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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 24 out of 862

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VAERS ID: 1978795 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Wisconsin  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101813253

Write-up: This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team for a Pfizer sponsored program (163738). A 20 year-old male patient received bnt162b2 (COMIRNATY) (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: Bnt162b2 (DOSE: 1), for COVID-19 immunization. The following information was reported: MYOCARDITIS (medically significant), outcome "recovered", described as "Developed myocarditis after his second COVID vaccine". The lot number for bnt162b2 was not provided and will be requested during follow up.; Sender''s Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the event myocarditis and BNT162B2. 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, as appropriate.


VAERS ID: 1980786 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: California  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-25
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 INC202101780678

Write-up: myocarditis; This is a spontaneous report received from a non-contactable reporter (Consumer or other non HCP) from medical information team. A child female patient received bnt162b2 (COMIRNATY) (Lot number: unknown) as single dose 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". Reporter was fully vaccinated. Reporter''s daughter received all the booster everything Pfizer she was in her 40 they were all fine. Reporter''s question was about the booster for the 5-11 years old, and the reason that, and reporter wanted to find out if there was, now reporter understand that 5 million children received this Pfizer vaccine reporter didn''t know how many, if that was the right number but on the news, reporter was just assuming. Since the schools were mandating many of the private schools were mandating the vaccine by 15Feb2021. Reporter was concerned about myocarditis, had there been any myocarditis case, caused reporter knew one family that who child (patient) got it like a few days ago, that was why was worried about reporter''s grandchildren getting it. Patient was a girl, reporter''s daughter just told. Reporter''s grandchildren would be vaccinated, so reporter asked if there had been any adverse effects from children ages 5-11. Reporter asked if there had been like one or two or there had been a lot of people with myocarditis who are ages 5-11. No follow up attempts are possible; Information about lot/batch number cannot be requested. No further information is expected.


VAERS ID: 1980903 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Cardiac failure, Cardiac failure congestive, Cardiac valve disease, Cardiac valve prosthesis user, Carditis, Cerebral haemorrhage, Cerebrovascular accident, Chest pain, Computerised tomogram thorax, Dyspnoea, Echocardiogram abnormal, Fatigue, Intensive care, Myocarditis, Troponin increased
SMQs:, Cardiac failure (narrow), Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Myocardial infarction (narrow), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? Yes
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: CT scan of chest, troponin elevated, echocardiogram showed heart failure,
CDC Split Type:

Write-up: November my mom began having problems with fatigue, shortness of breath and chest pain. She went to ER and had elevated troponins and more cardiac work up revealed valvular heart failure. She required a mechanical valve in December, and then had a stroke and brain bleed. She is in a medical center. She likely had myocarditits causing heart inflammation and heart valve failure that caused her to go into congestive heart failure.


VAERS ID: 1995330 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Wisconsin  
Vaccinated:2021-02-01
Onset:2021-02-01
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-12-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EN6202 / 2 LA / -

Administered by: Other       Purchased by: ?
Symptoms: Fatigue, Inappropriate schedule of product administration, Lymphadenopathy, Malaise, Myocarditis, Night sweats, Pyrexia, Weight decreased
SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Cardiomyopathy (broad), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (narrow), 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Milk allergy; Reaction to food additive
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101804347

Write-up: myocarditis; tiredness for 2 months; fever; night sweats; feeling unwell; swollen lymph glands; lost 15 pounds; dose 1 on 26Feb2021, dose 2 in Feb2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 81 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date Feb2021 (Batch/Lot number: EN6202) as dose 2, single for covid-19 immunisation in Clinic. The patient was not pregnant when administration. Known allergies: dairy & preservatives. Other medical history: some digestive. The patient took some vitamins & Blood pressure, & coloresterol pre in 2 weeks. The patient didn''t receive other vaccines in 4 weeks. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3242, Location of injection: Arm Left), administration date: 26Feb2021 01:30 PM, when the patient was 81 years old, for COVID-19 immunization. The patient was not diagnosed with COVID-19 prior to vaccination. The patient has not been tested for COVID-19 post vaccination. The following information was reported: MYOCARDITIS (medically significant) with onset 01Mar2021 14:00, outcome "recovered", described as "myocarditis"; FATIGUE (non-serious) with onset 01Mar2021 14:00, outcome "recovered", described as "tiredness for 2 months"; PYREXIA (non-serious) with onset 01Mar2021 14:00, outcome "recovered", described as "fever"; NIGHT SWEATS (non-serious) with onset 01Mar2021 14:00, outcome "recovered", described as "night sweats"; MALAISE (non-serious) with onset 01Mar2021 14:00, outcome "recovered", described as "feeling unwell"; LYMPHADENOPATHY (non-serious) with onset 01Mar2021 14:00, outcome "recovered", described as "swollen lymph glands"; WEIGHT DECREASED (non-serious) with onset 01Mar2021 14:00, outcome "recovered", described as "lost 15 pounds". The events "myocarditis", "fever", "night sweats", "feeling unwell", "swollen lymph glands" and "lost 15 pounds" were evaluated at the emergency room visit. It was unknown if therapeutic measures were taken as a result of myocarditis, fatigue, pyrexia, night sweats, malaise, lymphadenopathy, weight decreased. The lot number for bnt162b2 was not provided and will be requested during follow up.


VAERS ID: 1995529 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Wisconsin  
Vaccinated:0000-00-00
Onset:2021-12-01
Submitted: 0000-00-00
Entered: 2021-12-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 LA / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Bell's palsy, Chills, Myocarditis, Palpitations
SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hearing impairment (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? Yes
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: COVID-19
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101821246

Write-up: Heart palpitations; chills; myocarditis; Bells Palsy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47-year-old adult male received the first dose of intramuscular BNT162b2 (solution for injection; batch/lot reported as unknown expiry not provided) as a single dose in the left arm on an unspecified date in 2021 for COVID-19 immunisation. Relevant medical history included COVID-19 (diagnosed prior to vaccine). There were no concomitant medications reported. The patient denied receiving any other vaccine within four weeks of receiving this vaccine. The patient denied being tested for COVID since receiving the vaccine. On 01Dec2021 the patient experienced heart palpitations, chills, and myocarditis; which resulted/required visit(s) to Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care and Hospitalization, Life threatening illness (immediate risk of death from the event), Disability or permanent damage. A few days later, on an unspecified date in Dec2021, the patient experienced Bell''s Palsy: which resulted/required visit(s) to Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care and Hospitalization, Life threatening illness (immediate risk of death from the event), Disability or permanent damage. The patient received unspecified treatment. The outcome of the events heart palpitations, chills, myocarditis, and Bell''s Palsy was unknown.


VAERS ID: 1995605 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: California  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-12-31
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101843451

Write-up: the patient had an episode of pericarditis 10 days after the initial second dose; This is a spontaneous report received from a contactable reporter(s) (Physician) from information team for a sponsored program (159558). A 41 year-old male patient received bnt162b2 (BNT162B2) (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: Bnt162b2 (1st dose), for COVID-19 immunization. The following information was reported: PERICARDITIS (medically significant), outcome "unknown", described as "the patient had an episode of pericarditis 10 days after the initial second dose". The lot number for bnt162b2 was not provided and will be requested during follow up.; Sender''s Comments: As there is limited information in the case provided, the causal association between the event pericarditis with the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available.


VAERS ID: 2017686 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: New York  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2022-01-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Feeling abnormal, Neuralgia, Pericarditis
SMQs:, Peripheral neuropathy (narrow), Systemic lupus erythematosus (broad), Dementia (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: USMODERNATX, INC.MOD20214

Write-up: Had inflammation around his heart; Had bad nerve pain from head to toes; Felt terrible from head to toes; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 23-Dec-2021 and was forwarded to Moderna on 23-Dec-2021. This spontaneous case was reported by a consumer and describes the occurrence of PERICARDITIS (Had inflammation around his heart) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. 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 PERICARDITIS (Had inflammation around his heart) (seriousness criterion medically significant), NEURALGIA (Had bad nerve pain from head to toes) and FEELING ABNORMAL (Felt terrible from head to toes). At the time of the report, PERICARDITIS (Had inflammation around his heart), NEURALGIA (Had bad nerve pain from head to toes) and FEELING ABNORMAL (Felt terrible from head to toes) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant information was not provided. It was reported that the patient was a pharmacist and experienced side effects that were really bad. Treatment information was not provided. Company Comment This case concerns a patient of an unknown age with no previous relevant medical history reported. The event occurred on an unknown date after a dose of COVID-19 Vaccine Moderna (mRNA-1273). Very limited information regarding this event has been provided at this time. Clinical course with diagnostic workup and treatment details were not provided. The benefit-risk relationship of COVID-19 Vaccine Moderna (mRNA-1273) is not affected by this report.; Sender''s Comments: This case concerns a patient of an unknown age with no previous relevant medical history reported. The event occurred on an unknown date after a dose of COVID-19 Vaccine Moderna (mRNA-1273). Very limited information regarding this event has been provided at this time. Clinical course with diagnostic workup and treatment details were not provided. The benefit-risk relationship of COVID-19 Vaccine Moderna (mRNA-1273) is not affected by this report.


VAERS ID: 2018444 (history)  
Form: Version 2.0  
Age:   
Sex: Unknown  
Location: Unknown  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2022-01-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

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:
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC202101836638

Write-up: pericarditis; This is a spontaneous report received from a non-contactable reporter (Consumer) from medical information team. A patient (no qualifiers provided) received bnt162b2 (COMIRNATY) (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 (DOSE 1; MANUFACTUERER UNKNOWN), for COVID-19 Immunization. The following information was reported: PERICARDITIS (medically significant), outcome "unknown", described as "pericarditis". A patient was suffering from pericarditis three days after receiving the second dose of the vaccine. Consumer inquired if they can receive the booster dose of the vaccine. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.


VAERS ID: 2018459 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Utah  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2022-01-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Magnetic resonance imaging heart, Myocarditis, Oedema due to cardiac disease, Troponin
SMQs:, Cardiac failure (broad), Pulmonary hypertension (broad), Haemodynamic oedema, effusions and fluid overload (narrow), 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: Test Name: Cardiac magnetic resonance images; Result Unstructured Data: Test Result:focal inferolateral wall edema; Test Name: Troponin; Result Unstructured Data: Test Result: elevated
CDC Split Type: USPFIZER INC202101837611

Write-up: Myocarditis; focal inferolateral wall edema; This is a literature report for a Pfizer sponsored program Background: Rare cases of myocarditis have been reported in adults following COVID-19 vaccination, with most cases occurring in males <30 years old. Since the authorization to administer the Pfizer-BioNTech COVID-19 vaccine in those as young as 12 years of age, suspected myocarditis temporally related to the vaccine has also been reported in adolescents. Myocarditis has been associated with other vaccines, such as smallpox and influenza, though data are limited regarding symptoms, clinical course, and short-term outcomes of suspected myocarditis following COVID-19 vaccination. On June 23, 2021, the Centers for Disease Control and Prevention''s (CDC) Advisory Committee on Immunization Practices reported a likely link between mRNA COVID-19 vaccination and myocarditis, particularly in those


VAERS ID: 2018463 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Utah  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2022-01-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 2 - / -

Administered by: Unknown       Purchased by: ?
Symptoms: Electrocardiogram, Magnetic resonance imaging heart, Myocarditis, Troponin
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: Test Name: Electrocardiogram; Result Unstructured Data: Test Result:Diffuse ST elevation; Test Name: Cardiac magnetic resonance images; Result Unstructured Data: Test Result:Subepicardial and mid-wall enhancement; Comments: characteristics of myocarditis.; Test Name: Troponin levels; Result Unstructured Data: Test Result:Elevated
CDC Split Type: USPFIZER INC202101837752

Write-up: This is a literature report for the following literature source (Clinically Suspected Myocarditis Temporally Related to COVID-19 Vaccination in Adolescents and Young Adults). Background: Rare cases of myocarditis have been reported in adults following COVID-19 vaccination, with most cases occurring in males <30 years old. Since the authorization to administer the Pfizer-BioNTech COVID-19 vaccine in those as young as 12 years of age, suspected myocarditis temporally related to the vaccine has also been reported in adolescents. Myocarditis has been associated with other vaccines, such as smallpox and influenza, though data are limited regarding symptoms, clinical course, and short-term outcomes of suspected myocarditis following COVID-19 vaccination. On June 23, 2021, the Centers for Disease Control and Prevention''s (CDC) Advisory Committee on Immunization Practices reported a likely link between mRNA COVID-19 vaccination and myocarditis, particularly in those


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