National Vaccine
Information Center

Your Health. Your Family. Your Choice.

MedAlerts Home
Search Results

From the 10/15/2021 release of VAERS data:

Found 4,148 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



Case Details

This is page 9 out of 415

Result pages: prev   1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18   next


VAERS ID: 1514452 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Texas  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-07-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT

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: USMODERNATX, INC.MOD20212

Write-up: heart inflammation; This spontaneous case was reported by a consumer and describes the occurrence of MYOCARDITIS (heart inflammation) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced MYOCARDITIS (heart inflammation) (seriousness criterion medically significant). At the time of the report, MYOCARDITIS (heart inflammation) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported. No treatment information was provided. Very limited information regarding this event has been provided at this time. Further information has been requested.; Sender''s Comments: Very limited information regarding this event has been provided at this time. Further information has been requested.


VAERS ID: 1514465 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Pennsylvania  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-07-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Pericarditis
SMQs:, Systemic lupus erythematosus (broad), Chronic kidney disease (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: Comments: No medical history was provided.
Allergies:
Diagnostic Lab Data:
CDC Split Type: USMODERNATX, INC.MOD20212

Write-up: Pericarditis; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by an other health care professional and describes the occurrence of PERICARDITIS (Pericarditis) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No medical history was provided. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PERICARDITIS (Pericarditis) (seriousness criterion medically significant). At the time of the report, PERICARDITIS (Pericarditis) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was provided. Patient commented saying that while she may not have been evaluated for pericarditis as of yet, she has heard of others who have and ER nurses have also mentioned this to her. Very limited information regarding the events has been provided at this time; Sender''s Comments: Very limited information regarding the events has been provided at this time


VAERS ID: 1514469 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Ohio  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-07-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Blood pressure measurement, Body temperature, Catheterisation cardiac, Computerised tomogram, Computerised tomogram coronary artery, Echocardiogram, Ejection fraction, Electrocardiogram, Heart rate, Investigation, Magnetic resonance imaging heart, Myocarditis, Oxygen saturation, Respiratory rate, SARS-CoV-2 test, Troponin, Ultrasound scan
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? Yes
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: SARS-CoV-2 infection (approximately two months prior to the onset of his symptoms); Tobacco user
Allergies:
Diagnostic Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:121/54 mmHg; Test Name: Body temperature; Result Unstructured Data: Test Result:98.4 Fahrenheit; Comments: orally; Test Name: heart catherization; Result Unstructured Data: Test Result:whichwas unremarkable.; Test Name: Cardiac computed tomography; Result Unstructured Data: Test Result:showed a coronary artery calciumscore of zero and; Comments: showed a coronary artery calcium score of zero and no pathology.; Test Name: coronary artery calcium score; Result Unstructured Data: Test Result:zero; Test Name: Inpatient echocardiogram; Result Unstructured Data: Test Result:showed left ventricular ejection fraction (LVEF) 5; Comments: showed left ventricular ejection fraction (LVEF) 59% with no other abnormalities; Test Name: left ventricular ejection fraction; Test Result: 59 %; Test Name: electrocardiogram; Result Unstructured Data: Test Result:ST segment elevation; Comments: diffuse concave ST segment elevations; Test Name: heart rate; Result Unstructured Data: Test Result:113; Comments: beats per minute; Test Name: examination; Result Unstructured Data: Test Result:pain worsened with sitting and improved while lyin; Comments: pain worsened with sitting and improved while lying flat.; Test Name: Cardiac magnetic resonance imaging; Result Unstructured Data: Test Result:positive for myocarditis; Test Name: SpO2; Test Result: 100 %; Comments: on room air.; Test Name: respirations; Result Unstructured Data: Test Result:20; Comments: breaths per minute; Test Name: PCR/SARS CoV-2; Test Result: Negative ; Test Name: SARS-CoV-2; Test Result: Positive ; Test Name: troponin; Result Unstructured Data: Test Result:89 ng/ml; Comments: which increased on repeat examination; Test Name: troponin; Result Unstructured Data: Test Result:108 ng/ml; Comments: increased to a maximum; Test Name: ultrasound; Result Unstructured Data: Test Result:revealed a small pericardial effusion without evid; Comments: revealed a small pericardial effusion without evidence of tamponade, which supported the diagnosis.
CDC Split Type: USPFIZER INC202100910810

Write-up: Myocarditis; This is a literature report. A 20-year old male with no prior medical history presented to the emergency department (ED) with a chief complaint of midsternal chest pain that radiated to the left side. The pain started in the morning and remained while resting. The patient also complained of mild shortness of breath secondary to pain. Upon examination, pain worsened with sitting and improved while lying flat. The patient had received his second dose of the Pfizer-BioNTech (BNT 162b2) vaccination two days prior to the onset of chest pain. The patient denied history of venous thromboembolism or family history of cardiovascular disease. The patient had a history of tobacco use. Approximately two months prior to ED presentation, the patient tested positive for SARS-CoV-2 and recovered with no sequalae. In the ED his initial troponin was 89 ng/L and increased to a maximum of 108 ng/L. The patient tested negative for SARS CoV-2 by PCR. Vital signs revealed blood pressure 121/54 mm/Hg, heart rate 113 beats per minute, temperature 98.4 degree F orally, respirations 20 breaths per minute, SpO2 100% on room air. The patient''s electrocardiogram showed diffuse concave ST segment elevations with PR depressions. (Fig. 1, Note the somewhat diffuse concave ST elevations with PR depressions (V5-V6, II, aVF).). Myocarditis was suspected and bedside ultrasound revealed a small pericardial effusion without evidence of tamponade, which supported the diagnosis. The patient was subsequently given a dose of colchicine 0.6 mg and then admitted to the hospital for further evaluation. Inpatient echocardiogram showed left ventricular ejection fraction (LVEF) 59% with no other abnormalities. The patient underwent left heart catherization which was unremarkable. Cardiac computed tomography showed a coronary artery calcium score of zero and no pathology. Cardiac magnetic resonance imaging was positive for myocarditis. After his chest pain resolved, the patient was discharged with colchicine 0.6 mg for three months, metoprolol XL 12.5 mg daily for three months, and ibuprofen 600 mg three times daily for two weeks. Myocarditis is most often caused by a viral infection; however, other causes include idiopathic, autoimmune, and hypersensitivity. When there is an infectious etiology, patients typically present with flu-like symptoms in addition to chest pain. Myocarditis has also been reported following live viral vaccinations, most notably the smallpox vaccine. From the early 1950s until 2003, six cases of cardiac complications following smallpox vaccination were reported. A campaign to vaccinate personnel against smallpox with the Dry Vax vaccine between 2002 and 2003 resulted in 67 cases of myocarditis or pericarditis out of the 540,824 personnel vaccinated. Due to concern for cardiac complications following smallpox vaccination, a study was conducted to evaluate risk of myocarditis and pericarditis in live viral vaccinations. Of the 416,629 vaccinated adults studied, only one case of pericarditis and zero cases of myocarditis were identified following vaccination. The authors concluded there was no increased risk of myopericarditis following live viral vaccination. While this case demonstrates a clear temporal association of vaccine-related myocarditis and other potential causes of myo-carditis are unlikely, a true cause-and-effect relationship could not be established nor determined. The author hope this case provides emergency medicine physicians additional information on evaluating potential post COVID-19 vaccination myocarditis. Information about lot/batch number cannot be obtained.; Sender''s Comments: Based on the current available information and a possible contributory role of the suspect product BNT162B2 to the development of event myocarditis cannot be totally 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 RAs, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 1514481 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Vermont  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-07-30
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 INC202100917570

Write-up: Myocarditis; This is a spontaneous report from a contactable physician through a Pfizer sales representative. A patient of an unspecified age and gender received BNT162B2 (Pfizer-Biontech Covid-19 Vaccine) at single dose, on an unspecified date, for COVID-19 immunisation. Relevant medical history and concomitant medications were unknown. On an unspecified date, after the vaccination the patient experienced myocarditis. Treatment was received. Clinical outcome of the adverse event was unknown at time of this report. 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 current available limited information and the plausible drug-event association, a possible contributory role of the suspect product BNT162B2 to the development of the event cannot be fully excluded.


VAERS ID: 1517882 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: New York  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-07-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Aortic valve incompetence, Blood bicarbonate, Blood creatine phosphokinase, Blood creatinine, Blood culture, Blood lactic acid, Blood pressure measurement, Body mass index, C-reactive protein, Death, Echocardiogram, Electrocardiogram, Heart rate, Incorrect dose administered, Myocarditis, Off label use, Oxygen saturation, PCO2, PO2, Procalcitonin, Pulmonary arterial wedge pressure, Renal impairment, Respiratory failure, Respiratory rate, Septic shock, Troponin, pH body fluid
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (narrow), Anaphylactic reaction (broad), Retroperitoneal fibrosis (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (broad), Torsade de pointes, shock-associated conditions (broad), Hypovolaemic shock conditions (broad), Toxic-septic shock conditions (narrow), Anaphylactic/anaphylactoid shock conditions (broad), Hypoglycaemic and neurogenic shock conditions (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Hypersensitivity (broad), Tumour lysis syndrome (broad), Respiratory failure (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypokalaemia (broad), Sepsis (narrow), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? Yes
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 8 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: Multiple sclerosis
Preexisting Conditions: Comments: Unknown
Allergies:
Diagnostic Lab Data: Test Name: Heart rate; Result Unstructured Data: 145 bpm; Test Name: Heart rate; Result Unstructured Data: 125 BPM; Test Name: Blood pressure; Result Unstructured Data: 117/70 mmHg; Test Name: Respiratory rate; Result Unstructured Data: 39; Test Name: Body mass index; Result Unstructured Data: 27.5; Test Name: Electrocardiogram; Result Unstructured Data: sinus tachycardia; Test Name: Blood culture; Result Unstructured Data: Negative for all viruses; Test Name: Procalcitonin; Result Unstructured Data: 185.71 ng/mL; Test Name: Troponin; Result Unstructured Data: 1.260-2.050 ng/mL; Test Name: Transthoracic echocardiogram; Result Unstructured Data: 2+ aortic regurgitation and diffuse left ventricular hypokinesis; Test Name: Echocardiogram; Result Unstructured Data: Diffuse left ventricular hypokinesis with severely reduced contraction; Test Name: Pulmonary arterial wedge pressure; Result Unstructured Data: 14 mmHg; Test Name: Creatinine; Result Unstructured Data: 1.21 mg/dL; Test Name: Bicarbonate; Result Unstructured Data: 16 mmol/L; Test Name: Troponin; Result Unstructured Data: <0.010 ng/mL; Comments: reference range =0010 ng/mL; Test Name: Creatine phosphokinase; Result Unstructured Data: 53 U/L; Test Name: Procalcitonin; Result Unstructured Data: 0.07 ng/mL; Test Name: C-reactive protein; Result Unstructured Data: 7.2 mg/L; Test Name: pH; Result Unstructured Data: 7.02; Test Name: Partial pressure CO2; Result Unstructured Data: 94 mmHg; Test Name: PaO2; Result Unstructured Data: 27 mmHg; Test Name: Lactate; Result Unstructured Data: 8.3 mmol/L; Test Name: Creatinine; Result Unstructured Data: worsening; Test Name: Oxygen saturation; Result Unstructured Data: 75 %
CDC Split Type: USJNJFOC20210754113

Write-up: VACCINE INDUCED MYOCARDITIS (VIRAL MYOCARDITIS); ACUTE HYPOXIC HYPERCAPNIC RESPIRATORY FAILURE; SEPTIC SHOCK; DECLINE IN RENAL FUNCTION; 2+ AORTIC REGURGITATION; PATIENT ADMINISTERED WITH 2 DOSES OF VACCINE; OFF LABEL USE; DEATH; This spontaneous report was received from literature: Case report with literature review. This report concerned a 70 year old female. The patient''s height, and weight were not reported. The patient''s concurrent conditions included multiple sclerosis. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown, expiry: unknown), frequency 2 total doses, start therapy date were not reported for prophylactic vaccination. The batch number was not reported and has been requested. No concomitant medications were reported. On an unspecified date, after two days post second dose (inappropriate dose of vaccine administered and off label use) the patient experienced developed dyspnea at home and eventually required an ambulance for hospital transfer. The vital signs on arrival included a heart rate of 145 bpm, a 75% oxygen saturation level on room air, a blood pressure of 117/70 mmHg, a respiratory rate of 39, and a BMI of 27.5. The electrocardiogram (ECG) on admission revealed sinus tachycardia with a heart rate of 125bpm and T-wave inversions in leads V4-V6 without any ST-segment change. The patient arrived at the emergency department in severe respiratory distress that warranted immediate intubation. She was admitted to the intensive care unit (ICU) with the provisional diagnoses of acute hypoxic hypercapnic respiratory failure and septic shock. The laboratory screening and blood culture proved negative for all viruses, Mycoplasma pneumonia, and chlamydophila pneumonia. A repeat investigation revealed marked elevations in procalcitonin [185.71(ng/mL)] and troponin [1.260-2.050 ng/mL] levels on the second day of admission. The patient required multiple vasopressors to maintain the mean arterial pressure above 65 mmHg. The transthoracic echocardiogram on admission revealed 2+ aortic regurgitation and diffuse left ventricular hypokinesis with severely decreased left ventricular ejection fraction (10%). A repeat echocardiogram with contrast medium showed diffuse left ventricular hypokinesis with diagnostic monitoring via Swanz-Ganz catheter revealed a pulmonary wedge pressure (PWP) of 14mmHg. The patient continued receiving vasopressors and antibiotic therapy, while her renal function deterioration since admission warranted the prompt administration of renal replacement therapy. Further decline in renal function was marked by oliguria and worsening of creatinine levels. The patient declined cardiac catheterization and remained. On an unspecified date the patient was hospitalized and it was for 8 days. On unspecified date patient died with vaccine induced myocarditis (viral myocarditis) on eighth day of admission to hospital. The exact cause of death was not reported and it was unknown whether autopsy was performed. The other laboratory data includes, Creatinine (NR: 0.05 - 1.20) 1.21 mg/dL, Bicarbonate (NR: 22 - 29) 16 mmol/L, Creatine phosphokinase (NR: 20 - 190) 53 U/L, Procalcitonin (NR: 0.02 - 0.10) 0.07 ng/mL, C-reactive protein (NR: 0 - 3.00) 7.2 mg/L, pH (NR: 7.35 - 7.45) 7.02 (units unspecified), Partial pressure CO2 (NR: 35 - 48) 94 mmHg, Lactate (NR: 0.6 - 1.4) 8.3 mmol/L, PaO2 (NR: 83 - 108) 27 mmHg, The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of vaccine induced myocarditis (viral myocarditis), acute hypoxic hypercapnic respiratory failure, septic shock, decline in renal function, 2+ aortic regurgitation, patient administered with 2 doses of vaccine, off label use was not reported. This report was serious (Death, Life Threatening, and Hospitalization Caused / Prolonged).; Sender''s Comments: V0: 20210754113-covid-19 vaccine ad26.cov2.s - Death, vaccine induced myocarditis, acute hypoxic hypercapnic respiratory failure, septic shock, decline in renal function, 2+ aortic regurgitation. 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).; Reported Cause(s) of Death: UNKNOWN CAUSE OF DEATH


VAERS ID: 1521986 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: California  
Vaccinated:2021-06-25
Onset:2021-06-01
Submitted: 0000-00-00
Entered: 2021-08-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Arrhythmia, Blister, Cardiac disorder, Chest discomfort, Chest pain, Dizziness, Dyspnoea, Fatigue, Feeling abnormal, Furuncle, Initial insomnia, Irritability, Lethargy, Myocarditis, Pain in extremity, Palpitations, Pericarditis
SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Hostility/aggression (broad), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow), Depression (excl suicide and self injury) (broad), Vestibular disorders (broad), Chronic kidney disease (broad), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (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: ADVILGEL
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Foot surgery
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202100929242

Write-up: when she lays down to go to sleep and her heart starts going boom boom boom; not able to fall asleep very easily because her heart is beating like that, it energizes her and keeps her awake; the heart palpitations are worse when she lays down; chest pains; have a blister/boil on their leg; have a blister/boil on their leg; myocarditis; pericarditis; felt kind of tired, just lethargic; felt kind of tired, just lethargic; arm pain; arrhythmias/ constant arrhythmia; would feel a little bit dizzy; couldn''t quite catch a full breath/ not quite breathing deeply enough or getting enough oxygen; felt a heaviness in her chest; feels lightheaded; crabby; brain fog; This is a spontaneous report from a Pfizer-sponsored program, received from contactable consumer or other non-hcp (Patient). A 65-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection; Batch/Lot Number: Unknown, Expiration date: Unknown) via intramuscular route of administration in Left Arm on 25Jun2021 as dose 1, single for COVID-19 immunization.Medical history included foot operation (surgery once on her foot) from an unknown date and unknown if ongoing.Concomitant medication included ibuprofen (ADVILGEL).In Jun2021, the patient experienced arrhythmias/ constant arrhythmia, would feel a little bit dizzy, couldn''t quite catch a full breath/ not quite breathing deeply enough or getting enough oxygen, felt a heaviness in her chest, feels lightheaded, crabby, brain fog. On an unspecified date, patient experienced myocarditis, pericarditis, when she lays down to go to sleep and her heart starts going boom boom boom, not able to fall asleep very easily because her heart is beating like that, it energizes her and keeps her awake, the heart palpitations are worse when she lays down, chest pains, have a blister/boil on their leg.On 25Jun2021, patient had arm pain.On 26Jun2021, the patient felt kind of tired, just lethargic. The event arrhythmia lead to visit Physician Office. She had a surgery once on her foot where they had to cut her open and the expected time later, they went to take the stitches out and her skin hadn''t even started to mend so they made a mistake. Caller stated this is a big shock to everybody even as she was saying that they need to make sure they look at her and not what they expect to happen to her, and they never listen to her until that happened one day and of course she''s not in a proper place to have her skin opened up left open. Family history None, caller stated there''s no heart arrhythmia issues in her family. Caller stated she didn''t even know what it was until now. Caller stated literally until yesterday when she looked it up. Caller stated her doctor said it sounds like an arrhythmia so she looked it up and every single symptom was like check, check, all of them and what was really interesting to her was that this article specified as WEBMD, specified that its worse, the heart palpitations are worse when she lays down and it was very specific about where she feels the pressure and pain and it said in the middle of the chest, up where the heart is and right below it where the solar plexus is and she''s thinking oh that makes sense, if it''s her heart muscle that''s swollen or the lining that''s swollen and its sitting on her sternum then that makes sense, that area of the sternum has to do with her breast, her lungs too, taking an actual breath. Caller stated it doesn''t feel like her lungs, it''s her heart/chest area, that was interesting to her that its worse when she lays down and that''s when she''s trying to sleep, that'' the nightmare of it. Caller stated she talked to her doctor and a couple of people and they suggested that she call Pfizer to ask these questions because Pfizer knows. Caller stated she knows it''s a work in progress, but the doctors aren''t on top of everything. Caller stated initially, the day after the vaccine, she felt arm pain, felt kind of tired and maybe not even sick just lethargic. Caller stated she wanted to nap a lot, which she did because she kind of didn''t have a choice. Caller stated on 25Jun2021, caller stated her arm started hurting on that same day. Caller stated her being tired started the next day 26Jun2021 and is ongoing and persisting. Caller stated and she has more symptoms and now with the symptoms that have progressed to the arrhythmia. Caller stated along with tiredness, she would feel a little bit dizzy, there was one day she felt like she was going to faint, but she didn''t. Caller stated she felt like she couldn''t quite catch a full breath and then it was a week later. Caller stated it kept going, symptoms got worse, then she felt a heaviness in her chest, she felt like, she''s still feeling it now, like she can''t quite get enough breaths, her lungs don''t bother her, just feels more like chest and solar plexus that area, just feels really heavy and so during the day she feels tired, like she''s not quite breathing deeply enough or getting enough oxygen or something. Caller stated then at night when she lays down to go to sleep and she''s tired, her heart starts going boom, boom and she goes what is that and that''s been going on pretty much every night, what is it a couple of weeks now. Caller stated it happened last night, so she''s not able to fall asleep very easily because her heart is beating like that, it energizes her and keeps her awake and that''s where they are today. Caller stated it all started right after the vaccine. Call confirms all symptoms began in Jun2021. Caller stated for the vaccine, she has never had an arrhythmia in her life. Caller stated this is happening and so because she doesn''t fit into the standard population that''s getting these symptoms, she feels like her doctor just dismissed it because oh it must not be happening to her. Caller stated as she''s talking, she feels lightheaded, dizzy, her chest is heavy, she''s tired and she''s a healthy person otherwise as far as exercise and diet and how she takes care of herself and so this is hard. Caller stated the only antidote she would add is that she does have a history since childhood to present of not being able to process medications very quickly and also, she has a very slow, her ability to heal things is very slow, but she heals, but she''s kind of like the antidotal patient that people don''t understand, they look at her and appear healthy. Caller stated so this is her, this is her life, and she was actually kind of nervous about getting the vaccine because she''s like she wants to protect herself and it took her a really long time to decide if she should get it or not, she thought long and hard and she is the person in the 1 or 2%. Caller stated when everybody was trying to convince her to get the vaccine, they said most people don''t have this, that and the other side effects and she is usually not in the most people category. Caller stated so now she''s in a position where she is having a situation and she doesn''t know what to do. Caller stated she doesn''t know. Caller stated her common sense tells her first she needs to deal with what''s happening and heal and then is it a good idea for her to get vaccine number two when she is still having these problems? Caller stated her common sense says no but she hasn''t been able to get anything concrete, the nurse that just transferred her over didn''t know she had to look it up. Caller stated she wants to talk to somebody that she can talk to. Caller stated she feels like she''s falling through the cracks and that''s not necessary. Caller stated she thought, alright, this is going to pass at some point then a week after that she started feeling more. Caller stated it''s not a good loop, if the call handler doesn''t know and Medical doesn''t know then obviously nobody knows. Caller stated she has to figure out who then does she talk to? Caller stated pharmacists are going to go off what Pfizer knows, so it''s all really stemming from what she doesn''t know and that this is a work in progress and as Pfizer gets new information then Pfizer puts out new information. Caller stated her situation is registered with the CDC and with Pfizer as a side effect so yes this is a side effect then with that A) What''s causing this side effect? B) Will she heal from this and will it work its way out? C) Is it safe for her to get another dose? D) What''s the longest she can wait? Caller stated those are the kind of questions, relevant questions for her and she absolutely needs to get answers to them. Caller asking who does she talk to? Caller stated she needs to escalate, she''s in a tier and nobody''s able to answer. Caller stated they told her 6 weeks, but they didn''t tell her if they could go beyond 6 weeks because she brought it up. Caller stated in country, they are actually recommending for Pfizer 12 weeks, isn''t that odd? Caller stated their version of our head Dr. that they have a medical health whatever person figure head, and that lady is recommending 12 weeks and saying that there''s all kinds of information saying that if Pfizer will actually have a better effect if people wait longer between doses whereas in country, we are getting them between 3 and 6 weeks and if people go longer, Pfizer is saying they can''t guarantee that it''s going to be effective. Caller stated its two contradictory pieces of information that doesn''t make sense. Caller stated she doesn''t want to hurt her heart anymore. Caller stated she doesn''t want to hurt herself; she doesn''t want to get Covid, the delta variant, but she''s starting to feel frustrated and pissed off like she feels like she needs better information and she''s not getting it from the source. Caller stated she also feels crabby, it''s persisting. Patient stated I had a side effect after the first dose of the vaccine; she questioned If I should I get the second dose. The outcome of arrhythmias/ constant arrhythmia, felt kind of tired, just lethargic, would feel a little bit dizzy, couldn''t quite catch a full breath/ not quite breathing deeply enough or getting enough oxygen, felt a heaviness in her chest, feels lightheaded, crabby, brain fog was not resolved ; while the outcome of all other events was unknown. Information about lot/batch number has been requested.


VAERS ID: 1534072 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Maine  
Vaccinated:2021-07-18
Onset:2021-07-01
Submitted: 0000-00-00
Entered: 2021-08-07
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Blood pressure abnormal, Blood pressure measurement, Chest pain, Heart rate, Heart rate increased, Myocarditis
SMQs:, Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Hypertension (broad), Cardiomyopathy (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 Date: 202107; Test Name: Blood Pressure; Result Unstructured Data: Test Result:Not stable; Comments: Blood pressure is not stable.; Test Date: 202107; Test Name: Heart beat; Result Unstructured Data: Test Result:fast
CDC Split Type: USPFIZER INC202100950916

Write-up: myocarditis; chest hurt; fastheart beat; blood pressure is not stable; This is a spontaneous report from a contactable consumer (patient) via Pfizer sponsored program. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 18Jul2021 (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. On an unspecified date in Jul2021, after a couple of days the patient felt side effects like myocarditis, chest hurt, fast heart beat and blood pressure was not stable. The outcome of the events was unknown. Information on lot/batch number has been requested.


VAERS ID: 1534078 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Florida  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-08-07
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 INC202100951577

Write-up: myocarditis; This is a spontaneous report from a contactable nurse reported for a patient via a Pfizer company representative. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via unspecified route of administration on an unspecified date (batch/lot number and expiry date unknown) as dose number unknown, single for covid-19 immunization. The patient''s medical history and concomitant medications were not reported. The nurse reported "Verbatim question: for the covid vaccine, 12 and up, they encountered myocarditis. Can you please send/call her about this. She''s a pediatrician. She would like more info.". The outcome of the event was unknown. The lot number for the vaccine, bnt162b2, was not provided and will be requested during follow up.; Sender''s Comments: Based on available information and known drug profile, a possible causal relationship cannot be excluded between the suspect product bnt162b2 and the reported event myocarditis. 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: 1536701 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-08-09
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Pericarditis
SMQs:, Systemic lupus erythematosus (broad), Chronic kidney disease (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: USJNJFOC20210809585

Write-up: PERICARDITIS; This spontaneous report was received from literature: Myocarditis and Pericarditis After Vaccination for COVID-19. 2021 Aug 04. This report concerned multiple patients. 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: Unknown expiry: unknown) dose, start therapy date were not reported, 1 total administered for prophylactic vaccination. The batch number was not reported. Per procedure, no follow up will be requested for this case. No concomitant medications were reported. On an unspecified date, the patient experienced pericarditis. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of pericarditis was not reported. This report was serious (Other Medically Important Condition).; Sender''s Comments: V0: 20210809585-COVID-19 VACCINE AD26.COV2.S-pericarditis. This event is considered unassessable. The event 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.


VAERS ID: 1594430 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-08-21
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (JANSSEN)) / JANSSEN UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Pericarditis
SMQs:, Systemic lupus erythematosus (broad), Chronic kidney disease (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: USJNJFOC20210836454

Write-up: PERICARDITIS; This spontaneous report received from a consumer via a company representative through (social media) news article spells out which cardiac conditions warrant caution with vax concerned two patients of unknown age, sex. The patients weight, height, and medical history were not reported. The patients received covid-19 vaccine ad26.cov2.s (suspension for injection, route of admin not reported, batch number: unknown, expiry: unknown) dose, 1 total, start therapy date were not reported for prophylactic vaccination. The batch number was not reported. Per procedure, no follow-up will be requested for this case. No concomitant medications were reported. On an unspecified date, the patients experienced pericarditis. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of pericarditis was not reported. This report was serious (Other Medically Important Condition).; Sender''s Comments: V0: 20210836454-covid-19 vaccine ad26.cov2.s -pericarditis. This event is considered unassessable. The event 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.


Result pages: prev   1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18   next

New Search

Link To This Search Result:

https://medalerts.org/vaersdb/findfield.php?EVENTS=ON&PAGENO=9&SYMPTOMS[]=Acute_endocarditis_%2810049001%29&SYMPTOMS[]=Atypical_mycobacterium_pericarditis_%2810055036%29&SYMPTOMS[]=Autoimmune_myocarditis_%2810064539%29&SYMPTOMS[]=Bacterial_pericarditis_%2810004050%29&SYMPTOMS[]=Carditis_%2810062746%29&SYMPTOMS[]=Endocarditis_%2810014665%29&SYMPTOMS[]=Endocarditis_bacterial_%2810014666%29&SYMPTOMS[]=Endocarditis_enterococcal_%2810014671%29&SYMPTOMS[]=Endocarditis_noninfective_%2810062608%29&SYMPTOMS[]=Endocarditis_staphylococcal_%2810014684%29&SYMPTOMS[]=Endocarditis_viral_%2810061837%29&SYMPTOMS[]=Eosinophilic_myocarditis_%2810014961%29&SYMPTOMS[]=Fungal_endocarditis_%2810017529%29&SYMPTOMS[]=Giant_cell_myocarditis_%2810083635%29&SYMPTOMS[]=Immune-mediated_myocarditis_%2810082606%29&SYMPTOMS[]=Lupus_endocarditis_%2810058225%29&SYMPTOMS[]=Lyme_carditis_%2810078417%29&SYMPTOMS[]=Meningococcal_carditis_%2810027270%29&SYMPTOMS[]=Myocarditis_%2810028606%29&SYMPTOMS[]=Myocarditis_bacterial_%2810065218%29&SYMPTOMS[]=Myocarditis_infectious_%2810066857%29&SYMPTOMS[]=Myocarditis_septic_%2810028615%29&SYMPTOMS[]=Myopericarditis_%2810028650%29&SYMPTOMS[]=Pericarditis_%2810034484%29&SYMPTOMS[]=Pericarditis_constrictive_%2810034487%29&SYMPTOMS[]=Pericarditis_infective_%2810062491%29&SYMPTOMS[]=Pericarditis_lupus_%2810058149%29&SYMPTOMS[]=Pericarditis_meningococcal_%2810034492%29&SYMPTOMS[]=Pericarditis_rheumatic_%2810034496%29&SYMPTOMS[]=Pericarditis_tuberculous_%2810055069%29&SYMPTOMS[]=Pleuropericarditis_%2810059361%29&SYMPTOMS[]=Purulent_pericarditis_%2810051071%29&SYMPTOMS[]=Streptococcal_endocarditis_%2810073742%29&SYMPTOMS[]=Subacute_endocarditis_%2810042276%29&SYMPTOMS[]=Viral_myocarditis_%2810047470%29&SYMPTOMS[]=Viral_pericarditis_%2810047472%29&VAX=COVID19&VAXTYPES=COVID-19&WhichAge=range&LOWAGE=(-1)&HIGHAGE=(-1)

Government Disclaimer on use of this data


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