndrome, Lethargy, Loss of consciousness, Malaise, Mental disorder, Myocarditis, Nausea, Pain, Palpitations, Pyrexia, Sinus arrhythmia, Sleep disorder, Somnolence, Suspected COVID-19, Weight, Weight decreased, X-ray
SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Lack of efficacy/effect (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Disorders of sinus node function (narrow), Conduction defects (narrow), Dementia (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Depression (excl suicide and self injury) (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Dehydration (narrow), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (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:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Anxiety; Hair thinning; Hyperthyroidism (stress induced, disappeared with beta blocer); Immunocompromised; Insomnia; Obesity; Stress
Allergies:
Diagnostic Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:she didn''t see it as inflammation; Test Name: stress test; Result Unstructured Data: Test Result:Unknown Results; Comments: Had two past, stress test; Test Name: echo; Result Unstructured Data: Test Result:unknown result; Test Name: EKG; Result Unstructured Data: Test Result:sinus arrhythmia; Test Name: body weight; Result Unstructured Data: Test Result:lost 5 pounds; Test Name: x-ray; Result Unstructured Data: Test Result:she didn''t see it as inflammation
CDC Split Type: USPFIZER INC202101313532

Write-up: It was honestly- covid. Being sick and miserable.; It was honestly- covid. Being sick and miserable.; passed out; , myocarditis that to her personally is what she feels she had; tired like I have always am because of lack of sleep and sleeping problems; feel more dehydrated that I do from the beta blocker; I feel every day I feel hot; my heart rate periodically goes up; I starts to sweat; I go very sick/feel sick; my mouth gets very dry; I get very dry; I am getting even less sleep than I normally get; feel more lethargic; higher heart rate; has sweats; light fever; a little sleepy; got chills hot and cold; ached; heart pounding; felt crappy; nauseous; Yeast infection so much; mental breakdowns, crying hysterically; mental breakdowns, crying hysterically; lost her appetite; immobilized; sinus arrhythmia; she had lost 5 pounds; showed AV block; chest pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A female patient received bnt162b2 (BNT162B2) (Batch/Lot number: unknown) as dose 1, single and (Batch/Lot number: unknown) as dose 2, single for covid-19 immunisation. Relevant medical history included: "stress" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "hyperthyroid" (unspecified if ongoing), notes: stress induced, disappeared with beta blocer; "obese" (unspecified if ongoing); "hair thin" (unspecified if ongoing); "insomnia" (unspecified if ongoing); "immunocompromised" (unspecified if ongoing). The patient''s concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant), outcome "recovered" (Jan2021) and all described as "It was honestly- covid. Being sick and miserable."; LOSS OF CONSCIOUSNESS (medically significant), outcome "recovered" (Jan2021), described as "passed out"; MYOCARDITIS (medically significant), outcome "recovered" (Jan2021), described as ", myocarditis that to her personally is what she feels she had"; FATIGUE (non-serious), outcome "recovered" (Jan2021), described as "tired like I have always am because of lack of sleep and sleeping problems"; DEHYDRATION (non-serious), outcome "recovered" (Jan2021), described as "feel more dehydrated that I do from the beta blocker"; FEELING HOT (non-serious), outcome "recovered" (Jan2021), described as "I feel every day I feel hot"; HEART RATE INCREASED (non-serious), outcome "recovered" (Jan2021), described as "my heart rate periodically goes up"; HYPERHIDROSIS (non-serious), outcome "recovered" (Jan2021), described as "I starts to sweat"; MALAISE (non-serious), outcome "recovered" (Jan2021), described as "I go very sick/feel sick"; DRY MOUTH (non-serious), outcome "recovered" (Jan2021), described as "my mouth gets very dry"; DRY SKIN (non-serious), outcome "recovered" (Jan2021), described as "I get very dry"; SLEEP DISORDER (non-serious), outcome "recovered" (Jan2021), described as "I am getting even less sleep than I normally get"; LETHARGY (non-serious), outcome "recovered" (Jan2021), described as "feel more lethargic"; HEART RATE INCREASED (non-serious), outcome "recovered" (Jan2021), described as "higher heart rate"; HYPERHIDROSIS (non-serious), outcome "recovered" (Jan2021), described as "has sweats"; PYREXIA (non-serious), outcome "recovered" (Jan2021), described as "light fever"; SOMNOLENCE (non-serious), outcome "recovered" (Jan2021), described as "a little sleepy"; CHILLS (non-serious), outcome "recovered" (Jan2021), described as "got chills hot and cold"; PAIN (non-serious), outcome "recovered" (Jan2021), described as "ached"; PALPITATIONS (non-serious), outcome "recovered" (Jan2021), described as "heart pounding"; FEELING ABNORMAL (non-serious), outcome "recovered" (Jan2021), described as "felt crappy"; NAUSEA (non-serious), outcome "recovered" (Jan2021), described as "nauseous"; FUNGAL INFECTION (non-serious), outcome "recovered" (Jan2021), described as "Yeast infection so much"; MENTAL DISORDER (non-serious), CRYING (non-serious), outcome "recovered" (Jan2021) and all described as "mental breakdowns, crying hysterically"; DECREASED APPETITE (non-serious), outcome "recovered" (Jan2021), described as "lost her appetite"; IMMOBILISATION SYNDROME (non-serious), outcome "recovered" (Jan2021), described as "immobilized"; SINUS ARRHYTHMIA (non-serious), outcome "recovered" (Jan2021), described as "sinus arrhythmia"; WEIGHT DECREASED (non-serious), outcome "recovered" (Jan2021), described as "she had lost 5 pounds"; ATRIOVENTRICULAR BLOCK (non-serious), outcome "recovered" (Jan2021), described as "showed AV block"; CHEST PAIN (non-serious), outcome "recovered" (Jan2021), described as "chest pain". The patient underwent the following laboratory tests and procedures: blood test: she didn''t see it as inflammation; cardiac stress test: unknown results, notes: Had two past, stress test; electrocardiogram: sinus arrhythmia; x-ray: she didn''t see it as inflammation; echocardiogram: unknown result.. Patient took the booster and regrets taking it when she did and she went through similar side effect tha she had when she first took the vaccine and then it subsided. Patient first took it and then it subsided but unfortunately patient took it when patient took the fresh pack of birth control that patient hadnt taken in a while, its a full strength of birth control because the pharmacy sent me sun damaged birth control and patient was stupid and dumb and put trash in my body. And the same week patient got the booster patient started the birth control and patient have been feeling really sick obviously when, in my early 40s but patient dont believe patient am going to menopause but usually when you dont have enough estrogen in your body is when you are going to be sick but patient am feeling sick when patient am taking full strength of the birth control (Unspecified birth control pills). So thats strange and it doesnt make sense and patient dont know whats going on with my body ever since patient got the shot. Patient have been feeling, patient mean actually patient felt better after certain day and then Friday after patient took it on Tuesday patient had a really bad side effect, patient was hot and cold, hot and cold, and then patient had a really bad blood effect. Patient took it on Tuesday and then on Friday patient was sweating profusely and then ever since then patient just keep sweating every day and sweating and then the sweating stopped and then patient just started, after the sweating stopped patient am just hot. And my heart rate keep going up and it keep waking me up, my heart rate is pounding out of my chest and its hurting my chest and so, patient dont know if it was the birth control that was causing it but everybody is like oh no usually when you dont have enough estrogen that''s when your body is going to go crazy and have these symptoms, not when you starts putting the estrogen back into your body. And so patient don''t (voice not clear) for million years, patient didn''t take too much not being one (voice not clear) for 2 month. But unfortunately patient took your dose right when patient started the fresh pack after 2 month patient didnt have the vaccine (incomplete sentence). So, patient got your shot the same time when patient resume taking my birth control and ever since patient took it patient feel more dehydrated that patient do from the beta blocker (Unspecified medications) that patient take for anxiety not for low blood pressure and patient feel every day patient feel hot throughout the day even though my body temperature is normal patient am feeling hot, but then my heart rate periodically goes up when patient starts to sweat, and patient go very sick and my mouth gets very dry, patient get very dry. And no matter who patient call, if patient go hospital, if patient go there to find out whats going on. Patient hope to god this isnt a permanent side effect, patient am hoping it''s the birth control not the vaccine because patient did so well with it the first time and it was many months before patient took it again, so patient am just stuck in a bad place patient am just miserable and patient cant get better. No one can tell me what to do, patient didn''t take my birth control for 1 day which patient guess is not enough to get it out of my system, if the birth control is causing this but that will be strange for the birth control to cause hot flush, and a higher heart rate and thats usually signs of not getting enough estrogen, so patient am just totally lost and confused, patient dont know what to do. Patient know your machine said you cant give medical advice. So patient dont know if it is even going to benefit me at all since reporting this to you guys. The pharmacy that patient even got this didn''t report patient had to call one of the other location and talk to them and they are like you have to call that pharmacy and report it, they need to report it and them (incomplete sentence). Patient getting even less sleep than patient normally get and patient just feel sick and patient just feel hot and patient just feel like patient cant do anything and its just that patient go to sleep and if patient am lucky enough to fall asleep patient am waking up with my heart pounding. But the pharmacy that patient called right now gave me you guys information but patient wish they, the other pharmacy would have given it to me because then patient would have called you earlier then patient would have been able to get transferred to medical info, now patient have to wait and it''s not fun, its very hard on me. (Voice not clear) has been hard on my body and now oh my god patient rushed to get this when patient should have patient should have been more patience and patient should have been myself, feel more lethargic and tired like patient have always am because of lack of sleep and sleeping problems. And now patient am suffering with pill and patient might, if this is something that''s going to be permanent for rest my life patient am going to like, this is like misery my beta blocker patient take at 3 oclock and then nearly by 7 in morning my heart is pounding out of my chest. And birth control is usually when you dont have estrogen in your body you get the effects not when you are putting that. You seems very noticeable and patient appreciate that and patient am sorry patient am very overwhelmed and nobody will see me nobody will talk to me, nobody will see me, everybody is like just wait it out like how much longer to wait it out. If patient didnt take the birth control yesterday and patient know one day is probably not enough to take it out of my body, it is birth control, it will take more days to take it out of my system but patient am just overwhelmed patient never expected it to happen patient am just really sad right now. Patient am sorry patient am really exhausted. Consumer stated, patient have to start all over again, okay alright patient appreciate your patience letting me to get this out, patient just really wish patient waited, patient really wish patient was afraid patient wouldnt be able to get it and patient am living with 2 geriatric people and patient was afraid patient wouldn''t be able to get it, patient possible just ran, patient should have sit in shower and relax but patient didn''t and now patient am suffering consequences of not listening and taking sun damage birth control for 2 months. Now patient dont know, everybody is like it could be Pfizer, it could be birth control or combination of two, patient just want to feel better, patient just want to feel normal even my normal is so horrible and patient barely, patient don''t get enough sleep and patient feel sick on my beta blockers, at least my normal is lot better that my normal as now. Investigation: EKG (Date: Unspecified, Result / Units: sinus arrhythmia) Additional Context: Report 1 of 2 on caller. Caller is not sure what happened to her, something did and has been to many doctor visits since thinking that she was going into early menopause and she went to OB checked out and is not in early menopause States she has sweats and higher heart rate and whatever that was. States the vaccine is the only other thing States she has been to so many doctor offices and still has to see neurologist and others States she is getting better and she has a suspicion something was done at the pharmacy. With the 1st 2 vaccine she had mild fever, chills and ached and that stopped and everything was fine in early Jan2021, no issue or problems States she has soreness with whole cycle opposed to the last week and she started taking Beta blockers too and thought that so she stopped the birth control that gave soreness, every day she took Advil and she stopped it as well and doesn''t think that was related to that may have been body getting older and OB said lot of people come in with messed up cycles. Has been to cardiology multiple times and has follow up in a few months. Her heart rate went up 1.5 years before and didn''t get it addressed because of Covid and started beta blockers for higher heart rate due to stress She gets heart palpitations and sweats, heart rate 99 in BP cuff and lower when not paying attention so started small dose beta blocker for some relief and did help Caller states she has a lot of stress and anxiety and with her 1st 2 doses in Jan2021 she had side effects for 2 days and they went away, just stopped and was fine and everything was great. States she is considered obese and had no other underlying issues, hyperthyroid is stress induced but that disappeared with beta blocker, her hair is still thin but magically cured and she thinks it''s wrong and inaccurate and didn''t have insurance at the time. She got insurance and was put on T4 drugs subclinical TSH high and T3 T4 low but in range. States on Levoxyl and hair grew back and skin is normal after 1 month and 3 months her hair is thicker and back and then told to stop taking as too high of a dose and she had insomnia but has hair, she tries to go back and forth, she is still under 10 and has thinner hair. States the bloodwork TSH lower than stress induced hyperthyroid and total T4 really high and has never happened before. States she has been tested 2 times since she started the beta blocker and the vaccine and doesn''t think that would change her thyroid it would be the beta blocker. States they gave her the beta blocker for hyper to slow it down so she doesn''t have too much thyroid. States she wishes she had naturally done a decrease for her heartrate because she is sick, weak, foggy and feels dumb and stupid.States they switched her beta blocker and she has less side effects but it doesn''t block her anxiety as well, that stress lowers immunity and the reason she wanted the vaccine was to go out to dinner and she was close to her 8 month vaccine mark. On 21Sep2021, she went to Pharmacy 2 days before it was approved and signed papers saying she was immunocompromised and wasn''t and knows that is wrong and they gave her an intrusive questionnaire and she doesn''t have to divulge information about her health and the tech said she didn''t have to sign or fill out, she could tell she wasn''t happy about her getting the vaccine and she isn''t immunocompromised but she wanted to feel safe before her birthday. She said she was keeping the paperwork and put it in her purse, she is not required to complete it and got a lot of backlash for it and told the tech they had been giving shots a long time. She overheard them talking at the window and the pharmacist said patient know she signed the papers and you have to give it and she was still having issues with her giving the vaccine. All those red flags, she didn''t feel like she should be getting the vaccine, a gut feeling she should change her mind and cancel and didn''t and wishes she had. She went into the room and looked at the vaccine and she knows it''s supposed to be off white and it looked different and may have been her nervousness and feeling like it''s not right It was administered at 6:30pm and she went home like the 1st time and had a light fever and was a little sleepy this time and didn''t mind, she slept a 3 hour nap, she was grateful for that she doesn''t sleep that long. She got chills hot and cold not as bad and Wed felt crappy. Thursday the fever was done and she felt perfectly normal like the 1st time and she thought she was back to where she should be Something happened Friday morning, she woke up and was in a pool of sweat not similar to the vaccine and was drenched in sweat, she was still kind of asleep but aware and was like fighting it and her head was left and right and she passed out and woke up and doesn''t know what time she woke up at noon Still having that sweat all over and her heart rate wasn''t being controlled like it had been since Jan2021 and the same dose for several months, it''s the 2nd beta blocker Atenolol 37.5mg, before that it was half as she wants to take as little as possible. Medication affects her different, less works so why take more she gets less side effects and her doctor gave her permission, he prescribed 50mg once a day and said she could take half. Information provided by caller is discrepant.She had an echo when she went to a sleep pulmonologist and he asked why she is on beta blocker and she said for stress and heart palpitations and sweats at night but they are not the same after the booster She would wake up from those sweats and would go back to normal and be fine, no hot sensation or like she was on fire. Everyone said it was hot flashes, premenopause and they can''t do anything about hot flashes. Something happened and pulmonology did an echo before it all happened and it was perfect, nothing showing at all on that or EKG. She doesn''t sleep a lot with stress with her crazy family. She got the vaccine Tuesday and Wed and Thursday was fine and Friday was burning up and heart rates went in the 90''s and wondered why since she takes a beta blocker and had no control of her heart rate all of a sudden. Caller called her pharmacy and asked if anyone else had a weird reaction from the same vial and was told no no one had a reaction, she did for some reason and it was the entire day her body temperature was 97.8 but she felt completely hot and she couldn''t cool down, she was extremely nauseous and has a fan on her and she didn''t think to take 50 she was on 37.5. Her heart rate is in the 90''s when she wakes up and thank goodness she is on a beta blocker or it would be way over what it is. She is sweating and nauseous and has Promethazine to take as needed with anxiety and IBS and is taking more often that she would have like, it caused dehydration and she is drinking fluids like crazy nonstop to stay hydrated. Was told it lasts 2 weeks in the system and to give it 2 weeks and she was miserable with mental breakdowns, crying hysterically miserable about why her heart rate keeps going up. Everyday it''s like clockwork then down to the 80''s but still feels sick and don''t know why. She couldn''t take it anymore and took 50mg and felt better and didn''t wake up as bad and her heart rate went down for 2 glorious days then next day right back up, it''s not anxiety she knows what that feels like this was heartrate just going up no reason and don''t know why. It has gotten better it''s hard to control it, she has to avoid stress, doesn''t drink a lot of caffeine, she stopped that, reduced sugar intake, hasn''t lost weight with reduced food intake as she lost her appetite. Each day she is sweating so much it''s hard to get mobile or move or anything, she felt immobilized. She saw her primary and was tired and couldn''t communicate that she took 50mg and he ran out of the room so quick so she went to the ER something was wrong. They did EKG and blood and didn''t examine her physically but it''s in the paperwork with wrong symptoms and it was her 1st dose. Had an EKG that had sinus arrhythmia. She was stupid to go to the ER that day, she took more than 50 that day and it didn''t work in a span of 6 hours she took 50 at night and took 2 quarter doses for total of 75mg and went to the ER and it''s cold there so that helped and she was laying down and tired and out of it. She had a slight arrhythmia, not a big deal she was told. She was admitted and they kept coming and saying do you see normal heart rate and yes she because she took 75mgof the blocker of it wouldn''t be normal.Now it has stopped but she had a weird beat and it wasn''t a hand on the chest feeling laying there it was like static over her heart buzzing and buzzing and she can''t read, watch TV or anything the heart rate is so annoying and tried elevating on pillows. She hasn''t had that sensation in a long time.It was very annoying and didn


VAERS ID: 1938750 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Texas  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Angiogram, Blood pressure measurement, C-reactive protein, Chest X-ray, Electrocardiogram, Heart rate, Magnetic resonance imaging, Myocarditis, Oxygen saturation, Physical examination, Red blood cell sedimentation rate, Respiratory rate, Troponin, Ultrasound scan, Vital signs measurement
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? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: coronary computed tomography angiogram (CCTA); Result Unstructured Data: Test Result:high suspicion for myocarditis; Comments: low suspicion for acute coronary syndrome; Test Name: coronary computed tomography angiogram (CCTA); Result Unstructured Data: Test Result:normal coronary origins; Comments: with a coronary artery calcium score of 0; Test Name: Blood pressure; Result Unstructured Data: Test Result:119/79 mmHg; Test Name: Chest x-ray; Result Unstructured Data: Test Result:no acute cardiopulmonary abnormalities; Test Name: C- reactive protein; Test Result: 1.9 mg/dl; Comments: elevated; Test Name: ECG; Result Unstructured Data: Test Result:sub-1-mm lateral ST elevations; Comments: with sub-1-mm depression in lead III; Test Name: ECG; Result Unstructured Data: Test Result:reciprocal depression in lead III; Comments: 1-mm elevations in leads I and aVL; Test Name: Heart rate; Result Unstructured Data: Test Result:90; Comments: Beats/min; Test Name: Cardiac magnetic resonance imaging; Result Unstructured Data: Test Result:diffuse; Comments: subepicardial delayed gadolinium enhancement of the anterior and lateral wall of the left ventricle, with corresponding heterogeneous T1 signal prolongation and increased short tau inversion recovery signal consistent with a high-risk pattern for myocarditis; left ventricular ejection fraction was preserved at 55%; Test Name: Pulse oximetry; Test Result: 97 %; Comments: on room air; Test Name: Physical exam; Result Unstructured Data: Test Result:benign; Comments: including lungs clear to auscultation, no murmurs/rubs/gallops on cardiac examination, and non-reproducible chest pain; Test Name: Erythrocyte sedimentation rate; Result Unstructured Data: Test Result:normal at 14; Comments: mm/h; Test Name: Respiration rate; Result Unstructured Data: Test Result:16; Comments: breaths/min; Test Name: Initial troponin; Result Unstructured Data: Test Result:0.08 ng/ml; Comments: elevated; Test Name: Trended troponins; Result Unstructured Data: Test Result:0.39 ng/ml; Comments: continued to rise, with a peak value of 0.39 ng/mL.; Test Name: Trended troponins; Result Unstructured Data: Test Result:down trended ng/ml; Test Name: Troponin; Result Unstructured Data: Test Result:0.22 ng/ml; Test Name: Ultrasound; Result Unstructured Data: Test Result:trace pericardial effusion; Comments: without wall motion abnormalities; Test Name: Vitals; Result Unstructured Data: Test Result:within normal limits
CDC Split Type: USPFIZER INC202101666566

Write-up: focal myocarditis/chest pain and exertional dyspnea; This is a literature report for the following literature source(s): "STEMI Mimic: Focal Myocarditis in an Adolescent Patient After mRNA COVID-19 Vaccine.", A 17 year-old male patient received bnt162b2 (BNT162B2), administration date 2021 (Batch/Lot number: unknown) as dose 2, single for covid-19 immunisation. The patient''s relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (first dose; manufacturer unknown), for covid-19 immunisation. The following information was reported: MYOCARDITIS (hospitalization, medically significant) with onset 2021, outcome "unknown", described as "focal myocarditis/chest pain and exertional dyspnea". The patient was hospitalized for myocarditis (hospitalization duration: 1 day(s)). The events "focal myocarditis/chest pain and exertional dyspnea" were evaluated at the physician office visit and emergency room visit. In June of 2021, a thin, otherwise healthy 17-year-old male presented to the Emergency Department with 3 days of progressively worsening substernal chest pain and exertional dyspnea that began 1 day after his second BNT162b2 vaccination. He had no family history of premature coronary artery disease. Upon presentation, the patient''s vitals were within normal limits; blood pressure 119/79 mm Hg, heart rate 90 beats/min, respiration rate 16 breaths/min, and pulse oximetry 97% on room air. His physical examination was benign, including lungs clear to auscultation, no murmurs/rubs/gallops on cardiac examination, and non-reproducible chest pain. The patient''s chest x-ray study showed no acute cardiopulmonary abnormalities. The initial electrocardiogram (ECG) showed sub-1-mm lateral ST elevations with sub-1-mm depression in lead III. Bedside ultrasound showed a trace pericardial effusion without wall motion abnormalities. Initial troponin was elevated, at 0.08 ng/mL (normal [nl] < 0.03 ng/mL). Repeat ECG demonstrated 1-mm elevations in leads I and aVL, with reciprocal depression in lead III. At this time, Cardiology was consulted, and a code STEMI was called, given localizing ECG changes meeting STEMI criteria. The patient was given 324 mg of aspirin and sublingual nitroglycerin without improvement in the patient''s chest pain. Intra- venous diltiazem was then administered for concerns of possible coronary vasospasm, without improvement in the patient''s chest pain or normalization of the patient''s ECG. Cardiology elected to obtain a coronary computed tomography angiogram (CCTA), as there was high suspicion for myocarditis and low suspicion for acute coronary syndrome given the patient''s age and lack of risk factors. The CCTA showed normal coronary origins with a coronary artery calcium score of 0. Repeat troponin returned at 0.22 ng/mL. The patient was then admitted to the Cardiology service for suspected myocarditis. C-reactive protein was noted to be elevated at 1.9 mg/dL (nl


VAERS ID: 1938821 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 3 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Chest pain, Dyspnoea, Electrocardiogram, Heart rate, Heart rate increased, Immunisation, Myocarditis, Pericarditis, Troponin
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: EKG blood levels; Result Unstructured Data: Test Result:Unknown results; Test Name: fast beating and heart rate; Result Unstructured Data: Test Result:Unknown results; Test Name: Troponin; Result Unstructured Data: Test Result:Unknown results
CDC Split Type: USPFIZER INC202101732474

Write-up: This is a spontaneous report from a contactable consumer or other non-health care professional via medical information team for a sponsored program. The reporter is the patient. A male patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number: not reported), via unspecified route of administration on unspecified date as DOSE 3 (BOOSTER), SINGLE for COVID-19 immunization. Patient previously received BNT162B2 ((PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number: not reported), via unspecified route of administration on unspecified date as DOSE 1, SINGLE and DOSE 2, SINGLE for COVID-19 immunization. Patient medical history and concomitant medication were not reported. On an unspecified date the patient experienced Pericarditis, Myocarditis, Booster dose, chest pain, shortness of breath, fast beating and heart rate. The patient underwent the following laboratory tests and procedures which includes electrocardiogram, heart rate and troponin with unknown results. Reporter quired for how does the symptoms of chest pain, shortness of breath, fast beating and heart rate associated with Pericarditis and Myocarditis differ from Anxiety. Reporter stated that he received his third dose of the Pfizer Covid-19 vaccine and had no underlying medical condition. Reporter stated that he was trying to figure out how to reliably differentiate these symptoms. Reporter queried for what was the onset or time frame for an individual to develop these condition. Reporter queried for when to seek medical help when they experience such symptoms, to which health care professional does he need to consult with. In response to the query it was provided that referred to health care professional to assess and evaluate his symptoms. Advised the reporter on the likelihood of having Myocarditis based on PI Warnings and attached document. Post marketing data demonstrate increased risks of myocarditis and pericarditis, particularly within 7 days following the second dose. Outcome of events was unknown.


VAERS ID: 1941863 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Michigan  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Cardiac stress test, Echocardiogram, Ejection fraction, Electrocardiogram, Fatigue, Investigation, Magnetic resonance imaging heart, Myocarditis, Pain in extremity, SARS-CoV-2 test negative, Troponin T
SMQs:, Cardiomyopathy (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad), COVID-19 (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? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Name: exercise stress test; Result Unstructured Data: Test Result:normal; Test Name: transthoracic echocardiogram; Result Unstructured Data: Test Result:left ventricular systolic function within normal; Comments: range (ejection fraction of 58%), with no regional wall motion abnormalities and no pericardial effusion; Test Name: transthoracic echocardiogram; Result Unstructured Data: Test Result:normal; Test Name: ejection fraction; Test Result: 58 %; Test Name: ejection fraction; Test Result: 67 %; Test Name: electrocardiography; Result Unstructured Data: Test Result:diffuse ST segment elevation; Test Name: electrocardiography; Result Unstructured Data: Test Result:Normal; Comments: done 4 days after presentation; Test Name: 7 day ambulatory rhythm monitor; Result Unstructured Data: Test Result:25 isolated ventricular ectopic beats; Test Name: cardiac magnetic resonance image; Result Unstructured Data: Test Result:small area of subepicardial late gadolinium; Comments: enhancement but no definite signs of active myocardial inflammation; Test Name: SARS-CoV-2 polymerase chain reaction; Test Result: Negative ; Test Name: cardiac troponin T; Result Unstructured Data: Test Result:1029 pg/mL; Test Name: cardiac troponin T; Result Unstructured Data: Test Result:1273 pg/mL; Test Name: cardiac troponin T; Result Unstructured Data: Test Result:10 pg/mL; Comments: 1 month later was within normal range
CDC Split Type: USPFIZER INC202101627751

Write-up: nonradiating chest pain/ Myocarditis; 1 day of fatigue and arm soreness after vaccination; 1 day of fatigue and arm soreness after vaccination; The initial case was missing the following minimum criteria: unspecified suspect product. Upon receipt of follow-up information on 26Nov2021, this case now contains all required information to be considered valid. This is a literature report. A previously healthy 19-year-old man presented with sudden onset of severe, nonradiating chest pain 3 days after receiving a second dose of a messenger RNA (mRNA) SARS-CoV-2 vaccine. He noted 1 day of fatigue and arm soreness after vaccination, which resolved before the onset of chest pain. There was no associated dyspnea, nausea, or vomiting. Work-up included a negative SARS-CoV-2 polymerase chain reaction test result, electrocardiography with diffuse ST-segment elevation, and high-sensitivity cardiac troponin T level of 1029 pg/mL (reference range, 0 to 19 pg/mL). A transthoracic echocardiogram showed left ventricular systolic function within normal range (ejection fraction of 58%), with no regional wall motion abnormalities and no pericardial effusion. He was admitted and received ibuprofen and colchicine. His pain resolved by the following morning. Troponin T levels peaked the day after presentation at 1273 pg/mL; repeated measure of troponin T level 1 month later was within normal range (10 pg/mL). Echocardiography done 4 days after presentation was normal, with an ejection fraction of 67%. Three months after presentation, the patient was asymptomatic. A 7-day ambulatory rhythm monitor showed 25 isolated ventricular ectopic beats. An exercise stress test was normal. A cardiac magnetic resonance image (MRI) showed a small area of subepicardial late gadolinium enhancement but no definite signs of active myocardial inflammation.; Sender''s Comments: Based on the currently available information the possibility of causal association between the event myocarditis and the suspect drug BNT162B2 cannot be ruled out. 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.


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