VAERS Reports 320308D

VAERS 2644626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: -
Alter: 28,0
Geschlecht: M
Eingang: 13.06.2023
Impfdatum: 27.10.2021
Beginn: 09.12.2022
Tage bis Beginn: 408,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Hypoxia Symptom recurrence

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA 12/16/2022 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2633023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: MN
Alter: 91,0
Geschlecht: F
Eingang: 17.05.2023
Impfdatum: 10.11.2021
Beginn: 09.02.2023
Tage bis Beginn: 456,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiac failure Cardiac failure congestive Dyspnoea SARS-CoV-2 test positive Wheezing

Symptomtext

The patient was brought to the ED by EMS on 2/9/23 for evaluation of shortness of breath and difficulty breathing that has been going on for the past few days. EMS reports she had 88% SpO2 on room air with wheezes, so they administered a nebulizer treatment and placed the patient on 4L supplemental O2 with improvement. A COVID PCR test performed in the ED resulted positive. She was admitted 2/9/23 - 2/21/23 for acute hypoxic respiratory failure, COVID-19 pneumonia, and decompensated newly diagnosed congestive heart failure. She was started on diuretics and steroids during admission. The patient has received the primary COVID vaccine series and one booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2628990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: -
Alter: 58,0
Geschlecht: M
Eingang: 09.05.2023
Impfdatum: 23.09.2022
Beginn: 11.10.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute myocardial infarction

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE UNSPECIFIED

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2623940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 28.01.2021
Beginn: 30.04.2023
Tage bis Beginn: 822,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 Chills Cough Multiple sclerosis Nausea Pain Pneumonia bacterial Vomiting

Symptomtext

Pt has a cough, body aches, chills, nausea, and vomiting for 10 days. She is admitted with COVID-19 with acute hypoxic respiratory failure, secondary bacterial pneumonia, and MS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2614762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: CA
Alter: 55,0
Geschlecht: M
Eingang: 13.04.2023
Impfdatum: 26.10.2021
Beginn: 20.12.2021
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Blood test abnormal Computerised tomogram thorax abnormal Deep vein thrombosis Fibrin D dimer Laboratory test normal Pulmonary embolism Thrombosis Ultrasound scan

Symptomtext

I developed DVT and PE blood clot issues. No family history. Non smoker, non drinker. Physically active daily.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: 2022-02-08: Blood test and ultrasound. D-Dimer 10+ 2022-02-08: Hospital: Blood and CT chest scan indicating PE. Hospitalized 2022-02-09: Hospital: Blood tests for Type V mutation negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi vitamin, Vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 2587324

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 320308D

kritisch

Staat: -
Alter: 99,0
Geschlecht: F
Eingang: 25.02.2023
Impfdatum: 10.11.2021
Beginn: 15.01.2023
Tage bis Beginn: 431,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Back pain COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram head normal Coronary artery disease Cough Dementia Fall Fracture Fractured sacrum Headache Hypertensive heart disease Hypoxia Malaise Pneumonia bacterial SARS-CoV-2 test positive

Symptomtext

FINAL DIAGNOSIS: 1. COVID-19 PNA 2. Acute Hypoxemic Respiratory Failure 3. Fall 4. Acute Sacral Fracture 5. Chronic Lumbar Compression Fx 6. Dementia 7. Hypertensive Disease with CAD 8. Headache REASON FOR HOSPITALIZATION AND ADMITTING DIAGNOSIS: Fall and Back Pain Fall [W19.XXXA] Hypoxia [R09.02] Closed fracture of sacrum, unspecified portion of sacrum, initial encounter [S32.10XA] COVID [U07.1] HOSPITAL COURSE: Patient is a 101 y.o. female who presented to Hospital 1/15/2023 with fall 1. COVID-19 pneumonia with superimposed bacterial pneumonia 1. Onset of symptoms this 1 week prior to presentation symptoms included hypoxemia and cough. COVID test was positive on January 15, 2023. Patient has received 3 vaccinations for COVID. Chest x-ray demonstrated superimposed likely bacterial pneumonia. Patient discharged on completing course of Augmentin. Oxygen requirements 3 L nasal cannula will be discharged with arrangements for home oxygen. ID was consulted did not recommend remdesivir or Paxlovid at this time. 2. Acute hypoxemic respiratory failure 1. Arrangements being made for discharge with oxygen at home 3. Fall, unwitnessed 1. Mechanical fall PT OT followed during hospitalization 4. Acute sacral fracture 1. Ortho reports sacral fractures nonsurgical recommended continuation of PT OT and weightbearing as tolerated 5. Chronic lumbar compression fractures 1. Symptomatic management 6. Dementia 1. Returning to memory care unit 7. Hypertensive heart disease with CAD 1. Management per PCP on discharge 8. Headache 1. CT head ruled out any acute intracranial process

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2526329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: OH
Alter: 85,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 13.03.2021
Beginn: 01.02.2022
Tage bis Beginn: 325,0
Dosis: 2
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anxiety Condition aggravated Death Dizziness Pulmonary embolism

Symptomtext

dizziness, increased anxiety pulmonary embolism DEATH

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Clinic-Feb 2022 through June 2022
Aktuelle Erkrankungen: -
Vorgeschichte: remission Lymphoma Chronic Anxiety GI irritable bowl syndrome Hospitalized on Feb 2022 with blood clots in bilateral legs and pulmonary embolism, direct cause of MRNA injections x 3. Heart failure, blood clots Tried to convince patient not to take the shot, but she would not listen. Too many side effects known early 2021.
Andere Medikamente: Anti Diareal OTC OTC Tums OTC Nexium 1st Pfizer shot 3/13/21 Lot # EN6207, exp. 7/31/21 2nd Pfizer shot on 4/3/2021 - at 9:45 am #320308D, Lot # ER8733, exp. 7/31/2021 Pfizer Booster shot on 10/28/21-#320308D, no expiration date documented
Allergien: -
Vorherige Impfungen: -

VAERS 2526329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: OH
Alter: 85,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 13.03.2021
Beginn: 01.02.2022
Tage bis Beginn: 325,0
Dosis: 3
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anxiety Condition aggravated Death Dizziness Pulmonary embolism

Symptomtext

dizziness, increased anxiety pulmonary embolism DEATH

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Clinic-Feb 2022 through June 2022
Aktuelle Erkrankungen: -
Vorgeschichte: remission Lymphoma Chronic Anxiety GI irritable bowl syndrome Hospitalized on Feb 2022 with blood clots in bilateral legs and pulmonary embolism, direct cause of MRNA injections x 3. Heart failure, blood clots Tried to convince patient not to take the shot, but she would not listen. Too many side effects known early 2021.
Andere Medikamente: Anti Diareal OTC OTC Tums OTC Nexium 1st Pfizer shot 3/13/21 Lot # EN6207, exp. 7/31/21 2nd Pfizer shot on 4/3/2021 - at 9:45 am #320308D, Lot # ER8733, exp. 7/31/2021 Pfizer Booster shot on 10/28/21-#320308D, no expiration date documented
Allergien: -
Vorherige Impfungen: -

VAERS 2520897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: KY
Alter: 59,0
Geschlecht: M
Eingang: 01.12.2022
Impfdatum: 19.12.2021
Beginn: 16.03.2022
Tage bis Beginn: 87,0
Dosis: 1
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient had breakthrough infection and later passed away from complications.

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Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: Positive COVID test on 2/8/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: DM type 2 COPD Colon/rectal cancer Asthma Emphysema CAD HTN MI Angina Hyperlipidemia
Andere Medikamente: Montelukast Dofetilide Albuterol sulfate Clopidogrel Omeprazole Apixaban Nitroglycerin aspirin Symbicort Metoprolol succinate Atorvastatin Cholecalciferol Digoxin Furosemide Loratadine Tizanidine Zolpidem Ranolazine Hydromorphone
Allergien: Codeine Flu virus vaccine
Vorherige Impfungen: -

VAERS 2368879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 14.07.2022
Impfdatum: 31.01.2021
Beginn: 12.07.2022
Tage bis Beginn: 527,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Asthenia COVID-19 COVID-19 pneumonia Dyspnoea SARS-CoV-2 test positive Sepsis

Symptomtext

Pt arrived to the hospital with shortness of breath. He reports that he has had no energy. He has had a history of flash pulmonary edema, and was found to be COVID positive. Pt was admitted for acute hypoxic respiratory failure and sepsis and COVID pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2338786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: TN
Alter: 66,0
Geschlecht: M
Eingang: 28.06.2022
Impfdatum: 20.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: SYR / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute kidney injury COVID-19 pneumonia Death Diarrhoea Endotracheal intubation Exposure to SARS-CoV-2 Haemofiltration Mechanical ventilation Shock

Symptomtext

Patient presented to Medical Center on 01/10/2022 for 1 week of diarrhea. Patient stated family members in house have tested positive for Covid-19. Admitted for AKI, given multiple fluid boluses in ED, started on a sodium bicarb qtt. On 01/15/2022 patient was intubated and ventilated with severe covid PNA. Placed on pressors, sedation and bicarb. Patient received CRRT. 01/21/2022, patient refractory shock, unable to maintain perfusion pressure despite maximum vasopressors, unable to oxygenate or ventilate. Patient expired on 1/21/22.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2311641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 07.06.2022
Impfdatum: 12.11.2021
Beginn: 30.05.2022
Tage bis Beginn: 199,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure Angiogram pulmonary abnormal Aortic dilatation Arteriosclerosis Arteriosclerosis coronary artery Asthenia Atelectasis Bandaemia Blood lactic acid Bronchial secretion retention Bronchial wall thickening Bronchitis COVID-19 COVID-19 pneumonia Cardiac failure congestive Chest X-ray abnormal Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal

Symptomtext

Still admitted (8) days. Patient is a 82 y.o. male with severe O2 dependent chronic obstructive pulmonary disease, who was hospitalized about 6 weeks ago for chronic obstructive pulmonary disease exacerbation with bronchitis. He was doing well until yesterday when he developed cough productive of dark colored mucus, and fever. During the night he woke up and was in respiratory distress and had severe weakness, and his wife called an ambulance and had him brought to the emergency room. In the emergency department he was found to be hypoxemic at 84%. He had tachycardia and increased respiratory rate, but normal blood pressure. Labs revealed leukocytosis and bandemia, as well as lactic acidosis at 2.3. D-dimer was elevated at 2000. COVID PCR was positive. Procalcitonin was significantly elevated at 6. Chest x-ray showed bilateral pulmonary infiltrates left greater than right. CT angiogram of the chest excluded pulmonary embolism, and confirmed bilateral left greater than right pulmonary infiltrates. ASSESSMENT / PLAN: * Bilateral pneumonia Assessment & Plan Community-acquired pneumonia with high risk for Gram-negative infection. Recent MRSA screen was negative. Treat with cefepime and doxycycline. Mucinex and Acapella to help clear prominent pulmonary secretions. Sputum culture requested Severe sepsis Assessment & Plan Severe sepsis criteria with sepsis parameters of tachycardia increased respiratory rate leukocytosis and bandemia, and severe sepsis criteria of lactic acidosis. 2 L saline bolus (30 mL/kg) and maintenance IV fluids. Antibiotics for pneumonia Acute on chronic respiratory failure with hypoxia Assessment & Plan Patient is normally on 2 L of oxygen mainly at night, needing 2 L continuous now COVID-19 virus infection Assessment & Plan COVID positive. Checking inflammatory markers, but I believe this is not contributing to a lot of his symptoms. Patient will receive IV Solu-Medrol for chronic obstructive pulmonary disease and COVID. Also treat with remdesivir COPD (chronic obstructive pulmonary disease) Assessment & Plan Severe chronic obstructive pulmonary disease. Do not appreciate wheezing on admission exam. Treat with Solu-Medrol. Treat with long and short-acting inhalers. Coronary artery disease involving native coronary artery of native heart without angina pectoris Assessment & Plan Maintain aspirin and statin therapy Essential hypertension Assessment & Plan On Hyzaar. This will be held temporarily due to severe sepsis Protein-calorie malnutrition, severe Assessment & Plan Body mass index less than 20. To be followed by nutrition Elevated d-dimer Assessment & Plan D-dimer 2000 on admission. CTA of chest excluded pulmonary embolism. Will add upper and lower extremity venous ultrasounds to screen for DVT. DVT prophylaxis with Lovenox.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: Procedure Component Value Ref Range Date/Time DR CHEST SINGLE VIEW Resulted: 06/07/22 0959 Order Status: Completed Updated: 06/07/22 1001 Narrative: EXAMINATION: Single View Chest EXAM DATE: 6/7/2022 9:19 AM TECHNIQUE: Single view chest INDICATION: chf, pna, copd COMPARISON: June 5, 2022 most recent ENCOUNTER: Subsequent _________________________ FINDINGS: Severe emphysematous changes redemonstrated. Multifocal interstitial thickening predominantly basilar and left midlung again present and not significantly changed. _________________________ Impression: 1. No significant change CV Echo Limited with Contrast Collected: 06/06/22 1521 Order Status: Completed Updated: 06/07/22 0928 Narrative: LIMITED ECHOCARDIOGRAPHY REPORT Name: Study Date: 06/06/2022 Patient Location: Patient Class: Inpatient Gender: Male Ordering Physician: Age: 82 yrs Referring Physician: Height: 183 cm Performed By: Weight: 62 kg Resting HR: 65 BSA: 1.8 m2 Resting BP: 125/68 mmHg Reason For Study: Dyspnea on exertion (DOE), ., CHF s/p viral pneumonia, severe pulmonary HTN signs on CT History/Symptoms: Covid-19, COPD, Coronary artery disease, Hypertension, Influenza A, COPD, shortness of breath, Pneumonia, Hyperglycemia, Former smoker Electronically signed by: MD on 06/07/2022 09:27 AM Interpretation Summary Very limited views overall left ventricular function appeared normal left ventricular cavity size grossly normal. Overall wall thickness appeared normal No obvious mitral stenosis the anterior leaflet appeared calcified but move normally subvalvular chordal structures appeared calcified no obvious obstruction Due to limited acoustic windows, Definity was administered. The right ventricle is moderately dilated. The aortic valve is not well visualized. There is no comparison study available. STUDY PERFORMED/QUALITY: AORTIC VALVE: A two-dimensional transthoracic The aortic valve is not well echocardiogram with color flow and visualized. spectral flow Doppler was performed in limited views only. The technical MITRAL VALVE: quality of the exam was limited due to The mitral valve is not well suboptimal acoustic windows. Due to visualized. No obvious mitral stenosis limited acoustic windows, Definity was the anterior leaflet appeared administered. Location: Portable. calcified but move normally subvalvular chordal structures LEFT VENTRICLE: appeared calcified no obvious Very limited views overall left obstruction. ventricular function appeared normal left ventricular cavity size grossly normal. Overall wall thickness TRICUSPID VALVE: appeared normal. The tricuspid valve is not well visualized. There was insufficient tricuspid regurgitation envelope LEFT ATRIUM: detected to calculate right The left atrium is normal in size. ventricular systolic pressure. RIGHT ATRIUM: PULMONIC VALVE: Right atrium not well visualized. The pulmonic valve is not well visualized. RIGHT VENTRICLE: The right ventricle is not well visualized. The right ventricle is moderately dilated. PERICARDIUM/PLEURAL: No pericardial effusion. INFERIOR VENA CAVA: The inferior vena cava was not visualized during the exam. Reference Table: Normal Mild ModerateSevere Men LVEF > 52% 41-51% 30-40% <30% Women LVEF > 54% 41-53% 30-40% <30% Men LVIDd 4.2-5.8 5.9-6.3 6.4-6.8 >6.8 Women LVIDd 3.8-5.2 5.3-5.6 5.7-6.1 >6.1 LA Volume (ml/m^2) < 34 35-41 42-48 >48 LVEDVI (mL/m2) Male 34-74 75-89 89-100 >100 LVEDVI (mL/m2) Female 29-61 62-70 70-80 >80 ______________________________________________________________________________ Electronically signed by: MD on 06/07/2022 09:27 AM All sources of data reside in the Cardiology CT THORAX WITH IV CONTRAST Resulted: 06/05/22 1251 Order Status: Completed Updated: 06/05/22 1254 Narrative: EXAMINATION: CT Chest with IV Contrast EXAM DATE: 6/5/2022 12:30 PM TECHNIQUE: Standard protocol CT imaging of the chest with intravenous contrast was performed. Coronal and sagittal images were reconstructed. CONTRAST: 75 cc Isovue-370 QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Cough, persistent, Pneumonia, effusion or abscess suspected, xray done, Dyspnea, chronic, unclear etiology, Respiratory illness, nondiagnostic xray, Not improving COMPARISON: Several prior studies dating back to 7/16/2021, the most recent comparison examination done 5/30/2022 ENCOUNTER: Not applicable ____________________ FINDINGS: Base of Neck & Axillae: Unremarkable. No axillary or supraclavicular lymphadenopathy. Mediastinum & Hila: Several shotty mediastinal lymph nodes. No hilar or mediastinal lymphadenopathy. Cardiovascular: Normal heart size. No pericardial effusion. Ectatic aorta. Moderate/severe atherosclerotic disease. No thoracic aortic aneurysm or dissection. Dilated pulmonary arteries likely incident to secondary pulmonary arterial hypertension. Lungs & Airways: Severe COPD/pulmonary emphysema. Mild fibrotic changes. No airspace consolidation. Pleural Space: Small right and tiny left pleural effusions. No pneumothorax. Upper Abdomen: Several bilateral renal cysts. Otherwise unremarkable upper abdomen as seen. Chest Wall & Musculoskeletal: Mild/moderate arthrosis/spondylosis. No lytic or blastic bony lesions. No acute bony findings. ____________________ Impression: 1. Severe COPD/pulmonary emphysema. 2. Dilatation of the pulmonary arteries likely incident to secondary pulmonary arterial hypertension. 3. Small right and tiny left pleural effusions. Question some mild fluid overload. 4. No obvious pneumonia. 5. Small bilateral renal cysts. DR CHEST SINGLE VIEW Collected: 06/05/22 0946 Order Status: Completed Updated: 06/05/22 0951 Narrative: EXAMINATION: Single View Chest EXAM DATE: 6/5/2022 9:04 AM TECHNIQUE: Single view chest INDICATION: Inspiratory and expiratory view with A/P chest to rule out PTX as compared to this morning's earlier CXR, severe COPD, increased dyspnea COMPARISON: 6/5/2022 ENCOUNTER: Not applicable _________________________ FINDINGS: Cardiac size is normal. Advanced emphysematous changes are seen. Patchy opacities are again seen in the left mid lung and bilateral lung bases and to a lesser extent the right midlung. _________________________ Impression: Stable patchy bilateral opacities and emphysematous changes. Electronically signed by: MD on 6/5/2022 9:50 AM. DR CHEST SINGLE VIEW Collected: 06/05/22 0644 Order Status: Completed Updated: 06/05/22 0752 Narrative: EXAMINATION: Single View Chest EXAM DATE: 6/5/2022 6:15 AM TECHNIQUE: Single view chest INDICATION: Pneumonia, dyspnea COMPARISON: 6/3/2022 ENCOUNTER: Subsequent _________________________ FINDINGS: Extensive emphysematous changes. Left midlung and bibasilar interstitial and reticular opacities with some superimposed airspace opacities persist, not significantly changed. Probable bilateral skinfold artifact, less likely interval bilateral pneumothoraces. No interval consolidates or effusions _________________________ Impression: 1. Probable bilateral skinfold artifacts; doubtful pneumothoraces however repeat chest x-ray with inspiratory expiratory views recommended. 2. Extensive emphysematous changes with persistent lung opacities overall not significantly changed. 3. The orange significant findings protocol was initiated on 6/5/2022 7:03 AM. The presence of a significant findings result is to be communicated with a clinician and/or clinical staff by support staff. Electronically signed by: DO on 6/5/2022 7:04 AM. DR CHEST SINGLE VIEW Resulted: 06/03/22 1002 Order Status: Completed Updated: 06/03/22 1004 Narrative: EXAMINATION: Single View Chest EXAM DATE: 6/3/2022 9:32 AM TECHNIQUE: Single view chest INDICATION: Hypoxia, severe COPD, COVID 19 pneumonia, MSSA pneumonia, pleural effusion, weight gain COMPARISON: 6/1/2022 ENCOUNTER: Not applicable _________________________ FINDINGS: Slight interval increase in patchy right basilar airspace opacities. Left mid lung airspace opacities are also slightly increased. Ill-defined airspace opacities in the left lower lung are stable. Stable small right pleural effusion. No definite pneumothorax. Stable cardiomediastinal silhouette. _________________________ Impression: Slight interval increase in patchy airspace opacities in the right lung base and left midlung. DR CHEST SINGLE VIEW Resulted: 06/01/22 0737 Order Status: Completed Updated: 06/01/22 0739 Narrative: EXAMINATION: Single View Chest EXAM DATE: 6/1/2022 6:16 AM TECHNIQUE: Single AP upright chest INDICATION: bacterial pneumonia, Covid-19 infection COMPARISON: 5/30/2022 ENCOUNTER: Not applicable _________________________ FINDINGS: No supporting lines or tubes. There is no evidence of pneumothorax. Heart size remains within normal limits. No change in pulmonary vasculature or hilar regions. No mediastinal widening. Stable aorta. Infiltrate bilaterally greater on the left and right in the mid to lower lung on the left and in the base of the right with minimal change from yesterday. Trace right effusion suspected. Severe COPD. Osseous structures are unchanged. ________________________ Impression: 1. Bilateral infiltrates, left greater than right, suspicious for pneumonia without significant change from yesterday. 2. Severe COPD. 3. Trace right pleural effusion. USV Venous Upper Extremity Duplex Bilateral Resulted: 05/31/22 1116 Order Status: Completed Updated: 05/31/22 1118 Narrative: EXAMINATION: Complete Bilateral Upper Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 5/31/2022 11:07 AM TECHNIQUE: Real-time B-mode imaging with and without compression was used to evaluate the right and left upper extremity for deep venous thrombosis (DVT). Duplex Doppler with color and spectral Doppler was used. INDICATION: increased d-dimer, covid COMPARISON: None _____________________ Right Upper Extremity Findings: Right Internal Jugular Vein: No thrombus. Right Subclavian Vein: No thrombus. Right Axillary Vein: No thrombus. Right Brachial Vein: No thrombus. Right Radial Vein: No thrombus. Right Ulnar Vein: No thrombus. Superficial Veins: Right Basilic Vein: No thrombus. Right Cephalic Vein: No thrombus. Left Upper Extremity Findings: Left Internal Jugular Vein: No thrombus. Left Subclavian Vein: No thrombus. Left Axillary Vein: No thrombus. Left Brachial Vein: No thrombus. Left Radial Vein: No thrombus. Left Ulnar Vein: No thrombus. Superficial Veins: Left Basilic Vein: No thrombus. Left Cephalic Vein: No thrombus. ADDITIONAL FINDINGS: Normal cardiac pulsatility is present in the subclavian veins. _____________________ Impression: There is no deep venous thrombosis in the visualized deep veins of the right or left upper extremity. USV Venous Lower Extremity Duplex Bilateral Resulted: 05/31/22 1116 Order Status: Completed Updated: 05/31/22 1118 Narrative: EXAMINATION: Complete Right and Left Lower Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 5/31/2022 11:06 AM TECHNIQUE: Real-time B-mode imaging with and without compression was used to evaluate the right and left lower extremity for deep venous thrombosis (DVT). Duplex Doppler with color and spectral Doppler was used. INDICATION: increased d-dimer, covid COMPARISON: None _____________________ Right Lower Extremity Findings: Right Common Femoral Vein: No DVT. Right Femoral Vein: No DVT. Right Popliteal Vein: No DVT. Right Posterior Tibial Veins: No DVT. Right Peroneal Veins: No DVT. Right proximal Greater Saphenous Vein: No thrombus. Left Lower Extremity Findings: Left Common Femoral Vein: No DVT. Left Femoral Vein: No DVT. Left Popliteal Vein: No DVT. Left Posterior Tibial Veins: No DVT. Left Peroneal Veins: No DVT. Left proximal Greater Saphenous Vein: No thrombus. Duplex Doppler: Spectral Doppler demonstrates bilateral normal respirophasic waveforms in the common femoral veins. Additional Findings: None. _____________________ Impression: There is no deep venous thrombosis in the visualized deep veins of the right or left lower extremity. * CT ANGIO THORAX WITH IV CONTRAST Resulted: 05/30/22 0723 Order Status: Completed Updated: 05/30/22 0725 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 5/30/2022 7:07 AM TECHNIQUE: Standard protocol CT angiogram images were obtained through the chest following the administration of intravenous contrast. Coronal and sagittal MIP 3-D reformations were performed. CONTRAST: The amount and type of contrast are recorded in the medical record. QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: PE suspected, low/intermediate prob, positive D-dimer. COMPARISON: PET/CT imaging 5/17/2022 ENCOUNTER: Not applicable ____________________ FINDINGS: Base of Neck & Axillae: No adenopathy or mass in the base of the neck. Thyroid unremarkable. No axillary adenopathy. Mediastinum & Hila: Small hilar and mediastinal nodes appear stable to slightly increased in prominence. These may be reactive. There is no definitive evidence of suspicious adenopathy or other mass. Esophagus unremarkable. Cardiovascular: Normal heart size without significant pericardial effusion. Small amount of fluid demonstrated. Moderate calcified coronary artery plaque. No thoracic aortic aneurysm or dissection. Stable atherosclerotic changes. There is no evidence for significant right heart strain. Pulmonary Arteries: No evidence of pulmonary embolism. Central pulmonary arteries normal caliber. Lungs & Airways: Severe emphysema. Central airways patent. There is some mucus plugging and bronchial wall thickening in the left lower lobe and there is moderately extensive consolidation now demonstrated in the left lower lobe. Less extensive but similar changes are seen in the right lower lobe. This partially obscures posterior subpleural nodules which were seen on 5/17/2022. No gross change of these nodular findings. Chronic scarring demonstrated in the left upper lobe. The upper lobes in the right middle lobe do not have significant consolidation. No new pulmonary nodule. Pleural Space: No pleural effusion or pneumothorax. Upper Abdomen: Limited upper abdominal images appear grossly unchanged from recent PET/CT imaging. Chest Wall & Musculoskeletal: No acute osseous finding. Chest wall soft tissues unremarkable. ____________________ Impression: 1. No evidence of pulmonary embolism. 2. Severe emphysema. 3. Bilateral lower lobe pneumonia left greater than right. DR CHEST SINGLE VIEW Collected: 05/30/22 0642 Order Status: Completed Updated: 05/30/22 0646 Narrative: EXAMINATION: Single View Chest EXAM DATE: 5/30/2022 6:07 AM TECHNIQUE: Single view chest INDICATION: sob, cold like symptoms COMPARISON: None. ENCOUNTER: Not applicable ________________________ FINDINGS: Heart size is normal. Lungs are hyperinflated. Bilateral lower lobe atelectasis or infiltrates have developed since the prior study of 4/18/2022. Linear scarring in the left mid and upper lung is unchanged. There is no pneumothorax. _________________________ Impression: Bilateral lower lobe infiltrates, more pronounced on the left. Pulmonary hyperinflation. Electronically signed by: DO on 5/30/2022 6:45 AM
Aktuelle Erkrankungen: -
Vorgeschichte: Hospital Severe sepsis COVID-19 virus infection Elevated d-dimer Chronic obstructive pulmonary disease with acute exacerbation Coronary artery disease involving native coronary artery of native heart without angina pectoris Essential hypertension Protein-calorie malnutrition, severe Bilateral pneumonia Acute on chronic respiratory failure with hypoxia Hyperglycemia, drug-induced Pleural effusion Non-Hospital Acute bronchitis Chronic cough Elevated bilirubin Hemoptysis Influenza A Shortness of breath COPD exacerbation COPD, severe Hyperlipidemia History of bladder cancer Preoperative cardiovascular examination Malignant neoplasm of anterior wall of bladder
Andere Medikamente: albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ascorbic acid (VITAMIN C) 500 MG tablet aspirin 81 MG chewable tablet B Complex Vitamins (VITAMIN B
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2287834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: -
Alter: 98,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 02.11.2021
Beginn: 14.05.2022
Tage bis Beginn: 193,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 Fatigue Headache Pain Productive cough

Symptomtext

COVID 19 that lead to hospitalization. Had acute hypoxic respiratory failure. He had aches, headache fatigue and a productive cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2277731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

kritisch

Staat: CA
Alter: 76,0
Geschlecht: M
Eingang: 14.05.2022
Impfdatum: 11.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 51,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Blindness unilateral Cerebrovascular accident Magnetic resonance imaging head abnormal

Symptomtext

partial loss of sight in right eye due to stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: mri 4/19/22
Aktuelle Erkrankungen: NONEDM2
Vorgeschichte: DM2 HTN, HYPERLIPIDEMIA,
Andere Medikamente: METFORMIN, METOPROLOL,ROSUVASTATIN,COQ10
Allergien: NONE
Vorherige Impfungen: -

VAERS 2257010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

kritisch

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 04.11.2021
Beginn: 16.12.2021
Tage bis Beginn: 42,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Acute myocardial infarction Electrocardiogram abnormal Intracardiac thrombus Stent placement

Symptomtext

Blood clot to heart NSTEMIE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 3,0
Labordaten: EKG STENT
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure
Andere Medikamente: Cholorhalidone and diltiazem
Allergien: None
Vorherige Impfungen: -

VAERS 2137153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 25.09.2021
Beginn: 21.02.2022
Tage bis Beginn: 149,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 pneumonia

Symptomtext

Pt has a past medical history of type II IDDM, history of uterine malignancy, and obesity. She was transferred from facility for severe COVID pneumonia and acute hypoxic respiratory failure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2112933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: TN
Alter: 82,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 07.12.2021
Beginn: 24.01.2022
Tage bis Beginn: 48,0
Dosis: 3
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Fully vaccinated with 3 doses of Pfizer. Tested positive for COVID 19 on 01/24/2022. Admitted to Hospital on 01/08/2022. Expired on 02/08/2022 while still hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2096021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: MD
Alter: 57,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 05.11.2021
Beginn: 10.01.2022
Tage bis Beginn: 66,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Arthralgia Back pain COVID-19 Chest pain Condition aggravated Deep vein thrombosis Dyspnoea Echocardiogram Fatigue Imaging procedure Pain in extremity Peripheral swelling Pulmonary embolism SARS-CoV-2 test positive

Symptomtext

On 01/10/2022 - SOB and fatigue. and continued on the 01/11/2022. On 01/12/2022 severe SOB, sever fatigue, sharp chest pains. 01/13/2022- leg pain and swelling, added to what was already existing, shoulder pain and back pain and that kind of continued. On 01/24/2022- I was sent to the ER, by my doctor. I was admitted immediately and I had deep Vein thrombosis, blood clot on my right leg and pulmonary embolism in the lungs. 4 days of heparin through IV in the hospital from 01/24 - 01/27/2022, I was in the hospital. I would say unknown . I am under going current treatment for 6 months. I have to go every week to get images done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: long list scans and test done I went through a series of test when I was admitted. leg images, chest images taken on 01/24/2022 Then I was admitted to the hospital and they did cardio echograms on 01/24/2022 On 01/14/2022 - COVID -19 test- positive 01/24/2022 COVID-19 test - confirmed positive again
Aktuelle Erkrankungen: no
Vorgeschichte: high blood pressure
Andere Medikamente: lisinopril 20 mg bd amlodipine 10mg od testosterone 125 mg twice a week ibuprofen 400 mg twice a week prn glucosamine vitamin D dhea
Allergien: no
Vorherige Impfungen: -

VAERS 2039990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: WI
Alter: 67,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 31.10.2021
Beginn: 15.01.2022
Tage bis Beginn: 76,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

Death related to COVID 19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSC: Multiple myeloma; CKD Stage 4; acute on chronic systolic CHF
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1919646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 05.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Back pain Blood pressure increased Blood pressure measurement Blood test Chest X-ray Chest pain Dyspnoea Fatigue Immunisation Inflammation Magnetic resonance imaging Malaise Myocardial infarction Near death experience Pain Pain in extremity Peripheral swelling Product use issue

Symptomtext

she thought she was dying.; chest pains; She thought it was a heart attack; under her arm was hurting badly, like a throbbing pain; feeling sick; worn out/tired; back were hurting bad; got the booster; blood clots/right leg doppler of her leg/ calf and found the blood clot; got the booster and got the flu shot; the pain woke her up and it was horrible; blood pressure was up; shortness of breath; Under her arm was swollen and bulged out/one leg was bigger than the other; inflammation from the shot; the pain woke her up; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (159558). The reporter is the patient. A 54 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 05Nov2021 (Lot number: 320308D) at the age of 54 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), administration date 05Nov2021 (Batch/Lot number: unknown) as dose number unknown, single for immunisation. Relevant medical history included: "High blood pressure", start date: 2016 (ongoing); "Chronic kidney disease", start date: 2014 (ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (first dose; Lot number: EP7533), administration date: 01Apr2021, when the patient was 53 years old, for Covid-19 immunization, reaction(s): "broke out in hives", "itched"; Bnt162b2 (second dose; Lot number: EW0171), administration date: 22Apr2021, when the patient was 53 years old, for Covid-19 immunization, reaction(s): "Really ill", "Weak", "Tired", "Body aches", "Headaches", "Really bad chills", "She was in bed for 2 days", "Numbing in her leg and foot". The following information was reported: IMMUNISATION (medically significant) with onset 05Nov2021, outcome "unknown", described as "got the booster"; THROMBOSIS (medically significant) with onset 05Nov2021, outcome "unknown", described as "blood clots/right leg doppler of her leg/ calf and found the blood clot"; PAIN (medically significant) with onset Nov2021, outcome "unknown", described as "the pain woke her up and it was horrible"; NEAR DEATH EXPERIENCE (medically significant) with onset 07Nov2021 02:00, outcome "unknown", described as "she thought she was dying."; CHEST PAIN (medically significant) with onset 06Nov2021, outcome "unknown", described as "chest pains"; MYOCARDIAL INFARCTION (medically significant) with onset 06Nov2021, outcome "unknown", described as "She thought it was a heart attack"; PAIN IN EXTREMITY (non-serious) with onset 06Nov2021, outcome "unknown", described as "under her arm was hurting badly, like a throbbing pain"; MALAISE (non-serious) with onset 06Nov2021, outcome "unknown", described as "feeling sick"; FATIGUE (non-serious) with onset 06Nov2021, outcome "unknown", described as "worn out/tired"; BACK PAIN (non-serious) with onset 06Nov2021, outcome "unknown", described as "back were hurting bad"; BLOOD PRESSURE INCREASED (non-serious) with onset Nov2021, outcome "unknown", described as "blood pressure was up"; DYSPNOEA (non-serious) with onset Nov2021, outcome "unknown", described as "shortness of breath"; PERIPHERAL SWELLING (non-serious) with onset Nov2021, outcome "unknown", described as "Under her arm was swollen and bulged out/one leg was bigger than the other"; INFLAMMATION (non-serious) with onset Nov2021, outcome "unknown", described as "inflammation from the shot"; SLEEP DISORDER (non-serious) with onset Nov2021, outcome "unknown", described as "the pain woke her up"; PRODUCT USE ISSUE (non-serious) with onset 05Nov2021, outcome "unknown", described as "got the booster and got the flu shot". The events "blood clots/right leg doppler of her leg/ calf and found the blood clot", "the pain woke her up and it was horrible", "she thought she was dying.", "chest pains", "she thought it was a heart attack", "under her arm was hurting badly, like a throbbing pain", "feeling sick", "worn out/tired", "back were hurting bad", "blood pressure was up", "under her arm was swollen and bulged out/one leg was bigger than the other", "inflammation from the shot" and "the pain woke her up" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: (Nov2021) up; blood test: (Nov2021) positive for blood clot; chest x-ray: (05Nov2021) normal; (Nov2021) negative; magnetic resonance imaging: (05Nov2021) normal; (Nov2021) negative; troponin: (05Nov2021) positive for a blood clot; ultrasound doppler: (05Nov2021) blood clot; (Nov2021) blood clot. Therapeutic measures were taken as a result of pain, near death experience, myocardial infarction, sleep disorder and treatment included muscle relaxer. The pain stopped after patient took a muscle relaxer, but a few hours later she had pain again. The pain was horrible and she could not forget about it. She said that she got up around 0700. Patient laid in bed and thought it would go away, and around 1200-1230 she went to the hospital because she couldn't bare the pain. Patient clarified that she was not admitted to the hospital. Prior vaccinations (within 4 weeks) reported as none.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Date: 202111; Test Name: blood pressure; Result Unstructured Data: Test Result:up; Test Date: 202111; Test Name: Blood tests; Result Unstructured Data: Test Result:positive for Blood clot; Test Date: 20211105; Test Name: Chest X-ray; Result Unstructured Data: Test Result:Normal; Test Date: 202111; Test Name: Chest X-ray; Test Result: Negative ; Test Date: 20211105; Test Name: MRI; Result Unstructured Data: Test Result:Normal; Test Date: 202111; Test Name: MRI; Test Result: Negative ; Test Date: 20211105; Test Name: Troponin; Result Unstructured Data: Test Result:Positive for a blood clot; Test Date: 20211105; Test Name: right leg doppler of her leg/ calf; Result Unstructured Data: Test Result:Blood clot; Test Date: 202111; Test Name: right leg doppler of her leg/ calf; Result Unstructured Data: Test Result:Blood clot
Aktuelle Erkrankungen: Blood pressure high; Chronic kidney disease
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1915921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: GA
Alter: 52,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 05.11.2021
Beginn: 04.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anaemia Blood cholesterol Cardiac stress test Chills Constipation Decreased appetite Enzyme level test Fatigue Feeling of body temperature change Fibrin D dimer Fibrin D dimer increased Gastrointestinal disorder Hepatic enzyme increased Hiatus hernia Illness Immunisation Movement disorder Myalgia

Symptomtext

Dose number=3; feeling like I was having a heart attack; a little tired; chills; no appetite; muscles hurt; fever; hot/cold; couldn't move a lot; constipated; constipation worse; digestive tract felt like it shut down; sick; D-dimer was high; Liver levels were a little high; anemic; hiatal hernia attack; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 52 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Nov2021 02:30 (Lot number: 320308D) at the age of 52 years as dose 3 (booster) single for covid-19 immunisation; influenza vaccine inact sag 3v (FLUCELVAX), administered in arm right, administration date 04Nov2021 (Lot number: Quad 2021-2022 syr) as dose number unknown, single for immunisation. Relevant medical history included: "Only one kidney" (unspecified if ongoing); "hiatal hernia" (unspecified if ongoing); "anemia" (unspecified if ongoing); "obesity" (unspecified if ongoing). No known allergies. Concomitant medications included: GABAPENTIN; SINGULAIR; PROTONIX [OMEPRAZOLE]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL9264, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 05Feb2021, when the patient was 52 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL1283, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 15Jan2021, when the patient was 52 years old, for Covid-19 immunization. Facility type vaccine was hospital. No other vaccine in four weeks. The following information was reported: IMMUNISATION (hospitalization) with onset 05Nov2021, outcome "unknown", described as "Dose number=3"; MYOCARDIAL INFARCTION (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "feeling like I was having a heart attack"; FATIGUE (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "a little tired"; CHILLS (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "chills"; DECREASED APPETITE (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "no appetite"; MYALGIA (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "muscles hurt"; PYREXIA (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "fever"; FEELING OF BODY TEMPERATURE CHANGE (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "hot/cold"; MOVEMENT DISORDER (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "couldn't move a lot"; CONSTIPATION (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "constipated"; CONSTIPATION (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "constipation worse"; GASTROINTESTINAL DISORDER (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "digestive tract felt like it shut down"; ILLNESS (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "sick"; FIBRIN D DIMER INCREASED (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "D-dimer was high"; HEPATIC ENZYME INCREASED (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "Liver levels were a little high"; ANAEMIA (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "anemic"; HIATUS HERNIA (hospitalization) with onset 04Nov2021 21:00, outcome "recovering", described as "hiatal hernia attack". The patient was hospitalized for immunisation, myocardial infarction, fatigue, chills, decreased appetite, myalgia, pyrexia, feeling of body temperature change, movement disorder, constipation, constipation, gastrointestinal disorder, illness, fibrin d dimer increased, hepatic enzyme increased, anaemia, hiatus hernia (hospitalization duration: 1 day(s)). The events "feeling like i was having a heart attack", "a little tired", "chills", "no appetite", "muscles hurt", "fever", "hot/cold", "couldn't move a lot", "constipated", "constipation worse", "digestive tract felt like it shut down", "sick", "d-dimer was high", "liver levels were a little high", "anemic" and "hiatal hernia attack" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood cholesterol: (04Nov2021) 177; cardiac stress test: (04Nov2021) normal; enzyme level test: (04Nov2021) little high; fibrin d dimer: (04Nov2021) high; sars-cov-2 test: (07Nov2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of myocardial infarction, fatigue, chills, decreased appetite, myalgia, pyrexia, feeling of body temperature change, movement disorder, constipation, constipation, gastrointestinal disorder, illness, fibrin d dimer increased, hepatic enzyme increased, anaemia, hiatus hernia. No covid prior vaccination. Clinical course: The day of everything seemed normal was a little tired. The day after had chills, no appetite, muscles hurt, fever, hot/cold, couldn't move a lot. Called into work. Was constipated. Patient's digestive tract felt like it shut down. Went to work the next day, but was still really sick. Same symptoms, constipation worse. The third day (Sunday) woke feeling like she was having a heart attack. Went to the emergency room, was tested for a heart attack. Pains subsided, but D dimer was high, Liver levels were a little high, was anemic. Was admitted to the hospital for a day. The doctors found very little wrong other than maybe a hiatal hernia attack. Even did a stress test which was normal. Put patient on Lipitor, but even her cholesterol levels were 177. After two weeks, things seem to be getting better. The doctors don't believe her, though, that this could be shot-related. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 1,0
Labordaten: Test Date: 20211104; Test Name: cholesterol levels; Result Unstructured Data: Test Result:177; Test Date: 20211104; Test Name: stress test; Result Unstructured Data: Test Result:normal; Test Date: 20211104; Test Name: Liver levels; Result Unstructured Data: Test Result:little high; Test Date: 20211104; Test Name: D-Dimer; Result Unstructured Data: Test Result:high; Test Date: 20211107; Test Name: SARS-CoV-2 PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anemia; Hiatal hernia; Obesity; Renal agenesis
Andere Medikamente: GABAPENTIN; SINGULAIR; PROTONIX [OMEPRAZOLE]
Allergien: -
Vorherige Impfungen: -

VAERS 1829677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

kritisch

Staat: WA
Alter: 58,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Adverse reaction Anaphylactic shock Dizziness Extra dose administered Hyperhidrosis Nausea Pharyngeal swelling Rash Syncope

Symptomtext

Patient was administered third Pfizer vaccine 10/29/21 at 3:25pm. Within 5 minutes of the vaccine, patient's husband reported patient was having an adverse reaction. Patient reported syncope, lightheadedness, sweating, and nausea but did not report symptoms swelling in the throat, rash, etc that would be typical of a anaphylactic shock. At this point, EMS was called. Patient was instructed to lay down to help resolve symptoms for a couple minutes with little improvement so we decided to bring her in to counseling room to do a blood pressure reading but by that time EMS had arrived and taken over the situation. Patient was eventually taken to hospital by ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1828445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

kritisch

Staat: OH
Alter: 84,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

observed resident to be passed away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NA on Hopsice
Aktuelle Erkrankungen: on Hospice for dementia with life expectancy of 6 months or less
Vorgeschichte: on Hospice for dementia with life expectancy of 6 months or less demetina, malignant neoplasm kidney, HTN, hyperlipidemia, dysphagia, constipation, squamous cell carcinoma to nose, depression, anxiety, cognitive decline, low back pain, DM
Andere Medikamente: tramadol,fentanyl patch, miralax,colace, Depakote, Tylenol,norvasc, fluoxetine, trazodone, exelon
Allergien: codeine, hydrocodone,propoxyphene,tetracycline,clinoril,darvon,indocin,phenergan,vasotec,tap
Vorherige Impfungen: -

VAERS 2711566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: MA
Alter: 35,0
Geschlecht: M
Eingang: 08.11.2023
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Full blood count Malaise Metabolic function test Syncope

Symptomtext

syncope. He was not feeling well, went to the bathroom and felt weak and syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: hospitalization; cbc, bmp
Aktuelle Erkrankungen: none
Vorgeschichte: adrenal insufficiency
Andere Medikamente: fludrocortisone
Allergien: none
Vorherige Impfungen: -

VAERS 2624656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 02.05.2023
Impfdatum: 08.11.2021
Beginn: 21.05.2022
Tage bis Beginn: 194,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Deep vein thrombosis Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE DVT, UNSPECIFIED VEIN 6/7/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2598690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: NY
Alter: 35,0
Geschlecht: M
Eingang: 17.03.2023
Impfdatum: 29.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Cardiac failure Chest pain Computerised tomogram Dyspnoea Echocardiogram Electrocardiogram Fatigue Hypersensitivity Magnetic resonance imaging Myocarditis Pruritus Pulmonary function test Swelling Urticaria

Symptomtext

between 6-10 days after the initial dose i had allergic reactions ranging from hives, swelling, itching, etc, followed by 2 visits to the ER. By the 2nd dose i exhibited more frequent reactions also including SOB, fatigue, and chest pain. I was later diagnosed with Myocarditis, which led to moderate heart failure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG, Echocardiograms, MRI's, PFT, CT Scan
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2581495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 14.02.2023
Impfdatum: 14.12.2021
Beginn: 13.02.2023
Tage bis Beginn: 426,0
Dosis: 3
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute kidney injury Alanine aminotransferase normal Anion gap Aspartate aminotransferase normal Asthenia Atelectasis Bacterial test positive Base excess increased Basophil count decreased Basophil percentage decreased Bilirubin urine present Bladder scan Blood albumin normal Blood alkaline phosphatase normal Blood bicarbonate increased Blood bilirubin increased Blood calcium decreased Blood chloride normal

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: DO on February 13, 2023 07:40 Verified By: DO on February 13, 2023 07:40 Encounter Info: Hospital, Inpatient, 02/12/23 - * Final Report * Chief Complaint syncope/loc History of Present Illness/Subjective This is a 71-year-old female with a history of diabetes, COPD, chronic arthritis, hypertension, obesity, breast cancer who presents after syncopal episode. Husband states that she has been generally weak, has had a cough, and has been feeling short of breath for about 2 days. Home COVID test prior to arrival was positive. This evening, the patient was using her lift chair going from a lying to an upright position when she had a syncopal episode. She endorses dizziness prior to passing out. She denies any symptoms currently including abdominal pain, increased back pain above baseline, chest pain, or headache. She did not fall to the floor or hit head. In the ED workup revealed hypercapnia, cxr suggest possible aspiration pneumonia vs pneumonitis, ua shows likely UTI, covid test was +, lactate was elevated, and she had an AKI. With fluid administration lactate normalized, and aki improved overnight. This patient is critically ill due to metabolic, hemodynamic and/or respiratory instability. They require high complexity evaluation, decision making, and care. They require ICU level of care and monitoring due to high risk of clinical decompensation with high risk of morbidity and mortality. Critical care time includes, but is not limited to, bedside assessment, review of medical record, radiographic and laboratory results, ventilator and/or respiratory management, review of ekg and/or cardiac monitoring, critical decision making, coordination of care with consultants and/or care team, and documentation of critical intervention/plans, and consultation with patient and/or family. Time excludes any procedural time. I spent greater than 60 minutes in the evaluation and management of this patient with more than 50% of the time spent counseling and/or coordinating care. I counseled the patient and/or family about the findings, differential diagnoses, my assessment, recommendations, and plan. I coordinated care with the multidisciplinary healthcare team. Review of Systems A complete, 13-system review was performed and was negative except for as noted in the HPI. Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 36.5 (36.5-36.5) Temp (FAHR) 97.7 (97.7-97.7), BP 129/55 (104-152)/(44-93), HR 51 (51-77), RR 20 (13-20), O2Sat 95 (92-95) Neurologic (most recent and range for last 24 hours) GCS 14(14-15) Patient Weight Current Daily Weight: 119.6 kg 02/13/23 Previous Daily Weight: 119.6 kg 02/13/23 BMI: 43.9 02/13/23 Morbid Obesity (BMI > = 40) Patient Height Constitutional: Alert. _no acute distress, well-nourished. Chronically ill-appearing, obese Eye: PERRLA, EOMI, normal conjunctiva, visually fixates and follows HENT: Normocephalic and atraumatic. External ears normal bilaterally, oral mucosa moist, no pharyngeal erythema. Normal nose. Neck: Supple, no lymphadenopathy. Normal ROM. No meningismus. Respiratory: Coarse bilaterally with bibasilar crackles. Mild respiratory distress. Ventimask in place. Breath sounds are equal, symmetrical chest wall expansion. Cardiovascular: Sinus bradycardia, no murmur, no gallop, good pulses equal in all extremities, normal peripheral perfusion, no edema Genitourinary: Deferred Gastrointestinal: Soft, non-tender, non-distended, normal bowel sounds, no organomegaly, no masses Lymphatics: No lymphadenopathy Musculoskeletal: Normal range of motion, normal strength, no tenderness, no swelling, no deformity, normal gait, spine straight. No TTP to TL spine. Integumentary: Warm, dry, intact, no rashes. Capillary refill < 3 seconds Neurologic: Alert. Oriented to person, place, and time. Moves all 4 extremities and follows commands. Gross motor function and sensation intact in all 4 extremitis. No gross focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Sepsis A41.9 2. Hypercapnic respiratory failure J96.92 3. COVID U07.1 4. Pneumonia J18.9 5. Syncope R55 6. UTI (urinary tract infection) N39.0 -admit to ICU for new bipap therapy -likely 2/2 uti and or pneumonia as well as covid. -follow cx, adjust abx prn, will cover for both uti and cap with rocephin doxy -begin dexamethasone -resp assessment, svns -obtain inflammatory markers -trend lactate until it normalizes -trend wbc and procal to monitor response -will not start remdesivir in view of aki -supplemental O2 -bipap prn -serial vbg -syncope most likely 2/2 orthostatic hypotension given the severity of her dehydration when she arrived -obtain echo to rule out alternative causes of syncope -maintain telemetry Gastro-esophageal reflux disease without esophagitis K21.9 cont home meds Ordered: pantoprazole, 40 mg, Orally, Tab, Delayed Rel, Daily, 02/13/23 9:00:00 Generalized osteoarthritis of multiple sites M15.9 cont home meds Ordered: gabapentin, 300 mg, Orally, Capsule, 4 Times Daily, 02/13/23 9:00:00 Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 02/12/23 23:49:00 albuterol, 2 Puff, Inhalation, Aerosol, MDI/DPI Inhaler Treatment, Q4H, PRN, Dyspnea, 02/13/23 2:05:00 albuterol, 2.5 mg, Neb Inhal, Inhalation SOLN, Aerosol Treatment, Q6H, PRN, Wheezing, 02/13/23 0:36:00, RT Care Assessment and Protocol per Policy albuterol, 2.5 mg, Neb Inhal, Inhalation SOLN, Aerosol Treatment, Q4H, PRN, Dyspnea, 02/13/23 2:04:00, RT Care Assessment and Protocol per Policy allopurinol, 100 mg, Orally, Tablet, Daily, 02/13/23 9:00:00 aspirin, 81 mg, Orally, Tab, Chewable, Daily, 02/13/23 9:00:00 atorvastatin, 40 mg, Orally, Tablet, At Bedtime, 02/13/23 21:00:00 carvedilol, 6.25 mg, Orally, Tablet, BID, 02/13/23 9:00:00 ceftRIAXone, 1 GM, IVPB, Injection, Q24H, Indication: UTI, 02/13/23 0:00:00, 100 mL/hr, Infuse Over 30 minutes, Total Volume (mL) = 50 dexamethasone, 6 mg, IV Push, Injection, Q24H, NOW, 02/12/23 23:49:00, for 10 Days, 02/21/23 23:49:00 Dextrose 10% in Water 500 mL, Total Volume (mL) = 500, IV, 02/12/23 23:49:00, PRN - See Comments, Clinical Weight docusate, 100 mg, Orally, Capsule, BID, 02/13/23 9:00:00 doxycycline, 100 mg, Orally, Capsule, Q12, Indication: Pneumonia - CAP, 02/13/23 10:00:00 fentaNYL, 1 Patch, Topical, Patch, Q72H, 02/13/23 1:00:00 fluticasone-vilanterol, 1 Puff, Inhalation, Aerosol Powder, MDI/DPI Inhaler Treatment, Daily, 02/13/23 9:00:00 glucagon, 1 mg, IM, Injection, Unscheduled, PRN, Hypoglycemia, 02/12/23 23:49:00 glucose, Per Glucose Level, IV Push, Injection, Unscheduled, PRN, Low Blood Sugar, 02/12/23 23:49:00 heparin, 5,000 Units, Subcutaneous, Injection, Q8H, Routine, 02/13/23 0:00:00 insulin lispro, Sliding Scale, Subcutaneous, Injection, With Glucose Testing, PRN, Serum Glucose, 02/12/23 23:49:00 Lactated Ringers 1,000 mL, Total Volume (mL) = 1,000, IV, 02/12/23 23:49:00, 60 mL/hr, Clinical Weight leveTIRACetam, 250 mg, Orally, Tablet, BID, 02/13/23 9:00:00 ondansetron, 4 mg, IV Push, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 02/12/23 23:49:00 OXYcodone-acetaminophen, 1 Tablet, Orally, Tablet, Q4H, PRN, Pain, Moderate to Severe, 02/13/23 1:30:00 rOPINIRole, 0.25 mg, Orally, Tablet, TID, 02/13/23 9:00:00 sacubitril-valsartan, 4 Tablet, Orally, Tablet, BID, 02/13/23 9:00:00 Sodium Chloride 0.9% 500 mL, Total Volume (mL) = 500, IV, 02/12/23 23:50:00, Other - See Comments, Clinical Weight spironolactone, 25 mg, Orally, Tablet, Daily, 02/13/23 9:00:00 tiZANidine, 4 mg, Orally, Tablet, At Bedtime, 02/13/23 21:00:00 torsemide, 20 mg, Orally, Tablet, Daily, 02/13/23 9:00:00 umeclidinium, 1 Puff, Inhalation, Aerosol Powder, MDI/DPI Inhaler Treatment, Daily, 02/13/23 9:00:00 180 gm Carb per day Diet Admit to Inpatient CAH Auto Diff Basic Metabolic Panel BIPAP Intermittent Bladder Scan Call (Specify) Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Oxygen Need Greater Than Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature Call Urine Output CBC w/Differential CBC w/Differential CK SerPl QN CRP SerPl QN D-Dimer Pl QN Fall Precautions Ferritin SerPl QN Fluid Intake Requirement Gluc-Strip POC Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Oxygen Protocol Initiate Respiratory Protocol Initiate Skin and Wound Care Protocol Intake + Output Strict Interleukin 6 QN L pneumophila Ag Ur QL LDH SerPl QN Level of Care Lipid Panel SerPl QN Magnesium SerPl QN Medical Service Medication Message to Nursing Message to Nursing Message to Nursing No NSAIDS (includes COX-2 Inhibitors) Notify Provider Notify Provider Notify Provider Peripheral IV Insertion Reason for Not Ordering Long-acting Insulin Resp CX + Stn Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Single Oxygen Saturation Strep pneumoniae Ag Urine Telemetry Class III 24hr Recommendation Vital Signs Weight Code Status Resuscitation Status - Ordered -- 02/12/23 23:49:00, Full Code Chronic Problem List Allergic asthma Arthralgia Diabetes mellitus with neurological manifestation Family history of breast cancer Foot callus History of cardiomyopathy in adulthood Hyperlipidemia Hypertension Low back pain Lymphedema Morbid obesity NASH (nonalcoholic steatohepatitis) Onychomycosis Osteoarthritis Personal history of breast cancer Spondylosis of cervical spine Tongue lesion Use of opiates for therapeutic purposes Procedure/Surgical History ?Diabetic retinal eye exam (06/20/2022) ?Bone density scan (09/18/2017) ?Cholecystectomy (11/27/2008) ?Carpal tunnel decompression ?Colonoscopy ?Heel spur ?Hip ?Hysterectomy ?Knee replacement ?Mastectomy ?Right shoulder ?Umbilical hernia Medications Home Medications (27) Active acetaminophen 650 mg, PRN, Orally, BID albuterol 2.5 mg/3 mL (0.083%) inhalation solution 2.5 mg = 3 mL, PRN, Neb Inhal, Q6H allopurinol 100 mg oral tablet 100 mg = 1 Tablet, Orally, Daily aspirin 81 mg oral tablet, chewable 81 mg = 1 Tablet, Orally, Daily atorvastatin 40 mg oral tablet 40 mg = 1 Tablet, Orally, At Bedtime Blood Glucose Meter Not Applicable, Other, Unscheduled, DX E11.9One Touch Meter Blood Glucose Test Strips Check one time daily, Other, Unscheduled, One Touch strips E11.65, not on insulin, testing one a day, fax carvedilol 6.25 mg oral tablet 6.25 mg = 1 Tablet, Orally, BID, stop metoprolol and change to coreg 6.25mg. DME Nebulizer Machine w/ Supplies Not Applicable, Other, Unscheduled Entresto 97 mg-103 mg oral tablet 1 Tablet, Orally, BID fentaNYL 50 mCg/hr transdermal film, extended release 1 Patch, Topical, Q72H Lancets Check one time daily, Other, Unscheduled, Sunmark True Metrix lancets E11.65, fax, not on insulin, testing once a day leveTIRACetam 250 mg oral tablet 250 mg = 1 Tablet, Orally, BID metFORMIN 1000 mg oral tablet 1,000 mg = 1 Tablet, Orally, BID, E11.9 Neurontin 300 mg oral capsule 300 mg = 1 Capsule, Orally, 4 Times Daily omeprazole 40 mg oral delayed release capsule 40 mg = 1 Capsule, Orally, Daily Percocet 10 mg-325 mg oral tablet 1 Tablet, Orally, Q6H Potassium Chloride (Eqv-Klor-Con M20) 20 mEq oral tablet, extended release See Instructions, 1 Tablet every other day predniSONE 5 mg oral tablet 10 mg = 2 Tablet, Orally, Daily, patient has a regimen of tapering every 2 weeks rOPINIRole 0.25 mg oral tablet 0.25 mg = 1 Tablet, Orally, TID, G89.4 spironolactone 25 mg oral tablet 25 mg = 1 Tablet, Orally, Daily tiZANidine 2 mg oral tablet 4 mg = 2 Tablet, Orally, At Bedtime torsemide 20 mg oral tablet 20 mg = 1 Tablet, Orally, Daily Trelegy Ellipta , Inhalation, Daily Trelegy Ellipta 200 mCg-62.5 mCg-25 mCg inhalation powder 1 Puff, Inhalation, Daily Ventolin HFA 90 mCg/inh inhalation aerosol 180 mCg = 2 Puff, Inhalation, 4 Times Daily, Every 4 - 6 hours as needed for shortness of breath and/or wheezing. Voltaren Topical 1% topical gel 2 GM, Topical, 4 Times Daily, Use dosing card to measure dose Active Scheduled Inpatient Medications allopurinol, Tablet, 100 mg, Orally, Daily, Start: 02/13/23 09:00:00 aspirin, Tab, Chewable, 81 mg, Orally, Daily, Start: 02/13/23 09:00:00 atorvastatin, Tablet, 40 mg, Orally, At Bedtime, Start: 02/13/23 21:00:00 ceftRIAXone, Injection, 1 GM, IVPB, Q24H, Indication: UTI, Start: 02/13/23 00:00:00 dexamethasone, Injection, 6 mg, IV Push, Q24H, Start: 02/12/23 23:49:00 docusate (docusate sodium), Capsule, 100 mg, Orally, BID, Start: 02/13/23 09:00:00 doxycycline, Capsule, 100 mg, Orally, Q12, Indication: Pneumonia - CAP, Start: 02/13/23 10:00:00 fentaNYL (fentaNYL 50 mCg/hr transdermal film, extended release), Patch, 1 Patch, Topical, Q72H, Start: 02/13/23 01:00:00 fluticasone-vilanterol (Breo Ellipta 100 mCg-25 mCg inhalation powder), Aerosol Powder, 1 Puff, Inhalation, Daily, Start: 02/13/23 09:00:00 gabapentin (Neurontin), Capsule, 300 mg, Orally, 4 Times Daily, Start: 02/13/23 09:00:00 heparin (heparin 5,000 units/0.5 mL injectable solution), Injection, 5,000 Units, Subcutaneous, Q8H, Start: 02/13/23 00:00:00 leveTIRACetam, Tablet, 250 mg, Orally, BID, Start: 02/13/23 09:00:00 pantoprazole, Tab, Delayed Rel, 40 mg, Orally, Daily, Start: 02/13/23 09:00:00 rOPINIRole, Tablet, 0.25 mg, Orally, TID, Start: 02/13/23 09:00:00 sacubitril-valsartan (Entresto 97 mg-103 mg oral tablet), Tablet, 4 Tablet, Orally, BID, Start: 02/13/23 09:00:00 spironolactone, Tablet, 25 mg, Orally, Daily, Start: 02/13/23 09:00:00 tiZANidine, Tablet, 4 mg, Orally, At Bedtime, Start: 02/13/23 21:00:00 torsemide, Tablet, 20 mg, Orally, Daily, Start: 02/13/23 09:00:00 umeclidinium (Incruse Ellipta 62.5 mCg inhalation powder), Aerosol Powder, 1 Puff, Inhalation, Daily, Start: 02/13/23 09:00:00 Lactated Ringers 1,000 mL IV 60 mL/hr 0 02/13/23 Dextrose 10% in Water 500 mL IV PRN - See Comments Sodium Chloride 0.9% 500 mL IV Other - See Comments 0 02/13/23 One-Time Medications Given 02/12/23 00:00:00 TO 02/13/23 07:40:26 atorvastatin, Tablet, 40 mg, Orally, ONCE, (1 DOSE 02/13/23 01:26:00) carvedilol, Tablet, 6.25 mg, Orally, ONCE, (1 DOSE 02/13/23 01:26:00) fentaNYL patch DISPOSAL, Dispose , Misc, ONCE, (1 DOSE 02/13/23 01:21:00) gabapentin, Capsule, 300 mg, Orally, ONCE, (1 DOSE 02/13/23 01:26:00) leveTIRACetam, Tablet, 250 mg, Orally, ONCE, (1 DOSE 02/13/23 01:26:00) rOPINIRole, Tablet, 0.25 mg, Orally, ONCE, (1 DOSE 02/13/23 01:26:00) sacubitril-valsartan (sacubitril-valsartan 97 mg-103 mg oral tablet), Tablet, 4 Tablet, Orally, ONCE, (1 DOSE 02/13/23 01:26:00) tiZANidine, Tablet, 4 mg, Orally, ONCE, (1 DOSE 02/13/23 01:26:00) PRN Medications (0600 - 0559) from 02/12 - 02/13 OXYcodone-acetaminophen, 1 Tablet, Orally, Q4H, 1 Dose(s) acetaminophen, 650 mg, Orally, Q4H, 0 Dose(s) albuterol, 2 Puff, Inhalation, Q4H, 0 Dose(s) albuterol, 2.5 mg, Neb Inhal, Q4H, 0 Dose(s) albuterol, 2.5 mg, Neb Inhal, Q6H, 0 Dose(s) glucagon, 1 mg, IM, Unscheduled, 0 Dose(s) glucose, Per Glucose Level , IV Push, Unscheduled, 0 Dose(s) insulin lispro, Sliding Scale , Subcutaneous, With Glucose Testing, 0 Dose(s) ondansetron, 4 mg, IV Push, Q6H, 0 Dose(s) Allergies Altace (Angioedema, allergic reaction) Vicks VapoRub (turns skin red) sulfa drugs (allergic reaction) Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School disability due to RA Home/Environment Lives with Spouse. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Arthritis: Mother and Father. Asthma: Mother and Father. Diabetes mellitus type 2: Mother. Diabetes..: Mother. Gout..: Mother. Heart disease: Mother. Heart disease..: Mother. Hyperlipidemia: Mother and Father. Hypertension: Mother and Father. Hypothyroid: Father. Osteoporosis: Mother and Father. Osteoporosis..: Mother and Father. Shortness of breath: Mother. Sleep apnea...: Mother and Father. Stroke: Mother and Father. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 15.7 k/cumm High (02/13/23 04:28:00) RBC: 3.62 million/cumm Low (02/13/23 04:28:00) Hgb: 11.2 GM/dL Low (02/13/23 04:28:00) Hct: 35.1 % (02/13/23 04:28:00) MCV: 97 fL (02/13/23 04:28:00) MCH: 30.9 pg (02/13/23 04:28:00) MCHC: 31.9 GM/dL Low (02/13/23 04:28:00) RDW: 16.2 % High (02/13/23 04:28:00) Platelet: 165 k/cumm (02/13/23 04:28:00) MPV: 8.3 fL (02/13/23 04:28:00) Neutrophils %: 96 % (02/13/23 04:28:00) Lymphocytes %: 3 % (02/13/23 04:28:00) Monocytes %: 1 % (02/13/23 04:28:00) Eosinophils %: 0 % (02/13/23 04:28:00) Basophils %: 0 % (02/13/23 04:28:00) Absolute Neutrophil: 15.1 k/cumm High (02/13/23 04:28:00) Absolute Lymphocyte: 0.5 k/cumm Low (02/13/23 04:28:00) Absolute Monocyte: 0.1 k/cumm (02/13/23 04:28:00) Absolute Eosinophil: 0 k/cumm (02/13/23 04:28:00) Absolute Basophil: 0 k/cumm (02/13/23 04:28:00) Chemistry: Sodium SerPl QN: 140 mmol/L (02/13/23 06:20:49) Potassium SerPl QN: 3.7 mmol/L (02/13/23 06:20:49) Chloride SerPl QN: 101 mmol/L (02/13/23 06:20:49) Carbon Dioxide SerPl QN: 30 mmol/L High (02/13/23 06:20:49) Anion Gap: 9 mmol/L (02/13/23 06:20:49) BUN SerPl QN: 46 mg/dL High (02/13/23 06:20:49) Creatinine SerPl QN: 1.48 mg/dL High (02/13/23 06:20:49) Estimated GFR (CKD-EPI, no race): 38 mL/min/1.73m2 Low (02/13/23 06:20:49) Estimated CRCL (CG): 45 mL/min Low (02/13/23 06:20:49) Glucose SerPl QN: 227 mg/dL High (02/13/23 06:20:49) Calcium Total SerPl QN: 8.2 mg/dL Low (02/13/23 06:20:49) Alkaline Phos SerPl QN: 46 Units/L (02/12/23 18:21:00) ALT SerPl QN: 18 Units/L (02/12/23 18:21:00) AST SerPl QN: 14 Units/L (02/12/23 18:21:00) Bilirubin Total SerPl QN: 1.2 mg/dL High (02/12/23 18:21:00) Total Protein SerPl QN: 6.2 GM/dL Low (02/12/23 18:21:00) Albumin SerPl QN: 3.6 GM/dL (02/12/23 18:21:00) Magnesium SerPl QN: 2.1 mg/dL (02/13/23 04:26:00) CK SerPl QN: 388 Units/L High (02/13/23 04:26:00) Troponin-I High Sensitivity: 32 ng/L High (02/12/23 19:23:00) BNP Pl QN: 82 pg/mL (02/12/23 18:21:00) Lactate Venous Pl QN: 1.6 mmol/L (02/12/23 20:51:00) pH Bld Venous QN: 7.35 (02/12/23 20:15:00) PCO2 Bld Venous QN: 58 mmHg (02/12/23 20:15:00) PO2 Bld Venous QN: 34 mmHg Low (02/12/23 20:15:00) Base Excess Bld Venous: 5 mmol/L High (02/12/23 20:15:00) Bicarb Bld Venous Calc: 32 mmol/L High (02/12/23 20:15:00) O2 Sat Bld Venous Calc: 62 % (02/12/23 20:15:00) Patient Temperature: 37 DegC (02/12/23 20:15:00) C-Reactive Prot SerPl QN: 31.6 mg/dL High (02/13/23 04:26:00) Coagulation: PT: 13.5 seconds (02/12/23 18:21:00) INR: 1.18 (02/12/23 18:21:00) D-Dimer Pl QN: 533 ng/mL DDU High (02/13/23 04:26:00) Urine Studies: Color: Yellow (02/12/23 19:38:00) Clarity: Clear (02/12/23 19:38:00) Specific Gravity: 1.020 (02/12/23 19:38:00) pH: 5.0 (02/12/23 19:38:00) Protein: 30 Abnormal (02/12/23 19:38:00) Glucose: NEGATIVE (02/12/23 19:38:00) Ketones: NEGATIVE (02/12/23 19:38:00) Bilirubin: SC Small Abnormal (02/12/23 19:38:00) Hgb Ur: MODERATE. Abnormal (02/12/23 19:38:00) Nitrite: NEGATIVE (02/12/23 19:38:00) Urobilinogen: NormalUro (02/12/23 19:38:00) Leukocyte Esterase Ur: SMALL. Abnormal (02/12/23 19:38:00) WBC: 11-20 Abnormal (02/12/23 19:38:00) RBC: 6-10 Abnormal (02/12/23 19:38:00) Bacteria: Moderate Abnormal (02/12/23 19:38:00) Squamous Epithelial: Few (02/12/23 19:38:00) All Other Labs: COVID 19 Specimen Source: Nasal (02/12/23 18:32:00) Coronavirus SARS-CoV2 Rapid: Detected Abnormal (02/12/23 18:32:00) Diagnostics Radiology Results - Last 24 hours Across Visits 02/12/2023 18:53 - XR Chest PA or AP Portable IMPRESSION: New opacity opacity and interstitial thickening in the right mid tolower lung since 2/1/2023 compatible with atelectasis and/orpneumonitis. The possibility of aspiration pneumonitis should beconsidered.Thank you for consulting our team of subspecialty emergencyradiologists at radiology. Healthcare providers wishing to discuss this case further can contactthe Health Emergency Radiology reading room. Signature Line Electronically Signed on 02/13/23 07:40 ________________________________________________________ DO

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CT
Alter: 65,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 04.11.2022
Beginn: 12.12.2022
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: unbekannt

Ataxia Blood cholesterol normal Bradycardia C-reactive protein normal Cardiac monitoring abnormal Cerebellar infarction Computerised tomogram head abnormal Electrocardiogram QT prolonged Fatigue Laboratory test normal Nausea Presyncope Red blood cell sedimentation rate normal Ventricular extrasystoles Vomiting White blood cell count normal

Symptomtext

Developed acute severe nausea, vomiting and ataxia on 12/12/22. Presented to the ER and administered IV fluids. EKG showed prolonged QT interval and labs were normal. Symptoms of N/V continued with several near syncopal episodes and ataxia. Admitted to the hospital on 12/30/22 after head CT revealed mulitple cerebellar infarcts. Placed on aspirin and statin dose was increased. Continuous cardiac monitoring ruled out Atrial fibrillation, but did show intermittent PVCs and bradycardia. There was no evidence of coagulation disorders. Cholesterol was normal as were all other labs (including normal CRP, ESR, WBC). Severe fatigue and nausea continues as of 1/16/23. No etiology for CVAs identified.

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Praegender Schweregrund: Presyncope
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: atorvastatin, calcium qday
Allergien: none
Vorherige Impfungen: -

VAERS 2554578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: NY
Alter: 82,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 09.06.2022
Beginn: 23.10.2022
Tage bis Beginn: 136,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest X-ray normal Hypoxia Loss of consciousness Oxygen saturation decreased Pickwickian syndrome SARS-CoV-2 test positive White blood cell count increased

Symptomtext

10/23/2022- Presents to Ed, passed out while on toilet. Covid + test. WBC-16.2. CXr- no infiltrates. Desat to 88% placed on 4L NC Admit acute hypoxia in setting of obesity hypoventilation. Started decadron. 10/24/2022-No events on tele., on RA now. Normal CXR. Given betelovimab 10/25/2022-VSS. om RA. WBC- 13.4 d/c to SNF.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Osteoathritis, afib, Obesity and HTN
Andere Medikamente: -
Allergien: Narcotics
Vorherige Impfungen: -

VAERS 2497763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CO
Alter: 52,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 04.04.2022
Beginn: 13.09.2022
Tage bis Beginn: 162,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chest X-ray Lung disorder Lymphadenopathy Pneumonia Pulmonary oedema SARS-CoV-2 test positive Sinusitis

Symptomtext

Tested positive on 9/13/22 for first time. Continue to have Covid related sinus infection and lung issues, filling with fluid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: Chest X-ray, use of inhalers, use of nebulizer. Sinus infection and pneumonia results
Aktuelle Erkrankungen: Swollen lymph nodes in armpits for one week prior to testing positive
Vorgeschichte: Osteoarthritis
Andere Medikamente: Estradiol, vitamin c, d, e, b, calcium, magnesium Low fat diet
Allergien: Penicillin
Vorherige Impfungen: Enlarged lymph nodes in armpit

VAERS 2481164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CO
Alter: 30,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Aphonia Blood test Chills Cough Decreased appetite Dyspnoea Electrocardiogram Epilepsy Fibromyalgia Headache Hyperhidrosis Insomnia Laboratory test Magnetic resonance imaging abdominal Magnetic resonance imaging head Magnetic resonance imaging neck Magnetic resonance imaging spinal Nausea

Symptomtext

Day of - chills, shakes, fever, sweats, body aches, headaches, difficulty breathing, insomnia Day 2 - same symptoms increased + cough, lost voice, lost appetite, nausea Day 3 - shakes, body aches, headaches, difficulty breathing, insomnia, lost appetite, nausea Day 4 - shakes, body aches, nausea, some difficulty breathing Moving forward - randomized moments of pain, shaking, nausea, headaches. By Jan 2022 I began experiencing seizures and pain which worsened, went through a variety of testing and hospitalization through Feb and was officially diagnosed with Epilepsy and fibromyalgia (no prior instances or genetic history) . I?m currently in pain management treatment, it?s unknown if anything COVID related like the vaccine directly caused or increased symptoms. I had a similar reaction to my first 2 as well.

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Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Nov ?21 - COVID swab test, asthma testing, blood panel Jan ?22 - blood panels, urine tests Feb ?22 - X-rays, MRIs (abdomen, back, cervical, head March/April - MRIs, EKG, ultrasound, urologist testing, rheumatology blood panels May ?22 - 72 hour EKG
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, chronic pain
Andere Medikamente: Sertraline
Allergien: None
Vorherige Impfungen: COVID Pfizer dose 1 & 2 same symptoms

VAERS 2438744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: TN
Alter: 45,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 17.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Angina pectoris Blood pressure increased Cardiac stress test normal Catheterisation cardiac abnormal Chest pain Coronary artery occlusion Dizziness Echocardiogram abnormal Fatigue Feeling hot Hypoaesthesia Pain Pericarditis Pubic pain Scan with contrast abnormal Stent placement Throat irritation

Symptomtext

10/31/2021 Sharp pain in lower right pubic area. Throbbing on right side of chest. 12/10/2021-1/23/2022 Multiple (12) occurrences - Heart pain, burning chest and lower part of throat, struggling to keep steady flow of oxygen, face is hot. Occurs for 5-10 minutes with lingering numbness in face and chest. Elevated blood pressure, dizziness, heart pain, burning chest, tiredness, jaw and face numbness for month and ongoing. Pericarditis diagnosed in February 2022, Medication prescribed. High blood pressure diagnosed in April 2022 Medication prescribed. Blocked artery diagnosed June 2022, Emergency Room Visit- worsened symptoms Heart Catheterization - Stent inserted, 6/24/2022, Blockage had erupted. Ongoing symptoms- Same as above Heart Catheterization- 8/9/2022. Microvascular disease a possibility - on medications

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Praegender Schweregrund: Pericarditis
Hospital-Tage: 3,0
Labordaten: February 2022 Stress test- normal. February 2022 Echocardiogram - pericarditis. June 2022 CT scan with contrast- Blocked Mid LAD.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Elderberry, women's 1 a day vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2379239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: MN
Alter: 63,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 06.04.2021
Beginn: 14.06.2022
Tage bis Beginn: 434,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 COVID-19 pneumonia Hypoxia Loss of consciousness SARS-CoV-2 test positive

Symptomtext

ALTERED LOC, COVID PNEUMONIA, HYPOXIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 3,0
Labordaten: POSITIVE COVID TEST 6/14/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Alcoholic hepatitis Alcohol-induced chronic pancreatitis Exocrine pancreatic insufficiency Pancreatic duct calculus Arthritis Asthma Bipolar affective disorder Chronic back pain Chronic obstructive pulmonary disease Coronary artery disease Depressive disorder Gastroesophageal reflux disease HTN (hypertension) Hyperlipidemia Insomnia Migraine Neurologic disorder Polysubstance abuse PTSD (post-traumatic stress disorder) Schizoaffective disorder Seasonal allergies Seizures Type 2 diabetes mellitus Viral gastroenteritis
Andere Medikamente: Albuterol Hfa (Proventil;Ventolin Hfa) 90 Mcg/Actuation Inhl Inhaler Budesonide 160 Mcg-formoterol 4.5 Mcg (Symbicort) 160-4.5 Mcg/Actuation Inhl Hfaa Inhaler Cholecalciferol (Vitamin D3) 25 Mcg (1,000 Unit) Oral Cap
Allergien: Haldol [Haloperidol Lactate] Amoxicillin Ampicillin Pollen
Vorherige Impfungen: -

VAERS 2245620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 12.11.2021
Beginn: 01.02.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Thrombosis

Symptomtext

Developed a blood clot in left lung; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), on 12Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "COPD in bottom lung Diagnosed with a long time ago" (ongoing), notes: The caller has a preexisting condition in the lungs.; "Had Pneumonia 5 times in bottom left lung" (unspecified if ongoing), notes: Had Pneumonia 5 times in bottom left lung and the left lung doesn't work; "the left lung doesn't work" (unspecified if ongoing), notes: Had Pneumonia 5 times in bottom left lung and the left lung doesn't work. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (First dose: 26Mar2021 , lot: ER8730, NDC: Unknown, expiration: Unknown , Route of administration: left arm), administration date: 26Mar2021, when the patient was 62-year-old, for COVID-19 immunization, reaction(s): "couldn't breathe"; BNT162b2 (First dose: 26Mar2021 , lot: ER8730, NDC: Unknown, expiration: Unknown , Route of administration: left arm), administration date: 26Mar2021, when the patient was 62-year-old, for Covid-19 Immunization, reaction(s): "Dry drowning in lung", "got worse in lungs", "except for taste and smell"; BNT162b2 (First dose: 26Mar2021 , lot: ER8730, NDC: Unknown, expiration: Unknown , Route of administration: left arm), administration date: 26Mar2021, when the patient was 62-year-old, for COVID-19 Immunization, reaction(s): "except for taste and smell"; BNT162b2 (Second dose: 16Apr2021 , lot: EW0170, NDC: unknown , expiration: unknown , Route of adminstration: left arm, the caller had no reaction to the second dose), administration date: 16Apr2021, when the patient was 62-year-old, for Covid-19 Immunization, reaction(s): "had no reaction to the second dose". The following information was reported: THROMBOSIS (medically significant) with onset Feb2022, outcome "unknown", described as "Developed a blood clot in left lung". Clinical course: Caller states prior to receiving the first dose Unknown Pfizer Vaccine, the caller had no lung issue and no cold, did not have Pneumonia or bronchitis, nothing. Developed a blood clot in left lung: The caller developed a blood clot in the left lung.never had a blood clot before. The blood clot was found in Feb2022 but doesn't know when the blood clot occurred. The caller had never had blood clots before. Eventually, later down the road the caller was in the hospital five times. Caller not able to provide dates for hospitalization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: COPD (The caller has a preexisting condition in the lungs.)
Vorgeschichte: Medical History/Concurrent Conditions: Lung disorder (Had Pneumonia 5 times in bottom left lung and the left lung doesn't work); Pneumonia (Had Pneumonia 5 times in bottom left lung and the left lung doesn't work)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2134617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CA
Alter: 33,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 22.11.2021
Beginn: 20.01.2022
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Angiogram normal Anticoagulant therapy Cardio-respiratory distress Chest X-ray abnormal Chest discomfort Cold sweat Dyspnoea Echocardiogram abnormal Ejection fraction normal Electrocardiogram abnormal Hypoaesthesia Laboratory test Magnetic resonance imaging normal Myocarditis Pain Paraesthesia Troponin increased

Symptomtext

On the morning of January 20th, I developed extreme tightening sensation in my chest. My right arm went tingly and then numb. I sat down for a few minutes and when I stood up my left arm went tingly and numb. I then broke out in a cold sweat and then started having difficulty breathing. I called EMS and was rushed to the ER in cardiac distress. I was given aspirin, nitro, and blood thinner in the ambulance and ER. The pain and symptoms were the worst in the ambulance which was roughly 30 minute after the onset of symptoms. After it was established I was not having a heart attack, they determined I had Myocarditis. I was admitted to the hospital and stayed overnight and was discharged around 7:30pm on January 21st.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory distress
Hospital-Tage: 2,0
Labordaten: ECG - 01/20/22 - Abnormal ECG - 01/20/22 - Abnormal ECG - 01/20/22 - Abnormal ECG - 01/20/22 - Abnormal ECG - 01/20/22 - Abnormal Chest X-ray - 01/20/22 - FINDINGS: The heart is normal in size. The pulmonary vasculature is normal. There are no focal areas of pulmonary consolidation or pleural effusions. There may be mild right pulmonary infiltrate. IMPRESSION: 1. Question of mild right pulmonary infiltrate. Correlate for clinical evidence of pneumonia. Echocardiogram - 01/20/22 - Slight inflammation of the myocardium Angiogram - 01/20/22 - Normal Lab Tests - 01/20/22 - All normal ranges except Troponin level at 624.5 pg/ml Lab Tests - 01/21/22 - All normal ranges (Troponin not tested) MRI - 01/21/22 - FINDINGS: Situs is normal. There is no pleural or pericardial effusion or pulmonary infiltrate. There is no evidence of a dysplasia or any definite focal wall motion abnormality. Left ventricular ejection fraction is lower limits of normal at 55 percent. Stroke volume is 100 cc. Cardiac output is 7.6 L/m. Right ventricular ejection fraction is 53 percent. Stroke volume is 93 cc. Cardiac output is calculated at 7.1 L/m. There is a focus of delayed hyperenhancement in the inferolateral wall, that would be consistent with myocarditis. It occupies approximately 5.4 percent of the left ventricular myocardium. It is a full-thickness area of hyperenhancement but has an amorphous appearance and is not typical of an infarct, and myocarditis would be the most likely diagnosis. There is no aortic or pulmonary insufficiency or stenosis. The Qp/Qs is normal at 1.1, there is no evidence of shunt. IMPRESSION: 1. Small focal area of delayed hyperenhancement in the inferolateral wall, small in size, but quite compatible with a focus of myocarditis. It does not have typical appearance of an infarct, and the age of the patient would be against any coronary artery disease. 2. In this region, I do not see any definite wall motion abnormality. This region is quite small and likely is not of sufficient size that it would affect wall motion to any significant degree. 3. The left ventricular ejection fraction is lower limits of normal at 55 percent.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Fluoxetine 40mg once daily
Allergien: N/A
Vorherige Impfungen: -

VAERS 2110347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: NH
Alter: 43,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Anaphylactic reaction Chills Fatigue Food allergy Hypoaesthesia oral Lip swelling Pain Paralysis Pyrexia Rash Swelling face

Symptomtext

First dose was a 103 fever and body aches, chills, overall fatigue. Second dose I was paralyzed for 2 hours about 12 hours after the injection. Also had 103 fever, chills and body aches with overall fatigue. I had a rash for a week following the second dose. The 3rd dose I became anaphylactic allergic to soy, peanuts, lima beans and peas. I never had a food allergy before. I ate peanut butter and my lips swelled. As the week went on every time I ate soy or peanuts the reaction worsened until my face swelled and tongue and lips went numb. I now have an epi pen and avoid soy and peanuts. I also had a fever, body aches, fatigue and chills with my 3rd dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: I saw my physician
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: After my booster I am now dangerously allergic to soy, peanuts, lima beans, peas
Vorherige Impfungen: -

VAERS 2071399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: VA
Alter: 29,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Chills Communication disorder Cough Dyspnoea Feeling abnormal Generalised tonic-clonic seizure Headache Pain Pyrexia Suspected COVID-19

Symptomtext

Seizures similar to partial grand mal and grand mal seizures; Full COVID-19 symptoms; High fever; Difficulty breathing/ Shortness of breath; Cough; Chills; Extreme head pain; Extreme body aches; Brain fog; Inability to follow conversation or form sentences; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29-year-old female patient (not pregnant) received BNT162B2 (BNT162B2), administered in arm left, administration date 26Oct2021 18:45 (Lot number: 320308D) at the age of 29 years as dose 1, single for COVID-19 immunization. Relevant medical history included: "COVID-19", start date: Feb2020 (unspecified if ongoing). The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The following information was reported: GENERALISED TONIC-CLONIC SEIZURE (disability, medically significant, life threatening) with onset 27Oct2021, outcome "recovering", described as "Seizures similar to partial grand mal and grand mal seizures"; SUSPECTED COVID-19 (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "Full COVID-19 symptoms"; PYREXIA (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "High fever"; DYSPNOEA (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "Difficulty breathing/ Shortness of breath"; COUGH (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "Cough"; CHILLS (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "Chills"; HEADACHE (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "Extreme head pain"; PAIN (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "Extreme body aches"; FEELING ABNORMAL (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "Brain fog"; COMMUNICATION DISORDER (disability, life threatening) with onset 27Oct2021, outcome "recovering", described as "Inability to follow conversation or form sentences". The events "seizures similar to partial grand mal and grand mal seizures", "full covid-19 symptoms", "high fever", "difficulty breathing/ shortness of breath", "cough", "chills", "extreme head pain", "extreme body aches", "brain fog" and "inability to follow conversation or form sentences" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of generalised tonic-clonic seizure, suspected covid-19, pyrexia, dyspnoea, cough, chills, headache, pain, feeling abnormal, communication disorder. Clinical course: Adverse reactions occurred to first shot. Seizures similar to partial grand mal and grand mal seizures, and also full COVID-19 symptoms including high fever, difficulty breathing, cough, chills, extreme head pain, extreme body aches, shortness of breath, brain fog, inability to follow conversation or form sentences. Already had COVID-19 in Feb2020, with antibodies in T-cells, prior to vaccination. Seizures continued multiple times a day for nearly 3 weeks, then decreased. The patient received the second dose in the right arm on 18Nov2021 18:30 (lot number: 3302680). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: IL
Alter: 29,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood magnesium normal Blood thyroid stimulating hormone C-reactive protein normal Chest pain Echocardiogram abnormal Full blood count normal Metabolic function test Palpitations Pericardial effusion Pericarditis Red blood cell sedimentation rate normal

Symptomtext

Pt w/sharp chest pain 1 day after vaccination + palpitations. Chest pain worse with laying back. Symptoms persisting into 1/13/22, though much improved. Echo 1/13/22 reveals trivial pericardial effusion. Suspect vaccine-induced pericarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: CBC/CMP/Mag/TSH/ESR/CRP all wnl. Echo revealing trivial pericardial effusion.
Aktuelle Erkrankungen: None
Vorgeschichte: chronic allergic rhinits, mild intermittent asthma w/o complication
Andere Medikamente: Azelastine nasal spray, hydroxyzine prn, cetirizine, albuterol prn, lactobacillus probiotic
Allergien: None
Vorherige Impfungen: -

VAERS 2018658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: WI
Alter: 49,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Immunisation Pericarditis SARS-CoV-2 test

Symptomtext

Dose number:03; pericarditis; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 49 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 11Nov2021 (Lot number: 320308D) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Migraine" (unspecified if ongoing); "Insulin resistance" (unspecified if ongoing); "Depression" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN; TOPAMAX; LEVOTHYROXINE; TRINTELLIX. Past drug history included: Known_allergies:clindamycin, reaction(s): "Drug allergy". Vaccination history included: Bnt162b2 (Dose Number: 1, rev_dose_lot_number=ek5730, prev_dose_vaccine_location= Left arm), administration date: 07Jan2021, when the patient was 48 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 2, prev_dose_lot_number=el1283, prev_dose_vaccine_location= Left arm), administration date: 28Jan2021, when the patient was 48 years old, for COVID-19 Immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. The following information was reported: IMMUNISATION (hospitalization, medically significant) with onset 11Nov2021, outcome "unknown", described as "Dose number:03"; PERICARDITIS (hospitalization, medically significant) with onset 22Dec2021 08:00, outcome "recovering", described as "pericarditis". The patient was hospitalized for immunisation (start date: Dec2021); for pericarditis (start date: Dec2021, discharge date: Dec2021, hospitalization duration: 2 day(s)). The event "pericarditis" was evaluated at the emergency room visit. Since the vaccination, the patient has been tested for COVID-19. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (22Dec2021) negative. Therapeutic measures were not taken as a result of pericarditis. Device Date: 25Dec2021. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the available reported information, the causal association between the events immunization and pericarditis and the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available. 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Test Date: 20211222; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Insulin resistance; Migraine
Andere Medikamente: METFORMIN; TOPAMAX; LEVOTHYROXINE; TRINTELLIX
Allergien: -
Vorherige Impfungen: -

VAERS 2010639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Loss of consciousness Syncope

Symptomtext

vasovagal syncope - passed out for 20 seconds then recovered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: ibuprofen 200 mg
Allergien: none
Vorherige Impfungen: -

VAERS 2002948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: IN
Alter: 84,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 29.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Asymptomatic COVID-19 Computerised tomogram head abnormal Dizziness Echocardiogram Ejection fraction normal Myocardial ischaemia Orthostatic hypotension SARS-CoV-2 test positive Subdural haematoma Syncope Troponin increased

Symptomtext

Syncopal episode at home, occurred after standing up quickly, no loss of consciousness, no head trauma, no chest pain, no shortness of breath. CT head shows chronic subdural hematoma. Reported dizziness, likely orthostatic hypotension Patient incidentally noted to be COVID positive, asymptomatic received vaccine and booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 2,0
Labordaten: 1/3/22 Troponin level 63 1/3/22 Transthroacic echocardiogram - Ejection fraction 55-60%, mitral valve, aortic valve and tricuspid valve: no significant regurgitation. 1/3/2022 Atrial-sensed ventricular spaced rhythm Cardiac consult: elev troponin, very mildly elevated likely demand ischemia without issues. 1/3/2022 COVID19 rapid test is positive
Aktuelle Erkrankungen: -
Vorgeschichte: Pulmonary embolism diabetes dementia AV block s/p pacemaker
Andere Medikamente: Xarelto
Allergien: Beta Blockers
Vorherige Impfungen: -

VAERS 2001077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: MA
Alter: 71,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood test Chest X-ray Culture urine Electrocardiogram Seizure

Symptomtext

Full seizure (with hospitalization) within 24 EKG, hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: EKG, chest x-ray, blood and urine samples
Aktuelle Erkrankungen: None
Vorgeschichte: Epilepsy A-fib
Andere Medikamente: Eliquis Atorvastatin Levetiracetam Multaq
Allergien: None
Vorherige Impfungen: -

VAERS 1988289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: NE
Alter: 35,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 18.11.2021
Beginn: 22.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test C-reactive protein increased Chest pain Dyspnoea Echocardiogram abnormal Electrocardiogram normal Feeling abnormal Infection Mobility decreased Neck pain Oropharyngeal pain Pain Pericardial effusion Pericarditis Pulmonary oedema Ultrasound chest

Symptomtext

Pericarditis. Awful. Started feeling some slight chest pain on 12/22. Felt it more or less continuously for a few days, but nothing severe, until the evening of 12/24. I woke up at 11 pm with severe pain and difficulty lying down and taking a deep breath. Severe chest pains and pain throughout my neck and throat. Went to the ER. They did an EKG and ran some blood tests. My CRP was at a 5, leading them to think I had some sort of infection. EKG was normal, didn't show that I had or was having a heart attack or anything, thank God. They sent me home. Next day, I saw a cardiologist who performed an ultrasound and that showed pericardial effusion around the heart and some fluid buildup around the lungs. Diagnosed it as pericarditis. Prescribed ibuprofen -- 3 pills 3 x a day -- with food. Went back on 12/28 and the fluid around my heart was gone and the fluid around my lungs had diminished from 20 mm to 16 mm. On 12/28, Cardiologist, along with pulmonologist, reduced my ibuprofen to 2 (400 mg tablets) 2x a day. Feeling much better than on 12/24, when I thought I might be having a heart attack despite no history of heart problems in my family at such a young age.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: EKG. Blood tests. 12/24/21 and 12/25/21 Ultrasound on my chest and lungs. 12/25/21 and again on 12/28. I have more or less recovered although I still have some pain. It will likely take me another week or two to completely recover and return to my normal life. I am to be on 2 400mg ibuprofen 2x a day until 1/7/21.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D pills, just one a day
Allergien: No
Vorherige Impfungen: -

VAERS 1981883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Guillain-Barre syndrome Hypoaesthesia Laboratory test abnormal Muscular weakness Pain Paraesthesia

Symptomtext

Numbness, tingling and weakness of my lower extremities. Legs feel as if they will give out. Severe throbbing/pulsating sensation. Symptoms worsened after second dose on 11/26/2021 tingling and weakness moved up towards my hands and upper body. Diagnosed with Guillain Barre Syndrome on 12/15/2021 and currently receiving 30 grams of IVIG daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: Labs 12/10/21 12/15/2021 Diagnosed with GBS
Aktuelle Erkrankungen: Thrombocytosis
Vorgeschichte: Thrombocytosis
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1920786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: UT
Alter: 53,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anaphylactic reaction Chest pain Dizziness Nausea Throat tightness Urticaria

Symptomtext

Anaphylaxis (hives, throat tightening, chest pain, dizziness, nausea) after booster dose with Pfizer-BioNTech COVID-19 vaccine. Took patient to urgent care. Gave diphenhydramine 50 mg IV. Gave epinephrine and glucagon 1 mg IV. Contacted EMS. EMS gave additional dose of epinephrine and transported patient to ED. Limited data from outside ED, but looks like patient was discharged in stable condition with instructions to return if symptoms return. Given home EpiPen prescription.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Atrial fibrillation
Vorgeschichte: -
Andere Medikamente: -
Allergien: Many allergies listed in the patient's chart. Patient had a similar reaction to the first dose, but premedicated for the second dose, and didn't have a reaction.
Vorherige Impfungen: -

VAERS 1905682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: VA
Alter: 34,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Hyperhidrosis Loss of consciousness Paraesthesia Presyncope

Symptomtext

Pt stated they were anxious at seeing vaccinator assemble needle. Vaccine given and pt reported tingling sensation down arm and then across chest. Pt with vaso vagal response and unconscious for a few seconds, awoke sweaty, following commands. Stated first vaccine he had tingling in lips. EMS called and pt agreed to hospital transport. VSWNL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Denies
Andere Medikamente: None
Allergien: NKDA, NKFA
Vorherige Impfungen: Tingling to lips s/p first COVID vaccination

VAERS 1902841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: SC
Alter: 34,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 26.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anaphylactic reaction

Symptomtext

Anaphylaxis: 0.3mL EPI 1:1 via IM, Benadryl 50mg via IM, Seek Eval at ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Unknown.
Aktuelle Erkrankungen: None Reported
Vorgeschichte: Hyperlipidemia
Andere Medikamente: Vitamin D
Allergien: Sulfa drugs and Pertussis Vaccine
Vorherige Impfungen: -

VAERS 1887884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: AZ
Alter: 28,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting/Unresponsive-Mild, Additional Details: Patient experienced lightheadedness and required EMS due to passing out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1885046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: SC
Alter: 49,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood glucose Blood magnesium Dyspnoea Electrocardiogram Full blood count Hypotonia Seizure

Symptomtext

11/18/2021, at 1:17 pm: Received Pfizer (1st dose). 11/18/2021, at 1:25 pm: She had trouble breathing. Assisted to a nearby chair closer to the treatment room, then directly assisted to a treatment room a few feet away. Blood pressure being taken when she became limp. Immediately assisted to the floor. 911 called. B/P 184/71-97- 98 percent O2 SAT. She had 4 seizures before ambulance service arrived. 11/18/2021, at 1:32 pm ambulance arrived. VS taken: B/P 145/78-113-O2 SAT 98 %. She is conscious, brought pocketbook to her. Family notified by phone. Patient on stretcher and transferred to ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: CBC, MG, Glucose, EKG.
Aktuelle Erkrankungen: Anxiety disorder
Vorgeschichte: Unknown. Co-worker stated patient has a tumor on the spine and went to the hospital in August for seizures.
Andere Medikamente: Hydrochlorothiazide 25mg by mouth for high BP; Flonase 2 sprays each nostril (inflammation of nose due to allergy); Valacyclovir 500mg tab; Ascorbic acid, Vitamin C 100mg tablet daily by mouth; Cholecalciferol, Vitamin D3 25mcg (1.000 unit
Allergien: Morphine (hives)
Vorherige Impfungen: -

VAERS 1881125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: NC
Alter: 19,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Syncope

Symptomtext

Patient fainted the day following vaccine after waking up. Symptoms resolved quickly and patient was resting in bed when caregiver called.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1874405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: MO
Alter: 29,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Confusional state Pallor Syncope Unresponsive to stimuli Vomiting

Symptomtext

Patient was prepped to receive Pfizer Covid-19 vaccine, vaccine was administered and in approximately 2 minutes patient experienced vasovagal syncope, fainting. Pharmacist tried to alert patient who remained non-responsive for approximately 2 minutes and EMS was called. When patient regained consciousness, patient was confused and pale. Patient became more alert and within approximately 5 minutes began to vomit. EMS arrived and took over care of patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 1871125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anxiety Fear Hypotension Syncope

Symptomtext

Patient fainted after getting her first dose of covid-19 vaccine Pfizer, pharmacy called paramedic and paramedic informed us that patient had low blood pressure, and needed to be observed for a period of time. Pharmacy called mother and was told that paramedic told her she had anxiety attack due to fear of vaccine but not allergic to covid-19, mother also informed pharmacy there's no medication given to her daughter by paramedic, and patient was doing fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1869794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: NY
Alter: 63,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Chest X-ray Condition aggravated Pain in extremity Seizure

Symptomtext

WITHIN AN HOUR PATIENT HAD A SEIZURE, AND HAD 2 ADDITIONAL SEIZURES ABOUT 15 MINUTES AFTER THAT. STATED THAT ARM AND LEGS WERE ALSO HURTING. USED A HEATING PAD FOR THE PAIN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 1,0
Labordaten: PATIENT WAS HOSPITALIZED. CHECKED FOR HEART ATTACK, X-RAYS
Aktuelle Erkrankungen: NONE
Vorgeschichte: SEIZURE DISORDER
Andere Medikamente: FELBAMATE AT NOON, PHENOBARBITAL
Allergien: PENICILLIN
Vorherige Impfungen: COVID - PFIZER

VAERS 1869703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Electrocardiogram abnormal Myocarditis Pyrexia Troponin increased

Symptomtext

Reports 11/12 with fever to 103.5 resolved 24 hours. On 11/15 woke with chest pain, evaluation at hospital with ECG mild ST elevations, elevated troponin. Probable vaccine associate myopericarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: 11/15: ECG with SR w mild ST elevations diffuse Troponin T 198 (nl 0-21 ng/L)
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: albuterol inhaler, symbicort
Allergien: sulfa drugs
Vorherige Impfungen: -

VAERS 1869268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: PA
Alter: 83,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 02.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

C-reactive protein increased Chills Computerised tomogram thorax abnormal Fibrin D dimer increased Interstitial lung disease Lung opacity Mental status changes Pain Pneumonia Positive airway pressure therapy Procalcitonin Respiratory distress SARS-CoV-2 test negative White blood cell count

Symptomtext

83-year-old female presented to the emergency department with respiratory distress, chills, body aches and altered mental status 10 days after receiving her third dose of the Pfizer-BioNTech SARS-CoV-2 vaccination on 11/2/2021. Doses from her primary Pfizer series were administered on 2/27/2021 and 3/20/2021. Prior to presenting to the emergency department, on post-vaccine day 4, the patient was seen by her PCP and was diagnosed with pneumonia; oral outpatient antibiotics were initiated empirically. On arrival to the emergency department the patient was found to be in severe respiratory distress with a pulse oximetry of 55% on room air. Supplemental oxygen and ultimately BiPAP were initiated and pulse oximetry increased to the 90s. After admission, supplemental oxygen via high-flow nasal cannula at rates of 40-50 liters per minute was required to maintain oxygen saturations. Chest CT showed severe diffuse ground-glass and interstitial opacities through all lung fields bilaterally. She was swabbed nasopharyngeally for SARS-CoV-2 on admission and the results were negative. White blood cells was 9800 per microliter, D-dimer was 955 ng/mL, C-reactive protein was 4.3 mg/dL, procalcitonin was reported as <0.05 (undetectable). The patient remained afebrile and hemodynamically stable. Corticosteroids were initiated in the form of dexamethasone 6 mg IV q12h for treatment of presumed drug-induced interstitial lung disease caused by the COVID-19 vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: 10,0
Labordaten: 83-year-old female presented to the emergency department at the hospital with respiratory distress, chills, body aches and altered mental status 10 days after receiving her third dose of the Pfizer-BioNTech SARS-CoV-2 vaccination on 11/2/2021. Doses from her primary Pfizer series were administered on 2/27/2021 and 3/20/2021. Prior to presenting to the emergency department, on post-vaccine day 4, the patient was seen by her PCP and was diagnosed with pneumonia; oral outpatient antibiotics were initiated empirically. On arrival to the emergency department the patient was found to be in severe respiratory distress with a pulse oximetry of 55% on room air. Supplemental oxygen and ultimately BiPAP were initiated and pulse oximetry increased to the 90s. After admission, supplemental oxygen via high-flow nasal cannula at rates of 40-50 liters per minute was required to maintain oxygen saturations. Chest CT showed severe diffuse ground-glass and interstitial opacities through all lung fields bilaterally. She was swabbed nasopharyngeally for SARS-CoV-2 on admission and the results were negative. White blood cells was 9800 per microliter, D-dimer was 955 ng/mL, C-reactive protein was 4.3 mg/dL, procalcitonin was reported as <0.05 (undetectable). The patient remained afebrile and hemodynamically stable. Corticosteroids were initiated in the form of dexamethasone 6 mg IV q12h for treatment of presumed drug-induced interstitial lung disease caused by the COVID-19 vaccine.
Aktuelle Erkrankungen: -
Vorgeschichte: Atrial fibrillation Anxiety Arthritis Depression Dyslipidemia GERD (gastroesophageal reflux disease) Hypertension Hypothyroidism
Andere Medikamente: -
Allergien: pollen
Vorherige Impfungen: -

VAERS 1865719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Feeling abnormal Loss of consciousness Seizure Unresponsive to stimuli

Symptomtext

About after 5 minutes after received the Covid vaccine, patient passed out and had seizure. She became conscious after about a minute. She doesn't respond when we tried to talk to her. She became unconscious/conscious couple times before the ambulance came. Ambulance employees said all her vitals signs is normal. But she seems like she does not aware of her surrounding. Ambulance took her to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: UNKNOWN
Allergien: NO ALLERGY
Vorherige Impfungen: -

VAERS 1864808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: WI
Alter: 41,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Anaemia Colon adenoma Colonoscopy abnormal Gastrointestinal haemorrhage Haematocrit decreased Haemoglobin decreased Haemorrhage Haemorrhoidal haemorrhage Haemorrhoids Large intestine polyp Mean cell haemoglobin concentration normal Mean cell haemoglobin normal Mean cell volume normal Mean platelet volume normal Packed red blood cell transfusion Pathology test Platelet count increased Polypectomy

Symptomtext

Pt received Vaccine and then on 10/30 had developed syncope from GI bleed. received transfusion of 2 units of PRBC. Colonoscopy 10/31/2021 showed grade 3 prep right colon grade 2 prep left and transverse. 1 sigmoid polyp was removed, he was noted to have large internal hemorrhoids with 1 column of hemorrhoids with stigmata of recent bleeding. 1 hemorrhoid had evidence of prior banding in 1 had stigmata of recent bleeding. No active bleeding up to the TI. PATH of polyp was fragments of tubular adenoma He was hospitalized again for anemia received transfusion again and was rehospitialized for bleeding .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: Results for patient as of 11/12/2021 09:33 11/10/2021 17:44 HEMOGLOBIN: 7.1 (L) HEMATOCRIT: 21.4 (L) 11/11/2021 01:02 HEMOGLOBIN: 7.5 (L) HEMATOCRIT: 23.3 (L) 11/11/2021 05:23 WHITE BLOOD CELL COUNT: 4.6 RED BLOOD CELL COUNT: 2.90 (L) HEMOGLOBIN: 8.0 (L) HEMATOCRIT: 23.6 (L) MEAN CORPUSCULAR VOLUME: 81.3 (L) MEAN CORPUSCULAR HGB: 27.4 (L) MEAN CORPUSCULAR HGB CONCENTRN: 33.7 RED CELL DISTRIBUTION WIDTH: 16.6 (H) PLATELET COUNT: 415 MEAN PLATELET VOLUME: 7.2 11/11/2021 05:24 11/11/2021 12:44 HEMOGLOBIN: 7.9 (L) HEMATOCRIT: 24.2 (L) 11/11/2021 15:00 11/11/2021 15:01 RETIC NUMBER X 10^6: 0.1303 (H) RETICULOCYTE PERCENTAGE: 4.1 (H) 11/11/2021 23:21 HEMOGLOBIN: 7.7 (L) HEMATOCRIT: 23.1 (L) 11/12/2021 08:20 WHITE BLOOD CELL COUNT: 4.5 RED BLOOD CELL COUNT: 3.32 (L) HEMOGLOBIN: 8.9 (L) HEMATOCRIT: 27.0 (L) MEAN CORPUSCULAR VOLUME: 81.3 (L) MEAN CORPUSCULAR HGB: 26.7 (L) MEAN CORPUSCULAR HGB CONCENTRN: 32.9 RED CELL DISTRIBUTION WIDTH: 16.1 (H) PLATELET COUNT: 447 MEAN PLATELET VOLUME: 7.5
Aktuelle Erkrankungen: common cold
Vorgeschichte: none
Andere Medikamente: Calcium-Magnesium-Zinc Muscle Relaxation Formula Nutritional Supplements (LIVER DEFENSE) Omega-3 Fatty Acids (FISH OIL) 1000 MG capsule 1Q day vitamin E (TOCOPHERYL) 400 units capsule Take 400 Units by mouth daily.
Allergien: none
Vorherige Impfungen: -

VAERS 1864517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: IL
Alter: 19,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cardiac disorder Chest X-ray Chest discomfort Pericarditis

Symptomtext

Systemic: Cardiac Disorder (diagnosed by MD)-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Additional Details: patient was diagnosed with mild pericarditis following chest xray and given antiinflammatory medications and order to avoid exercise until feeling well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1861843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cold sweat Fear of injection Hyperhidrosis Pallor Syncope

Symptomtext

Brought to my attention that patient had syncopal episode and was escorted to exam room table. When I initially saw patient, she was awake, pale, diaphoretic but was alert and oriented to time, place, and situation. We observed her for 30 minutes, and she became more pink, less diaphoretic but still clammy, and she had drank 4 oz water and had a lollipop in mouth. I checked initially for any bleeding of mouth, no obvious head injury. She was stable upon discharge. I suspect trypanophobia given patient's history with needles. Still encourage 2nd dose but inform injector, stay for 30 minutes observation, and 15 grams of sugar such as a soda or juice carton. She was driven home in private car with an accompanied older female adult relative. Instructed on emergency care immediately for any increased difficulty breathing, chest pain, or increased weakness. Otherwise, anticipate common reactions, such as fever, body aches, and arm injection site pain to be treated with fluids, rest, and Tylenol as needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Vitals on 11/11/21 at 3:00 PM were, BP 94/62, HR 84, RR 16, SpO2 98%, BG 105 g/dL. @3:30 PM, BP 95/66, HR 65, SpO2 98%, BG 90 g/dL.
Aktuelle Erkrankungen: Gatsroesophageal Reflux Disease (GERD)
Vorgeschichte: Denies, although admits she does get lightheaded or has passed out during previous vaccinations or venous blood draws.
Andere Medikamente: No current medications.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1855080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: TX
Alter: 18,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Syncope

Symptomtext

Patient received vaccine approximately 5:15pm. Patient was sitting in waiting room and at approximately 5:25pm patient reached for something on the ground and fainted onto the ground. 911 was called. Police and EMT arrived at the scene. Patient refused to go to the hospital. He called his family to come pick him up. Patient left with out notifying anyone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1851220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: CT
Alter: 19,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Nausea Seizure

Symptomtext

about 1 minute after receiving the vaccine, the patient began feeling nauseous and appeared to have a seizure/convulsions. She was assisted and was lying down in the waiting room until paramedics arrived

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1847367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: PA
Alter: 12,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Confusional state Pallor Seizure Syncope

Symptomtext

about 10 seconds after administration patient convulsed twice and fainted lasting 5-7 seconds. was confused and pale but alert. recovered within minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: HPV

VAERS 1846814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Loss of consciousness Nausea Syncope Tension

Symptomtext

client fainted/ loss consciousness with both tension in both arms and eyes open staring blankly for approx 10 to 20 seconds post vaccination at 3:13pm. client stated that they did not eat all day as they "just woke up" and reported feeling "nauseous" right before incident. Client recieved food from brother after incident. No other treatments given. Vitals after eating stable. @3:14pm BP 78/35 HR 52 @3:16PM BP 86/58 HR 61 @3:26 PM BP 90/55 HR 73 @3:56PM BP 106/52 HR 81 @3:56PM BP 107/74 HR 89 O2 100% THROUGH COURSE OF INCIDENT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1843710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: OK
Alter: 35,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cold sweat Dyskinesia Pallor Syncope

Symptomtext

After receiving his Covid vaccine, patient sat with me for about 5 minutes and then moved to an observation chair. As he sat down he had a brief syncope event with jerks. Was aware and coherent afterwards but pale, and cold sweat. Called 911. Took bp and it was 84/50. Paramedics were on seen in roughly 5 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Paramedics took him to ambulance for treatment and observation, total time about 30 minutes on 11/3/2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1842387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: NJ
Alter: 32,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chest pain Confusional state Injection site pain Loss of consciousness Nausea Pyrexia Seizure Syncope Tinnitus Vision blurred

Symptomtext

Aside from experiencing typical vaccine side effects of fever, pain at injection site, and joint pain, around 15 hours post vaccine I became nauseous followed by blurred vision, chest pain and ringing in my ears. I either fainted or had a seizure but no way to confirm which as I was alone at the time. I did awake on the floor after being unconscious though and was very confused for approximately 30 minutes or so.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None.
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1841211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: GA
Alter: 50,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anaphylactic reaction Burning sensation Dyspnoea Heart rate increased Hypoaesthesia Pain Peripheral coldness Throat tightness Tremor

Symptomtext

Patient had expressed concerns about reacting to the vaccine prior to coming to the pharmacy. She has had reaction to epidural and to the flu shots many years before and has not gotten a vaccine since. She had spoken to her doctor who advised her to be monitored for 30 minutes after vaccination. She informed the pharmacist prior to administration. Approximately 5 minutes after the vaccine, she reported experiencing a burning sensation, increased heart rate, and numbness in the left arm as well as pain under the left breast. She also started feeling cold in the hands, particularly the left hand. She was given Benadryl 50 mg about 7-10 minutes after the vaccine. She started shaking all over. She was asked if she wanted the pharmacy to call 911 but she wanted to wait until the Benadryl kicked in to see if it helped. Then she reported experiencing throat tightness and difficulty breathing, with short and gasping breaths. 911 was called and she was given one dose of 0.3 mg EpiPen in the left leg about 15 minutes after vaccination. She reported being able to breathe better and tightness going away, though the shaking and anxiousness remained. EMS arrived about 10 minutes later, and she was evaluated. She went to the ER to be monitored. At the ER, they diagnosed her with an anaphylaxis reaction the covid-19 Pfizer vaccine. She was given a prescription for EpiPen for future use and prednisone after discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: -
Allergien: n/a
Vorherige Impfungen: flu vaccine

VAERS 1839977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: PA
Alter: 39,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 21.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anticoagulant therapy Deep vein thrombosis Pain in extremity Ultrasound Doppler abnormal

Symptomtext

Pain in left calf that continued to get worse over 5 days. Dr ordered ultrasound and found DVT. No prescribed blood thinners (xeralto)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound performed on November 2, 2021
Aktuelle Erkrankungen: No
Vorgeschichte: High cholesterol and high blood pressure
Andere Medikamente: Lipitor and bystollic
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1832399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood glucose normal Dizziness Loss of consciousness

Symptomtext

pt came in to receive the booster dose for covida19 Pfizer and Flu vaccine. He stated that he had experienced dizziness after getting blood drawn. Stated he didn't have problem after getting the Covid 19 Janssen in March 2021. Covid vaccine was administered first on the left arm and flu shot was on the right arm. Immediately after the flu vaccine, pt passed out in the chair. I kept tapping on his shoulder and called his name but he didn't answer. I told my staff to call emergency immediately and kept tapping on his shoulder. After maybe 4 or 5 seconds or maybe loner, pt slowly regained consciousness. Pt was in the chair at all time. Paramedic arrived, took his BP and checked blood sugar from finger prick. Glucose was 85. Paramedic asked pt to sign waiver that he didn't want to go to the Er in the ambulance, advised pt to not drive and go see his doctor as soon as possible. Pt was contacting family members but no one came and he said he had to go home and he could drive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: pt stated he has anxiety
Andere Medikamente: pt reported he takes anxiety medication
Allergien: nkda
Vorherige Impfungen: -

VAERS 1831679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: PA
Alter: 20,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Dizziness Flushing Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

Systemic: Abdominal Pain-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1829680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: IL
Alter: 22,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Incontinence Loss of consciousness Nausea Seizure Syncope

Symptomtext

about five min after getting shot pt passed out, hit his head, started having a seizure and incontance issues. he was unconscious for several minutes. after waking up he was dizzy, nausous, and light-headed. paramedics wetre called and checked him out. he refused to go with them and his parents came and picked him up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none, pt refused medical care
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1828911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: PR
Alter: 49,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Blood test Decreased appetite Dizziness Nausea Pain Peripheral swelling Pyrexia Syncope Vomiting

Symptomtext

After vaccine at around 9PM, I started feeling nauseous, body ache, feverish, dizziness, I fainted on the floor, vomiting. Monday 10/25/2021 I woke up with swollen left arm. All this week I've been feeling weak and haven't been eating much. I know this vaccine has given me every symptom since 10/22/2021 when I received it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Bloodwork
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Sabella Vortioxetine Neurontin
Allergien: Oxycodone Paracetamol
Vorherige Impfungen: -

VAERS 1818924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: TN
Alter: 83,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Mental impairment Syncope

Symptomtext

Patient fainted after her third covid Pfizer vaccine. She became alert after several minutes. She drank some water and applied cold wet paper towels to her neck. After several minutes of being alert she was not able to answer questions consistently. At that time we called the ambulance. The paramedics arrived and Patient was feeling much better and was consistently able to answer questions. Patient did not require attention from the paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Hydrocortisone 20 mg twice a day
Allergien: No know allergies
Vorherige Impfungen: -

VAERS 1818519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: FL
Alter: 22,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chest pain Dehydration Dyspnoea Fatigue Myalgia Pain in extremity Panic attack Paraesthesia Syncope Tearfulness Tremor

Symptomtext

Complained of L arm pain and tingling about an hour after administration but stated this was a reaction he had in past to flu vaccine. Several hours later he complained of chest pain and feeling short of breath. Visibly shaking and tearful. Able to speak in full sentences. Emergency services was called. O2 sat was normal. No hives/rashes. He was sent to an urgent care via emergent transport (fire dept) where he was monitored for several hours. He was told he had a panic attack with dehydration and syncope. Today, 10/26 he is only complaining of usual symptoms of increased fatigue and muscle aches. He is working today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Unsure what they did at urgent care but telemetry was applied when EMS arrived 10/25.
Aktuelle Erkrankungen: Reactions to other vaccines.
Vorgeschichte: Reported to me he has IBS disease.
Andere Medikamente: Advair inhaler as needed
Allergien: PCN, peanuts, shellfish
Vorherige Impfungen: Flu- date unknown

VAERS 1818152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 01.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Hyperhidrosis Syncope

Symptomtext

Faint, sweating, dizzy spells

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1813698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 20.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Epistaxis Haemorrhage Thrombosis

Symptomtext

Woke up in middle of the night as felt wet on pillow- pillow soaked with blood which was bright red with clots covering a very large portion of my pillow. I got up and went to the bathroom- spit out atleast 3 large blood clots that were almost the size of ?? an apricot. The bleeding continued for 40 minutes. I applied pressure at the nostrils and bridge of nose. When it did not stop, applied a very cool compress to the nose and face while husband held pressure on the bridge of my nose. At 45 minute mark, the bleeding went to only light red when dabs my nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: I chose to not go to the ER as blood was everywhere. I had bloodwork done the month prior-9/2/21 RBC 4.87, platelets 228
Aktuelle Erkrankungen: diabetes, kidney disease stg1, lumbar disc herniation and radiculopathy
Vorgeschichte: diabetes, kidney disease stg1, lumbar disc herniation and radiculopathy
Andere Medikamente: align probiotic, daily womans multivite and apple cider vinegar gummies
Allergien: erythromycin- swells throat
Vorherige Impfungen: -

VAERS 1809015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: PA
Alter: 21,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blindness Hypoacusis Loss of consciousness Nausea Vomiting

Symptomtext

about 5 to 10 minutes after getting the vaccination patient started to have trouble seeing "blacked out" was unable to see and was having trouble hearing for about 3 to 5 minutes. He then came through and felt nauseous and threw up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: multivitamin
Allergien: n/a
Vorherige Impfungen: -

VAERS 1808042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: MD
Alter: 18,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dizziness Feeling hot Loss of consciousness Pallor Visual impairment

Symptomtext

Patient recieved the vaccine into her left deltoid. Within minutes, reported seeing black spots, feeling dizzy and hot/pale. She then lost consciousness and the pharmacist/bystander held her head to prevent her from collapsing onto the floor. She regained consciousness shortly after and was able to sit up in the chair. The pharmacist took her BP (100/61 mmHg) and she was given water/monitored. EMS were called and arrived within 5-10 minutes. Patient was then taken to ER with EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP reading : 100/61 mmHg
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Mili birth control, doxycycline monohydrate
Allergien: n/a
Vorherige Impfungen: -

VAERS 1802585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

schwer

Staat: KS
Alter: 21,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Disorientation Dizziness Loss of consciousness Nervousness Paraesthesia

Symptomtext

Patient after receiving vaccine had a moment of passing out and felt dizzy and disorientated. Patient felt tingly and shaky. EMS was called and patient recovered over a period of time. EMS measured blood pressure and found patient to have normal BP and pulse. Patient was accompanied by mother and was 'normal' on departure from pharmacy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None reported
Vorgeschichte: No known health conditions
Andere Medikamente: Patient reports no drug/medication use
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1775176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

schwer

Staat: WI
Alter: 14,0
Geschlecht: F
Eingang: 09.10.2021
Impfdatum: 09.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Loss of consciousness Pain in extremity

Symptomtext

Patient was given vaccination as usual and vaccine was confirmed and accurate. No previous reactions were reported prior to administration. Patient expressed the vaccine hurt more on her arm that dose 1 as she was returing to her mother in the waiting area. She began to state she was passing out as she reached her chair in which her mother was attending to her and had her in chair safe. Pharmacist was alerted immediately and patient was moving and responsive when he arrived but past out shortly after arrival. technician retrieved blanket and bottle of water as patient was safely lowered to ground by pharmacist and mother after assessing she was safe but unconscious. patient was responsive to name and mom state

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: unknown result but was awake and stable. believed to be transported out of caution
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Clindamycin/BPO gel topical
Allergien: -
Vorherige Impfungen: -

VAERS 2673581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 05.11.2021
Beginn: 08.08.2023
Tage bis Beginn: 641,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Atelectasis COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Pneumonia Pneumonia bacterial White blood cell count normal

Symptomtext

COPD exacerbation secondary to COVID-19 infection, suspected bacterial Community-acquired pneumonia: Chest x-ray with left basilar subsegmental atelectasis Currently afebrile, no leukocytosis, WBC WNL Completed course of Rocephin and azithromycin to cover possible superimposed bacterial infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, paroxysmal atrial fibrillation on chronic anticoagulation with Coumadin, history of bi p
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2673504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 18.08.2023
Impfdatum: 05.11.2021
Beginn: 03.03.2023
Tage bis Beginn: 483,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2635558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: CT
Alter: 50,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Arthralgia Dehydration Diarrhoea Headache Injection site pain Injection site swelling Oedema peripheral Pyrexia Vomiting

Symptomtext

On 11/8/2021, I went to get my Pfizer COVID-19 booster at my PCP's office. At first, I had just swelling and pain at the injection site, but that's nothing unusual for me. I then rapidly developed a fever of 102-103. I then had severe swelling in both armpits, and this didn't go away until about a week later or longer. I took Tylenol every four hours to treat the fever, but the fever always returned. I also quickly developed severe pain in all of my joints. I woke up in the early hours of 11/9/2021. I had a high fever, severe diarrhea, a headache, and ceaseless vomiting. I then went to the ER, because I had become dehydrated, and the Tylenol wouldn't bring the fever down. At the ER, I was given Zofran, which stopped the vomiting. I was given several IV bags to treat the dehydration. I think they also gave me Tylenol. I was eventually discharged and sent home. They prescribed me Zofran to take at home. The fever ended up lasting for about a week before it finally resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Interstitial Cystitis; Hypothyroidism; Rheumatoid Arthritis; Psoriatic Arthritis; Sjogren's Syndrome; Mitral Valve Prolapse; Hypertension; Irritable Bowel Syndrome
Andere Medikamente: Vitamin D; Atenolol; Alprazolam; Levothyroxine; Tylenol
Allergien: Amoxicillin; Penicillin; Ciprofloxacin; Vancomycin; Aspirin; NSAIDs; Latex; Bee Stings; Most Adhesives; Gluten Sensitivity; Sulfa Drugs; Contrast Dye; Influenza Vaccine
Vorherige Impfungen: -

VAERS 2624205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 20.10.2021
Beginn: 30.11.2021
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthma Hypotension

Symptomtext

I95.9 HYPOTENSION 12/10/2021 HX OF ACUTE KIDNEY INJURY I95.9 HYPOTENSION 12/10/2021 ASTHMA, UNSPECIFIED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2556132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: OK
Alter: 14,0
Geschlecht: M
Eingang: 10.01.2023
Impfdatum: 11.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Atrioventricular block Blood test Cardiac pacemaker insertion Cardiac resynchronisation therapy Dizziness Echocardiogram Electrocardiogram Electrocardiogram ambulatory Gene mutation identification test Hypoaesthesia Influenza virus test negative Loss of personal independence in daily activities Magnetic resonance imaging heart Malaise Mononucleosis heterophile test negative Palpitations SARS-CoV-2 test negative Sinus node dysfunction

Symptomtext

A few days after getting a second dose of COVID-19 vaccine, Patient began to feel generally unwell. He experienced numbness in his legs, dizziness and heart palpitations. We took him to the doctor a few times, but his Flu, COVID and Mono tests were all negative. Over the course of the month, his symptoms became worse, causing him to miss school and sports. In October, Patient's primary care doctor, Dr., referred Patient to Hospital Cardiology after an EKG reveals his resting heart rate was 31. We followed up with Dr. at Hospital. Another EKG showed his heart rate in the 30s. Patient underwent an echo and then wore a 24-hour holter monitor a few different times. After it was discovered the electrical system in his heart wasn't working properly, he was referred to Dr. who subsequently diagnosed Patient with sinus node dysfunction and heart block. Dr. continued to monitor Patient's symptoms, which did not significantly improve. In October of 2022, his symptoms again became worse. It was decide Patient would best benefit with a dual chamber pacemaker implant. A pacemaker was implanted on Nov. 7, 2022, and a lead revision was performed Nov. 22, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: 3,0
Labordaten: ECG (10/25/2021; 9/12/2022) Echocardiogram (10/25/2021; 2/8/2021) Cardiac MRI (3/4/2022) Holter monitor (10/25/2021; 1/5/2022; Blood tests (11/9/2021; 2/8/2021 Genetic testing (9/12/2022)
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal allergies
Andere Medikamente: None
Allergien: Amoxycillin
Vorherige Impfungen: -

VAERS 2510789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: ID
Alter: 36,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 03.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Echocardiogram Magnetic resonance imaging head Migraine Tachycardia

Symptomtext

I had the vaccine in November of 2021 and in January of 2022 I developed Migraines and Tachycardia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Echocardiogram done on 03/24/22 MRI of Brain on 10/26/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Factor V leiden Hypothyroidism
Andere Medikamente: Levothyroxine 100 mcg daily
Allergien: PCN: hives
Vorherige Impfungen: -

VAERS 2431081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MN
Alter: 59,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 12.03.2021
Beginn: 26.07.2022
Tage bis Beginn: 501,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: POSITIVE COVID TEST 7/26/22
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia essential hypertension hypertriglyceridemia nasal polyps obesity OSA colon polyp GERD nonalcoholic fatty liver sinus tachycardia tobacco dependence in remission chronic bronchitis COPD
Andere Medikamente: Diltiazem fluticasone Claritin albuterol Singulair Protonix prednisone rosuvastatin Trelegy Ellipta venlafaxine
Allergien: Beta-blockers
Vorherige Impfungen: -

VAERS 2415698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NC
Alter: 55,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Allergy to vaccine Alopecia Blood pressure measurement Burning sensation Dyspepsia Feeling hot Hot flush Hypertension Pharyngeal swelling Throat tightness

Symptomtext

fire in my arm; High blood pressure; body feel hot; hair has fallen out at an alarming rate; hot flashes; severe heartburn; allergic to your vaccine; Throat swelled closed; Throat swelled closed; The initial case was missing the following minimum criteria: ICH- Unspecified product. Upon receipt of follow-up information on (16Aug2022), this case now contains all required information. This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. The reporter is the patient. A 55-year-old female patient received BNT162b2 (BNT162B2), on 28Oct2021 as dose 1, single (Lot number: 320308D) at the age of 55 years for covid-19 immunisation. The patient's relevant medical history included: "post menopausal" (unspecified if ongoing), notes: had been hot flash free for 2 years. The patient took concomitant medications included Vitamins. The following information was reported: PHARYNGEAL SWELLING (medically significant), THROAT TIGHTNESS (medically significant) all with onset 28Oct2021, outcome "not recovered" and all described as "Throat swelled closed"; ALLERGY TO VACCINE (medically significant) with onset 28Oct2021, outcome "not recovered", described as "allergic to your vaccine"; DYSPEPSIA (non-serious) with onset 04Nov2021, outcome "not recovered", described as "severe heartburn"; HOT FLUSH (non-serious) with onset 11Jan2022, outcome "not recovered", described as "hot flashes"; ALOPECIA (non-serious) with onset 21Mar2022, outcome "not recovered", described as "hair has fallen out at an alarming rate"; BURNING SENSATION (non-serious), outcome "unknown", described as "fire in my arm"; HYPERTENSION (non-serious), outcome "recovering", described as "High blood pressure"; FEELING HOT (non-serious), outcome "unknown", described as "body feel hot". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: High. Therapeutic measures were taken as a result of allergy to vaccine included Benadryl, pharyngeal swelling, throat tightness, dyspepsia, hot flush, alopecia. Clinical course reported as: consumer stated she was allergic to the vaccine. Throat swelled closed. Therefore she could not get a second dose. The first vaccine also gave her severe heartburn within couple of weeks. She had never had it before. She was struggling with it. She was post menopausal and had been hot flash free for 2 years. The hot flashes also returned after the vaccine. Her hair has fallen out at an alarming rate which she hadn't had this bad in the past. She could not take PPI's- Now she was allergic to those. Where she had never had allergic reactions to med before. She did not go to the hospital. Treated on site. The right side of her throat now swells some or feels now if I had other seasonal allergies. She had never had any health issues in the past. Since she had first COVID vaccine, she had a lot more issues with her health. Her throat would bother her on right with foods and drink. High blood pressure showed up but it was going back to normal. If her mouth got dry more it was the right-side 1st heartburn bothered her severely. Now she could not take PPIs for undecipherable, it brothered and made her throat and tongue swell store. She had limited what she could eat, When she received the Pfizer vaccine. It was like fire in her arm and her throat started swelling instantly. The shot made her whole body feel hot. Allergist said she had an allergic reaction to vaccine and does not recommend her get another one.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: blood pressure; Result Unstructured Data: Test Result:High
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Menopausal (had been hot flash free for 2 years)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2410016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 60,0
Geschlecht: M
Eingang: 12.08.2022
Impfdatum: 30.09.2021
Beginn: 10.08.2022
Tage bis Beginn: 314,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

COVID-19 Condition aggravated Dyspnoea Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

Pt to ED 8/9 for SOB, productive cough and fever worsening over the last few days. Pt COVID+ 8/10, continue decadron, to start remdesivir. 8/11 No new complaints noted; stable; no acute cardiac issues. Pt is sitting comfortably in bed AOx4, on RA not in distress, denies pain or SOB. Pt discharged 8/12.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Acute respiratory failure with hypoxia (CMS/HCC); COPD exacerbation (CMS/HCC) RSV bronchitis HCAP (healthcare-associated pneumonia) Pneumonia due to COVID-19 virus Major depression, recurrent Depression Coughing Tobacco dependence Nodule of right lung Depression with anxiety Chronic midline low back pain with right-sided sciatica SOB (shortness of breath)
Andere Medikamente: benzonatate (TESSALON PERLES) 100 MG PO Cap citalopram (CELEXA) 40 MG PO Tab dexamethasone 6 MG PO Tab hydrocodone-acetaminophen (NORCO) 10-325 MG PO Tab methocarbamol (ROBAXIN) 500 MG PO Tab omeprazole (PRILOSEC) 20 MG PO CAPSULE DELAYED R
Allergien: None
Vorherige Impfungen: -

VAERS 2403011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 02.03.2021
Beginn: 04.08.2022
Tage bis Beginn: 520,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Pneumonia SARS-CoV-2 test positive Sepsis

Symptomtext

Pt was admitted on 7/26 for sepsis and hospital-acquired pneumonia. He tested negative for COVID at that time. He was retested for COVID on 8/4 due to his wife testing positive the day prior and having been visiting him in the hospital. He was positive at that time.

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Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1845958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: FL
Alter: -
Geschlecht: U
Eingang: 03.07.2022
Impfdatum: 04.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac failure Chest pain Expired product administered Chest X-ray normal Computerised tomogram normal Dizziness Dyspnoea Fibrin D dimer increased Monocyte count normal Monocyte percentage increased Product storage error

Symptomtext

heart failure; had mistakenly given me an expired dose that was in the throw away batch; severe chest pains; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP), Program ID: (005570). The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 04Nov2021 as dose number unknown (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization completed, Manufacturer unknown), for Covid-19 immunization. The following information was reported: CARDIAC FAILURE (medically significant), outcome "unknown", described as "heart failure"; EXPIRED PRODUCT ADMINISTERED (non-serious), outcome "unknown", described as "had mistakenly given me an expired dose that was in the throw away batch"; CHEST PAIN (non-serious), outcome "unknown", described as "severe chest pains". Clinical course: Hello, I was given a COVID booster shot on 04Nov2021. The pharmacist called me a couple of hours later to inform me the nurse had mistakenly given me an expired dose that was in the throw away batch. Twenty four hours later I started having severe chest pains. I have been under the doctors care since then and (8 months later) was recently diagnosed with heart failure. I was told by the company at fault to contact Pfizer because you all were at fault due to my adverse reaction. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2347522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: ME
Alter: 54,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cardiac stress test abnormal Chest discomfort Congestive cardiomyopathy Dyspnoea Echocardiogram abnormal Electrocardiogram ambulatory abnormal Influenza like illness Laboratory test Palpitations SARS-CoV-2 test negative

Symptomtext

So the day after I had some chest pressure and that lasted a couple days and it got less and less. I thought that was it but then I started getting heart palpitations around the holidays. I was due for a physical in March and mention to my doctor about that and shortness of breath at times, kind off and on flu like symptoms and been tested for COVID many times all resulted NEGATIVE. My provider had me wear a heart monitor for 2 weeks then it showed some abnormalities. SO then she had me do a stress test and echocardiogram. Results were lower then it should be so she sent me to a Cardiologist. First appointment was yesterday 6/30/2022. I was diagnosed with dilated Cardiomyalphay and the dr. is sending me for more labs and another echocardiogram plus a cardiac MRI. 2nd Cariology appoint. more labs and echo on 7/12/2022. No date for the cardiac MRI yet, waiting on call.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Listed above. Cardiologist Dr.
Aktuelle Erkrankungen: NO
Vorgeschichte: Hypothyroid, High Blood Pressure, Mild Asthma
Andere Medikamente: Centrium Silver, Fish Oil, Valtrex, HTZ, Synthroid, Vit.D3
Allergien: NO
Vorherige Impfungen: -

VAERS 2344862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: GA
Alter: 42,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 19.03.2021
Beginn: 28.11.2021
Tage bis Beginn: 254,0
Dosis: 3
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Abdominal pain Adnexal torsion Cholelithiasis Musculoskeletal chest pain Ovarian operation Pain Pelvic pain Ultrasound biliary tract abnormal Ultrasound scan vagina abnormal

Symptomtext

10 days after getting my 3rd dose (booster) of the vaccine I ended up in the ER in excruciating abdominal pain. I was having crippling pain on the right side of the abdomen (lower pelvic area and upper under ribs). I was given 2 ultrasounds. The trans-vaginal ultrasound revealed I have an ovarian torsion that required emergency surgery. I was transported to another hospital immediately to have the surgery. The ER had also done an ultra-sound of my gallbladder and found gallstones. I had another surgery to have those removed on 1/19/22.

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Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: Ultrasounds given 11/28/21 at the local Emergency Room. I don't remember if I had any other tests like CT scans or such. I was in a lot of pain and given pain medication.
Aktuelle Erkrankungen: none
Vorgeschichte: Migraines Asthma
Andere Medikamente: Xyzal for seasonal allergies Maxalt as needed for migraines
Allergien: none
Vorherige Impfungen: -

VAERS 2328950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MN
Alter: 75,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 27.12.2021
Beginn: 26.05.2022
Tage bis Beginn: 150,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Cardiac failure congestive Dyspnoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient presented to the emergency department via EMS on 5/26/2022 with shortness of breath, subsequently admitted from 5/26-5/31. Tested COVID-19 positive via PCR on 5/26. CHF. This meets criteria for vaccine breakthrough case review.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2318921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: VA
Alter: 32,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Condition aggravated Dizziness Electrocardiogram normal Exercise tolerance decreased Palpitations

Symptomtext

I was already having palpitations, dizziness, and light headedness prior to getting the vaccine, but it was only when I was on my menstrual my cycle. In the last 6 months starting in January 2022 or February 2022 they have increased. I cant workout the week of or after my cycle. These symptoms are still present and more frequent now. I started noticing in March 2022 and April 2022 that i was having the symptoms even when I wasn't on my cycle. I would just maybe be sitting at my desk then it starts happening or even in the grocery store it would happen. I had a follow up with my rheumatologist. Then I went to see my PCP. She referred me to see a cardiologist. to see if I am having a cardiac issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG- normal (6/14/2022) Bloodwork- awaiting results (6/14/2022)
Aktuelle Erkrankungen: none
Vorgeschichte: Polycystic Ovarian Syndrome
Andere Medikamente: Lomaira, Topiramate, Avelastine, Flonase, Zyrtec, Allergy Eye Drops, Natures Bounty Quick Dissolve B12, Nature Wise Vitamin D3, Copaiba, Chelated Zinc, Vegan Micro Plex, EO Mega Essential Oils, Alpha CRS Plus
Allergien: Outside Allergies
Vorherige Impfungen: -

VAERS 2310176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 06.06.2022
Impfdatum: 18.10.2021
Beginn: 30.05.2022
Tage bis Beginn: 224,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Angiogram pulmonary abnormal Anticoagulant therapy Atrial fibrillation Blood creatinine increased Blood culture negative Blood potassium decreased COVID-19 Cardiac monitoring Chronic kidney disease Condition aggravated Cough Dyspnoea Echocardiogram abnormal Ejection fraction normal Essential hypertension Foreign travel Gastrooesophageal reflux disease Hyperlipidaemia

Symptomtext

Discharge Provider: DO Primary Care Provider at Discharge: MD Admission Date: 5/30/2022 Discharge Date: 6/3/2022 DISCHARGE DIAGNOSES: 1. Sepsis due to bilateral, bacterial community-acquired pneumonia 2. COVID-19 infection 3. New onset atrial fibrillation 4. Hypokinesis of basal to mid inferior wall of left ventricle 5. Benign essential hypertension 6. Hyperlipidemia 7. Type 2 diabetes mellitus 8. Hypokalemia 9. GERD 10. Hypothyroidism 11. Stage 3a CKD HOSPITAL COURSE: Patient is a 62-year-old male with history of hypertension, hyperlipidemia, type 2 diabetes mellitus, GERD, hypothyroidism and stage 3a CKD who presented to the ED with worsening shortness of breath. He had recently traveled for a 2 week trip, and after returning home, developed upper respiratory symptoms and tested positive for COVID-19 on a home test. He was seen by his PCP, who prescribed him Paxil that at that time. Beginning on 05/28, he developed low-grade fevers, worsening shortness of breath and dry cough. Due to worsening symptoms, he presented to the emergency department for further evaluation. In the emergency department, he was tachycardic and found to be in new onset atrial fibrillation. Troponins were elevated at 89 and 87, respectively. Labs revealed a potassium of 3.1, creatinine 1.51 and WBC count 17.7. EKG was done in the emergency department, and confirmed atrial fibrillation. CTA thorax with contrast showed bilateral lung consolidation, worse at the right than left, suspicious for infectious pneumonia. He was given potassium and IV Rocephin in the emergency department, and admitted to the hospitalist service for further care. Upon admission, the patient remained stable on room air. He was continued on IV Rocephin and continued on oral minocycline for suspected community-acquired pneumonia. Blood cultures have remained negative, and patient was unable to produce sputum for sputum culture. I did add prednisone 30 mg daily due to ongoing dyspnea, which did provide symptomatic benefit. He will complete a 5 day course of antibiotic, with transition to Ceftin at discharge. He will be placed on 3 more days of prednisone at discharge, for a total of 5 days. For his atrial fibrillation, he was started on Eliquis 5 mg twice daily and Cardizem 30 mg four times daily. Cardizem was transition to Cardizem CD 120 mg daily by time of discharge. He did convert out of atrial fibrillation to normal sinus rhythm prior to discharge. An echocardiogram was performed during hospitalization, which revealed an ejection fraction of 52% with evidence of hypokinesis involving the basal to mid inferior wall. Given wall motion abnormalities, Cardiology was consulted. They recommended continued rate control with Cardizem and anticoagulation with Eliquis. They recommend outpatient cardiac MRI and 14 day cardiac monitor at discharge. He was felt stable for discharge home on 06/03/2022. He should follow-up with his PCP in 1 week. He should follow-up with Cardiology in 2 weeks. ZIO patch was placed prior to discharge. He will be continued on Eliquis 5 mg twice daily and Cardizem CD 120 mg daily at discharge. Amlodipine to be discontinued. Will defer timing of cardiac MRI to Cardiology in the outpatient setting. He will be placed on 2 days of Ceftin and 3 days of prednisone at discharge to complete 5 days of therapy of each.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: Foot Swelling 9/24/2021
Vorgeschichte: GERD (gastroesophageal reflux disease) Hx of hiatal hernia Primary osteoarthritis of left hip Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin Morbid obesity with BMI of 40.0-44.9, adult Stage 3 chronic kidney disease, unspecified whether stage 3a or 3b CKD Vaccine counseling Back pain Intractable back pain Post-operative nausea and vomiting Closed fracture of lamina of lumbar vertebra Subacute osteomyelitis, other site History of penicillin allergy Community acquired pneumonia, bilateral Atrial fibrillation (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aluminum, magnesium & simethicone (MAALOX EX) 400-400-40 M
Allergien: PenicillinsAnaphylaxis, Shortness of Breath, Swelling, Throat swelling
Vorherige Impfungen: -

VAERS 2287183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 19.11.2021
Beginn: 12.05.2022
Tage bis Beginn: 174,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Asthenia Blood chloride increased Blood creatinine increased Blood glucose normal Blood potassium increased Blood sodium normal Blood urea increased Breath sounds abnormal COVID-19 Carbon dioxide decreased Chest X-ray normal Cough Dyspnoea Dyspnoea exertional Full blood count normal General physical condition abnormal Hepatic enzyme

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: DNP, A-GNP Admission Date: 5/12/2022 Discharge Date: 5/14/2022 PRESENTING PROBLEM: Acute kidney injury due to COVID-19 (HCC) COVID-19 HPI: 85-year-old female with a history of hypertension, hyperlipidemia, previous CVA with left-sided weakness, chronic kidney disease stage 3. Patient presents to the emergency room with complaints of weakness for over a month. Much worse over the last week. Last night she had a cough which would not allow her to sleep, nonproductive. She denies any fevers or chills. No chest pain. She does states she has been short of breath for the last week or 2, particularly with exertion. Patient presented to the emergency room today as her cough was worsening. On arrival she was hemodynamically stable, satting 97% on room air. She was mildly ill appearing but pleasant and conversant. Lungs show diminished breath sounds at the bases heart was regular rate and rhythm abdomen was benign. Extremities showed 1+ edema with chronic venous stasis changes bilaterally. Sodium 138 potassium 5.1 chloride 110 CO2 16 BUN 72 creatinine 2.16 (baseline creatinine is around 1.3). Glucose 152 liver enzymes normal complete blood count was normal. Chest x-ray showed no acute disease. Patient has COVID-19 came back positive. Patient states she has had slight decreased oral intake over the last week. She denies taking NSAIDs. Patient also has a chronic ileostomy, history of Crohn's disease. Currently not on medications. HOSPITAL COURSE: Patient did well. She was gently hydrated with IV fluids and her acute kidney injury continue to improve, creatinine now 1.4. She was eating well, having reasonable urine output. Vital signs have been stable. She has been on room air oxygen throughout this admission, not showing any signs or symptoms of COVID-19 pneumonia. Patient is stable for discharge. On day of discharge she reports that she feels stronger today than she has in over a month. Patient will continue with COVID 19 discharge instructions, also encourage good oral intake. Patient to follow-up with primary care provider next week. Patient does have a mild persistent metabolic acidosis, which can be followed up as outpatient with repeat BMP next week. Patient advised to return should she develop any shortness of breath or any other problems

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Hyperlipidemia Urge incontinence DJD (degenerative joint disease) of knee Senile osteoporosis Osteoarthrosis, unspecified whether generalized or localized, pelvic region and thigh CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) Stroke, lacunar (HCC) Arthritis Weakness Artificial opening status, unspecified (HCC) Spastic hemiplegia of left nondominant side as late effect of cerebral infarction (HCC) Crohn's disease of small intestine with complication (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 10 MG tablet cholecalciferol (VITAMIN D3) 100 MCG (4000 UT) CAPS Multiple Vitamins-Minerals (MULTIVITAMIN PO) Omega-3 Fatty Acids (FISH OIL) 1000 MG capsule TURMERIC PO zinc g
Allergien: ClindamycinHives Alendronic Acid Peanut-derived Products Penicillin [Aspartame And Phenylalanine]Hives PenicillinsSkin Rashes/Hives, Rash Pneumococcal VaccineSkin Rashes/Hives, Swelling Prinivil [Lisinopril] Remicade [Infliximab] Shellfish Allergy Vitamin B ComplexNausea and Vomiting
Vorherige Impfungen: -

VAERS 2270814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 25.03.2021
Beginn: 22.02.2022
Tage bis Beginn: 334,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Nausea Palpitations SARS-CoV-2 test positive

Symptomtext

02/22/22 presents to ED for "palpitations and persistent nausea". PMHx of "diabetes, CKD, hypertension, obstructive sleep apnea and atrial fibrillation on warfarin"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 02/22/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2269040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MO
Alter: 18,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 29.01.2021
Beginn: 26.04.2022
Tage bis Beginn: 452,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Airway secretion clearance therapy Bronchial disorder COVID-19 Chest X-ray abnormal Cough Dyspnoea Hypoxia Lung hypoinflation Lung opacity Malaise Physiotherapy chest Pneumonia SARS-CoV-2 test positive

Symptomtext

admitted for increased work of breathing with hypoxemia to 88% in the setting of a positive COVID rapid antigen test. Her symptoms began 4/25 with positive test on 4/26. Fully vaccinated x3. CXR showed hypoinflated with bronchovascular crowding and hazy bilateral airspace opacities consistent with infection. She follows with pulmonology and is on airway clearance protocol with chest physiotherapy, cough assist, and albuterol twice daily which is increased to 4 times daily during infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: COVID+ 4/26/22
Aktuelle Erkrankungen: -
Vorgeschichte: history of cerebral palsy, cortical blindness, G-tube dependence, neuromuscular scoliosis, and chronic cough with ineffective airway clearance
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2273266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 02.12.2021
Beginn: 21.02.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 COVID-19 pneumonia Chronic obstructive pulmonary disease Dyspnoea SARS-CoV-2 test positive

Symptomtext

Narrative: Admission Diagnosis:COVID-19 pneumonia, COPD exacerbation DIAGNOSIS: Primary Diagnosis: Pneumonia Secondary diagnosis: COVID-19, dyspnea, COPD

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Vital Signs * Temperature 98.6 (37 C) Pulse 84 Respirations 22 Blood Pressure 135/78 Pain scale recorded: 0 Pulse Oximetry 88 Room Air COVID positive 2/22/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2260405

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MN
Alter: 86,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 04.03.2021
Beginn: 28.04.2022
Tage bis Beginn: 420,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia COVID-19 Dyspnoea Feeling cold Hyperhidrosis SARS-CoV-2 test positive

Symptomtext

WEAKNESS, COLD, DIAPHORETIC, SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST 5/28/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Angina pectoris Aortic aneurysm Arthritis, degenerative BPH CAD COPD Essential hypertension, benign Ganglion cyst of wrist, left Malignant neoplasm of upper lobe of left lung Mixed Hyperlipidemia Type II diabetes mellitus Unilateral inguinal hernia, right Vitamin D deficiency PVD Iliac artery aneurysm, bilateral AAA Allergic rhinitis Sepsis Multifocal pneumonia Moderate malnutrition Nonrheumatic aortic valve stenosis
Andere Medikamente: ? albuterol HFA (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler Inhale 2 puffs every 4 (four) hours as needed for shortness of breath or Wheezing. ? albuterol-ipratropium, conc: 3-0.5mg/3mL, (DUO-NEB) Inhl nebulizer solution Nebulize
Allergien: Cefdinir Codeine Flexeril [Cyclobenzaprine] Latex Levaquin [Levofloxacin] Lisinopril Penicillin V
Vorherige Impfungen: -

VAERS 2250638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: OH
Alter: 20,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 17.11.2021
Beginn: 05.02.2022
Tage bis Beginn: 80,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute psychosis Antiacetylcholine receptor antibody Autoimmune encephalopathy Condition aggravated Immunoglobulin therapy Metabolic function test abnormal Mycoplasma test Pneumonia mycoplasmal

Symptomtext

In late January/early February 2022, experienced an episode of acute psychosis thought to result from AutoImmune encephalitis by specialist. Mycoplasma pneumonia infection possibly contributing as a trigger. Being treated by Psychiatric Nurse Practioner, and Immunologist including ivig treatment. Having to take medical leave from college after hospitalization and currently at home concentrating on improving health.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 19,0
Labordaten: Cunningham panel elevated results on February 2022 Acetylcholine Receptor Ganglionic (Alpha 3) borderline on 2/8/22 Mycoplasma IGM value 2.68 on 2/7/22
Aktuelle Erkrankungen: Tinea versicolor, eczema
Vorgeschichte: Autoimmune encephalitis, eczema.
Andere Medikamente: Paliperidone ER, Azelastine, Trazodone, Zyrtec, Fish oil, S. Boulardii, Megasporbiotic, Magnesium Oxide, Gi Detox, B12, D-Hist, Vitamin A.
Allergien: Risperdal, Benadryl, Zyprexa
Vorherige Impfungen: -

VAERS 2236041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 15.04.2022
Impfdatum: 26.10.1981
Beginn: 27.10.2021
Tage bis Beginn: 14.611,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Furuncle Pruritus Scar Scratch Skin ulcer

Symptomtext

AS PER PT, NIGHT AFTER RECEIVING THE VACCINE SHE STARTED GETTING ITCHY ON HER LEFT HAND. EVENTUALLY SHE ALSO STARTED GETTING SORES/BOILS AND THEY WOULD POP. UPON EXAMINATION, SKIN IS SCARRED FROM BOILS AND SCRATCHING. PT DOES NOT HAVE INSURANCE SO DID NOT GET SEEN. THEY ALSO DID NOT REPORT UNTIL NOW BECAUSE IT HAS GOTTEN WORSE AND POTENTIALLY SPREAD TO HER RIGHT HAND.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: None stated
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2227684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 12.04.2022
Impfdatum: 02.12.2021
Beginn: 21.02.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 COVID-19 pneumonia Chronic obstructive pulmonary disease Condition aggravated Dyspnoea SARS-CoV-2 test positive

Symptomtext

Narrative: Admission Diagnosis:COVID-19 pneumonia, COPD exacerbation DIAGNOSIS: Primary Diagnosis: Pneumonia Secondary diagnosis: COVID-19. dyspnea, COPD

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Vital signs *Temperature 98.6 F (37C) Pulse 84 Respirations 22 Blood Pressure 135/78 Pain scale recorded: 0 Pulse Oximetry 88 Room Air COVID positive 2/22/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2189947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: SC
Alter: 42,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Breast pain Chest discomfort Electrocardiogram normal Mobility decreased Muscular weakness Injection site muscle weakness Myalgia Vaccination site movement impairment Vaccination site pain

Symptomtext

Not able to use left arm fully as I once did, losing strength in arm, upper left side aches, vaccine location=left arm; Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm; Ongoing sore muscle; Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Nov2021 (Lot number: 320308D) at the age of 42 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulfur" (unspecified if ongoing); "Known allergies: Shellfish" (unspecified if ongoing). Concomitant medication(s) included: IRON; WELLBUTRIN. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FE3590, Location of injection: Arm Left), administration date: 27Oct2021, when the patient was 42 years old, for Covid-19 immunization. The following information was reported: VACCINATION SITE PAIN (disability) with onset 21Nov2021, outcome "not recovered", described as "Not able to use left arm fully as I once did, losing strength in arm, upper left side aches, vaccine location=left arm"; VACCINATION SITE MOVEMENT IMPAIRMENT (disability), INJECTION SITE MUSCLE WEAKNESS (disability) all with onset 21Nov2021, outcome "not recovered" and all described as "Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm"; MYALGIA (disability) with onset 21Nov2021, outcome "not recovered", described as "Ongoing sore muscle". The events "not able to use left arm fully as i once did, losing strength in arm, upper left side aches, vaccine location=left arm", "not able to use left arm fully as i once did, losing strength in arm, /vaccine location=left arm", "ongoing sore muscle" and "not able to use left arm fully as i once did, losing strength in arm, /vaccine location=left arm" were evaluated at the physician office visit. Therapeutic measures were taken as a result of vaccination site pain, vaccination site movement impairment, myalgia, injection site muscle weakness. Treatment includes Upcoming physical therapy. No covid prior vaccination. Not covid tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shellfish allergy; Sulfonamide allergy
Andere Medikamente: IRON; WELLBUTRIN
Allergien: -
Vorherige Impfungen: -

VAERS 2189947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: SC
Alter: 42,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Breast pain Chest discomfort Electrocardiogram normal Mobility decreased Muscular weakness Injection site muscle weakness Myalgia Vaccination site movement impairment Vaccination site pain

Symptomtext

Not able to use left arm fully as I once did, losing strength in arm, upper left side aches, vaccine location=left arm; Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm; Ongoing sore muscle; Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 21Nov2021 (Lot number: 320308D) at the age of 42 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Sulfur" (unspecified if ongoing); "Known allergies: Shellfish" (unspecified if ongoing). Concomitant medication(s) included: IRON; WELLBUTRIN. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: FE3590, Location of injection: Arm Left), administration date: 27Oct2021, when the patient was 42 years old, for Covid-19 immunization. The following information was reported: VACCINATION SITE PAIN (disability) with onset 21Nov2021, outcome "not recovered", described as "Not able to use left arm fully as I once did, losing strength in arm, upper left side aches, vaccine location=left arm"; VACCINATION SITE MOVEMENT IMPAIRMENT (disability), INJECTION SITE MUSCLE WEAKNESS (disability) all with onset 21Nov2021, outcome "not recovered" and all described as "Not able to use left arm fully as I once did, losing strength in arm, /vaccine location=left arm"; MYALGIA (disability) with onset 21Nov2021, outcome "not recovered", described as "Ongoing sore muscle". The events "not able to use left arm fully as i once did, losing strength in arm, upper left side aches, vaccine location=left arm", "not able to use left arm fully as i once did, losing strength in arm, /vaccine location=left arm", "ongoing sore muscle" and "not able to use left arm fully as i once did, losing strength in arm, /vaccine location=left arm" were evaluated at the physician office visit. Therapeutic measures were taken as a result of vaccination site pain, vaccination site movement impairment, myalgia, injection site muscle weakness. Treatment includes Upcoming physical therapy. No covid prior vaccination. Not covid tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shellfish allergy; Sulfonamide allergy
Andere Medikamente: IRON; WELLBUTRIN
Allergien: -
Vorherige Impfungen: -

VAERS 2196655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NH
Alter: 74,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 28.10.2021
Beginn: 30.11.2021
Tage bis Beginn: 33,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia Cardiovascular evaluation Cervical spinal stenosis Chest pain Immunoglobulin therapy Intervertebral disc protrusion Magnetic resonance imaging spinal abnormal Muscular weakness Myelitis transverse Paraesthesia Vertebral lesion

Symptomtext

Pt presented with chest pain and was getting cardiac workup. Pt developed who has paresthesia and left leg and right arm weakness on exam. He had sudden onset of weakness since 11/29/2021. Evaluated by Neurology and neurosurgery. Working diagnosis is transverse myelitis vs compressive myelopathy (symptoms inconsistent with NMO); unclear etiology (possibly related to COVID-19 vaccine booster). Most likely infectious or inflammatory in nature. Compressive myopathy ruled out by neurosurgery evaluation. Pt treated with IVIG 50 gram (0.5 g/kg/day) IV daily x 4 days, and methylprednisolone 1 gram IV daily x 5 days. Generalized weakness improved over next 10 days, with new onset upper and lower extremity weakness on 12/9/2021; evaluated by neurology and neurosurgery however no evidence for acute spinal cord compression. At discharge to skilled nursing facility, his generalized weakness was improving; pt progressing well with physical therapy and occupational therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 16,0
Labordaten: He had MRIs which showed T2 hyperintense lesion from C5-7 and T1-3 he does have several bulging discs with spinal stenosis in cervical region, but no recent fall or truama. He had abnormal enhancement in cervical cord lesion and thoracic cord.
Aktuelle Erkrankungen: episodes of toe and fingertips numbness that would "come and go" but patient was never diagnosed with peripheral neuropathy
Vorgeschichte: hypertension, hyperlipidemia, gout, TMJ, diabetes Pt reported baseline numbness/tingling in hands/feet for some time, but was never weak (unclear from history how long this peripheral neuropathy affecting him, may be secondary to diabetes)
Andere Medikamente: allopurinol, amlodipine, aspirin, atorvastatin, lisinopril, metoprolol, oxybutynin, voltaren topical gel
Allergien: nkda
Vorherige Impfungen: -

VAERS 2192071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MN
Alter: 81,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 09.11.2021
Beginn: 21.03.2022
Tage bis Beginn: 132,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest pain Dyspnoea Influenza A virus test positive SARS-CoV-2 test positive Tachypnoea

Symptomtext

SOB, TACHYPNEA, CHEST PAIN; FLU A AND COVID POSITIVE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ESRD ON DIALYSIS, NSTEMI, DM, HTN
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2128022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 21.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Alopecia Antibody test Blister Blood pressure measurement Hypertension Back pain Deafness Dizziness Headache Insomnia Laboratory test Malaise Hypoaesthesia Pain Paraesthesia Peripheral swelling Rash Swelling

Symptomtext

blood pressure was too high; numbness; tingling in my face; After a while I started just not feeling well especially when I went to work; hives; blistered; pain; hair loss; My right arm started swelling up so I went to the doctor; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 45 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid right, administration date 21Oct2021 (Lot number: 320308D) at the age of 45 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Lupus" (ongoing); "kidney cancer" (ongoing); "Partial surgery (R) Nephrectomy", start date: 2019 (unspecified if ongoing); "HTN" (ongoing); "GERD" (ongoing); "Constip." (ongoing); "Stool softener" (ongoing). Concomitant medication(s) included: HCTZ taken for hypertension (ongoing); K-LOR taken for hypertension (ongoing); PROTONIX [OMEPRAZOLE] taken for gastrooesophageal reflux disease (ongoing); COLACE taken for constipation, faeces hard (ongoing). Vaccination history included: Bnt162b2 (Dose: 1st, Anatomical site of injection: R Deltoid, Route of administration: Intramuscular, Batch/lot number: FF2589), administration date: 23Sep2021, when the patient was 45 years old, for Covid-19 Immunization, reaction(s): "light headache", "felt like I was gonna collapse", "I was very shaky". The following information was reported: HYPERTENSION (non-serious), outcome "recovered with sequelae", described as "blood pressure was too high"; HYPOAESTHESIA (non-serious), outcome "recovered with sequelae", described as "numbness"; PARAESTHESIA (non-serious), outcome "recovered with sequelae", described as "tingling in my face"; MALAISE (non-serious), outcome "recovered with sequelae", described as "After a while I started just not feeling well especially when I went to work"; URTICARIA (non-serious), outcome "recovered with sequelae", described as "hives"; BLISTER (non-serious), outcome "recovered with sequelae", described as "blistered"; PAIN (non-serious), outcome "recovered with sequelae", described as "pain"; ALOPECIA (non-serious), outcome "recovered with sequelae", described as "hair loss"; PERIPHERAL SWELLING (non-serious), outcome "recovered with sequelae", described as "My right arm started swelling up so I went to the doctor". The events "blood pressure was too high", "numbness", "tingling in my face", "after a while i started just not feeling well especially when i went to work", "hives", "blistered", "pain", "hair loss" and "my right arm started swelling up so i went to the doctor" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of hypertension, hypoaesthesia, paraesthesia, malaise, urticaria, blister, pain, alopecia, peripheral swelling. Additional information: Patient didn't had prior vaccination within 4 weeks. After 1st dose of covid-19 Pfizer vaccine I was light headache so I reported this when I went for my 2nd dose. So I was told to take Tylenol and drink plenty of fluids. 1 and 1/2 hour after leaving the pharmacy I felt like I was gonna collapse so I ran home and took some Benadryl. I was very shaky. I've tried to bed as, I was off from work. I kept taking the Benadryl and going to sleep because I wouldn't have that feeling of my body being overwhelmed. I had a routine visit with one of my doctors but she kept telling my blood pressure was too high and gave me blood pressure medications. I tried telling her my body was overeating to the vaccine but she said I was just complaining. I tried the blood pressure medications but started having numbness and tingling in my face. So I discontinued the medications and continue taking Benadryl. After a while I started just not feeling well especially when I went to work, I started with hives, blistered and pain and increased hair loss. My right arm started swelling up so I went to the doctor. The swelling disappeared then returned about 3-4 days later. I went to urgent care where I got steroids and to continue antihistamine until seen by Rheumatologist. I returned home for PCP for follow up visit - (name withheld) RN. Autopsy information: NA No follow-up attempts are possible. No further information is expected. Sender's Comments: Based on the available information, there is a reasonable possibility of a causal relationship between the suspect vaccine BNT162B2 (COMIRNATY) and reported events which cannot be fully assessed/excluded. The case will be reassessed if additional information becomes available. 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: platelet factor IV; Result Unstructured Data: Test Result:Thromboembolic Events with Thrombocytopenia; Comments: Thromboembolic Events with Thrombocytopenia; Test Name: blood pressure; Result Unstructured Data: Test Result: high.
Aktuelle Erkrankungen: Constipation; GERD; Hypertension; Kidney cancer; Lupus enteritis; Stools hard.
Vorgeschichte: Medical History/Concurrent Conditions: Nephrectomy.
Andere Medikamente: HCTZ; K-LOR; PROTONIX [OMEPRAZOLE]; COLACE.
Allergien: -
Vorherige Impfungen: -

VAERS 2179420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: WA
Alter: 36,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 28.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Autonomic nervous system imbalance Postural orthostatic tachycardia syndrome

Symptomtext

Re-emergence of dysautonomia/POTS symptoms.; Re-emergence of dysautonomia/POTS symptoms.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 36-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 28Oct2021 (Lot number: 320308D) at the age of 36 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (INFLUENZA), administration date 28Oct2021 (Batch/Lot number: unknown) as dose number unknown, single. Relevant medical history included: "Crohns disease" (unspecified if ongoing), notes: I have crohn's disease; "Interchange of vaccine products" (unspecified if ongoing). Family history included: "Dysautonomia/POTS symptoms." (Unspecified if ongoing), notes: -Originally dx at age 17 with POTS but have not had tachycardia or needed medication for it in the last 10 years., -My sister developed a severe case of dysautonomia/ POTS.; "Autoimmune Issues" (unspecified if ongoing), notes: Have family history of autoimmune issues. Concomitant medication(s) included: APRISO; WELLBUTRIN; LOESTRIN; VIT D [COLECALCIFEROL]. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: 007M20A), administration date: 29Jan2021, when the patient was 35 years old, for COVID-19 Immunization; Moderna (Dose Number: 1, Batch/Lot No: 037K20A), administration date: 01Jan2021, when the patient was 35 years old, for COVID-19 Immunization. The following information was reported: AUTONOMIC NERVOUS SYSTEM IMBALANCE (non-serious), POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME (non-serious) all with onset 04Nov2021, outcome "not recovered" and all described as "Re-emergence of dysautonomia/POTS symptoms.". Therapeutic measures were not taken as a result of autonomic nervous system imbalance, postural orthostatic tachycardia syndrome. Additional information: Seriousness criteria was no according Results in death, not Life threatening, did not Caused/prolonged no hospitalization, no Disabling/Incapacitating, no Congenital anomaly/birth defect. the patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Reported Event: Re-emergence of dysautonomia/POTS symptoms. Originally dx at age 17 with POTS but have not had tachycardia or needed medication for it in the last 10 years. Began having symptoms again shortly after booster. Has not resolved. Have family history of autoimmune issues. I have Crohn's disease. My sister developed a severe case of dysautonomia/ POTS in Apr after completing Moderna vaccines. My other sister has a history of Guillain-Barre. No Known allergies. Prior to vaccination, the patient did not diagnose with COVID-19. Since the vaccination, the patient did not get tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Postural orthostatic tachycardia syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Autoimmune disorder (Have family history of autoimmune issues); Crohn's disease (I have crohn's disease); Interchange of vaccine products; Postural orthostatic tachycardia syndrome.
Andere Medikamente: APRISO; WELLBUTRIN; LOESTRIN; VIT D [COLECALCIFEROL].
Allergien: -
Vorherige Impfungen: -

VAERS 2179175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: FL
Alter: 57,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 09.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Condition aggravated Neck pain Oropharyngeal pain Pain in extremity Tinnitus

Symptomtext

sore arm that went up her shoulder and to her neck; sore arm that went up her shoulder and to her neck; sore arm that went up her shoulder and to her neck; Sore throat; Ringing in ears/ My ears has been ringing; sore arm that went up her shoulder and to her neck was reported as worsened/ Sore throat was reported as worsened; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202101557359 (Pfizer). A 57 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 09Nov2021 11:00 (Lot number: 320308D) at the age of 57 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: Flu vaccine (she has a reaction to a flu vaccine 17 years ago). The following information was reported: PAIN IN EXTREMITY (non-serious), ARTHRALGIA (non-serious), NECK PAIN (non-serious) all with onset 09Nov2021, outcome "not recovered" and all described as "sore arm that went up her shoulder and to her neck"; OROPHARYNGEAL PAIN (non-serious) with onset 09Nov2021, outcome "not recovered", described as "Sore throat"; TINNITUS (non-serious) with onset 09Nov2021, outcome "not recovered", described as "Ringing in ears/ My ears has been ringing"; CONDITION AGGRAVATED (non-serious) with onset Nov2021, outcome "not recovered", described as "sore arm that went up her shoulder and to her neck was reported as worsened/ Sore throat was reported as worsened". Therapeutic measures were not taken as a result of pain in extremity, arthralgia, neck pain, oropharyngeal pain, tinnitus, condition aggravated. Additional information: Patient is taking Multi Vitamins. She wanted to know if ever she receives the 2nd dose, will the ringing of ears be worse and if it will go away. Any AE(s) did not require a visit to Emergency Room/Physician Office. No Prior Vaccinations (within 4 weeks). Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NJ
Alter: 42,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Myalgia Neuralgia Pain Pain in extremity Paraesthesia Peripheral swelling

Symptomtext

My arm was almost doubled in size; Arm Pain which hitting nerve, affecting neck shoulder trap, lateral basically everything that has to do with shoulder; Muscle pain; My fingertips my pointer and my thumb I feel pins and needles; Arm Pain which hitting nerve, affecting neck shoulder trap, lateral basically everything that has to do with shoulder; My fingertips my pointer and my thumb I feel pins and needles; Arm Pain which hitting nerve, affecting neck shoulder trap, lateral basically everything that has to do with shoulder; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 30Oct2021 12:00 (Lot number: 320308D) at the age of 42 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "car accident", start date: Apr2021 (unspecified if ongoing), notes: car accident. There were no concomitant medications. Vaccination history included: Flu shot (last time I took a Flu shot it was 6 months ago, so I am not about shots.), administration date: 2021, for immunization. The following information was reported: PERIPHERAL SWELLING (non-serious) with onset 31Oct2021, outcome "recovering", described as "My arm was almost doubled in size"; PAIN IN EXTREMITY (non-serious), ARTHRALGIA (non-serious) all with onset 2021, outcome "not recovered" and all described as "Arm Pain which hitting nerve, affecting neck shoulder trap, lateral basically everything that has to do with shoulder"; NEURALGIA (non-serious) with onset 31Oct2021, outcome "not recovered", PARAESTHESIA (non-serious), PAIN (non-serious) all with onset 2021, outcome "unknown" and all described as "My fingertips my pointer and my thumb I feel pins and needles"; MYALGIA (non-serious) with onset 31Oct2021, outcome "not recovered", described as "Muscle pain". The events "my arm was almost doubled in size", "arm pain which hitting nerve, affecting neck shoulder trap, lateral basically everything that has to do with shoulder", "arm pain which hitting nerve, affecting neck shoulder trap, lateral basically everything that has to do with shoulder", "arm pain which hitting nerve, affecting neck shoulder trap, lateral basically everything that has to do with shoulder", "my fingertips my pointer and my thumb i feel pins and needles", "muscle pain" and "my fingertips my pointer and my thumb i feel pins and needles" were evaluated at the physician office visit. Therapeutic measures were taken as a result of peripheral swelling, pain in extremity, neuralgia, arthralgia, paraesthesia, myalgia, pain. Additional information: arm was swollen for about 2 and a half weeks just 2-3 days went down but have this annoying pain on arm which is hitting a nerve, so it affecting neck shoulder trap, lateral like basically everything that has to do with shoulder. And then fingertips pointer and thumb feel pins and needles, so he know its hitting the nerve. just going through this pain but this swelling went down, this pain is not going away. Its hitting up the part of arm where it is affecting his whole arm and neck, so say if he turn his face to the right and then he try to extend his arm to the left excruciating pain its hitting the nerve in that area right where shoulder blade and trap is. had muscle pain and the swelling happened the day after. the next day arm started getting swollen it was basically by the end of the week arm was almost doubled in size, he was soaking the hot and cold water, he is not that irritable, so he tried soaking with cold and hot water besides that important. he have to do with liquid, the watery hot or watery cold works better that the actual using a hot compress or using an ice compress (treatment). Pressure on the nerve all the way to the two fingers, thumb and pointer, goes to shoulder, bicep, tricep and trap: was taking antiinflammatory from doctor. had to see somebody and was taking methylprednisolone 4mg dose pack. took Methylprednisolone 4mg dose pack first and it was working. The medication ended shortly, only 6 days of taking the Methylprednisolone. doctor was on vacation. Prednisone: Another doctor gave the caller another medication that did not do anything. states the other medication that did not do anything was prednisone 5mg tablets. Methylprednisolone: The caller finished the Methylprednisolone and that was helping. The caller states he started taking Methylprednisolone 5 or 6 weeks after the caller was already in pain. thought the pain was going to subside. The caller doesn't take flu shots or anything like that. No prior vaccination within four weeks. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Accident (car accident)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NJ
Alter: 47,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Arrhythmia Bone pain Condition aggravated Diarrhoea Heart rate increased Migraine Myalgia Pyrexia Vomiting

Symptomtext

Heart arrhythmia two days after administration heart rate at 150 (normal resting heart rate for patient is 40). Other symptoms include migraine, muscle ache, fever, muscle and bone pain, diarrhea, vomiting one day after administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Heart arrhythmia confirmed via ECR on Watch, Symptoms subsided before being admitted to ER. However ventricular unusual heart patterns continued for two weeks and were confirmed during ER admission on October 27, 2021.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Received COVID-19 vaccinations on March 30, 2021 and April 17, 2021 and patient have both times symptoms of migraine, muscle ach

VAERS 2152154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: AK
Alter: 37,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 14.03.2021
Beginn: 11.04.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Antinuclear antibody Blood folate Blood magnesium Blood phosphorus Blood thyroid stimulating hormone Blood zinc Burning sensation Differential white blood cell count Full blood count Haemoglobin Laboratory test Lipids Low density lipoprotein Lyme disease Metabolic function test Neuropathy peripheral Pain in extremity Paraesthesia

Symptomtext

First Covid 19 vaccine administered March 2021. Starting ~ April 2021 (unfortunately cannot remember exact date) noticed tingling in right pinky toe. Shortly after noticed tingling in left pinky toe as well. Over time tingling progressed to involve multiple toes and then hands (symptoms in both hands and feet noted by June 2021). Severity of tingling waxed and waned throughout day. By August 2021 also noticed pain in right calf (burning, intermittent), and intermittent, short-lived, shooting, shock-like pain in single digit on left foot (observed when walking down stairs). Was evaluated at clinic on June 17, 2021 and had CBC/Diff, CMP, Cardiovascular risk assessment, Vit B6, Hemoglobin A1cL, LDL cholesterol, Lipoid panel with LDL/HDL Ratio, magnesium, phosphorus, TSH+Free T4, vitamin B12 and folate, Vitamin D levels checked - all WNL. Also spoke with OB/GYN as gave birth vaginally- no differentials given at that time. Referral to Neuro recommended. Moved cross country, saw new PCP. Had zinc, Vit B12, ESR, ANA, Intrinsic factor, Sjogren antibody panel, protein electrophoresis, UA, brain MRA, celiac disease panel, cervical radiographs, and lyme testing performed between August and December 2021 - all within normal limits. Had telemedicine consult with Neurologist January 17, 2022. Diagnosed with presumptive peripheral neuropathy. Spinal tap and EMG recommended, but have not been performed yet as would require travel and I elected to wait until weaning my infant to travel due to Covid. NO CAUSE OF PERIPHERAL NEUROPATHY HAS BEEN DETERMINED, SO I DO NOT YET KNOW IF RELATED TO VACCINE. Did not report until now as I recently read that peripheral neuropathies have been reported post vaccination. Currently, pain has resolved. Tingling in fingers and toes persists, continues to wax and wane, but is overall much more mild than it was previously. May be worse when dehydrated/after lying down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Prenatal vitamin Calcium supplement Sunflower lecithin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2151017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NY
Alter: 36,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 05.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blister Blood test COVID-19 Cough Crepitations Dizziness Dyspnoea Fatigue Hand-foot-and-mouth disease Impaired work ability Onychomadesis Oral mucosal blistering Oropharyngeal blistering Oropharyngeal pain Pain Pneumonia Pyrexia Rash

Symptomtext

I had the symptoms of hand foot and mouth on 11-13-2021. This included a rash with bumps on my hand feet and chest with a really high fever of 103.1. I was off work sick until November 19, 2021. The bumps turned into blisters that were extremely painful and it stretched to my face, mouth, nose and throat and tongue. I saw the doctor on 11-13-2021 and was diagnosed with hand foot and mouth. The doctor advised me to gargle with salt water and use OTC Aquaphor to treat. All my nails fell off. I am still losing the nails on my toes. I communicated this information thru my chart. All the blisters and bumps healed. I got my 2nd dose of the vaccine on November 26, 2021-(fj875-Pfizer). After this, I started getting sore throat and I was tired with congestion on February 15, 2022. The symptoms got worse daily with a fever as high as 102.8. I was diagnosed with pneumonia On February 19, 2022. I took a PCR test negative for COVID 19. However my at home kit tested positive on February 17,2022. I am currently undergoing a lot of treatments now. I started amoxicillin on February 20th and was only on it 1 day when the doctor prescribed prednisone, clarithromycin benzoate and a probiotic. I still have a lot of wheezing chest cracking and its hard to breath. I am dizzy tired and very short of breath. I am going for a chest x-ray and a pulmonary function test on Friday. I am still unable to return to symptoms. On February 09, 2022, I had to go to a cardiologist for breathing issues and was diagnosed with Premature ventricular contraction. No treatment was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood work, chest x-ray.
Aktuelle Erkrankungen: Fever and cough on 11-11-2021
Vorgeschichte: -
Andere Medikamente: Vitamin C and D, Women's 1 a day multivitamin, Norethindrone
Allergien: Dairy, Latex, Sumatriptan, Doxycycline, Augmentin, Zithromax, Fluconazole, Keflex, Levaquin, Cipro, Max Alt, Ethochloride, Dilaudid, Bioxen
Vorherige Impfungen: -

VAERS 2123974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MO
Alter: 64,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 02.11.2021
Beginn: 10.02.2022
Tage bis Beginn: 100,0
Dosis: 2
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain upper Asthenia COVID-19 Chest pain Dehydration Diarrhoea Eye pain Fatigue Headache Incontinence Influenza Pain SARS-CoV-2 test positive Urinary tract infection Vomiting

Symptomtext

Flu and UTI, stomach pain, severe vomiting, diarrhea, dehydration, fatigue, weakness, headache, bodyaches, eye pain, chest pain, incontinence

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: COVID-19 PCR (+)
Aktuelle Erkrankungen: not known/recalled at time of vaccinations
Vorgeschichte: COPD, RA, seizure hx, chronic back pain, early onset dementia
Andere Medikamente: Pt on many Rx related to chronic health factors, POA could not name them all treated for UTI and Flu at time of this event/hospitalization
Allergien: sulfates; no other known allergies
Vorherige Impfungen: -

VAERS 2118734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: KS
Alter: 45,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Dizziness Swollen tongue Tongue discomfort Tongue pruritus

Symptomtext

tongue is swollen, it itching and burns; tongue is swollen, it itching and burns; tongue is swollen, it itching and burns; chest hurts; Dizzy; 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. Other Case identifier(s): US-PFIZER INC-202101427342 (Pfizer). A 45-year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 22Oct2021 10:10 (Lot number: 320308D) at the age of 45 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: SWOLLEN TONGUE (non-serious), TONGUE DISCOMFORT (non-serious), TONGUE PRURITUS (non-serious) all with onset 22Oct2021 10:40, outcome "unknown" and all described as "tongue is swollen, it itching and burns"; CHEST PAIN (non-serious) with onset 22Oct2021 10:40, outcome "unknown", described as "chest hurts"; DIZZINESS (non-serious) with onset 22Oct2021 10:40, outcome "unknown", described as "Dizzy". Additional information Prior Vaccinations (within 4 weeks) never had any vaccines other than when she was a child. AE(s) following prior vaccinations was none. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available) was none. The patient reporting on the Pfizer Covid vaccine and who states she was just forced to take the first dose by her job and now her tongue is swollen, it is itching and burns. Her chest hurts and she feels dizzy. She got the shot about 30 minutes ago and it just started. There was nothing was wrong with her before getting the shot. She wants to report this and know what she is supposed to do. The events did not result in Emergency Room nor Physician Office visit. Relevant Tests was none No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2201173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 12.11.2021
Beginn: 03.01.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Atelectasis Atypical pneumonia COVID-19 Chest X-ray abnormal Chills Cough Decreased appetite Headache Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 01/13, Pfizer, dose #1 02/03, Pfizer, dose #2, Pfizer, dose #3 pt cc: exposure: unknown 01/03 pt admit to ED cc: COUGH/CONGESTION/DECREASED/DECREASED APPETITE, CHILS AND MILD HEADACHE dx: COVID-19 INFECTION, ATYPICAL PNEUMONIA LOS: 1 day 01/03 CXR impression: Bibasilar brochovascular crowding and atelectasis with no discrete focal airspace consolidation.

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Praegender Schweregrund: Atypical pneumonia
Hospital-Tage: -
Labordaten: 01/03 COVID swab, result: detected 01/10 COVID swab, result: detected 01/03 pt cc: exposure: unknown 01/03 CXR impression: bibasilar brochivascular crowding and atelectasis with no discrete focal airspace consolidation.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2092577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MN
Alter: 38,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 11.11.2021
Beginn: 19.01.2022
Tage bis Beginn: 69,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Angiogram normal Arteriogram coronary abnormal Bipolar disorder Blood creatinine increased Blood pressure increased COVID-19 Cardiomyopathy Chronic kidney disease Computerised tomogram head normal Condition aggravated Echocardiogram abnormal Fibrin D dimer Hypertension Hypertensive emergency Hypokinesia Left ventricular dysfunction Low density lipoprotein increased Magnetic resonance imaging normal

Symptomtext

PROGRESS NOTE 2/06/2022 38 y.o. female with no significant past cardiac history, history of hypertension, depression and chronic kidney disease. Patient was admitted with COVID-19 infection on 1/19/2022. Her blood pressure was markedly elevated at 220/145. Troponin level was increased. Echocardiogram showed reduced left ventricular systolic function with wall motion abnormality. Reason for cardiology follow-up is newly diagnosed cardiomyopathy, wall motion abnormality and elevated troponin. Subjective: No new symptoms Objective: Blood pressure 126/87, pulse 85, temperature (!) 95.7 ?F (35.4 ?C), resp. rate 19, height 5' 1.5" (1.562 m), weight 80 kg (176 lb 5.9 oz), SpO2 99 %, not currently breastfeeding. General: comfortable, in no acute distress. PLAN: Hypertensive emergency H/o noncompliance. Last se een by nephrology on an outpatient HTN/ chronic kidney disease in 12/2021. They suspect that the etiology of her chronic kidney disease could be related to hypertensive nephrosclerosis and she did have some mild proteinuria. Given her young age, they recommended work-up and follow-up for secondary causes Resume Coreg 25 mg p.o. twice daily, chlorthalidone 25 mg p.o. daily, hydralazine 25 mg p.o. 3 times daily, and lisinopril 40 mg p.o. daily, Held BP meds in 2/4 BP on lower side. Held lisinopril ( Cr bumped) , Restarted Coreg 2/5 , Hydralazine PRN 24-hour urine for catecholamines and metanephrines pending Renal artery ultrasound unremarkable Acute LLE weakness / pain R/o CVA ,decreased motor and sensation LLE unknown onset Discuss with Neurology seen MRI / MRA w./o Cer w negative Admit CT head no acute finding US BLE r/o DVT PT/ OT , nurse report patient was able to ambulate to bathroom today Elevated troponin Likely acute myocardial injury/strain from hypertensive emergency. Echo mildly decreased, estimated LVEF 45-50%.Inferolateral and anterolateral hypokinesis. Aspirin, Coreg. LDL 88 ( 3/18/20) Consulted Cardiology ?Coronary angiogram ( Cr 1.9 ) CKD stage III Suspected due to hypertension Last seen by Nephrology 12/21 Cr 1.5- 1.7 for the last few years Admit Cr 1.68 -- > Cr 1.93 Avoid nephrotoxic meds COVID-19 Multiple constitutional symptoms Not on O2 currently no indication for steroids Ddimer 5.34 , US LE negative. heparin Supportive cares History of seizure disorder Continue Trileptal 300mgBIDPTA ( on 600mg BID PTA ) Bipolar disorder Continue Risperdal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: 38-year-old female with history of chronic kidney disease, hypertension, depression, chronic anemia, and history of noncompliance Past Medical History: Diagnosis Date ? Anemia Iron deficient, on Iron replacement ? Back pain second to MVA, for the most part treated and resolved. ? CKD (chronic kidney disease) stage 2, GFR 60-89 ml/min 10/18/2014 ? Depression ? Herpes simplex type 2 infection genital, buttock ? HTN (hypertension) ? Migraine ? Obesity ? Other immediate postpartum hemorrhage, unspecified as to episode of care ? Preeclampsia with first pregnancy ? Reactive airway disease - cold temp . induced 12/9/2013 ? Seasonal allergies ? Seizure disorder - ??? - 15 per psychiatry ? SOB (shortness of breath)
Andere Medikamente: -
Allergien: Banana; Metronidazole; Prochlorperazine; Acyclovir; Adhesive; Adhesive tape-silicones; Amlodipine; Augmentin [amoxicillin-pot clavulanate]; Cigarette smoke; Citalopram; Compazine [prochlorperazine edisylate]; Dust/dust mites; Escitalopram; Green pepper; Kiwi; Kiwi; Latex; Latex, natural rubber; Red (food color); Rubber-non latex; Seasonale [levonorgestrel-ethinyl estrad]; Sertraline; and Tape-adhesive porous
Vorherige Impfungen: -

VAERS 2065649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood test normal Chest X-ray normal Chest pain Electrocardiogram normal

Symptomtext

Received Pfizer booster on Friday at 5:00pm, after work. Onset of chest pains at 10:00am the next morning. Increasing pain by 3:00pm. Went to hospital to report worsening chest pains. Blood work taken, chest x-rays taken and EKG monitoring for several hours. Blood work, x-rays and EKG showed no issues with my heart. Was finally given Nitroglycerin (3 times) and chest pain subsided somewhat. I was admitted to hospital over-night for monitoring. Released the next morning with an RX for Nitroglycerin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: 10/29/2021 - EKG, CHEST X-RAYS, BLOOD WORK. 10/30/2021 - EKG, CHEST X-RAYS, BLOOD WORK
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes
Andere Medikamente: Atorvastatin 20 mg tablet, Bumetanide 1 mg tablet, Bystolic 10 mg tablet, Cetirizine 10 mg, Levothyroxine 100 mcg tablet, NovoLog U100, Quinapril 20 mg tablet, Tiadylt ER 240 mg capsule
Allergien: Tetracycline, sulfonamides
Vorherige Impfungen: -

VAERS 2065381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: SC
Alter: 46,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chest discomfort Dyspnoea Swollen tongue

Symptomtext

Patient received covid vaccine at 1542. While sitting in observation, patient complained of a "heaviness" in her chest and used her rescue inhaler, 2 puffs at 1612. I offered to call EMS for her: however she refused, stated "I don't want to go to the Emergency Room". She also reacted to her first two doses of the Covid vaccine. 1615 patient took 50 mg of Benadryl that she brought with her to the clinic. 1616 patient was having difficulty breathing and heaviness was worse. Patient agreed for EMS to be called. 1617 EMS called and patient self administered her epi pen. 1618 Patient breathing easier and stated, "the heaviness is getting better". 1621 EMS arrived and took over care and monitoring of patient to transport to Emergency Department. Patients parents were with her at the clinic and were going to meet her at the Emergency Room. Emergency Visit: Dr."This is a 46-year-old chief complaint allergic reaction. 46-year-old who apparently got her first Covid shot a while ago had some itching afterwards got her second 1 and had quite a bit itching took some Benadryl decided to get a booster shot now and when she did it today she said she started getting short of breath and feel like she her tongue was swelling so she gave herself an epi shot took some Benadryl and came in she denies any other complaints" Dr., "Please note patient is feeling much better I do think some of this was anxiety I explained to her to use her EpiPen she has an extra 1 I will send her home with some prednisone tell her to take Benadryl to I did not get any vaccinations with a Covid type in the future as this could cause a severe anaphylactic reaction" Prescription for Prednisone 80 mg po daily x5 days. Medications received in the ED: ATIVAN, PEPCID, Solumedrol, Benadryl injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Medical History from ED Chart: Asthma, MS, GERD, Sciatica, Disc Disease, Peripheral Neuropathy, Anxiety and Depression
Andere Medikamente: Aspirin, Bacolfen, Zyrtec, Doxcycline, Cymbalta, Gabapentin, Norco, Epi Pen, Benadryl, Rescue Inhaler, Antivert, Mobic, Singular, and Mysoline
Allergien: Pencillin
Vorherige Impfungen: itching after first and second dose of COVID vaccine

VAERS 2052287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: UT
Alter: 35,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 23.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angiogram Artificial crown procedure Computerised tomogram normal Discomfort Ear discomfort Ear pain Endodontic procedure Eye pain Eyelid function disorder Facial pain Magnetic resonance imaging normal Mobility decreased Neuralgia Pain Toothache Trigeminal neuralgia X-ray dental

Symptomtext

On 3/25 two days after my vaccine, I had a sharp searing, burning pain in my tooth, right side of face and pressure in my right ear. I went to the dentist and after an exam, he referred me to have a root canal. The pain continued to worsen and eventually in May I had a root Canal when they had an opening. The pain only got worse and began to involve my eye, ear, tooth. Some days was hard to get out of bed. I went back and after an exam he decided to repeat the root canal. Again, it only made it worse. The pain was burning, shooting, pressure and affecting my eyelid. The dentist then proceeded to place a crown. Both the dentist and endondontist never saw any reason to require a root canal only based on exam. My dentist referred me to a neurologist. I had a MRI, MRA, CTA, CT? all vessels look great and no impingement on my trigeminal nerve. My neurologist named it an atypical trigeminal neuralgia / nerve pain and we started trying different medications. None seemed to help or the side effects were too much. In December, the pain slowly started to improve. I have not had a reoccurrence.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: MRI, mra, CT, CTA, Two Root Canals, Dental X-rays
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Imitrex as needed, baclofen as needed for migraines, progesterone (birth control)
Allergien: Celiac
Vorherige Impfungen: -

VAERS 2051024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 49,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 16.11.2021
Beginn: 19.01.2022
Tage bis Beginn: 64,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Dyspnoea Palpitations SARS-CoV-2 test

Symptomtext

palpitations, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS-COV-2 (COVID-19), NAA, Routine
Aktuelle Erkrankungen: -
Vorgeschichte: Cholecystitis 2011 ? Endometriosis ? IBS (irritable bowel syndrome) 2010 ? Pulmonary embolism (CMS/HCC) ? SVT (supraventricular tachycardia)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2047569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MN
Alter: 45,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 05.03.2021
Beginn: 18.01.2022
Tage bis Beginn: 319,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Ear pain Eye pruritus Headache Migraine Nasal congestion Pyrexia Sinus congestion Sneezing Upper-airway cough syndrome

Symptomtext

headache, has migraines, fever-98.6-99.9, chills, ear pain, sinus congestion, nasal congestion, post nasal drainage, sneezing, itchy eyes. starting 1/18/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Bee sting anaphylactic reaction, Reflex sympathetic dystrophy, Left arm - MAPS, Depression/Anxiety, Nicotine abuse, one-half per day since age 21, History of painful left cesarean scar margin - MAPS injection x2 partially effective, Recurrent sinusitis, Hypertension, Recurrent low back pain/DDD, Reactive airway disease, Migraines - following with neurolog, Dyslipidemia, Hashimoto's thyroiditis/hypothyroidism, Occipital neuralgia.
Andere Medikamente: Taking fentaNYL Cit-Ropivacaine-NaCl 0.2-0.2-0.9 MG/100ML Solution as directed Epidural , Taking Melatonin 5 MG Tablet 3 tablets in the evening Orally Once a day, Taking Ibuprofen 200 MG Tablet 1-2 tablets Orally every 6 hrs, Notes: as need
Allergien: Bee: anaphylaxis - Allergy, Sulfa: hives - Allergy, Cipro: rash - Allergy, Erythromycin Base: GI upset - Allergy, Keflex: hives - Allergy, Doxycycline Hyclate: GI upset - Allergy, Adhesives : rash - Allergy, Seafood: vomiting - Allergy, Septra: rash - Side Effects, Aerospan: vomiting - Allergy, Clindamycin HCl: vomiting, Clarithromycin: vomiting - Side Effects, PENICILLIN DRUGS: hives - Allergy, Hydrocodone-Acetaminophen: throat swelling - Allergy, Verapamil HCl: dizziness - Side Effects, Lisinopril: vomiting, cough - Side Effects.
Vorherige Impfungen: -

VAERS 2039914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NH
Alter: 43,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 10.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Rash

Symptomtext

Trouble breathing and body rash. Allergy medication and steroids were administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: None
Allergien: Latex
Vorherige Impfungen: -

VAERS 2036124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: IL
Alter: 59,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 12.10.2021
Beginn: 30.12.2021
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chest X-ray abnormal Pneumonia bacterial SARS-CoV-2 test positive

Symptomtext

I tested positive for Covid-19 on 1/3/22. I had a sore throat, light congestion. About a week into it, I developed a fever of 101.80, and chills. went to doc to get a chest x-ray and it revealed mild bacterial pneumonia. took antibiotics for that and am feeling good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia bacterial
Hospital-Tage: -
Labordaten: PCR test for Covid Chest x-ray for pneumonia
Aktuelle Erkrankungen: No
Vorgeschichte: Pulmonary sarcoidosis, high blood pressure
Andere Medikamente: 2 mg prednisone, lisinipol/HTCZ. gabapentin, vitamins, fish oil
Allergien: no
Vorherige Impfungen: -

VAERS 2034906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: FL
Alter: 53,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 10.05.2021
Beginn: 10.01.2022
Tage bis Beginn: 245,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest X-ray normal Chills Computerised tomogram thorax abnormal Cough Dyspnoea Lung infiltration Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st Vaccine received on 04/19/2021. 53 y/o PMH Asthma, COPD, Metastatic Breast Cancer/Left mastectomy, OSA, Diastolic HF, CAD, Pulm emboli presents to ED with 1 day history of c/o SOB, dry cough, sore throat, fevers, chills and generalized body aches. CXR negative. CT chest with multifocal patchy groundglass infiltrates RLL. Pt requiring O2 at 2L NC sats 94%. Treated with IV Steroids/IV ABX and Remdesivir.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS CoV 2 PCR Covid19-Detected 01/10/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Stage IV Metastatic Breast Cancer/Left mastectomy, COPD, OSA, Diastolic HF, CAD, Pulm emboli
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2018752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Asthenia Chest discomfort Cough Dyspnoea Fatigue Headache Immunisation Lacrimation increased Rales SARS-CoV-2 test Sinus congestion Sneezing

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 28Nov2021 12:00 (Lot number: 320308D) at the age of 58 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ZOLPIDEM. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8729, Location of injection: Arm Left, Vaccine Administration Time: 02:30 PM), administration date: 08Apr2021, when the patient was 58 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER2613, Location of injection: Arm Left, Vaccine Administration Time: 10:30 AM), administration date: 19Mar2021, when the patient was 58 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 28Nov2021 12:00, outcome "unknown", described as "Dose Number: 3"; FATIGUE (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "Extreme fatigue"; COUGH (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "chronic cough"; HEADACHE (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "headache"; RALES (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "chest/lung rattles"; DYSPNOEA (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "shortness of breath at times"; SINUS CONGESTION (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "sinus congestion"; ASTHENIA (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "general weakness"; SNEEZING (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "occasional sneezing"; LACRIMATION INCREASED (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "eyes tearing up"; CHEST DISCOMFORT (non-serious) with onset 29Nov2021 02:00, outcome "not recovered", described as "chest tightness". The events "extreme fatigue", "chronic cough", "headache", "chest/lung rattles", "shortness of breath at times", "sinus congestion", "general weakness", "occasional sneezing", "eyes tearing up" and "chest tightness" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of fatigue, cough, headache, rales, dyspnoea, sinus congestion, asthenia, sneezing, lacrimation increased, chest discomfort. Additional information: Patient did not receive any other vaccines within 4 weeks PRIOR to the COVID-19 vaccine. Patient had no allergy. Prior to vaccination, was the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. The patient received treatment with Steroids, antibiotics, nebulizer, inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20211201; Test Name: PCR Covid Test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20211220; Test Name: PCR Covid Test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: No known allergies. Other Medical history : No
Andere Medikamente: ZOLPIDEM
Allergien: -
Vorherige Impfungen: -

VAERS 2018319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: FL
Alter: 71,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Immunisation Product use issue Sleep disorder Tinnitus

Symptomtext

buzzing/humming and hissing sound in ears; It affects sleep patterns; it became much worse within 24-48 hours after this 3rd dose; booster vaccine; Other vaccine same date vaccine date 19Nov2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Nov2021 11:00 (Lot number: 320308D) at the age of 71 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine inact sag 4v (FLUAD QUAD), administered in arm right, administration date 19Nov2021 (Batch/Lot number: unknown) as dose 3, single. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0171, Location of injection: Arm Left, Administration date:28Apr2021, Vaccine Administration Time: 11:00 AM), administration date: 28Apr2021, when the patient was 71 years old, for COVID-19 Immunization, reaction(s): "buzzing and humming sounds in ears"; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0185, Location of injection: Arm Left, Administration date:05May2021, Vaccine Administration Time: 10:45 AM, Adverse event start date: 08May2021), administration date: 05May2021, when the patient was 71 years old, for COVID-19 Immunization, reaction(s): "buzzing and humming sounds in ears", "First dose: 28Apr2021; Second dose: 05May2021". The following information was reported: IMMUNISATION (non-serious) with onset 19Nov2021 11:00, outcome "unknown", described as "booster vaccine"; PRODUCT USE ISSUE (non-serious) with onset 19Nov2021, outcome "unknown", described as "Other vaccine same date vaccine date 19Nov2021"; TINNITUS (non-serious), outcome "not recovered", described as "buzzing/humming and hissing sound in ears"; SLEEP DISORDER (non-serious), outcome "not recovered", described as "It affects sleep patterns"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "it became much worse within 24-48 hours after this 3rd dose". Therapeutic measures were not taken as a result of tinnitus, sleep disorder. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications in two weeks. The patient had no known allergies. Within 14 days of vaccine #1 on 28Apr2021 had buzzing and humming sounds in ears. Stayed about same even after vaccine dose #2 on 19May2021. Was an annoyance for most part but something new that I did not have until after the 1st Pfizer vaccine. However, after the booster vaccine on 19Nov2021 it became much worse within 24-48 hours after this 3rd dose. It persists to this date and is louder with buzzing/humming and hissing sound in ears. At times seems to be more piercing sound. I looked on internet and did find that some Covid vaccine recipients experienced these sounds and even tinnitus with ringing in ears. I am not sure if I would describe it ringing, but it is a very annoying sound and is constant. It affects sleep patterns due to this persisting sound when everything should be quiet and ready to sleep. I take no medications or prescriptions, but I would say this is a side effect of the vaccines, much like some people taking meds have side effects. No Treatment was received. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2001565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 21,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Dyspnoea Palpitations

Symptomtext

Episodes of racing heart, periodic feelings of chest pressure (worse when lying down) --occasional difficulty breathing or getting a full breath of air. She says she has no idea how many times a day nor how long it lasts - it builds gradually until she notices it's been happening, then subsides gradually.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None available. Called dr's office, dr on vacation, they suggested calling health dept. or going to urgent care; no appointments available in near future. Health dept suggested calling or going to urgent care (one hour drive from home). Because of Omicron surge we called urgent care rather than going. Nurse from urgent care called us - she did not think these symptoms could be related to a vaccination. She said not to bother coming in unless we felt she was in crisis, and that they couldn't do any tests that would help her anyways. Next nearest hospital 3 hours away and also overloaded. she is going overseas for school in two weeks, we decided not to pursue any further.
Aktuelle Erkrankungen: none
Vorgeschichte: Low blood pressure; episodes of vasovagal syncope. Reynaud's syndrome, patulous Eustachian tube. Possible (undiagnosed) athsma.
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1999048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 17,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Palpitations

Symptomtext

Intermittent racing heart for the next 24 hours. Contacted family doctor (who was on vacation), doctor's office suggested contacting health dept, who advised rest, fluids and Tylenol. Resolved in ~ 24 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: flu 2-3 weeks previous to vaccination
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 1999032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 17,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Palpitations

Symptomtext

A FEW EPISODES OF RACING HEART, AND OCCASIONAL SENSE OF TIGHTNESS IN CHEST. CALLED DOCTOR (ON VACATION) AND HEALTH DEPT., THEY RECOMMENDED TYLENOL AND REST. CONTINUED INTERMITTENTLY ~24 HOURS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: flu about 2-3 weeks previous to vaccination
Vorgeschichte: none
Andere Medikamente: none
Allergien: possible allergy to bee stings
Vorherige Impfungen: -

VAERS 1993426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: OH
Alter: 45,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Chest pain Dyspnoea Dyspnoea exertional Erythema Fatigue Lymph node pain Musculoskeletal discomfort Nausea Pain in extremity Painful respiration Peripheral swelling Skin warm Vomiting

Symptomtext

I started with fatigue day after receiving vaccine. Last night my glands started hurting and i was short of breath wth exertion. Today, I am extremely short of breath and pain and pressure in chest and back when I take a deap breath.I have had nausea and vomitting since i got the vaccine. Also, my arm was sore, red, swollen, and hot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid arthritis, asthma, SVT, Hypertension, migraines, hyperlipidemia, anxiety, allergies
Andere Medikamente: Lisinopril, metoprolol, zetia, provastatin, ibuprofen otc, zoloft, buspar, albuterol inhaler, ativan
Allergien: ERythromyocin
Vorherige Impfungen: pain and swelling at injection site

VAERS 1989477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MS
Alter: 38,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 01.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 25,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Arthralgia Back pain Mobility decreased Pain in extremity

Symptomtext

Arm pain that's still hurting til this day. Back pain. Can not raise arm. Shoulder hurts also.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Went to the urgent care clinic.
Aktuelle Erkrankungen: Na
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: Pfizer

VAERS 1978684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: KY
Alter: 34,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoacusis Hypoaesthesia Immunisation Paraesthesia Tinnitus

Symptomtext

side of her face started going numb and tingling/numbness, tingling, and ringing in her ear was occurring on the right side; side of her face started going numb and tingling/numbness, tingling, and ringing in her ear was occurring on the right side; Ears started ringing/ringing in her ear was occurring on the right side; She just got the Pfizer Covid-19 booster; can't hear out of her ear good and it is like it is full of water; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 34-year-old female patient received bnt162b2 (BNT162B2, Solution for injection), administered in arm left, administration date 06Dec2021 16:30 (Lot number: 320308D) at the age of 34 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1, single, Batch/Lot number: EL9267, Expiry: May2021), administration date: 19Feb2021, when the patient was 33 years old, for COVID-19 immunization; Bnt162b2 (Dose 2, single, Batch/Lot number : EN6202, Expiry date : 30Jun201), administration date: 12Mar2021, when the patient was 33 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 06Dec2021 16:30, outcome unknown, described as She just got the Pfizer Covid-19 booster; TINNITUS (non-serious) with onset 06Dec2021 16:45, outcome not recovered, described as Ears started ringing/ringing in her ear was occurring on the right side; PARAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 06Dec2021 16:50, outcome not recovered and all described as side of her face started going numb and tingling/numbness, tingling, and ringing in her ear was occurring on the right side; HYPOACUSIS (non-serious) with onset 06Dec2021, outcome not recovered, described as can't hear out of her ear good and it is like it is full of water. Additional information: Caller is a consumer that reported that she just got the Pfizer Covid-19 booster dose at 1630 and about 15 minutes after she got it she left and was driving home and reported that her ears started ringing when she left at 1645. HCP: Caller declined. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MA
Alter: 63,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 28.10.2021
Beginn: 04.12.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

COVID-19 Computerised tomogram thorax abnormal Dyspnoea Lung opacity Neutropenia SARS-CoV-2 test positive

Symptomtext

Patient was admitted prior to this admission for covid 19 infection iso neutropenia and tested positive for covid on 11/27/21. Patient presented to Hospital on 12/4/21 with worsening SOB and was started on 5 days of remdesivir. Patient was also continued on home oncologic treatment. Patient is fully vaccinated for covid. Patient was discharged on 12/10/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 6,0
Labordaten: covid positive on 12/5/21. 12/4 CT chest impression: No evidence for PE. small peripheral pulmonary groundglass opacities and consolidations likely related to patient's known covid 19 infection
Aktuelle Erkrankungen: N/A
Vorgeschichte: mantle cell lymphoma c/b babesia
Andere Medikamente: acalabrutinib, acyclovir, allopurinol, vitamin d3, melatonin, venetoclax
Allergien: penicillin G, benzathin, procain
Vorherige Impfungen: -

VAERS 1955383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: AZ
Alter: 40,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 30.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest discomfort Chest scan Cognitive disorder Disturbance in attention Feeling abnormal Headache Impaired work ability Migraine Scan brain Screaming Tremor Vomiting

Symptomtext

I had covid late 2020. I tested my antibodies and had a lot of antibodies a year later. I received the pfizer vaccine despite having natural immnity 2 days later I was reading then all of a sudden I had severe migraine pain and physically couldn't read anymore like my brain stopped working. I laid down and started uncontrollably shaking. Migraine pain so bad that I was screaming in agony. I was driven to the hospital. I puked 3 times in the hospital from the pain. I was giving chest scans and sent home with diagnosis of "headache". I was unable to work for two weeks due to my inability to even perform my job due to decreased cognitive ability and severe migraines. I have had tightness in chest, brain fog and migraines ever since the vaccine. Never have I had ever these symptoms in my life before the vaccine. Everyday is a struggle at work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Brain and chest scan. Brain scan and chest scan
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1935417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Abdominal pain Dysphagia Dyspnoea Injected limb mobility decreased Injection site erythema Injection site induration Injection site nodule Injection site pain Injection site swelling Pyrexia Throat tightness

Symptomtext

Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Abdominal Pain-Medium, Systemic: Fever-Mild, Additional Details: pt states that arm was sore or tender for few days. then became very painful and feels like there is hard knot in there with redness swelling. not hotness to touch. pt states that it is so painful it has limited to her mobility. she did get slight fever (that night after administration) and stomach pain (few days after administration) above the belly button.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MO
Alter: 49,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Condition aggravated Fatigue Immunisation Muscular weakness Myalgia Pain in extremity Vaccination site pain Weight

Symptomtext

Arm was sore all the way down into the forearm; She received the booster dose; Humeral elbow pain; elbow pain) tried to massage it, but it ended up getting worse and it felt more sore.; Tired; She still has humeral elbow pain. She said it doesn't feel like arthritis, but more of a nagging, annoying, and burning sensation; She said it makes her right arm so weak; Joint pain; Pain at the injection site; Muscle pain; Pain in extremity; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team. The reporter is the patient. A 49 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 25Oct2021 (Lot number: 320308D) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Second dose, lot: EN6204, NDC: Unknown, Expiration: Unknown, Route of administration: right arm), administration date: 18Mar2021, when the patient was 48 years old, for COVID-19 immunization, reaction(s): "sore arm"; Bnt162b2 (First dose, Expiration: 30Jun2021 , lot: EN6198, NDC: Unknown , Route administration: left arm), for COVID-19 immunization, reaction(s): "sore arm"; Shingles vaccine (shingles vaccine in the left arm, two weeks prior to receiving the booster dose Pfizer Covid Vaccine.); Hepatitis d vaccine, reaction(s): "bad". The following information was reported: IMMUNISATION (non-serious) with onset 25Oct2021, outcome "unknown", described as "She received the booster dose"; ARTHRALGIA (non-serious) with onset 2021, outcome "not recovered", described as "Humeral elbow pain"; CONDITION AGGRAVATED (non-serious) with onset 2021, outcome "unknown", described as "elbow pain) tried to massage it, but it ended up getting worse and it felt more sore."; PAIN IN EXTREMITY (non-serious) with onset 25Oct2021, outcome "not recovered", described as "Arm was sore all the way down into the forearm"; FATIGUE (non-serious) with onset 2021, outcome "unknown", described as "Tired"; ARTHRALGIA (non-serious) with onset 2021, outcome "unknown", described as "She still has humeral elbow pain. She said it doesn't feel like arthritis, but more of a nagging, annoying, and burning sensation"; MUSCULAR WEAKNESS (non-serious) with onset 2021, outcome "unknown", described as "She said it makes her right arm so weak"; ARTHRALGIA (non-serious) with onset 2021, outcome "unknown", described as "Joint pain"; VACCINATION SITE PAIN (non-serious) with onset 2021, outcome "unknown", described as "Pain at the injection site"; MYALGIA (non-serious) with onset 2021, outcome "unknown", described as "Muscle pain"; PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "unknown", described as "Pain in extremity". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of arthralgia, condition aggravated, pain in extremity, arthralgia. Additional information: A 49-year-old female pharmacist said she received the booster dose of the Pfizer-BioNTech Covid-19 Vaccine. She said it has already been over two weeks, but she still has humeral elbow pain. She said it doesn't feel like arthritis, but more of a nagging, annoying, and burning sensation. She said it is painful when she has her arm bent for too long so she has to keep it straight all the time. She said it makes her right arm so weak. Reporter said she is not sure if this is because of the way the pharmacist administered the vaccine to her, and that maybe she hit a nerve. She said that instead of administering it to the center, the pharmacist administered it to the side a bit. Afterwards, she felt pain all the way down to her forearm. Description of complaint: Caller reported arm was sore all the way down into the forearm after receiving booster dose Pfizer Covid Vaccine. She had a sore arm after receiving first and second dose Pfizer Covid Vaccine. sore arm was gone in less than a week after receiving first and second dose Pfizer Covid Vaccine. She thought her arm soreness all the way down into forearm was improving but she was doing stuff like putting a heating pad around the elbow and taking Ibuprofen. It has been two weeks and tired of doing that and feels like now it was getting worse. The caller is not even sure, thinks may have taken Ibuprofen and was taking Tylenol right after booster dose Pfizer Covid Vaccine and may have switched to Ibuprofen. Reported that joint pain, pain at the injection site, muscle pain, and pain in extremity have been reported after administration of the booster dose, but not specific to the elbow. Caller stated that she gained a bunch of weight that the weight gain was just from being sedentary nothing due to vaccine. Reporter stated that she received shingles vaccine in the left arm, two weeks prior to receiving the booster dose Pfizer Covid Vaccine. Shingles Vaccine: NDC/lot/expiration: The caller does not have this information to provide but is sure withheld has the information, withheld is where the caller received the shingles vaccine. Indication: The caller has a daughter going to college in withheld and started using the airline quite a bit to fly home back and forth, received to prevent infections with colic daughter traveling. The caller has seen the doctor once because the caller had shingles at the beginning of the year. Clarified that she had shingles prior to receiving any dose of the Pfizer Covid Vaccine. Reporter wanted to know if there have been reports of elbow pain after receiving the booster dose, and if it resolves over time. Reporter seriousness for Booster dose: Arm was sore all the way down into the forearm: Unspecified Event: Booster dose: Arm was sore all the way down into the forearm was reported as worsened. Source of assessment: Primary Source Reporter Method of assessment: Regulatory Authority Drug result: Unknown

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Weight; Result Unstructured Data: Test Result:gained a bunch of weight
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1924539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: OH
Alter: 32,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Arthralgia Back pain Chills Feeling cold Headache Hyperhidrosis Insomnia Neck pain Tremor

Symptomtext

Woke up at 2AM with uncontrollable chills/shaking, couldn't get warm, headache, neck pain, hip pain, lower back pain, sweating (despite being really cold), and couldn't sleep. Insomnia every night since getting dose 2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Multivitamin
Allergien: Latex, environmental
Vorherige Impfungen: -

VAERS 1923854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: WI
Alter: 54,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 08.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Back pain Chest pain Computerised tomogram abnormal Culture Differential white blood cell count Electrocardiogram Full blood count Hypopnoea Laboratory test Lipase Metabolic function test Pain Pleural effusion Troponin Urine analysis

Symptomtext

Dose was the booster on 10/8/2021. Felt pain on Sunday, 10/10/2021. Delayed going to Dr. as I was waiting for a regular appointment scheduled (3-4 weeks later). After waiting 1 week, opted to go to urgent care (10/18/2021) due to constant pain in left chest with shifting forward (bending) causes more pain. Pain also radiates to back and breathing was a bit more shallow. Urgent care sent me to ER the same day. ER notes indicated incorrect date in notes, indicating "just a date sometime close is fine". Outcome: Trace left pleural effusion (was not on any prior CTs).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: All occurred on 10/18/2021: Review of symptoms/vitals, EKG 12- Lead, Labs, CT scan. Lab tests CBC W Auto Differential, comprehensive metabolic panel, istat troponin, lipase blood,
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2565298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 28,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Palpitations

Symptomtext

Palpitations chest discomfort Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1923240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 01.10.2021
Beginn: 17.11.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cardiac flutter Chest discomfort Dyspnoea Palpitations SARS-CoV-2 test negative

Symptomtext

Heart palpitations, flutter, chest pressure, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Covid-19 test negative
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D3 1000 iu
Allergien: None
Vorherige Impfungen: -

VAERS 1920270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: VA
Alter: 56,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Paraesthesia Pharyngeal swelling Pruritus

Symptomtext

Facial tingling, facial itching, throat swelling (within 30 mins of vaccine administration)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Norethindrone .35mg (birth control) OTC Claritin, Flonase for season allergies
Allergien: Codeine, Amoxicillin, Bactrum, Levaquin, Tramdol (hives and facial swelling), Omnicef, Cipro (all hives)
Vorherige Impfungen: -

VAERS 1910081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NM
Alter: 54,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 16.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: UN / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Limb discomfort Mobility decreased Pain in extremity

Symptomtext

I began having pain/soreness/heaviness in my right arm/shoulder approximately 4 days after the second vaccination. It is not constant but is still with me. It seems to be worse when I wake up from sleep. I go to the gym 3-4 times a week and I feel the soreness especially when working out. I also do not lift as much weight due to the soreness. It has been going on for approximately a week and a half.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Zyrtec
Allergien: N/A
Vorherige Impfungen: -

VAERS 1909792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NY
Alter: 34,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 27.10.2021
Beginn: 04.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angiogram Chest discomfort Chest pain Stress echocardiogram

Symptomtext

Pt began having chest pain and tightness 6 days after vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: pending CTA and STress Echo
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension, Hyperlipidemia, Gout
Andere Medikamente: Crestor, Synthroid, Hydrodiuril
Allergien: Copper
Vorherige Impfungen: -

VAERS 1903761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dyspepsia Erythema Feeling hot Pruritus Tremor Urticaria Wheezing

Symptomtext

severe heart burn; face very hot red over nose and cheeks; face very hot red over nose and cheeks; itchy hives on chest; wheezing and tremors in her legs; wheezing and tremors in her legs; has redness and itching on her cheeks chest; has redness and itching on her cheeks chest; This is a spontaneous report from a contactable nurse (patient) via medical information team. A 59-year-old female patient received first dose of bnt162b2 (COMIRNATY, Solution for injection, Batch number: not reported/ Lot Number: 320308D) via an unspecified route of administration, administered in arm left (reported as left arm) on 27Oct2021 08:30 (also reported as three weeks ago tomorrow) (at the age of 59-year-old) as dose 1, single for covid-19 immunization administered in across from clinic. Patient's relevant medical history included, diagnosed allergies, compromised immune status, respiratory illness, genetic/chromosomal abnormalities, endocrine abnormalities (including diabetes), obesity, allergies to medications and thyroid cancer no thyroid, all from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. Historical vaccine included patient previously received flu vaccine (unknown manufacturer) on an unspecified date and patient was not allergic to the flu vaccine. Historical vaccine included patient previously received pneumovax vaccine (unknown manufacturer) and hepatitis vaccine (unknown manufacturer) on an unspecified date and experienced allergies. Prior vaccination within 4 weeks was noted as no. Additional vaccines administered on same date of the Pfizer suspect was noted as no. It was reported that the side effects started about 12 hours after the vaccine. On 27Oct2021 21:00, patient woke up with severe heart burn. Her face was very hot and red over her nose and cheeks. She had itchy hives on her chest. She was wheezing. She took Benadryl. She did not take anything prior. It lasted a few hours. She took the Benadryl in response to what was going on. The Benadryl helped. She didn't feel febrile, but she did have some tremors in her legs. Her legs were shaking, but she didn't feel chilled. She had recovered completely. Patient reported she had redness and itching on her cheeks chest that comes and goes on an unspecified date in 2021. It had been a few weeks out now (at the time of the report). She responded to Benadryl. Patient thought that was medically significant, and related. No adverse events required to visit emergency room or physician office. The patient was due for her second shot on 17NOv2021 (reported as tomorrow). She was wondering if she can pre-medicate for the second dose based on what happened 3 weeks ago. She was wondering if there was anything she could do to avoid some of the symptoms. Relevant tests was noted as no. Outcome of the events has redness and itching on her cheeks chest was unknown and outcome of rest of other events was recovered on 27Oct2021. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on limited information in the case , a possible causal association between the reported events heart burn, feeling hot , face red, hives, tremor limb, wheezing, erythema ,itching and the suspect drug BNT162B2 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy multiple; Chromosome abnormality; Diabetes; Drug allergy; Endocrine disorder; Immunocompromised; Obesity; Respiratory disorder; Thyroid cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1902211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NM
Alter: 18,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Alanine aminotransferase increased Aphonia Aspartate aminotransferase increased Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Cough Dyspnoea Fatigue Hepatic enzyme increased Hepatosplenomegaly Lymphadenopathy Myalgia Oropharyngeal pain Pyrexia Rhinorrhoea Tachycardia

Symptomtext

11/09/2021: low grade fever and myalgias 11/12/2021: into Urgent Care as symptoms worsened; loss of voice, rhinorrhea, dry cough, sore throat, intermittent low grade fevers that would subside with antipyretic; given Augmentin BID X 10 days, flonase and received a steroid shot in office. 11/16/2021: fever and tachycardia remain, fatigue, shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11/23/2021 liver enzymes elevated; AST 263, ALT 721 11/24/2021 CT abdomen shows hepatosplenomegaly and lymphadenopathy; CT chest shows adenopathy
Aktuelle Erkrankungen: Tachycardia Allergic Rhinitis eczema
Vorgeschichte: -
Andere Medikamente: Vitamin D3 Flaxseed oil Cetirizine
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1899323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: CO
Alter: 73,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Immunisation Tinnitus

Symptomtext

her tinnitus is really really bad; her tinnitus is really really bad; Booster; This is a spontaneous report from a contactable consumer (patient). A 73-years-old female patient received third dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: 320308D), via an unspecified route of administration, administered in Arm Right on 04Nov2021 at 13:45 (at the age of 73-years-old) as dose 3 (booster), single for covid-19 immunisation. Medical history included ongoing tinnitus. Concomitant medication included influenza vaccine inact sag 4v (FLUAD QUAD, Lot number: 312828), received within 4 weeks prior to the vaccination, administered in right arm taken for an unspecified indication on 18Oct2021. The patient previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EK4231), via an unspecified route of administration on 30Jan2021 (at the age of 72-years-old) as dose 1, single and received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: ENU207), via an unspecified route of administration on 20Mar2021 (at the age of 72-years-old) as dose 2, single both doses for covid-19 immunisation. The patient did not receive any other additional vaccine on same date of the pfizer suspect. On 06Nov2021, the patient experienced her tinnitus was really really bad. Her tinnitus WAS really really bad was reported as worsened. Patient stated since she got that shot on 04Nov2021, her tinnitus was really really bad. She has had tinnitus for at least 20 years but it has been mild and then it has increased and was really loud. The patient did not required emergency room or physician office visit. Patient Stated that the tinnitus was ongoing and had been at a steady loud rate and that was noticed on 06Nov2021 after the booster vaccine. The outcome of the event was not recovered. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Tinnitus (Verbatim: Tinnitus Had for at least 20 years)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1895113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 23,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Menstrual disorder Menstruation irregular Mobility decreased Pain in extremity Pyrexia

Symptomtext

Menstrual cycle completely out of sync; have been hormonally grossly imbalanced since my anticipated period on the 1st of November (incidentally the same date of my first intramuscular vaccine injection). An irregular period has never happened to me in my life. I got a fever of 101 degrees F which has persisted to this moment; my arms were so debilitatingly sore I can no longer lift them up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: N/A
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1894212

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NJ
Alter: 65,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 21.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Burning sensation Dyspnoea Injection site pain

Symptomtext

I have Burning at Site of Injection, near Pacemaker, Heart, and Shoulder Feel shortness of Breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: I have a Pacemaker for AFIB and also in January 2020, My Heart Valves were repaired. I started feeling a burning sensation near Pacemer and Shoulder after the vaccine
Vorgeschichte: None
Andere Medikamente: Xeralto 20 MG Cardizem (Diltizem) 120 MG Montelukkasr Sodium 10 MG
Allergien: None
Vorherige Impfungen: -

VAERS 1890704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NC
Alter: 46,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Heart rate increased Paraesthesia Paraesthesia oral

Symptomtext

Patient called asking for advice regarding adverse effects she was having an hour to several hours after receiving the vaccine. She reported tingling in her lips, arms, shoulder. She also reported a rapid heart rate that had been ongoing for at least an hour. Pharmacist recommended visiting the ER and to take an aspirin which the patient reported that she had already taken. Follow up call the next day was not answered and the patient has not called us back to let us know the outcome/how she is currently doing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Latex Iodine
Vorherige Impfungen: -

VAERS 1888062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: VA
Alter: 52,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 03.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tachycardia

Symptomtext

Tachycardia when standing or with little activity starting five days post-vaccine and continuing to date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: POTS; Migraines
Andere Medikamente: Metoprolol Vitamin D Vitamin B12 Magnesium Multivitamin
Allergien: Penicillin; Keflex; Gentamicin; Gadnolinium; Sulfa; Aspirin; Tylenol; Cyclogyl; Shellfish; Spearmint
Vorherige Impfungen: -

VAERS 1885164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 01.03.2021
Beginn: 15.11.2021
Tage bis Beginn: 259,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Dyspnoea Fatigue SARS-CoV-2 test positive

Symptomtext

Pt received pfizer vaccines on 03/01/2021, 03/22/2021, and 11/04/2021. Pt presented to the ED on 11/15/21 with complaints of feeling fatigued with SOB. Pt was found to be COVID positive

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, DM, COPD, CKD, obesity,
Andere Medikamente: Zyloprim, lipitor, jardiance, lexapro, neurontin, lantus, pril
Allergien: Hydrochlorothiazide, metformin, saxagliptin
Vorherige Impfungen: -

VAERS 1884304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: AZ
Alter: 43,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Decreased appetite Dizziness Dyspnoea Headache Hypersensitivity Myalgia Nausea Pain Pain in extremity Pain of skin

Symptomtext

Headache, body aches, sore skin, muscles, joints, dizziness, breathlessness, nausea, loss of appetite, tips of fingers hypersensitive sending pain through my fingers and hands, similar sharp shooting pain in toes and feet - nothing like I have ever felt before. All subsided after one week except for the pain in my hands, arms, feet, and legs - weird, unusual pain unlike anything I?ve experienced before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No.
Aktuelle Erkrankungen: No.
Vorgeschichte: No.
Andere Medikamente: Vitamins D & C, Multivitamin, Probiotic
Allergien: Latex.
Vorherige Impfungen: -

VAERS 1881093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Erythema Headache Hypertension Hypoaesthesia oral Paraesthesia oral Pharyngeal hypoaesthesia Pharyngeal paraesthesia Urticaria

Symptomtext

53 year old female complained of headache, had hives and redness on neck and chest, and numbness and tingling on her lip and throat. 1745 Blood pressure at 191/98, patient given Benadryl 50 mg IM to left deltoid. 1753 Blood pressure 206/109 and pulse 93, per unit manager hold epi pen due to high blood pressure. Called 911 services due to high blood pressure at 1800 blood pressure 224/118. Patient taken to ER via ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1877355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

moderat

Staat: OH
Alter: 36,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 14.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anosmia Blood pressure increased Burning sensation Diarrhoea Dizziness Fatigue Migraine Nausea Pyrexia

Symptomtext

extreme fatigue, extreme migraine, dizzyness, nausea, diarrhea, cant smell certain things, burning sensation throughout body no fever, increase in blood pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: lexopril
Allergien: -
Vorherige Impfungen: -

VAERS 1873393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NJ
Alter: 38,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 29.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Atypical pneumonia Breath sounds abnormal Electrocardiogram normal Fatigue Headache Influenza virus test negative Nasal congestion Oropharyngeal pain Pyrexia Respiratory tract congestion Respiratory tract infection SARS-CoV-2 test negative

Symptomtext

Sore Throat within first 36 hours progressed to fatigue and headache within 48 hours. Further progression led to nasal congestion and chest congestion. Within 4 days, fever and increased chest congestion with headache and general fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atypical pneumonia
Hospital-Tage: -
Labordaten: EKG results normal. Rapid tested for COVID and Influenza - both negative. Diminished lung sounds with no cracking or popping. Doxycycline and Albuterol prescribed for respiratory infection (walking pneumonia)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1867830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 26.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood thyroid stimulating hormone Electrocardiogram Fibrin D dimer Full blood count Metabolic function test Paraesthesia Troponin

Symptomtext

Left arm paresthesia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CBC, CMP, TSH, D-dimer, Trop, EKG.
Aktuelle Erkrankungen: -
Vorgeschichte: Glaucoma.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 1864866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NJ
Alter: 37,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Breast pain Chest X-ray Chest discomfort Chest pain Echocardiogram Electrocardiogram Inflammation Pain in extremity

Symptomtext

Chest pressure, pain in chest, at times pain under breasts and by under arms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/5/2021 had EKG, blood work and chest x-ray done 11/10/2021 had EKG, blood work, chest x-ray, and echo ultrasound Doctors said it could be inflammation due to the vaccine.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 1864787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: FL
Alter: 36,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood pressure increased Chest discomfort Chest pain Heart rate increased Impaired work ability

Symptomtext

Reported complaints of sternal chest pain beginning the afternoon of vaccination administration. States he was unable to lie flat that night and experienced pain the following day as well. He left work due to the discomfort, but did not seek medical attention. Reported slightly elevated heart rate and blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1860814

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: FL
Alter: 44,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Condition aggravated Ear pain Extra dose administered Fatigue Headache Lymphadenopathy Nausea Pain Pain in jaw Pyrexia Sensitive skin

Symptomtext

Extreme skin sensitivity, body aches, headache, fever, chills, nausea and fatigue as well as swollen lymph nodes in my left under arm. This lasted 24 hours. Since those extreme symptoms dissipated, i have minor pain in my ears and jaw, a continued headache and continued swollen lymph nodes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: women's multivitamin
Allergien: sulfa and pineapple
Vorherige Impfungen: 2nd COVID Pfizer vaccine with similar symptoms with the addition of vertigo

VAERS 1857124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MD
Alter: 58,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Headache Heart rate increased Hypertension Myalgia

Symptomtext

High heart rate for at least 8 hours. 135 bpm normal 85. BP over ten points higher top and bottom. Major headache muscle pains for 3 days. Tiredness continues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pfyser

VAERS 1854034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: PA
Alter: 54,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 23.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal distension Chills Dysmenorrhoea Headache Menopausal symptoms Menopause Migraine Pain

Symptomtext

This was a booster shot, and the third shot from Pfizer for the Covid Vaccine. I had the same reactions to all three shots. The first day after shot, severe body aches, chills, and headache. I am also perimenopausal, I hadn't had menstrual periods for 6 months, but weeks after getting the first shot, I got severe PMS symptoms including migraines, bloating, etc, that I normally got before menstrual period. The day of second shot, I got a menstrual period with severe cramping, along with the body aches, chills in the reaction. After that cycle, I stopped having PMS symptoms and menstrual periods again. After third shot, 2 weeks later I'm experiencing severe PMS symptoms again, with migraines, bloating, etc.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: none.
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, allergies
Andere Medikamente: Claritin 24; nasacort; symbcort
Allergien: no allergies to medications, food or other products, seasonal and animal allergies.
Vorherige Impfungen: -

VAERS 1851809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: NY
Alter: 47,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 01.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Diarrhoea Genital herpes Injected limb mobility decreased Injection site pain Nausea

Symptomtext

Mild diarrhea within 1 hour of 1st vaccine Pfizer shot. Mild intermittent nausea, no vomiting. Severe injection site upper arm pain, difficulty lifting the arm for 2 days. Genital herpes outbreak within 4 hours of 1st shot, pre-existing condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Endometriosis, genital herpes
Andere Medikamente: Triamterene 37.5 mg (started taking 10 days prior to vaccine), cetirizine hydrochloride 10 mg antihistamine, daily multivitamin
Allergien: None known
Vorherige Impfungen: -

VAERS 1851021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dysarthria Dyspnoea Periorbital oedema

Symptomtext

COVID booster given. Patient stated she had Benadryl in her car. She went to her car to get Benadryl and came back inside. On the elevator, a nurse noticed that she was having shortness of breath, slurred speech, and per-orbital edema. Vital signs were checked, oxygen applied. Benadryl had already been taken. EpiPen administered. 911 called, and patient was taken to ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1850469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 01.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Dementia Exposure to SARS-CoV-2 Hallucination Hypoxia

Symptomtext

hx of dementia at the hospital with worsening dementia and hallucinations and covid concern. Son had covid recently. she was hypoxic to 70s per ems. She was placed on O2. She is vaccinated and had received the 3rd dose previous week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1848974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: OH
Alter: 25,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dry skin Hyperhidrosis Posture abnormal Tremor

Symptomtext

Patient received the Pfizer vaccine on 11/6/2021 at 11:55am at 12 noon., he slumped over in his chair. He was shaky and sweaty. Brought gurney over and transferred patient. vital signs: 12:07 133/88.73 12:13 99/64 , 81 12:25 122/73 55 12:35 107/40 53, Spo2 100% This was patients first dose. He never had an adverse reaction to any other vaccines. NKDA. Only Seasonal allergies No other illnesses at time of vaccination No chronic health conditions at time of vaccination Patient was accompanied by friend (who is a MA) Patient instructed to let nurse know that when he gets second vaccine what happened and that we would administer on cart. He had two bottles of water. V.S stable, color good, skin dry

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: n/a
Allergien: Seasonal only
Vorherige Impfungen: -

VAERS 1846059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MI
Alter: 31,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Bedridden Erythema Fatigue Feeling hot Hyperhidrosis Nausea Palpitations Tremor

Symptomtext

Patient instantly became hot and shaky. She began sweating and her face became red. She stated she felt nauseous and felt as though her heart was racing. I followed up with the patient 2 days after the incident to see how she was doing. she claimed to be bed ridded for the rest of the day after her vaccination and felt extremely tired and not herself for 2 days. pt claimed to finally begin feeling like herself again on day 3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Blood pressure was taken twice 15 minutes apart. 1st read was taken shortly after symptom onset and was 118/83, the second reading was 123/86.
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: Pt claims to take Spironolactone.
Allergien: None reported
Vorherige Impfungen: -

VAERS 1844732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: TX
Alter: 29,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Heart rate increased Heart rate irregular Palpitations Pyrexia

Symptomtext

First two days after the vaccine was normal Fever like symptoms, has developed into fast beating, irregular, pounding heart beats with shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: Multi vitamin, fish oil
Allergien: N/A
Vorherige Impfungen: -

VAERS 1836677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: OH
Alter: 39,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 25.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia Decreased appetite Dehydration Diarrhoea Fatigue Headache Hypoaesthesia Paraesthesia

Symptomtext

Left knee numbness/tingling, dehydration, headache, diarrhea, tiredness, weakness, loss of appetite?symptoms started around 2:30 am on 10/28 didn?t subside until 11/01? knee is still tingling

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control
Allergien: None
Vorherige Impfungen: -

VAERS 1833794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MD
Alter: 26,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain upper Cough Diarrhoea Dyspnoea Feeling hot Hyperhidrosis Somnolence

Symptomtext

A few hours after the injection I started to get hot sweats that lasted about 15 mins per session 4 times the first day only then i got diarrhea that was nearly completely watery and lasted roughly 3 days in length giving way to extreme stomach pains every hour until bathroom occurred also gave me a cough that has lasted from the injection date to current date with cough episodes lasting 15 mins per time and often nothing comes up and nearly leaves me breathless difficulty falling asleep lasted one the first night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Currently going to contact nurse advice line for more information
Aktuelle Erkrankungen: Cold
Vorgeschichte: None
Andere Medikamente: Escitalopram
Allergien: N/A
Vorherige Impfungen: -

VAERS 1831839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: KS
Alter: 56,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Dyspnoea

Symptomtext

Patient states her chest was getting tight and shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Patient stated she has severe asthma.
Vorgeschichte: Asthma
Andere Medikamente: None that I am aware of.
Allergien: Aspirin and Sulfa drugs.
Vorherige Impfungen: -

VAERS 1826272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MO
Alter: 54,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Paraesthesia

Symptomtext

Patient reports tingling in arms from elbows to fingertips and legs from knees to toes that has persisted for last 7 hours. Recommended visit to urgent care facility as I could not find similar reports.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1818443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Decreased appetite Diarrhoea Dizziness Feeding disorder Lethargy Migraine Musculoskeletal stiffness Pyrexia Tremor Vomiting

Symptomtext

Stiff arm (almost immediately and still ongoing) **After about 10 hours the following developed** Extreme Lethargy (lasting 3 days) Migraine (lasting 2 days) Vomiting - Could not even consume liquids (24 hours) Loss of appetite (ongoing) Fever (24 hours) Chills (48 hours) Uncontrollable body shakes (48 hours) diarrhea (24 hours) dizziness (ongoing)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Tooth infection leading to root canal and crown lengthening procedure
Vorgeschichte: Kidney infection from ongoing asymptomatic UTI
Andere Medikamente: 800mg Ibuprofen 500mg Amoxicillin
Allergien: Minocycline Pertussis Vaccine Lanolin
Vorherige Impfungen: -

VAERS 1808334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: MS
Alter: 20,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Paraesthesia

Symptomtext

patient received vaccination same day symptoms started. symptoms started 2 hours later with intermittent dizziness and tingling sensation to R shoulder

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1788013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: WI
Alter: 66,0
Geschlecht: M
Eingang: 15.10.2021
Impfdatum: 06.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SC / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Vertigo

Symptomtext

Intermittent chest pain: sharp/burning, mostly upper chest and under clavicles, improved with sitting up and/or leaning forward Intermittent vertigo, brought on by movement, episodes lasting < 60 seconds

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, osteoporosis, paroxysmal atrial fibrillation, scoliosis
Andere Medikamente: lisinopril, atorvastatin, melatonin, aspirin, forteo. acetaminophen
Allergien: none
Vorherige Impfungen: Age 65, Shringrix, malaise for 6-8 hours

VAERS 1775471

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

moderat

Staat: WI
Alter: 56,0
Geschlecht: F
Eingang: 10.10.2021
Impfdatum: 09.10.2021
Beginn: 10.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Dehydration Dizziness Extra dose administered Fatigue Hyperhidrosis Inappropriate schedule of product administration Insomnia Nausea Pain Pyrexia Tachycardia

Symptomtext

About 15 hours after getting booster shot began having high fever 102, chills, sweats, mild nausea, tachycardia and body aches. Also unable to sleep even before severe symptoms started, despite feeling tired. Quite significant as I had not had anything to this level with 1st or 2nd COVID vaccines. I am a health care worker in a hospital. My second COVID vaccine was 1/11/2021. Only injection site pain, fatigue and sleep problem with second dose. It is now 24 hours later. I took acetaminophen to try to break the fever. Feeling a bit better?no more fever but do have body aches, mild dehydration (tachycardia), dizziness and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: None. Did not seek medical attention.
Aktuelle Erkrankungen: None Did get Quadrivalent influenza vaccine on 10/5/21 (no adverse effects)
Vorgeschichte: Exercise/cold air induced wheezing
Andere Medikamente: Bupropion xl Buspirone Cetirizine Multivitamin Evening Primrose oil CoQ 10 Vitamin D
Allergien: No
Vorherige Impfungen: -

VAERS 2688243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: KY
Alter: 61,0
Geschlecht: F
Eingang: 28.09.2023
Impfdatum: 21.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache

Symptomtext

another one she got a killer headache with that Tylenol could not get rid of; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient received bnt162b2 (BNT162B2), on 21Oct2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 61 years for covid-19 immunisation. The patient's relevant medical history included: "GERD" (ongoing), notes: GERD; "Had gall bladder removed" (unspecified if ongoing). Concomitant medication(s) included: ESOMEPRAZOLE taken for gastrooesophageal reflux disease (ongoing). Vaccination history included: bnt162b2 (DOSE 1, SINGLE, Lot: EN6202, Expiry: 30Jun2021), administration date: 05Mar2021, when the patient was 60-year-old, for COVID-19 Immunization, reaction(s): "She was exhausted", "felt awful for a few days in a row", "She threw up in the middle of the night", "She got a killer headache"; bnt162b2 (DOSE 2, SINGLE, Lot: EP6955 , Expiry: 30Jun2021), administration date: 26Mar2021, when the patient was 60-year-old, for COVID-19 Immunization, reaction(s): "She was exhausted", "felt awful for a few days in a row", "She threw up in the middle of the night", "She got a killer headache". The following information was reported: HEADACHE (non-serious) with onset Oct2021, outcome "recovered" (Oct2021), described as "another one she got a killer headache with that Tylenol could not get rid of". Therapeutic measures were taken as a result of headache. Additional information: She got a killer headache with that Tylenol could not get rid of and had that a day or two and then after the immunization, she would feel better the next day after 2-3 days of misery, she would wake up feeling perfectly normal the next day.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300311369 same reporter/patient, differnet vaccine dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: GERD (GERD)
Vorgeschichte: Medical History/Concurrent Conditions: Gallbladder removal
Andere Medikamente: ESOMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2528586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OR
Alter: 29,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Lip swelling Peripheral coldness Peripheral swelling Pyrexia SARS-CoV-2 test negative Swelling Temperature intolerance

Symptomtext

The day after the shot, my left hand fingertips swole up for a few days straight. I had a fever for about 12 hours, and a bit of a headache, but the swelling in my hand persisted for days after. Ever since then, I'll experience swelling in my hands and feet if they're exposed to cold temperatures for more than a few minutes, and sometimes the swelling will last for hours. I've had my 4th dose, and I'm getting more random swelling (a weird spot on my butt, occasionally my lip). The internet says this is what chilblains are? I've never experienced anything like this in my life, and until I experienced it, I didn't know you could experience allergic reactions to cold temperatures.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: I'd taken covid tests (often rapid antigen tests) when I suspected it could be covid, but every test I took gave a negative result. The chilblains are not related to active covid infections.
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown, if any
Andere Medikamente: None
Allergien: NSAIDs
Vorherige Impfungen: -

VAERS 2503191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OH
Alter: 66,0
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 07.05.2022
Beginn: 29.08.2022
Tage bis Beginn: 114,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On 08/29/2022, I woke up with a runny nose. Later in the morning, I developed a slight fever of 100.5. I took some Tylenol, and the fever only lasted a total of around 6 hours. I took an at home COVID-19 test, and it was positive. I never had to take any additional Tylenol. My only symptoms were that short lived fever and a runny nose. The only reason I tested myself and discovered that I was positive was because I had a wedding to attend. The runny nose lasted for around 5 days. I continued testing myself and was still positive at 5 days. I tested again at 7 days and was negative. I took an additional test on the 9th day, and it was also negative. I continued to isolate at home for the additional day for a total of 10 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 29AUG2022- At Home COVID-19 Test- Positive; 03SEP2022- At Home COVID-19 Test- Positive; 05SEP2022- At Home COVID-19 Test- Negative; 07SEP2022- At Home COVID-19 Test- Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; High Cholesterol
Andere Medikamente: Flonase; Pulmicort Flex Haler; Fluticasone Propanoate; Atorvastatin; Vitamin D; Calcium; Vitamin C; Vitamin E
Allergien: NSAID Pain Relievers; Asparagus
Vorherige Impfungen: Fatigue lasting several weeks after all vaccines.

VAERS 2490048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: PA
Alter: 36,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 24.10.2021
Beginn: 13.07.2022
Tage bis Beginn: 262,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Fatigue Feeling abnormal Headache Oropharyngeal pain Paranasal sinus discomfort Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Throat clearing

Symptomtext

On 7/13/2022 I started feeling like a headache, a little bit of congestion, that got progressively worse. I was feeling feverish. On the 7/14/22 it got worse. On 7/14/2022 I tested positive for COVID-19. On 7/15, I was very tired, and I had a lot of sinus pressure in my head about 7/18 or 7/19 I started developing a sore throat, the pain was significant. I had a visit with my doctor on 7/20/22 and was prescribed a steroid, Prednisone. it relieved the sore throat. and the other symptoms started to subside. Once that started to clear up, I had a dry cough that went through the 30th of July. I was tired the week of the July 25. On 8/3 I started not to feel too much pain. but I felt like I had to clear my throat. I also had a little bit of brain fog on the 1st week of August. kind of like a daze. I started feeling like myself by September 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 7/13/ rapid COVID-19 test - negative 7/14 rapid COVID-19 test - positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Anxiety
Andere Medikamente: Sertraline; Collagen; Whey Protein; Multivitamin; Vitamin D supplement; Lorazepam
Allergien: N/A
Vorherige Impfungen: -

VAERS 2485670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: SC
Alter: 78,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 26.04.2022
Beginn: 22.09.2022
Tage bis Beginn: 149,0
Dosis: 4
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia Anosmia Asthenia Blood magnesium decreased Blood sodium decreased Body temperature increased Diarrhoea Headache Oropharyngeal pain Pain

Symptomtext

temp sore throat diarra headache ache all over no smell or taste weakl

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 4,0
Labordaten: hospital 4 days fluids given sodium & magnesmum low
Aktuelle Erkrankungen: diabetic heart stent
Vorgeschichte: diabetic
Andere Medikamente: Levothyroxine telmisartan simvastatin omeprazole basagler insulin metoprolol aspirin vit d 3 magnesium potassium vit b 12
Allergien: pencil codine lisinopril morphine
Vorherige Impfungen: -

VAERS 2476935

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Body temperature Heart rate Hypersensitivity Interchange of vaccine products Lethargy Pain in extremity Scleroderma

Symptomtext

a severe reaction with Pfizer booster; soreness in the left arm; felt lethargic; scleroderma; 1st dose of Moderna COVID-19 Vaccine on 2Feb2021, 2nd dose on 02Mar2021 and Pfizer booster on 29Oct2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP and Other HCP). The reporter is the patient. Other Case identifier(s): MOD22-025755 (Moderna). A female patient received BNT162b2 (BNT162B2), on 29Oct2021 as dose 3 (booster) single (Lot number: 320308D, Expiration Date: Feb2022), in left arm for covid-19 immunisation. The patient's relevant medical history included: "food and other products" (unspecified if ongoing); "chocolate" (unspecified if ongoing); "Acute and Chronic illnesse" (unspecified if ongoing); "asthma" (unspecified if ongoing), notes: since she was a child; "hyperparathyroidism", start date: Apr2021, stop date: Apr2021, notes: she had a surgery to remove the thyroid. Concomitant medication(s) included: OMEPRAZOLE; FLU [INFLUENZA VACCINE], on 15Oct2021 as dose number unknown, single. Past drug history included: Avelox for allergy, reaction(s): "Allergy: Avelox", notes: Allergy: Avelox; Caffeine, reaction(s): "Allergy: caffeine", notes: Allergy: caffeine; Monosodium gluconate for allergy, reaction(s): "Allergy: monosodium gluconate", notes: Allergy: monosodium gluconate. Vaccination history included: moderna (Dose: 1, date: 02Feb2021, Lot number: 004M20A, Route Intramuscular), administration date: 02Feb2021, for COVID-19 immunization, reaction(s): "soreness in left arm", "patient felt lethargic"; BNT162b2 (Dose: 2, date: 02Mar2021, Lot number: 026L20A), administration date: 02Mar2021, for COVID-19 immunization, reaction(s): "her pulse was 90", "she felt so bad", "she felt so hot and her temperature was 102?F", "she had some difficulty breathing but not enough to go to the hospital". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 29Oct2021, outcome "unknown", described as "1st dose of Moderna COVID-19 Vaccine on 2Feb2021, 2nd dose on 02Mar2021 and Pfizer booster on 29Oct2021"; SCLERODERMA (medically significant) with onset Nov2021, outcome "unknown"; HYPERSENSITIVITY (non-serious), outcome "unknown", described as "a severe reaction with Pfizer booster"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "soreness in the left arm"; LETHARGY (non-serious), outcome "unknown", described as "felt lethargic". The event "a severe reaction with pfizer booster" required emergency room visit. Clinical course: Caller stated she did not have history of myocarditis or pericarditis Patient mentioned she had a severe reaction with Pfizer booster and she had to go to urgent care, but with Moderna it was only a slight reaction. For both Moderna vaccines patient did not take any treatment. Patient wanted to know if it would be possible for Safety Team to tell her symptoms that she reported are severe or moderate, for her to take an informed decision about getting the bivalent booster. patient had not ever COVID + test or diagnosis. Condition 2: Scleroderma(start Date: Nov2021, Recent change in status such as improvement or worsening: no). patient experienced a similar event in the past - it was a food related thing. Concomitant: Vitamins. The patient underwent the following laboratory tests and procedures: Body temperature: 102 Fahrenheit; Heart rate: 90. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Test Name: temperature; Result Unstructured Data: Test Result:102 Fahrenheit; Test Name: pulse; Result Unstructured Data: Test Result:90
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (since she was a child); Food allergy; Hyperparathyroidism (she had a surgery to remove the thyroid); Illness
Andere Medikamente: OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2469396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MA
Alter: 71,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: ja

Body temperature Growth retardation Interchange of vaccine products Investigation Rash Weight

Symptomtext

Caller provides this rash was from head to toe; Dose 1 and dose 2 is of moderna and dose 3 of pfizer; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 71-year-old female patient received BNT162b2 (BNT162B2), on 29Oct2021 as dose 3 (booster), single (Lot number: 320308D, Expiration Date: Feb2022) at the age of 71 years for covid-19 immunisation. The patient's relevant medical history included: "Hyperparathyroidism", start date: 2021 (unspecified if ongoing); "Allergies: chocolate" (unspecified if ongoing), notes: it gives her palpitations specifically she experiences SVT's; "Allergies: caffeine" (unspecified if ongoing), notes: it gives her palpitations specifically she experiences SVT's; "Palpitations" (unspecified if ongoing), notes: it gives her palpitations specifically she experiences SVT's; "SVT's." (unspecified if ongoing), notes: it gives her palpitations specifically she experiences SVT's; "MSG" (unspecified if ongoing), notes: it gives her palpitations specifically she experiences SVT's. There were no concomitant medications. Past drug history included: Avelox antibiotic, reaction(s): "Allergies: She has no allergies but the only medication she has something with was Avelox antibiotic". Vaccination history included: moderna covid vaccine (Moderna First Dose: Date 02Feb2021, Caller is unsure if the Lot number is 004M20A or 009M20A), administration date: 02Feb2021, when the patient was 70-year-old, for COVID-19 Immunization; moderna covid vaccine (feeling very sick, Moderna Second Dose: Date 02Mar2021 Lot 026L20A.), administration date: 02Mar2021, when the patient was 70-year-old, for COVID-19 Immunization, reaction(s): "feeling very sick", "102?F temperature". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 29Oct2021, outcome "unknown", described as "Dose 1 and dose 2 is of moderna and dose 3 of pfizer"; RASH (disability, medically significant) with onset 07Nov2021, outcome "recovered" (16Nov2021), described as "Caller provides this rash was from head to toe". The event "caller provides this rash was from head to toe" required emergency room visit. The patient underwent the following laboratory tests and procedures: Body temperature: 102 Fahrenheit; Growth retardation: 5 feet 4 inches, notes: about 5 feet 4 inches, she has shrunk, she was 5 feet 6 inches; 5 feet 6 inches; they did all this testing: everything came back negative; Weight: 162lbs or 163lbs at that time.. Therapeutic measures were taken as a result of rash. Clinical course: The patient stated that she was calling about the Pfizer covid Booster, not the new one with the omicron. She was in the process of signing up to have booster, she was hoping to do the Pfizer Covid Bivalent vaccine. Her first 2 COVID vaccines were Moderna, but her last covid booster was by Pfizer on 29Oct2021. The reason she was calling because she tried to sign up, and she did have a reaction but she never reported it, it was 10 days after the Pfizer COVID booster vaccine from head to toe she had a rash she went to urgent care, they prescribed her Benadryl and a steroid dose pack. She had the steroid for a week, and it took like a week for the rash to go away. The doctor said it had nothing to do with the vaccine, but then another said it had to do with the booster. She never reported it. The pharmacist said she needed to check with the doctor as it could have been a severe reaction. She then read on the CDC information that it was a side effect; it did say severe reaction side effect and that she should have reported it. The patient wanted to know it was considered a severe reaction. she wanted information; she has already called the doctor, but she doubted they would come back. The patient reported about rash: The rash stopped about a week after around 16Nov2021, once the itch was gone, she felt like she recovered. Seriousness Criteria: It was disabling also because she was on Benadryl every 4-6 hours and when she is on that she could not function, it made her sleepy, so if she had to drive, she would have not been able to. The patient got a Tetanus shot because she stepped on a nail, this was well after the rash, she got the tetanus shot in either Apr2022 or May2022. Medical Conditions: last year she got diagnosed with Hyperparathyroidism, she was diagnosed in an arthritis clinic in either Oct2021 or Sep2021. She also would like to add that she went to the clinic in Nov2021 after the rash, it was an arthritis clinic, they were looking for autoimmune diseases, they did all this testing and everything came back negative, however she is a little over average for scleroderma, she has not been diagnosed with scleroderma but they have been watching her for 2 more symptoms, if she experienced that then she needs to call, right now it was unknown if she has an autoimmune disease. The patient was probed for the Benadryl Lot number, she responded saying that with the Benadryl she had no problems, she was told to take it every 4 - 6 hours, when she was itching, she also put on Caladryl. Benadryl Lot is unknown, she another that is unused, but she does not have the one she consumed. Allergies: She had no allergies but the only medication she has something with was Avelox antibiotic, she also cannot eat chocolate, caffeine, or MSG as it gives her palpitations specifically, she experienced SVTs.; Sender's Comments: Based on possible temporal association the causal association of suspect drug BNT162b2 and for the reported events -Rash and interchange of vaccine products- 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 RAs, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Name: 102?F temperature; Result Unstructured Data: Test Result:102 Fahrenheit; Test Name: she has shrunk; Result Unstructured Data: Test Result:5 feet 4 inches; Comments: about 5 feet 4 inches, she has shrunk, she was 5 feet 6 inches; Test Name: she has shrunk; Result Unstructured Data: Test Result:5 feet 6 inches; Test Name: they did all this testing; Result Unstructured Data: Test Result:everything came back negative; Test Name: weight; Result Unstructured Data: Test Result:162lbs or 163lbs at that time.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to chemicals (it gives her palpitations specifically she experiences SVT's); Caffeine allergy (it gives her palpitations specifically she experiences SVT's); Food allergy (it gives her palpitations specifically she experiences SVT's); Hyperparathyroidism; Palpitations (it gives her palpitations specifically she experiences SVT's); Supraventricular tachycardia (it gives her palpitations specifically she experiences SVT's)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2388337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: FL
Alter: 69,0
Geschlecht: M
Eingang: 25.07.2022
Impfdatum: 21.01.2021
Beginn: 01.03.2021
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Dermatomyositis Myalgia Rash

Symptomtext

Muscle aches and rash later diagnosed with Dermatomyositis.

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Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia
Andere Medikamente: rosuvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2329025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MN
Alter: 67,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 07.12.2021
Beginn: 26.05.2022
Tage bis Beginn: 170,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Fatigue Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

Patient presented to the emergency department for nausea, vomiting, fatigue, and weakness on 5/26/2022. Tested positive for COVID-19 via PCR that day and subsequently admitted for her symptoms. Patient was discharged on 5/27/2022. This meets criteria for vaccine breakthrough case review.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2319312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MN
Alter: 80,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 15.02.2021
Beginn: 25.05.2022
Tage bis Beginn: 464,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Confusional state Cough Pyrexia SARS-CoV-2 test positive

Symptomtext

WEAKNES, CONFUSION, DRY COUGH, FEVER,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: 6,0
Labordaten: POSITIVE COVID TEST 5/25/2022
Aktuelle Erkrankungen: -
Vorgeschichte: A-fib Angina pectoris (HCC) Arthritis Arthritis of carpometacarpal (CMC) joint of right thumb Asthma, mild intermittent, well-controlled Colon polyps COPD (chronic obstructive pulmonary disease) (HCC) Degenerative arthritis of thumb, right Heartburn HTN (hypertension) Colonic polyps Late onset Alzheimer's disease without behavioral disturbance (HCC) Malignant neoplasm of upper-outer quadrant of right breast in female, estrogen receptor positive (HCC) Right carpal tunnel syndrome Rosacea
Andere Medikamente: acetaminophen (TYLENOL) 500 mg oral tablet ammonium lactate 12% (LAC-HYDRIN) 12 % Top cream cream anastrozole (ARIMIDEX) 1 mg oral tablet ARNUITY ELLIPTA 200 mcg/actuation Inhl DsDv inhaler ascorbic acid 500 mg Oral
Allergien: Barbiturates Phenobarbital
Vorherige Impfungen: -

VAERS 2302596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AZ
Alter: 33,0
Geschlecht: F
Eingang: 30.05.2022
Impfdatum: 31.10.2021
Beginn: 02.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Arthropathy Bone pain Cyst Joint range of motion decreased Loss of personal independence in daily activities Magnetic resonance imaging abnormal X-ray normal

Symptomtext

First thing I noticed was a pain like my humorous was going to snap in half while moving in bed. Within a few more days I started to lose range of motion and constant pain in my shoulder. I was unable to put my bra on or reach across or stretch my left arm out. By the time week 2 rolled around, I struggled to be able to prepare dinner plates for my children. I sit with a heat pad on my should constantly for some relief. Finally went to my dr and he gave a cortisone shot. This was roughly a month after the vaccine. Cortisone shot was great at first. I finally was pain free and able to move around. My dr recommended physical therapy. First cortisone shot lasted 1 week. Went to physical therapy. Physical therapist agrees that there was something going on with the lose of range of motion. Went bad to dr to follow up with report from PT. Was given a second cortisone shot. Lasted 2 weeks. Dr ordered xray, which came back clear. Requested MRI. MRI shows tear in Labrum and an adjacent 1cm cyst. Referred to pain management and to an orthopedic surgeon. Appt with Orthopedic Surgeon is June 23 2022 for next steps. Possible surgery to repair tear.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Xray- normal; MRI- tear on shoulder Labrum with adjacent 1 CM cyst.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Advil.
Allergien: Hydroxycloriqune & Morphine.
Vorherige Impfungen: -

VAERS 2294114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: -
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 05.11.2021
Beginn: 26.11.2021
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Allergy test Allergy to animal Blood immunoglobulin E Blood immunoglobulin E increased Dermatitis Eczema Laboratory test abnormal Photosensitivity reaction Polymorphic light eruption Pruritus Rash Rash macular SARS-CoV-2 antibody test Skin disorder Viral rash

Symptomtext

eczema; her eruption seemed to localize on the sun-exposed area of her skin; pruritus; Photodermatitis; polymorphous light eruption; photodermatitis; Dog dander 11.3 KU/L high level/ Cladosporium herbarum(m2) IgE very low level/ Dermatophagoides 20.6 KU/L very high level/ Farinae (d2), pteronyssinus 26.0 KU/L very high level; immunoglobulin E 576 KU/L; upper arms with few spots; more severe viral exanthem rash; neck rash 26Nov2021; This is a spontaneous report received from a contactable reporter(s) (Physician). A 32-year-old female patient received BNT162b2 (BNT162B2), on 05Nov2021 as dose 3 (booster), single (Lot number: 320308D) intramuscular, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "Mild eczema" (ongoing), notes: Intermittent; "Hay fever" (ongoing), notes: Childhood. The patient's family history included: "Hay Fever" (ongoing), notes: Father and grandmother - Hay fever. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Time: 14:30, Site and route of injection: Left deltoid, Route of administration: Intramuscular, Batch/Lot number: EP6955), administration date: 10Mar2021, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Time: 14:30, Site and route of injection: Left Deltoid, Route of administration: Intramuscular, Batch/Lot number: ER8734), administration date: 31Mar2021, for COVID-19 immunization. The following information was reported: RASH (medically significant) with onset 26Nov2021, outcome "not recovered", described as "neck rash 26Nov2021"; VIRAL RASH (medically significant) with onset 10Feb2022, outcome "not recovered", described as "more severe viral exanthem rash"; ECZEMA (non-serious), outcome "unknown"; SKIN DISORDER (non-serious), outcome "not recovered", described as "her eruption seemed to localize on the sun-exposed area of her skin"; PRURITUS (non-serious), outcome "unknown"; PHOTOSENSITIVITY REACTION (non-serious), outcome "not recovered", described as "Photodermatitis"; POLYMORPHIC LIGHT ERUPTION (non-serious), outcome "not recovered", described as "polymorphous light eruption"; DERMATITIS (non-serious), outcome "not recovered", described as "photodermatitis"; LABORATORY TEST ABNORMAL (non-serious), outcome "unknown", described as "Dog dander 11.3 KU/L high level/ Cladosporium herbarum(m2) IgE very low level/ Dermatophagoides 20.6 KU/L very high level/ Farinae (d2), pteronyssinus 26.0 KU/L very high level"; BLOOD IMMUNOGLOBULIN E INCREASED (non-serious), outcome "unknown", described as "immunoglobulin E 576 KU/L"; RASH MACULAR (non-serious), outcome "unknown", described as "upper arms with few spots". The events "eczema", "her eruption seemed to localize on the sun-exposed area of her skin", "pruritus", "photodermatitis", "polymorphous light eruption" and "photodermatitis" required physician office visit. The event "more severe viral exanthem rash" required emergency room visit. The patient underwent the following laboratory tests and procedures: Allergy test: (15Feb2022) Unknown results; (unspecified date) 0.13 kU/L, notes: Very low level; (unspecified date) 20.6 kU/L, notes: very high level; (unspecified date) 26.0 kU/L, notes: Very high level; Allergy to animal: (unspecified date) 11.3 kU/L, notes: High level; Blood immunoglobulin E: (unspecified date) 576 kU/L, notes: Standard range: 114 or less kU/L; SARS-CoV-2 antibody test: (16Jan2022) Positive. Therapeutic measures were taken as a result of viral rash, eczema, skin disorder, pruritus, photosensitivity reaction, polymorphic light eruption, dermatitis, rash macular. Therapeutic measures were not taken as a result of rash. Clinical information: Patient has developed an eruption on her face, neck, chest and hands about 3 weeks after her recovery from Covid-19 in Jan2022. Patient was treated as eczema by her primary care M.D with Desonide, Fluocinenide and protopic without improvement. The distribution of her eruption seemed to localize on the sun-exposed area of her skin (face, neck, "v" of chest doral hands and upper arms with few spots) and she was taking Zyrtec for her pruritus. The pattern suggested a possibility of Rx induced photodermatitis or polymorphous light eruption. Patient was advised to d/c Zyrtec and avoid sun exposure. Patient eruption was clear but only for only then it received + became persistent. Patient was seen by a dermatologist and subsequently she was treated with a 2 week tapering course of prednisone 60 mg. Patient was clear while on prednisone, but 2 days after her prednisone course, the eruption recurred on her face, neck, chest and upper extremities and also spreaded to her trunk and lower extremities. Patient eruption has persisted without change over the last few weeks.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the events and suspect drug BNT162B2 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Test Date: 20220215; Test Name: Childhood Allergy test; Result Unstructured Data: Test Result:Unknown results; Test Name: Cladosporium herbarum (m2) IgE; Result Unstructured Data: Test Result:0.13 kU/L; Comments: Very low level; Test Name: Dermatophagoides; Result Unstructured Data: Test Result:20.6 kU/L; Comments: very high level; Test Name: Farinae (d2), pteronyssinus; Result Unstructured Data: Test Result:26.0 kU/L; Comments: Very high level; Test Name: Dog dander; Result Unstructured Data: Test Result:11.3 kU/L; Comments: High level; Test Name: Immunoglobin E; Result Unstructured Data: Test Result:576 kU/L; Comments: Standard range: 114 or less kU/L; Test Date: 20220116; Test Name: Covid Test; Test Result: Positive
Aktuelle Erkrankungen: Eczema (Intermittent); Hay fever (Father and grandmother - Hay fever); Hay fever (Childhood)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2280811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MN
Alter: 83,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 04.03.2021
Beginn: 09.05.2022
Tage bis Beginn: 431,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

FEVER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: 4,0
Labordaten: POSITIVE COVID TEST 5/7/22
Aktuelle Erkrankungen: -
Vorgeschichte: ? Acute cystitis 4/4/2019 ? Acute heart failure, unspecified heart failure type (HCC) ? Acute kidney insufficiency 7/14/2013 ? AKI (acute kidney injury) (HCC) 7/14/2013 ? Alzheimer's type dementia with late onset without behavioral disturbance (HCC) 6/16/2021 ? Anemia 7/25/2019 ? Chronic indwelling Foley catheter 6/16/2021 ? Cystitis ? Diarrhea urgency for 5 months ? Dyslipidemia 1/31/2022 ? Essential hypertension 7/27/2020 ? Headache(784.0) 7/14/2013 ? History of rectal cancer 9/27/2017 ? Hydronephrosis of right kidney 3/11/2021 ? Hypercholesteremia 7/16/2009 ? Hypothyroidism 2/18/2009 ? Malignant neoplasm of rectum (HCC) 10/6/2008 1. Continuous infusional 5FU and concurrent pelvic radiotherapy given neoadjuvant and completed on November 18, 2004. 2. Low anterior resection and diverting loop ileostomy on December 13, 2004. Pathology showed a 1 cm adenocarcinoma which invaded into the muscularis propria with six negative nodes. 3. Takedown of loop ileostomy and resection of small bowel with reanastomosis on December 30, 2004 ? Microscopic hematuria 7/14/2013 ? Neuropathy bilateral feet ? Osteopenia 9/21/2011 ? PONV (postoperative nausea and vomiting) ? Poor nutrition ? Pulmonary nodule seen on imaging study 7/14/2013 ? Rectal Cancer (2004) 10/6/2008 radiation and chemo ? Rectal carcinoma (HCC) ? Recurrent UTI 9/2/2021 ? Retention of urine 3/11/2021 ? S/P ureteral stent placement 6/16/2021 ? Seborrheic keratosis 11/2/2009 ? Sepsis 7/14/2013 ? Sepsis (HCC) 4/4/2019 ? Stage 1 chronic kidney disease 1/18/2019 ? Suspected HAP/VAP (gram negative or MRSA pneumonia) 12/30/2020 ? TIA (transient ischemic attack) "TIA years ago-completely recovered"
Andere Medikamente: ? acetaminophen (TYLENOL) 325 mg oral tablet Take 325 mg by mouth once daily. ? amLODIPine (NORVASC) 2.5 mg oral tablet TAKE 1 TABLET EVERY DAY (Patient taking differently: Take 2.5 mg by mouth once daily.) ? ascorbic acid, vitamin C, 500
Allergien: Augmentin [Amoxicillin-Pot Clavulanate] Doxycycline Doxycycline Calcium Iodinated Contrast Media Xray Dyes (Nic)
Vorherige Impfungen: -

VAERS 2278363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 12.11.2021
Beginn: 07.05.2022
Tage bis Beginn: 176,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case of COVID-19: I had congestion and sore throat. I had a virtual appointment and the doctor prescribed benzonatate and guaiatussin. I took three take home rapid test and one PCR test.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: PCR COVID-19 test positive.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2271010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MO
Alter: 67,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 07.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Conjunctivitis Eye pain Herpes zoster Intraocular pressure increased Ocular discomfort Photophobia Uveitis

Symptomtext

I got my Pfizer booster on 11/7/2021, and early in December 2021, I started having eye pain and severe light sensitivity in the right eye, which resulted in my visiting the local emergency room on 12/11/2021. They gave me ointment for conjunctivitis and referred me to an eye doctor at the eye care center. The eye doctor started me on steroid eye drops. My condition didn't get better, and I probably visited the eye doctor every week in December. They eventually diagnosed me with Uveitis, and they gave me a round of steroid eye drops. I had three rounds, and every time a round was completed, I had rebound symptoms. My last round was completed 3/17/2022. After I got off the steroids, I took Ibuprofen at least once a day to manage the pain. In April 2022, I was referred to a doctor. The doctor diagnosed me with Shingles, and she gave me a 14-day course of Valtrex, steroid eye drops and Celebrex. I also experienced increased pressure in the right eye, and I took Timolol eye drops to treat it. I completed the therapy on 5/6/2022. I felt fine for one day, but I started to have pain in the right eye again on 5/8/2022. I started taking Celebrex again. I left a message for the doctor to inform her of the situation, and at the time of this writing, I have not yet heard back from her. I have a follow-up appointment on 5/24/2022. I am still having discomfort in the right eye, though it's not as severe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension Type II Diabetes Asthma Osteoarthritis
Andere Medikamente: Cardizem Spironolactone Hydrochlorothiazide Zyrtec Flonase Nasal Spray Flonase Inhaler Metformin Lipitor Centrum Silver for Women
Allergien: Penicillin Tetanus Vaccine Percocet
Vorherige Impfungen: I have a negative reaction to Tetanus shots.

VAERS 2270911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 07.04.2021
Beginn: 13.02.2022
Tage bis Beginn: 312,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Pain in extremity SARS-CoV-2 test positive

Symptomtext

02/13/22 presents to EC ED for "right foot pain". PMHx of "depression and GERD".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: 02/13/22 SARS-CoV-2 (COVID-19) detected.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2265994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: WI
Alter: 72,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 03.11.2021
Beginn: 30.04.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia COVID-19 Chills Nasopharyngitis Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive Sleep disorder

Symptomtext

The first day I just had a sore throat. The second day I had cold like symptoms - runny nose, chills, achy and like I had a real bad cold. Then Tuesday morning I had a at home COVID-19 test and it was positive. I had no energy to do anything and couldn't sleep. Severity was like a really bad cold. I suspected it was COVID-19 because I was on an airplane and in the airport without a mask. Now I'm isolating. I called my Doctor and I wasn't anywhere near my home and that afternoon they told me they had antivirals but it was hard to find and I should take vitamin D, C and Zinc. Once I got home I went and got the antiviral prescription 2x day for 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home COVID-19 test - positive.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Synthroid Calcium
Allergien: Sulfur Macrobid Penicillin
Vorherige Impfungen: After 3rd dose COVID-19 vaccine - I felt dizzy, chills, extreme hunger for the 1st couple of days.

VAERS 2257011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MO
Alter: 65,0
Geschlecht: F
Eingang: 28.04.2022
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Rash Rash pruritic Skin warm

Symptomtext

On 11/11/2021 I had a rash around my neck going down my chest. It was hot and itchy. It got worse overnight so I got a hold of my doctor the next morning. She prescribed 30mg of Prednisone for 3 days 20mg for 3 days, 10mg for 3 days. At the same time I was also prescribed 20mg of Pepcid a day and 10mg of Zyrtec daily. It did clear up the rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Synthroid 0.075mg Daily, Lipitor 10mg daily, Hormone Patch Lyllana 0.0375mg, Estring 2mg Vaginal ring. I also take Vitamin D 2000 IU daily and Calcium 1200mg daily.
Allergien: Codeine and I have had a reaction to Shingrix, Euflexxa and Synvisc.
Vorherige Impfungen: Shingrix gave me a similar reaction. Rash around my neck and I did go to ER. 04/18/ 2018. Rash occurred next day 04/19/2018. I

VAERS 2254645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: TX
Alter: 59,0
Geschlecht: M
Eingang: 27.04.2022
Impfdatum: 26.10.2021
Beginn: 15.03.2022
Tage bis Beginn: 140,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache Lacrimation increased Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test

Symptomtext

I thought I had allergies, but my Nasacort and Allegra were not relieving my symptoms. I took a rapid test on the 15th, and I spoke to my doctor who recommended that I take the monoclonal antibodies which I did. The symptoms were congestion body ache, headache, runny nose and watery eyes. I was symptom free within 18 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Monoclonal antibodies
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; High Cholesterol
Andere Medikamente: Does not wish to provide
Allergien: None
Vorherige Impfungen: Shingles-sore shoulder for 24 hours

VAERS 2248096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 05.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Eye pain Fatigue Headache Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

After a few months out from receiving my Dose 3 Pfizer, 11/05//2021 I was diagnosed with COVID positive on COVID positive 01/04/2022 . I was feeling unwell from 01/03/2022 -01/07/2022 head ache, fever, sore eyes, and fatigue. I went to urgent care who provided testing and diagnosis. I was advised that it was okay to take the over the counter medication that I had on hand at home. I feel that I have fully recovered from this issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: Tested at Urgent with the test with results the next day.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2238044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: TN
Alter: 58,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 20.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity X-ray

Symptomtext

Within days, after my first dose, I started having really bad pain in my hands and thumb area with a lot of weakness. I went to an orthopedic Dr. and he diagnosed me with arthritis and gave some medication and a topical cream. He also gave me a hand splints. Plus he gave me a steroid shot in my wrist area. The pain went away a little and then it came back after my second dose. It started to go away and I got my 3rd shot and it came back with a vengeance. I am still dealing with this at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: X-ray
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Omeprazole
Allergien: Macrobid
Vorherige Impfungen: -

VAERS 2233813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AZ
Alter: 51,0
Geschlecht: M
Eingang: 14.04.2022
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Headache Night sweats Pyrexia Sleep disorder Somnolence

Symptomtext

-Extreme fatigue began about 4 hours after booster shot. -Feverish with sweating during sleeping. -Fatigue/sleepiness would occur mid-day for the next 3 days. -Persistent headache occurred during sleeping. Headache was severe and would wake me up usually in the early morning. Headache began near base of skull on left side and arc over left side to left upper forehead. Headache would persist unless I took shallow breaths and sat up slowly. Headache would subside after about 30 minutes. This headache occurred consistently for 3 months, About mid-January 2022 headache no longer occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: No testing performed.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Bronchitis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2233721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MN
Alter: 66,0
Geschlecht: F
Eingang: 14.04.2022
Impfdatum: 22.10.2021
Beginn: 12.04.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Pyrexia

Symptomtext

Fever

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple myeloma undergoing chemo priming
Andere Medikamente: acyclovir (ZOVIRAX) 800 MG tablet, allopurinol (ZYLOPRIM) 300 MG tablet, amLODIPine (NORVASC) 5 MG tablet, blood glucose test (GLUCOSE BLOOD) strips, cefpodoxime (VANTIN) 200 MG tablet, diclofenac sodium (VOLTAREN) 1 % Gel, enoxaparin ANTIC
Allergien: Pencillin
Vorherige Impfungen: -

VAERS 2225980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: FL
Alter: 51,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 02.11.2021
Beginn: 19.01.2022
Tage bis Beginn: 78,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Nasopharyngitis Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I just started having regular cold symptoms and I didn't think I had COVID but my wife insisted and I went and got tested so she would stop nagging me and I had a sore throat, cough, and runny nose. I didn't have any other symptoms and I went and got tested and I was positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID Test Positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Polyhymnia; Hypertension
Andere Medikamente: Losartan 50 mg
Allergien: None
Vorherige Impfungen: -

VAERS 2204076

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 320308D

mild

Staat: MO
Alter: 35,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 12.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Allergy test positive Angioedema Chronic spontaneous urticaria

Symptomtext

Chronic spontaneous idiopathic urticaria (Hives) covering my entire body, angioedema in lips and fingers, has been continuous since start date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chronic spontaneous urticaria
Hospital-Tage: -
Labordaten: Allergy tests showed some sort of antagonizer but nothing else.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lutera, Famotidine, Citalopram
Allergien: Sulpha, Phenolbarbitol
Vorherige Impfungen: -

VAERS 2179114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CT
Alter: 40,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 28.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Lymphadenopathy Pain in extremity

Symptomtext

Swollen lymph nodes under left arm; Painful and noticeably swollen compared to area under right arm; This is a spontaneous report from a contactable consumer. This 40-year-old female consumer (patient) reported for herself that: Serious: (NO) Seriousness criteria-Results in death: (NO) Seriousness criteria-Life threatening: (NO) Seriousness criteria-Caused/prolonged hospitalization: (NO) Seriousness criteria-Disabling/Incapacitating: (NO) Seriousness criteria-Congenital anomaly/birth defect: (NO) Race ethnicity information available. patient occupation: None of the above Start Date/Time: [Pfizer] 28Oct2021 12:30 PM Location of injection for vaccine received same date: Flu Shot (Afluria Quad PF) - Right Arm Dose received: 3 most_recent_dose_details: Product=COVID 19, brand=Pfizer, Brand unknown=False, lot number=320308D, lot unknown=False, Administration date=28Oct2021, Administration time=12:30 PM, dose_number=3, vaccine location=Left arm Previous dose details: Prev dose product=COVID 19, prev dose brand=Pfizer, prev dose brand unknown=False, prev dose lot number=EW0167, prev dose lot unknown=False, prev dose administration_date=29Apr2021, prev dose dose number=2, prev dose vaccine location=Left arm}, {prev dose product=COVID 19, prev dose brand=Pfizer, prev dose brand unknown=False, prev dose lot number=ER8732, prev dose lot unknown=False, prev dose administration date=01Apr2021, prev dose dose number=1, prev dose vaccine location=Left arm Other vaccine same date details: Other vaccine same date product= Flu Shot (Afluria Quad PF), other vaccine same date vaccine date=28Oct2021, other vaccine same date dose number=1, other vaccine same date vaccine location=Right Arm facility type vaccine: Pharmacy or Drug Store facility name and address: Withheld other medications in two weeks: D-Amphetamine, Escitalopram, Tri-Sprintec, Vit D adverse event: Swollen lymph nodes under left arm. Painful and noticeably swollen compared to area under right arm. adverse event start date: 30Oct2021 adverse event country: US AE resulted in: None of the above if patient recovered: Recovered if treatment ae: No Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store Did the patient receive any other vaccines within 4 weeks prior to the COVID vaccine: No Prior to vaccination, was the patient diagnosed with COVID-19?:No Since the vaccination, has the patient been tested for COVID-19?:No Device Date : 02Nov2021 known allergies: no other medical history: no No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: DEXTROAMPHETAMINE [DEXAMFETAMINE]; ESCITALOPRAM; VIT D [COLECALCIFEROL]; TRI-SPRINTEC
Allergien: -
Vorherige Impfungen: -

VAERS 2176563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NJ
Alter: 29,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 29.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Biopsy COVID-19 Macule Rash

Symptomtext

spreading rash on both arms and both legs; tiny red dot with a darkish middle; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old male patient received bnt162b2 (BNT162B2), administration date 08Mar2021 20:00 (Lot number: ER8733) as dose 1, single and administration date 29Mar2021 18:00 (Lot number: 320308D) as dose 2, single for covid-19 immunisation. Relevant medical history included: "covid" (unspecified if ongoing), notes: If covid prior vaccination: Yes. There were no concomitant medications. The following information was reported: RASH (non-serious) with onset 30Mar2021 18:00, outcome "unknown", described as "spreading rash on both arms and both legs"; MACULE (non-serious) with onset 30Mar2021 18:00, outcome "unknown", described as "tiny red dot with a darkish middle". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash, macule. Additional information: Age at vaccination: 29 Years. Patient received 3rd dose of pfizer covid-19 vaccine on 01Nov2021, 10:00 AM, Lot number=EN6205, Vaccine location=Left arm for covid-19 immunisation. Adverse event: I have developed a spreading rash on both arms and both legs. They are tiny red dots with a darkish middle. They continue to spread across my body. If treatment ae: Antibiotic, Antiviral, Biopsy, Antiseptic, etc. patient was not covid tested post vaccination. Facility where the most recent COVID-19 vaccine was administered: Pharmacy or Drug Store. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Other medications in two weeks: None. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Biopsy; Result Unstructured Data: Test Result:unknown; Test Name: Covid-19; Result Unstructured Data: Test Result:Prior to vaccination, was the patient diagnosed wi; Comments: Prior to vaccination, was the patient diagnosed with COVID-19?:Yes
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: UT
Alter: 63,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Decreased appetite Diarrhoea Fatigue Lymphadenopathy Myalgia Nausea SARS-CoV-2 test

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 63-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 22Oct2021 11:00 (Lot number: 320308D) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "asthma" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "sulfonamide allergy" (unspecified if ongoing), notes: known allergies: sulfa. Concomitant medication(s) included: FLU taken for immunisation, administration date 12Oct2021. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EL0140, Location of injection: Arm Right, Vaccine Administration Time: 11:00 AM, Route of Administration: Intramuscular), administration date: 08Jan2021, when the patient was 63 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3248, Location of injection: Arm Right, Vaccine Administration Time: 11:00 AM, Route of Administration: Intramuscular), administration date: 26Jan2021, when the patient was 63 years old, for Covid-19 Immunization, reaction(s): "I didn't feel well with nonspecific symptoms", "Got a very unusual headache". The following information was reported: DIARRHOEA (non-serious) with onset 23Oct2021, outcome "recovering", described as "explosive watery diarrhoea x 2"; MYALGIA (non-serious) with onset 23Oct2021, outcome "recovering", described as "muscle aches"; CHILLS (non-serious) with onset 23Oct2021, outcome "recovering", described as "chills"; NAUSEA (non-serious) with onset 23Oct2021, outcome "recovering", described as "nausea"; FATIGUE (non-serious) with onset 23Oct2021, outcome "recovering", described as "fatigue"; LYMPHADENOPATHY (non-serious) with onset 23Oct2021, outcome "recovering", described as "I have bilateral, right > left axillary lymphadenopathy"; DECREASED APPETITE (non-serious) with onset 23Oct2021, outcome "recovering", described as "loss of appetite". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of diarrhoea, myalgia, chills, nausea, fatigue, lymphadenopathy, decreased appetite. Additional information: Patient was not pregnant at the time of Vaccination. Patient received FLU vaccine in right arm (other vaccine in four weeks). Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. In early Sep. patient was exposed to PCR proven COVID through someone who lived in their home. Patient subsequently developed a bad sinus infection but had a negative COVID test, nasal PCR. They went away for 4 days to an isolated place, so no more testing was done, but there was good chance they both had a mild case of breakthrough COVID. I did not feel well with nonspecific symptoms and got a very unusual headache for 2 days. Sinus infection was treated with 2 courses of antibiotics (As reported). Seriousness reported as no. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 202109; Test Name: COVID-19; Test Result: Negative; Comments: nasal PCR.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Hypertension; Sulfonamide allergy (known allergies: sulfa).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: FL
Alter: 31,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 19.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Loss of personal independence in daily activities Vision blurred

Symptomtext

My eyes started to feel blurry after injection date/ reduced ability to see or read documents; Tiredness; unwanting to work; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 19Oct2021 19:00 (Lot number: 320308D) at the age of 31 years as dose 1, single and intramuscular, administered in arm left, administration date 09Nov2021 (Lot number: FH8028) as dose 2, single for covid-19 immunization. Relevant medical history included: "Schizophrenia diagnosed by doctor; but not confirmed or accepted by patient" (unspecified if ongoing), notes: Schizophrenia diagnosed by doctor; but not confirmed or accepted by, patient. There were no concomitant medications.The following information was reported: VISION BLURRED (non-serious) with onset 20Oct2021, outcome "recovered", described as "My eyes started to feel blurry after injection date/ reduced ability to see or read documents"; FATIGUE (non-serious) with onset 2021, outcome "recovered", described as "Tiredness"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 2021, outcome "recovered" (2021), described as "unwanting to work". Therapeutic measures were not taken as a result of vision blurred. Additional information: Patient did not take other vaccine in four weeks or other medications in two weeks.The patient did not test positive for COVID prior vaccination and post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Schizophrenia (Schizophrenia diagnosed by doctor; but not confirmed or accepted by patient)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2157756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AL
Alter: 35,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 19.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 43,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ageusia Anosmia Asthenia COVID-19 Fatigue Feeling abnormal Gastrointestinal disorder Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

About six weeks after my third dose a family member tested positive and about two days afterward I lost my sense of smell over night and the other symptoms came right after. I had sounded a little congestion the day before. The other symptoms were body aches and I lost my sense of taste. I had some GI problems. I was extremely tired for a week. My sense of taste returned after two days. I got an antibody infusion on the fifth day and the next day my sense of smell returned. I had more energy after the infusion as well. About three days after the infusion I felt almost normal. My totally recovered after about seven days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Dose 1:02/10/2021-EM9809. Dose 2:03/03/2021-EN6205. COVID-19 Positive: 01/01/2022-Rapid test.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2122598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: FL
Alter: 42,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 23.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity Pyrexia Tenderness

Symptomtext

low grade fever; soreness in my left arm; On 10/25 and 10/26 I experience tenderness under my left armpit.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 23Oct2021 16:00 (Lot number: 320308D) at the age of 42 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU, administration date 09Oct2021; LEXAPRO. Past drug history included: No. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6205, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM), administration date: 15Apr2021, when the patient was 41 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL9267, Location of injection: Arm Left, Vaccine Administration Time: 01:00 PM), administration date: 25Mar2021, when the patient was 41 years old, for COVID-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset 25Oct2021, outcome "not recovered", described as "low grade fever"; PAIN IN EXTREMITY (non-serious) with onset 25Oct2021, outcome "not recovered", described as "soreness in my left arm"; TENDERNESS (non-serious) with onset 25Oct2021, outcome "not recovered", described as "On 10/25 and 10/26 I experience tenderness under my left armpit.". Therapeutic measures were not taken as a result of pyrexia, pain in extremity, tenderness.Prior to vaccination, the patient was not diagnosed with covid-19 and since the vaccination, patient was not diagnosed with covid-19. No follow-up attempts are possible. No further information is expected. Device Date : 26Oct2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: LEXAPRO
Allergien: -
Vorherige Impfungen: -

VAERS 2118757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MA
Alter: 53,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Axillary pain Body temperature Fatigue Pain Pyrexia Vaccination site pain

Symptomtext

Within 6 hrs pain at injection site and in armpit (lymph nodes); Within 6 hrs pain at injection site and in armpit (lymph nodes); fatigue; general body aches; fever which peaked at 101.4F; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 22Oct2021 13:30 (Lot number: 320308D) at the age of 53 years as dose 3(booster) , single for covid-19 immunisation. Relevant medical history included: "A fib" (unspecified if ongoing); "prediabetic" (unspecified if ongoing). Concomitant medication(s) included: FLU VACCINE VII, start date: 22Sep2021, stop date: 22Sep2021; FAMOTIDINE; ATORVASTATIN; METFORMIN; ASPIRIN [ACETYLSALICYLIC ACID]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 01:45 PM), administration date: 15Mar2021, when the patient was 53 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EL3247, Location of injection: Arm Left, Vaccine Administration Time: 02:45 PM), administration date: 22Feb2021, when the patient was 53 years old, for COVID-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious), AXILLARY PAIN (non-serious) all with onset 22Oct2021 23:00, outcome "recovered" (Oct2021) and all described as "Within 6 hrs pain at injection site and in armpit (lymph nodes)"; FATIGUE (non-serious) with onset 22Oct2021 23:00, outcome "recovered" (Oct2021), described as "fatigue"; PAIN (non-serious) with onset 22Oct2021 23:00, outcome "recovered" (Oct2021), described as "general body aches"; PYREXIA (non-serious) with onset 22Oct2021 23:00, outcome "recovered" (Oct2021), described as "fever which peaked at 101.4F". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of vaccination site pain, axillary pain, fatigue, pain, pyrexia. Additional information: Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination the patient has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Test Date: 20211022; Test Name: fever; Result Unstructured Data: Test Result:101.4 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation; Pre-diabetic
Andere Medikamente: FLU VACCINE VII; FAMOTIDINE; ATORVASTATIN; METFORMIN; ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2113082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: VA
Alter: 48,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 26.11.2021
Beginn: 10.01.2022
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Asthenia Diarrhoea Dissociation Fatigue Feeling abnormal Headache Pyrexia SARS-CoV-2 test negative Vomiting

Symptomtext

Lot number is either 320308D or 3203080 I had vomiting, Diahrrea for 5 hrs. on January 10, 2022 Also weakness, headache, disconnected 101 fever for several days. I took 2 home tests that were negative. I had a telehealth visit with Dr. office and I was told I had a presumptive positive based off my symptoms and it was treated as such. I was prescribed Tessalon Perles and Zofran. I did recover from Covid but still have fatigue. I do not feel 100% My joint pain has been worse than normal. Things have been harder to do.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 2 home tests did come back negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: 1. Tetanus vaccine 2. Penicillin 3. Moxifloxacin and all Quinolones medication 4. Neosporin 5. Onion 6. Latex Sensitivity 7. Gluten
Vorherige Impfungen: Tetanus booster shot. 2017 I got mild hives and Doctor recovered.

VAERS 2201221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 12.11.2021
Beginn: 27.12.2021
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Myalgia Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/04, Pfizer, dose #1 02/22, Pfizer, dose #2 11/12, Pfizer, dose 3 12/27 COVID swab, result: detected 12/27 pt cc: cough, fatigue myalgias, sore throat, exposure, family

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 12/27 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2101839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OR
Alter: 66,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 24.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Tinnitus

Symptomtext

Headache and Tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Working with ENT for other allergy ear related problems, which may also be related to the Tinnitus.
Aktuelle Erkrankungen: None
Vorgeschichte: Allergies to animals, grass and trees.
Andere Medikamente: Thyrox
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2093583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 28.01.2022
Beginn: 29.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Burning sensation Rash Rash erythematous Rash macular Rash pruritic Skin tightness

Symptomtext

Full body rash; started off spotty the day after my vaccination. When I woke up the following morning, it was a full body rash that appeared like a sunburn. It was itchy, tight, and burning. I was seen at the Urgent Care Sunday 1/29/2022 and was prescribed methylprednisolone for 6 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: No tests were done.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Tylenol, imitrex PRN
Allergien: NKDA
Vorherige Impfungen: I had a similiar reaction to the Moderna COVID vaccine (the 2nd in my series) on 02/04/2021 lot # 037K20A. Similar burning rash

VAERS 2203713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 05.02.2022
Impfdatum: 10.11.2021
Beginn: 25.12.2021
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cough Diarrhoea Headache Inappropriate schedule of product administration Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 03/31, Pfizer, dose #1 04/21, Pfizer, dose #2 11/10, Pfizer, dose #3 12/27 COVID swab, result: detected 12/25 pt cc: cough, diarrhea, headache, rhinorrhea, sore throat exposure: unknown 12/30 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2202378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 10.11.2021
Beginn: 25.12.2021
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cough Diarrhoea Headache Inappropriate schedule of product administration Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 03/31, Pfizer, dose #1 04/21, Pfizer, dose #2 11/10, Pfizer #3 12/27 COVID swab, result: detected 12/25 pt cc: cough, diarrhea, headache, rhinorrhea, sore throat exposure: unknown 12/30 clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 07.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Arthritis reactive

Symptomtext

4 days after Booster Pfizer, left hip pain started. No injury prior. Then knee pain and ankle pain. Diagnosed as reactive arthritis to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: pending
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2076044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 08.10.2021
Beginn: 27.12.2021
Tage bis Beginn: 80,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abdominal pain COVID-19 SARS-CoV-2 test positive Urinary retention

Symptomtext

12/27/21 presents to EC ED for "urinary retention and abdominal pain". PMHx of "recent PID DX (currently on day 8 of 10 of doxy/flagyl), POD4 from abortion c/b retained products requiring a D&C".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 12/28/21 SARS-CoV-2 (COVID-19) by NAA detected.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2074363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 25.10.2021
Beginn: 01.10.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthritis Asthma Eating disorder Interchange of vaccine products Pain Pain in extremity Weight Weight decreased

Symptomtext

She lost weight; She eats a lot more; Right leg causing a lot of problems and hurting/ Sometimes she gets pain to her thigh and it goes down to right leg.; They got the J&J and then got the Pfizer booster; Upset her asthma; Arthritis in hands got worse; She has had a lot of pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 25Oct2021 (Lot number: 320308D) at the age of 70 years as dose 2 (booster), single for covid-19 immunisation. Relevant medical history included: "compound fracture" (unspecified if ongoing), notes: She had a compound fracture 9 years ago and had a titanium rod and screws in that leg; "has a lot of arthritis in her hands" (unspecified if ongoing); "She gained a lot of weight ahead of time" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: J&j covid-19 vaccine (dose 1, Lot: 1805020, expiration is unknown, Anatomical location: right arm.), administration date: 09Mar2021, when the patient was 70 years old, for COVID-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 25Oct2021, outcome "unknown", described as "They got the J&J and then got the Pfizer booster"; ASTHMA (non-serious) with onset 25Oct2021, outcome "not recovered", described as "Upset her asthma"; ARTHRITIS (non-serious) with onset Oct2021, outcome "not recovered", described as "Arthritis in hands got worse"; PAIN (non-serious) with onset Oct2021, outcome "not recovered", described as "She has had a lot of pain"; WEIGHT DECREASED (non-serious), outcome "not recovered", described as "She lost weight"; EATING DISORDER (non-serious), outcome "unknown", described as "She eats a lot more"; PAIN IN EXTREMITY (non-serious) with onset 25Oct2021, outcome "not recovered", described as "Right leg causing a lot of problems and hurting/ Sometimes she gets pain to her thigh and it goes down to right leg.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain, pain in extremity. Additional Information: Received call from consumer regarding the Pfizer COVID Booster shot. She got it and she looked it up and read article. It has been causing her a lot of problems. Her legs were hurting. She had a compound fracture 9 years ago and had a titanium rod and screws in that leg. She also has a lot of arthritis in her hands. She read an article about Pfizer giving compensation and she was seeking compensation for her issues. She would like to know how to receive compensation. She said her weight fluctuates and was between 97-100. She gained a lot of weight ahead of time. They got the J&J and then got the Pfizer booster. Her mother also got it and had no issues. She lost weight after the Pfizer booster dose. She eats a lot more than anybody in the world dose and she cannot gain any weight back. She was up to 104. She did not provide her height. She has had a lot of pain and has been living on Tylenol, she wants to be compensated for serious issues she was having. Her leg was giving her a fit. It upset her Asthma. It caused a lot of health issues for her. Sometimes she gets pain to her thigh and it goes down to right leg. She was just saying there was nothing she can do about it and it was in her system. She has a doctor's appointment at 3pm and did not have time to answer additional questions. No further details provided. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Name: weight; Result Unstructured Data: Test Result:97-100; Comments: weight fluctuates and is between 97-100
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Compound fracture (She had a compound fracture 9 years ago and had a titanium rod and screws in that leg); Hand arthritis; Weight gain
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2072021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: GA
Alter: 50,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 26.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Biopsy Breast cancer female Inflammation Lymphadenopathy Mammogram Pain in extremity Ultrasound scan

Symptomtext

My side effects were pain under my left arm where I had gotten inflammation. The pain comes and goes. I had a mammogram on 10/26/2021, and then the doctor called me and told me that one of lymph nodes was swollen. Then I had a biopsy on December 9, 2021. I was diagnosed with breast cancer. I still have pain in my arm, but it doesn't last all day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Mammogram (10/26/2021) Ultrasound- lymph nodes were inflamed (11/2/2021)
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Aurovela 24 Fe Syntac Zolpidem
Allergien: Diclofenac
Vorherige Impfungen: -

VAERS 2071930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 21.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache

Symptomtext

started having continuous headaches about a week after the vaccine, I take Tylenol and that relieves them for a little bit and there right back again. I Have a headache everyday all day long unless I take Tylenol, and again it only last about 3-4 hours and the headache is back again, I have never suffered from headaches until I took this booster shot....

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: high blood pressure thyroid disease depression gerd nerve pain psoriasis
Andere Medikamente: abilify, Pristiq, Trazodone, Estradiol patch, Levothyroxine, omeprazole, vit D3, Biotin, Losarton, Hydralazine, Lyrica Humira injection, topamax, adipex , zinc, vit c,
Allergien: celebrex
Vorherige Impfungen: -

VAERS 2065902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: WA
Alter: 48,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 23.10.2021
Beginn: 14.01.2022
Tage bis Beginn: 83,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Adverse event Herpes zoster Hypoaesthesia Rash

Symptomtext

I started noticing the numbness on a Friday, 01/14/2022. The bumps appeared on Monday, 01/17/2022. On 01/18/2022- I chatted with Dr. over an app. She said it sounded like I had shingles. She prescribed, Valacyclovir. I picked it up on 01/18/2022, I took 3 pills a day, for 7 days, and the last dose was 01/25/2022. My 1st time having shingles. I never had it before. No, I have not recovered from the AE, it is not completely cleared up yet, but it's getting better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: asthma hole in the heart between the upper 2 chambers I take an anti-depressant
Andere Medikamente: sertraline generic for Zoloft famodoline generic for Pepcid Montelukast generic for Singulair Zyrtec low dose aspirin glucosamine with msn fish oil magnesium L-theanine vitamin B-5 ashwagan dha vitamin D
Allergien: I don't do well with halothane
Vorherige Impfungen: -

VAERS 2065681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Pain Product preparation error

Symptomtext

Patient was given undiluted Pfizer vaccine - .3 ml in am on 1/18/2022. Patient experienced aching and chills that evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2062921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CT
Alter: 97,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 03.11.2021
Beginn: 24.01.2022
Tage bis Beginn: 82,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain upper Fatigue Headache Oropharyngeal pain SARS-CoV-2 test

Symptomtext

Headache, Stomach pain, fatigue, sore throat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: Rapid Test 01/24/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Bradycardia, Muscle Weakness, Athersclerotic Heart Disease of Native Coronary Artery, Hyperlipidemia, Essential Hypertension, Hypothyroidism, Orthostatic, Hypotension
Andere Medikamente: Acetaminophen, Asprin, Atorvastatin Calcium, Carboxymethylcellulose Sodium, Cyanocobalamin, Ergocalciferol, Furosemide, Levothyroxine Sodium, Metoprolol Sucinate ER, Multivitamin Adult, prednisone, Sulfamethoxazole-Trimethoprim, Tamsulosin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2039593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NY
Alter: 80,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 04.11.2021
Beginn: 12.01.2022
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Fall Pain in extremity

Symptomtext

CHIEF COMPLAINT: Pt. arrives via EMS from home c/o pain to the left femur after falling at home. Pt. denies hitting his head, as well no blood thinners. HISTORY OF PRESENT ILLNESS: Presents with: _lef fum pain Duration: _ Onset: _ Course: _ Location Pain Onset: _ Location Pain at Present: _ Pain Radiation: _ Pain Quality: _

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: CKD, Hypertension
Andere Medikamente: Unknown
Allergien: N/A
Vorherige Impfungen: -

VAERS 2039555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 25.10.2021
Beginn: 25.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal discomfort Angiogram Cardiac stress test Echocardiogram Electrocardiogram Flushing Headache Heart rate increased Pain in extremity

Symptomtext

She got her vaccine, her arm was sore, had a really bad headache, a little bit sick to her stomach and her heart was beating rapidly and she was flushed. Has a history of AFib. She has medicine that she takes for her A-fib and took that, and continued to take a 3rd dose which resolved it. All of the time that she has been on that medicine as needed she has only had to take it in that way once in 15 years. This has happened a couple of times since taking the booster shot, but does resolve with medication. These have been lasting longer in duration since the vaccine. She has been to her cardiologist and had testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: She had EKG, echocardiogram, Cardiolyte nuclear stress test which showed something and had a PET nuclear dye stress test, which they again saw something. She had angiogram on 1/13/22, and the results showed no blockage. She was diagnosed with some inflammation.
Aktuelle Erkrankungen: None.
Vorgeschichte: A-fib, thyroid disease, high blood pressure.
Andere Medikamente: Multivitamin, vitamin D, calcium, Levothyroxine, Hydrochlorothiazide, Benzopril, Eliquis, Atenolol, Amlodipine, Propanefenone.
Allergien: Bentyl, Epinephrine. Latex.
Vorherige Impfungen: -

VAERS 2038282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: NC
Alter: 26,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Breast pain Breast tenderness Headache Muscle spasms Neck pain Pain Vaginal haemorrhage

Symptomtext

Full body left side pain from 5:30pm 1/11/2022-current as of 1/16/22. Sore tender breast as of 1/12/2022- current as of 1/16/2022. Spotting/ light bleeding and cramping since 1/12/2022 (unrelated to period, not pregnant) Headache and neck pain since 1/11/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: None done
Aktuelle Erkrankungen: None
Vorgeschichte: Lower back pain
Andere Medikamente: zoloft 100mg and bupropion 300mg
Allergien: Amoxicillin, penicillin, Hydroxizine
Vorherige Impfungen: First and 2nd covid vaccine. Left arm pain for 2 months after vaccines in April 2021

VAERS 2038250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: IL
Alter: 47,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Headache Oropharyngeal pain Pyrexia Trismus

Symptomtext

I had lock jaw for 24 hours following my 1st dose in addition to fever, sore throat and headache, as well as tightening of the chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2036614

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 20.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ageusia Anosmia Chills Feeling abnormal Pain Pyrexia

Symptomtext

Severe aches and pins, shivering, low grade fever starting within 24 hours. i nearly went to urgent care it was so bad, much worse than the first two shots. then after i felt better several days later, i found that i could not smell or taste anything. this lasted for 6 or 7 weeks. now my ability to smell/taste is intermittent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, obesity, sleep apnea
Andere Medikamente: estradiol, spironolactone, bupropion, omeprazole, singulair, finasteride, progesterone
Allergien: mild food allergies (apples, bananas)
Vorherige Impfungen: -

VAERS 2028704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AL
Alter: 44,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Pruritus Swollen tongue

Symptomtext

Patient arrived to the Immunizations clinic to receive his Covid Booster. Patients information was verified and he was asked if he has any food or drug allergies and if he has ever had an adverse event to any previous vaccinations. The patient stated no to all questions. Patient then received his Covid Booster and was advised to wait 15min post inoculation. Failure to comply, the patient called an hour after vaccination and stated that he is experiencing an itchy face and swollen tongue shortly after arriving home. Pt was referred to contact the Nurse Advice Line to get an off-base ER/Urgent Care referral. Pt understood and had no further questions or concerns.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Cetirizine -10mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1843408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: WI
Alter: 8,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Product administered at inappropriate site Product administered to patient of inappropriate age Incorrect dose administered Incorrect route of product administration No adverse event

Symptomtext

Fatigue; Daughter received the adult dose of the Pfizer COVID vaccine instead of the pediatric dose; Patient received BNT162B2 in the right thigh; This is a spontaneous report received from a contactable reporter (Pharmacist) from medical information team. The reporter is the parent. An 8-year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in thigh right, administration date 04Nov2021 11:00 (Batch/Lot number: unknown) at the age of 8 years as dose 1, 30 ug single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious) with onset 04Nov2021, outcome "unknown", described as "Daughter received the adult dose of the Pfizer COVID vaccine instead of the pediatric dose"; PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 04Nov2021, outcome "unknown", described as "Patient received BNT162B2 in the right thigh"; FATIGUE (non-serious) with onset 05Nov2021, outcome "recovered", described as "Fatigue". Therapeutic measures were not taken as a result of product administered to patient of inappropriate age, product administered at inappropriate site, fatigue. Additional information: The patient's mother stated her 8-year-old daughter received the adult dose of the Pfizer COVID vaccine instead of the pediatric dose. A pharmacy student administered a 30-mcg adult COVID-19 vaccine dose to the patient instead of the 10-mcg dose by accident. The patient's mother asked what side effects she should look out for and if her daughter should receive a second dose. Regarding the seriousness, it was reported as unknown, the patient's mother monitored her for the first hour and there was nothing unusual with her, but the patient's mother did not know what to expect. When querying dose, the patient's mother stated she thought her daughter received 0.3ml since that dose was intended for the patient's mother's booster dose, but instead it was given to her daughter. There were no additional vaccines administered on the same date of the Pfizer suspect. The adverse events did not require a visit to the emergency room or a physician office. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. There were no adverse events following prior vaccinations. There was no family medical history relevant. There were no relevant tests taken (specific relevant test for thromboembolic events with thrombocytopenia: none). The patient's mother consider that the Pfizer product had a casual effect to the adverse event. The patient received the second dose (Lot number: FK5127) on 26Nov2021 at 11:00 in the right deltoid intramuscularly. There were no side effects after the second dose. The lot number for bnt162b2 was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: NONE
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: WI
Alter: 31,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 10.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chest X-ray abnormal Lung opacity Pneumonitis Pulmonary pain

Symptomtext

Lung pain and inflammation. X-ray revealed "Hazy groundglass opacity at the left lung base projecting over the left anterior sixth rib"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary pain
Hospital-Tage: -
Labordaten: Lat Chest Radiograph 10/18/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma diagnosed in childhood. No incidents or symptoms in over a decade
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2018186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AL
Alter: 33,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 22.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Head discomfort Heart rate Heart rate increased

Symptomtext

slight pressure in the front of my head; lightheaded spells; fast heart beat; 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 33 year-old male patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 22Oct2021 15:00 (Lot number: 320308D) at the age of 33 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "High blood pressure" (unspecified if ongoing), notes: Verbatim: High blood pressure. The patient took concomitant medications. The following information was reported: HEAD DISCOMFORT (non-serious), outcome "unknown", described as "slight pressure in the front of my head"; DIZZINESS (non-serious), outcome "unknown", described as "lightheaded spells"; HEART RATE INCREASED (non-serious), outcome "unknown", described as "fast heart beat". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of head discomfort, dizziness, heart rate increased. Additional information The patient had been having since the first shot just over 2 weeks ago slight pressure in the front of head and lightheaded spells. He did experience a fast heart beat when had the lightheaded spells. No treatment and this has been going on since that shot its been constant for 2 weeks. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Name: heart beat; Result Unstructured Data: Test Result:fast
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Verbatim: High blood pressure)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2010102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MN
Alter: 58,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 24.11.2021
Beginn: 18.12.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Dry mouth Ear pain Fatigue Oropharyngeal pain Pain in jaw Pyrexia Rash erythematous SARS-CoV-2 test Sinus congestion

Symptomtext

I has a sore throat, and I had a lot of sinus congestion. My Chest felt tight, and I had to use my Inhaler 3 times a day. I was fatigued. My jaw and my ear hurt. At night, I had severe dry mouth and I developed a rash on my forehead and Chin. I had a fever of 100 degrees for about 9 or 10 days. I went to see my doctor on 12/27/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: Covid Test Exam
Aktuelle Erkrankungen: NONE
Vorgeschichte: Asthma, Chronic pain, Type 2 Diabetes
Andere Medikamente: Crestor; Zoloft; Vistaril; Losartan; Advil; Cough Syrup with Codeine, Xopenex, Ozempic, Insulin
Allergien: Penicillin, Sulfa, Aspirin, Benadryl, Latex, Peanuts
Vorherige Impfungen: -

VAERS 2000427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: UT
Alter: 48,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 25.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Blood test normal Immobile Inflammation Laboratory test normal Magnetic resonance imaging normal Ultrasound scan normal Weight bearing difficulty X-ray normal

Symptomtext

Pain in ankle, difficulty putting weight on foot, inflammation in ankle and foot, became immobile. Went to medical facility and they inspected the foot and took X-rays. They recommended we go to ER for additional assessments. Went to ER, they took additional X-rays, took a blood panel, and drew fluid from the inflammation spot. All tests came back negative, we were released and given a specialist referral. I went to the specialist a few days later they took additional X-rays and recommended an ultrasound and MRI. The ultrasound came back negative, and MRI didn't show cause. 12/21 we saw Dr. and we are still working on finding a cause. As of todays date 1/3/22 cause is unknown inflammation has gone down and I can walk on it but it flares up and is still painful at times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 10/31/21 - X-rays 10/31/21 - X-rays, blood panel, fluid tap 11/3/21 - X-rays 11/6/21 - Ultrasound 11/12/21 - MRI
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1998883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OK
Alter: 58,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Lethargy Lymphadenopathy Pain Pyrexia

Symptomtext

Lethargic, body aches, low-grade fever and extreme lymph node swelling in left armpit approximately 3". Lymph node swelling took about two weeks to go away. Other symptoms subsided after four days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1992504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: GA
Alter: 42,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 17.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Abdominal discomfort Abdominal pain Abdominal pain lower Appendicitis perforated Bladder pain Computerised tomogram abdomen abnormal Constipation Drain placement Drainage Laboratory test abnormal Nausea Pelvic pain Surgery Vomiting White blood cell count increased

Symptomtext

Started with upset stomach and constipation on Monday. Tuesday had pain on either side of bellybutton and nausea and continued constipation. Wednesday pain at bladder area, upset stomach, nausea, vomiting, leading to excruciating pain in afternoon then relief. About 1:30 am excruciating pain in right lower quadrant/pelvis and bladder area leading me to ER. CT showed ruptured appendix and they decided on emergency surgery at 7:30am. Left a drain and kept me in the hospital with antibiotics and IV pain meds because the drain was cloudy and had pus and my pain was not controlled. Was finally discharged Saturday with the drain. Continued antibiotics at home and had drain removed the following Wednesday. Still recovering from the surgery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 3,0
Labordaten: CT in ER 12/16 showing ruptured appendix. Lab work in ER showing elevated WBCs 12/16, 12/17,12/18.
Aktuelle Erkrankungen: Gallbladder disease
Vorgeschichte: hypertension, high cholesterol
Andere Medikamente: Lisinopril 40 mg, Simvastatin 40 mg, Omeprasole 20 mg
Allergien: Codeine, dilaudid, tessalon pearles
Vorherige Impfungen: -

VAERS 1992126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: VA
Alter: 41,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 08.11.2021
Beginn: 14.12.2021
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia COVID-19 Chills Cough Oropharyngeal pain Pain SARS-CoV-2 test positive Sinus congestion Sinus disorder

Symptomtext

On 12/14, I developed a sore throat, congested head which felt like a sinus infection, a dry cough, but it was only in my throat area. Body aches, chills and loss of taste and on 12/16 I tested positive to Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19-positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Vit D3, Valtrex, Wellbutrin, Vistaril, Prozac, Pepcid, Allertec
Allergien: Penicillin, Avocados
Vorherige Impfungen: Pfizer COVID-19

VAERS 1985257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IL
Alter: 68,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 04.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dental operation Urticaria

Symptomtext

This may or may not have been related to the vaccine. I broke out in hives. In addition to the booster, had a flu vaccine at a HCF on 11/18 and had multiple doses of no I and for a dental procedure on 11/18, and had Steroid injections in my knees through joint relief institute on Monday, 11-22-21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: No tests but went to the doctor for medication.
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, diverticulosis, irregular heart rhythm
Andere Medikamente: Irbesartan, simvastati, low dose aspirin, vit D,
Allergien: Cipro, Flagil, penicillin
Vorherige Impfungen: -

VAERS 1984743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AZ
Alter: 47,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 30.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Fatigue Hypoaesthesia Lethargy Pain in extremity Paranasal sinus discomfort Restlessness Rhinorrhoea Sinus congestion Sinus disorder

Symptomtext

The day after I received vaccine shot 2 on 3/30/21, I had terrible sinus issues. Pressure, congestion, runny nose, worse if I sat down or laid down. Tried allergy meds, sinus pressure meds, nasal sprays by Mucinex and Xlear. Issues worsened after Covid booster on 12/7/21. After the booster I have not felt myself. Lethargic for the past 3 weeks, tired, restless, on 12/22/21 I thought I was having the onset of a heart attack. Numbmess and pain in left arm, shoulder, hands. I got up from bed, walked around, sat up for a good hour, subsided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I have not been to a Dr. I do not have insurance and have just dealt with the symptoms at home with over the counter meds.
Aktuelle Erkrankungen: No illness. I have asthma and high blood pressure and take medication daily for both.
Vorgeschichte: Asthma, high blood pressure.
Andere Medikamente: Lisinopril, Advair, Ventolin, Amlodipin, Pravastatin, Montelukast, Gabapentin.
Allergien: None
Vorherige Impfungen: -

VAERS 1982061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: VA
Alter: 33,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 23.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Lymphadenopathy Neck pain Oropharyngeal pain

Symptomtext

Lymph node swelling on left side, pain on left side neck. Left sided headache, sore throat left sided

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Ginger tea, Goody's powder
Allergien: none
Vorherige Impfungen: PPD skin test

VAERS 1979236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IN
Alter: 67,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angina pectoris Arthralgia Blood test Chest X-ray Electrocardiogram

Symptomtext

Shoulder pain, Heart pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: EKG Chest x-ray Blood work
Aktuelle Erkrankungen: Cough
Vorgeschichte: Blood pressure , Cholesterol, Diabetes
Andere Medikamente: Lisinopril , Jardiance, Janumet , Simvistation , Sertraline
Allergien: None
Vorherige Impfungen: 66 2-11-2021 & 3-11-2021 Headaches Body aches Chills Moderna

VAERS 1978689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: FL
Alter: -
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Body temperature Electrocardiogram Fatigue Headache Immunisation Musculoskeletal stiffness Pain Pyrexia Vaccination site pain

Symptomtext

Booster; Pain and stiffness in injection arm; Felt feverish but temperature never rose above 98.4; stiffness in injection arm; body aches; fatigue; headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69 year-old male patient received bnt162b2 (BNT162B2) (Lot number: 320308D, Expiration Date: 15Nov2021) as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Ulcerative colitis", start date: 2005 (ongoing), notes: 4 colonoscopies; "Osteoporosis", start date: 2017 (ongoing), notes: Dexa scans lifeline screenings (Hospital name); "Heart block", start date: 2019 (ongoing), notes: One stay (Hospital name) no treatment tests done EKG ECHs etc. Concomitant medication(s) included: 6-MERCAPTOPURINE MONOHYDRATE taken for colitis ulcerative, start date: Nov2005 (ongoing); ALENDRONATE taken for osteoporosis, start date: 2017 (ongoing). Vaccination history included: Bnt162b2 (Dose 1 , Prior vaccinations: Covid-19 vaccine vial, Manufacturer: Pfizer, Anatomical Site of Injection: Left arm, No. of previous doses: 2, Date: 16Nov2021), for COVID-19 Immunization; Bnt162b2 (Dose 2, Prior vaccinations: Covid-19 vaccine vial, Manufacturer: Pfizer, Anatomical Site of Injection: Left arm, No. of previous doses: 2, Date: 16Nov2021), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious), outcome "unknown", described as "Booster"; VACCINATION SITE PAIN (non-serious), outcome "recovered", described as "Pain and stiffness in injection arm"; PYREXIA (non-serious), outcome "recovered", described as "Felt feverish but temperature never rose above 98.4"; MUSCULOSKELETAL STIFFNESS (non-serious), outcome "recovered", described as "stiffness in injection arm"; PAIN (non-serious), outcome "recovered", described as "body aches"; FATIGUE (non-serious), outcome "recovered", described as "fatigue"; HEADACHE (non-serious), outcome "recovered", described as "headache". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: He had no private car and take city buses 5-6 days week. Took third COVID-19 Vaccination. Felt feverish but temperature never rise above 98.4 was not disturbed during sleep this time. Pain and stiffness in injection arm body aches fatigue headache. All symptoms resolved in about 30 hours. Now ready for omicron booster. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: Feverish; Result Unstructured Data: Test Result:Never rise above 98.4; Test Date: 2019; Test Name: EKG Echocardiogram; Result Unstructured Data: Test Result:Heart block; Comments: Asymptomatic currently
Aktuelle Erkrankungen: Heart block (One stay (Hospital name) no treatment tests done EKG ECHs etc.); Osteoporosis (Dexa scans lifeline screenings (Hospital name)); Ulcerative colitis (4 colonoscopies)
Vorgeschichte: -
Andere Medikamente: 6-MERCAPTOPURINE MONOHYDRATE; ALENDRONATE
Allergien: -
Vorherige Impfungen: -

VAERS 1970828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308 D

mild

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea Immunisation

Symptomtext

Diarrhea for about 10 days; Booster; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 74 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 29Nov2021 09:45 (Lot number: 320308 D) at the age of 74 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ATORVASTATIN; OXYBUTYNIN; CALCIUM CITRATE. Past drug history included: Erythromycin, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Vaccine Administration Time: 08:30 AM, DOSE 2, SINGLE, Batch/Lot No: EN 6205, Location of injection: Arm Right), administration date: 15Mar2021, when the patient was 74 years old, for Covid-19 Immunization; Bnt162b2 (Vaccine Administration Time: 08:30 AM, DOSE 1, SINGLE, Batch/Lot No: EL 9266, Location of injection: Arm Left), administration date: 22Feb2021, when the patient was 73 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 29Nov2021 09:45, outcome "unknown", described as "Booster"; DIARRHOEA (non-serious) with onset 01Dec2021, outcome "not recovered", described as "Diarrhea for about 10 days". Therapeutic measures were taken as a result of diarrhoea. Additional information: No other vaccine was administered in four weeks. Patient's concomitant medication included multivitamin. The patient was treated with BRAT diet, Pedialyte, and occasionally with Immodium for Diarrhea. The patient did not have covid prior to vaccination. The patient was not tested covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ATORVASTATIN; OXYBUTYNIN; CALCIUM CITRATE
Allergien: -
Vorherige Impfungen: -

VAERS 1968017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: WV
Alter: 55,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Chills Cough Decreased appetite Disturbance in attention Headache Pain Vision blurred Vomiting

Symptomtext

12/18/2021 02:30 am Awoke from sleep and began vomiting. Over the course of the next 10 or so hours I vomiting at least 30 times. I developed a severe headache on 12/18/2021 around noon that lasted about 1.5 hours and was a 10 on the pain scale. Through out 12/18/2021 and 12/19/2021 I experienced abbreviated symptoms of Covid 19....chills, loss of appetite, body aches, cough and tightness in chest. On 12/20/2021 I found it very hard to focus on work and my vison was very blurry. This finally subsided by noon on 12/20/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1966863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: KS
Alter: 83,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Immunisation Influenza like illness Overdose Pain Pain in extremity Product preparation error Swelling

Symptomtext

sore arm; red swollen; red swollen; painfull; Flu-like symptoms; Dose: 3rd; the undiluted vial was administered to a patient with 0.3 mL; the undiluted vial was administered to a patient with 0.3 mL; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). An 83 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in deltoid left, administration date 28Oct2021 11:45 (Lot number: 320308D, Expiration Date: 28Feb2022) at the age of 83 years as dose 3 (booster), 0.3 ml single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for covid-19 immunization; Bnt162b2 (DOSE 2, SINGLE), for covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 28Oct2021 11:45, outcome "unknown", described as "Dose: 3rd"; OVERDOSE (non-serious), PRODUCT PREPARATION ERROR (non-serious) all with onset 28Oct2021, outcome "unknown" and all described as "the undiluted vial was administered to a patient with 0.3 mL"; PAIN IN EXTREMITY (non-serious) with onset 29Oct2021, outcome "unknown", described as "sore arm"; ERYTHEMA (non-serious), SWELLING (non-serious) all with onset 29Oct2021, outcome "unknown" and all described as "red swollen"; PAIN (non-serious) with onset 29Oct2021, outcome "unknown", described as "painfull"; INFLUENZA LIKE ILLNESS (non-serious) with onset 29Oct2021, outcome "unknown", described as "Flu-like symptoms". Additional information: Booster dose due to high risk of frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 complications). The patient had provided information regarding the reported adverse event(s) with the use of the product, the Pfizer product had a causal effect to the adverse event. NDC number of COVID-19 Vaccine: 59267100001. It was unknown that prior vaccinations within 4 weeks. It was unknown that there was specific relevant test for thromboembolic events with thrombocytopenia. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1962855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: PA
Alter: 40,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Lip swelling Pruritus Swelling face Urticaria

Symptomtext

BODY COVERED IN HIVES FROM BOTTOM OF FEET TO TOP OF HEAD LASTED ONE WEEK 2 ER VISIT MULTIPLE SHOTS OF EPPI STEROIDS BENEDRYL PEPCID AND 2 EPPI PENS TO HAVE AT HOME BECAUSE OF THE SWELLING TO FACE AND LIPS OUT OF CONTROL ITCHING LEAVING ME TO RUBBING THE SKIN OFF OF MY BODY UNTIL I GOT TO THE ER AND THEY GAVE ME IV MEDS AND SHOTS OF EPPI HIVES AND ITCHING DISAPPEARED AFTER A WEEK WITH HELP OF EPPI AND STEROIDS BENEDRYL AND PEPCID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1955683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OR
Alter: 61,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Computerised tomogram normal Headache Sleep disorder

Symptomtext

This was my second PFIZER vaccine, but I received the Johnson and Johnson vaccine first. On 11/3/2021 I had a thunderclap of a headache that would not go away. It seemed to get a little better with ALEVE. IT was waking me up at night for a few nights in a row. 11/7/2021 I went to the ER and had a CT scan done. It was normal. The doctors believed it was a vaccine response. They referred me to a neurologist. I talked to my internist who told me to take ALEVE around the clock. It felt better but did not go away. On 11/17/2021 I saw the neurologist and he suggested I add a muscle relaxant to my routine. The headache did not completely go away until end of November or early December.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: CT scan 11/7/2021 normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1952244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OR
Alter: 69,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea Eructation Nausea Rhinorrhoea Vomiting

Symptomtext

For the first 2 days she had the normal reaction. After that she stated she became stuff with a lot of mucus. She had a lot of burping way more than usual. She also had a bad case of diarrhea and nausea vomitting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: venlafaxine, atorvastatin,
Allergien: no
Vorherige Impfungen: -

VAERS 1944444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IL
Alter: 48,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Bacterial infection Injection site pain Injection site pruritus Injection site swelling Injection site warmth Sleep disorder

Symptomtext

Bacterial infection and swollen shoulder at the site of injection. It was itchy and extremely hot-to-touch! She could not sleep on the side and could not wear a long sleeve shirt to cover the arms because it hurt so much. She went to urgent care and got prescribed clindamycin 300mg 1 cap 3 times daily for 10 days. She followed-up with the urgent care center Friday 12/10/2021 after being on the antibiotic for 2 days since Tuesday 12/07/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1944420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MO
Alter: 57,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 02.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood test Erythema Pain in extremity Swelling

Symptomtext

Patient developed pain in right arm on 11/5/2021 with soreness that crossed over to left arm. Red big square noted and was raised and swollen. Referred to personal doctor or urgent care. Daycare sent her to Urgent care facility. She was evaluated and placed on Septra 800/160mg one tablet every 12 hours by mouth x 7 days. She was advised to drink plenty of fluids and take medication with food.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Blood test taken and antibiotics ordered.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1942076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MA
Alter: 66,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Abdominal pain upper Arthralgia Bone pain Contusion Decreased appetite Diarrhoea Dysgeusia Feeling hot Feeling jittery Glossodynia Headache Insomnia Joint range of motion decreased Lip pain Malaise Oral discomfort Pain in extremity Psychomotor hyperactivity

Symptomtext

1) Metallic taste within 30 minutes after shot; metallic taste lasted for about four hours. This was followed by pain and burning feeling on tongue and burning and stinging feeling on lips, which continues to be a problem as of today?s date. Tongue also feels swollen but does not visually appear swollen. 2) Feeling of hyperactivity, jitteriness and insomnia immediately after shot, which still persists. 3) Loss of appetite and weight loss immediately after shot, which persists. Stomach pain developed about one week after second dose on November 26, 2021. 4) Blurry vision immediately after shot and remains intermittent. 5) Pain in bones and joints, including knees, elbows, shoulder, hips, feet, which developed about one week after shot and persist today. Limitation in shoulder mobility developed immediately after second dose and has only improved slightly after two weeks. 6) Intermittent feeling of burning up but no fever. 7) Intermittent headaches, which developed about one week after shot, and persist today. 8) Unexplained bruising, which developed about one week after second dose on November 26, 2021. 9) General feeling of being unwell within 30 minutes of first shot and persists today. 10) Intermittent diarrhea within one day of shot and symptom continues intermittently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin, zyrtec
Allergien: Pitocin,prednisone, Demerol, adhesive
Vorherige Impfungen: Loss of consciousness at age 8 from unknown vaccine, persistent cough after whooping cough vaccine in 2015

VAERS 1904194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: MD
Alter: 28,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Balance disorder Dizziness Fatigue Gait disturbance Neurological examination abnormal Immunisation Interchange of vaccine products Nystagmus Off label use Product use issue Vertigo Vestibular neuronitis

Symptomtext

moderna 1st&2nd dose, pfizer booster dose; moderna 1st&2nd dose, pfizer booster dose; vestibular neuritis; could not walk to the bathroom without losing my balance; I was diagnosed with Vertigo in the ED; developed nystagmus; feeling dizzy it lasted for about 10 minutes; booster; Location of injection for vaccine received same date: Influenza: AFLURIA QUAD 2021-22 (3YR UP) - right deltoid; Initially after that vaccination I just had generalized fatigue for two days; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 28 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 31Oct2021 14:00 (Lot number: 320308d) at the age of 28 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient no known allergies. Concomitant medication(s) included: AFLURIA QUAD, start date: 31Oct2021, stop date: 31Oct2021. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: Unknown. Unable to locate or read the details, Vaccine Administration Time: 09:00 AM), administration date: 08Feb2021, when the patient was 27 years old, for Covid-19 immunization; Moderna (Dose Number: 1, Batch/Lot No: Unknown. Unable to locate or read the details, Vaccine Administration Time: 09:00 AM), administration date: 09Jan2021, when the patient was 27 years old, for Covid-19 immunization. The following information was reported: OFF LABEL USE (medically significant), INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown" and all described as "moderna 1st&2nd dose, pfizer booster dose"; IMMUNISATION (medically significant) with onset 31Oct2021 14:00, outcome "unknown", described as "booster"; VESTIBULAR NEURONITIS (medically significant) with onset 21Nov2021, outcome "recovering", described as "vestibular neuritis"; PRODUCT USE ISSUE (non-serious) with onset 31Oct2021, outcome "unknown", described as "Location of injection for vaccine received same date: Influenza: AFLURIA QUAD 2021-22 (3YR UP) - right deltoid"; FATIGUE (non-serious) with onset 31Oct2021, outcome "recovered" (02Nov2021), described as "Initially after that vaccination I just had generalized fatigue for two days"; DIZZINESS (non-serious) with onset 16Nov2021 05:00, outcome "recovered" (16Nov2021 05:10), described as "feeling dizzy it lasted for about 10 minutes", On 20Nov2021 she had another episode of dizziness that lasted about 20-30 minutes and then went away; BALANCE DISORDER (non-serious) with onset 21Nov2021, outcome "recovering", described as "could not walk to the bathroom without losing my balance"; VERTIGO (non-serious) with onset 21Nov2021, outcome "recovering", described as "I was diagnosed with Vertigo in the ED", The neurologist said it could be from vestibular neuritis; NYSTAGMUS (non-serious) with onset 21Nov2021, outcome "recovering", described as "developed nystagmus". The events "vestibular neuritis", "initially after that vaccination i just had generalized fatigue for two days", "feeling dizzy it lasted for about 10 minutes", "could not walk to the bathroom without losing my balance", "i was diagnosed with vertigo in the ed" and "developed nystagmus" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of vestibular neuronitis, fatigue, dizziness, balance disorder, vertigo, nystagmus included Meclazine, zofran, and vestibular exercises. Initially after receiving the booster vaccination she did not develop a fever, ear pain, or ear pressure, was very active, healthy and rarely get sick. The patient did not have any medical problems. The patient had no prior vaccination, not tested for covid post vaccination. No other vaccine administered in four weeks and no other medications in two weeks.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the reported events Off label use, Interchange of vaccine products, Immunisation, Vestibular neuronitis and suspect drug BNT162B2 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 re-sponse, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: AFLURIA QUAD
Allergien: -
Vorherige Impfungen: -

VAERS 1904194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: MD
Alter: 28,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Balance disorder Dizziness Fatigue Gait disturbance Neurological examination abnormal Immunisation Interchange of vaccine products Nystagmus Off label use Product use issue Vertigo Vestibular neuronitis

Symptomtext

moderna 1st&2nd dose, pfizer booster dose; moderna 1st&2nd dose, pfizer booster dose; vestibular neuritis; could not walk to the bathroom without losing my balance; I was diagnosed with Vertigo in the ED; developed nystagmus; feeling dizzy it lasted for about 10 minutes; booster; Location of injection for vaccine received same date: Influenza: AFLURIA QUAD 2021-22 (3YR UP) - right deltoid; Initially after that vaccination I just had generalized fatigue for two days; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 28 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 31Oct2021 14:00 (Lot number: 320308d) at the age of 28 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient no known allergies. Concomitant medication(s) included: AFLURIA QUAD, start date: 31Oct2021, stop date: 31Oct2021. Vaccination history included: Moderna (Dose Number: 2, Batch/Lot No: Unknown. Unable to locate or read the details, Vaccine Administration Time: 09:00 AM), administration date: 08Feb2021, when the patient was 27 years old, for Covid-19 immunization; Moderna (Dose Number: 1, Batch/Lot No: Unknown. Unable to locate or read the details, Vaccine Administration Time: 09:00 AM), administration date: 09Jan2021, when the patient was 27 years old, for Covid-19 immunization. The following information was reported: OFF LABEL USE (medically significant), INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown" and all described as "moderna 1st&2nd dose, pfizer booster dose"; IMMUNISATION (medically significant) with onset 31Oct2021 14:00, outcome "unknown", described as "booster"; VESTIBULAR NEURONITIS (medically significant) with onset 21Nov2021, outcome "recovering", described as "vestibular neuritis"; PRODUCT USE ISSUE (non-serious) with onset 31Oct2021, outcome "unknown", described as "Location of injection for vaccine received same date: Influenza: AFLURIA QUAD 2021-22 (3YR UP) - right deltoid"; FATIGUE (non-serious) with onset 31Oct2021, outcome "recovered" (02Nov2021), described as "Initially after that vaccination I just had generalized fatigue for two days"; DIZZINESS (non-serious) with onset 16Nov2021 05:00, outcome "recovered" (16Nov2021 05:10), described as "feeling dizzy it lasted for about 10 minutes", On 20Nov2021 she had another episode of dizziness that lasted about 20-30 minutes and then went away; BALANCE DISORDER (non-serious) with onset 21Nov2021, outcome "recovering", described as "could not walk to the bathroom without losing my balance"; VERTIGO (non-serious) with onset 21Nov2021, outcome "recovering", described as "I was diagnosed with Vertigo in the ED", The neurologist said it could be from vestibular neuritis; NYSTAGMUS (non-serious) with onset 21Nov2021, outcome "recovering", described as "developed nystagmus". The events "vestibular neuritis", "initially after that vaccination i just had generalized fatigue for two days", "feeling dizzy it lasted for about 10 minutes", "could not walk to the bathroom without losing my balance", "i was diagnosed with vertigo in the ed" and "developed nystagmus" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of vestibular neuronitis, fatigue, dizziness, balance disorder, vertigo, nystagmus included Meclazine, zofran, and vestibular exercises. Initially after receiving the booster vaccination she did not develop a fever, ear pain, or ear pressure, was very active, healthy and rarely get sick. The patient did not have any medical problems. The patient had no prior vaccination, not tested for covid post vaccination. No other vaccine administered in four weeks and no other medications in two weeks.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the reported events Off label use, Interchange of vaccine products, Immunisation, Vestibular neuronitis and suspect drug BNT162B2 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 re-sponse, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: AFLURIA QUAD
Allergien: -
Vorherige Impfungen: -

VAERS 1939807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 15.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain Rash Urticaria

Symptomtext

Patient got her second dose vaccine Pfizer on 11-15-2021 and on 12-2-2021 came to the pharmacy to report an adverse reaction that she got 3 days after her second dose. Patient stated that she got hives on her arms, legs, elbows, thighs and joint. she had aches as well. she saw a doctor and gave her a steroid treatment for it. The patient said this rash was related to the vaccine, however, the doctor did not saying anything about this rash was related to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: unknow.
Aktuelle Erkrankungen: none
Vorgeschichte: None
Andere Medikamente: None.
Allergien: None
Vorherige Impfungen: -

VAERS 1939407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IN
Alter: 62,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Chills Headache Injection site pain Movement disorder

Symptomtext

Joint pain all over my body. Chills. Slight headache, sore at injection site. No problems date of injection, next morning, couldn't hardly move from the joint pain. Lasted until about 6:00pm that evening. Chills lasted all day until about 9:00pm. Headache lasted all day until 9:00pm. Arm injection site is still sore today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Metamucil
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1938714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IN
Alter: 60,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Cough Fatigue Immunisation Influenza like illness Pyrexia Rhinorrhoea

Symptomtext

Flu like symptoms; horrific cough; Feverish; I was so fatigue I could not get out of it; runny nose; I am blowing a lot, it is nothing but a clear mucous; armpit very bad soreness under the ''shot arm'' and it actually traced over to my right arm, which was not the ''shot arm''; soreness really bad on to my left armpit; got the Pfizer booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 60-year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 17Nov2021 (Lot number: 320308D, Expiration Date: 28Feb2022) at the age of 60 years as dose 3 (booster), single for covid-19 immunisation; dulaglutide (TRULICITY), subcutaneous (Batch/Lot number: unknown) as 1.5 mg, weekly. Relevant medical history included: "Type II Diabetic" (unspecified if ongoing), notes: Verbatim: Type II Diabetic. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1), administration date: Mar2021, when the patient was 59 years old, for Covid-19 immunization, reaction(s): "I had no issue"; Bnt162b2 (Dose: 2), administration date: Mar2021, when the patient was 59 years old, for Covid-19 immunization, reaction(s): "I had no issue"; Flu shot (I got the Flu shot (Unspecified Flu shot) yeah in Oct2021.), administration date: Oct2021, when the patient was 60 years old, for Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 17Nov2021, outcome "unknown", described as "got the Pfizer booster"; AXILLARY PAIN (non-serious) with onset 18Nov2021, outcome "recovering", described as "armpit very bad soreness under the ''shot arm'' and it actually traced over to my right arm, which was not the ''shot arm''; soreness really bad on to my left armpit"; INFLUENZA LIKE ILLNESS (non-serious) with onset 19Nov2021, outcome "recovering", described as "Flu like symptoms"; COUGH (non-serious) with onset 19Nov2021, outcome "recovering", described as "horrific cough"; PYREXIA (non-serious) with onset 19Nov2021, outcome "recovering", described as "Feverish"; FATIGUE (non-serious) with onset 19Nov2021, outcome "recovering", described as "I was so fatigue I could not get out of it"; RHINORRHOEA (non-serious) with onset 19Nov2021, outcome "recovering", described as "runny nose; I am blowing a lot, it is nothing but a clear mucous". Therapeutic measures were taken as a result of axillary pain, influenza like illness, cough, pyrexia, fatigue, rhinorrhoea. Additional information: Patient had received Robitussin cough syrup as treatment for the cough. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type II diabetes mellitus (Verbatim: Type II Diabetic)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1935103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MA
Alter: 41,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Erythema Immunisation Lymphadenopathy Pruritus

Symptomtext

Swollen lymph nodes on my left arm the next day, lasting for 3 days; A red dotted rash on my left inner thigh about 2inches*2inch, the dots were itchy they have lasted 3 weeks and progressively gotten better; A red dotted rash on my left inner thigh about 2inches*2inch, the dots were itchy they have lasted 3 weeks and progressively gotten better; Dose_number=3; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 26Oct2021 19:00 (Lot number: 320308D) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU, administration date 07Oct2021. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8729, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 03Apr2021, when the patient was 40 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6207, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 13Mar2021, when the patient was 40 years old, for COVID-19 immunization.The following information was reported: IMMUNISATION (non-serious) with onset 26Oct2021 19:00, outcome "unknown", described as "Dose_number=3"; LYMPHADENOPATHY (non-serious) with onset 27Oct2021, outcome "recovered" (2021), described as "Swollen lymph nodes on my left arm the next day, lasting for 3 days"; ERYTHEMA (non-serious), PRURITUS (non-serious) all with onset 27Oct2021, outcome "recovered" (2021) and all described as "A red dotted rash on my left inner thigh about 2inches*2inch, the dots were itchy they have lasted 3 weeks and progressively gotten better".Therapeutic measures were not taken as a result of lymphadenopathy, erythema, pruritus.Prior to vaccination, the patient was not diagnosed with COVID-19 and Since the vaccination, the patient has not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1924583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: TN
Alter: 56,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 03.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: UN / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Dizziness Pain in extremity Pyrexia Tenderness

Symptomtext

Chills, fever, lightheaded, sore arm, tender under arm/left breast area

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Lexapro
Allergien: none
Vorherige Impfungen: -

VAERS 1923989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: GA
Alter: 46,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 20.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest discomfort Discomfort Fatigue Peripheral swelling Skin discolouration Contusion

Symptomtext

Patient came to pharmacy on 12/6 and showed me his left arm, which is bruised and swollen from shoulder to hand. He states that it is a reaction to his vaccine on 11/20, but that the reaction didn't start until 12/1. He states that he has not had any other trauma to the arm, he has no allergies, and can think of no other reason why his arm would look like that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Patient went to the emergency room on 12/2, and was advised by them to rest and ice the arm, but that they could not offer him any treatment.
Aktuelle Erkrankungen: none, verified by patient
Vorgeschichte: -
Andere Medikamente: -
Allergien: none, verified by patient
Vorherige Impfungen: -

VAERS 1920831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CT
Alter: 62,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Feeling abnormal Headache Myalgia Nausea Pain in extremity Tinnitus

Symptomtext

Tinnitus started the morning after. Very sore arm. Stomach a little queasy. Achy muscles. Mild headache and brain fogginess. All symptoms started the morning after, except the sore arm, which started the evening of the shot(7-9 hours later)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None known
Vorherige Impfungen: Age 62, similar symptoms

VAERS 1920179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: SC
Alter: 53,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Chills Erythema Fatigue Inflammation

Symptomtext

Chills, fatigue. Soreness, and redness in the shoulder. Inflamed armpit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Men's one a day; Occasional Advil
Allergien: None
Vorherige Impfungen: Same effects

VAERS 1919684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Chills Illness Nasal congestion Pain Pain in extremity Pyrexia Somnolence

Symptomtext

sick/ Really Sick; chills; fever; body aches; stuffy nose; Weakness; her arm was a little sore; sleepy; 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 39 year-old female patient received bnt162b2 (COMIRNATY), administered in arm right, administration date 15Nov2021 18:30 (Lot number: 320308D) at the age of 39 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: ILLNESS (life threatening) with onset 18Nov2021 04:00, outcome "not recovered", described as "sick/ Really Sick"; CHILLS (life threatening) with onset 18Nov2021 04:00, outcome "not recovered", described as "chills"; PYREXIA (life threatening) with onset 18Nov2021 04:00, outcome "not recovered", described as "fever"; PAIN (life threatening) with onset 18Nov2021 04:00, outcome "not recovered", described as "body aches"; ASTHENIA (life threatening) with onset 18Nov2021, outcome "not recovered", described as "Weakness"; NASAL CONGESTION (life threatening) with onset 18Nov2021 04:00, outcome "not recovered", described as "stuffy nose"; PAIN IN EXTREMITY (non-serious) with onset 15Nov2021, outcome "not recovered", described as "her arm was a little sore"; SOMNOLENCE (non-serious) with onset 15Nov2021, outcome "not recovered", described as "sleepy". Therapeutic measures were taken as a result of illness, chills, pyrexia, pain, asthenia, nasal congestion, pain in extremity, somnolence. Clinical course: Patient stated that on Monday she was sleepy and her arm was a little sore. On Thursday at 4:00AM she woke up with chills, fever, body aches and stuffy nose - she stated she was really sick and still feels sick and it varies, she feels different everyday. She clarifies by feels really sick she means chills, fever, body aches, and stuffy nose. Treatment received was Tylenol and Theraflu. No family medical history relevant to AE and no history of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available). No additional Vaccines Administered on Same Date of the Pfizer Suspect. No AE(s) require a visit to Emergency Room or considering going to the doctors office. No prior vaccinations within 4 weeks. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's Medical History (including any illness at time of vaccination)? None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1919650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: DE
Alter: 72,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Fatigue Immunisation Peripheral swelling Psoriasis Psoriatic arthropathy

Symptomtext

Psoriatic arthritis more intense; extremely tired; swelling of legs feet; extreme pain in joints; psoriasis which became much more severe; dose received: 3; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 72 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 29Oct2021 (Lot number: 320308D) at the age of 72 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Psoriasis" (unspecified if ongoing); "psoriatic arthritis" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6207, Location of injection: Arm Left), administration date: 15Mar2021, when the patient was 71 years old, for Covid-19 immunization, reaction(s): "flu like symptoms"; Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8729, Location of injection: Arm Left), administration date: 12May2021, when the patient was 72 years old, for Covid-19 immunization, reaction(s): "administration date=15Mar2021/ dose administration date=12May2021". No other vaccine in four weeks. No covid prior vaccination, no covid tested post vaccination. The following information was reported: IMMUNISATION (medically significant) with onset 29Oct2021, outcome "unknown", described as "dose received: 3"; PSORIATIC ARTHROPATHY (medically significant) with onset 30Oct2021, outcome "recovering", described as "Psoriatic arthritis more intense"; FATIGUE (non-serious) with onset 30Oct2021, outcome "recovering", described as "extremely tired"; PERIPHERAL SWELLING (non-serious) with onset 30Oct2021, outcome "recovering", described as "swelling of legs feet"; ARTHRALGIA (non-serious) with onset 30Oct2021, outcome "recovering", described as "extreme pain in joints"; PSORIASIS (non-serious) with onset 30Oct2021, outcome "recovering", described as "psoriasis which became much more severe". The events "psoriatic arthritis more intense", "extremely tired", "swelling of legs feet", "extreme pain in joints" and "psoriasis which became much more severe" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of psoriatic arthropathy, fatigue, peripheral swelling, arthralgia, psoriasis. These events finally calm down 18Nov2021 and Outcome was reported as recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Psoriasis; Psoriatic arthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1910280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: TN
Alter: 55,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Insomnia Sleep disorder Throat irritation Tinnitus

Symptomtext

Continuos fatigue through out the day Difficulty during sleep and staying sleep Ringing in the ear My body is in overdrive specifically when sleeping Continuous itching of the throat after booster shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: I didn't go to health center to see my doctor. Because, I don't know what he can do for me.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: HCTZ 25mg daily Metoprolol sr 25mg daily
Allergien: None
Vorherige Impfungen: -

VAERS 1909367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: PA
Alter: 28,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 16.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Activated partial thromboplastin time Back pain Chlamydia test Dizziness Fatigue Full blood count Gram stain Impaired work ability International normalised ratio Metabolic function test Neisseria test Pelvic pain Perineal pain Prothrombin time Smear vagina Ultrasound abdomen Ultrasound scan vagina Urine analysis

Symptomtext

2 days after receiving the vaccine on 11/18/21 I began to have heavy vaginal bleeding and pelvic pain. today is day 13 of pelvic pain, vaginal bleeding and clots. I was seen in the Emergency Room on saturday 11/27/21 because the pain had become worse, i was feeling lightheaded and fatigued. i was unable to report to work that day and on sunday 11/28/21 due to the pain. the pain is mostly located on my left lower pelvic region but at times refers to my left lower back and throughout my pelvic and perineal region.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: 11/27/21 at the emergency room i was ordered a urinalysis, CBC w/ diff, CMP, transvaginal and abdominal ultrasound, aPTT, PT/INR, gonorrhea/chlamydia screen, and gram stain/wet mount of vagina.
Aktuelle Erkrankungen: none at time of vaccination
Vorgeschichte: endometriosis, GERD
Andere Medikamente: Nexium, vitamin D, vitamin C, Loestrin Fe birth control, Wellbutrin XL, Zyrtec
Allergien: Cashews, penicillin
Vorherige Impfungen: -

VAERS 1904536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: DE
Alter: 63,0
Geschlecht: M
Eingang: 28.11.2021
Impfdatum: 08.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Cough Drainage Headache Oropharyngeal pain Pain Productive cough SARS-CoV-2 test negative Secretion discharge

Symptomtext

11/18/2021: Severe chills to the core, causing shivering for about 20 minutes in afternoon; 11/19-21: Dull headache, and body aches (muscular) for next few days; 11/19-24: Upper respiratory drainage with slight sore throat and cough; 11/20: Received Covid-19 test at pharmacy; 11/23: Test results received: NEGATIVE; 11/22 - present (11/28/2021): Very thick, sticky clear mucus in lungs with productive coughs with frequency of coughing and mucus improving. Recovery anticipated. Treatment was taking 2 aspirins per day for 2-days on 11/19-20.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 11/20/2021 Baseline Covid-19 test at pharmacy (Reference ID 2324445504). Negative result received 11/23/2021
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma (controlled)
Andere Medikamente: Olmesartan Medoxomil 20mg; Rosvastatin Calciu 10mg; Flovent H
Allergien: none
Vorherige Impfungen: -

VAERS 1904352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 32 0308 D

mild

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 28.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Alanine aminotransferase increased Anion gap normal Arthralgia Aspartate aminotransferase increased Blood albumin normal Blood alkaline phosphatase increased Blood bicarbonate normal Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatine phosphokinase normal Blood creatinine decreased Blood creatinine normal Blood glucose normal Blood potassium Blood urea increased Chills Chromaturia

Symptomtext

Rigors for 3 hours begininng abiut 6 hours after (this was a booster, original series given 12/20/2020 and 01/09/2021 with minimal body aches and fatigue after second does). Severe myalgias and arthralgias for 48 hour after rigors stopped; brown urine onset 2.5 days after dose evening of 11/22, which continued for several more days. Labs drawn 11/24/2021 below

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 11/24/2021 CK 176 (nl 20-180U/L. Anion gap 12.0 (3.0-18.0) BUN/Cr 29 (5-37). Globulin 3.0 (2.4-4g/dl)glucose 90 (70-100 mg/dl) ***BUN 20 (7-18 mg/dl) Cr 0.69 , K+ 3.9, Cl 107. **CO2 24, Ca 8.4, Albumin 4.0, total bili 0.6 ***Alk Phos 180 (33-152), ***AST 60 (7-45), ***ALT/SGPT 188 (10-60) CBC essentially normal slight increase in Hgb from concentration
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: sulfa antibiotics
Vorherige Impfungen: -

VAERS 1904169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: NY
Alter: 12,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Cytokine test Full blood count Metabolic function test Rash SARS-CoV-2 antibody test Total complement activity test Tryptase

Symptomtext

approx. 1 hr after vaccination developed rash L shoulder, back, chest. Had Benadryl before ed evaluation, at time of my evaluation rash was not raised but mother describes as initially hives like. no swelling mouth or face, no rash to face, no resp symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: cbc, cmp,covid spike, tryptase, complement total ch50, c3-c9, cytokine panel
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: pcn
Vorherige Impfungen: -

VAERS 1899991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: PR
Alter: 71,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Inflammation Pruritus Somnolence

Symptomtext

About 4-5 hours after injection, my hands, feet, shoulders and elbows suddenly became inflamed and excessively itchy. Very excessively. I took a cold shower and washed well with over the counter soap. No relief. Applied Benadryl ointment. No relief. Sprayed effected areas with Off insect spray. Instant relief and instant sleepiness. Instant. Slept 8 hours. All symptoms gone. Very weird.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Thyroxizione 40, cholesterol med
Allergien: Tetracycline, prolonged exposure to betadine
Vorherige Impfungen: -

VAERS 1897988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Rash Rash pruritic Urticaria

Symptomtext

Received her first Covid-19 Vaccine Pfizer on 10/30/21. The day after (10/31/2021) she started experiencing allergic reaction (mild skin bumps only similar to hives but without redness or welts) through out her chest, arms and legs. Bumps were itchy, but no color and lasted for 24 hours. She received her 2nd dose 11/23/2021. During vaccination, patient was given loratadine 10mg tablet. She was also given diphenhydramine 25mg cap for night time with proper counseling (drowsiness). She was instructed to seek medical help as necessary. She waited 30 minutes in the pharmacy and experienced no symptoms. Upon follow up night of 11/23/21 and morning of 11/24/21, she mentioned no allergic reaction occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1895325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 21.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Injection site pain Pruritus

Symptomtext

Itching after1hr continues days using benadryl alternate Atarax face legs chest head Pain injection site and multi joint achiness On going day3

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Hx sle 40 yrs
Vorgeschichte: Osteoporosis. Sle.fibromylgia.hypertension gastroparesis
Andere Medikamente: Vitamin d.50,000.
Allergien: Neomycin.colymycin.penicillin. milk.tape.vibramycin Keflex ampicillin
Vorherige Impfungen: Same reactionphfizer

VAERS 1894781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Headache Pain

Symptomtext

Body ache, chills, headache, fatigue. Taking Tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity
Andere Medikamente: Claritin (allergy), Biotin, Vitamin D, Glucosamine Chondrotin, Multivitamin, Krill Oil.
Allergien: None
Vorherige Impfungen: Covid Pfizer 2nd dose

VAERS 1894762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: CO
Alter: 6,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Immediate post-injection reaction Incorrect dose administered Vomiting

Symptomtext

Pt was given 0.3ml of Pfizer adult dose, rather then childs dose. Pt immediately vomited

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: none, pt was watched in clinic after examined by Dr.
Aktuelle Erkrankungen: None
Vorgeschichte: Esotropia of left eye
Andere Medikamente: vitamin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1894718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: KY
Alter: 53,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 16.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

11/23/21 Reported fever, seen by PCP 11/23/21 Regeneron infusion given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 11/23/21 SARS-CoV-2 PCR -detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: No history listed
Andere Medikamente: Lipitor 20mg daily
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1890461

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 320308D

mild

Staat: GA
Alter: 25,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pruritus Rash Skin irritation

Symptomtext

Right over 24 hours after administration of vaccine, severe itching began on both arms and quickly escalated to both legs, abdomen and back over the following days. Severe irritation with rash that is unrelieved with antihistamine cream occurred as the itching increased. I am still taking Benadryl and using topical creams to relieve the symptoms, but the rash has continued to worsen 6 days post vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prenatal vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1890040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MO
Alter: 76,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood pressure increased Fatigue Feeding disorder Headache Heart rate increased Pyrexia

Symptomtext

Extreme fatigue, headache, wouldn't eat or drink because she was to tired. Elevated BP, elevated pulse and fever.- as described by daughter. Taken to hospital to be evaluated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: NO
Vorherige Impfungen: -

VAERS 1888975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IN
Alter: 57,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pruritus

Symptomtext

patient received 2nd Pfizer vaccination 11/20/21 and called pharmacy 11/21/21 to complain of adverse reaction("itching from head to toe"). Patient informed me that the reaction also happened after the 1st dose on 10/26/21 and the itching has never stopped. She did not report the adverse reaction until 11/21/21. I asked if she was having difficulty breathing and she she no. I recommended benadryl every 6 hours and she said she has been taking benadryl since the 1st vaccination. I told her to call her primary care physician.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: no allergies on file
Vorherige Impfungen: -

VAERS 1887445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 53,0
Geschlecht: M
Eingang: 20.11.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Cough Headache Injection site pain Insomnia Pain Parosmia Respiratory tract congestion

Symptomtext

It began (11pm on the day of injection) with sever pain in both injection site (Covid vaccine in left shoulder & Flu vaccine in right shoulder) that prevented my ability to sleep until 4:30 am. In the morning additional symptoms developed (continual pain in both shoulder, chest congestion, general body ache, mild headache, persistent smell of cigarette smoke (no one smokes) and low grade cough. Symptoms present at time of reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension & High Cholesterol
Andere Medikamente: Atorvastatin 40mg, Lasartan 50mg & Amlodipine 10mg & Flu vaccine given at the same time as the Pfizer Covid Booster shot
Allergien: NA
Vorherige Impfungen: -

VAERS 1880655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: MS
Alter: 27,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SC / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Exposure during pregnancy Fatigue Pain Pruritus

Symptomtext

I am 5 months pregnant. Have body aches. Tired and itching everywhere. No redness or rash. Just persistent itch that won?t go away. I have had 3 Benadryl and am seeing a doctor

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sjogrens Fibromyalgia Migraines Raynaud?s Displaced jaw TMJ
Vorgeschichte: Fibromyalgia Raynauds Sjogrens Migraines ADHD
Andere Medikamente: Cymbalta Adderall Prenatal vitamin Vitamin d3 Calcium Zyrtec Baby aspirin Pepcid Plaquenil Tylenol Zofran
Allergien: Niacin sensitive, avelox allergy
Vorherige Impfungen: Covid pfizer 1

VAERS 1880591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MN
Alter: 27,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Feeling cold Flushing Hypoaesthesia Hypoaesthesia eye Hypoaesthesia oral Pruritus Swollen tongue Throat irritation Throat tightness Tongue pruritus

Symptomtext

Patient came in today to receive her Covid-19 vaccine Pfizer dose #1 for a requirement for her EMS participation. She had a medical exception to Covid-19 vaccine in the past but her doctors recently decided that she could get the vaccine. She does report having a shellfish allergy with anaphylactic reaction so she was recommended to wait for 30 minutes post vaccination. She reports being nervous to get the vaccine due to the concern of having a reaction. Pfizer, 0.3mL Lot # 320308D was given at approximately 10:40am in her left deltoid. At 10:45 a.m. this was approached reporting that she was getting an itchy throat and tongue. She was escorted to a cot to rest and given 1 diphenhydramine tablet (25mg) orally with water at 10:45 am. Blood pressure was 167/119 and pulse 85. No flushing or paleness noted. She reports that her throat was starting to tighten some and feeling itchy, but she could still breathe without issue, "slowly". She chose to sit on the cot vs. lie down. Patient reports needing to keep her breathing calm to prevent anxiety from setting in. They offered to call the ambulance and she responded that she thought that would be good. 911 was called at 10:48 a.m. to dispatch ambulance. 10:50 a.m. She reports that her tongue also felt like it was swelling and her face was starting to feel itchy. She continues to deny increased difficulty with breathing. 10:54 a.m. BP was 165/124 and patient's face is now red/flushed. She reports increased numbness and it moving to her tongue, lips, sinuses/eyes and forehead. She adds that this is what it felt like when she reacts to shellfish. They can hear ambulance sirens, but then they go away.They discussed administering epinephrine to her and she states that she needs to have epi administered now since she is familiar with how her body reacted and felt with her shellfish reaction in the past. 10:59 a.m.they administered 0.3mg epinephrine IM in mid-outer left thigh. Patient reports that she is also feeling very cold now. 11:00 a.m. facility hears ambulance sirens again and the ambulance arrives with a minute or 2 after the administration of epi reports off to the ambulance crew who then took over her care and the ambulance took her away in their rig.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: only BP and pulse were taken at the vaccine site until the ambulance arrived. She was transported Emergency Room. Unknown what tests were completed there.
Aktuelle Erkrankungen: She voiced that she had another medical reason that she gets injections every 12 weeks for that was allowing her medical exception of Covid-19 vaccine up until recently but the doctors released her to get her Covid-19 vaccine.
Vorgeschichte: unknown. States was (or is) getting injections every 12 weeks but unknown what it was for.
Andere Medikamente: unknown
Allergien: shellfish, latex, unknown if additional
Vorherige Impfungen: -

VAERS 1880347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IN
Alter: 29,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain Pyrexia

Symptomtext

Body aches and fever for 36+ hours. Onset of side effects took almost 11 hours post vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sinus infection coupled with ear infection
Vorgeschichte: Rheumatoid arthritis
Andere Medikamente: Sprintec 28 day (OCT). All other medications stopped 5 days before vaccine per rheumatoid arthritis specialist doctors recommendation.
Allergien: -
Vorherige Impfungen: -

VAERS 1880066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Nausea

Symptomtext

Systemic: Nausea-Mild, Additional Details: gave water and asked to sit still and was ok. Patients mom said he is fine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1873313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: FL
Alter: 55,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Headache Hypoaesthesia Injection site mass Musculoskeletal stiffness Pruritus

Symptomtext

Lump at injection site, itching in the evening of vaccine recieved. This morning 11:30am. Left arm numbness, tightness lump at injection site still, no fever, headache, tired at 1:15pm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, heart condition
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1870415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: FL
Alter: 16,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 03.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Miliaria Rash

Symptomtext

pt woke up with a heat rash with white bumps on face after 2 days getting vaccinated. pt got rash again 10 days after vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no covid back in july 2021
Vorgeschichte: -
Andere Medikamente: no
Allergien: no allergies
Vorherige Impfungen: -

VAERS 1869415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AL
Alter: 31,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 11.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Eye discharge Eye pain Eye swelling Ocular hyperaemia Pruritus

Symptomtext

Swollen left eye, pain, redness, draining. Redness and itchiness in between fingers, arms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: Metformin 1000mg per day
Allergien: Iodine
Vorherige Impfungen: -

VAERS 1868485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IL
Alter: 43,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Herpes zoster Pruritus Rash Rash erythematous

Symptomtext

around 6pm ( 5 or so hours after vaccination) i felt itching under my right shoulderblade. that worsened overnight and turned to red rash. this slowly spead to the middle of my upper back and then to just under my right breast. after a few days it spread to the middle of my chest. today it is spreading to the top of my right breast.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Dr identified it as shingles.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1868266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IN
Alter: 57,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pain Peripheral coldness Pyrexia

Symptomtext

Mild fever and body ache. Oddly, I had an intermittent feeling of something cold touching the inside of my right forearm, as if I had spilled cold water or brushed up against a cold piece of metal on clothing, but in fact no cold water or metal were present; it was a phantom sensation. I had never experienced such a thing before. All symptoms subsided in a little over 24 hours without treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Mild heart condition ? I forget the name for it, but a valve does not close all the way and some blood moves back into the other chamber on each heartbeat.
Andere Medikamente: none
Allergien: Levaquin
Vorherige Impfungen: 2nd dose of Pfizer COVID vaccine, lot EW0153, 4/13/21, fever and body ache

VAERS 1868099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: -
Alter: 25,0
Geschlecht: M
Eingang: 14.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Disturbance in attention Dizziness Fatigue Feeling abnormal Lymph node pain Lymphadenopathy

Symptomtext

Fatigue within hours of vaccination. Slept through the afternoon and late into the next day. Shivering while in bed with sweatshirt, sweatpants, multiple blankets and room temperature of 75. Swollen lymph node in the armpit of the arm I got the vaccination in (about golf ball size with soreness over the next 2-3 days). Dizziness over the next few days following vaccination. Foggy thinking and trouble focusing in the week or more following vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None. I don't have a doctor and was forced to get vaccinated to keep my job
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Daily multivitamin, None other
Allergien: None
Vorherige Impfungen: -

VAERS 1868007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: TN
Alter: 49,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 06.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Diarrhoea Dizziness Fatigue Headache Lymphadenopathy Malaise Neck pain Pyrexia Rash Rhinitis allergic

Symptomtext

Swollen lymph node under left arm for 6 days; headache for 4 days; neck pain for 7 days; rash on chest for 1 day; shoulder pain for 7 days; dizziness for 7 days; general feeling of feeling sick for 6 days; nausea for 5 days; diarrhea for 1 day; fatigue for 6 days; 99 fever for 1 day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Na
Vorgeschichte: Hashimotos
Andere Medikamente: Tirosint 88mcg
Allergien: Na
Vorherige Impfungen: 03/22/2021; covid doses 1 & 2; same side effect as dose 3 except no diarrhea or swollen lymph node

VAERS 1867793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: GA
Alter: 66,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pain in extremity Shoulder injury related to vaccine administration

Symptomtext

Patient said she had arm pain starting the day after vaccination. She was diagnosed with SIRVA. The Dr prescribed Medrol Dosepack 4mg on 11/1/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1865220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Headache Joint range of motion decreased Nausea Pain Pain in extremity Pyrexia

Symptomtext

Adverse event: High fever (101+) with headache and extreme soreness on right side of body (arm, shoulder, back, leg all the way to foot.) Queasy stomach, no vomiting. Extreme pain at inside of right elbow, causing throbbing in right hand. These symptoms lasted 40 hours before they began to receded. I took 2 pills Excedrin migrane at noon on October 27 (day after vaccination, day one of symptoms) I took 1 low dose asprin on October 28th at 10 am. I drank a LOT of water the entire time. Currently (November 12, 2021) still experiencing continuing soreness in right shoulder, limiting rotation motion. Pain seems to come from front side of shoulder at joint.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none - I don't have insurance
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Lavender, Vitamin D 2000iu, B12 complex
Allergien: no
Vorherige Impfungen: First dose Pfizer COVID-19 vaccine in February 2021. Left arm shot, resulted in deep and severe pain in shoulder joint. Pain beg

VAERS 1864033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IN
Alter: 72,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Immunisation Pain Pyrexia

Symptomtext

Intense pain from face to feet on left side; Fever; Chills; The patient received the third/booster dose of BNT162b2; This is a spontaneous report from a contactable consumer, the patient. A 72-year-old non-pregnant female patient received the third (booster) dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: 320308D) in the left arm on 04Nov2021 at 11:30 (at the age of 72-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient received other vaccines within four weeks prior to the vaccination which included influenza vaccine (flu) (MANUFACTURER UNKNOWN) on 20Oct2021 for immunization. Concomitant medications included levothyroxine (MANUFACTURER UNKNOWN) and doxepin (MANUFACTURER UNKNOWN), both for an unknown indication from an unknown date and unknown if ongoing. The patient previously received thiomersal (THIMEROSAL) and experienced drug allergy. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL3246) in the left arm on 08Feb2021 (at the age of 71-years-old) and also received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6200) in the left arm on 01Mar2021 (at the age of 72-years-old) as a single dose for COVID-19 immunisation. On 04Nov2021 at 12:00, the patient experienced intense pain from face to feet on left side, fever and chills. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events intense pain from face to feet on left side, fever and chills were resolving at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LEVOTHYROXINE; DOXEPIN
Allergien: -
Vorherige Impfungen: -

VAERS 1862540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CO
Alter: 68,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal discomfort Arthralgia Dizziness Dysstasia Fatigue Gait disturbance Headache Limb discomfort Myalgia

Symptomtext

Day 2: severe headache; bad pain in joints and muscles; trouble walking and standing, legs and arms felt very heavy; Day 3: fatigue Day 6: severe dizziness from 7am to 1pm; sick at stomach but no vomiting; could not walk--had to crawl, fatigue rest of day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None. Called online nurse on Day 7
Aktuelle Erkrankungen: -
Vorgeschichte: asthma
Andere Medikamente: Dulara (asthma), ibuprofen
Allergien: -
Vorherige Impfungen: -

VAERS 1861326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OH
Alter: 48,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Flushing Injection site pain Lymph node pain Lymphadenopathy Pelvic pain Radiotherapy

Symptomtext

I experienced a flushing, an increase in pain and erythema in the pelvic area where I had received radiation therapy approximately 5 hours after administration of the vaccine. The following 2 days, the lymph nodes in my groin (also previously radiated) were swollen and tender, this was unexpected. My right arm was sore at the site of the injection (which I expected). Today, Thursday Nov. 11th, mild pelvic skin erythema and tenderness persist, but have not gotten worse. Left groin lymph node still feels tender, is no longer swollen or palpable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: Diagnosed with anal cancer July 15, 2020- underwent chemoradiation for 6 weeks from Aug 24- Oct 5th 2020
Andere Medikamente: Ristela twice daily, collagen powder daily, amberen daily, vitamin d 1,000 units daily, vitamin c 1,000 mg daily, miralax daily, metamucil daily
Allergien: none
Vorherige Impfungen: -

VAERS 1860479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: SC
Alter: 24,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 02.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dysmenorrhoea Headache Heavy menstrual bleeding

Symptomtext

I am on kyleena for birth control. I have had it for a few years. My periods have almost completely stopped since having this IUD. I experience slight spotting every now and then but haven?t seen actual blood in about half a year or longer. I got the Covid shot on November 2, 2021 and on November 4, 2021 I started a full heavy bleeding cycle. During this cycle I have experienced severe cramping. One cramp sent me to the floor it was so bad. It is now November 11, 2021 and I am still bleeding. The bleeding has slowed down but still there and I am still experiencing mild cramping today. I have been taking ibuprofen for pain and using a heating pad. I will be scheduling an appointment with my OBGYN in the morning. I have also experienced more frequent headaches since receiving the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Kyleena
Allergien: None
Vorherige Impfungen: -

VAERS 1860338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Decreased appetite Hypersomnia Pain in extremity

Symptomtext

sleeping 10 hours a night; right arm is still very sore; has very poor appetite; This is a spontaneous report from a contactable consumer (patient). A 73-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Right on 21Oct2021 13:45 (lot number: 320308D; expiry date: unknown) at the age of 73-years-old, as dose 3 (BOOSTER), single for Covid-19 immunization. The patient had no relevant medical history and family history and was not taking concomitant medications. She had no change in medications, no change in nutritional intake and no significant change in nutritional intake. Patient does not smoke. There were no changes in medical conditions or her health and no exposure to anything. The vaccine was administered in a pharmacy grocery store. The patient previously received 1st dose BNT162B2 on 31Mar2021 (lot number: EP7533) and the 2nd dose on 21Apr2021 (lot number: EN6204) both administered in the right arm for COVID-19 immunization. After the 1st dose she had absolutely no side effects and may have slept well that night and then after the 2nd dose she had nothing regarding no side effects. The patient did not receive other vaccines on the same date as BNT162B2. The patient previously received influenza vaccine (FLUZONE) for immunisation. She had the flu shot for seniors 3 weeks before the 3rd dose of the Pfizer COVID Vaccine and the flu shot was Fluzone HD 65 plus and has the lot number on it of PF2021-22 injection 0.7mL with NDC 49281-0121-65 and it was administered on 28Sep2021. She had received flu shots for many years and never had any side effects from any vaccine or from the flu shots. Patient stated that she had her 3rd dose on 21Oct2021 which was last Thursday, and her right arm was still very sore. She was still sleeping 10 hours a night and only getting up one time and still has very poor appetite. She does not have nausea and does not have fever but still has the sore arm and was still sleeping which was very nice but thought she should do her part and report this. Her arm soreness was a little better and was in her right arm where all three doses of the Pfizer COVID vaccines were administered. She got the 3rd dose of the vaccine at 1:45pm or 1:50pm and by 6:00pm at night was when she started noticing the poor appetite and it was a little better today. The events did not require emergency room and Physician's Office visit. Outcome of the event sleeping 10 hours a night was not recovered, while for the other events was recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: NONE
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1859038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: VA
Alter: 36,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cluster headache Hyperhidrosis Myalgia Pain in extremity

Symptomtext

Severe ache in muscles and headaches and sweating profusely lasted for approximately 48 hours and arm is still sore over week later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cluster headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergy to shrimp
Vorherige Impfungen: -

VAERS 1859033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Genital rash Herpes zoster Rash Rash erythematous Rash pruritic Rash vesicular

Symptomtext

Rash on left groin appeared within 2-3 hours of shot. Was itchy and red for a couple days then began to blister. Started becoming painful a 3-4 days later. Day 5 went to doctor at local office and it was diagnosed as Shingles.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Genital rash
Hospital-Tage: -
Labordaten: Office Visit with M.D. on Wednesday November 10, 2021. Diagnosed was: Herpes Zoster (Shingles)
Aktuelle Erkrankungen: Miscarried at 9 weeks pregnant, 2 weeks prior to vaccine.
Vorgeschichte: None
Andere Medikamente: Prenatal vitamins Calcium & iron supplements
Allergien: None
Vorherige Impfungen: -

VAERS 1859025

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: -
Alter: 15,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Cough Injection site vesicles Pain

Symptomtext

The following morning after the shot (11/7/21), the patient woke up with a strange blister that popped on his shoulder in the arm where he received the covid shot. The next day (11/8/21), the patient felt radiating pain from his armpit down the side of his body. In addition, he developed a deep cough. Patient went to his doctor's office on 11/8/21 to determine if these were complications of the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site vesicles
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1859015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OR
Alter: 43,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness

Symptomtext

Felt dizzy. Orange juice given and encourage fluids (water). Persisted symptom and was sent home. On follow up check at 550pm - she is feeling better and not dizzy anymore. Encouraged to see her doctor if not better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1858051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Urticaria

Symptomtext

Hives

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Mitral valve replaced - on warfarin
Andere Medikamente: Warfarin
Allergien: None
Vorherige Impfungen: -

VAERS 1857613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MI
Alter: 51,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Oedema peripheral

Symptomtext

Patient reports a swelling in armpit that began approximately 21 hours after injection. At this time it is about 3 inches in diameter, and is very painful. Patient will follow up with MD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1857140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: ME
Alter: 50,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Arthritis Back pain Neck pain Pelvic pain

Symptomtext

Almost immediately after the vaccination I had excessive and painful inflammation in both knees, both shoulders, my neck, pelvis, and back for 3 days. It felt as if it was contorting my body into a deformed ball. With no present injury to these sites prior to the injection it was pretty clear that this was targeting issues I had had with these area in my past. It was inflammation pumped directly into those locations. Very painful. After 3 days I was back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lexapro Omeprazole DHEA Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1854459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Feeling abnormal Headache Lethargy Pain Pain in extremity

Symptomtext

Excessive, pronounced exhaustion. Body aches, chills & strong headache throughout the night. Went to bed at 10:00pm 11/8/21 & did not wake until 10:30am on 11/9/21. Strong pain in entire upper left arm, painful to move around in bed. Ate 3 very healthy meals on 11/8/21 & hydrated with water throughout the day & night. Took (1) Extra Strength Tylenol @ 11:30am on 11/9/21 to relieve the headache. I remain quite foggy & lethargic. I did not experience any of these markedly elevated side affects with either of my first 2 Pfizer shots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: Codine - strong headaches
Vorherige Impfungen: -

VAERS 1853430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: UT
Alter: 41,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Anosmia Chills Decreased appetite Fatigue Headache Malaise Pain Pain in extremity Pyrexia Taste disorder

Symptomtext

Fever, chills, headache, body ache, lack of apetite, impaired sense of smell and taste, extremely sore arm, significant fatigue. It's been more than one week, arm is still sore and still suffer from significant fatigue and overall lower feeling of wellbeing. Also sense of taste and smell still impaired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Demarol
Vorherige Impfungen: -

VAERS 1851412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MS
Alter: 33,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Rash Vomiting

Symptomtext

Patient first experienced a rash consisting of raised bumps on the skin of both arms. About 15-20 minutes later, patient vomited several times, though this resolved after another 15-20 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known
Vorgeschichte: None known
Andere Medikamente: None known by pharmacy administering vaccine
Allergien: None known
Vorherige Impfungen: -

VAERS 1850377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MA
Alter: 48,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 26.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal discomfort Arthralgia Computerised tomogram abdomen abnormal Endoscopy Feeling abnormal Gastritis Gastrointestinal wall thickening Hepatobiliary scan Injection site pain Pain Sleep disorder Ultrasound abdomen

Symptomtext

I received the vaccine on Tuesday, mid-morning, on October 26, 2021. It felt like I was having an inflammatory response by the afternoon. The soreness at the injection site increasingly grew in intensity and the joints throughout my body were radiating pain. I felt awful. I contracted Covid in June of 2021, but this felt worse than the actual symptoms. I self-medicated with 600 mg of Ibuprofen and would alternate with Tylenol. These feelings persisted and by Saturday, October 30, 2021, I started having an upset stomach. I didn't make the connection, and ate lightly the rest of the day. The next day, Sunday, it felt like my entire abdomen was on fire. I tried every home remedy I could think of. Taking Tums, Mylanta, Miralax, and I went on a liquid diet, but nothing helped. I could not sleep Sunday or Monday night because the pain was so intense. Early Tuesday morning, around 4am, I drove to our local Emergency Room. They gave me IV, administered anti-inflammatory medication, calcium, and performed a CAT scan. The CAT scan revealed the thickening of my colon lining, but no blockages or life threatening issues, so I was discharged. with a prescription for Pepcid. I went to my PCP the next day, and she prescribed Prilosec. When that didn't provide relief, I went back to the hospital on Wednesday and was admitted until Friday, and discharged with gastritis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: 2,0
Labordaten: ultrasound, CAT scan, endoscopy, nuclear medicine tests on the gallbladder
Aktuelle Erkrankungen: 10/08/21 - 10/13/21 I experienced a raw sore throat, post nasal drip, low grade fever, chest heaviness. Tested negative for Covid, PCR test.
Vorgeschichte: High blood pressure, allergies, allergic rhinitis, and history of anaphylaxis to certain foods and Singulair medicine
Andere Medikamente: cetirizine 10 mg daily, metoprolol succinate 25 mg daily, multivitamin, culturelle probiotic
Allergien: Singulair, hazelnut, tree fruits, oak, dander, dust, mold, grass
Vorherige Impfungen: -

VAERS 1849374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: UT
Alter: 27,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Lethargy Lymphadenopathy Nausea Pain Pruritus

Symptomtext

The same day of the vaccine (2nd dose on 11/2/21) I had itchy palms and itchy feet for a few hours which is unusual for me. The following day I had body aches, a headache, swollen lymph nodes, and nausea. I also experienced lethargy. The nausea & lethargy lasted for a few days afterward. The lymph node under my ear, next to my jaw on the left side has been swollen since the first vaccine and rock hard. It has not decreased still (a month later).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None.
Allergien: None
Vorherige Impfungen: -

VAERS 1849323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MD
Alter: 55,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Extra dose administered Hypoaesthesia Injection site pain Pain in extremity Peripheral swelling Tenderness

Symptomtext

This Pfizer shot was my booster, after receiving the Janssen vaccine in March 2021. I had no adverse reactions to Jansseen but with this booster my left underarm has swollen, it is somewhat painful (not extreme) but very tender to touch. Basically, I have a small ball under my left arm. The injection site is a little tender but the real reaction seems to be underneath the arm/armpit. My entire left arm - at times, not consistently -feels a little numb. I received the booster shot two days ago and the symptoms are still with me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Thyroid NP (60 mg); DIM SGS +; iodine; ADK 10; Progesterone compounded (100 mg)
Allergien: None
Vorherige Impfungen: -

VAERS 1849118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Decreased appetite Disturbance in attention Fatigue Headache Insomnia Nausea Pain Sensory disturbance Swollen tongue Tinnitus

Symptomtext

Within 1 hr following vaccine, noticed mouth felt weird and tongue slightly swollen (took benedryl as precaution, no further swelling) Within 14 hrs of vaccine, felt all over general aches and joint pains, loss of appetite, trouble focusing on tasks but still able to complete them After 30 hrs, suffered insomnia (1 night), with shooting aches and pains and headache At ~ 40 hours the pains included loss of concentration, unfocus on tasks and unable to complete them, total loss of appetite, nausea, severe headache, tinnitus, severe body and joint aches and lethargy. At this point I cancelled my work day because I couldn?t function. The pain was miserable. Day 3 after vaccine - a little sore, aches in places that don?t usually ever hurt and usual spots hurting about double, a little tired, smaller appetite than usual but eating.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Pineapple, kiwi, mango, walnuts
Vorherige Impfungen: -

VAERS 1848650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: NE
Alter: 37,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dysphagia Flushing Hyperhidrosis Pruritus Throat tightness

Symptomtext

Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Flushed / Sweating-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1846843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: OH
Alter: 22,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Heart rate increased Hyperhidrosis Vomiting

Symptomtext

Patient began to become sweating and ended up throwing up about 10 minutes after the vaccination. The patient pulse was high, but never lost consciousness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sertraline 100 mg and Nuvaring
Allergien: No known medications
Vorherige Impfungen: -

VAERS 1845946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: RI
Alter: 48,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Lymph node pain Lymphadenopathy

Symptomtext

Swollen and painful lymph gland under left armpit

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity, hip arthritis, plantar fasciitis
Andere Medikamente: Aspirin, GABA, oil of oregano, turmeric curcumin with bioperine, vitamin D3, glucosamine, chondroitin, MSM, multivitamin, chelated iron, vitamin C
Allergien: Amoxicillin, aspartame, duck feathers, duck down, erythromycin, inulin, MSG, morphine, oxymetazoline HCl, penicillin, phenylalanine
Vorherige Impfungen: Chills, fever, body aches, fatigue, pain around site of injection

VAERS 1844710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: VA
Alter: 67,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site pruritus Nausea

Symptomtext

Itching and redness for 4 inches around injection site starting about an hour after injection. Nausea 1 day after injection. Still have mild nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Pre-diabetes Obesity S/P Pituitary adenoectomy
Andere Medikamente: Metformin,500 mg daily Hydrocortisone 10 mg daily Thyroxine 0.1 mg daily Glucosamine/Chondroitin Vitamin D 50,000 units weekly
Allergien: ? Aspirin Tape Allergy
Vorherige Impfungen: -

VAERS 1839610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: IL
Alter: 55,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Amnesia Blood test Computerised tomogram head Disturbance in attention Dizziness Feeling abnormal Headache Laboratory test Vision blurred

Symptomtext

Extreme headaches (progressive from 1st dose) Dizzy/haze/foggy feeling Loss of Memory/difficult focus & remembering simple things that I did before

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Emergency Room (Brain CT) Labs (blood) Shot of Toradol
Aktuelle Erkrankungen: High Blood Pressure
Vorgeschichte: Back (Mil) Upper Gastric Hearing Shoulder Blood Pressure Sleep Apnea (CPCP) Celiac Disease
Andere Medikamente: Lisinopril Nefedapine Rosuvastatin Tramadol
Allergien: Gluten
Vorherige Impfungen: -

VAERS 1837685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: VA
Alter: 35,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 31.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Peripheral swelling Pyrexia Rash Swelling Swelling face

Symptomtext

The day after 2nd dose of vaccine, pt reported fever and rash/swelling on face, torso, arms. Pt came to pharmacy and reported this 2 days after vaccine dose and no longer had fever but still had rash and some swelling. Pt was taking cetirizine to self treat. Pt was recommended to instead take diphenhydramine and follow up with urgent care, especially if reaction does not get better or gets worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Pt had fever after first pfizer dose

VAERS 1836805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MN
Alter: 66,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Interchange of vaccine products Nausea Pain Pyrexia Somnolence

Symptomtext

She had moderna for 1 and 2. Had pfizer for her booster on 10/29. Had low grade fever and achiness the day after. 17 hours later developed light headed, felt like she was going to pass out. Had some nausea. Felt like her blood pressure was really low. Checked her blood pressure a while later and her blood pressure was 96/64 - doesn't remember pulse. O2 was 96% and thinks pulse was in 80's on oximeter. She then fell immediately asleep and woke up 1.5 hours later and then felt much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Seen virtual visit 11/2/2021 but no testing done as feeling well now
Aktuelle Erkrankungen: NA
Vorgeschichte: intermittent SVT, osteopenia, idiopathic pancreatitis
Andere Medikamente: miralax, zenpep, tylenol prn, albuterol prn, melatonin 2.5mg at bedtime
Allergien: almonds, apples, cherries, penicillins
Vorherige Impfungen: -

VAERS 1834608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: VA
Alter: 41,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 26.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Axillary pain Extra dose administered Lymphadenopathy Malaise Pyrexia

Symptomtext

Robust swelling/pain noted in right armpit glands approximately 48 hours after vaccine received i right deltoid. Also feverish, achy joints, generally felt unwell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: migraines
Vorgeschichte: Hypercholestremia, hypertension, pancreatic/liver lesions, chronic pain
Andere Medikamente: Ibuprofen
Allergien: Grifulvin, Atorvastatin
Vorherige Impfungen: Jan 2021, received 1st and 2nd dose of Pfizer Covid 19 vaccine with low grade fevers, body aches, headaches etc following admini

VAERS 1834466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AZ
Alter: 71,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Body temperature increased Bone pain Extra dose administered Fatigue Feeling cold Malaise Myalgia Pain of skin

Symptomtext

Fourteen hrs after receiving the Covid booster vaccine, my bones, muscles and skin started hurting quite severely. At the same time I was freezing and my temp was 101.8. This came on very quickly and lasted 22 hours and for the next 24 hrs I was extremely fatigued. I have never felt so sick in my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Benazepril 40 mg Hydrochlorothiazide 25 mg Calcium One A Day Multiple Vitamin
Allergien: Pain Pills
Vorherige Impfungen: -

VAERS 1832297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: WA
Alter: 34,0
Geschlecht: M
Eingang: 31.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Dizziness Fatigue Headache Musculoskeletal stiffness Pain Pyrexia

Symptomtext

Severe fatigue Severe headache Fever Chills Whole body soreness Whole body stiffness Dizziness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes melitus Asthma Hypertension Persistent depressive disorder Generalized anxiety disorder
Andere Medikamente: Sertraline Hydrochloride 50mg Bupropion Hydrochloride ER 150mg Buspirone Hydrochloride 10mg Levocetirizine dihydrochloride 5mg Lisinopril 20mg Aripiprazole 2mg
Allergien: Sulfa Montelukast sodium
Vorherige Impfungen: -

VAERS 1832290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: KS
Alter: 45,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary mass Axillary pain

Symptomtext

Patient reported a dime size lump under the left arm ampit that is painful a day after the shot. No pain at the injection site. Pain worsened after putting an ice pak on it. Lump was not there prior to getting the covid booster shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: n/n
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1832099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NH
Alter: 53,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain upper Diarrhoea Injection site pain

Symptomtext

Approx. 4 hours after injection, I experienced terrible arm pain at injection site. Now 24 hours later, it's still there just not as bad. Approx. 12 hours after injection, I developed upper left abdomen pain which also happened last time with injection #2 Approx. 24 hours after injection, along with the abdomen pain, I developed diarrhea which also happened last time with injection #2 (in which I needed to go to the hospital & colitis had been found - no previous colitis & everything resolved in a month or so). Now approx. 28 hours after injection, the upper left abdomen pain is tolerable but the diarrhea is persistent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: SVT (Supraventricular Tachycardia) Diabetes 1.5 (Stable, not on meds at this time) NASH, NAFLD, Cirrhosis Hypotension Hypothyroid Hashimoto?s GERD IBS Osteoarthritis
Andere Medikamente: Levothyroxin Metoprolol Bayer Aspirin Crestor
Allergien: Medication allergies: Percocet, Dilaudid, Doxy, Clindamycin, PPI, Erythro, Augm, Amox, Macrobid, Budesonide
Vorherige Impfungen: -

VAERS 1831930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NY
Alter: 24,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Axillary pain Extra dose administered Fatigue Grip strength decreased Injection site pain Muscular weakness Myalgia Pain

Symptomtext

After booster shot, I woke up next morning with weakness in my left arm (injection arm). I had difficulty opening my medication bottle and experienced weakness throughout the day. Injection site was sore and tender (as it was for my previous shots). I had unusual sharp and dull pain in my left arm pit. I had muscle aches throughout my body, which subsided after taking Advil. Pain got worse as the day progressed and is still currently present. I also felt tired throughout the day (as I did after previous shots). The arm weakness and armpit pain did not occur after my first 2 doses though.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Sensory integration disorder, chronic fatigue syndrome (remission), andemia, hashimoto?s hypothyroidism, ADHD
Andere Medikamente: Vyvanse, propranolol, bupropion, levothyroxine, fish oil, vitamin D, vitamin B12, vitamin B2, feosol, Claritin, magnesium, melatonin
Allergien: -
Vorherige Impfungen: -

VAERS 1831906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Headache Influenza like illness Pain Skin discolouration

Symptomtext

Purple armpit and under arm. Flu like symptoms. Headache chills body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Pfizer covid 19 1st dose

VAERS 1831608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NJ
Alter: 48,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 28.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia Dizziness Lethargy

Symptomtext

I felt dizzy and lethargic after the shot but now I have lost my sense of taste less that 24 hours after taking the Pfizer. It is not listed as a side effect as I thought I would have much more adverse reaction due to the fact that my body does not agree with medicines and or drugs. But nothing I can do because I can?t afford to lose my job and be outcast from society.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lasinapril. Metformin
Allergien: Eggs protein
Vorherige Impfungen: -

VAERS 1829115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 84,0
Geschlecht: M
Eingang: 29.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Myalgia

Symptomtext

Extreme muscular soreness, left shoulder and arm, not specifically at the site of the injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: COVID-19 booster shot
Aktuelle Erkrankungen: None
Vorgeschichte: Gaucher's Disease, Gilbert Syndrome, High Blood Pressure, Glaucoma, Osteoporosis
Andere Medikamente: Lisinopril, Timolol and multivitamins taken earlier in the day.
Allergien: None
Vorherige Impfungen: Flu vaccine 1962

VAERS 1828770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MD
Alter: 48,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site swelling Lymphadenopathy

Symptomtext

Swelling under arm and at injection site and redness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hbp, asthma, pre diabetes
Andere Medikamente: Daily vitamin, notethindrone, estradiol, vitamin d3, biotin, lisinopril hctz.
Allergien: N/a
Vorherige Impfungen: Pfizer 3/10/21, 4/7/21 age 48. Injection

VAERS 1826442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MA
Alter: 44,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Erythema Injection site erythema Injection site mass Injection site pain Injection site pruritus Injection site swelling Pruritus

Symptomtext

Severe itching that started at injection site to my whole body. Pain, swelling, redness, and lump at injection site also. Noticed a big red circle on opposite arm (left) that was very itchy. The itching started maybe an hour or so when I took bandaid off after injection to present, just not as bad. Took Benedryl per pharmacist and spoke with triage nurse at doctor's office. Also been in contact w/ Dr. via portal. Advised to call office the next am if needed (too late to be seen) and/or go to ER if throat closes or sob. Dr. Sent script for Hydroxyzine for the itching. As of today, 10/23, feeling much better. Some itching but very mild. Lump on arm going down as well as redness and swelling. Left arm appears to have improved also.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety/Depression, GERD, HBP, Endometriosis, CKD, Gallstones, Migraines, history of kidney stones, history of PEs, Factor VIII, previous diagnosed w/ Left Ventricular Hypertrophy while treated for PEs.
Andere Medikamente: Aspirin Pantoprazole Bupropion Paroxetine Lorazepam Verapamil Potassium Citrate Norethindrone BCP Hydrochlorothiazide Vitamin B6 Vitamin B12
Allergien: Morphine, Lactose Intolerant
Vorherige Impfungen: -

VAERS 1826308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: -
Alter: 29,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 22.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Fatigue Headache

Symptomtext

Headache, fatigue begginning several hours after the injection around 6:00 pm lasting until the next morning

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cold
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1825847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 27.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dizziness Hypoaesthesia Hypoaesthesia oral Laboratory test Neurological symptom

Symptomtext

Patient experienced dizziness, numbness of tongue/mouth and spreading to body, stroke-like symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Patient had tests done in er on 10/27/21 and tests ordered by md on 10/28/21. Results are not reported to pharmacy.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: High blood pressure, diabetes, hypothyroidism
Andere Medikamente: Farxiga 10mg, Levothyroxine 88mcg, Losartan 50mg, Metformin 500mg, Zylet ophth drops
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1825397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: FL
Alter: 49,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 26.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Discomfort Lymphadenopathy Sleep disorder

Symptomtext

Severe pain in armpit (right arm), apparently lymph nodes are swollen. This pain woke me up out of my sleep and is severe. The skin appears normal and is not impacted, however the pain is severe below skin surface and not able to get comfortable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Chronic back and neck pain
Andere Medikamente: Hydrocodone, Flexeril, Alprazalom, Zolpidem
Allergien: NA
Vorherige Impfungen: -

VAERS 1824855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: DC
Alter: 57,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 19.10.2021
Beginn: 19.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Injection site pain Insomnia Joint range of motion decreased Loss of personal independence in daily activities Pain

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: pain and limited range of motion-Medium, Systemic: Joint Pain-Medium, Systemic: Unable to Sleep-Medium, Additional Details: Per patient...his head was turned while vaccine was given, but complained to nurse that it hurt really badly and pain continued for next 48hrs and affected his sleep and daily activities. Now the pain is a 3 out of 10 (worst), but it radiates from his shoulder to his wrist even at rest. He has limited range of motion. He believes vaccine was given in shoulder nerves and not deltoid and nerves damaged. He wants $5K from pharmacy for his time for doctor visits he may need. He has not seen doctor yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1820976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MS
Alter: 47,0
Geschlecht: M
Eingang: 27.10.2021
Impfdatum: 25.10.2021
Beginn: 26.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Body temperature increased Diarrhoea Fatigue Headache Pain

Symptomtext

woke up Tuesday am with 102F (orally), generalized body aches, fatigue, headache and diarrhea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1818381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 23.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Urticaria

Symptomtext

Patient showed hives on both of her upper thighs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1814800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: WI
Alter: 51,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Headache Myalgia

Symptomtext

Headache. Severe, crippling muscle pain and weakness throughout entire body. Started about 11:30 pm Friday 10/22/2021 lasted until Monday 10/25/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, High BP, Cholesterol, Chronic back lumbar back pain w\bilateral leg pain. neuropathy, Raynaud disease
Andere Medikamente: Omeprazole, Gabapentin, Lisinopril, Fenofibrate, Diazepam, Nadolol, Cyclobenzapr, Jardiance, Lavaza
Allergien: Pravastatin, Relpax, Effexor, Savella, Cymbalta, Amitryptline, Atorvostatin, Meloxicam, Topamax, Livalo
Vorherige Impfungen: -

VAERS 1814203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CO
Alter: 53,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Chills Headache Nausea Pyrexia Vomiting

Symptomtext

Shot received morning of 10/21. Mild headache developed evening of 10/21. Morning of 10/22, headache became severe and fever developed. Began at 99F and climbed throughout day; reached 103.6 overnight 10/22. Chills, weakness, and very severe headache. Fever broke morning of 10/23, but severe headache continued. Nausea and vomiting during day 10/23. Severe headache and nausea continued overnight and through 10/24. Fluids, ice, and NSAIDs did not provide any relief from headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, obesity, depression
Andere Medikamente: Wellbutrin Duloxetine Gabapentin Klonopin Trileptal
Allergien: Zythromycin
Vorherige Impfungen: -

VAERS 1814187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: UT
Alter: 47,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 22.10.2021
Beginn: 23.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Induration Lymph node pain Lymphadenopathy Pain in extremity

Symptomtext

The lymph nodes under my left arm haven swollen up and become hard and painful. It hurts to lower my arm or have any pressure there at all. The entire area under my arm is swollen and protruding. It is much worse than a typical swollen lymph node when getting sick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid arthritis
Andere Medikamente: Diclophenac, hydroxychloroquine, escitalipram
Allergien: Penicillins, amoxicillin, keflex
Vorherige Impfungen: -

VAERS 1814185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: UT
Alter: 52,0
Geschlecht: M
Eingang: 24.10.2021
Impfdatum: 22.10.2021
Beginn: 22.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site pain

Symptomtext

Arm pain at and around injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/a
Vorgeschichte: Celiac
Andere Medikamente: Naproxen
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1813984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: AR
Alter: 50,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 22.10.2021
Beginn: 24.10.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood glucose increased Fatigue Oral contusion Tongue biting Urinary incontinence Vomiting

Symptomtext

Woke this morning with a brused tongue (bitten), vomited. Patient also said she had urinated on herself while sleeping. vomited a few more times after. Felt really tired all day after that. Patient states her blood sugar was a little high as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: high blood sugar (in the 200's)
Aktuelle Erkrankungen: none
Vorgeschichte: diabetes, Heart disease, triple bypass
Andere Medikamente: Clopidogrel, lisinopril, ozempic 1mg, 2 tylenol 325mg, novolog,
Allergien: gluten intolerance,
Vorherige Impfungen: -

VAERS 1813782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

mild

Staat: KS
Alter: 55,0
Geschlecht: F
Eingang: 24.10.2021
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chills Dizziness Headache Pain in extremity Pharyngeal swelling Swollen tongue

Symptomtext

Within the first 24 hours: Chills, sore arm, mild headach, and light-headed. On Tuesday 10/19/2021, the same side effects continued. On Wednesday, 10/20/21, patient had to go to ER because throat began to swell. Went to ER twice that day. On Thursday, patient went to ER twice again. On Friday, patient again returned to the ER. On Saturday, patients throat and tongue began to swell. On Saturday, patient picked up an epi-pen and prednisone from the pharmacy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: obesity, high blood pressure
Andere Medikamente: hydroxychloroquine 200 mg tablet, potassium 8meq tablet, ezetimibe 10mg tablet, carvedilol 6.25mg tablet, Vitamin C 250mg tablet, aspirin 81mg tablet, atorvastatin 80mg tablet, and Lotrel 5/10 capsule.
Allergien: nkda
Vorherige Impfungen: -

VAERS 1807985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: PA
Alter: 33,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Pruritus

Symptomtext

Patient started itching about 15 to 20 minutes after injection was given. She was immediately give diphenhydramine hcl capsule (25mg) but when the reaction continues, intramuscular diphenhydramine hcl 50mg/ml (0.5ml) was injected on her right deltoid muscle. The adverse effect stopped about 30 minutes after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: NONE
Vorgeschichte: ANXIETY
Andere Medikamente: UNKNOWN
Allergien: NO KNOWN ALLERGY
Vorherige Impfungen: -

VAERS 1804320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: NY
Alter: 84,0
Geschlecht: M
Eingang: 21.10.2021
Impfdatum: 21.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Vomiting

Symptomtext

Vomiting uncontrollably

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: APAP 325 mg Amlodipine 5 mg Atorvastatin 10 mg Bupropion 75 mg Docusate 100 mg Donepezil 10 mg Fenofibrate 145 mg Memantine ER 28 mg Montelukast 10 mg
Allergien: -
Vorherige Impfungen: -

VAERS 1801779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: CA
Alter: 19,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 20.10.2021
Beginn: 20.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Feeling cold Vomiting

Symptomtext

Patient received his first dose of Pfizer COVID-19 vaccine and about ten minutes after, he reported light-headedness and felt cold. Shortly after, he started throwing up. He felt better after throwing up and had paramedics check him before he was safely released to go home from the pharmacy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1800760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: MA
Alter: 26,0
Geschlecht: F
Eingang: 20.10.2021
Impfdatum: 17.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Menstrual disorder

Symptomtext

Started having my period, which I don?t normally have at all because of my birth control. I haven?t missed a pill or had anything else that would cause this (not sexually active, live alone). Also have had abdominal pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine, high blood pressure, asthma, PMDD, MDD, ADHD
Andere Medikamente: Ashlyna birth control, 0.5 mg melatonin, omeprazole, wellbutrin 150mg XR, vyvanse 30 mg, prazosin 2 mg, propranolol 80mg, Botox 200 units every 60 days, 2 capsules of ritual brand multivitamins
Allergien: None
Vorherige Impfungen: -

VAERS 1787900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

mild

Staat: PR
Alter: 69,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 08.10.2021
Beginn: 09.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site erythema Injection site induration

Symptomtext

Area red and hard.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2716066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 21.11.2023
Impfdatum: 09.11.2021
Beginn: 13.06.2022
Tage bis Beginn: 216,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; Dose #1: Pfizer/ Dose#2: Pfizer/ Dose #3: Pfizer/ Dose #4: Moderna; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 66-year-old male patient received bnt162b2 (BNT162B2), on 26Mar2021 as dose 1, single (Lot number: ER8727), on 18Apr2021 as dose 2, single (Lot number: EW0161) and on 09Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 64 years for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 13Jun2022 as dose 4 (booster), single (Lot number: 014B22A) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. No known allergies. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 13Jun2022, outcome "recovered", described as "Dose #1: Pfizer/ Dose#2: Pfizer/ Dose #3: Pfizer/ Dose #4: Moderna"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovered" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid from 26Oct2023 to 31Oct2023. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2713546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CT
Alter: -
Geschlecht: F
Eingang: 14.11.2023
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

COVID-19; COVID-19; Dose Number: 1 and Dose Number: 2: Moderna; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 63-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 29Oct2021 as dose 3 (booster), single (Lot number: 320308D) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 12Jan2021 as dose 1, single (Lot number: 013420A), on 09Feb2021 as dose 2, single (Lot number: 016M20A), on 08Apr2022 as dose 4 (booster), single (Lot number: 065K21A) and on 13Sep2022 as dose 5 (booster), single (Lot number: AS7144B), in left arm for covid-19 immunisation; elasomeran (SPIKEVAX), on 02Oct2023 at 10:00 as dose 6 (booster), single (Lot number: AU3832B), in left arm for covid-19 immunisation. The patient's relevant medical history included: "HTN" (unspecified if ongoing); "Hyperlipidemia" (unspecified if ongoing); "Multinodular Goiter" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 29Oct2021, outcome "unknown", described as "Dose Number: 1 and Dose Number: 2: Moderna"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Oct2023, outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19: the patient received treatment with Paxlovid from 26Oct2023 to 30Oct 2023 (lot number GJ7157).; Sender's Comments: The contributory role of the suspect product to the reported event drug ineffective cannot be excluded as the efficacy of a drug varies individually and may be affected by different factors including drug potency. Considering interchange of vaccine, the contributory role of company suspect drug BNT162b2 to all the reported events drug ineffective, covid-19 cannot be excluded completely.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hyperlipidemia; Hypertension; Multinodular goiter
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2707063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: WA
Alter: 47,0
Geschlecht: M
Eingang: 31.10.2023
Impfdatum: 18.10.2021
Beginn: 15.03.2022
Tage bis Beginn: 148,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Interchange of vaccine products SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; Dose #1: Pfizer/ Dose #2: Pfizer/ Dose #3: Pfizer/ Dose #4: Moderna/ Dose #5: Moderna; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old male patient received bnt162b2 (BNT162B2), on 24Mar2021 as dose 1, single (Lot number: ER8732), in left arm, on 14Apr2021 as dose 2, single (Lot number: EW0161), in left arm and on 18Oct2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 47 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 15Mar2022 as dose 4 (booster), single (Lot number: 048L21A), in left arm and on 15Sep2022 as dose 5 (booster), single (Lot number: AS7145B), in left arm for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Penicillin" (unspecified if ongoing); "known allergies: sulfa drugs" (unspecified if ongoing); "known allergies: cashews, Peanuts, tree nuts" (unspecified if ongoing); "Seasonal allergies" (unspecified if ongoing); "pre-diabetes" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Zithromax, reaction(s): "known allergies: Zithromax". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 15Mar2022, outcome "unknown", described as "Dose #1: Pfizer/ Dose #2: Pfizer/ Dose #3: Pfizer/ Dose #4: Moderna/ Dose #5: Moderna"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: product- COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19 with Paxlovid from 14Oct2023 to 18Oct2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Treatment of COVID-19; Test Result: Positive ; Comments: product- COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts; Penicillin allergy; Pre-diabetes; Seasonal allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2705242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 28.10.2023
Impfdatum: 08.11.2021
Beginn: 15.10.2023
Tage bis Beginn: 706,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 08Nov2021 as dose number unknown, single (Lot number: 320308D) at the age of 33 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 15Oct2023, outcome "not recovered" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2674170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 21.08.2023
Impfdatum: 01.11.2021
Beginn: 03.01.2022
Tage bis Beginn: 63,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Hypersensitivity

Symptomtext

ALLERGIC REACTION, INIT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypersensitivity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: -
Geschlecht: M
Eingang: 11.07.2023
Impfdatum: 16.01.2021
Beginn: 23.11.2022
Tage bis Beginn: 676,0
Dosis: 4
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID positive test; COVID positive test; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 73-year-old male patient received BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FN2908) for 1 day, in left arm, as dose 3 (booster), single (Lot number: 320308D) for 1 day, in left arm, as dose 2, single (Lot number: EM98910) for 1 day, in left arm, on 16Jan2021 as dose 1, single (Lot number: EL8982), in left arm and (Batch/Lot number: unknown) for COVID-19 immunisation. The patient's relevant medical history included: "Heart failure" (unspecified if ongoing). Concomitant medications included: ALOPURINOL; CALCIUM; DAILY VITAMINS; OMEPRAZOLE. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 23Nov2022, outcome "unknown" and all described as "COVID positive test". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (23Nov2022) Positive. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300245529 same patient and drug; different dose and event;US-PFIZER INC-202300247071 same patient and drug; different dose and event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221123; Test Name: COVID-19 test (nasal swab); Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Heart failure
Andere Medikamente: ALOPURINOL; CALCIUM; DAILY VITAMINS; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2650818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 29.06.2023
Impfdatum: 19.10.2021
Beginn: 23.11.2022
Tage bis Beginn: 400,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 3/11/21 lot# EN6207; Pfizer 4/1/21 Lot#Er8732; Pfizer 10/19/21 lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2645279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 14.06.2023
Impfdatum: 18.11.2021
Beginn: 20.01.2023
Tage bis Beginn: 428,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 2 vaccines Janssen 3/18/21 lot# 1802068; Pfizer 11/18/21 Lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2639137

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 31.05.2023
Impfdatum: 23.10.2021
Beginn: 16.08.2022
Tage bis Beginn: 297,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 2 vaccines Pfizer 3/24/21 lot# EN6204; Pifzer 10/23/21 lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2626565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MO
Alter: 77,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 03.11.2021
Beginn: 25.03.2023
Tage bis Beginn: 507,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Unevaluable event

Symptomtext

Unknown. Unable to speak with case due to hospitalization on 03/25/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Unknown. Unable to speak with case due to hospitalization on 03/25/2023.
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2623985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 20.05.2022
Beginn: 21.08.2022
Tage bis Beginn: 93,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Obstructive sleep apnoea syndrome

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE OBSTRUCTIVE SLEEP APNEA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2619807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MO
Alter: 91,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 11.11.2021
Beginn: 17.04.2023
Tage bis Beginn: 522,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Unevaluable event

Symptomtext

Unable to complete case investigation or speak with case due to hospitalization.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2619475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: IL
Alter: 61,0
Geschlecht: M
Eingang: 23.04.2023
Impfdatum: 26.10.2021
Beginn: 27.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tinnitus

Symptomtext

Rapid increase/onset of bilateral tinnitus on the morning after my second COVID-19 booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: audiologist visit/hearing examination 4/27/21 in response to persistent, mild tinnitus found no structural/medical issue
Aktuelle Erkrankungen: none
Vorgeschichte: mild hypertension mycosis fugoides (in remission since 2008)
Andere Medikamente: 81 mg children's aspirin daily 10 mg lisinopril daily 2 puffs/nostril fluticasone daily 50 mcg vitamin D3 daily
Allergien: none
Vorherige Impfungen: -

VAERS 2614096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 15.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 15May2021 as dose 1, single (Lot number: FW0172), in left arm and on 15Nov2021 as dose 2, single (Lot number: 320308D) at the age of 55 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing); "Multiple Sclerosis" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing); "pre-diabetes" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Ceftriaxone, reaction(s): "Known allergies: Ceftriaxone". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of drug ineffective, covid-19.; Sender's Comments: Based on available information, a lack of efficacy with the suspect vaccine BNT162B2 in this patient cannot be completely excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism; Multiple sclerosis; Penicillin allergy; Pre-diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2604861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MO
Alter: 73,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 31.10.2022
Beginn: 24.03.2023
Tage bis Beginn: 144,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Unevaluable event

Symptomtext

unable to speak with case due to hospitalization on 0324/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 3,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2597558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: FL
Alter: 27,0
Geschlecht: F
Eingang: 16.03.2023
Impfdatum: 04.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Activated partial thromboplastin time Appendicectomy Appendix disorder Blood glucose Blood test Body temperature increased Culture urine Differential white blood cell count Fear Feeling abnormal Full blood count Gingival swelling Magnetic resonance imaging normal Pollakiuria Pregnancy test urine Prothrombin time SARS-CoV-2 test Swelling

Symptomtext

Hours after receiving the first dose the left side of my tongue began to swell, along with my gum on the left side of my face, it eventually subsided. However four days after my appendix began to swell and I was rushed into an emergency surgery where it had to be removed. I shared my concern with all the doctors attending to me at Hospital that the vaccine caused the swelling within my body and every one of them dismissed my concern regarding the allergic reaction. I was released after surgery and was scared to take the second dose, none of the doctors documented my concerns so I reluctantly took the second dose 2 weeks later. When I returned more symptoms began to develop. I started to pee way more frequently than normal, my body temperature was always higher than normal and between October 2021 to January 2022 I lost a lot of weight. My doctor ordered me to do a MRI and ultrasound which both returned normal however the symptoms remained until around March of 2022 when I began to feel like myself again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Activated partial thromboplastin time
Hospital-Tage: 2,0
Labordaten: 10/08/2021 2:05 PM 10/08/2021 2:14 PM CBC WITH DIFFERENTIAL 10/08/2021 2:05 PM 10/08/2021 2:18 PM UA W/Cult Reflex 10/08/2021 2:05 PM 10/08/2021 2:45 PM Biochemical Profile (BP-12) 10/08/2021 3:14 PM 10/08/2021 3:15 PM POC UR PREG 10/08/2021 3:48 PM 10/08/2021 4:06 PM Prothrombin Time (PT) 10/08/2021 3:48 PM 10/08/2021 4:06 PM Activated PTT 10/08/2021 3:48 PM 10/08/2021 4:16 PM COVID19 AG NPUI 10/09/2021 12:31 AM 10/09/2021 12:32 AM Glucose by Monitoring Device 10/09/2021 4:59 AM 10/09/2021 6:43 AM Biochemical Profile (BP-7) 10/09/2021 4:59 AM 10/09/2021 6:58 AM CBC WITH DIFFERENTIAL
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2592440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

gering

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 07.03.2023
Impfdatum: 07.11.2021
Beginn: 06.03.2023
Tage bis Beginn: 484,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 3/4/21 Pfizer Lot# EN62052; Pfizer 3/25/21 Lot# EP6955; Pfizer 11/7/21 Lot# 320308d

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2589981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 63,0
Geschlecht: F
Eingang: 02.03.2023
Impfdatum: 26.10.2021
Beginn: 09.05.2022
Tage bis Beginn: 195,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Pfizer vaccine: 26Oct2021 and Moderna vaccine: 09May2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Oct2021 as dose number unknown, single (Lot number: 320308D) at the age of 63 years for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 09May2022 as dose number unknown, single (Lot number: 057M21A) for covid-19 immunisation. The patient's relevant medical history included: "IBS" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 09May2022, outcome "unknown", described as "Pfizer vaccine: 26Oct2021 and Moderna vaccine: 09May2022"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Feb2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Irritable bowel syndrome
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 10.11.2021
Beginn: 23.04.2022
Tage bis Beginn: 164,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 3/8/21 Lot# EN6299 ; Pfizer 3/29/21 Lot# Er8732; Pfizer 11/10/21 Lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2554678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 19.11.2021
Beginn: 05.01.2023
Tage bis Beginn: 412,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 3/18/21 Lot# EN6207; Pfizer 4/8/21 Lot# ER8732; Pfizer 11/19/21 Lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2552486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge 320308D

gering

Staat: AZ
Alter: 79,0
Geschlecht: M
Eingang: 06.01.2023
Impfdatum: 26.10.2022
Beginn: 16.12.2022
Tage bis Beginn: 51,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 test positive

Symptomtext

Tested positive for Covid on December 16. My wife also tested positive on that date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: At home Covid test on 12/16/2022. My wife had her Covid test in the doctor's office. She still tested positive on January 3., 2023.
Aktuelle Erkrankungen: None
Vorgeschichte: Pace Maker for Sinus Bradycardia, Glaucoma
Andere Medikamente: Atorvastatin, Lumigan, Timolol, Oxybutyin, Pepcid, MultiVitamin, Fish Oil, Glucosamine, Aspirin,
Allergien: Mild allergy to penicillin
Vorherige Impfungen: -

VAERS 2518795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 86,0
Geschlecht: F
Eingang: 29.11.2022
Impfdatum: 16.11.2021
Beginn: 26.11.2022
Tage bis Beginn: 375,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after three vaccines Pfizer 2/10/21 Lot# EL9267; Pfizer 3/3/21 Lot# En6205; Pfizer 11/16/21 Lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2515333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 20.11.2021
Beginn: 22.11.2022
Tage bis Beginn: 367,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after three vaccines Pfizer 4/9/21 Lot# EW0150; Pfizer 4/30/21 Lot# EW0172; Pfizer 11/20/21 Lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2514035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 61,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 14.10.2022
Beginn: 12.11.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test positive

Symptomtext

Positive COVID test on 11/14/22 (first symptoms 11/12/22)

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home COVID test 11/14/22
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Zyrtec (Cetirizine Hdrochloride 10mg), Psyllium Husk capsules 1,500 mg), Multivitamin with Biotin Collagen Keratin B Vitamins and Bamboo Extract, "Full Spectrum" CBD oil
Allergien: Steroids, all caines, nickel, methylparaben
Vorherige Impfungen: -

VAERS 2512596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 50,0
Geschlecht: M
Eingang: 20.11.2022
Impfdatum: 02.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Blood glucose increased Electromyogram abnormal Glycosylated haemoglobin increased Hyperglycaemia Impaired work ability Muscular weakness Neuropathy peripheral Type 2 diabetes mellitus

Symptomtext

I developed acute onset hyperglycemia. On 11/21/21 I was diagnosed with type II diabetes with a fasting glucose of 369 and HbA1C of 9.9. Subsequently I have also developed acute onset neuropathy of unknown etiology. Neuropathy has continued to worsen over the last year resulting in significant weakness that involve bilateral lower legs and arms resulting in difficulty with work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood glucose increased
Hospital-Tage: -
Labordaten: Fasting sugars and HbA1C abnormal EMG findings consistent with severe neuropathy
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2510907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 30.11.2021
Beginn: 12.11.2022
Tage bis Beginn: 347,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after three vaccines Pfizer 3/18/21 Lot# EN6207; 4/13/21 Pfizer Lot# Ew0158; Pfizer 11/30/21 Lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: external COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2499741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CT
Alter: 57,0
Geschlecht: M
Eingang: 05.11.2022
Impfdatum: 27.10.2021
Beginn: 19.08.2022
Tage bis Beginn: 296,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; Vaccine brand other: Moderna,Vaccine administration date: 19Aug2022; Vaccine brand: Pfizer / BioNTech, Vaccine administration date: 27Oct2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 58-year-old male patient received BNT162b2 (BNT162B2), on 27Oct2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 57 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 19Aug2022 as dose 4 (booster), single (Lot number: 053B22A), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Celiac disease" (unspecified if ongoing), notes: other medical history: Celiac Sprue. There were no concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 19Aug2022, outcome "not recovered", described as "Vaccine brand other: Moderna,Vaccine administration date: 19Aug2022; Vaccine brand: Pfizer / BioNTech, Vaccine administration date: 27Oct2021"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 01Nov2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (26Oct2022) Negative; (01Nov2022) Positive; (unspecified date) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: It was reported that, other medication in 2weeks was No. It was reported that, the patient was tested positive again 01Nov2022 after negative test 26Oct2022. Symptoms worse-sinus and chest infection. No known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221026; Test Name: Covid test; Test Result: Negative ; Test Date: 20221101; Test Name: Covid test; Test Result: Positive ; Test Name: Covid-19 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Celiac disease (other medical history: Celiac Sprue)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

gering

Staat: CA
Alter: 64,0
Geschlecht: M
Eingang: 02.11.2022
Impfdatum: 06.11.2021
Beginn: 30.04.2022
Tage bis Beginn: 175,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Interchange of vaccine products SARS-CoV-2 test Vaccination failure

Symptomtext

COVID-19; COVID-19; vaccine brand other=Moderna; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 65-year-old male patient received BNT162b2 (BNT162B2), on 11Mar2021 at 09:00 as dose 1, single (Lot number: El3247), in left arm, on 08Apr2021 at 09:00 as dose 2, single (Lot number: Ew0151), in left arm and on 06Nov2021 at 12:00 as dose 3 (booster), single (Lot number: 320308d) at the age of 64 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 30Apr2022 at 12:00 as dose 4 (booster), single (Lot number: 056m21a), in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 30Apr2022, outcome "unknown", described as "vaccine brand other=Moderna"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: COVID 19 Treatment; (18Oct2022) Negative, notes: a negative test on 18Oct2022; (28Oct2022) Positive, notes: Tested positive with symptoms 10 days after last dose of Paxlovid. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient received Paxlovid from 13Oct2022 to 18Oct2022 for treatment of COVID-19. Paxlovid rebound. Patient was tested positive with symptoms 10 days after last dose of Paxlovid and a negative test on 18Oct2022. Event did not resulted in emergency room visit or physician office visit. No treatment received for Paxlovid rebound. No known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Virus test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 20221018; Test Name: COVID-19 Virus test; Test Result: Negative ; Comments: a negative test on 18Oct2022; Test Date: 20221028; Test Name: COVID-19 Virus test; Test Result: Positive ; Comments: Tested positive with symptoms 10 days after last dose of Paxlovid
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2494094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 22.10.2021
Beginn: 29.10.2022
Tage bis Beginn: 372,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after three vaccines Pfizer 2/22/21 Lot# EN6200; Pfizer 3/25/21 Lot# EN6199; Pfizer 10/22/21 Lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: AK
Alter: 40,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 03.12.2021
Beginn: 01.08.2022
Tage bis Beginn: 241,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 41-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 03Dec2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 40 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 08Jan2021 as dose 1, single (Lot number: 029L20A), in left arm and on 06Feb2022 as dose 2, single (Lot number: 029L20A), in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ARMOUR THYROID. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "recovering" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19; Positive, notes: Positive rapid Ag test after 2 negative tests 48hrs apart; Negative, notes: Positive rapid Ag test after 2 negative tests 48hrs apart; Negative, notes: Positive rapid Ag test after 2 negative tests 48hrs apart. Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Name: rapid Ag test; Test Result: Positive ; Comments: Positive rapid Ag test after 2 negative tests 48hrs apart; Test Name: rapid Ag test; Test Result: Negative ; Comments: Positive rapid Ag test after 2 negative tests 48hrs apart; Test Name: rapid Ag test; Test Result: Negative ; Comments: Positive rapid Ag test after 2 negative tests 48hrs apart
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ARMOUR THYROID
Allergien: -
Vorherige Impfungen: -

VAERS 2440796

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 320308D

gering

Staat: MN
Alter: 39,0
Geschlecht: M
Eingang: 12.09.2022
Impfdatum: 03.12.2021
Beginn: 07.09.2022
Tage bis Beginn: 278,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient vaccinated against then tested positive for COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 30.11.2021
Beginn: 29.08.2022
Tage bis Beginn: 272,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Inappropriate schedule of product administration SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 2 vaccines Pfizer 9/15/21 Lot# FF2588; Pfizer 11/30/21 Lot# 320308D

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2421048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: KS
Alter: 36,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product administration error

Symptomtext

This is an administration error in which the patient did not report any adverse events. The patient's first covid vaccine was Janssen administered on 03/25/2021 and she received Pfizer on 06/28/2021. Patient received 0.3 mL of Pfizer (booster) after receiving J&J as primary series before booster had been approved for the general population. On the consent form, the patient had indicated that she had never received a covid19 vaccine prior. Patient then returned on 10/31/2021 to complete the pfizer series (prior J&J vaccine still unknown by pharmacy staff) to which she did receive a 2nd dose. It was disclosed to the pharmacy today, 8/26/22, that she had originally received her first vaccine in March of 2021 resulting in 2 administration errors and patient receiving a booster at 2 separate occasions in which they were not yet approved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administration error
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2409508

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: AL
Alter: -
Geschlecht: U
Eingang: 12.08.2022
Impfdatum: 28.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Investigation Therapeutic response unexpected

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 84-year-old patient received BNT162b2 (BNT162B2), on 28Oct2021 as dose 3 (booster), single (Lot number: 320308D) for covid-19 immunisation. The patient's relevant medical history included: "canker sores in my mouth and on my tongue " (unspecified if ongoing), notes: I have had canker sores in my mouth and on my tongue on a constant basis. This began as young as 4 years old. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose: 1, Lot: EL1283), administration date: 01Feb2021, for COVID-19 immunization, reaction(s): "a potential solution to the treatment of Canker Sores"; BNT162b2 (Dose: 2, Lot: EN6210), administration date: 22Feb2021, for COVID-19 immunization, reaction(s): "a potential solution to the treatment of Canker Sores". The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "unknown", described as "a potential solution to the treatment of Canker Sores". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Almost all my life I have had Canker Sores in my mouth and on my tongue on a constant basis. This began as young as 4 years old. Through my childhood I was examined and treated by several Dentist. There were times the Dentist told me and my Parents that I had as many as 21 Canker Sores with some of them as large as a Dime. They could never eliminate them. Through my adult life this continued and caused me extreme discomfort. I always have had at least 4 to 5 Canker Sores in my mouth. I was born and raised in (withheld) and over the years have lived in (addresses withheld). Since the Vaccinations I have only had 3 Canker Sores and all 3 occurred where I bit my cheek or tongue while eating. I thought you might be interested in this as a potential solution to the treatment of Canker Sores. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Investigation
Hospital-Tage: -
Labordaten: Test Name: examined; Result Unstructured Data: Test Result: Unknown results; Comments: Through my childhood I was examined and treated by several Dentist.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Canker sores oral (have had canker sores in my mouth and on tongue on a constant basis. began as young as 4 years old.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2408243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 49,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 25.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Oct2021 as dose 2 (booster), single (Lot number: 320308D) at the age of 49 years for covid-19 immunisation; janssen coviD-19 vaccine (JANSSEN COVID-19 VACCINE), on 01Apr2021 as dose 1, single (Lot number: 042A21A) for covid-19 immunisation. The patient's relevant medical history included: "seronegative spondyloarthropathy" (unspecified if ongoing), notes: Other medical history: seronegative spondyloarthropathy. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Spondyloarthropathy (Other medical history: seronegative spondyloarthropathy)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2395857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: -
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: 10.11.2021
Beginn: 20.06.2022
Tage bis Beginn: 222,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Body temperature COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

he believe we got it from the hospital/we tested, we got the results of COVID test/we got the result on 22 which was positive; he believe we got it from the hospital/we tested, we got the results of COVID test/we got the result on 22 which was positive; This is a spontaneous report received from contactable reporter(s) (Nurse). A male patient received BNT162b2 (BNT162B2), on 11Feb2021 as dose 1, single (Lot number: EL9262), on 08Mar2021 as dose 2, single (Lot number: EN6199) and on 10Nov2021 as dose 3 (booster), single (Lot number: 320308D) for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 20Jun2022, outcome "unknown" and all described as "he believe we got it from the hospital/we tested, we got the results of COVID test/we got the result on 22 which was positive". The event "he believe we got it from the hospital/we tested, we got the results of covid test/we got the result on 22 which was positive" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Jun2022) Positive, notes: we got the test on 20Jun2022 and we got the result on 22Jun2022; Body temperature: (Jun2022) had a slight rise in temperature. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Unfortunately that the patient's wife believed and he (physician) believed he and his wife got it from the hospital. The patient was in the emergency in 05Jun2022 to 15Jun2022 because the patient's wife had been in the emergency. The patient was discharged on the 20Jun2022, he spent days in the hospital. On 20Jun2022, Monday, the patient's wife decided to move back from the emergency. On 20Jun2022, the patient had been discharged. On 20Jun2022, they had flu like symptoms like runny nose, sore throat and something like that they thought may be like and they thought it was like sinus and the patient's wife doctor told that the patient got the Covid test, the patient's wife did not really have a lot of symptoms but the patient had a slight rise in temperature, so they got the test on 20Jun2022 and they got the result on 22Jun2022. They started to have symptoms on 20Jun2022 and they tested, they got the results of COVID test on 22Jun2022, they got the result on 22Jun2022 which was positive, so they received it while they were at the hospital, so they received it together at the hospital. The patient was admitted in the emergency room at the hospital before they got the symptoms. Anyway the patient's wife told her primarily physician doctor, the patient did not get any kind of that because they ordered the request at Pharmacy. What happened was the patient did not get the nirmatrelvir; ritonavir (PAXLOVID) even if he did have a prescription for him but he never got it because the pharmacist told him that there was drug interaction which considered severe if the patient was taking anything but the physician had an prescription for the patient's wife. The patient never got nirmatrelvir; ritonavir from the guy. The patient wanted to go ahead and take nirmatrelvir; ritonavir but he never did the drug because there was such a big issue with drug interaction because the pharmacist, nobody told the doctor, the patient's wife knew he (pharmacist) did what he said, he said the ways into the benefit and the patient was taking some hmg coa reductase inhibitors (STATINS) and he was taking some flomax (name of medication not clarified). The patient's wife was so glad because the patient was not into that, the patient's wife was the one, that was strongly suggested to take nirmatrelvir; ritonavir.; Sender's Comments: The reported COVID-19 infection was considered as vaccination failure with bnt162b2 (COMIRNATY), as full dosing received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Body temperature
Hospital-Tage: -
Labordaten: Test Date: 202206; Test Name: Temperature; Result Unstructured Data: Test Result:had a slight rise in temperature; Test Date: 20220622; Test Name: Covid-19 test; Test Result: Positive ; Comments: we got the test on 20Jun2022 and we got the result on 22Jun2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2387408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 10.11.2021
Beginn: 20.06.2022
Tage bis Beginn: 222,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure Weight

Symptomtext

got the result on 22 which was positive; got the result on 22 which was positive/flu like symptoms like runny nose, sore throat; This is a spontaneous report received from contactable reporter (Nurse). The reporter is the patient. A 74-year-old female patient received BNT162b2 (BNT162B2), on 11Feb2021 as dose 1, single (Lot number: EL9262), on 08Mar2021 as dose 2, single (Lot number: EN6199) and on 10Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 74 years for covid-19 immunisation. The patient's relevant medical history included: "Osteoarthritis" (unspecified if ongoing), notes: Comments: Osteoarthritis; "Hypertension" (unspecified if ongoing), notes: Comments: Hypertension; "Eczema" (unspecified if ongoing), notes: Comments: Eczema; "arthritis" (unspecified if ongoing), notes: Celebrex 200 mg (not taking it daily because she was doing very fine).; "EGR Reflux" (unspecified if ongoing); "heartburn" (unspecified if ongoing), notes: Dexilant for support for heartburn and its for acidity.; "acidity" (unspecified if ongoing), notes: Dexilant for support for heartburn and its for acidity.; "gas relief" (unspecified if ongoing), notes: it is a gas relief Simethicone 75. Concomitant medication(s) included: DEXILANT taken for dyspepsia, gastrooesophageal reflux disease; LOSARTAN/HYDROCHLOORTHIAZIDE; CELEBREX taken for arthritis; PROTEX [TRICLOSAN]; SIMETHICONE taken for flatulence; ALLEGRA taken for eczema. The following information was reported: VACCINATION FAILURE (medically significant) with onset 20Jun2022, outcome "unknown", described as "got the result on 22 which was positive"; COVID-19 (medically significant) with onset 20Jun2022, outcome "unknown", described as "got the result on 22 which was positive/flu like symptoms like runny nose, sore throat". The events "got the result on 22 which was positive" and "got the result on 22 which was positive/flu like symptoms like runny nose, sore throat" required emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Jun2022) Positive, notes: got the test on 20Jun2022 and we got the result on 22Jun2022; Weight: (unspecified date) 155 to 158, notes: weigh around 155 to 158. Therapeutic measures were taken as a result of vaccination failure, covid-19 included Pfizer Paxlovid on 24Jun2022 by her primary physician to help the patient previous and help she to improve. Clinical course: the physician said to her that she was positive. Unfortunately that she believe and he (physician) believe she and her husband got it from the hospital. Her husband was in the emergency in 05Jun2022 to 15Jun2022 because she had been in the emergency. He (her husband) was discharged on the 20Jun2022, he spent days in the hospital. On 20Jun2022, Monday, she decided to move back from the emergency. In 20Jun2022, he (her husband) had been discharged. On 20Jun2022 they had flu like symptoms like runny nose, sore throat and something like that they thought may be like and they thought it was like sinus and her doctor told that her husband got the Covid test, the patient did not really have a lot of symptoms but her husband had a slight rise in temperature, so they got the test on 20Jun2022 and they got the result on 22Jun2022. They started to have symptoms on 20Jun2022 and they tested, we got the results of COVID test on 22Jun2022, they got the result on 22Jun2022 which was positive, so they received it while they were at the hospital, so they received it together at the hospital. Her husband was admitted in the emergency room at the hospital before they got the symptoms.; Sender's Comments: Based on plausible dose -event relationship post vaccination and no other alternate explanation the causal role of BNT162B2 cannot be excluded for the reported LOE events

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220622; Test Name: Covid-19; Test Result: Positive ; Comments: got the test on 20Jun2022 and we got the result on 22Jun2022.; Test Name: weight; Result Unstructured Data: Test Result:155 to 158; Comments: weigh around 155 to 158.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (esophageal); Acid reflux (oesophageal) (Dexilant for support for heartburn and its for acidity.); Arthritis (Celebrex 200 mg (not taking it daily because she was doing very fine).); Eczema (Comments: Eczema); Gas (it is a gas relief Simethicone 75.); Heartburn (Dexilant for support for heartburn and its for acidity.); Hypertension (Comments: Hypertension); Osteoarthritis (Comments: Osteoarthritis)
Andere Medikamente: DEXILANT; LOSARTAN/HYDROCHLOORTHIAZIDE; CELEBREX; PROTEX [TRICLOSAN]; SIMETHICONE; ALLEGRA
Allergien: -
Vorherige Impfungen: -

VAERS 2387387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 75,0
Geschlecht: M
Eingang: 24.07.2022
Impfdatum: 10.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

we got the result on 22 which was positive; we got the result on 22 which was positive; This is a spontaneous report received from a contactable reporter(s) (Nurse) from product quality group. A 75-year-old male patient received BNT162b2 (BNT162B2), on 11Feb2021 as dose 1, single (Lot number: EL9262), on 08Mar2021 as dose 2, single (Lot number: EN6199) and on 10Nov2021 as dose 3 [booster], single (Lot number: 320308D) at the age of 75 years for covid-19 immunisation; tamsulosin hydrochloride (FLOMAX [TAMSULOSIN HYDROCHLORIDE]); epoetin alfa (ESPOGEN); tamsulosin (TAMSULOSIN). The patient's relevant medical history included: "CABG" (unspecified if ongoing), notes: CABG; "COPD" (unspecified if ongoing), notes: COPD. Concomitant medication(s) included: ADVAIR. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "we got the result on 22 which was positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (20Jun2022) positive. The action taken for tamsulosin hydrochloride, epoetin alfa and tamsulosin was unknown. clinical course: When probed if patient has experienced any side effects: Reporter stated, Yes, I want to document it because this is emergency use medication and it was prescribed to me by my Primary Physician. Side effects: Reporter stated, I took all the prescribed Pfizer Paxlovid on 24Jul (Later clarified as 24Jun, 2022) by my primary physician to help me previous and help me to improve and he said to me that I am positive. Unfortunately that I believe and he believe we got it from the hospital, I think too because my husband was in the emergency in 05June to 15Jul (Later clarified as 05Jun to 15Jun) because I have been in the emergency. He was discharged on the 20Jul (Later clarified as 20Jun), he spent days in the hospital. On 20Jul (Later clarified as 20Jun), Monday, I decided to move back from the emergency. In 20Jul , he had been discharged (Later clarified as 20Jun). On 20Jul (Later clarified as 20 Jun) we had flu like symptoms like runny nose, sore throat and something like that we thought may be like and we thought it was like sinus and my doctor told that he got the Covid test, I did not really have a lot of symptoms but he has a slight rise in temperature, so we got the test on 20 and we got the result on 22. We started to have symptoms on 20July (Later clarified as 20June) and we tested, we got the results of COVID test on the 21 next day, we got the result on 22 which was positive, so we received it while we were at the hospital, so we received it together at the hospital. He was admitted in the emergency room at the hospital before we got the symptoms. Anyway I told my primarily physician doctor, my husband did not get any kind of that because we ordered the request at Pharmacy. What happened was my husband did not get the Paxlovid even if he did have a prescription for him but he never got it because the pharmacist at pharmacy told him that there is drug interaction which considered severe if my husband is taking anything but he has an prescription for me. I think there is nothing elaborated so he was telling me that he wants me to take the Paxlovid and I did ask is there any kind of side effect or are you sure this is safe, he assured me that it is going to be fine, he said I would rather give it to you because of my age, I am 74 but I have vaccine both doses and the booster, we both had it and we get better. What happen was I took the first dose on the evening of 24Jul (Later clarified as 24Jun). We ordered it from, so he ordered that and my husband never got it from the guy, he did not get it but he said I should take it. LOT# (Pfizer COVID-19 Vaccine): Reporter stated, And ever since we are having problems with you know and I had to fill up the report. Before we end this call I just want to ask you something you know as a drug safety person. For me the first is a Pfizer COVID Vaccine the LOT# is EL9262, I received this in 11Feb2021. The second is the Pfizer COVID also the LOT is EN6199, I received this on 08Mar2021. Yeah, we have the same LOT# for the first and the second, both of us have the same one and then did you want the booster which is the third one? Okay, the booster was received in the store, retail store they have the pharmacy there. Its the LOT# is for me to receive is 320308D I received this in 10Nov2021 and then my husband he also got this from the store it same date but the LOT# 320308D so, its the same LOT# same time, the same date, the same store. No follow-up attempts are possible. No further information is expected.; Sender's Comments: As there is limited information in the case provided, the causal association between the Reported events and the suspect drug cannot be excluded. The case will be reassessed once new information is available.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220620; Test Name: the test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: CABG; COPD
Andere Medikamente: ADVAIR; FLOMAX [TAMSULOSIN HYDROCHLORIDE]; ESPOGEN; TAMSULOSIN
Allergien: -
Vorherige Impfungen: -

VAERS 2387163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 13.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27Feb2021 as dose 1, single (Lot number: EN6203), in right arm, on 20Mar2021 as dose 2, single (Lot number: ER2613), in right arm and on 13Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 49 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Allergies" (unspecified if ongoing); "chronic bronchitis" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown results, notes: Paxlovid rebound; (12Jul2022) Positive, notes: Return of symptoms and positive test. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: Patient received no other medication in 2 weeks. No follow-up attempts are needed. No further information is expected.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown results; Comments: Paxlovid rebound.; Test Date: 20220712; Test Name: COVID-19 test; Test Result: Positive ; Comments: Return of symptoms and positive test.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Asthma; Chronic bronchitis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2374848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 08.12.2021
Beginn: 13.07.2022
Tage bis Beginn: 217,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19

Symptomtext

covid

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2371519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 12.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Nurse). The reporter is the patient. A 44-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 17Dec2020 as dose 1, single (Lot number: EJ1685), in left arm, on 09Jan2021 as dose 2, single (Lot number: EL0142), in left arm and on 12Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 43 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "known allergies allergic to penicillin" (unspecified if ongoing); "known allergies allergic to sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Vicodin, reaction(s): "known allergies vicodin". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. No follow-up attempts are possible. No further information is expected.; Sender's Comments: The causal association between the events and suspect vaccine cannot be excluded based on known safety profile. Case will be reassessed on receipt of more information.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Penicillin allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2359406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 26.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31Dec2020 as dose 1, single (Lot number: EL1284), in right arm, on 19Jan2021 as dose 2, single (Lot number: EL3302), in right arm and on 26Oct2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 41 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Sulfa" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results, notes: Indication: Covid-19 treatment; negative; positive; negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Additional information: Rebound COVID occurred at 4 days following completion of Paxlovid treatment and was confirmed through home antigen test. Previous negative home antigen and negative PCR tests were received 4 days following initial infection on the date Paxlovid treatment was completed (6/26). Current symptoms include headache, sore throat, body aches, running nose, congestion and fatigue. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the information provided, known drug safety profile and plausible temporal association, the causality between BNT162B2 and the drug ineffective, covid-19 cannot be completely excluded.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid/PCR tests; Result Unstructured Data: Test Result:Unknown results; Comments: Indication: Covid-19 treatment; Test Name: Covid/PCR tests; Test Result: Negative ; Test Name: home antigen test; Test Result: Positive ; Test Name: home antigen test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2357695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MN
Alter: 28,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 30.11.2021
Beginn: 01.07.2022
Tage bis Beginn: 213,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Interchange of vaccine products

Symptomtext

J&J vaccine 4/2/21. Pfizer 11/30/22. Hospitalized with COVID infection 7/1/22

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Praegender Schweregrund: COVID-19
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: OR
Alter: 21,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 25.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Pfizer / BioNTech dose 3 / Treatment of COVID-19; Pfizer / BioNTech dose 3 / Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 21-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Oct2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 21 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Anxiety" (unspecified if ongoing); "autism" (unspecified if ongoing); "adhd" (unspecified if ongoing); "seasonal allergies" (unspecified if ongoing); "asthma" (unspecified if ongoing); "vocal cord dysfunction" (unspecified if ongoing); "known allergies: Almonds" (unspecified if ongoing), notes: known allergies: Almonds; "Allergy" (unspecified if ongoing); "Birth control pill" (unspecified if ongoing). Concomitant medication(s) included: ZYRTEC ALLERGY taken for hypersensitivity, start date: 22Aug2014. The following information was reported: DRUG INEFFECTIVE (medically significant), outcome "not recovered", COVID-19 (medically significant), outcome "recovered" and all described as "Pfizer / BioNTech dose 3 / Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results; Negative; Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: The patient received other medication in 2weeks. The patient received COVID 19 Treatment, (Paxlovid) from 03Jun2022 to 07Jun2022 for treatment of COVID-19. Adverse event I am experiencing rebound symptoms. I am day 12 of my covid illness and was symptom free since day 6. I tested negative day 10, but test positive day 12 after having new onset of symptoms (runny nose, sneezing, congestion, headache, fatigue, SOB). I likely exposed 4 different people today. The information on the batch/lot number for [BNT162B2] has been requested and will be submitted if and when received; Sender's Comments: As there is limited information in the case provided, the causal association between the event and the suspect drug cannot be excluded. The case will be reassessed once new information is available.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid; Result Unstructured Data: Test Result:Unknown results; Test Name: Covid; Test Result: Negative ; Test Name: Covid; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: ADHD; Allergy; Anxiety; Asthma; Autism; Food allergy (known allergies: Almonds); Seasonal allergy; Vocal cord dysfunction; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: ORAL CONTRACEPTIVE NOS
Andere Medikamente: ZYRTEC ALLERGY
Allergien: -
Vorherige Impfungen: -

VAERS 2315247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CT
Alter: 53,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 05.11.2021
Beginn: 02.05.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Tested positive; Tested positive; This is a spontaneous report received from contactable reporter (Consumer). The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Apr2021 as dose 1, single (Lot number: ER8732), in left arm, on 26Apr2021 as dose 2, single (Lot number: GR8731), in left arm and on 05Nov2021 as dose 3 (boosster), single (Lot number: 320308D) at the age of 53 years, in left arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 24Apr2022 as dose 4 (booster), single (Lot number: 057M21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Sulfa". There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 02May2022, outcome "recovered" (20May2022) and all described as "Tested positive". Patient became sick with Covid. Tested positive on 02May2022. Experienced symptoms before testing positive. Symptoms included fever, chills, vomiting, diarrhea, sore throat, cough, and then secondary infection which was treated with Azithromycin, albuterol, benzonatate. Strange thing was patient seemed to improve, tested negative for three days in May2022, and then her symptoms returned on 13May and she tested positive again for more than a week. Adverse event treatment included received Paxlovid then other meds after rebound.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: I tested positive again for more than a week.; Test Date: 20220502; Test Name: Covid-19 test; Test Result: Positive ; Test Date: 202205; Test Name: Covid-19 test; Test Result: Negative ; Comments: tested negative for three days; Test Date: 202205; Test Name: Covid-19 test; Test Result: Negative ; Comments: tested negative for three days; Test Date: 202205; Test Name: Covid-19 test; Test Result: Negative ; Comments: tested negative for three days
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2315121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: NY
Alter: 47,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 11.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47-year-old female patient received BNT162b2 (BNT162B2), on 11Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 47 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Nsaids" (unspecified if ongoing), notes: Nsaids. The patient's concomitant medications were not reported. Past drug history included: Aspirin, reaction(s): "Known allergies Aspirin", notes: known allergies Aspirin. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Negative, notes: 2 negative covid rapid tests; (unspecified date) Negative, notes: 2 negative covid rapid tests; (04Jun2022) Positive, notes: tested positive again on rapid tests on day 5 post paxlovid; (unspecified date) Unknown results, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid treatment, start date: 26May2022 and Stop date: 30May2022 Clinical course: Bad taste while taking Paxlovid; Rebound Covid symptoms started 3 days after Paxlovid (after 2 negative covid rapid tests) and tested positive again on rapid tests on day 5 post paxlovid. Patient was recovering from symptoms and did not take treatment. No other medication reported in 2weeks. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: covid rapid tests; Test Result: Negative ; Comments: 2 negative covid rapid tests; Test Name: covid rapid tests; Test Result: Negative ; Comments: 2 negative covid rapid tests; Test Date: 20220604; Test Name: covid rapid tests; Test Result: Positive ; Comments: tested positive again on rapid tests on day 5 post paxlovid.; Test Name: Covid test; Result Unstructured Data: Test Result:Unknown results; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to NSAIDs (Nsaids)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2309582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 44,0
Geschlecht: M
Eingang: 04.06.2022
Impfdatum: 30.11.2021
Beginn: 14.05.2022
Tage bis Beginn: 165,0
Dosis: 3
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Drug ineffective Polymerase chain reaction SARS-CoV-2 test

Symptomtext

COVID Infection; COVID Infection; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 44-year-old male patient received BNT162b2 (BNT162B2), on 21Mar2021 as dose 1, single (Lot number: EN6208), in left arm, on 02Apr2021 as dose 2, single (Lot number: ER9737), in left arm and on 30Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 44 years, in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Prior to vaccination, the patient was not diagnosed with COVID-19; and since the vaccination, has been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The following information was reported: DRUG INEFFECTIVE (medically significant) with onset 14May2022, outcome "recovered", COVID-19 (medically significant) with onset 14May2022, outcome "recovered" and all described as "COVID Infection". The patient underwent the following laboratory tests and procedures: Polymerase chain reaction: (19May2022) Positive, notes: Nasal Swab; SARS-CoV-2 test: (29May2022) Negative, notes: Other; (16May2022) Positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of drug ineffective, covid-19.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200792657 same patient and drug, different event separated in time.

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220519; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab; Test Date: 20220529; Test Name: AG Rapid Test Saliva; Test Result: Negative ; Comments: Other; Test Date: 20220516; Test Name: Rapid Test Binax; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2309572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 04.06.2022
Impfdatum: 01.11.2021
Beginn: 11.05.2022
Tage bis Beginn: 191,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID infection; COVID infection; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 37-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Mar2021 as dose 1, single (Lot number: EL3247), on 29Mar2021 as dose 2, single (Lot number: EP6955) and on 01Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 36 years for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 11May2022, outcome "recovered" (May2022) and all described as "COVID infection". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (13May2022) Positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220513; Test Name: COVID- test; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2295859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 03.12.2021
Beginn: 01.05.2022
Tage bis Beginn: 149,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Drug ineffective Suspected COVID-19

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An elderly female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Feb2021 as dose 1, single (Lot number: EN6203), in left arm, on 22Mar2021 as dose 2, single (Lot number: Er8727), in left arm and on 03Dec2021 as dose 3 (booster), single (Lot number: 320308D), in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: CETIRIZINE HYDROCHLORIDE, start date: Jan2021. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant) all with onset May2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of suspected covid-19. Clinical course included: The patient received Paxlovid (Lot number: Gc0466) from 17May2022 to 19May2022 for the treatment of COVID-19. No known allergies. The patient was not recovered. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Drug ineffective
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None Known allergies: No
Andere Medikamente: CETIRIZINE HYDROCHLORIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2294240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 67,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 27.10.2021
Beginn: 18.05.2022
Tage bis Beginn: 203,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 15Feb2021 at 14:00 as dose 1, single (Lot number: EN6201), in right arm, on 08Mar2021 at 14:00 as dose 2, single (Lot number: EN6199), in left arm and on 27Oct2021 at 14:00 as dose 3 (booster), single (Lot number: 320308D) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hypothyroidism" (unspecified if ongoing); "menopausal symptoms" (unspecified if ongoing). Concomitant medication(s) included: CLARITIN [CLARITHROMYCIN], start date: 03Jan2022, stop date: 09May2022; LEVOTHYROXINE, start date: Jan1982; ESTRADIOL, start date: Sep2010; CITRACAL + D [CALCIUM CITRATE;COLECALCIFEROL], start date: Jan2010. Other medication in 2weeks brand: Ameal, start date Jan1982, Teva, start date Sep2010, Multivitamin, other medication in 2weeks brand: various. Past drug history included: Fexofenadine, reaction(s): "Allergy". The following information was reported: VACCINATION FAILURE (medically significant) with onset 18May2022, outcome "unknown", COVID-19 (medically significant) with onset 18May2022, outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18May2022) Positive. Therapeutic measures were taken as a result of covid-19. It was reported that, COVID symptoms returned 18May2022 and rapid antigen test strong positive. Conclusion: The complaint for a Lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot 32030BD was investigated. The investigation included reviewing incoming quality and manufacturing batch records, deviation investigations, an analysis of the complaint history for the reported lot and product type and final release assay testing. This product is received as preformulated bulk and is manufactured, labeled and packaged by Pfizer. The final scope was determined to be lot 32030BD. No quality issues were identified during the investigation. There is no impact on product quality. An NTM was not issued for the complaint. No regulatory were held as a result of this complaint. The complaint condition of lack of effect was not confirmed, therefore the root cause cannot be attributed to manufacture or vendor processes. The root cause was not determined to be manufacture or vendor related as incoming quality component testing and the results of all analytical tests performed at the time of lot release confirmed that the batch met potency specifications. No corrective or preventative actions are required as the complaint condition was not determined to be manufacture or vendor related and there are quality systems in place to detect defects prior any lot being released to the market. No further investigation required. The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot EN6199 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EN6199, fill lot EN5331, and the formulated drug product lot EN5320 and finished goods lot EN6201, fill lot EN5333, and the formulated drug product lot EN5322. A complaint sample was not returned, and photographs were not received. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220518; Test Name: Rapid antigen; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism; Menopausal symptoms
Andere Medikamente: CLARITIN [CLARITHROMYCIN]; LEVOTHYROXINE; ESTRADIOL; CITRACAL + D [CALCIUM CITRATE;COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2294113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MN
Alter: -
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 08.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Drug ineffective Suspected COVID-19

Symptomtext

COVID 19; COVID 19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient received BNT162b2 (BNT162B2), on 08Nov2021 as dose 3 (booster), single (Lot number: 320308D), in left arm for covid-19 immunization; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 20Mar2021 as dose 1, single (Lot number: 007M20A) and on 20Feb2021 as dose 2, single (Lot number: 011A21A), in left arm for covid-19 immunization. The patient's relevant medical history included: "Known allergies: sulfa" (unspecified if ongoing), notes: Known allergies: sulfa; "hypothyroidism" (unspecified if ongoing); "Interchange of vaccine products" (unspecified if ongoing), notes: Dose3 Pfizer, Dose 2 an 1 Moderna. Concomitant medication(s) included: LEVOTHYROXINE (100MCG); VITAMIN C [ASCORBIC ACID] 1000; VITAMIN D3 (2000 IU); VITAMIN B12 [CYANOCOBALAMIN](5000mcg); ZINC (50mg); MAGNESIUM (250mg); CALCIUM CITRATE (600mg); SELENIUM (200mcg); PROBIOTICS [BIFIDOBACTERIUM LONGUM;LACTOBACILLUS ACIDOPHILUS;LACTOBACILLUS RHAMNOSUS]; COLLAGEN + BIOTIN 6000mg. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19". Therapeutic measures were taken as a result of drug ineffective, suspected covid-19. Covid-19 treatment included Paxlovid from 04May2022 to 09May2022 of lot number GA1519 for the indication treatment of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Drug ineffective
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism; Interchange of vaccine products (Dose3 Pfizer Dose 2 an 1 Moderna); Sulfonamide allergy (Known allergies: sulfa)
Andere Medikamente: LEVOTHYROXINE; VITAMIN C [ASCORBIC ACID]; VITAMIN D3; VITAMIN B12 [CYANOCOBALAMIN]; ZINC; MAGNESIUM; CALCIUM CITRATE; SELENIUM; PROBIOTICS [BIFIDOBACTERIUM LONGUM;LACTOBACILLUS ACIDOPHILUS;LACTOBACILLUS RHAMNOSUS]
Allergien: -
Vorherige Impfungen: -

VAERS 2266886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

gering

Staat: MA
Alter: 57,0
Geschlecht: F
Eingang: 07.05.2022
Impfdatum: 18.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Apr2021 as dose 1, single (Lot number: EW0153), in left arm, on 01May2021 as dose 2, single (Lot number: ER8736), in left arm and on 18Nov2021 as dose 3 (booster), single (Lot number: 320308d) at the age of 57 years, in right arm for Covid-19 immunisation. The patient's relevant medical history included: "Parkinson's disease" (unspecified if ongoing); "known allergies: Penicillin tetanus" (unspecified if ongoing), notes: known allergies: Penicillin tetanus. Concomitant medication(s) included: CARBIDOPA AND LEVODOPA. Vaccination history included: Tetanus (known allergies: Penicillin tetanus), for Immunization, reaction(s): "known allergies: Penicillin tetanus". The following information was reported: VACCINATION FAILURE (medically significant), outcome "unknown", COVID-19 (medically significant), outcome "not recovered" and all described as "Covid-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) positive; (unspecified date) Negative; (30Apr2022) Positive. Therapeutic measures were taken as a result of Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid Test; Test Result: Positive; Test Name: Covid Test; Test Result: Negative; Test Date: 20220430; Test Name: Covid Test; Test Result: Positive.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Parkinson's disease; Penicillin allergy (known allergies: Penicillin tetanus)
Andere Medikamente: Carbidopa and Levodopa
Allergien: -
Vorherige Impfungen: -

VAERS 2265723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: OH
Alter: 67,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 02.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective

Symptomtext

Product=COVID 19 Treatment, brand=Paxlovid/vaccine brand=Pfizer; Product=COVID 19 Treatment, brand=Paxlovid/vaccine brand=Pfizer; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 11Mar2021 as dose 2, single (Lot number: EN6204), in right arm and on 02Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 67 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: penicillin" (unspecified if ongoing), notes: Known allergies: penicillin; "Known allergies: tree nuts" (unspecified if ongoing), notes: Known allergies: tree nuts; "Known allergies: peanuts" (unspecified if ongoing), notes: Known allergies: peanuts; "Known allergies: coconut" (unspecified if ongoing), notes: Known allergies: coconut. Concomitant medication(s) included: AMITRIPTYLINE; ARMOUR THYROID; ROSUVASTATIN. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Product=COVID 19 Treatment, brand=Paxlovid/vaccine brand=Pfizer". Therapeutic measures were taken as a result of covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts (Known allergies: tree nuts); Food allergy (Known allergies: coconut); Peanut allergy (Known allergies: peanuts); Penicillin allergy (Known allergies: penicillin)
Andere Medikamente: AMITRIPTYLINE; ARMOUR THYROID; ROSUVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2203559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: NJ
Alter: 13,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 05.11.2021
Beginn: 20.12.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Alopecia areata Inappropriate schedule of product administration SARS-CoV-2 test Alopecia Blood test normal

Symptomtext

Hi, patient got her 2nd COVID 19 Pfizer vaccine on 05Nov2021. Patient started losing noticeable hair from December but then in January, I noticed an approximate 3x3 bald spot on her right side on her head. We got an appointment with her pediatrician and she diagnosed it as Alopecia Areata. We had started her on Steroid injection treatments since March 2022 but the bald spot is coming on new sites on her scalp. Patient has lost approximately 30% of her hair. She is continuing to loss her hair. No one in my or my husbands family has history of hair loss or hair thinning. All her blood work is done & her results are within normal range including hormone levels.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia areata
Hospital-Tage: -
Labordaten: Please see the comments in section item 18.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2259744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: NC
Alter: -
Geschlecht: F
Eingang: 30.04.2022
Impfdatum: 28.10.2021
Beginn: 16.04.2022
Tage bis Beginn: 170,0
Dosis: 3
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Vaccination failure; Breakthrough covid-19 infection; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 48-year-old female patient received BNT162b2 (BNT162B2), on 30Mar2021 as dose 1, single (Lot number: EL3247), in right arm, on 20Apr2021 as dose 2, single (Lot number: EL3247), in right arm and on 28Oct2021 as dose 3 (booster), single (Lot number: 320308D), in right arm, all intramuscular for covid-19 immunisation. The patient had not received any other vaccines within 4 weeks prior to the BNT162B2 vaccine. The patient's relevant medical history and concomitant medications were not reported. The patient had not experienced Covid-19 prior vaccination. The following information was reported: COVID-19 (medically significant) with onset 16Apr2022, outcome "recovered with sequelae", described as "Breakthrough covid-19 infection"; VACCINATION FAILURE (medically significant) with onset 16Apr2022, outcome "recovered with sequelae". The events "vaccination failure" and "breakthrough covid-19 infection" required physician office visit. Patient's clinical course was the following: Breakthrough COVID-19 infection. Mild headache, runny nose, cough, fever, chills, general fatigue and loss of taste and smell. Most symptoms lasted about 3 days. Cough, runny nose and loss of taste and smell persisted for over a week. Slight recovery of taste and smell about 1.5 weeks post infection. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (16Apr2022) Positive, notes: Clinitest Rapid Ag test; (25Apr2022) Positive, notes: BinaxNOW Rapid Ag test. Therapeutic measures were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220416; Test Name: COVID 19 test, Nasal Swab; Test Result: Positive ; Comments: Clinitest Rapid Ag test; Test Date: 20220425; Test Name: COVID 19 test, Nasal Swab; Test Result: Positive ; Comments: BinaxNOW Rapid Ag test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2252028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: FL
Alter: 28,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 27.10.2021
Beginn: 25.04.2022
Tage bis Beginn: 180,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Unevaluable event

Symptomtext

patient hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2249392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: NY
Alter: 57,0
Geschlecht: M
Eingang: 23.04.2022
Impfdatum: 04.11.2021
Beginn: 17.04.2022
Tage bis Beginn: 164,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Tested positive for Covid on Sunday, 17Apr2022; Tested positive for Covid on Sunday, 17Apr2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old male patient received BNT162b2 (BNT162B2), on 23Jan2021 as dose 1, single (Lot number: EK4176), on 15Feb2021 as dose 2, single (Lot number: EL9266) and on 04Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 57 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: COVID-19 (medically significant) with onset 17Apr2022, outcome "unknown", VACCINATION FAILURE (medically significant), outcome "unknown" and all described as "Tested positive for Covid on Sunday, 17Apr2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (17Apr2022) positive. Therapeutic measures were taken as a result of covid-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220417; Test Name: COVID-19 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2248107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

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Staat: AZ
Alter: 72,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 13.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Asthenia Tinnitus

Symptomtext

PERSISTENT RINGING IN EARS, TINNITUS (debilitating, extremely loud)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: NONE
Vorgeschichte: Type II Diabetes (A1C normal - under control)
Andere Medikamente: Tamsulosin (0.4mg) Vitamin D3 (5,000 IU)
Allergien: NONE
Vorherige Impfungen: -

VAERS 2248055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

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Staat: WA
Alter: 74,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 27.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: UN / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Acoustic stimulation tests abnormal Deafness bilateral Sleep disorder Tinnitus

Symptomtext

Roughly 2 days after my booster vaccine, I was at work at and suddenly had a very loud ringing in my ears. Within a few hours, I had complete hearing loss on my left and 75% on my right ear. I sought care from an ENT specialist. I was given 3 injections in my eardrum which has not helped. In addition I have Tinnitus in my left ear which is keeping me from sleeping, There is a 30% chance of recovery of my hearing. However the condition has remained the same and in fact has worsened within the past few months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests abnormal
Hospital-Tage: -
Labordaten: Several Hearing Tests
Aktuelle Erkrankungen: A1C is greater than 7 / Borderline Diabetic
Vorgeschichte: None
Andere Medikamente: Multi vitamins, Pioglitazone 15mgs x day, Atorvastatin 40mgs x day.
Allergien: None
Vorherige Impfungen: -

VAERS 2243434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

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Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 05.03.2021
Beginn: 03.07.2021
Tage bis Beginn: 120,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

7/3/21 PMH of DVT on eliquis, L carotid aneurysm, HTN, skin cancer, hypothyroid; presented for a CC of unresponsive episode

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 7/3/21 SARS-CoV-2 (COVID-19) by NAA Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: WV
Alter: 63,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 23.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tinnitus

Symptomtext

Ringing in my ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: Saw my PCP who referred me to an ENT Doctor.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish Oil and a multi-vitamin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2237750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: WI
Alter: 72,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 15.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Therapeutic response unexpected

Symptomtext

The first Pfizer Covid Vaccine helped her breathing/Pfizer Covid Vaccine booster dose and the same thing happened, her breathing was fine again, better.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old female patient received BNT162b2 (BNT162B2), on 26Feb2021 as dose 1, single (Lot number: EN6202), in right arm and on 15Nov2021 as dose 3 (booster), single (Lot number: 320308D) at the age of 72 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "COPD" (ongoing), notes: Onset date unknown other than years ago. She has been on inhalers for years and years for COPD.; "Vitamin D deficiency" (unspecified if ongoing), notes: She thinks she had a vitamin D deficiency but that was before all of this. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 2, SINGLE. Batch/Lot No. Unknown, Expiry: Unknown, Upper Arm.), administration date: 26Mar2021, when the patient was 72-year-old, for COVID-19 Immunization. The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "unknown", described as "The first Pfizer Covid Vaccine helped her breathing/Pfizer Covid Vaccine booster dose and the same thing happened, her breathing was fine again, better.". Additional Information: There was product complaint to report (product is not suspect product) with Description of Product Complaint as patient has been on inhalers for years and years for COPD. After first Pfizer Covid Vaccine noticed whenever went to take Advair inhaler in the morning would start to cough. So patient stopped taking Advair Inhaler. Patient was not using Advair inhaler for like 6 months after getting first Pfizer Covid Vaccine, After about 6 months started having a bit of a problem breathing again. When booster came out she went and got the Pfizer Covid Vaccine booster dose and the same thing happened, her breathing was fine again, better. She tried to get off inhalers numerous times on her own prior to this and never could. Would only last maybe 2-3 days at the most and then have to take the inhaler again. Reporter did not provide any additional inhaler product names regarding been on inhalers for years and years; tried to get off inhalers; only provided Advair inhaler. Description of complaint of the product Advair inhaler, Manufacturer name Glasko Smith Kline with NDC no. 0173-0717-20 for lot K35H with Expiry as 20Aug2022. Follow-up (07Apr2022): This is a spontaneous follow-up report received in response to the mail trail sent regarding the confirmation below mentioned query. The response included the lot number for the booster dose was 320308D. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Therapeutic response unexpected
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: COPD (Onset date unknown other than years ago. She has been on inhalers for years and years for COPD.)
Vorgeschichte: Medical History/Concurrent Conditions: Vitamin D deficiency (She thinks she had a vitamin D deficiency but that was before all of this.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2226397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: PR
Alter: 34,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 27.11.2021
Beginn: 24.12.2021
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal discomfort Bowel movement irregularity COVID-19 Deafness unilateral Feeling abnormal SARS-CoV-2 test positive

Symptomtext

I woke up and I couldn't hear well from my right ear. I didn't have any other symptoms like sneezing, mucus, or coughing. That first day I just felt strange. The next day I started having stomach issues. I was going to the bathroom very frequently. I didn't have any serious symptoms. I kept working from home. I kept not hearing well for 2 or 3 days. The stomach issues lasted for about 5 or 6 days. It took me a couple of weeks to feel 100% completely recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal discomfort
Hospital-Tage: -
Labordaten: COVID Test- Positive (12/23/2021)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2220509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: AZ
Alter: 68,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 19.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Acoustic stimulation tests Tinnitus

Symptomtext

Tinnitus to the hearing, no treatment, high pitch sound constant

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests
Hospital-Tage: -
Labordaten: Saw ENT Doctor, he did a hearing test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Eliquis, Metoprolol ER Succinate, Alendronate, Baby Aspirin, Calcium, Vitamin D3 & B-Complex
Allergien: None
Vorherige Impfungen: -

VAERS 2209341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: VA
Alter: 62,0
Geschlecht: M
Eingang: 31.03.2022
Impfdatum: 03.11.2021
Beginn: 01.01.2022
Tage bis Beginn: 59,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tinnitus

Symptomtext

Tinnitus - mild onset becoming progressively more severe. Initial doctor visit 03/11/2022. Referred to ear, nose, throat doctor 03/14/2022. Ears and hearing appeared normal . Diagnosis Tinnitus. No treatment recommended . Ear ringing continues daily

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: 03/14/2022 Hearing test normal
Aktuelle Erkrankungen: n/a
Vorgeschichte: high blood pressure
Andere Medikamente: 10 mg Lisinopril
Allergien: n/a
Vorherige Impfungen: -

VAERS 2203495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 9,0
Geschlecht: M
Eingang: 29.03.2022
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Erythema SARS-CoV-2 test Vaccination site mass Vaccination site swelling Vaccination site warmth

Symptomtext

Red, hot, swollen, hard lump around the injection site; Red, hot, swollen, hard lump around the injection site; Red, hot, swollen, hard lump around the injection site; Red, hot, swollen, hard lump around the injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 9 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 30Nov2021 (Lot number: 320308D) at the age of 9 years 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 Number: 1, Batch/Lot No: FH8028, Location of injection: Arm Right), administration date: 04Nov2021, for covid-19 immunisation. The following information was reported: ERYTHEMA (non-serious), VACCINATION SITE WARMTH (non-serious), VACCINATION SITE SWELLING (non-serious), VACCINATION SITE MASS (non-serious) all with onset 30Nov2021, outcome "recovered" and all described as "Red, hot, swollen, hard lump around the injection site". The event "red, hot, swollen, hard lump around the injection site", "red, hot, swollen, hard lump around the injection site", "red, hot, swollen, hard lump around the injection site" and "red, hot, swollen, hard lump around the injection site" was evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of erythema, vaccination site warmth, vaccination site swelling, vaccination site mass. It was reported that the patient did not have covid prior to vaccination. The patient was tested for covid post vaccination. The patient had no Known allergies and had no Other medical history. The patient did not have any vaccine in four weeks. Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Erythema
Hospital-Tage: -
Labordaten: Test Date: 20211217; Test Name: PCR; Test Result: Negative ; Comments: Nasal swab; Test Date: 20211221; Test Name: PCR; Test Result: Negative ; Comments: Nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2188128

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: NV
Alter: 34,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 29.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Axillary mass Swelling

Symptomtext

Waking up swollen in the morning. Felt swollen and went to take a shower then noticed golf balls sized masses under armpits. Took Tylenol and and drank lots of fluids, then it resolved in about 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary mass
Hospital-Tage: -
Labordaten: Also received flu shot 2 days before booster. (10/29/2021)
Aktuelle Erkrankungen: None
Vorgeschichte: Viral induced Asthma
Andere Medikamente: Prozac Generic 40mg
Allergien: Amoxicillin, all Penicillin, Bactrim, Cephalexin
Vorherige Impfungen: -

VAERS 2180119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

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Staat: CO
Alter: 19,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 26.03.2021
Beginn: 23.08.2021
Tage bis Beginn: 150,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Basedow's disease Blood thyroid stimulating hormone Hyperthyroidism Ultrasound scan abnormal

Symptomtext

Graves Disease - Hyper-thyroid

Weitere VAERSDATA-Felder

Praegender Schweregrund: Basedow's disease
Hospital-Tage: -
Labordaten: TSH <0.008 uIU/mL and ultrasound came back consistent with Graves disease,
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bicuspid Aortic Valve
Andere Medikamente: Losartin 25mg Multi-vitamin Vitamin D Supplement
Allergien: N/A
Vorherige Impfungen: -

VAERS 2179849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 23.02.2021
Beginn: 02.02.2022
Tage bis Beginn: 344,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Unevaluable event

Symptomtext

ADMITTED TO HOSPITAL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

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Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 23.10.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Alopecia

Symptomtext

Hair loss; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (159558). The reporter is the patient. A 58 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 23Oct2021 10:15 (Lot number: 320308D) at the age of 58 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Type II Diabetes" (unspecified if ongoing), notes: Diagnosed 6-7 years ago. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose no=1 at 18:30 , Lot FF2589,, Injected in left arm in the muscle), administration date: 01Oct2021, when the patient was 58 years old, for COVID-19 Immunization. The following information was reported: ALOPECIA (non-serious), outcome "recovering", described as "Hair loss". Additional Information: Warm transfer from (Name withheld), Support, 159558 She has a consumer on the line who just received Series from Pfizer in Oct2021 and since then has noticed hair loss.Patient confirmed information above. She works in the medical field, but is not a healthcare professional. She received her first dose on 01Oct2021, which was a Friday, and by Monday or Tuesday, she realized her hair was coming out quite a bit and for the next 2-3 weeks, she was losing a lot of hair.She never had a hair problem before.It did not dawn on her until she talked to a friend last night.It was embarrassing and she looked it up online and saw articles where a few patients had hair loss with it. Since she noticed it at first, over 2-3 weeks, it was more and more, but now it has slowed down a bit.She thought that it was due to getting the shot and it does lower your immune and didn't know if that were it. She did look at the vaccine before he gave it to her, even though she is not a nurse. The second dose of the Pfizer COVID vaccine was last Saturday.By then, she had considerably less hair on her head.She provided lot 320308D, Expiration unknown. Date was 23Oct2021, and it was injected in right arm in the muscle. She got it for her job and she wants to travel and have no restrictions for travel. She did not wish to provide her primary care doctor's name or contact details. Additional Vaccines Administered on Same Date of the Pfizer Suspect reported as None. Any AE(s) require a visit to Emergency Room and Physician Office reported as No. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) reported as none. Patient's Medical History (including any illness at time of vaccination) reported as None or Unknown Family Medical History Relevant to AE(s) and Relevant Tests reported as None. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type II diabetes mellitus (Diagnosed 6-7 years ago.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2177663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 14.03.2022
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Interchange of vaccine products

Symptomtext

Initial COVID vaccine Moderna, second and third COVID vaccine Pfizer. Incorrect vaccine given for second injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2177657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: IL
Alter: 76,0
Geschlecht: M
Eingang: 14.03.2022
Impfdatum: 19.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Interchange of vaccine products

Symptomtext

First COVID vaccine Moderna. Second COVID vaccine Pfizer. Third COVID vaccine Pfizer. Incorrect medication given on second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2151239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 52,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Asthenopia Hypoaesthesia Somnolence

Symptomtext

Systemic: Numbness (specify: facial area, extremities)-Moderate, Systemic: drowsy-Moderate, Additional Details: Pt did not want to get the COVID shot / employer mandated. States she had an anaphylactic reaction to the flu shot and had numerous allergies. I administered the shot, had her sit down. I came back in about 2 minutes. She said she felt numb and kept trying to close her eyes. I told the other pharmacist to call 911. I stayed with the pt and made her talk to me the entire time until EMS arrived. They took her off in a stretcher

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenopia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2124216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 29.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Breast cyst Mammogram Ultrasound breast

Symptomtext

Ten days after receiving Pfizer booster discovered two benign cysts in left breast that had not been present before booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast cyst
Hospital-Tage: -
Labordaten: Mammogram and breast ultrasound.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish oil. Multi vitamin.
Allergien: Coconut
Vorherige Impfungen: -

VAERS 2116425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 28.11.2021
Beginn: 15.02.2022
Tage bis Beginn: 79,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Vaccine breakthrough infection

Symptomtext

Fully vaccinated, not boosted, COVID infection breakthrough

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2640704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 69,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

EXPIRED VACCINE GIVEN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: -----
Vorgeschichte: -----
Andere Medikamente: hydroCHLOROthiazide, MECLAZINE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2102035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MO
Alter: 76,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 05.11.2021
Beginn: 23.01.2022
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia COVID-19 Fall SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Received notification from Hospital. Limited information was given. Admitted to Hospital on 1/23/22 at nursing home, weakness, possible head injury. Nursing home name/information was not given in notification. Other symptoms are unknown and it was not disclosed whether the patient has any underlying medical conditions or is taking any systemic immunosuppressive therapy or medications. CDC Investigation form disclosed that he was not admitted to ICU and did not require any mechanical ventilation. Discharge from the hospital was reported to have been 1/25/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: 2,0
Labordaten: 1/23/22 RT-PCR COVID 19 POSITIVE
Aktuelle Erkrankungen: None listed
Vorgeschichte: None listed
Andere Medikamente: None listed
Allergien: None listed
Vorherige Impfungen: -

VAERS 2098658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: PA
Alter: 62,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 05.11.2021
Beginn: 07.01.2022
Tage bis Beginn: 63,0
Dosis: UNK
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Nasopharyngitis SARS-CoV-2 test positive Sinusitis

Symptomtext

Head cold and sinusitis, went to facility on January 15 and was to I was Covid positive

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Covid test January 15 came back positive
Aktuelle Erkrankungen: None
Vorgeschichte: Dvt High blood pressure Fibromyalgia Kidney disease Diabetes
Andere Medikamente: Multivitamin Super B Complex Ventolin HFA Xarelto Famotidine Levothyroxin Venlafaxine ER Fenofibrate Aripiprazole Solifenacin Pravastatin Tradjenta Amlodipine
Allergien: Any drug with Sulfa
Vorherige Impfungen: -

VAERS 2095387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 22.10.2021
Beginn: 07.02.2022
Tage bis Beginn: 108,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

covid vaccine breakthrough dose 1 1/29/21 EL9265 dose 2 2/18/21 EL9265

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ test 2/7/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2082500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: WA
Alter: 82,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 04.02.2021
Beginn: 27.01.2022
Tage bis Beginn: 357,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Infection

Symptomtext

Patient was admitted due to progressive decline in functional status likely due to active COVID-19 infection on 01/27/22. This is considered a breakthrough case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2074553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 46,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 29.10.2021
Beginn: 12.11.2021
Tage bis Beginn: 14,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Contusion Fibrin D dimer normal Metabolic function test Vitamin D

Symptomtext

Bruising started about 2 weeks after the booster and then I started to accumulate them. I thought it was the blood thinner I was on. They had me stop it but they still continued and ran bloodwork for my presurgery check. Then added a vitamin d just to be sure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: Pre surgery screening results done on 1/17/22 including a d dimer that was normal and a basic metabolic. A few outliers but basically all normal for me. They then checked my d it was also normal. They changed up my blood thinner to be extra cautious. This time limit does not allow me to add all the bloodwork. I would have been able to upload a pic though. D was taken on 1/18/22
Aktuelle Erkrankungen: -
Vorgeschichte: [ ] Allergies to adhesives, dyes and medal [ ] Random hives [ ] Dry issues, eye, mouth etc [ ] Other eye issues [ ] Gross cracked feet weekly self pedicures to maintain daily aquafor on feet. Per podiatrist instructions [ ] dysautonomia [ ] Asthma [ ] Hernia [ ] Acid reflux [ ] Throat problems [ ] Csf leak blood patch Feb 2021 [ ] Hydrocephalus secondary to brain cyst [ ] Pelvic congestion syndrome [ ] Venous Malformation brain [ ] Eagle syndrome [ ] Prolapse [ ] Painful bladder syndrome [ ] Pain with sex [ ] Precancerous polyps removed 11/2021 [ ] Chronic sinus infections currently being controlled with immunology team and ent etc. [ ] Recent scan shows neck fusion problem [ ] Chronic muscle spasms [ ] Chronic dislocations and subluxations [ ] Chronic pain [ ] Random bowel leakage [ ] Hypothyroidism Hormone support
Andere Medikamente: ? Np thyroid 60 1x day ? Omeprazole 20 1x day ? Methocarbamol 750 mg as needed ? Azelastine 2x day ? Neilmed sinus rinse 2x day ? Adk 1x day A5000-k500mcg-d5000 ? Probiotic 1x day ? Allegra 1x day ? Testosterone pellet bio identical
Allergien: Penicillin Tremadol Codeine Surgical tape adhesive NSAIDs Vicodin Nickel Disperse blue Quarternium Foods Wheat Soy Walnuts Peanuts Avocado Almond Pineapple Corn
Vorherige Impfungen: -

VAERS 2072071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CT
Alter: 18,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 27.10.2021
Beginn: 27.01.2022
Tage bis Beginn: 92,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asymptomatic COVID-19 SARS-CoV-2 test positive

Symptomtext

Asymptomatic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: PCR - 1/27/22
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2068945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: PA
Alter: 39,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

No adverse event Product preparation issue

Symptomtext

Pfizer vaccine diluted incorrectly, patient reports no symptoms of adverse effect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2058856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MN
Alter: 25,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Patient was administered a booster dose past the BUD. Expiration was 1/20/22 at 1700. Vaccine was administered on 1/21/22 at 0830

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2037628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 40,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Drug ineffective Immunisation SARS-CoV-2 test Suspected COVID-19

Symptomtext

Patient tested positive for COVID after receiving the 3rd dose of the vaccine; Patient tested positive for COVID after receiving the 3rd dose of the vaccine; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 40 year-old male patient received bnt162b2 (BNT162B2), administration date 28Nov2021 (Lot number: 320308D) at the age of 40 years as dose 3 (booster), single, administration date 23Apr2021 (Lot number: EW0161) as dose 2, single and administration date 31Mar2021 (Lot number: ER8734) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. The following information was reported: DRUG INEFFECTIVE (medically significant) with onset 04Jan2022, outcome "unknown", SUSPECTED COVID-19 (medically significant) with onset 04Jan2022, outcome "recovering" and all described as "Patient tested positive for COVID after receiving the 3rd dose of the vaccine"; IMMUNISATION (medically significant) with onset 28Nov2021, outcome "unknown", described as "Booster". The event "patient tested positive for covid after receiving the 3rd dose of the vaccine" was evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: Inteliswab test: (04Jan2022) positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of drug ineffective, suspected covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Drug ineffective
Hospital-Tage: -
Labordaten: Test Date: 20220104; Test Name: Inteliswab test; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2035257

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MN
Alter: 27,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 06.04.2021
Beginn: 31.12.2021
Tage bis Beginn: 269,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ageusia Cough Nasopharyngitis Respiratory tract congestion

Symptomtext

ith cold symptoms: cough, congestion, loss of taste. starting 12/31/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ageusia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Attention deficit; seasonal allergies
Andere Medikamente: Taking tylenol 1 tab Oral , Taking Ibuprofen 400 MG Tablet Orally once a day, Taking Vitamin B-Complex - Tablet as directed Orally , Taking Magnesium 250 MG Tablet 1 tablet with a meal Orally Once a day, Taking Loratadine 10 MG Tablet 1 tab
Allergien: none
Vorherige Impfungen: -

VAERS 2034548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: RI
Alter: 45,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Drug ineffective Immunisation Suspected COVID-19

Symptomtext

COVID infections; COVID infections; Booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administration date 04Nov2021 (Lot number: 320308D) at the age of 45 years as dose 3 (booster), single, administration date 24Mar2021 (Lot number: EP6955) as dose 2, single and administration date 01Mar2021 (Lot number: EL3247) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: IMMUNISATION (medically significant) with onset 04Nov2021, outcome "unknown", described as "Booster"; DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant) all with onset 03Jan2022, outcome "recovering" and all described as "COVID infections". Therapeutic measures were not taken as a result of drug ineffective, suspected covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Drug ineffective
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 21,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 18,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and State recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 19,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and State recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 19,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and State recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 16,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and State of MA recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 18,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and State recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 16,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and State of MA recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 20,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and State recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 17,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and state recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 20,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 17,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 21,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 19,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 3 weeks after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and state recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 17,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 16 days after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 17,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine was administered 16 days after beyond use date and is less effective. Treatment: Pt returning to our office for additional vaccine based on Pfizer and state recommendations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2031447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 21,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date, less effective. Treatment: Pt will return to our office to get additional vaccine, as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 16,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 17,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer and the state.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 16,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered Immunisation

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 17,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 30,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 34,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer and the state they live in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 18,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 17,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MS
Alter: 16,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 16 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 19,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 6 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 23,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 6 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 93,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 6 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer and the state.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 23,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 6 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer and the state of MA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MS
Alter: 21,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Vaccine administered 6 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 32,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 6 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer and the state.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: NJ
Alter: 20,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 2 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 35,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 2 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2028033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 35,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Adverse event Product storage error

Symptomtext

Adverse event: Vaccine administered 2 days after beyond use date and less effective. Treatment: Pt is receiving another dose in office as recommended by Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2027871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MA
Alter: 18,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Adverse event: Pt was administered vaccine that was 2 days past the beyond use date in fridge. Treatment: Pt will be receiving another booster in office as beyond use date vaccine is less effective.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2026256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CT
Alter: 39,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 07.11.2021
Beginn: 08.12.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Menstrual disorder

Symptomtext

Missed period. Cycle lasted 44 days. Started 12/8/2021. Current cycle is 35 days as of 1/11/2022. Still no period. Previously my period has been normal/regular for past year prior to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Menstrual disorder
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1995981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: OR
Alter: 16,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Inappropriate schedule of product administration

Symptomtext

patient was given second dose of Pfizer vaccine too soon (13 days apart from the fist dose)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: second dose of Pfizer vaccine was given too soon (13 days apart from the 1st dose)
Allergien: -
Vorherige Impfungen: -

VAERS 1836442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308d

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Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Alopecia

Symptomtext

Losing lots of hair; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 12 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 29Oct2021 12:00 (Lot number: 20021) at the age of 12 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: ALOPECIA (non-serious) with onset 30Oct2021 12:00, outcome "recovering", described as "Losing lots of hair". It was unknown if therapeutic measures were taken as a result of alopecia. Additional information: other vaccine same date lot number=32030BD, other vaccine same date vaccine date=29Oct2021, other vaccine same date dose number= 30. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: UT
Alter: 58,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 30.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tinnitus

Symptomtext

Mild, high pitched, tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Cholelithiasis, biliary colic
Vorgeschichte: ME/Chronic Fatigue
Andere Medikamente: none
Allergien: allergies to several antibiotics including penicillin family, first generation cephalosporins
Vorherige Impfungen: -

VAERS 1972079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: AK
Alter: 11,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Incorrect dose administered

Symptomtext

Minor patient too young for dose given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1968048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: IL
Alter: 68,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Extra dose administered No adverse event

Symptomtext

Patient came into the pharmacy on 12-19-2021 and requested to received Pfizer vaccination. Patient filled out a vaccination consent form where he signed and reported that he received a dose of Janssen Johnson COVID-19 vaccination on 04/16/2021. His CDC card also reported that he received Janssen Johnson COVID-19 only. The pharmacist made the clinical decision that it would be appropriate to administer Pfizer COVID-19 vaccine as a booster shot to the patient. Patient was monitored for 15 minutes and did not report any adverse health effects. Patient was healthy after her received the vaccination and left the pharmacy. Later, the pharmacist discovered that patient received Moderna COVID-19 vaccination at another pharmacy. Pharmacist called the patient to inform that it is no recommended by the CDC to receive 3 doses of each covid-19 vaccines and Pfizer vaccine that was received on 12-19-21 was inappropriate because it was not recommended by the CDC. Patient admitted that he wanted to get a booster of Pfizer because he is afraid of the COVID-19 virus. Patient deceived the pharmacy team because he did not report verbally or in written language anywhere that he received Moderna on 10-26-2021 at another Pharmacy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: No medical tests, no adverse events reported
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes and Heart Disease
Andere Medikamente: None reported
Allergien: None reported
Vorherige Impfungen: -

VAERS 1966932

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 22.10.2021
Beginn: 03.12.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abortion spontaneous Physical examination

Symptomtext

she had lost her baby; there was no more heart beat; This is a spontaneous report received from a contactable reporter (Pharmacist). The reporter is the parent. A 32 year-old female patient (pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 22Oct2021 (Lot number: 320308D) at the age of 31 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing), notes: no medical history. The patient was 7 weeks pregnant at the event onset. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose no: 1, LOT of 1st dose: 301558A), administration date: 04Oct2021, when the patient was 31 years old, for COVID-19 Immunization. The following information was reported: ABORTION SPONTANEOUS (medically significant) with onset 03Dec2021, outcome "unknown", described as "she had lost her baby; there was no more heart beat". The pregnancy resulted in spontaneous abortion. The fetal outcome is intrauterine death. The patient underwent the following laboratory tests and procedures: physical examination: (03Dec2021) there was no more heart beat, notes: The doctor measured that the baby could be 7 weeks. The patient just had a physical check with the obstetrician but no lab work. The patient received a vaccine on her first trimester and upon checking with her doctor 3 days ago she has lost the child that she is carrying and she had a vaccine second dose on 22Oct2021 (the patient received the first dose 20 days before). The reporter stated that it makes a sense because the baby was still around and the patient just had a check with the doctor to ensure that she was pregnant and that was on 24Oct2021 when she made an announcement that she was pregnant, so the baby was still there. She checked again on 03Dec2021 and there was no more heart beat. The doctor measured that the baby could be 7 weeks. The patient just a physical check with the obstetrician but no lab work.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the reported events Abortion spontaneous and suspect drug BNT162B2 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-202101739119 baby case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abortion spontaneous
Hospital-Tage: -
Labordaten: Test Date: 20211203; Test Name: physical check; Result Unstructured Data: Test Result: there was no more heart beat; Comments: The doctor measured that the baby could be 7 weeks. The patient just a physical check with the obstetrician but no lab work.
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No, Comment: no medical history.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1962225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: MD
Alter: 48,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 13.11.2021
Beginn: 10.12.2021
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Herpes zoster

Symptomtext

Shingles on left arm where vaccination was given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1958630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 21.10.2021
Beginn: 08.12.2021
Tage bis Beginn: 48,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19

Symptomtext

Patient was admitted to Hospital on 12/8/2021 for COVID related symptoms. This is considered a breakthrough case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1954939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: UT
Alter: 42,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Needle issue Underdose

Symptomtext

During vaccine administration the syringe and needle separated. It is unknown how much of the vaccine the patient received as some liquid came out of the syringe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Needle issue
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: bupropion, quetiapine, sertraline, nicotine lozenge, ibuprofen, bictegravir/emtricitabine/tenofovir.
Allergien: nka
Vorherige Impfungen: -

VAERS 1951664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: NY
Alter: 28,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 22.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Lymphadenopathy

Symptomtext

Swollen lymph nodes under right arm a few days after both the 1st & 2nd shot was administered. I'm scheduled to see a general physician in a few days to assess the issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymphadenopathy
Hospital-Tage: -
Labordaten: N/A, haven't' seen a physician yet
Aktuelle Erkrankungen: N/A
Vorgeschichte: Neurological issues/abnormalities
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Chills, joint pain, pins & needles sensations over body (around 2009-2010, exact dates & brand of vaccines cannot be recalled)

VAERS 1951569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 51,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

No symptomatic / adverse events reported. Expired 0.3 mL Pfizer 12+ older dose administered. Expired by 5 days. Directed by Dept of Health and Pfizer to file VAERS report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Unknown.
Vorgeschichte: Fibromyalgia, liver hemangioma, elevated alpha fetoprotein, polycythemia, vitamin D deficiency, insomnia, chronic pain syndrome, depression, benign thyroid cyst, bulging of cervical intervertebral disc without myelopathy, connective tissue disease, hemangioma, IBS, MTHFR mutation, stress incontinence in female, elevated hemoglobin, hypothyroidism
Andere Medikamente: Celebrex 200 mg, Vitamin D3, Flexeril 10 mg, Pristiq 50 mg, Dexilant 30 mg, Cymbalta 20 mg, Famvir 500 mg, Allegra 180 mg, Flonase Nasal, Neurontin 100 mg, Probiotic 10 billion cell cap, Protonix 20 mg, Progesterone oral, Transderm-SCOP pat
Allergien: Hydromorphone
Vorherige Impfungen: -

VAERS 1951543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 31,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

No adverse event Product storage error

Symptomtext

No symptomatic / adverse events reported. Expired 0.3 mL Pfizer 12+ older dose administered. Expired by 5 days. Directed by Dept of Health and Pfizer to file VAERS report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Unknown.
Vorgeschichte: None.
Andere Medikamente: Sprintec 0.25 mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1951527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 27,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

No symptomatic / adverse events reported. Expired 0.3 mL Pfizer 12+ older dose administered. Expired by 5 days. Directed by CO Dept of Health and Pfizer to file VAERS report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Unknown.
Vorgeschichte: Exercise-induced asthma, Migraine with Aura, Tree nut allergy
Andere Medikamente: Albuterol inhaler, Biotin, Epipen, Nexplanon implant, Ferrous sulfate, Omega-3 417 mg
Allergien: Nuts, Peanuts, Tree nuts, Duocet, Hydrocodone
Vorherige Impfungen: -

VAERS 1951498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 64,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

No symptomatic / adverse events reported. Expired 0.3 mL Pfizer 12+ older dose administered. Expired by 5 days. Directed by Dept of Health and Pfizer to file VAERS report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Unknown.
Vorgeschichte: Essential hypertension, COPD, Bipolar 2 disorder, Endogenous depression, Renal cell carcinoma, ADHD, Hx of Unilateral Nephrectomy, GERD, History of Hep C infection
Andere Medikamente: Albuterol inhaler, Norvasc 10 mg, Wellbutrin 300 mg, Voltaren gel, Hydrodiuril 12.5 mg, Micardis 80 mg
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1951486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CO
Alter: 25,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

No adverse event Product storage error

Symptomtext

No symptomatic / adverse events reported. Expired 0.3 mL Pfizer 12+ older dose administered. Expired by 5 days. Directed by Dept of Health and Pfizer to file VAERS report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: -
Vorgeschichte: ADHD, Anxiety
Andere Medikamente: Adderall 10 mg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1910467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 18.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Magnetic resonance imaging head Transient ischaemic attack

Symptomtext

Had a TIA; This is a spontaneous report received from contactable Consumer. The reporter is the patient. A 63 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 18Nov2021 12:00 (Lot number: 320308D) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (dose 2, Left arm,lot number EW0169), administration date: 20Apr2021, when the patient was 63 years old, for COVID-19 immunization; Bnt162b2 (dose 1, Left arm, lot number ER8733), administration date: 30Mar2021, when the patient was 63 years old, for COVID-19 immunization. The following information was reported: TRANSIENT ISCHAEMIC ATTACK (medically significant) with onset 21Nov2021 10:15, outcome "recovered" (Nov2021), described as "Had a TIA". The event "had a tia" was evaluated at the physician office visit. Therapeutic measures were taken as a result of transient ischaemic attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Magnetic resonance imaging head
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1910467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 18.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Magnetic resonance imaging head Transient ischaemic attack

Symptomtext

Had a TIA; This is a spontaneous report received from contactable Consumer. The reporter is the patient. A 63 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 18Nov2021 12:00 (Lot number: 320308D) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (dose 2, Left arm,lot number EW0169), administration date: 20Apr2021, when the patient was 63 years old, for COVID-19 immunization; Bnt162b2 (dose 1, Left arm, lot number ER8733), administration date: 30Mar2021, when the patient was 63 years old, for COVID-19 immunization. The following information was reported: TRANSIENT ISCHAEMIC ATTACK (medically significant) with onset 21Nov2021 10:15, outcome "recovered" (Nov2021), described as "Had a TIA". The event "had a tia" was evaluated at the physician office visit. Therapeutic measures were taken as a result of transient ischaemic attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Magnetic resonance imaging head
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: SC
Alter: 9,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Incorrect dose administered Product administration error

Symptomtext

Patient was given the >12year old product instead of the 5-11 year old product. Error was recognized after the vaccine was administered when healthcare professional went to document. Pharmacist that was contacted, recommended to keep child in office and observe for at least 30 minutes. Advised that likelihood of side effects common but harm not likely. Advised to treat any fever or symptoms to treat with acetaminophen or ibuprofen. Patient left the office after 30 minutes. No further issues reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: none
Andere Medikamente: None in chart
Allergien: Clindamycin
Vorherige Impfungen: -

VAERS 1939703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 41,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use 11/29/21, vaccine given 12/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 40,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 49,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 30,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 53,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 65,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 24,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 03.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/3/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 34,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 02.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/2/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 12,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 02.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/2/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 45,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 02.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given 12/2/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 67,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 01.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given on 12/1/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 65,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 01.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given on 12/1/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1939442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 320308D

gering

Staat: TN
Alter: 80,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 01.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

beyond use date 11/29/21, vaccine given on 12/1/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -