VAERS Reports #FE3594

VAERS 2728670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 29.12.2023
Impfdatum: 16.12.2021
Beginn: 13.11.2023
Tage bis Beginn: 697,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory distress syndrome Acute respiratory failure Anaemia Azotaemia Blood creatinine normal Blood glucose normal Blood urea increased COVID-19 Cellulitis Chronic obstructive pulmonary disease Computerised tomogram abnormal Computerised tomogram limb Computerised tomogram thorax abnormal Condition aggravated Culture wound negative Disease complication Electrocardiogram abnormal Endotracheal intubation

Symptomtext

Patient is a 62 y.o. male, nursing home resident with history of end-stage COPD on 4L NC at home, hypertension, hyperlipidemia, CHF, alcohol abuse, diabetes mellitus type 2, who presented to Country Hospital with respiratory distress and hypoxia then transferred to General Hospital. Goal of care Palliative following, pt with very poor prognosis, advanced COPD on Vent due to COVID with multiple complications. Discussed with family and code status changed to DNR CC, compassion extubation done 11/22. Pt to be admitted to inpt hospice. Comfort medication ordered. Acute on chronic hypoxic hypercapnic respiratory failure Acute COPD exacerbation COVID 19 with ARDS MRSA cavitary pneumonia Possibly COPD exacerbation precipitated by COVID infection. Patient oxygen home requirement on 4 L nasal cannula. Required BIPAP and later intubated at County before transferring to on 11/13. Sputum culture 11/14 + MRSA Antibiotics changed from Rocephin and azithromycin to vancomycin. Cefepime clinda started on 11/20 for arm cellulitis Received remdesevir and dexamethasone. CT chest repeated today (11/20) Multiple cavitating lesions in the right lung, probable cavitating pneumonia Pulmonary following Off pressors since 11/16 Compassion extubation 11/22/23 Left upper extremity cellulitis Noted worsening erythema and edema of LUE 11/20. CT arm Multiple foci of air density are identified within the soft tissues along the medial aspect of the left upper arm, findings suspicious for necrotizing infection with a gas-forming organism/necrotizing fasciitis Surgery took pt to OR, no clear signs of Nec fasc, I&D done 11/20. Wound cultures negative Received Cefepime, clinda, Vancomycin Wound care Thrombocytopenia Chronic anemia Platelets remains low at 122k, no signs of bleeding. Hb stable ~11 Due to acute illness monitor Uremia Ongoing uremia, BUN improving 58. normal Cr I/O overall even, but -1.5L in the last 24 hrs. Monitor for now HFpEF, chronic Hypertension EKG showed sinus tachycardia with no acute ischemic changes. Initial hypotension requiring pressors, now resolved. Metoprolol initiated 11/17 Diabetes mellitus type 2 complicated with peripheral neuropathy Blood glucose 120, and last A1c 14%. HA1C 7.4. Continue Lantus and Monitor blood glucose and start SSI during admission. Continue home gabapentin. Alcoholic liver cirrhosis with Ascites History of alcohol abuse hold home lasix and spironolactone. schizoaffective disorder Bipolar disorder History of seizure Continue home Abilify, and Keppra. Morbid obesity BMI 32.77 kg/M2. Lifestyle modification is recommended.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2649401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: -
Alter: 20,0
Geschlecht: M
Eingang: 26.06.2023
Impfdatum: 07.12.2021
Beginn: 27.04.2023
Tage bis Beginn: 506,0
Dosis: 3
Route/Site: IM / LA

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

Deep vein thrombosis Pneumonia Pulmonary embolism

Symptomtext

I26.99 ACUTE PULMONARY EMBOLISM 4/27/2023 PNEUMONIA I82.442 ACUTE DVT OF LEFT TIBIAL VEIN 4/27/2023 PNEUMONIA

Weitere VAERSDATA-Felder

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

VAERS 2639899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MD
Alter: 60,0
Geschlecht: M
Eingang: 01.06.2023
Impfdatum: 13.12.2021
Beginn: 23.09.2022
Tage bis Beginn: 284,0
Dosis: 3
Route/Site: - / LA

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

Cerebrovascular accident

Symptomtext

Stroke; 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 male patient received BNT162b2 (BNT162B2), on 13Dec2021 as dose 3 (booster), single (Lot number: FE3594) at the age of 60 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Enlarged prostate" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin. Concomitant medication(s) included: TAMSULOSIN; LATANOPROST; DORZOLAMIDE. Vaccination history included: BNT162b2 (DOSE 2, SINGLE, Batch/Lot number: ER8732, Anatomical location: Left Arm), administration date: 30Mar2021, for Covid-19 immunization; BNT162b2 (DOSE 1, SINGLE, Batch/Lot number: EN1699, Anatomical location: Left Arm), administration date: 03Mar2021, for Covid-19 Immunization. The following information was reported: CEREBROVASCULAR ACCIDENT (hospitalization) with onset 23Sep2022 at 15:30, outcome "recovered with sequelae", described as "Stroke". The patient was hospitalized for cerebrovascular accident (hospitalization duration: 2 day(s)). The event "stroke" required emergency room visit. Therapeutic measures were taken as a result of cerebrovascular accident. Clinical course included: AE treatment: Stroke treatment & clot buster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Enlarged prostate; Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: TAMSULOSIN; LATANOPROST; DORZOLAMIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2631204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 12.05.2023
Impfdatum: 17.12.2021
Beginn: 09.04.2022
Tage bis Beginn: 113,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction Aortic valve stenosis

Symptomtext

I21.11 ACUTE ST ELEVATION MI, RIGHT CORONARY ARTERY 4/9/2022 ACUTE ST ELEVATION MI, UNSPECIFIED AORTIC VALVE STENOSIS I21.3 ACUTE ST ELEVATION MI, UNSPECIFIED 4/9/2022 ACUTE ST ELEVATION MI, UNSPECIFIED AORTIC VALVE STENOSIS

Weitere VAERSDATA-Felder

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

VAERS 2623213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 13.12.2021
Beginn: 27.07.2022
Tage bis Beginn: 226,0
Dosis: 2
Route/Site: - / -

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

Hypoxia Obstructive sleep apnoea syndrome Pulmonary embolism

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE OBSTRUCTIVE SLEEP APNEA ACUTE PULMONARY EMBOLISM HYPOXEMIA

Weitere VAERSDATA-Felder

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

VAERS 2522931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 23.12.2021
Beginn: 18.03.2023
Tage bis Beginn: 450,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Anticoagulant therapy Cardiac stress test normal Chest pain Echocardiogram abnormal Echocardiogram Ejection fraction Fluid intake restriction Fraction of inspired oxygen Hypokalaemia Laboratory test Lung infiltration Medical diet Obesity

Symptomtext

Admission Date: 3/18/2023 Discharge Date: Mar 21, 2023 PRESENTING PROBLEM: Chest pain [R07.9] HOSPITAL COURSE: 67-year-old with past medical history significant for COPD, T2DM, HLD, CHF, HTN, OSA, alcoholic liver cirrhosis initially presented from Ludington on 03/14 for cardiology evaluation of nonexertional typical chest pain on 3/18. Was recently discharged after treatment for COVID-19 from 03/8-3/11. Presented back to the emergency department on 03/14/2023 with substernal chest pain. Was diuresed and discharged home on bronchodilators. Presented to the emergency department again on 03/17/2023 with similar symptoms, labs showed mild elevation tropes (17->59) and chest x-ray showing pulmonary vascular congestion. Patient was diuresed with IV Bumex and given nebulizers. Case was discussed with Cardiology who recommended starting the patient on heparin and transferring to Butterworth for additional recommendations. Repeated troponins were flat. Echo on 3/19 with EF 65% and no WMA however suboptimal acoustic windows. Etiology recommended stress test. Lexiscan on 3/21 with no evidence for myocardial ischemia. Cardiology felt that elevated troponins was likely myocardial and really related to recent COVID infection. Did not recommend any further cardiac workup or follow-up at this time. Chest pain resolved. Patient was transitioned back to home Bumex with continued good diureses. Patient discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: 12/22/2021 - 12/23/2021 (31 hours) Acute on chronic respiratory failure with hypoxia Principal problem
Vorgeschichte: Mixed type COPD (chronic obstructive pulmonary disease) Primary hypertension Other hyperlipidemia Type 2 diabetes mellitus with diabetic polyneuropathy, without long-term current use of insulin Presence of biventricular AICD Thrombocytopenia Diet-controlled diabetes mellitus Simple chronic bronchitis Obstructive sleep apnea Acute on chronic respiratory failure with hypoxia and hypercapnia Alcoholic cirrhosis of liver without ascites Sleep-related hypoventilation due to pulmonary parenchymal pathology Leukopenia Morbid obesity with BMI of 45.0-49.9, adult Fall from standing Chronic obstructive pulmonary disease with (acute) exacerbation Splenomegaly Hypokalemia COVID-19 Pneumonia due to infectious organism Chronic diastolic heart failure Peripheral vascular disease AKI (acute kidney injury) Chest pain
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ALBUTEROL 108 (90 Base) MCG/ACT inhaler aspirin EC 81 MG enteric coated tablet baclofen (LIORESAL) 10 MG tablet budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler bumetanide (BUMEX) 2 MG tablet
Allergien: None
Vorherige Impfungen: -

VAERS 2522931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 23.12.2021
Beginn: 18.03.2023
Tage bis Beginn: 450,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Anticoagulant therapy Cardiac stress test normal Chest pain Echocardiogram abnormal Echocardiogram Ejection fraction Fluid intake restriction Fraction of inspired oxygen Hypokalaemia Laboratory test Lung infiltration Medical diet Obesity

Symptomtext

Admission Date: 3/18/2023 Discharge Date: Mar 21, 2023 PRESENTING PROBLEM: Chest pain [R07.9] HOSPITAL COURSE: 67-year-old with past medical history significant for COPD, T2DM, HLD, CHF, HTN, OSA, alcoholic liver cirrhosis initially presented from Ludington on 03/14 for cardiology evaluation of nonexertional typical chest pain on 3/18. Was recently discharged after treatment for COVID-19 from 03/8-3/11. Presented back to the emergency department on 03/14/2023 with substernal chest pain. Was diuresed and discharged home on bronchodilators. Presented to the emergency department again on 03/17/2023 with similar symptoms, labs showed mild elevation tropes (17->59) and chest x-ray showing pulmonary vascular congestion. Patient was diuresed with IV Bumex and given nebulizers. Case was discussed with Cardiology who recommended starting the patient on heparin and transferring to Butterworth for additional recommendations. Repeated troponins were flat. Echo on 3/19 with EF 65% and no WMA however suboptimal acoustic windows. Etiology recommended stress test. Lexiscan on 3/21 with no evidence for myocardial ischemia. Cardiology felt that elevated troponins was likely myocardial and really related to recent COVID infection. Did not recommend any further cardiac workup or follow-up at this time. Chest pain resolved. Patient was transitioned back to home Bumex with continued good diureses. Patient discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: 12/22/2021 - 12/23/2021 (31 hours) Acute on chronic respiratory failure with hypoxia Principal problem
Vorgeschichte: Mixed type COPD (chronic obstructive pulmonary disease) Primary hypertension Other hyperlipidemia Type 2 diabetes mellitus with diabetic polyneuropathy, without long-term current use of insulin Presence of biventricular AICD Thrombocytopenia Diet-controlled diabetes mellitus Simple chronic bronchitis Obstructive sleep apnea Acute on chronic respiratory failure with hypoxia and hypercapnia Alcoholic cirrhosis of liver without ascites Sleep-related hypoventilation due to pulmonary parenchymal pathology Leukopenia Morbid obesity with BMI of 45.0-49.9, adult Fall from standing Chronic obstructive pulmonary disease with (acute) exacerbation Splenomegaly Hypokalemia COVID-19 Pneumonia due to infectious organism Chronic diastolic heart failure Peripheral vascular disease AKI (acute kidney injury) Chest pain
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ALBUTEROL 108 (90 Base) MCG/ACT inhaler aspirin EC 81 MG enteric coated tablet baclofen (LIORESAL) 10 MG tablet budesonide/formoterol (SYMBICORT) 160-4.5 MCG/ACT inhaler bumetanide (BUMEX) 2 MG tablet
Allergien: None
Vorherige Impfungen: -

VAERS 2587393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: KY
Alter: 69,0
Geschlecht: F
Eingang: 26.02.2023
Impfdatum: 03.01.2022
Beginn: 02.08.2022
Tage bis Beginn: 211,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury COVID-19 Cerebrovascular accident Chronic kidney disease Condition aggravated Death Gastrointestinal haemorrhage SARS-CoV-2 test positive

Symptomtext

PATIENT ADMITTED TO HOSPITAL ON 7/9/22 FROM OUTSIDE FACILITY FOR AN AKI ON TOP OF HER CKD. SHE WAS COVID-19+ AT TIME OF ADMISSION AND REQUIRING OXYGEN. PATIENT HAD RECURRENT STROKES, GI BLEED, AND ACUTE ON CKD. PATIENT DECLINED DURING ADMISSION AND WAS TRANSITIONED TO DNR/DNI AND THEN MADE COMFORTABLE. PATIENT DIED 8/2/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: COVID-19 SPECIMEN COLLECTED ON 7/6/2022 - POSITIVE VIA PCR
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: PMH CAD; CHF; CKD; HTN; TYPE 2 DIABETES; HLD; ANEMIA; AND GALLBLADDER DISEASE;
Andere Medikamente: ASPIRIN; DICLOFENAC SODIUM; ALLOPURINOL; FERROUS SULFATE; NITROGLYCERIN; ATORVASTATIN; ATORVASTATIN; CITALOPRAM; COLESEVELAM; GLIPIZIDE; HYDRALAZINE; ISOSORBIDE MONONITRATE; METOPROIOL SUCCINATE; SITAGLIPTIN; ZETIA; TICAGRELOR;
Allergien: INFLUENZA VACCINE; PENICILLINS; POVIDONE-IODINE; SOAP; SULFAMETHOXAZOLE; TRIMETHOPRIM;
Vorherige Impfungen: -

VAERS 2162830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 27.12.2021
Beginn: 01.02.2023
Tage bis Beginn: 401,0
Dosis: 2
Route/Site: - / -

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

Abdominal distension Acute respiratory failure Ammonia normal Blood gases normal Blood pressure increased Acute respiratory distress syndrome COVID-19 COVID-19 pneumonia Computerised tomogram thorax normal Hypoxia Chest X-ray abnormal Cough Blood thyroid stimulating hormone normal Cardiomegaly Computerised tomogram abdomen normal Computerised tomogram head normal Diuretic therapy Dyspnoea

Symptomtext

Admission Date: 2/1/2023 Discharge Date: 2/16/23 PRESENTING PROBLEM: Acute respiratory insufficiency Acute respiratory failure with hypoxia HOSPITAL COURSE: Patient is a 51-year-old female with PMH significant for hypertension, OSA/CPAP, epilepsy on antiepileptics, type 2 diabetes, history of malignant brain tumor status post excision/VP shunt, thyroid cancer, anoxic brain injury/developmental delay and right hemiplegia with associated dysphagia/feeding tube, nonverbal/non communicative, wheelchair-bound complete care at baseline at home with mom as being primary caregiver, hypothyroidism presents to the hospital on 2/1---with complaints of increased blood pressure at home, facial swelling, abdominal distension and labored breathing. Patient was noted to be hypoxic in ER at 88%, tachypneic, needing supplemental oxygen and chest x-ray showing cardiomegaly and pulmonary congestion. Patient was admitted with suspicion for pulmonary congestion related to uncontrolled blood pressures, echo without any significant findings, was given diuretics. Echo showed EF of 70%. Blood pressure medications were further adjusted resulting in better control. Patient developed fever and 2/6 and with continued hypoxia further workup with chest x-ray that showed infiltrates, CT thorax/abdomen and pelvis without any acute changes. Urinalysis was negative. Patient did not have any meningeal signs. Ultimately she did test positive for COVID-19 on film array and interestingly her film array was negative at admit with prior COVID infection in Dec 2022. Patient was started on remdesivir and antibiotics discontinued. Her hypoxia and respiratory status worsened so she was started on dexamethasone with gradual improvement. Patient also developed increased lethargy around 2/5 of unclear etiology. Further workup with CT head without any acute changes, TSH, VBG, ammonia, B12 were all normal. Neurology consultation was obtained who recommended MRI brain (no acute changes), EEG (which was abnormal with occasional LR DA and GRDA and interictal epileptiform discharges) her home Keppra and Tegretol doses were increased. She had significant improvement with steroids. She was weaned down to RA and ultimately discharged home is stable conditions with plans to continue increased dose of BP meds and to finish steroids. It was discussed to the mother/caregiver to return if respiratory status worsened after stopping steroids for covid with the possibility of post-covid ILD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) History of brain tumor Cognitive impairment Hypokalemia Postsurgical hypothyroidism Mild persistent asthma with acute exacerbation Allergic rhinitis due to pollen History of papillary thyroid carcinoma Fatty liver Dysphagia Multifactorial functional impairment Constipation by delayed colonic transit Seborrhea capitis Primary hypertension Localization-related symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus (HCC) VP (ventriculoperitoneal) shunt status Insomnia At risk for falls OSA (obstructive sleep apnea) Morbid obesity (HCC) Lip swelling Excessive cerumen in both ear canals Discharge of right eye Difficult to control oropharyngeal secretions in evaluation for tracheostomy, not yet placed Right hemiplegia (HCC) Uses feeding tube Cough COVID-19 intermittent irregular breathing Skin lesion of face DM type 2 with diabetic dyslipidemia (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 10 MG tablet budesonide (PULMICORT) 1 MG/2ML nebulizer suspension carBAMazepine (TEGRETOL) 100 MG/5ML suspension dex
Allergien: Latex Nystatin PenicillinsItching
Vorherige Impfungen: -

VAERS 2162830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 27.12.2021
Beginn: 01.02.2023
Tage bis Beginn: 401,0
Dosis: 2
Route/Site: IM / -

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

Abdominal distension Acute respiratory failure Ammonia normal Blood gases normal Blood pressure increased Acute respiratory distress syndrome COVID-19 COVID-19 pneumonia Computerised tomogram thorax normal Hypoxia Chest X-ray abnormal Cough Blood thyroid stimulating hormone normal Cardiomegaly Computerised tomogram abdomen normal Computerised tomogram head normal Diuretic therapy Dyspnoea

Symptomtext

Admission Date: 2/1/2023 Discharge Date: 2/16/23 PRESENTING PROBLEM: Acute respiratory insufficiency Acute respiratory failure with hypoxia HOSPITAL COURSE: Patient is a 51-year-old female with PMH significant for hypertension, OSA/CPAP, epilepsy on antiepileptics, type 2 diabetes, history of malignant brain tumor status post excision/VP shunt, thyroid cancer, anoxic brain injury/developmental delay and right hemiplegia with associated dysphagia/feeding tube, nonverbal/non communicative, wheelchair-bound complete care at baseline at home with mom as being primary caregiver, hypothyroidism presents to the hospital on 2/1---with complaints of increased blood pressure at home, facial swelling, abdominal distension and labored breathing. Patient was noted to be hypoxic in ER at 88%, tachypneic, needing supplemental oxygen and chest x-ray showing cardiomegaly and pulmonary congestion. Patient was admitted with suspicion for pulmonary congestion related to uncontrolled blood pressures, echo without any significant findings, was given diuretics. Echo showed EF of 70%. Blood pressure medications were further adjusted resulting in better control. Patient developed fever and 2/6 and with continued hypoxia further workup with chest x-ray that showed infiltrates, CT thorax/abdomen and pelvis without any acute changes. Urinalysis was negative. Patient did not have any meningeal signs. Ultimately she did test positive for COVID-19 on film array and interestingly her film array was negative at admit with prior COVID infection in Dec 2022. Patient was started on remdesivir and antibiotics discontinued. Her hypoxia and respiratory status worsened so she was started on dexamethasone with gradual improvement. Patient also developed increased lethargy around 2/5 of unclear etiology. Further workup with CT head without any acute changes, TSH, VBG, ammonia, B12 were all normal. Neurology consultation was obtained who recommended MRI brain (no acute changes), EEG (which was abnormal with occasional LR DA and GRDA and interictal epileptiform discharges) her home Keppra and Tegretol doses were increased. She had significant improvement with steroids. She was weaned down to RA and ultimately discharged home is stable conditions with plans to continue increased dose of BP meds and to finish steroids. It was discussed to the mother/caregiver to return if respiratory status worsened after stopping steroids for covid with the possibility of post-covid ILD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) History of brain tumor Cognitive impairment Hypokalemia Postsurgical hypothyroidism Mild persistent asthma with acute exacerbation Allergic rhinitis due to pollen History of papillary thyroid carcinoma Fatty liver Dysphagia Multifactorial functional impairment Constipation by delayed colonic transit Seborrhea capitis Primary hypertension Localization-related symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus (HCC) VP (ventriculoperitoneal) shunt status Insomnia At risk for falls OSA (obstructive sleep apnea) Morbid obesity (HCC) Lip swelling Excessive cerumen in both ear canals Discharge of right eye Difficult to control oropharyngeal secretions in evaluation for tracheostomy, not yet placed Right hemiplegia (HCC) Uses feeding tube Cough COVID-19 intermittent irregular breathing Skin lesion of face DM type 2 with diabetic dyslipidemia (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 10 MG tablet budesonide (PULMICORT) 1 MG/2ML nebulizer suspension carBAMazepine (TEGRETOL) 100 MG/5ML suspension dex
Allergien: Latex Nystatin PenicillinsItching
Vorherige Impfungen: -

VAERS 2162830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 27.12.2021
Beginn: 01.02.2023
Tage bis Beginn: 401,0
Dosis: 2
Route/Site: IM / AR

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

Abdominal distension Acute respiratory failure Ammonia normal Blood gases normal Blood pressure increased Acute respiratory distress syndrome COVID-19 COVID-19 pneumonia Computerised tomogram thorax normal Hypoxia Chest X-ray abnormal Cough Blood thyroid stimulating hormone normal Cardiomegaly Computerised tomogram abdomen normal Computerised tomogram head normal Diuretic therapy Dyspnoea

Symptomtext

Admission Date: 2/1/2023 Discharge Date: 2/16/23 PRESENTING PROBLEM: Acute respiratory insufficiency Acute respiratory failure with hypoxia HOSPITAL COURSE: Patient is a 51-year-old female with PMH significant for hypertension, OSA/CPAP, epilepsy on antiepileptics, type 2 diabetes, history of malignant brain tumor status post excision/VP shunt, thyroid cancer, anoxic brain injury/developmental delay and right hemiplegia with associated dysphagia/feeding tube, nonverbal/non communicative, wheelchair-bound complete care at baseline at home with mom as being primary caregiver, hypothyroidism presents to the hospital on 2/1---with complaints of increased blood pressure at home, facial swelling, abdominal distension and labored breathing. Patient was noted to be hypoxic in ER at 88%, tachypneic, needing supplemental oxygen and chest x-ray showing cardiomegaly and pulmonary congestion. Patient was admitted with suspicion for pulmonary congestion related to uncontrolled blood pressures, echo without any significant findings, was given diuretics. Echo showed EF of 70%. Blood pressure medications were further adjusted resulting in better control. Patient developed fever and 2/6 and with continued hypoxia further workup with chest x-ray that showed infiltrates, CT thorax/abdomen and pelvis without any acute changes. Urinalysis was negative. Patient did not have any meningeal signs. Ultimately she did test positive for COVID-19 on film array and interestingly her film array was negative at admit with prior COVID infection in Dec 2022. Patient was started on remdesivir and antibiotics discontinued. Her hypoxia and respiratory status worsened so she was started on dexamethasone with gradual improvement. Patient also developed increased lethargy around 2/5 of unclear etiology. Further workup with CT head without any acute changes, TSH, VBG, ammonia, B12 were all normal. Neurology consultation was obtained who recommended MRI brain (no acute changes), EEG (which was abnormal with occasional LR DA and GRDA and interictal epileptiform discharges) her home Keppra and Tegretol doses were increased. She had significant improvement with steroids. She was weaned down to RA and ultimately discharged home is stable conditions with plans to continue increased dose of BP meds and to finish steroids. It was discussed to the mother/caregiver to return if respiratory status worsened after stopping steroids for covid with the possibility of post-covid ILD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) History of brain tumor Cognitive impairment Hypokalemia Postsurgical hypothyroidism Mild persistent asthma with acute exacerbation Allergic rhinitis due to pollen History of papillary thyroid carcinoma Fatty liver Dysphagia Multifactorial functional impairment Constipation by delayed colonic transit Seborrhea capitis Primary hypertension Localization-related symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus (HCC) VP (ventriculoperitoneal) shunt status Insomnia At risk for falls OSA (obstructive sleep apnea) Morbid obesity (HCC) Lip swelling Excessive cerumen in both ear canals Discharge of right eye Difficult to control oropharyngeal secretions in evaluation for tracheostomy, not yet placed Right hemiplegia (HCC) Uses feeding tube Cough COVID-19 intermittent irregular breathing Skin lesion of face DM type 2 with diabetic dyslipidemia (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 10 MG tablet budesonide (PULMICORT) 1 MG/2ML nebulizer suspension carBAMazepine (TEGRETOL) 100 MG/5ML suspension dex
Allergien: Latex Nystatin PenicillinsItching
Vorherige Impfungen: -

VAERS 2569996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: -
Alter: 89,0
Geschlecht: M
Eingang: 28.01.2023
Impfdatum: 20.12.2021
Beginn: 07.01.2023
Tage bis Beginn: 383,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Anaemia Asthenia Benign prostatic hyperplasia Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cachexia Decubitus ulcer Dehydration Dementia Fall Gastrooesophageal reflux disease Haemoglobin decreased Hyponatraemia Leukocytosis Pyrexia Respiratory failure

Symptomtext

Acute on chronic respiratory failure with hypoxia COVID-19 pneumonia only Sepsis present on admission due to above Patient from SNF. Family stated patient was positive on 1/4, however unable to verify. Swabbed on 1/8 and was positive for COVID-19. Patient is febrile, tachycardic, has leukocytosis. Discussed goals of care at length with family yesterday and will continue to keep the patient comfortable. Patient will be discharged home with hospice likely tomorrow. Continue comfort measures for now Tylenol for fever Initially required 4 L O2 on admission. Titrate supplemental O2 for comfort 4L. Comfort measures in place including muscle relaxants, anxiety medication, pain medication. Elevated BNP, chronic BNP 2797, previously 28550 Hyponatremia, mild Due to dehydration Refrain from IVF resuscitation due to DNR cc Anemia, stable Hb 10.5, baseline Hb 9.1-9.9 BPH Continue flomax and proscar GERD Continue protonix Cachexia POA Debility Dementia Frequent falls Pressure sores buttock stage I POA Sacral pressure ulcer stage I POA Follow-up with hospice care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2528534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 11.12.2022
Impfdatum: 20.12.2021
Beginn: 05.12.2022
Tage bis Beginn: 350,0
Dosis: 3
Route/Site: IM / -

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

Cerebral haemorrhage Coma Intraventricular haemorrhage Respiratory failure Subarachnoid haemorrhage

Symptomtext

Patient in coma, respiratory failure 2/2 intracerebral hemorrhage, intraventricular hemorrhage, and subarachnoid hemorrhage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2494980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 01.04.2021
Beginn: 06.09.2022
Tage bis Beginn: 523,0
Dosis: 3
Route/Site: - / -

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

Death Pyrexia

Symptomtext

09/06/22 presents to ED for "fever". PMHx of "afib not on thinners, HTN, HLD"

Weitere VAERSDATA-Felder

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

VAERS 2453622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 05.01.2022
Beginn: 01.09.2022
Tage bis Beginn: 239,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Aspergillus test negative Asthenia Bronchial secretion retention Bronchiectasis Bronchopulmonary aspergillosis Bronchoscopy abnormal COVID-19 Cognitive disorder Computerised tomogram thorax abnormal Culture positive Lung consolidation Malaise Pneumonia pseudomonal Pulmonary mass Respiratory failure SARS-CoV-2 test positive Stenotrophomonas infection

Symptomtext

Patient with 3 COVID vaccines who admitted with complications r/t COVID. Provider d/c note "77 y/o female with history of COPD and Hypertension that presents following recent hospitalization for hypoxemia on 8/19. Bronchoscopy and subsequent BAL demonstrated aspergillus antigen. Culture from lavage showed stenotrophomonas, pseudomonas putida, candida, aspergillus. Patient admitted here on 9/1 for persistent hypoxemia found to be COVID positive, with symptoms starting on 8/30. Imaging significant for CT chest showing stable pulmonic nodules w/ new wedge-shaped atelectatic consolidation & traction bronchiectasis. Patient received seven days of Levaquin therapy, completed a remdesivir course, and was on prednisone 40mg day. Voriconazole for aspergillus also started. Hospital Course: No notes on file. These were her acute medical issues addressed: Acute on chronic hypercapnic, hypoxic respiratory failure: likely new baseline- likely due to acute COVID-19 infection, chronic mucus plugging, suspected Stenotrophomonas, Pseudomonas pneumonia- seen by Pulmonary team. Supplement oxygen with goal SpO2 of 88-92%- aggressive pulmonary toileting- completed 7 days of prednisone and Levaquin- completed Remdesivir treatment. Pulmonary Aspergillosis- continue voriconazole. Total of 3 months: thru 12/5/22- 1 3 beta glucan, aspergillosis galactomannan negative- will need infectious disease clinic follow-up in 4-6 weeks post discharge- will require CMP, complete blood count, voriconazole level around 10/7. Tobacco dependence- nicotine patch- smoking cessation counseling given. Hypertension- Aldactone, Lasix- Held lisinopril for now. Resume if hypertensive. Mild cognitive impairment. Code status: Do not resuscitate DNI. Discharged in frail condition, to local center for further rehab".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: COVID Detected PCR on 09/01/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Venous insufficiency, COPD exacerbation (*), Colon cancer screening, Age-related osteoporosis without current pathological fracture.
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2395945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: DE
Alter: 45,0
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: 16.12.2021
Beginn: 06.07.2022
Tage bis Beginn: 202,0
Dosis: 3
Route/Site: - / LA

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

Appendicectomy Investigation Pulmonary embolism Pulmonary thrombosis COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Since the vaccination, has the patient been tested for COVID-19?:Yes/Result: Positive; Since the vaccination, has the patient been tested for COVID-19?:Yes/Result: Positive; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old male patient received BNT162b2 (BNT162B2), on 02Mar2021 as dose 1, single (Lot number: EN6202), in left arm, on 30Mar2021 as dose 2, single (Lot number: ER8733), in left arm and on 16Dec2021 as dose 3 (booster), single (Lot number: FE3594) at the age of 45 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: LANSOPRAZOLE. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 06Jul2022, outcome "unknown" and all described as "Since the vaccination, has the patient been tested for COVID-19: Yes/Result: Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (06Jul2022) Positive, notes: COVID test type post vaccination: Nasal swab. Clinical Course: No other vaccine in four weeks. No COVID prior vaccination. COVID was tested post vaccination. Vaccination Facility Details available. No follow-up attempts possible. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Test Date: 20220706; Test Name: Rapid Antigen covid test; Test Result: Positive ; Comments: COVID test type post vaccination: Nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: LANSOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2361138

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: MI
Alter: 71,0
Geschlecht: M
Eingang: 07.07.2022
Impfdatum: 17.05.2021
Beginn: 01.08.2021
Tage bis Beginn: 76,0
Dosis: 3
Route/Site: SYR / -

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

Cognitive disorder Creutzfeldt-Jakob disease Death Feeding disorder Gait inability Impaired driving ability Impaired self-care Laboratory test Lumbar puncture abnormal Memory impairment

Symptomtext

My Dad started experiencing symptoms of CJD Creutfeldt Jakob Disease within months of the 2nd vaccine dose. He was unable to sleep, he also had coordination issues and double vision. After receiving his booster on 12/16/21, he went drastically downhill within one week, He became unable to walk unassisted, had memory and cognitive issues, had trouble feeding and caring for himself, He could no longer drive. or be left alone for long periods of time. After seeing multiple specialists through January 2022, he was hospitalized and a Lumbar punch was performed. Three weeks later on Feb 28th, 2022 his test results returned positive for CJD. My Dad came home from the hospital on hospice and passed on 4/21/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 22,0
Labordaten: A multitude of tests were run between Dec 2021 & Feb 2022. Dad's Lumbar punch was performed 2/8/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Iodine & Shellfish
Vorherige Impfungen: -

VAERS 2341733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 29.06.2022
Impfdatum: 20.12.2021
Beginn: 23.05.2022
Tage bis Beginn: 154,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Clostridium difficile infection Colon cancer metastatic Computerised tomogram abnormal Death Dyspnoea General physical health deterioration Hypotension Large intestinal haemorrhage Leukocytosis Metastatic neoplasm Peritoneal catheter insertion SARS-CoV-2 test positive Transfusion

Symptomtext

pt had a positive COVID test on 5/23/22 at SNF; was transported to Hospital for hypotension and leukocytosis; admitted and treated for hypotension and leukocytosis with ABX and vasopressors; peritoneal catheter placed with improvement; later, pt c/o dyspnea and was transferred to another Hospital for further evaluation and treatment; given O2 via NC; required multiple transfusions due to blood loss from colon CA; CT revealed metastatic colon CA with carcinomatosis; C. difficile, treated with ABX; dexamethasone and Baricitinib given for COVID; pt's condition declined; family decided on inpatient hospice, but pt expired prior to hospice

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM, Hypothyroidism, anemia, hepatic cirrhosis, CAD, HLD, PAD, osteoarthritis, morbid obesity, gout
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2335858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: TN
Alter: 63,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 15.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Death Dyspnoea Endotracheal intubation Haemoptysis Hypoxia Oxygen saturation decreased Positive airway pressure therapy Productive cough Pyrexia Swelling

Symptomtext

Patient brought to ED at a local HCF on 01/01/2022 for increased SOB after of diagnosis of Covid. She noted fever, increased swelling, increased shortness of breath and cough with mucus/blood. In the ED oxygen was in low 80;s on room air. She was placed on nonrebreather where she was at 86% oxygen. Due to continued hypoxia the patient was placed on BiPap. Patient admitted with acute hypoxic respiratory failure 2/2 Covid PNA. Patient started on bronchodilators, IV steroids, O2. Patient was intubated on 1/12/22, then developed refractory hypoxemia. Patient was made DNR and passed on 1/22/2022.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 21,0
Labordaten: Chest Xray 01/01/2022: multifocal covid PNA.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2228328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: CO
Alter: 75,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 17.03.2021
Beginn: 21.01.2022
Tage bis Beginn: 310,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Angiogram pulmonary normal Anticoagulant therapy COVID-19 COVID-19 pneumonia Chest X-ray abnormal Infection Lung opacity SARS-CoV-2 test positive

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient hospitalized for acute hypoxemic respiratory secondary to COVID-19 pneumonia. Received remdesivir, steroids, antibiotics, supplemental oxygen, and anticoagulation. Discharged to home medically stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: On admission: SARS-CoV-2: positive, CT pulmonary angiogram was negative for a pulmonary embolism, chest x-ray showed opacities consistent with infection.
Aktuelle Erkrankungen: None
Vorgeschichte: arthritis, breast cancer, osteoporosis, hypothroidism, hypertension
Andere Medikamente: acetaminophen, albuterol, glycerin, calcium, vitamin D3, etanercept, iron, hydrocortisone cream, levothyroxine, multivitamin, vitamin E
Allergien: strawberry
Vorherige Impfungen: -

VAERS 2082449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 12.08.2021
Beginn: 26.01.2022
Tage bis Beginn: 167,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Moraxella infection Pneumonia bacterial Respiratory failure SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Patient presented covid-19 positive on 01/26/22 with a mix of COVID-19 pneumonia as well as bacterial pneumonia secondary to Moraxella. Pt progressed to acute on chronic hypoxic respiratory failure. This is considered a breakthrough case.

Weitere VAERSDATA-Felder

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

VAERS 2079642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 21.12.2021
Beginn: 30.01.2022
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Alanine aminotransferase normal Albumin globulin ratio normal Analgesic drug level Analgesic drug level therapeutic Anion gap Aspartate aminotransferase normal Asthenia Basophil count normal Basophil percentage decreased Benzodiazepine drug level Bilirubin urine Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium normal Blood chloride increased

Symptomtext

1/30/22 65-year-old female with notable past medical history for anxiety/depression, osteoarthritis, mixed asthma/COPD, hypertension, seizure disorder, history of UTIs, history of pneumonia, and history of ovarian cancer in remission. Her ED attending and family, they report altered mental status at home and on initial evaluation in ED and patient was unable to provide much history. However bedside today patient is alert and oriented x2, place and self. She seems fatigued but can provide fairly reliable history. She states that yesterday she progressively felt more and more unwell throughout the day, noting initially pronounced fatigue and weakness eventually developing chills (but did not take temperature at home), cough, and mild shortness of breath. She states she also developed confusion stating she could not remember is that it happened, times, in order of events. She denies any chest pain, nausea, vomiting, or diarrhea. She is vaccinated against COVID-19, and denies recent travel or any known sick contacts. Today she states that she feels mildly better than she did at home. Review of Systems General: As above HEENT: Denies recent falls, head trauma, cold/URI symptoms, rhinorrhea, sore throat. CVS: Denies chest pain, palpitations, racing heart, edema. RS: Respiratory symptoms as above Abdominal: Denies abdominal pain, nausea, vomiting, diarrhea, constipation, hematemesis, melena, hematochezia. Genitourinary: Denies dysuria. Endocrine: Denies hot/cold flashes. Neurological: Denies headaches, visual disturbance, dizziness, syncope, falls, trauma. Psychiatric: Denies suicidal/homicidal ideation. All systems reviewed and negative except pertinent positives, which are as noted in history of present illness. Collection Time: 01/30/22 6:08 AM Result Value Ref Range White Blood Count 11.27 (H) 4.5 - 11.0 10*3/uL Red Blood Count 4.11 4.0 - 5.2 10*6/uL Hemoglobin 12.7 12.0 - 16.0 g/dL Hematocrit 39.9 36.0 - 46.0 % Mean Corpuscular Volume 97.1 80.0 - 100.0 fL Mean Corpuscular Hemoglobin 30.9 26.0 - 34.0 pg Mean Corpuscular HGB Conc 31.8 31.0 - 37.0 g/dL Red Cell Distribution Width-CV 12.4 12.0 - 16.8 % Platelet Count 244 140 - 440 10*3/uL Mean Platelet Volume 10.1 8.4 - 12.4 fL Diff Type Hospital CBC w/AutoDiff (Lab) Neutrophils % 86.3 (H) 45 - 80 % Lymphocyte % 5.9 (L) 15 - 50 % Monocyte % 5.0 0 - 15 % Eosinophil% 2.0 0 - 7 % BASO% 0.4 0 - 2 % Immature Granulocyte% 0.4 0.0 - 1.0 % Nucleated RBC % 0 0 /100(WBC) Neutrophil Abs 9.75 (H) 2.0 - 8.8 10*3/uL Lymphocyte-Absolute 0.66 (L) 0.7 - 5.5 10*3/uL Monocyte Absolute 0.56 0.0 - 1.7 10*3/uL EOS-Absolute 0.22 0.0 - 0.8 10*3/uL Basophil Abs 0.04 0.0 - 0.2 10*3/uL Immature Granulocyte Abs 0.04 0.00 - 0.10 10*3/uL Urinalysis Collection Time: 01/30/22 6:08 AM Result Value Ref Range Color-Urine Light yellow Clarity-Urine Clear Specific Gravity Urine 1.015 1.005 - 1.030 (Lab) pH-Urine 6.5 5.0 - 9.0 (pH) Protein-Urine 20 (A) Negative mg/dL Glucose-Urine Negative Negative mg/dL Ketone-Urine Negative Negative mg/dL Bilirubin-Urine Negative Negative mg/dL Occult Blood-Urine Negative Negative (Lab) Nitrite-Urine Negative Negative (Lab) Urobilinogen-Urine Normal Normal (Lab)/dL Leukocyte Esterase-Urine Negative Negative (Lab) Source-Urine Urine Midstream Reflex Microscopic? Macroscopic only performed Lactic Acid Collection Time: 01/30/22 6:08 AM Result Value Ref Range Lactic Acid 1.5 0.7 - 2.0 mmol/L Toxicology Screen, urine Collection Time: 01/30/22 6:21 AM Result Value Ref Range Amphetamines-Urine Scrn Negative Negative Barbiturates-Urine Screen Negative Negative Benzodiazepines-Urine Screen Negative Negative Cannabinoids-Urine Screen Negative Negative Cocaine-Urine Screen Negative Negative Opiates-Urine Screen Negative Negative Comprehensive Metabolic Panel(CMP) Collection Time: 01/30/22 8:41 AM Result Value Ref Range Sodium 143 136 - 145 mmol/L Potassium 3.6 3.5 - 5.1 mmol/L Chloride 108 (H) 98 - 107 mmol/L Carbon Dioxide 25 22 - 29 mmol/L Anion Gap 10 5 - 13 (arb'U) Glucose 123 (H) 74 - 99 mg/dL Blood Urea Nitrogen (BUN) 20 10 - 20 mg/dL Creatinine-Blood 1.23 (H) 0.55 - 1.02 mg/dL BUN/Creatinine Ratio 16.3 RATIO Estimated GFR 44 (L) >60 /1.73 m2 Estimated GFR if 53 (L) >60 /1.73 m2 Total Protein 6.8 6.2 - 8.0 g/dL Albumin 3.9 3.2 - 4.6 g/dL Globulin 2.9 1.5 - 4.5 g/dL Albumin/Globulin Ratio 1.3 1.1 - 2.5 RATIO Calcium 9.0 8.4 - 10.2 mg/dL Total Bilirubin 0.5 0.2 - 1.2 mg/dL AST/SGOT 18 5 - 34 U/L ALT/SGPT 7 0 - 55 U/L Alkaline Phosphatase 80 40 - 150 U/L Toxicology Screen Collection Time: 01/30/22 8:42 AM Result Value Ref Range Acetaminophen <18.0 <18.0 ug/mL Ethylalcohol <10 <10 mg/dL Salicylate <5.0 2.0 - 20.0 mg/dL CT Chest Wo Contrast: 1/30/22- IMPRESSION: Multifocal pneumonia most probably involving the left lower lobe. The findings are nonspecific. Although not the typical presentation of Covid 19 pneumonia, it is not excluded. XR Chest 1 Vw 1/30/22- IMPRESSION: Mild nonspecific perihilar infiltrates 2/1/22-Discharge note-65-year-old female with a past medical history of asthma, COPD, seizures, anxiety, bipolar disorder, depression, hypertension and hyperlipidemia who is mid to the hospital for acute respiratory failure secondary to COVID-19 pneumonia. She was also found to have an acute kidney injury. Upon hospitalization, a COVID-19 test was ordered which came back positive. CT chest was consistent with groundglass opacities. She was initially started on broad-spectrum IV antibiotics but since this was likely Covid, this was discontinued. Over the course of her hospitalization, Patient's condition remained stable. She is remained on room air, patient was back stable for discharge. She did not qualify for an IV steroids. Patient was discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: 1/30/22 COVID-19 Result Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Allergy history unknown o Anemia o Anxiety o Arthritis o Asthma o Blood transfusion o Cancer -ovarian o Cataract o Chronic back pain o Colon polyp o COPD (chronic obstructive pulmonary disease) o Depression o Hiatal hernia o Hypertension o Kidney stones o Kidney stones o Obesity o Pneumonia o Seasonal allergies o Seizures 2012 o Snoring o STD (sexually transmitted disease) o Urinary tract infection
Andere Medikamente: b complex-C-folic acid 1 CAP Take 1 capsule by mouth daily., b complex-C-folic acid 1 CAP Take 1 capsule by mouth daily., acidophilus-bulgaricus (FLORANEX) PACK Take 1 packet by mouth 3 (three) times daily with meals. !! albuterol HFA 10
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2069233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: PA
Alter: 39,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 19.01.2022
Beginn: 26.01.2022
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

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

Angiogram pulmonary abnormal Atelectasis Chest pain Computerised tomogram thorax abnormal Lung consolidation Lymph node calcification Pleural effusion Pulmonary embolism Scan with contrast abnormal

Symptomtext

Patient presented with chest pain and was ruled out for COVID. had CT chest: IMPRESSION: 1. Bilateral pulmonary emboli. 2. Normal heart ratio. 3. Bilateral lower lobe atelectasis and possible developing pulmonary infarcts. 4. Bilateral calcified axillary lymph nodes. PROCEDURE INFORMATION: Exam: CTA Chest With Contrast Exam date and time: 1/27/2022 3:06 PM Age: 39 years old TECHNIQUE: Imaging protocol: Computed tomographic angiography of the chest with contrast. 3D rendering (Not supervised by radiologist): MIP and/or 3D reconstructed images were created by the technologist. Radiation optimization: All CT scans at this facility use at least one of these dose optimization techniques: automated exposure control; mA and/or kV adjustment per patient size (includes targeted exams where dose is matched to clinical indication); or iterative reconstruction. Contrast material: OMNI350; Contrast volume: 100 ml; Contrast route: INTRAVENOUS (IV); COMPARISON: No relevant prior studies available. FINDINGS: Pulmonary arteries: Left lower lobe pulmonary emboli present. Right upper lobe segmental pulmonary emboli. Segmental pulmonary emboli in the right lower lobe. Aorta: Unremarkable. No aortic aneurysm. No aortic dissection. Lungs: Bilateral lower lobe atelectasis. Mild airspace disease and minimal consolidation right lung base. Pleural spaces: Small right pleural effusion. Heart: Unremarkable. No cardiomegaly. No pericardial effusion. Heart RV/LV ratio: RV/LV ratio 0.7. Lymph nodes: Bilateral axillary calcified lymph nodes. Right calcified axillary lymph node measures 22 mm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: He has no risk factors for PE, he is not obese, nonsmoker, no travel or immobilization. Family history negative except grandmother with DVT and hypercoagulable workup is pending.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2054555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: ME
Alter: 35,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 22.12.2021
Beginn: 16.01.2022
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

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

Amphetamines positive Angiogram cerebral Arteriogram carotid Blood glucose normal Cerebral infarction Coma Computerised tomogram head Echocardiogram Ejection fraction decreased Encephalopathy Endotracheal intubation Facial paresis Hemiparesis Leukoencephalopathy Lumbar puncture Magnetic resonance imaging head abnormal Mental status changes Muscle spasticity

Symptomtext

Presented 1/16 with left facial weakness, which progressed to left sided weakness, followed by altered mental status and intubation for severe encephalopathy. MRI brain with bilateral white matter changes consistent with either watershed infarcts versus leukoencephalopathy. He remains comatose and intubated with severe spasticity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coma
Hospital-Tage: 4,0
Labordaten: MRI brain w/wo contrast 1/18/22: bilateral restricted diffusion high-cortical white matter CT brain 1/19/22 CTA head and neck 1/18/22 MRI brain 1/16/22 TTE 1/18/22 mildly reduced EF with no PFO lumbar puncture 1/20/22: WBC 5, protein normal, glucose normal tox screen positive cocaine, amphetamines, thc
Aktuelle Erkrankungen: none
Vorgeschichte: asthma substance abuse
Andere Medikamente: albuterol inhaler prn ipratropium-albuterol nebulizers prn
Allergien: fluoxetine
Vorherige Impfungen: -

VAERS 2044621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

kritisch

Staat: WA
Alter: 76,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 28.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 8,0
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 Pneumonia bacterial SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 1/31/21 (lot # EN5318), 2/28/21 (lot # EN6198), and 12/28/21 (lot # FE3594). On 1/5/22, patient tested positive for COVID. On 1/16/22, patient admitted to our inpatient med/surg unit for acute respiratory failure with hypoxia secondary to COVID-19 pneumonia likely with superimposed bacterial pneumonia. As of today (1/18/22), patient is still admitted in our med/surg unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: COVID status positive 1/5/22.
Aktuelle Erkrankungen: -
Vorgeschichte: BPH, colon cancer, sleep apnea, dyslipidemia
Andere Medikamente: atorvastatin, cochicine, lidocaine patch, medical marijuana, omeprazole, PEG-3350, simvastatin, tamsulosin
Allergien: penicillins
Vorherige Impfungen: -

VAERS 2678401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 31.08.2023
Impfdatum: 30.12.2021
Beginn: 01.04.2023
Tage bis Beginn: 457,0
Dosis: 2
Route/Site: IM / RA

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

Basal ganglia stroke Ischaemic stroke

Symptomtext

I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 4/12/2023 ACUTE STROKE OF BASAL GANGLIA, UNSPECIFIED TYPE AND ARTERY I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 4/12/2023 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Basal ganglia stroke
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2669404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: -
Alter: 42,0
Geschlecht: M
Eingang: 10.08.2023
Impfdatum: 06.01.2022
Beginn: 22.01.2023
Tage bis Beginn: 381,0
Dosis: 2
Route/Site: IM / RA

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

Brain stem stroke Obstructive sleep apnoea syndrome

Symptomtext

OBSTRUCTIVE SLEEP APNEA ACUTE STROKE OF BRAINSTEM, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain stem stroke
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2624188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: -
Alter: 28,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 10.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: - / -

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

Myocarditis Neuropathy peripheral

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE PERIPHERAL NEUROPATHY MYOCARDITIS

Weitere VAERSDATA-Felder

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

VAERS 2620753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 26.05.2021
Beginn: 29.09.2022
Tage bis Beginn: 491,0
Dosis: 4
Route/Site: - / -

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 OF LEFT LEG, UNSPECIFIED VEIN ACUTE DVT OF LEFT FEMORAL VEIN 10/14/2022 --- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2618455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 20.04.2023
Impfdatum: 22.12.2021
Beginn: 21.04.2022
Tage bis Beginn: 120,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy Facial paresis

Symptomtext

LEFT BELLS PALSY LEFT FACIAL MUSCLE WEAKNESS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2610714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 06.04.2023
Impfdatum: 14.12.2021
Beginn: 29.06.2022
Tage bis Beginn: 197,0
Dosis: 3
Route/Site: IM / RA

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

Cardiac failure congestive Cardiogenic shock

Symptomtext

CARDIOGENIC SHOCK 6/29/2022 CHF (CONGESTIVE HEART FAILURE), UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2539054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 02.01.2021
Beginn: 28.09.2022
Tage bis Beginn: 634,0
Dosis: 3
Route/Site: - / -

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

Anticoagulant therapy Aspiration pleural cavity Atelectasis Bradycardia Bronchoscopy COVID-19 Computerised tomogram thorax abnormal Deep vein thrombosis Endobronchial ultrasound Fibrin D dimer increased High-resolution computerised tomogram of lung Hypoventilation Lymphadenopathy mediastinal Lymphocyte count Pleural effusion Pulmonary mass Resuscitation SARS-CoV-2 test positive

Symptomtext

74-year-old woman with a past medical history significant for breast CA 2010 status post RT and lumpectomy, dyspnea with associated weight loss and fatigue for the last 6 to 8 months, and hypertension who presented to the hospital for an outpatient bronchoscopy with EBUS. She underwent HRCT outpatient was found to have a large right pleural effusion and underwent thoracentesis on 9/16/2022 which revealed lymphocytic with negative cytology. The CT also revealed pulmonary nodules with right middle lobe atelectasis mediastinal lymphadenopathy requiring her to be scheduled for the EBUS bronchoscopy today. Prior to the bronchoscopy the patient was reportedly in her normal state of health. She denies shortness of breath was any different from her typical shortness of breath for the past 6 months. She also denied chest pain, fever, chills, abdominal pain, nausea or vomiting. She denies recent travel or sick contacts. She has never required home oxygen. She reports no history of lung disease ( other than recurrent pleural effusions recently) or cardiac disease. She has never smoked tobacco and only drinks alcohol socially. Post bronchoscopy today the patient experienced episode of bradycardia with heart rates in the 20s to 30s, atropine was given and the patient also received 4-5 chest compressions by anesthesia. She was reportedly hypoventilating throughout the procedure with low tidal volumes. The patient was also initially difficult to arouse postprocedure but she did became more alert and was able to be extubated and transitioned to supplemental oxygen via nasal cannula. Given the above scenario the patient was admitted to internal medicine for ongoing monitoring. COVID-19 positive. Medical team consulted, discussed with them. Patient is agreeable and wishes to start remdesivir if appropriate per recommendations. Decadron ordered by pulmonary medicine. Will monitor LFTs and HR. Discussed with medical team, plan to stop Remdesivir and isolation precautions as COVID-19 positivity is likely related to old infection. Elevated D-dimer in the setting of recent procedure, and chest compressions. Bilateral lower extremity venous duplex is ordered showing chronic DVT. VQ scan abnormal. Patient will need anticoagulation for at least 3 months and prefers to be on Eliquis despite the high cost does not want to be on Coumadin. Patient understands that she needs to follow-up with cardiology and her primary care provider for ongoing medication refills past the first 30 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: 9/28 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 28.12.2021
Beginn: 16.09.2022
Tage bis Beginn: 262,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain Acute kidney injury Anticoagulant therapy Ascites Asymptomatic COVID-19 Atelectasis Blood bilirubin increased Cancer pain Chest X-ray abnormal Coagulopathy Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Condition aggravated Confusional state Drain placement Electrolyte imbalance Fatigue Flatulence

Symptomtext

Hematologist/Oncologist: MD Primary Care Physician at Discharge: PRESENTING PROBLEM: Encephalopathy acute HOSPITAL COURSE: The patient is a very pleasant 58-year-old male with past medical history as listed above including pancreatic cancer, who presented to Emergency Department secondary to generalized fatigue, severe lower extremity edema and intermittent confusion. Initial laboratory studies and imaging can be found per Epic review. His encephalopathy was felt multifactorial secondary to toxic metabolic encephalopathy, AKI with electrolyte derangements, infections, and medications. COVID-19 was positive on presentation. Cycle threshold was 34.2. The patient was asymptomatic and not hypoxic. ID was consulted. No indication for treatment. Chest x-ray showed atelectasis and small bilateral pleural effusions. He underwent a CT chest, abdomen, and pelvis on presentation that showed progression including new air bubbles within the pancreatic lesion possibly reflecting necrosis or fistula formation with bowel most likely duodenum, superinfection of tumor cavity was also possible. Surgical Oncology and Gastroenterology were consulted. Surgical Oncology evaluated the patient, felt a small amount of gas within the pancreas most likely due to tumor necrosis and no surgical intervention offered regardless of the etiology of this foci of pancreatic air. GI felt the fistulization was likely due to tumor and could repeat imaging of worsening clinical status. The patient had increasing ascites on CT scan and underwent a paracentesis on September 19. Later, peritoneal drain was placed per IR. Gastritis was noted on CT and the patient was placed on a PPI 2 times a day. Nephrology was consulted for AKI and hyperkalemia. They felt this was likely due to prerenal azotemia and likely ATN in the setting of hemodynamic changes from sepsis and COVID-19 infection and likely would be further evolution of AKI due to contrast induced nephropathy with IV contrast dye administered on September 16th. There was no obstruction or hydronephrosis. He was given Lokelma, but this was ineffective. He was placed on a bicarb drip. He was started on IV albumin and this was continued until discharge. Given the grave prognosis of his metastatic pancreatic adenocarcinoma, CCRT would not improve his situation. Quality of life would most likely be worsened by it. Bilirubin was elevated throughout the hospital stay. CT did show stent in place. He had a coagulopathy and received vitamin K and FFP. He was placed on a heparin drip for a new portal vein and superior mesenteric vein thrombus as well as splenic infarct, however, this was discontinued with coagulopathy and increased risk for bleeding. Home Eliquis was also held. Palliative Care was consulted to assist with abdominal pain and cancer related pain. Overall, given progression of disease seen on imaging, hospice was recommended. Several goals of care, conversations we had had with the patient and the family and initially family wanted all aggressive treatment until his body gives up completely. On 09/19, further lengthy goals of care resulted in patient and family wishing to pursue hospice given the grave nature of his disease and he will be discharged home today 09/25/2022 in stable condition with plan to sign on with hospice at home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mesenteric vein thrombosis
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Fever in adult Cancer related pain Pancreatic cancer metastasized to liver (HCC) Constipation due to opioid therapy Nausea Ascending aortic aneurysm (HCC) Benign essential HTN Bile duct obstruction Dyslipidemia History of biliary duct stent placement Primary hyperaldosteronism (HCC) Barrett's esophagus without dysplasia Iron deficiency anemia Pancreatic cancer (HCC) Opiate analgesic use agreement exists Electrolyte abnormality Counseling regarding advance directives and goals of care Gram-negative bacteremia due to Klebsiella oxytoca, with recurrent fever Unspecified severe protein-calorie malnutrition (HCC) Hypertensive urgency Dyspnea, unspecified type Neoplastic (malignant) related fatigue COVID-19 virus detected Peritonitis (HCC)
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet acetaminophen (TYLENOL) 650 MG suppository amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet bisacodyl (DULCOLAX) 10 MG suppository calcium citrate-vitamin D (CITRACAL+D) 315-200 MG-UNIT per tab
Allergien: None
Vorherige Impfungen: -

VAERS 2444921

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 14.09.2022
Impfdatum: 01.01.2022
Beginn: 31.08.2022
Tage bis Beginn: 242,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Cardiac failure congestive Chest X-ray abnormal Cough Dyspnoea Hypertension Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

Discharge Provider: DO Primary Care Provider at Discharge: MD Admission Date: 8/31/2022 Discharge Date: 9/2/2022 HOSPITAL COURSE: The patient is a 70 y.o. female with past medical history significant for HFpEF, Afib (on eliquis), T2DM (requiring insulin), CKD IV, hypertension, and Von Willebrand disease, who presented to the ED with a chief complaint of cough and shortness of breath. Upon arrival to the ED patient was hypertensive of 179/64, remainder of vitals were stable. Saturations were 87% on room air with improvement to the mid 90s following 2 L nasal cannula. COVID-19 was noted to be positive. CXR revealed moderate pulmonary edema with CHF expected. While in the ED the patient did receive 1 L of normal saline as well as a 1-time dose of IV Lasix 40 mg. The patient was admitted to hospital medicine for further evaluation and management. Patient quickly improved with wean from oxygen. She remained on decadron while admitted, due to hx of DM and improvement in respiratory status, decadron was not continued on discharge. Patient aware to monitor blood glucose and blood pressure closely at home. He was discharged home in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: 12/25/2021 - 1/1/2022 (7 days) Hospital PRESENTING PROBLEM: Heart failure (HCC) [I50.9]
Vorgeschichte: PAF (paroxysmal atrial fibrillation) (HCC) Hyperlipidemia DJD (degenerative joint disease) Diabetes mellitus with neurological manifestation (HCC) Osteoarthritis, generalized Rheumatoid arthritis involving multiple sites with positive rheumatoid factor (HCC) Anemia in stage 4 chronic kidney disease (HCC) Bilateral carotid artery stenosis Essential hypertension Von Willebrand disease (HCC) Glaucoma Posterior vitreous detachment of both eyes Decreased visual acuity Secondary hyperparathyroidism of renal origin (HCC) Morbid obesity (HCC) Stage 4 chronic kidney disease (HCC) Coronary artery disease involving native coronary artery of native heart without angina pectoris LBBB (left bundle branch block) Mild mitral stenosis Mild aortic stenosis H/O: stroke with residual effects Pulmonary hypertension (HCC) PAD (peripheral artery disease) (HCC) Urinary incontinence Osteoporosis Mild intermittent asthma without complication Gastroesophageal reflux disease Diverticulosis of large intestine without hemorrhage Mild episode of recurrent major depressive disorder (HCC) Chronic diastolic heart failure (HCC) Vitamin D deficiency S/P carotid endarterectomy Tubular adenoma of colon Type 2 diabetes mellitus with diabetic neuropathy, with long-term current use of insulin (HCC) Intracranial hemorrhage (HCC) Abnormal CT scan, neck Requires assistance with activities of daily living (ADL)
Andere Medikamente: albuterol HFA (PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 10 MG tablet apixaban (ELIQUIS) 2.5 MG tablet atorvastatin (LIPITOR) 40 MG tablet Blood Glucose Monitoring Suppl MISC carvedilol (COREG) 25 MG tablet citalopram (
Allergien: Orencia [Abatacept]Hives, Itching Enbrel [Etanercept]Itching Humira Pen Starter [Adalimumab]Unknown MethotrexateUnknown TramadolNausea and Vomiting, Dizziness
Vorherige Impfungen: -

VAERS 2006222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: AZ
Alter: 20,0
Geschlecht: M
Eingang: 17.07.2022
Impfdatum: 30.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / AR

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

Blood creatinine Blood electrolytes Blood glucose Blood urea C-reactive protein Cardiac monitoring Chest pain Computerised tomogram Differential white blood cell count Dizziness Echocardiogram Electrocardiogram Laboratory test Dyspnoea Electrocardiogram abnormal Electroencephalogram abnormal Full blood count Haematocrit

Symptomtext

Patient went to the emergency room with chest pain, abnormal ekg/eeg, nausea, vomiting, dizziness, short of breath. He was admitted to the hospital with myocarditis. After he returned to university for Spring semester he started having severe leg pain. He was diagnosed by his PCP with sciatic nerve inflammation. He is still being treated and still has pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: This is not a comprehensive list of all tests ordered due to the adverse event: C-REACTIVE PROTEIN Jan 4, 2022 COMPREHENSIVE METABOLIC PANEL Jan 4, 2022 MRI Jan 3, 2022 SEDIMENTATION RATE, AUTOMATED Jan 3, 2022 Continuous Cardiac Monitoring Provider Unknown Jan 3, 2022 CBC Jan 3, 2022 TROPONIN I Jan 2, 2022 COMPREHENSIVE METABOLIC PANEL Jan 2, 2022 SEDIMENTATION RATE, AUTOMATED Jan 2, 2022 TROPONIN I Jan 2, 2022 Cardiac Echo Jan 2, 2022 TROPONIN I Jan 2, 2022 COMPREHENSIVE METABOLIC PANEL Jan 2, 2022 LIPID PANEL Jan 2, 2022 HIGH SENSITIVITY Jan 2, 2022 CT Scan Jan 2, 2022 CT Scan Jan 2, 2022 X-Ray Jan 2, 2022 PROTIME-INR Jan 2, 2022 ECG 12-LEAD Jan 2, 2022 COVID-19 MOLECULAR, ABBOTT ID Jan 2, 2022 CBC WITH DIFFERENTIAL Jan 2, 2022 POCT LYT-ICA-GLU-BUN-CR-HGB-HCT Jan 2, 2022 POCT TROPONIN I Jan 2, 2022 ECG 12-LEAD Jan 2, 2022
Aktuelle Erkrankungen: none
Vorgeschichte: none prior to booster shot
Andere Medikamente: none
Allergien: shellfish and tree nuts
Vorherige Impfungen: -

VAERS 2006222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: AZ
Alter: 20,0
Geschlecht: M
Eingang: 17.07.2022
Impfdatum: 30.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Blood creatinine Blood electrolytes Blood glucose Blood urea C-reactive protein Cardiac monitoring Chest pain Computerised tomogram Differential white blood cell count Dizziness Echocardiogram Electrocardiogram Laboratory test Dyspnoea Electrocardiogram abnormal Electroencephalogram abnormal Full blood count Haematocrit

Symptomtext

Patient went to the emergency room with chest pain, abnormal ekg/eeg, nausea, vomiting, dizziness, short of breath. He was admitted to the hospital with myocarditis. After he returned to university for Spring semester he started having severe leg pain. He was diagnosed by his PCP with sciatic nerve inflammation. He is still being treated and still has pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: This is not a comprehensive list of all tests ordered due to the adverse event: C-REACTIVE PROTEIN Jan 4, 2022 COMPREHENSIVE METABOLIC PANEL Jan 4, 2022 MRI Jan 3, 2022 SEDIMENTATION RATE, AUTOMATED Jan 3, 2022 Continuous Cardiac Monitoring Provider Unknown Jan 3, 2022 CBC Jan 3, 2022 TROPONIN I Jan 2, 2022 COMPREHENSIVE METABOLIC PANEL Jan 2, 2022 SEDIMENTATION RATE, AUTOMATED Jan 2, 2022 TROPONIN I Jan 2, 2022 Cardiac Echo Jan 2, 2022 TROPONIN I Jan 2, 2022 COMPREHENSIVE METABOLIC PANEL Jan 2, 2022 LIPID PANEL Jan 2, 2022 HIGH SENSITIVITY Jan 2, 2022 CT Scan Jan 2, 2022 CT Scan Jan 2, 2022 X-Ray Jan 2, 2022 PROTIME-INR Jan 2, 2022 ECG 12-LEAD Jan 2, 2022 COVID-19 MOLECULAR, ABBOTT ID Jan 2, 2022 CBC WITH DIFFERENTIAL Jan 2, 2022 POCT LYT-ICA-GLU-BUN-CR-HGB-HCT Jan 2, 2022 POCT TROPONIN I Jan 2, 2022 ECG 12-LEAD Jan 2, 2022
Aktuelle Erkrankungen: none
Vorgeschichte: none prior to booster shot
Andere Medikamente: none
Allergien: shellfish and tree nuts
Vorherige Impfungen: -

VAERS 2267583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: NM
Alter: 61,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 05.05.2022
Beginn: 05.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Agitation Blood pressure increased Erythema Feeling abnormal Loss of consciousness Pruritus Swelling

Symptomtext

I started itching on the face, chest and it was swollen and red. I started feeling very agitated. I then went to health clinic. I had an elevated blood pressure. I ended up going to ER, monitored me for a while. next morning, I felt fine for a few mins, then I started feeling really bad and passed out. I went back to ER, I waited or 2 hours and ended up leaving. BP ended up normalizing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: PTSD
Andere Medikamente: Levothyroxine Bupropion Claritin
Allergien: Naproxen (Aleve) CA flex Bees & wasps
Vorherige Impfungen: -

VAERS 2264629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MN
Alter: 35,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 10.12.2021
Beginn: 19.03.2022
Tage bis Beginn: 99,0
Dosis: 3
Route/Site: SYR / LA

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

Anticoagulant therapy Blood test Computerised tomogram abdomen Electrocardiogram Haemorrhage Menopause Nephrostomy Stent placement Surgery Thrombosis Thyroid function test Ultrasound Doppler abnormal

Symptomtext

Several months after the third dose, I had to have a right stint replaced from my ureter. After it was replaced I had to get bilateral nephrostomy tubes put in. I had those in for 3 months. I had a major surgery in mid March on multiple organ systems. I had 3 blot clots in my right calf and had to be put on blood thinners. I bled so much I almost had to have a blood transfusion and went back into the ER. I was put on progesterone and eventually a Depo Lupron shot for temporary Menopause. I am also still on the blood thinner Xarelto.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: Blood work Multiple Abdominal CT Scans Thyroid panel EKG Ultrasound Lower Extremity Bilateral
Aktuelle Erkrankungen: None
Vorgeschichte: Endometriosis Hydronephrosis of Kidneys
Andere Medikamente: CoQ10 Tylenol Motrin Aspirin
Allergien: Aloe Gluten and Dairy sensitivity
Vorherige Impfungen: -

VAERS 2216431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CO
Alter: 12,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 11.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain Acute kidney injury Alanine aminotransferase increased Anticoagulant therapy Aspartate aminotransferase normal Blood creatinine increased Blood fibrinogen increased C-reactive protein increased COVID-19 Chest pain Dyspnoea Echocardiogram abnormal Fibrin D dimer increased Headache Hypotension Immunoglobulin therapy Intensive care Laboratory test abnormal

Symptomtext

Patient developed symptoms of MISC on 12/16/21; fevers began on 12/17/21 with a Tmax of 40 degrees Celsius. Over the course of illness, symptoms and complications included fevers, shock, sinus tachycardia, hypotension, AKI, chest pain, shortness of breath, abdominal pain, rash, mucocutaneous lesions/conjunctivitis, headache, neck pain, and myalgias. Abnormal labs included elevated creatinine, elevated transaminases, thrombocytopenia, elevated NT-ProBNP, elevated CRP, elevated fibrinogen, elevated ferritin, and elevated D-dimer. ECHO studies showed pericardial effusion, pleural effusion, and trivial mitral regurgitation. Patient was admitted to the hospital on 12/20/21 and treated with IVIG, infliximab x 2, epinephrine, low flow nasal cannula, and aspirin. She was admitted to the ICU from 12/20/21 to 12/22/21. She was discharged on 12/24/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: Positive SARS-CoV-2 nucleocapsid IgG, 12/20/21; positive SARS-CoV-2 PCR, 12/20/21; peak fibrinogen 492 mg/dL, 12/20/21; peak CRP 23.9 mg/dL, 12/20/21; peak ferritin 283.00 ng/mL, 12/20/21; peak NT-ProBNP 1,560.0 pg/mL, 12/20/21; peak creatinine 1.52 mg/dL, 12/20/21; peak AST 45 U/L, 12/23/21; peak ALT 40 U/L, 12/22/21; peak D-dimer 7.16 mcg/mL, 12/20/21; lowest platelets 110 x 10^3/mcL, 12/23/21; ECHO 12/20/21 showed sinus tachycardia with occasional ectopy. ECHO 12/23/21 showed trivial pericardial effusion, trivial left pleural effusion, and trivial right pleural effusion. ECHO 12/24/21 showed trivial mitral regurgitation and trivial pericardial effusion.
Aktuelle Erkrankungen: unknown
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2199637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: FL
Alter: 19,0
Geschlecht: M
Eingang: 25.03.2022
Impfdatum: 17.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Back pain Cardiac imaging procedure normal Catheterisation cardiac normal Chest X-ray normal Chest pain Computerised tomogram thorax normal Echocardiogram Ejection fraction normal Electrocardiogram ST segment abnormal Electrocardiogram ST-T segment abnormal Electrocardiogram abnormal Lethargy Myocarditis Pain Pain in extremity Pain in jaw Palpitations

Symptomtext

12/21/21 - Woke up with severe pain in left arm and jaw, went to urgent care and then directed to go to ER. 12/21/21 - Severe chest pain 12/22/21 - Discharged from ER after an overnight stay, instructed to take NSAIDs for presumed myocarditis. 12/23/21-12/28/21 - Severe chest pain, lethargy, heart palpitations, tachycardia 12/28/21 - Diagnosed by cardiologist with myocarditis based off EKG abnormalities and high troponin levels. January 2022 - Moderate chest pain radiating to the back and shoulder, episodes of tachycardia on and off (prescribed metoprolol tartrate 25 mg for tachycardia on 1/15/22) February 2022 - Low levels of chest pain off and on, by the end of the month very low levels of pain or no pain at all. March 2nd 2022 - MRI reviewed, myocarditis diagnosis was agreed upon, considered fully recovered at this point.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: 12/21/21 - EKG revealed sinus tachycardia and abnormal ST-T segment. (Urgent Care) 12/21/21 - Several tests administered at the ER 6:29 PM Troponin I Cardiac - 2.39 ng/ml (normal value under 0.034) *Upon admission/triage, received a borderline EKG, ST segment abnormalities. 10:03 PM Troponin I Cardiac - 2.05 ng/ml COVID-19 Test - Negative (11:01 PM) CT Scan of Chest - No abnormalities seen X-Ray of Chest - No abnormalities 4:42 PM EKG Study - Sinus Tachycardia 6:40 PM EKG Study - Sinus Tachycardia, cannot rule out Anterior infarct , age undetermined 12/22/21 Hospital 2:50 AM Troponin I Cardiac - 1.32 ng/ml 10:52 AM Cardiac Catheterization Study - No coronary artery disease, no abnormalities. Echocardiogram - Not much abnormalities, normal EF of 60%. 12/24/21 - Troponin I Cardiac - 0.194 ng/ml (presented to ER for tachycardia, bpm of ~140 BPM) 1/15/22 - Presented to ER for tachycardia (presumed panic attack, at its height BPM of ~170 BPM) EKG Study - Sinus tachycardia, otherwise normal EKG Chest X-Ray - No abnormalities Troponin Test - 0.013ng/ml (normal value) 2/5/22 - Presented to ER with tachycardia (possible panic disorder) Troponin TNIH - 23.4ng/L (normal from 0-78.5) 2/28/22 - Cardiac MRI MRI revealed no delayed enhancement of left ventricular wall to suggest myocarditis. EF of 61%.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: - Cetirizine 10 mg
Allergien: None aware of.
Vorherige Impfungen: -

VAERS 2184618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fE3594

schwer

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain upper Dizziness Feeling abnormal Heart rate decreased Maternal exposure during pregnancy Muscle spasms Nausea Presyncope Syncope

Symptomtext

Approximately 4 weeks 6 days pregnant (EDD 8/19/2022). I woke up in the middle of the night after getting the vaccine that afternoon, and felt noticeably bad, stomach hurting, queasy, faint. Felt like I might pass out but also had to get up to go to the bathroom, where I nearly fainted, and eventually made it to the floor, where my partner monitored my pulse. I was on the edge of passing out/losing consciousness (but did not), without readily findable pulse in carotid, for almost 50 minutes. For most of the event, pulse oximeter on thumb could not detect pulse, and when it could, pulse was in the low 40s and pulse ox in the low 70s. Felt cramping in legs and stomach during this period too. Tried to elevate pulse by kicking and squeezing muscles which didn't work, until eventually the episode ended and pulse returned to normal, after about an hour total. As an aside -- something similar happened to my dad (age 78) after his second Pfizer dose. He also got up in the night to go to the bathroom, when he did lose consciousness briefly. Both of us have had occasional episodes of vasovagal syncope in the past.

Weitere VAERSDATA-Felder

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

VAERS 2050920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: TX
Alter: 68,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 01.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: - / RA

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

Dermatitis allergic Nausea Syncope Urticaria Vaccination complication Dermatitis Rash SARS-CoV-2 test Viral rash Vomiting

Symptomtext

acute rash/ weals rash; wheals inflamed rash urticarial weals arms, legs feet chest breasts bottom of feet; wheals inflamed rash urticarial weals arms, legs feet chest breasts bottom of feet; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date Dec2021 (Lot number: FE3594) at the age of 68 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Irritable bowel syndrome" (unspecified if ongoing); "Known allergies: pennicillen" (unspecified if ongoing). Concomitant medication(s) included: CYMBALTA; DULOXETINE. Past drug history included: Codeine, reaction(s): "Allergy"; Ibufrofen, reaction(s): "Allergy". Vaccination history included: Bnt162b2 (Dose Number: 1 at 01:15 PM (Batch/Lot No: pfizer FH8020) Location of injection: Right Arm), administration date: Dec2021, when the patient was 68 years old, for COVID-19 immunization. The following information was reported: RASH (non-serious) with onset 24Dec2021 14:30, outcome "not recovered", described as "acute rash/ weals rash"; URTICARIA (non-serious), DERMATITIS (non-serious) all with onset 24Dec2021 14:30, outcome "not recovered" and all described as "wheals inflamed rash urticarial weals arms, legs feet chest breasts bottom of feet". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash, urticaria, dermatitis. Additional information: Patient received second dose on unspecified date in Dec2021 at 02:30 PM at hospital. No other vaccine in four weeks. Adverse event: acute rash/ weals rash/ wheals inflamed rash urticarial weals arms, legs feet chest breasts bottom of feet. No Covid prior vaccination. Patient had Covid test post vaccination. Patient received Medrol prednisone 6 day dose pack/ hydroxyzine as treatment for adverse event. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20211230; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Irritable bowel syndrome; Penicillin allergy
Andere Medikamente: CYMBALTA; DULOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 2183031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 14.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 49,0
Dosis: 3
Route/Site: SYR / LA

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

Computerised tomogram abnormal Headache Thrombosis

Symptomtext

Early January I started to get really bad headaches, I went to the doctor on 2/25 around 5:30pm they ran a cat scan and found three blood clots. The doctor prescribed me to blood thinners and said I needed to take that for the next three months. Around the second week of taking the blood thinners I started to feel better but I am still on the blood thinners so it is still a ongoing issue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Cat scan.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Cystic Ovarian Tissue
Andere Medikamente: Birth Control Pills; Vitamins
Allergien: N/A
Vorherige Impfungen: -

VAERS 2162684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: VA
Alter: 62,0
Geschlecht: M
Eingang: 07.03.2022
Impfdatum: 21.01.2022
Beginn: 04.02.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Computerised tomogram thorax abnormal Dyspnoea Echocardiogram Pulmonary thrombosis

Symptomtext

Two weeks after receiving Booster I began to experience shortness of breath. I went to the local Emergency room Feb. 8, 2022. After blood was drawn and chest CAT was done it was determined I had developed blood clots in my lungs and was immediately admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 3,0
Labordaten: Feburary 8, 2022 Blood drawn and CAT of chest. ECHO Cardiagram
Aktuelle Erkrankungen: Gastrointestinal Disease
Vorgeschichte: Epilepsy, IBS, GERD
Andere Medikamente: Phenytoin, Xifaxin, Pantoprazole, Citrucil
Allergien: dairy
Vorherige Impfungen: 62 y.o. Toxic Phenytoin level despite no change in med dose after Phizer COVID vac April 29, May 20 2021

VAERS 2132010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 31.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Cluster headache Dizziness Echocardiogram Electrocardiogram Headache Heart rate increased Hypertension Loss of consciousness Magnetic resonance imaging Migraine Palpitations Vomiting

Symptomtext

Extreme dizziness to the point of puking and blacking out, headaches and migraines that come in clusters, racing heart palpitations, high blood pressure and heart rate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood test: 1/14/22, 2/7/22. Mri:2/11/22 Cardiogram: 2/11/22 Ekg: 2/1/22 and 2/7/22
Aktuelle Erkrankungen: No e
Vorgeschichte: Asd repair 2010, tumor removal 1996
Andere Medikamente: Probiotics, multi vitamin, green tea extract
Allergien: None
Vorherige Impfungen: -

VAERS 2108919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 14.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Dizziness Dysgeusia Facial paralysis Hypoaesthesia Lymphadenopathy Mouth swelling Nausea Paraesthesia Pharyngeal swelling Swollen tongue

Symptomtext

face numb and droopy; face still numb and tingly; face still numb and tingly; mouth/tongue still swollen; mouth/tongue still swollen; lymph nodes swelled; dizziness/lightheaded; nausea; heavy metal taste in mouth; throat swelled; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (COMIRNATY), administered in arm left, administration date 14Dec2021 09:00 (Lot number: FE3594, expiration date unknown) at the age of 53 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "migraine" (unspecified if ongoing); "allergy" (unspecified if ongoing), notes: Known allergies: other immunizations. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: fg3527, Location of injection: Arm Left, Vaccine Administration Time: 08:30 AM), administration date: 24Nov2021, for Covid-19 immunization, reaction(s): "lymph nodes swelled immediately", "Nausea", "Dizziness/lightheaded", "heavy metal taste in mouth". The following information was reported: FACIAL PARALYSIS (medically significant), outcome "not recovered", described as "face numb and droopy"; HYPOAESTHESIA (medically significant), PARAESTHESIA (medically significant), outcome "not recovered" and all described as "face still numb and tingly"; MOUTH SWELLING (non-serious), SWOLLEN TONGUE (non-serious), outcome "not recovered" and all described as "mouth/tongue still swollen"; LYMPHADENOPATHY (non-serious), outcome "not recovered", described as "lymph nodes swelled"; DIZZINESS (non-serious), outcome "unknown", described as "dizziness/lightheaded"; NAUSEA (non-serious), outcome "unknown", described as "nausea"; DYSGEUSIA (non-serious), outcome "not recovered", described as "heavy metal taste in mouth"; PHARYNGEAL SWELLING (non-serious), outcome "unknown", described as "throat swelled". Clinical course: First dose her lymph nodes swelled immediately, dizziness, lightheaded, heavy metal taste in mouth, nausea. Second dose, same symptoms but worse, then tongue swelled, throat swelled, face numb and droopy, lymph nodes swelled more than last time, metal taste now worse. After 1 month, still can't taste food because of metal taste, lymph nodes still swollen, face still numb and tingly, mouth/tongue still swollen. The events were evaluated at the emergency room visit. Therapeutic measures were taken as a result of all events and treatment included benadryl, prednisone, pepcid. There was no other vaccine in four weeks or other medications in two weeks. The patient had no covid prior vaccination or COVID tested post vaccination.; Sender's Comments: Based on the temporal association, a causal relationship between the events face numb and droopy and face still numb and tingly, and bnt162b2 (COMIRNATY) cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy (Known allergies: other immunizations); Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2095384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: PR
Alter: 7,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 23.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Seizure

Symptomtext

Mother of minor alleges that on the third day (12/23/2021) of receiving the second dose of Pfizer (0.2MG IM), the minor had an episode of seizure. The mother refers that she called the pediatrician of PT and followed medical orders.

Weitere VAERSDATA-Felder

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

VAERS 2091808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: ME
Alter: 32,0
Geschlecht: M
Eingang: 06.02.2022
Impfdatum: 16.12.2021
Beginn: 14.01.2022
Tage bis Beginn: 29,0
Dosis: 2
Route/Site: IM / LA

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

Deep vein thrombosis Thrombosis

Symptomtext

Blood clot leading to deep vein thrombosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: All tests on 01/18/22 No trace of familial history of blood clots.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2088977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 18.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Bell's palsy Sensory loss

Symptomtext

left facial decreased sensation, difficulty smiling on left side. Dx Bell's Palsy. prednisone 60 mg daily x 7 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2071429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MA
Alter: 29,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 29.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: - / LA

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

Bell's palsy SARS-CoV-2 test

Symptomtext

Bells Palsy, Left side of face; 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 29 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 29Dec2021 10:00 (Lot number: FE3594) at the age of 29 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Patient had no known allergies. Patient had no other vaccine in four weeks. There were no concomitant medications in two weeks. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8736, Expiration date: 31Jul2021, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 11May2021, when the patient was 28 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8737, Location of injection: Arm Left, Vaccine Administration Time: 09:00 AM), administration date: 13Apr2021, when the patient was 28 years old, for COVID-19 Immunization. Patient was not diagnosed with COVID-19, prior to vaccination. On 29Dec2021, patient had been tested for COVID-19 via polymerase chain reaction (PCR) test, result was negative. The following information was reported: BELL'S PALSY (medically significant) with onset 03Jan2022 08:00, outcome "recovering", described as "Bells Palsy, Left side of face". The event "bells palsy, left side of face" was evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: on 03Jan2022, patient had been for COVID-19 via nasal swab, result was negative and on 05Jan2022, patient had been for COVID-19 via nasal swab, result was negative. Therapeutic measures were taken as a result of bell's palsy and treatment included week of prednisone and anti-viral medication. The investigation results were reported and the investigation included reviewing manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot ER8737, fill lot EW3426, and the bulk formulated drug product lot EP8586 and lot ER8736, fill lot EP8688, and the bulk formulated drug product lot EP8585. A complaint sample was not returned. No related quality issues were identified during the investigation. There was no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Date: 20220103; Test Name: SARS-CoV-2 Nasal Swab; Test Result: Negative ; Test Date: 20220105; Test Name: SARS-CoV-2 Nasal Swab; Test Result: Negative ; Test Date: 20211229; Test Name: SARS-CoV-2 PCR Test; Test Result: Negative ; Comments: Other
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2065356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

schwer

Staat: IN
Alter: 63,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 21.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Blood test Computerised tomogram Dizziness Ischaemic stroke Ultrasound scan Vertigo X-ray

Symptomtext

Vertigo and dizziness started about 7 days after shot. On Jan 4 at 8:30am a Ischemic stroke on right side of brain occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 7,0
Labordaten: C scans. X rays. Blood work. Ultra sound
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Triamtererene_hctz Metoprolol succinate XL
Allergien: none
Vorherige Impfungen: -

VAERS 2063795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 30.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Back pain COVID-19 Cough Dizziness Head injury Headache Nausea SARS-CoV-2 test positive Syncope

Symptomtext

1/6/22 52-year-old female who is positive for COVID-19 as of 1/3/2022, who presents to the emergency department after a syncope episode that occurred this morning. Patient reports that she was sitting on the computer, felt a little lightheaded and had a syncope episode. She does report that she had the top of her head. She is on any blood thinners. No seizure activity. She denies any numbness or tingling. No focal weaknesses of her upper lower extremity. No speech changes. No vision changes. No gait issues. She denies any pain of her extremities. She does report that she has had a cough that is been ongoing since her development of Covid-19. She reports of right upper back pain that has been persistent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 1/3/22 COVID-19 Result Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis; o GERD (gastroesophageal reflux disease) 2012 Goiter, nontoxic, multinodular 0
Andere Medikamente: cyclobenzaprine (FLEXERIL) 10 MG tablet Take 1 tablet by
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2057172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: WA
Alter: -
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 05.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Decreased appetite Fatigue Headache Inappropriate schedule of product administration Investigation Malaise Myalgia Nausea Pain in extremity Presyncope Pyrexia SARS-CoV-2 test Vaccination site pain

Symptomtext

first dose was on 30Aug2021 and second shot: 05Jan2022; Injection site pain; Tiredness; Headache; Muscle pain; Fever; Nausea; Feeling unwell; Decreased appetite; Arm pain; I almost fell on the floor, I had like no control really on the body, I thought I was fainting; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 05Jan2022 (Lot number: FE3594, Expiration Date: Feb2022) as dose 2, 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: 01, Lot number: FC3183, Expiration date: Oct2021, Anatomical site of vaccine administration: Left arm), administration date: 30Aug2021, for COVID-19 Immunization, reaction(s): "I had COVID; The first Pfizer vaccine we got it on Monday and I came down with COVID on Sunday; We were tested and we had COVID". The following information was reported: PRESYNCOPE (non-serious) with onset Jan2022, outcome "unknown", described as "I almost fell on the floor, I had like no control really on the body, I thought I was fainting"; INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 05Jan2022, outcome "unknown", described as "first dose was on 30Aug2021 and second shot: 05Jan2022"; VACCINATION SITE PAIN (non-serious) with onset Jan2022, outcome "unknown", described as "Injection site pain"; FATIGUE (non-serious) with onset Jan2022, outcome "unknown", described as "Tiredness"; HEADACHE (non-serious) with onset Jan2022, outcome "unknown", described as "Headache"; MYALGIA (non-serious) with onset Jan2022, outcome "unknown", described as "Muscle pain"; PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "Fever"; NAUSEA (non-serious) with onset Jan2022, outcome "unknown", described as "Nausea"; MALAISE (non-serious) with onset Jan2022, outcome "unknown", described as "Feeling unwell"; DECREASED APPETITE (non-serious) with onset Jan2022, outcome "unknown", described as "Decreased appetite"; PAIN IN EXTREMITY (non-serious) with onset Jan2022, outcome "unknown", described as "Arm pain". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of presyncope, vaccination site pain, fatigue, headache, myalgia, pyrexia, nausea, malaise, decreased appetite, pain in extremity. Clinical course: Consumer stated, she was calling this number so she could mention the side effects of the Vaccine. She had the second Pfizer Vaccine, and here side effects that had been reported with the vaccine, she had 10 out of the 19. She had injection site pain, tiredness, headache, muscle pain, fever, nausea, feeling unwell, decreased appetite, arm pain. And also well it was not in there but she just felt she woke up early in the morning around 6 am in the morning went to the bathroom and coming back to her bed she almost fell on the floor, she had like no control really on the body and thank god she landed on the bed instead of the, she thought she was fainting. She did not know what they put in these vaccines, but the first one she had she was okay. But 5 days later her husband and she had COVID (Hence split made and PC Filed Conservatively). They said that should not be associated with COVID and okay fine. So they had the second one a few days ago on 5th and here they gave us this pages and they said side effects that had been reported with the vaccine, so all of those. And so, she wanted to report the side effects. When confirmed that the consumer got COVID after receiving Pfizer COVID 19 Vaccine, Consumer stated, "Yes, the first Pfizer vaccine they got it on Monday and on Saturday her husband came down with COVID and she did on Sunday and they were pretty sick. They were tested and they had COVID. Then they did monoclonal antibody, so they had to wait for 3 months and then they decided okay they will have the second Pfizer. Her husband reacted better, but she had all of this, she was feeling better now but out of the 21 side effects she had 10 and one that she just told that she almost fell on the ground, 11. So half of the side effects she had. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Monoclonal antibody; Result Unstructured Data: Test Result:unknown results; Comments: so we had to wait for 3 months and then we decided okay we will have the second Pfizer; Test Date: 202109; Test Name: COVID-19 Test; Result Unstructured Data: Test Result:Covid
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 2048583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: UT
Alter: 61,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 21.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 14,0
Dosis: UNK
Route/Site: IM / LA

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

Bell's palsy Eye pruritus Facial paralysis Nasopharyngitis Visual impairment

Symptomtext

1/4/2022 I stated with cold like symptoms a couple days later on 1/7/22 my left eye was very itchy and bothering me on that sunday 1/9/22 my eye felt like it was changing vision and collapsing on Monday we went to the ER because my left side of my face was droopy and i couldn't talk , eat, or drink well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 1/10/2022 ER diagnosed me with bell's palsy
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Metformin Glipizide ER Atrovasatatin Alogliptin
Allergien: -
Vorherige Impfungen: -

VAERS 2046443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: KY
Alter: 40,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Chest pain Dizziness Migraine Presyncope

Symptomtext

Approximately 10 minutes after 3rd COVID vaccine was administered, patient complained of dizziness and felt faint. Patient was given apple juice. BP 129/91. EMS was contacted and patient was transported to the ED after EMS evaluation. Patient does have a history of vasovagal syncope. Patient stated she felt pre syncopal but no true syncope. While in the ED, patient also complained that she had 2-3 days of N/V/D with cramping abdominal pain. While in the ED, patient then began having left side chest pain. No hx of CAD. Chest pain, dizziness, N/V/D have all resolved but it has now triggered a migraine headache which she has a history of. Denies f/c, cp, soa, abdominal pain, urinary symptoms. Patient was given anti-emetic and fluids. Patient and MD discussed that the booster vaccine caused a vasovagal dizziness and presyncope feeling. Patient had symptom relief and was discharged from the ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None listed
Aktuelle Erkrankungen: None
Vorgeschichte: ? Liver disease, unspecified Liver problem ? Other bacterial infections of unspecified site VRE (vancomycin-resistant Enterococci) ? Overweight Over weight ? Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism History of bleeding disorder ? Personal history of malignant neoplasm, unspecified History of malignant neoplasm ? Personal history of other diseases of the circulatory system History of hypertension ? Personal history of other diseases of the musculoskeletal system and connective tissue History of gout ? Personal history of other diseases of the respiratory system History of hyperventilation ? Personal history of other endocrine, nutritional and metabolic disease History of diabetes mellitus ? Personal history of other medical treatment Transfusion history ? Personal history of other mental and behavioral disorders History of depression ? Personal history of thrombophlebitis History of thrombophlebitis ? Renal tubulo-interstitial disease, unspecified Kidney infection ? Unspecified coma Loss of consciousness
Andere Medikamente: None listed
Allergien: Beeswax - anaphylaxis Ondansetron - anaphylaxis Wound dressing adhesive - rash banana - unknown Egg - no reaction listed morphine - no reaction listed
Vorherige Impfungen: -

VAERS 2045492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: FL
Alter: 16,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Confusional state Dizziness Flushing Headache Hyperhidrosis Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Medium, Systemic: Dizziness/Lightheadedness-Medium, Systemic: Fainting/Unresponsive-Medium, Systemic: Flushed/Sweating-Medium, Systemic: Headache-Medium, Systemic: Shakiness-Medium, Systemic: Weakness-Medium.

Weitere VAERSDATA-Felder

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

VAERS 2045467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: IN
Alter: 13,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Head injury Injection site swelling Syncope Thermal burn Unresponsive to stimuli

Symptomtext

Site: Swelling at Injection Site-Medium, Systemic: Fainting / Unresponsive-Severe, Additional Details: 14 year old child fainted following Pfizer vaccination. Hit head on carpet, leaving carpet burn on side of face. Was alert and up talking to me when I approached him. Patient was taken to local emergency room for evaluation.

Weitere VAERSDATA-Felder

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

VAERS 2042414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 15.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Body temperature Chills Fall Immunisation Ligament sprain Loss of consciousness Malaise Nausea Pain in extremity Pyrexia Tremor Weight Weight increased

Symptomtext

gained a few pounds; Passed out/ she was trying to get to the bathroom. She woke up on the floor/passed out again; fell; Everyday her knee reminds her of her adverse reaction/ She must have twisted her knee; Shakes; Got up feeling sick; Felt nauseous; Fever of 102/ really high fever; Chills; Booster; sore arm /couldn't touch her left arm or anything; The initial case was missing the following minimum criteria: unspecified adverse event. Upon receipt of follow-up information on [04Jan2022], this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable reporter (Consumer) from medical information team. The reporter is the patient. A 52-year-old female patient received bnt162b2 (PFIZER BIONTECH COVID-19 VACCINE), administered in arm left, administration date 15Dec2021 12:30 (Lot number: FE3594) at the age of 52 years as dose 3 (booster), single for covid-19 immunization. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1(lot number: EP6955)), administration date: 20Mar2021, when the patient was 51 years old for COVID-19 immunization. The patient was diagnosed with COVID 01Apr2021 (between the first and second dose). Then, had the 2nd dose (lot number: ER8735), administration date: 24Apr2021, when the patient was 52 years old. She did not have any type of side effects on the 2nd one. Then, received the booster dose on 15Dec2021 12:30. She passed out at 3 o'clock in the morning (16Dec2021) after getting the booster dose. She woke up nauseous and got up feeling sick. She felt nauseous, when she was trying to get to the bathroom. Then, she woke up on the floor. She was calling her husband and carried her to the toilet, but she passed out again. She must have twisted her knee when she fell so her knee reminds her every day of the adverse reaction. She also had a high fever of 102. She also had shakes and chills on 16Dec2021. She just decided to call because she was sitting there, and her knee almost gave out on her. She thought she was going to end up having to go to the doctor for it. She also had a very sore arm in Dec2021 for 3 days. She couldn't touch her left arm or anything for 3 days. She has gained a few pounds also noted on unknown date. The patient recovered from the events nauseous, got up feeling sick, high fever, shakes and chills on 18Dec2021; recovered from sore arm on unknown date and passed out on 16Dec201 while unknown for the remaining events. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20211216; Test Name: Fever; Result Unstructured Data: Test Result:102; Test Name: Weight; Result Unstructured Data: Test Result:Gained a few pounds
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2643887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: OH
Alter: 53,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 07.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Computerised tomogram thorax Fatigue Hypersomnia Laboratory test Oedema peripheral Thrombosis Ultrasound scan

Symptomtext

Patient states that on 1/8 he had low grade fever (99.8) and fatigue and he slept all day On 1/9/22 he woke up with a "baseball" sized swelling in his (L) armpit. He went to ER @ MC and was diagnosed with a superficial blood clot. Restarted on Eliquis. Inst'd to apply warm compresses up to 4x/day. States that swelling is "about the same" this morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Labs, Ultrasound of (L) armpit, CT scan of chest.
Aktuelle Erkrankungen: Denies
Vorgeschichte: Diabetes Type II,
Andere Medikamente: Eliquis, Lipozide, Citrazine, Lipropalol; Lisinopril; Cefalexin, Omeprazole, Rosuvistatin; Vit D3; One A Day Men's 50+
Allergien: Wellbutrin, Metformin
Vorherige Impfungen: -

VAERS 2033262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: WA
Alter: 46,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 29.12.2021
Beginn: 11.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Asthenia COVID-19 Chest X-ray normal Chronic kidney disease Hydronephrosis Hypophagia Hypovolaemic shock Nephrolithiasis SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 4/29/21 (lot # EW0171), 5/20/21 (lot # EW0182), and 12/29/21 (lot # FE3594). On 1/11/22, patient admitted to our inpatient facility with hypovolemic shock (in the setting of poor PO intake of 5 days), acute renal failure CKD stage II, and positive COVID test result (generalized weakness without any respiratory symptoms). During hospitalization, patient was also found to have calcific debris/small stones in distal left ureter with hydronephrosis, which will most likely pass per nephrology. As of today (1/13/22), patient is still hospitalized in our med/surg unit due to acute renal failure and without any respiratory COVID symptoms (CXR clear).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypovolaemic shock
Hospital-Tage: 2,0
Labordaten: COVID status positive 1/11/22.
Aktuelle Erkrankungen: -
Vorgeschichte: morbidly obese female with type 2 diabetes, hypertension, dyslipidemia, sleep apnea, V. fib arrest in 2020 and on evaluation found to have ST elevation MI status post cardiac catheterization with 90% occlusion in the right coronary artery status post PCI
Andere Medikamente: albuterol inh, baby aspirin, clopidogrel, dapagliflozin, docusate, eplerenone, hydrochlorothiazide, insulin glargine pen, insulin lispro pen, liraglutide inj, lisinopril, metoprolol xl, rosuvastatin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2028519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: WI
Alter: 34,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Cold sweat Dizziness Hyperhidrosis Loss of consciousness Pallor

Symptomtext

Dizzy, light headed, pale, sweating, clammy - patient did pass out for ~30-45 sec.

Weitere VAERSDATA-Felder

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

VAERS 2027313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: WA
Alter: 14,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Loss of consciousness

Symptomtext

Patient received her booster- and right after she received her vaccines about 2-3 minutes she reports feeling lightheaded and dizzziness- passed out for about 3-5 secwe lower her down the floor and elevated her legs to keep her pressure to vital organ- Checked her BP was within range- Heart rate 53, BP 113/66- alert and oriented-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP see above
Aktuelle Erkrankungen: vagal response to needles
Vorgeschichte: none
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2019771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: AZ
Alter: 12,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 09.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Vomiting

Symptomtext

Patient fainted and started to vomit 30 seconds after injection of Pfizer Covid-19 vaccine and symptoms lasted for 15 minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Patient fainted and started vomiting after 30 seconds of injection of Pfizer Covid-19 vaccine.
Allergien: NKA
Vorherige Impfungen: -

VAERS 2018570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Dizziness Headache Heart rate Immunisation Myocarditis

Symptomtext

myocarditis/chest pain, arrhythmia, shortness of breath, heartrate to the 160's,; headache; dizziness; Pfizer BTC vaccine (purple formula,12 and older) booster dose; This is a spontaneous report received from contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. A 38 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 13Dec2021 16:00 (Lot number: FE3594) at the age of 38 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Psoriasis", start date: 2013 (ongoing). Concomitant medication(s) included: CLOBETASOL taken for psoriasis, start date: 2013 (ongoing); VYVANSE, start date: 2015 (ongoing). Vaccination history included: Bnt162b2 (Dose 1, Lot: EK5730 , Received in the left arm), administration date: 05Jan2021, when the patient was 37 years old, for COVID-19 Immunization, reaction(s): "Achy", "Tired"; Bnt162b2 (Dose 2: , Lot: EL3248 , Received in the left arm), administration date: 22Jan2021, when the patient was 37 years old, for COVID-19 Immunization, reaction(s): "Achy", "Tired". The following information was reported: IMMUNISATION (medically significant) with onset 13Dec2021 16:00, outcome "unknown", described as "Pfizer BTC vaccine (purple formula,12 and older) booster dose"; MYOCARDITIS (medically significant) with onset 14Dec2021 08:00, outcome "recovered" (19Dec2021), described as "myocarditis/chest pain, arrhythmia, shortness of breath, heartrate to the 160's,"; HEADACHE (medically significant) with onset 14Dec2021, outcome "recovered" (19Dec2021), described as "headache"; DIZZINESS (medically significant) with onset 14Dec2021, outcome "recovered" (19Dec2021), described as "dizziness". The events "myocarditis/chest pain, arrhythmia, shortness of breath, heartrate to the 160's,", "headache" and "dizziness" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: heart rate: (14Dec2021) 160's, notes: heart rate to the 160's. Clinical course: The patient had no prior vaccinations (within 4 weeks) and no family medical history relevant to events. The patient used to take Adderall when she was child and switched to Vivance in 2015. The patient called and reported an adverse reaction that happened after the Covid-19 Vaccine booster dose for adults. The patient received the Pfizer BTC vaccine (purple formula,12 and older) booster dose on 13Dec2021. The symptoms only occurred with the booster dose; when she received her 1st and 2nd doses, she was only "achy and tired" that only lasted 12-24 hours. She received the vaccine (third dose), and she was having chest pain after the booster and that is why she went to the ER. Her PCP would not see her to do an EKG because she was having chest pain. She was sent to and ended up in the emergency department (ED). She thought she had myocarditis. The ED ruled out myocarditis. She was having heart rate elevation into the 160's, chest pain, shortness of breath, and arrhythmias. She had severe headache and dizziness when her heart rate elevated. She said that she had the Covid-19 booster on 13Dec2021 at 1600. Her chest pain started on 14Dec2021 at about 0800. Heart rate elevation started at around 0800 as well on 14Dec2021. Her heart rate situation was recorded on her phone because she has an Apple watch. Her shortness of breath (SOB) started at about noon. She stated that the shortness of breath was periodic and would accompany her heart rate elevations and arrhythmias. She said that it was obvious she had an arrhythmia because she would get dizzy when it would occur. No relevant tests done. The patient said that the ER physician said that he has seen plenty of people with the same kind of adverse events in the ER strictly from the Pfizer Booster.; Sender's Comments: The contributory role of the product bnt162b2 (COMIRNATY) to reported events myocarditis, headache and dizziness is possible. This case will be reassessed upon receipt of follow-up information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Date: 20211214; Test Name: Heart rate; Result Unstructured Data: Test Result:160's; Comments: heart rate to the 160's
Aktuelle Erkrankungen: Psoriasis
Vorgeschichte: -
Andere Medikamente: CLOBETASOL; VYVANSE
Allergien: -
Vorherige Impfungen: -

VAERS 2018523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 21.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / RA

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

Arrhythmia Chills Fatigue Headache Immunisation Loss of consciousness Pain in extremity Pyrexia

Symptomtext

Fever; Chills; I lost consciousness; Arrhythmia; Booster; Tiredness; Arm was sore; Little bit of headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non healthcare professional). The reporter is the patient. A 35 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 21Dec2021 (Lot number: FE3594) at the age of 35 years as DOSE NUMBER UNKNOWN (BOOSTER), SINGLE for covid-19 immunization. The patient had no relevant medical history. The patient had no any other vaccinations within 4 weeks. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (DOSE NUMBER UNKNOWN, Manufacturer Unknown), for COVID-19 Immunization. The following information was reported: IMMUNISATION (medically significant) with onset 21Dec2021, outcome "unknown", described as "Booster"; LOSS OF CONSCIOUSNESS (medically significant) with onset 22Dec2021, outcome "unknown", described as "I lost consciousness"; ARRHYTHMIA (medically significant) with onset 22Dec2021, outcome "unknown", described as "Arrhythmia"; FATIGUE (non-serious) with onset Dec2021, outcome "recovered" (Dec2021), described as "Tiredness"; PYREXIA (non-serious) with onset 22Dec2021, outcome "unknown", described as "Fever"; CHILLS (non-serious) with onset 22Dec2021, outcome "unknown", described as "Chills"; PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "unknown", described as "Arm was sore"; HEADACHE (non-serious) with onset 2021, outcome "unknown", described as "Little bit of headache". Therapeutic measure ibuprofen was taken as a result of pyrexia, pain in extremity, headache. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
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 2014903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: IN
Alter: 32,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 23.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: SYR / RA

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

Bell's palsy

Symptomtext

Bells palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Rheumatoid arthritis
Andere Medikamente: Enbrel Losartan hctz 50-12.5
Allergien: Vantan
Vorherige Impfungen: -

VAERS 2011616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: WA
Alter: 30,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 17.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

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

Bell's palsy Computerised tomogram head normal Ear pain Facial paralysis Hypoaesthesia oral Laboratory test normal Otitis media Scan with contrast normal Swelling

Symptomtext

Start of ear pain on 12/24/21. By 12/27/21 ear pain had not gone away and swelling was noticeable. At around 8pm that evening tongue started feeling numb. By around 6 am on 12/28/21 had partial facial paralysis most noticeable by lack of smile. Immediately went to ER . Upon clear CT scan and other tests was determine to have Bell?s Palsy and middle ear infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CT Head w/contrast
Aktuelle Erkrankungen: First week in December had a stuffy nose. Was tested for COVID-19 on 12/12/21 and was negative. Was feeling fine at time of vaccine
Vorgeschichte: None
Andere Medikamente: None
Allergien: Bacitracin
Vorherige Impfungen: -

VAERS 2004214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 84,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Blood glucose increased Cold sweat Drooling Eye movement disorder Syncope

Symptomtext

Patient was taken to bathroom, by caregiver of the board and care unit, after completing 15-minute recovery, post Pfizer COVID-19 booster shot. Patient did not have any complaints or symptoms, during the 15-minute recovery period. Per caregiver, after patient had large bowel movement, patient?s? eyes began rolling and she was drooling?. Caregiver called out for help. Upon arrival, health vaccination team nurses called out to patient, and patient made eye contact and was able to state full name. Patient?s skin was cool and clammy, BP = 85/53, P=55, R=16, O2 Sat= 98%, on 2L NC. Patient placed on mat on floor, alert and oriented to person and place. 911 called. Paramedics arrived at 1525 and took over care of patient. BP= 130/76, P= 64, R=18, O2 Sat=100 % on 2L NC, Blood Glucose Level = 174. Per paramedics, patient to be transported to hospital via ambulance. Patient transported at 1539 and was alert and talking during transfer. Per caregivers at board and care, patient had vasovagal/syncopal episode while in the shower, approximately 2 weeks ago

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Pending.
Aktuelle Erkrankungen: Per caregiver at board an care
Vorgeschichte: Hypertension
Andere Medikamente: Lorsartan, 50 mg, oral, daily
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1997458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Diplopia Headache VIth nerve paralysis

Symptomtext

6th cranial nerve palsy for 1 week, headache, double vision

Weitere VAERSDATA-Felder

Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MN
Alter: 15,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 30.12.2021
Beginn: 30.12.2021
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 upper Chest pain Hyperhidrosis Loss of consciousness Nausea Tremor

Symptomtext

The patient had left the room after vaccination and within 3 minutes had passed out, was shaky, sweating profusely. He was only out for a few seconds, came back to, and had stomach pain with nausea. I gave the patient water and glucose and he slowly improved over time. For 15 minutes he was sitting on the floor and had some mild chest pain that passed within a few minutes. No issues breathing. He stayed for 30 minutes and left with his grandmother with some persistent nausea.

Weitere VAERSDATA-Felder

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

VAERS 1991887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MO
Alter: 33,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Fear of injection Flushing Hyperhidrosis Pallor Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Shakiness-Mild, Additional Details: About 2-3 minutes after vaccine went back into vaccine area and pt was diaphoretic and pale and fainted post vaccine. Pt was assisted to a flat postions and she regained consciousness approx 15-30 seconds after she was flat. She was monitored in the pharmacy area for 30 minutes and given water. Pt reports that she is needle phobic.

Weitere VAERSDATA-Felder

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

VAERS 1991883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

schwer

Staat: TX
Alter: 18,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chills Headache Hypotension Nausea Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: Pt fainted few minutes after getting her first dose of the covid-19 vaccine.Nurse practitioner was immediately summoned who attended to her untill she was able to get back on her feet to go home

Weitere VAERSDATA-Felder

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

VAERS 1991883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

schwer

Staat: TX
Alter: 18,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Chills Headache Hypotension Nausea Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: Pt fainted few minutes after getting her first dose of the covid-19 vaccine.Nurse practitioner was immediately summoned who attended to her untill she was able to get back on her feet to go home

Weitere VAERSDATA-Felder

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

VAERS 1990029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: AZ
Alter: 17,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 26.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Loss of consciousness Pallor Syncope

Symptomtext

PATIENT FAINTED AND LOOSE CONSCIOUSNESS FOR ABOUT 30 SECONDS AND THEN REGAIN CONSCIOUSNESS BUT WAS VERY PALE AND WEEK. EMS TOOK PT TO HOSPITAL.

Weitere VAERSDATA-Felder

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

VAERS 1981569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: NC
Alter: 19,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 21.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain Drug screen negative Echocardiogram normal Ejection fraction normal Echocardiogram Electrocardiogram Myocarditis Troponin I Electrocardiogram T wave normal Electrocardiogram abnormal Haematocrit decreased Haemoglobin normal Influenza A virus test negative Oropharyngeal pain Pain Platelet count normal Respiratory syncytial virus test negative

Symptomtext

Per hospital records, on 12/24/2021, "Patient is a 19 year old male who presented to the ED with complaints of sore throat and chest discomfort. He had a Pfizer COVID booster vaccination 4 days ago then developed some body aches the following day. Those symptoms improved over the next day but today he began having some burning in his throat and chest area. The burning sensation began at about 7 am when he first woke up and was still present around 10 am. The sensation did not radiate and was not associated with any nausea, vomiting, dyspnea, palpitations, edema or dizziness. He denies recent heavy physical exertion. He has a history of depression. He denies smoking, vaping, ETOH or drug use. He denied fever, chills, cough, shortness of breath, abdominal pain, nausea vomiting or diarrhea. Currently he is not having any chest pain, burning, cough, or shortness of breath. In the ED, his temperature was 98.4 F, pulse 97, respirations 18, blood pressure 130/81, oxygen saturation 97% on room air. Labs revealed a white count of 7400, hemoglobin 14.3, hematocrit 41.8, platelets 215, high sensitive troponin I was elevated at 5790.9. Throat culture was negative for group A strep. SARS-CoV-2 PCR was negative. Influenza PCR negative and RSV PCR was negative. A 12 lead EKG revealed sinus tachycardia with a rate of 101. Normal AST T-wave as read by the ER physician. He received some IV fluids and Cardiology was notified. As soon as the the patient was transferred to medical floor, patient had no chest pain, shortness of breath or palpitations. Troponin went up to 7610 and then trended down to 3554. Echocardiogram was done that showed normal ejection fraction with no valvular disease and wall motion abnormality. Repeated EKG is also negative for acute ischemic changes and showed normal sinus rhythm. Cardiology evaluated the patient again today and did recommend that patient could be discharged to home but he needs to have a follow-up echocardiogram. Discharge plan is discussed with the patient and he agrees with the plan".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: Per hospital records, on 12/24/2021, "In the ED, his temperature was 98.4 F, pulse 97, respirations 18, blood pressure 130/81, oxygen saturation 97% on room air. Labs revealed a white count of 7400, hemoglobin 14.3, hematocrit 41.8, platelets 215, high sensitive troponin I was elevated at 5790.9. Throat culture was negative for group A strep. SARS-CoV-2 PCR was negative. Influenza PCR negative and RSV PCR was negative. A 12 lead EKG revealed sinus tachycardia with a rate of 101. Normal AST T-wave as read by the ER physician. He received some IV fluids and Cardiology was notified. As soon as the the patient was transferred to medical floor, patient had no chest pain, shortness of breath or palpitations. Troponin went up to 7610 and then trended down to 3554. Echocardiogram was done that showed normal ejection fraction with no valvular disease and wall motion abnormality. Repeated EKG is also negative for acute ischemic changes and showed normal sinus rhythm. Cardiology evaluated the patient again today and did recommend that patient could be discharged to home but he needs to have a follow-up echocardiogram. Discharge plan is discussed with the patient and he agrees with the plan". Per hospital discharge summary report, a urine drug screen was also performed on 12/24/2021 with negative results.
Aktuelle Erkrankungen: None
Vorgeschichte: Per hospital records, patient has "a history of depression".
Andere Medikamente: Per hospital records, Bupropion HCl 150 mg tablet PO daily and Sertraline 100 mg tablet PO daily.
Allergien: Per hospital records, no known allergies.
Vorherige Impfungen: -

VAERS 1986139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Generalised tonic-clonic seizure

Symptomtext

Grand Mal Seizure one episode lasting 2 minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: none yet
Aktuelle Erkrankungen: epilipsey
Vorgeschichte: Epilepsy seizure free for last 3.5 years
Andere Medikamente: LAMICTAL 150 MG IN THE Am and 100 mg in the PM
Allergien: nka
Vorherige Impfungen: -

VAERS 1985192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 37,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Condition aggravated Encephalopathy Mental status changes Partial seizures Seizure

Symptomtext

Patient give first dose of Pfizer COVID 19 vaccine 12/21/21 @ 1020. Around 1025, patient started having a seizure lasting 15 seconds. Ten minutes later patient appeared to have an additional seizure, lasting approximately one minute. Patient was back to his baseline within 5 minutes. Patient admitted for AMS, encephalopathy and focal seizures. Patient has been given anticonvulsants since admission. Seizures were similar to the ones he was experiencing during this admission. Neurologist notified and increased dose of Keppra and ordered extra 500mg dose x1. No further adverse reactions noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Partial seizures
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Focal seizure (R56.9: Unspecified convulsions) Headache (R51.9: Headache, unspecified) Intermittent, IV drug abuse, (F19.10: Other psychoactive substance abuse, uncomplicated)> Substance abuse Metabolic encephalopathy (G93.41: Metabolic encephalopathy)
Vorgeschichte: Focal seizure (R56.9: Unspecified convulsions) IV drug abuse, (F19.10: Other psychoactive substance abuse, uncomplicated)> Substance abuse
Andere Medikamente: -
Allergien: Diphenhydramine (reaction unknown), Haloperidol (reaction - mute)
Vorherige Impfungen: -

VAERS 1985124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: NY
Alter: 19,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Blood glucose normal Pallor Syncope

Symptomtext

19yo male patient who 5min after receiving the Pfizer booster had a syncope, episode lasted few seconds. He received J&J as the primary COVID vaccine. He was noted to be pale and weak but was easily arousable. Mother stated that this always happens when he gets shots, he does get anxious, nervous and faints and then self-recovers. Patient did not eat anything today. Initial VS: HR 115, RR 15, SpO2 98%, BP 107/65, Cap gluc 130. On PE AAO x 3, clear breath sounds bilaterally, RRR, Cap refill <2sec. He drank water. After a period of observation, he felt much better, was able to ambulate with no problems. Repeated set of Vital signs within normal limits. Patient was discharge home with complete resolution of symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1981784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: -
Alter: 18,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 21.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Myocarditis

Symptomtext

Myocarditis due to COvid19 vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1981238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

schwer

Staat: OH
Alter: 22,0
Geschlecht: F
Eingang: 26.12.2021
Impfdatum: 26.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope

Symptomtext

She went to the waiting area after receiving the vaccine and came up a few minutes later and said that she had fainted. She didn't hit the floor but dropped her phone and sweatshirt. She said this is common for her and has had this happen several times before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no known
Vorgeschichte: no known
Andere Medikamente: no known
Allergien: no known
Vorherige Impfungen: has passed out with several other vaccines

VAERS 1981118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: PA
Alter: 53,0
Geschlecht: M
Eingang: 26.12.2021
Impfdatum: 13.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

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

Bell's palsy

Symptomtext

Bell's palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: ER evaluation
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1980976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 21.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

C-reactive protein normal Myocarditis Troponin

Symptomtext

Post vaccine myocarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: CRP; 2.4, Troponin peaked: 7.44
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1979543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: TX
Alter: 12,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 24.12.2021
Beginn: 24.12.2021
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

a patient 12 years old came in for the second dose and after 5 minutes of giving her dose she had a split second syncope while she was waiting for her post vaccination observation time. She was ok after that split second and waited for 30 minutes with her dad. While waiting dad mentioned that she had experienced similar syncope last time with her non-covid vaccine as she gets very very nervous and anxious with immunizations. They were checked upon continuously and she was doing ok. After 30 minutes her dad confirmed she was ok and they left.

Weitere VAERSDATA-Felder

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

VAERS 1979270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

schwer

Staat: NY
Alter: 18,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 24.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nausea Syncope

Symptomtext

Synacope, pt briefly got light headed and slightly nauseated, almost fainted. Had history of fainting when receiving vaccination. Fully recovered w/o complaints within 15 minutes of onset.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Pt had fainting in past when receiving previous vaccinations, not specific to any particular vaccination

VAERS 1978969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MI
Alter: 17,0
Geschlecht: F
Eingang: 24.12.2021
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

Asthenia Confusional state Dizziness Fatigue Flushing Hyperhidrosis Lethargy Seizure Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Seizure-Medium, Systemic: Shakiness-Severe, Systemic: Weakness-Medium

Weitere VAERSDATA-Felder

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

VAERS 1978765

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: VT
Alter: 16,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Cold sweat Dizziness Fall Headache Immunisation Loss of consciousness Nasopharyngitis Pallor

Symptomtext

Passed out/Collapse; Really cold; Clammy; Headache; fall; feeling dizzy; Pale; booster; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the parent. A 16 year-old female patient received bnt162b2 (BNT162B2), administered in deltoid left, administration date 11Dec2021 (Lot number: FE3594) at the age of 16 years as dose number unknown (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (MANUFACTURER UNKNOWN, dose 1, single), for COVID-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 11Dec2021, outcome "unknown", described as "booster"; LOSS OF CONSCIOUSNESS (medically significant) with onset 12Dec2021 07:00, outcome "recovered" (12Dec2021), described as "Passed out/Collapse"; NASOPHARYNGITIS (non-serious) with onset 12Dec2021 07:00, outcome "recovered" (12Dec2021), described as "Really cold"; COLD SWEAT (non-serious) with onset 12Dec2021 07:00, outcome "recovered" (12Dec2021), described as "Clammy"; HEADACHE (non-serious) with onset 12Dec2021 07:00, outcome "recovered" (12Dec2021), described as "Headache"; FALL (non-serious) with onset 12Dec2021 07:00, outcome "unknown", described as "fall"; DIZZINESS (non-serious) with onset 12Dec2021 07:00, outcome "unknown", described as "feeling dizzy"; PALLOR (non-serious) with onset 12Dec2021 07:00, outcome "unknown", described as "Pale". Clinical course: There were no prior vaccinations within 4 weeks. The patient did not even get her flu shot yet. The patient received the booster yesterday around noon and this morning, she just, out of the blue, she just collapsed, she passed out and she was really cold and clammy. Also, she had a headache. This has never happened before. The mother made sure that she gets her fluids. She was really cold and clammy. She just had her lie down in bed actually for like half an hour and just monitored her. The patient was cold, clammy and pale and she was dizzy and she has never had that. She passed out. They were upstairs in our bedroom and she hit the floor, we heard her, we heard her fall, it was a big bang and it was her on the ground.; Sender's Comments: Based on known temporal association, there is reasonable possibility of causal association between the event Immunisation, Loss of consciousness, Nasopharyngitis, Cold sweat, Headache, fall, Dizziness, Pallor and the suspect drug BNT162B2. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
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 1975352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: DC
Alter: 25,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Anaphylactic reaction Dizziness Dysphagia Feeling abnormal Feeling hot Interchange of vaccine products Pharyngeal swelling Sensation of foreign body Swollen tongue Uvula deviation Throat irritation

Symptomtext

I was not expecting any immediate adverse symptoms, given that my first two doses of Moderna only produced mild flu like symptoms after more than 24 hours. Five minutes after taking the shot I began feeling a bit lightheaded and like they were waves of heat going through my body. I continued grocery shopping at the Safeway to dispense the shot, but eventually told my brother that I was feeling bad enough that I needed to go talk to the pharmacist about what I was feeling. As I was walking back to the pharmacy counter, I began noticing what felt like a growing ball in the back of my throat. I described my symptoms to them and they said they would like me to sit and watch me. I asked for water as it was becoming difficult to swallow. As the feeling grew stronger, I asked for the epipen wanting to make sure I would not get to the point of restricted breathing, and administered a dose. I had never had an anaphylactic reaction to anything before, but my younger brother has a severe allergy and I was familiar with the procedure. The pharmacist called the EMS unbeknownst to me and they convinced me to go to the emergency room. I was administered intravenous Benadryl and then more epinephrine after I mentioned it was beginning to feel like my tongue was too big for my mouth. After arriving at the hospital about 40 minutes later, I was feeling pretty fine and any noticeable swelling had abated but they kept me for observation for 4 hours. The only remark was that my uvula had stuck to the side of my throat, which may have increased a sensation of an anaphylactic response. I am not 100% confident that this was not a more mild response heightened by the power of suggestion to be completely honest. Though I will say that I had not read about any issues with tongue or throat swelling before I began experiencing it. No further issues have occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Unknown.
Aktuelle Erkrankungen: None.
Vorgeschichte: Arthritis in my thumbs.
Andere Medikamente: Dexadrine 20mg but none taken that day.
Allergien: No known allergies other than some cats and a very mild reaction to kiwis.
Vorherige Impfungen: -

VAERS 1977017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

schwer

Staat: OK
Alter: 17,0
Geschlecht: F
Eingang: 23.12.2021
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

Hyperhidrosis Loss of consciousness Pallor

Symptomtext

After administering the booster vaccination, the patient passed out and then regained consciousness and then passed out again. After she was alert, she was completely pale and lost color in her face and began to sweat. The ambulance was called.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: None
Vorherige Impfungen: -

VAERS 1975264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Disorientation Incoherent Loss of consciousness

Symptomtext

Minutes after the administration of the vaccine, the patient was sitting down and started losing consciousness. Seconds later, she came back. She was a little disoriented and incoherent. We immediately laid her down on a flat surface and observed her. She fully regained consciousness, was coherent and vocal. She explained that this happened to her before once when she was visiting someone at a hospital. She said sometimes it gets triggered with the smell of alcohol (i.e the alcohol swab). She stated that she was fine and felt like normal. I explained adverse events, what to expect and what to do in case of an emergency.

Weitere VAERSDATA-Felder

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

VAERS 1975000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: MO
Alter: 27,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

The patient briefly lost consciousness a few minutes after receiving the vaccine. The patient quickly regained consciousness and appeared to be alert. The event occurred in the hospital and the patient was taken admitted for further evaluation.

Weitere VAERSDATA-Felder

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

VAERS 1971805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Fall Loss of consciousness Syncope

Symptomtext

Child lost consciousness, fainted and fell to the floor within 10 seconds of receiving first vaccine dose. He regained consciousness within a few seconds. Paramedics were called as the nurses monitored his vital signs. He stabilized within 30 minutes or so and was cleared to go home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Augmentin - antibiotic
Vorherige Impfungen: -

VAERS 1971719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

Patient said he was nervous and after his first COVID dose he fainted in the chair. Last time he ate or drank anything was at 3am on 12/22/2021. Ambulance called and patient refused to go to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: Patient stated the last time he ate or drank anything was at 3AM.
Allergien: na
Vorherige Impfungen: -

VAERS 1971575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: RI
Alter: 57,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 11.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / RA

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

Bell's palsy Blood test Computerised tomogram

Symptomtext

Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Cat Scan and a bunch of blood tests including lyme disease
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: womans multi with Omega 3 Calcium - 500MG Prevagin
Allergien: Coedine
Vorherige Impfungen: -

VAERS 1971528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: IL
Alter: 34,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness

Symptomtext

Patient had vaccine and while sitting in waiting area , patient complained of feeling light headed. Patient soon had an episode of passing out while sitting in chair that lasted 15-20 seconds. Patient lowered to floor. Patient awake and alert after being lowered to floor. Responds appropriately and able to verbalize surroundings. Patient vitals taken 97.8-55-18, BP 103/68 right arm lying. Patient assisted up into sitting position after a few minutes. Then to standing to have a seat in chair. Patient monitored for an additional 30 minutes. She stated she felt better and may have been nervous about taking vaccine. Patient left clinic at 1125 am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: UNK
Vorgeschichte: UNK
Andere Medikamente: UNK
Allergien: UNK
Vorherige Impfungen: -

VAERS 1970962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: NC
Alter: 20,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Lethargy Nausea Seizure Syncope Unresponsive to stimuli

Symptomtext

Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Nausea-Medium, Systemic: Seizure-Severe

Weitere VAERSDATA-Felder

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

VAERS 1967135

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: IL
Alter: 43,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Blood pressure increased Dizziness Dizziness postural Flushing Hyperhidrosis Hypertension Syncope

Symptomtext

Systemic: Dizziness/Lightheadedness-Mild, Systemic: Elevated blood pressure-Mild, Systemic: Flushed/Sweating-Mild, Systemic: Hypertension-Medium, Additional Details: Patient felt syncope 10 minutes after vaccine administration. We gave bottle of water, orange juice and apple juice. Patient felt slightly better but felt dizzy upon standing. Took blood pressure 196/109 plus 90. Called 911. Patient alert and responsive/talking the whole time.

Weitere VAERSDATA-Felder

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

VAERS 1962300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

schwer

Staat: PA
Alter: 15,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Flushing Hyperhidrosis Loss of consciousness Malaise Nervousness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Severe, Systemic: The patient passed out 2 times-Severe, Systemic: Flushed / Sweating-Medium, Additional Details: The patient passed out 2 times after vaccination while waiting her 15 minutes. i called 911. emts came and her vitals were fine. the emts advised she not go to the er. emts called dr at hospital who advised she not come to er unless it happens again or she starts to feel unwell. emts thought she was nervous about getting the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1961942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: NE
Alter: 13,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Deafness Immediate post-injection reaction Pallor Presyncope Visual impairment

Symptomtext

Vasovagal response immediately after administration 1:05pm. Patient stated she could not hear and was seeing black spots within 1 minute of administration. Patient became very pale. Paramedics were called and arrived at 1:18pm and assessed patient as having vasovagal response. Patient fully recovered at 1:45pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None Known
Vorgeschichte: None known
Andere Medikamente: Unknown
Allergien: None Known
Vorherige Impfungen: -

VAERS 1961699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: AZ
Alter: 25,0
Geschlecht: M
Eingang: 18.12.2021
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

Dizziness Fall Hypotension Syncope Tinnitus Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Hypotension-Mild, Systemic: Tinnitus-Mild, Additional Details: Patient reported to NP about 5 min after receiving vaccine symptoms of ringing in ear and lightheadedness, then fainted and fell forward, NP caught patient and assisted to floor. No injury with fall. Patient regained consciousness within 5-10 seconds. He was able to sit up and aware of surroundings. call placed to 911. BP initially 86/58, rechecked and up to 94/60. HR 75, O2 98%. Pt reports improvement of sxs and drank water. EMS arrived, BP up to 126/82 while seated, not taken to ED

Weitere VAERSDATA-Felder

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

VAERS 1959253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

schwer

Staat: CA
Alter: 90,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac disorder Confusional state Hypotension Loss of consciousness Presyncope

Symptomtext

Systemic: Cardiac Disorder (diagnosed by MD)-Severe, Systemic: Confusion-Severe, Systemic: Hypotension-Severe, Additional Details: Suspected Vasovagal Reaction and loss of conciousness

Weitere VAERSDATA-Felder

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

VAERS 1959182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: IL
Alter: 28,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Confusional state Dizziness Nervousness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Severe, Additional Details: Pt given booster first and then flu shot into other arm. While getting up she got nervous, fainted, LOC for 4 seconds, woke up confused but was okay afew a few seconds. Juice, water, ice pack given, pt ok after 5 mins

Weitere VAERSDATA-Felder

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

VAERS 1947986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: WA
Alter: 25,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspnoea Hypoaesthesia oral Painful respiration Respiratory distress

Symptomtext

Friday, Dec.10th 2021 16:32 During a Vaccination clinic, Medical Teams staff/volunteers administered a 1st dose of Pfizer covid vaccine to a 25-year-old female. Approx. 5 minutes later a volunteer flagged me down and reported that the patient was having difficulty breathing. I immediately stopped the clinic. Upon seeing the patient, she was obviously in respiratory distress. I instructed volunteer to activate 911. I then drew up 0.3 mg of epinephrine and RN administered to patient via IM (1635). Patient was then placed supine on the ground and her legs were elevated. Post epi administration, patient vitals: pulse 120, BP, 120/100, resp rate 20. Patient reported that beathing became easier post epi administration, but pain on inspiration. After four minutes patient reported her tongue and lips were feeling numb. We had drawn up a second 0.3 ml of Epi, but fire had arrived on scene(1644). Report was given to paramedics, and patient was handed off and transported by paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1945101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: KY
Alter: 31,0
Geschlecht: U
Eingang: 13.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Dizziness Fear of injection Syncope

Symptomtext

pt stated on arrival phobia of needles. Pt states she "passes out" with all injections and vaccines. Pt laid down for vaccination. Pt laid on right side for 5 mins after vaccination, talking the entire time. AFter laying for five mins she sat at foot of bed for several minutes before trying to stand up. Pt walked to waiting room without difficulty stated she felt great - best she had ever done. Next thing PCT came to office to tell me pt lower herself to ground, was laying in lobby floor. Pt states she felt dizzy like she could pass out. Stated she sat on floor then laid down. Pt was awake the entire time. Vital signs WNL, able to have conversation. Pt layed on floor for approx 15 mins.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Pt Denied
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: pt states she "passes out" with all vaccinations

VAERS 1942017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 19,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Syncope Unresponsive to stimuli Visual impairment

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Visual Changes/Disturbances-Mild, Additional Details: Patient experienced syncopal episode soon after vaccine administered. Patient was helped to the ground. Patient did not experience any loss of consciousness, or seizure, or confusion. Patient does not have history of recent trauma, or Sx history, or DM, or CAD, or cerebrovascular accident, or GI bleeding, or infection. No report or observation of wheezing, or trouble breathing, or swelling/hives of face or lips or mouth, or increased sweating. Patient fully recovered.

Weitere VAERSDATA-Felder

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

VAERS 1942005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient experienced syncopal episode soon after vaccine administered. Patient was helped to the ground. Patient did not experience any loss of consciousness, or seizure, or confusion. Patient does not have history of recent trauma, or seizure history, or diabetes, or CAD, or cerebrovascular accident, or GI bleeding, or infection. No report or observation of wheezing, or trouble breathing, or swelling/hives of face or lips or mouth, or increased sweating. Patient fully recovered.

Weitere VAERSDATA-Felder

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

VAERS 1940274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

PATIENT RECEIVED VACCINE AT 230PM, AROUND 240PM, SHE APPEARED PALE AND SWEATING. PT STATED SHE FELT AS SHE WAS GOING TO FAINT. FAINTED MINUTES LATER. PROVIDED A INSTANT COLD PACK TO COOL PT, PT WOKE UP AND LAID DOWN, WHICH SHE STATED HELPED HER FEEL BETTER. EMS ARRIVED TO EVALUATE PT, PATIENT LEFT 30 MINUTES OR SO AFTER THE EVENT ALERT AND FINE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: NONE MENTIONED
Vorgeschichte: NONE MENTIONED
Andere Medikamente: UNKNOWN
Allergien: COMPAZINE
Vorherige Impfungen: -

VAERS 1938575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

schwer

Staat: NE
Alter: 18,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Eye movement disorder Hyperhidrosis Loss of consciousness Pallor Syncope Urinary incontinence

Symptomtext

A few minutes after receiving a second vaccination of pfizer covid vaccine, the patient became pale, white and her eyes rolled back and she fainted. She was momentarily passed out (unconscious) for approximately one minute. She also urinated in the immunization booth. I attended to her care and I shook her arms and I called her name. The mom was there and she shook the patient(her daughter) which woke her up. I applied ice packs to the patient's forehead and arms and her sit in relaxed position. I had her remove her jacket as she was dizzy and sweating a lot. After 10 minutes of applying the ice packs her skin color came back and she was acting normal without anymore symptoms. I monitored the patient for 20 more minutes and the mom said she was fine and they left the pharmacy area.

Weitere VAERSDATA-Felder

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

VAERS 2727653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 27.12.2023
Impfdatum: 22.12.2021
Beginn: 30.10.2023
Tage bis Beginn: 677,0
Dosis: 3
Route/Site: - / -

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

Blood culture negative Blood iron decreased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Condition aggravated Dyspnoea exertional Hypervitaminosis D Iron deficiency Legionella test Lung infiltration Pneumonia Procalcitonin normal Productive cough Pyrexia SARS-CoV-2 test positive Staphylococcus test negative Streptococcus test negative

Symptomtext

Patient is a 75 y.o. female patient of MD with history of anxiety and hypertension. She is admitted on 10/30/2023 with community-acquired pneumonia not improving with outpatient antibiotics. COVID-19 PNA Community-acquired pneumonia: Presenting with a week history of productive cough, dyspnea on exertion, and reported fevers. Chest x-ray with right middle lobe and left basilar infiltrate. Not improving with 3 days of outpatient Levaquin Bcx NGTD, MRSA swab NEG, Procalcitonin negative, Strep and Legionella negative COVID POSITIVE 10/30 ID consulted, recommendations appreciated. Past window for IV remdesivir and Paxlovid On day of discharge patient on room air with adequate saturation Received ceftriaxone and doxycycline while inpatient, discharged on 5 days of Augmentin and doxycycline Treated with IV dexamethasone while inpatient, per current recommendations stopped on discharge Iron deficiency anemia Thrombocytopenia Without signs of bleeding on admission Iron studies consistent with iron deficiency Continue home p.o. iron Follow-up hemoglobin outpatient Vitamin D deficiency, resolved Patient has hypervitaminosis D at this time with vitamin D level 148 Discontinue 50,000 IUs weekly Follow-up with primary care for continued management and appropriateness of lower dosage Anxiety: Continue home Xanax Hypertension: Continue home atenolol Losartan and Lasix discontinued outpatient due to hypotension and symptoms GERD PPI

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2697930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 18.10.2023
Impfdatum: 29.12.2021
Beginn: 17.09.2023
Tage bis Beginn: 627,0
Dosis: 3
Route/Site: - / -

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

Autonomic nervous system imbalance Bacteriuria Blood culture negative Blood potassium decreased COVID-19 Condition aggravated Constipation Culture urine positive Decreased appetite Dementia Encephalopathy Fatigue Hypertension Hypokalaemia Hypotension Malnutrition Mental status changes Parkinson's disease

Symptomtext

Patient is a 82 y.o. female with a history of parkinsons disease, orthostatic hypotension, and NIDDM who presented to Hospital 9/17/2023 with AMS. She was found to be COVID positive. ID econsulted, after discussion with patient/ family elected to pursue remdesivir, 9/18- 9/20. She has symptomatically improved, worked with therapy and is medically stable for discharge to a SNF. 1. COVID 19 infection, Improving: No hypoxia. Complicated by encephalopathy, and appears to be fatigued and hypotensive. ID followed- Paxlovid would interact with patient's quietapine, this was not given. Discussed with family who favored remdesivir, 9/18- 9/20. Follow up outpatient for monitoring of symptom resolution. Tessalon pearls PRN at disscharge. 2. Sepsis, Resolved: Likely 2/2 above with hypotension exacerbated by history of autonomic dysfunction. However, Vanc & Zosyn started on admission given significant hypotension, sepsis fluids, lactate. Blood cultures 9/18 no growth. Urine cultures with coagulase negative staph likely contaminant. She was deescalated to doxy/ rocephin for CAP coverage 9/18. These were discontinued 9/19 due to low concern for bacterial infection. Follow up outpatient for monitoring of resolution of COVID symptoms as above. 3. Hypokalemia: K 3.0 on admit, repleted as needed. Recommend repeat BMP in one week. Encourage good PO intake. 4. Parkinsons disease with dementia: Patient able to ambulate and talk at baseline. Home medications continued. 5. Autonomic dysfunction: Previous hospital admissions for syncope within the past year. Home midodrine provided with hold parameters for SBP >140, continue on discharge. 6. Bacteriuria: With >100k colonies coagulase negative staph on urine culture. With possible symptoms including dysuria/ increased frequency. Repeat UA without evidence of infection. Continue to monitor for s/s dysuria in the outpatient and repeat UA if needed. 7. NIDDM: on metformin, continue to address outpatient. 8. HTN: held amlodipine, ok to continue on discharge with hold parameters. 9. Constipation: Significant hx of constipation, continue home meds on discharge. 10. Moderate/non-severe, protein calorie malnutrition: related to chronic illness, per RD assessment. BMI 17.45, daughter reports loss of 5lbs over the past week PTA, poor appetite. Recommend Boost glucose control with breakfast and dinner. Encourage good PO intake.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2697086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 17.10.2023
Impfdatum: 23.12.2021
Beginn: 14.09.2023
Tage bis Beginn: 630,0
Dosis: 4
Route/Site: - / -

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

Affective disorder Angiogram cerebral normal Anticoagulant therapy Arteriogram carotid abnormal Arteriosclerosis Asthenia Atrial fibrillation Bipolar disorder Blood creatinine increased Blood lactate dehydrogenase normal Bradycardia COVID-19 Cardiac pacemaker replacement Cardiac telemetry Carotid artery stenosis Computerised tomogram normal Condition aggravated Depression

Symptomtext

Patient is a 76 y.o. male who presented from home on 9/14/2023 with unsteady gait, tremors and urinary symptoms. Tested positive for COVID-19. Behavioral medicine consulted due to patient's history of bipolar disorder for titration of medications. Patient was taken out of isolation for COVID. Gait instability - Etiology unclear. Likely weakness and decompensation from COVID-19. Unlikely cardiac in nature due to normal troponin. Unlikely stroke though unable to completely rule out as cannot have MRI - Patient uses cane and walker at baseline, since 2011 - Neuro exam unremarkable. Valproic acid level elevated but still within therapeutic range. - CT angio of the head and neck with no acute intracranial abnormality. Atherosclerosis present with moderate stenosis of the L vertebral artery, stenosis of the proximal cervical ICAs b/l. Orthostatics negative. -B12 normal -Unable to undergo MRI due to his cardiac device -Repeat CT negative; will monitor for any evidence of gait instability -He was clinically improving and ambulating better with therapy but then on 9/19 early morning had a fall - got up on own and tripped over bipap tubing - repeat ct stable -Imaging of lumbar spine 9/25 negative for any displacement of previous surgical hardware or acute fractures. Depression Bipolar disorder - Recently hospitalization for manic episode and meds adjusted. Per wife, patient sleeps often and is fatigued due to depression. -Also significantly improved on discharge. - Was started on Depakote for bipolar disorder 3 weeks ago. Continue inpatient; however dose reduced due to valproic acid level. Significantly improved mood. -Dose of Depakote reduced from 2000mg to 1500mg and started on Wellbutrin 150 daily per behavioral medicine recs on discharge. COVID-19 - Patient vaccinated with Moderna + booster. - Symptom onset day before admission. Patient satting well on room air. - ID consult for possible Paxlovid use; started on Paxlovid 9/15 and course completed - Given one-time Lasix on 9/16/23; lung exam much improved now and off O2 Thrombocytopenia - Baseline PLT count ~200. 98 upon admission. Likely due to COVID-19 infection. - LDH is normal, haptoglobin is normal - improved to nl range now xysmal atrial fibrillation - On home Xarelto 20 mg. Rate controlled in NSR - Changed to Eliquis while patient is on Paxlovid, now back on Xarelto. SA node dysfunction w/ pacemaker - Pacemaker battery last replaced on 9/4. Base pace rate is 45 bpm. - Continue to monitor via telemetry. Chronic kidney disease - Baseline Cr between ~1.5. Cr 1.60 upon admission. - Continue to monitor. - Was given one-time dose of Lasix on 9/16 given his congestion for dry lung strategy, tolerated this well HTN -On home Norvasc 5 mg, Carvedilol 25 BID at home, Losartan 50 mg. -BP controlled without Coreg, patient was bradycardic to 50-55 HR without Coreg. -continue home meds and monitor. Stop Carvedilol due to bradycardia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2677662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 29.08.2023
Impfdatum: 21.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Asthenia Condition aggravated Fatigue Headache Muscle spasms Pain Paraesthesia

Symptomtext

progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.; progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.; progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.; progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.; headache; new onset paresthesia in my legs while standing at work/paresthesia in my lower extremities from my buttocks to my feet; progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 67-year-old male patient received BNT162b2 (BNT162B2), on 21Nov2021 as dose 3 (booster), single (Lot number: FE3594) at the age of 65 years for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "Diabetes" (unspecified if ongoing); "High Cholesterol" (unspecified if ongoing); "Gout" (unspecified if ongoing); "if covid prior vaccination: Yes" (unspecified if ongoing), notes: if covid prior vaccination: Yes. Concomitant medication(s) included: AMLODIPINE;OLMESARTAN; JANUMET; CRESTOR; PROPANOLOL [PROPRANOLOL]. Past drug history included: Aspirin, reaction(s): "known allergies: Aspirin Intolerance", notes: known allergies: Aspirin Intolerance. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6207, Administrator route: Intramuscular; Location of injection: Arm Left), administration date: 06Apr2021, when the patient was 64-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: EW01050, Administrator route: Intramuscular; Location of injection: Arm Left), administration date: 27Apr2021, when the patient was 64-year-old, for COVID-19 Immunization, reaction(s): "Headache", "new onset paresthesia in my legs while standing at work", "progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.", "progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.", "progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.", "progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet", "progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.", "progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.". The following information was reported: ASTHENIA (non-serious), FATIGUE (non-serious), MUSCLE SPASMS (non-serious), PAIN (non-serious), CONDITION AGGRAVATED (non-serious), outcome "not recovered" and all described as "progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet."; HEADACHE (non-serious), outcome "not recovered"; PARAESTHESIA (non-serious), outcome "not recovered", described as "new onset paresthesia in my legs while standing at work/paresthesia in my lower extremities from my buttocks to my feet". The events "progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.", "headache" and "new onset paresthesia in my legs while standing at work/paresthesia in my lower extremities from my buttocks to my feet" required physician office visit. Therapeutic measures were not taken as a result of asthenia, fatigue, muscle spasms, pain, headache, paraesthesia, condition aggravated. Additional information: The following day after the 2nd dose, I suddenly developed a very severe headache and new onset paresthesia in my legs while standing at work, so bad that I had to call for assistance for support back to a chair. The symptoms resolved after a few minutes but that was the beginning of progressively worsening weakness/fatigue, cramps, deep pain, and paresthesia in my lower extremities from my buttocks to my feet.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300286687 Same patient/drug/AE, different dose.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: Yes); Diabetes; Gout; High cholesterol; Hypertension
Andere Medikamente: AMLODIPINE;OLMESARTAN; JANUMET; CRESTOR; PROPANOLOL [PROPRANOLOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2676549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 87,0
Geschlecht: F
Eingang: 25.08.2023
Impfdatum: 20.12.2021
Beginn: 08.03.2023
Tage bis Beginn: 443,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Hypoxia

Symptomtext

R09.02 HYPOXIA 3/23/2023 SHORTNESS OF BREATH

Weitere VAERSDATA-Felder

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

VAERS 2670156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 11.08.2023
Impfdatum: 22.12.2021
Beginn: 15.03.2023
Tage bis Beginn: 448,0
Dosis: 2
Route/Site: IM / RA

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 2659908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 24.07.2023
Impfdatum: 19.01.2022
Beginn: 16.07.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia COVID-19 Cough Faeces discoloured Hyponatraemia Loss of personal independence in daily activities Migraine Mobility decreased Myalgia Nausea Respiratory tract congestion SARS-CoV-2 test positive Vomiting

Symptomtext

"Patient is a 69 y/o female with a past medical history significant for sjogrens, hypothyroidism, HTN, asthma and depression. She presented to the ED due to weakness and nausea/vomiting. She states on Wednesday she had a migraine and was unable to get out of bed, she also had nausea with non bloody vomiting. The headache resolved but she continued to have nausea and vomiting with progressively worsening generalized weakness. She denies any abdominal pain. She does admit to 2 black stools, 2 days ago and yesterday, nothing today. She denies any frequent NSAID use. She felt too weak to shower today so she presented to the ED. She also admits to myalgias and congestion. She denies any shortness of breath but does admit to a dry cough. In ED patient was found to be hyponatremic so will be admitted for further evaluation. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: 6,0
Labordaten: Positive COVID test 7/16/2023 PCR
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2629830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 22.04.2022
Beginn: 01.07.2022
Tage bis Beginn: 70,0
Dosis: 4
Route/Site: - / -

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

Hypotension

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2629822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 70,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 22.04.2022
Beginn: 06.05.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: - / -

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

Hypotension

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2627491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 05.05.2023
Impfdatum: 15.04.2021
Beginn: 21.02.2023
Tage bis Beginn: 677,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/21/23 presents to ED for "cough" "shortness of breath". PMHx of "COPD, CKD, GERD, obesity, diabetes"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/21/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2595679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 13.03.2023
Impfdatum: 21.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Condition aggravated Muscle spasms

Symptomtext

I did not have an adverse reaction to the vaccine. I have had issues with my back for several years. Normally if I throw my back out, I will go for an adjustment, and I would be ok. My back went out and now I have muscle spasms on top of pain. I see pain specialist and get steroid injections into my back. I would occasionally take Advil or Tylenol to help with the pain.

Weitere VAERSDATA-Felder

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

VAERS 2548829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: FL
Alter: 32,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 02.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Blister COVID-19 Cough Herpes zoster Hypoaesthesia Migraine Oropharyngeal pain Pain in extremity Paraesthesia Pruritus Pyrexia Rash Rash pruritic Rhinorrhoea SARS-CoV-2 test positive Skin lesion Skin weeping

Symptomtext

I received my Pfizer COVID-19 booster on 1/2/2022. On 1/12/2022 or 1/14/2022, I woke up early in the morning with an itch on my right calf. When I turned on the light, I saw there was a painful, itchy rash on my calf. I took pictures of it and emailed them to my doctor, who messaged me back and told me that it looked like shingles. They prescribed me valaciclovir. About a day after the onset, I also had a rash on my left calf. My doctor thought it was a strange presentation of shingles, since only my calves were affected, but since I had pre-existing lupus and had recently received my booster for COVID-19, it wasn't entirely surprising. It took about 2 weeks for my shingles to subside, and during that time, my sores blistered and oozed. On 5/26/2022, I developed an itch on my right calf while I was in bed, and I immediately knew what it was. I went to the doctor later that day, and he told me it was a shingles recurrence and prescribed me valaciclovir. The presentation was exactly the same as it had been before. Both calves were affected, and the sores blistered and oozed. And again, it took about 2 weeks for the shingles to subside. On 12/28/2022, I developed a sore throat and runny nose. They continued on 12/29/2022. On 12/30/2022 at around 12:30PM, I developed a fever. At 1:25PM, my fever was 102, and I started to develop a cough. By 8:40PM, the fever 103.3, and my oxygen level was 92%. On 12/31/2022, my fever was 105.4 at 12:13AM. I took TYLENOL, which brought it down to 103.8. I slept with an ice pack for the rest of the night. When I took a home antigen test at 8:15AM on 12/31/2022, the result was positive. I then went to a pharmacy at 11:45AM to take a PCR test, which ultimately also yielded a positive result. For most of the day, the fever stayed at around 102, even though I took TYLENOL or ADVIL every 4 hours. At 10:00PM, it shot up to 103.7. I woke up at 5:30AM on 1/1/2023, and my temperature was 102.4. I then developed new symptoms that included a migraine on the left side of my head behind my eye, and my left foot and toes became numb and tingly. Both the migraine and leg numbness lasted for the entire day of 1/1/2023. At about 8:00PM that night, my fever dropped to 101. I slept most of the night that night. On 1/2/2023, I had a fever of 101 for almost the entire day. I would take a TYLENOL, which drop the temperature to only 100. When I woke up that morning, I had a migraine affecting both sides of my head that was concentrated behind my eyes, and it lasted all day that day until I went to sleep at about 8:00PM. At the time of this writing, I have no fever, but I still have a cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 12/31/2022 home antigen test positive result; 12/31/2022 PCR test positive result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Lupus; Meniere's Disease; Acid Reflux Disease; Antiphospholipid Syndrome; Sjogren's Syndrome; Thin Basement Membrane Disease (Both Kidneys); Polycystic Ovary Syndrome.
Andere Medikamente: PLAQUENIL; pantoprazole; CELLCEPT; lisinopril; CLARITIN; metaxalone; vitamin D; calcium; zinc; folic acid.
Allergien: Azithromycin; dust mites; shrimp; some adhesives.
Vorherige Impfungen: When I was about 5 or 6, I got a flu and tetanus shot in my left arm. I developed a fever and a baseball-sized swelling at the i

VAERS 2544579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NC
Alter: 35,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 17.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Exposure to SARS-CoV-2 Glucose tolerance impaired Hypertension Parosmia SARS-CoV-2 test positive Taste disorder

Symptomtext

I tested positive for COVID-19 on 12/22/2021. I didn't have symptoms at the time, but I knew that I had been exposed and decided to test. Later on, I developed loss of taste and smell. I was not prescribed medications for this health event. I also did not take any over-the-counter medications. I had these symptoms for about a month and a half. I still have altered smell and taste. Everything smells and taste kind of like onions. I have also developed high blood pressure and I am pre-diabetic. That does not run in my family or anything, so it is kind of strange to me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 22DEC2021 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2544369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: WA
Alter: 66,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Impaired work ability Injected limb mobility decreased Injection site pain Loss of personal independence in daily activities Musculoskeletal stiffness Wrong technique in product usage process

Symptomtext

The shot went in very hard. The person came at me with the needle, like a punch. I jumped off the table. It really hurt. I was unable to lift my arm above shoulder level. It was painful when driving home. It became very stiff. I could not do the usual activities of daily living, nor could I do farm and household chores. I was not able to perform my work in an active way. I am a personal trainer and group fitness instructor. I am a competitive swimmer. I am a runner and a biker. I have never ever had a sore shoulder. I saw my PCP Doctor. I got a referral for physical therapy. I went to 3 sessions. It took over 6 months to heal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Women's Multi-Vitamin, Vitamin D, Iron
Allergien: None
Vorherige Impfungen: -

VAERS 2513940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: ME
Alter: 60,0
Geschlecht: F
Eingang: 22.11.2022
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: ja ER: unbekannt Erholt: nein

Asthenia Dyskinesia Injected limb mobility decreased Loss of personal independence in daily activities Pain Pain in extremity Paraesthesia

Symptomtext

Left arm pain is constant, throbbing at times eleven months after receiving the vaccine. When the vaccine was administered, my whole arm tingled, and jumped, the person administering the shot said it was nothing and would go away. The pain has continued and sometimes throbs, almost a year later. It limits how I can use the arm, cannot carry heavy items in that hand, trouble lifting shirt off over my head.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi vitamin, Vitamin B12, Vitamin C, Vitamin D3, Quercetin
Allergien: None
Vorherige Impfungen: After my second Covid vaccine, I experienced some Shingles pustules.

VAERS 2501770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: WI
Alter: 24,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain

Symptomtext

Patient was here for her Bivalent booster on 11/4/2022. At the time of this appointment, she reported that after her 2nd and 3rd doses of the Pfizer vaccine, she experienced chest pain that lasted for 2 weeks. She described the chest pain as "feeling like a punch with superficial pain that was hard to pinpoint". She did not see a provider after experiencing the chest pain after either dose. There was no documentation of chest pain after the 2nd dose, so a 3rd dose was given by a paramedic at our clinic. Upon further review with a physician in our office, we did not administer the bivalent booster to this patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known
Vorgeschichte: None known
Andere Medikamente: None known
Allergien: None known
Vorherige Impfungen: Patient also reported having chest pain after her 2nd dose of the Pfizer Covid-19 vaccine. There was no documentation of this in

VAERS 2500166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3594

moderat

Staat: IN
Alter: 54,0
Geschlecht: M
Eingang: 06.11.2022
Impfdatum: 17.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 46,0
Dosis: 1
Route/Site: SYR / LA

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

Computerised tomogram thorax abnormal Dyspnoea Dyspnoea exertional Lung opacity Oxygen saturation decreased Pulmonary function test Total lung capacity decreased

Symptomtext

Shortness of breath, pulse oxygen dropped below 75, hospitalization for 7 days, given prednisone for 3 months to raise pulse oxygen, 100% gro7nd glass found in CT scan high res, still shortness of breath with any exertion or climbing stairs. 60% lung capacity left.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 7,0
Labordaten: Ct scan high res x3. Pulmonary function test.
Aktuelle Erkrankungen: None
Vorgeschichte: Ground glass, 60% lung capacity, shortness of breath, can no longer exercise. No longer bike ride, can?t climb multiple flights of stairs. Very tired
Andere Medikamente: Metformin , rosuvastatin, one a day 50, tramadol, clopidogrel, aspirin.
Allergien: -
Vorherige Impfungen: -

VAERS 2488479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 70,0
Geschlecht: U
Eingang: 25.10.2022
Impfdatum: 02.03.2021
Beginn: 02.09.2022
Tage bis Beginn: 549,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

09/02/22 presents to ED for "sharp chest pain". PMHx of "HTN, former smoker"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 09/03/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2487266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3594

moderat

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 14.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

Exostosis Inflammation Injected limb mobility decreased Injection site pain Magnetic resonance imaging Pain in extremity X-ray

Symptomtext

My arm was in extreme pain for many months after first injection. I had a hard time using it and lifting. I kept thinking that the pain would go away but after it did not subside, I eventually went and saw an orthopedist who did X-rays and eventually an mri. His findings were that the vaccine had triggered inflammation in my arm and the inflammation was rubbing on bone spurs. He injected me with the steroid injection which helped the inflammation. I still have pain in my left arm from where I was vaccinated the first time but at least my arm is usable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: 8/3/21 mri
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Birth control pill, multi-vitamin, Calcium, Dha, luetin
Allergien: -
Vorherige Impfungen: -

VAERS 2486170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 31.12.2021
Beginn: 16.10.2022
Tage bis Beginn: 289,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Asthenia Blood creatinine normal Bursitis COVID-19 Cellulitis Clostridium test negative Decreased appetite Dehydration Diarrhoea Hypophagia Mobility decreased Respiratory failure Ultrasound kidney normal

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 10/16/2022 Discharge Date: Oct 19, 2022 PRESENTING PROBLEM: Dehydration [E86.0] Weakness [R53.1] AKI (acute kidney injury) (HCC) [N17.9] HOSPITAL COURSE: Patient is a 76 y.o. male, with a PMH of ischemic cardiomyopathy, CHF, Afib, HTN, OSA, multiple myeloma, and primary appendiceal adenocarcinoma who presented to the ED with weakness. Patient was recently admitted from 10/8-10/12 with right septic olecranon bursitis/cellulitis treated with antibiotics, AKI and respiratory insufficiency due to COVID-19 infection. He was medically managed, weaned off oxygen, seen by PT/OT and discharged to home. At home he was not getting out of bed, not eating or drinking, and was weak without energy and brought back to the ER for further evaluation. On further interrogation he has been having diarrhea as well since starting Keflex and recent c.diff testing was negative. Given his weakness he was admitted to medicine for further evaluation. He was found to have AKI. Given small fluid bolus, but AKI persisted. Workup consistent with pre-renal etiology with poor intake and diarrhea. Renal US without signs of hydronephrosis. Given more IV fluids and had resolution of AKI back to baseline Cr. He was evaluated by PT/OT who recommended home with assist. Given his good improvement he was discharged home in stable condition on 10/19/2022. He tolerated Keflex while inpatient and should complete previous course of Keflex at home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: 12/27/2021 Family Practice Neck Pain
Vorgeschichte: Ischemic cardiomyopathy Coronary artery disease involving native coronary artery of native heart without angina pectoris Primary appendiceal adenocarcinoma (HCC) Arthritis Ascending aortic aneurysm Atrial fibrillation (HCC) Nephrolithiasis Essential hypertension Hearing loss Automatic implantable cardioverter-defibrillator in situ Multiple myeloma (HCC) Morbid obesity (HCC) Abdominal pain Valvular heart disease Aortic root aneurysm Shortness of breath Elevated diaphragm Acute bronchitis Acute colitis Polyneuropathy Chronic pain due to neoplasm Obstructive sleep apnea Treatment-emergent central sleep apnea Nocturnal hypoxia Diastolic dysfunction COVID Cellulitis of right elbow Unspecified severe protein-calorie malnutrition (HCC)
Andere Medikamente: aspirin 81 MG tablet carvedilol (COREG) 3.125 MG tablet cephalexin (KEFLEX) 500 MG capsule colchicine (COLCRYS) 0.6 MG tablet compounded topical medication misc diclofenac sodium (VOLTAREN) 75 MG delayed release tablet diphenoxylate-atropin
Allergien: Dilaudid [Hydromorphone]Hallucinations IsosorbideDizziness, Headache AspirinGI Upset CiprofloxacinMyalgia, Dizziness CodeineNausea and Vomiting, Other, Headache GabapentinMyalgia, Dizziness Hydrocodone-acetaminophenNausea and Vomiting, Headache IodineNausea and Vomiting Ivp Dye, Iodine ContainingNausea and Vomiting, Other
Vorherige Impfungen: -

VAERS 2477352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3594

moderat

Staat: AR
Alter: 36,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 24.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / -

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

Dizziness Feeling abnormal Headache Migraine Vision blurred

Symptomtext

Shortly after getting vaccine started getting headaches and dizziness intermittently, but frequently for the following 2 months. I thought it finally resolved, but I keep getting headaches/migraines intermittently. I've never had a problem with headaches or dizziness before (outside of acute illness like a cold or sinus infection) and never so persistently or intensely. Sometimes they make my vision blur and thoughts foggy. The dizziness isn't so bad or frequent anymore, primarily headaches/migraines now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine 50mcg daily
Allergien: Bactrim-rash
Vorherige Impfungen: -

VAERS 2461842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 41,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 06.01.2022
Beginn: 20.09.2022
Tage bis Beginn: 257,0
Dosis: 3
Route/Site: - / -

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

Asthenia Blood grouping COVID-19 Condition aggravated Convalescent plasma transfusion Diarrhoea Norovirus test positive Pneumonia Pneumonia bacterial Pyrexia SARS-CoV-2 antibody test negative SARS-CoV-2 test positive Stool analysis abnormal

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 9/20/2022 Discharge Date: 09/23/2022 Discharge Disposition: Transfer Discharge Provider: MD Primary Care Provider: MD Admission Date: 9/23/2022 Discharge Date: Sep 26, 2022 PRESENTING PROBLEM: Fever HOSPITAL COURSE: Patient is a 41-year-old female who was admitted on 09/20/2022 for fever. She has a history of renal transplant back in 2011 and is immunocompromised. She was diagnosed with COVID-19 followed by bacterial pneumonia in August of 2022. She continues to still be positive for COVID-19 we checked antibodies which were negative and does appear this is an active infection. Id has been consulted and they did initiate remdesivir yesterday we have continued her on doxycycline and cefepime to cover for bacterial pneumonia. Yesterday evening cycle threshold was low, ID recommended transfer to hospital for convalescent plasma today. Blood typing was obtained and consent for blood transfusion product, verified a plasma was applied at hospital for this patient. Patient overall has significantly improved in regards to her weakness. She has had no hypoxic episodes. We have continued her 5 mg daily prednisone. She has had diarrhea but chronically has this there was just increased recently, infectious studies are pending. PRESENTING PROBLEM: COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 41 y.o. female with PMH significant for kidney transplant and HTN who has been hospitalized at hospital from 9/20-9/23 for fever 2/2 COVID infection. Patient recently had COVID on 8/1/22 at which time she was treated with Paxlovid and has since had resolution of symptoms. She later had CAP which she was treated in August. Patient developed a fever on 9/16/22 which persisted several days, prompting ED presentation. While at hospital, she was found again positive for COVID with no COVID antibodies, suggesting this was an active infection. She was started on Remdesivir and ID was consulted and recommended convalescent plasma infusion so she was transferred to different Hospital. She tolerated well convalescent plasma infusion. She had no hypoxia. She received 5 doses of Remdesivir and was empirically treated w/ doxycycline and was discharged home on 9/26/22. During her time in the hospital, although she has chronic diarrhea, she also had stool studies obtained which came back positive for norovirus. She is immunocompromised due to antirejection meds for renal transplant and she also has chronic neutropenia with anemia which was slightly worse from her baseline, but was improving by time of discharge. Her CKD stage III was also stable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: End stage renal disease Other specified pre-operative examination Dysmenorrhea Heavy menses Orthopedic aftercare Right knee injury, initial encounter Acute pain of right knee Closed fracture of right proximal tibia Pelvic fluid collection Female pelvic peritoneal adhesion ESRD s/p Living related donor kidney transplant Renal insufficiency Bacterial sepsis Stage 3 chronic kidney disease Gastroesophageal reflux disease Hyperlipidemia Hypertension Hypomagnesemia Microscopic polyangiitis Osteoporosis Psychophysiological insomnia Renal osteodystrophy Secondary hyperparathyroidism Endometriosis Pelvic pain in female Acute nephritic syndrome Anemia in chronic kidney disease Arteritis Neutropenia Community acquired pneumonia of right lower lobe of lung COVID-19 Thrush, oral Diarrhea of presumed infectious origin Unspecified severe protein-calorie malnutrition Fever in immune-compromised patient Fever and neutropenia Norovirus
Andere Medikamente: BELATACEPT IV calcium citrate (CALCITRATE) 950 (200 Ca) MG tablet ergocalciferol (VITAMIN D2) 1.25 MG (50000 UT) capsule metoprolol succinate-XL (TOPROL-XL) 50 MG 24 hr tablet multivitamin (THERAGRAN) per tablet mycophenolate (MYFORTIC) 180
Allergien: PenicillinsHives TramadolNausea and Vomiting
Vorherige Impfungen: -

VAERS 2460589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 15.12.2021
Beginn: 11.09.2022
Tage bis Beginn: 270,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain upper Aortic valve incompetence Atrial fibrillation Blood sodium decreased Bradycardia COVID-19 Chest pain Condition aggravated Decreased appetite Echocardiogram abnormal Ejection fraction normal Electrocardiogram QT prolonged Hypokalaemia Hypomagnesaemia Hyponatraemia Hypophagia Hypophosphataemia Nausea

Symptomtext

"Patient with 3 COVID vaccines who admitted to hospital with complications from COVID and COVID detected PCR. Provider d/c note: ""85-year-old female presenting to the emergency department with epigastric pain that radiates to her sternum. This has been going on for 2 days. She is COVID positive via home test and has been started on Paxlovid. Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) See below note for details re: this current hospitalization. Hospital Course: No notes on file These were her acute medical issues addressed: Covid infection - 19 infection tested 9/11/22 - Holding paxlovid - No resp complaints, no hypoxia. - Vaccinated x 3 doses. Last booster dose 12/2021 - 10 days out from her first symptoms at discharge. A Fib with slow ventricular response, rates in 40-60'ss Hx of HTN Hx of PVC Diastolic heart failure Prolonged QTc - Echo 4/25/22: EF 70%, trace AR, mild - mod TR, RVSP 42mmHg - Held home Norvasc, chlorthalidone, Toprol, Valsartan given bradycardia and low normal BP on admission. - resume Norvasc, ARB at discharge. - continue to hold Chlorthalidone at DC. DC Toprol due to bradycardia. - Consult cardiology: Seen by Dr and Dr. She has declined PPM placement at this time. - on Pradaxa for chronic AF. Anorexia, nausea, resolved - General diet - Zofran prn, consider compazine if QTc prolonged. - may have contributed to hyponatremia. Hyponatremia - Sodium 108 on admission, corrected with IVF and salt tablets - Poor PO intake (COVID) +/- chlorthalidone use likely the main mechanism. Also may have had a component of SIADH, given nausea the preceding days. - no encephalopathy. Mentation maintained. -- IV NS + NaCl tabs. -- Na 129 at discharge. Hypomagnesemia Hypokalemic Hypophosphatemia - replace as needed DC home today with Home Health RN Will hold BB and Chlorthalidone at discharge."""

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 7,0
Labordaten: COVID Detected PCR on 9/11/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Varicose veins PVC (premature ventricular contraction) Pure hypercholesterolemia Hypertension Atrial fibrillation (*) AI (aortic insufficiency) MR (mitral regurgitation) Chronic diastolic heart failure (*) Chronic atrial fibrillation (*) Coronary artery disease of native artery of native heart with stable angina pectoris (*) Digestive Cholelithiasis Nausea and vomiting Psychological Episode of anxiety Urinary Urinary tract infection with hematuria Other CTS (carpal tunnel syndrome) Sensorineural hearing loss, asymmetrical Subjective tinnitus Dyslipidemia Hyponatremia
Andere Medikamente: -
Allergien: Readi-cat, Bactrim Cephalosporins, Dtp Toxoids Adsorbed, Penicillins, Pravastatin, Tetanus, Cephalexin, Sulfa
Vorherige Impfungen: -

VAERS 2454627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 62,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 22.12.2021
Beginn: 05.07.2022
Tage bis Beginn: 195,0
Dosis: 3
Route/Site: IM / LA

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

Alpha haemolytic streptococcal infection Angiogram pulmonary abnormal Asthenia Atelectasis Benign prostatic hyperplasia Blood culture positive Blood potassium decreased COVID-19 Computerised tomogram head normal Coronary artery stenosis Dehydration Electrocardiogram Fatigue Glycosylated haemoglobin increased Hypokalaemia Laboratory test Lung opacity Myocardial ischaemia

Symptomtext

Patient is a 63 y.o. male patient of CNP with history of CAD, essential tremor (status post brain stimulator), hypertension, DM type II presented with generalized weakness and found to have COVID-19. Covid-19 Virus Infection Date of onset of symptoms: 07/05/22 Symptoms present on admission: Generalized weakness, fatigue, fevers Date of covid positive test: 07/05/22 Vaccination status: vaccinated, including booster Imaging: CTPA showing reticular opacities in lung bases, likely atelectasis. Oxygen requirements on admission: None Medical therapy: not indicated Consultants following: None Anticipate end of isolation: 7/15/2022 Generalized weakness Not associated with focal neurologic deficits (chronic essential tremors as well as delayed speech) -- on primidone CT scan of brain w/o acute gross abnormalities. Likely multifactorial (COVID infection, dehydration) as other work up unremarkable PT/OT recommend upto 5, discharge to SNF Strep viridans bacteremia 1/2 sets of Bcx +viridans strep Likely contaminant -- repeat Bcx no growth so far Hold on Abx Hypokalemia - resolved K 3.2 (7/8) Replaced, replete 7/9 Elevated troponin due to demand ischemia CAD No chest pain or shortness of breath on presentation. Trop 30 -- > 48 -- > 53 EKG (reviewed) -- poor tremor artifact, NSR, no e/o acute ischemia CTPA without pulmonary embolism LHC (4/1/22) -- mild three vessel CAD, moderate RCA stenosis Restart home dose of beta-blocker and a statin. Aspirin was being held for TURP on 7/8 but resumed now as will push back procedure per Urology Essential tremors Status post brain stimulator placement Continue home gabapentin, primidone BPH Urinary retention Follows with Dr. and had TURP planned 7/8 Urology consulted -- rescheduled procedure Continue tamsulosin Required straight cath x1 for PVR >700cc Check PVR q8h with straight cath PRN -- > pt currently declining Foley and would prefer to monitor with straight caths for now PVRs have been 100-300s. DM type II, controlled A1c 7.3 Holding oral hypoglycemics. Lantus, SSI Hypertension Normotensive on admission. Continue home losartan, metoprolol

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: FL
Alter: 63,0
Geschlecht: M
Eingang: 09.09.2022
Impfdatum: 29.12.2021
Beginn: 01.08.2022
Tage bis Beginn: 215,0
Dosis: 3
Route/Site: SYR / UN

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

COVID-19 Dyspnoea

Symptomtext

Hospitalization for worsening shortness of breath due to COVID-19 on dates 8/1/2022-8/7/2022. Treated with vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Venlafaxine (anxiety), flecainide (needle-like feeling), niacin (affected eyesight)
Vorherige Impfungen: -

VAERS 2433601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 17.05.2021
Beginn: 24.08.2022
Tage bis Beginn: 464,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

08/24/22 presents to EC ED for "abdominal pain, shortness of breath". PMHx of "MS, CVA, recent fall and left rib fracture"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 08/24/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 88,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 20.03.2021
Beginn: 20.08.2022
Tage bis Beginn: 518,0
Dosis: 3
Route/Site: - / -

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

Agitation Amnesia Arthralgia Bladder catheterisation COVID-19 Chest tube insertion Cholelithiasis Computerised tomogram thorax abnormal Delirium Fall Haematoma Impaired driving ability Intentional medical device removal by patient Klebsiella test positive Magnetic resonance cholangiopancreatography Magnetic resonance imaging abdominal abnormal Mental status changes Mobility decreased

Symptomtext

Patient is a 89-year-old male admitted 8/20 for fever and AMS the patient found to have UTI with C/S positive for klepsiella& And COVID-positive with isolation removed on 8/24.On 8/23 Ct chest showed loculated left pleural effusion,chest tube was inserted on 8/24 pending results.MRCP abdomen showed Cholelithiasis. No evidence of acute cholecystitis and intraductal papillary mucinous neoplasms& GIT team recommended for F/U after discharge. The patient was admitted on 8/1 2/2 fall and left arm hematoma then he was discharged to SAR on 8/9. Geriatrics followed him during that hospital stay for delirium as well. He was started on Seroquel 12.5 mg qhs after several nights of needed PRN IV haldol. His mentation improved and when he was clinically stable he was d/c'd to hospital for SAR. Per documentation sent from hospital he was weaned off seroquel while he was there and did nto have any further behavior issues. Per the chart and RN notes the patient had episodes of delirium and non violet agitations over the last few days. Today morning he pulled out the chest tube. He kept trying to pull out foley catheter as well. He was verbally reoriented and put in 2 points restraints. Today the patient was seen laying down on his bed calm& Alert, orientedx3. He denied any pain and he stated that he feels comfortable. He stated that he is aware that he pulled the pigtail but he doesn't know why. His wife and his daughter were bedside. She says patient has been having short term memory loss for about the last 6 months, denies any sundowning or agitated behaviors at home. Says he gave up driving due to feeling unsure of himself and no longer does the finances either. He does manage his own medications at home, he uses a pill box. He is independent for all of his ADLs, she does help him get dressed due to arthritis pain and limited mobility (e.g. can't bend over to put his socks on).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 8/20 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2431031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 13,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 29.12.2021
Beginn: 07.08.2022
Tage bis Beginn: 221,0
Dosis: 1
Route/Site: - / -

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

Abdominal X-ray Abdominal distension Abdominal pain Aggression Agitation COVID-19 Condition aggravated Cough Crying Culture stool negative Decreased appetite Diarrhoea Endoscopy upper gastrointestinal tract abnormal Exposure to SARS-CoV-2 Faeces discoloured Head banging Intentional self-injury Quarantine

Symptomtext

13y.o. male with PMH of cerebral palsy, ARID1B-related (Coffin-Siris) syndrome-spectrum neurodevelopmental disorder, developmental delay, agitation/self-injurious behavior requiring protective helmet, encopresis with constipation and overflow incontinence of stool, aerophagia, and hx of GI perforation in 2020 who presented with worsening agitation, self-injurious behavior and mother's concern that this was secondary to abdominal pain. Patient was going to go to camp today, but mother was too concerned about his behavior and so brought him to the ED. Mother says that patient has worsening agitation and self-injurious behavior (crying excessively, banging head on items, hitting mother, etc.) in the past that has been a sign of abdominal pain. She say that these behaviors have increased recently. Per mother, patient is nonverbal and has not been able to demonstrate abdominal tenderness in the past. Mother says that his last BM was early yesterday (08/07/2022). She says that he typically has a lot of flatulence, but has not had much recently. She states that his appetite has been decreased for the last 6 weeks. Patient has a long history of encopresis with constipation and overflow incontinence of stool. He typically will use a diaper, however can sometimes sit on the toilet with assistance by his caretaker. Mother says that a few months ago, although previously he would produce occasional hard pebble balls, he was now experiencing explosive diarrhea. Mother says that she cut down his bowel regimen, stopping Colace, and decreasing Dulcolax to 15 from 30, while continuing Miralax. Diarrhea is brown/yellow in color. Patient was last seen by GI on 04/15/2022. There they recommended use of milk of mag, periactin, Levsin, speaking with a GI dietitian and trial of pecid. Currently patient is not taking of any of those medications. An abdomen XR on that same date, did show moderate gaseous distention. Their next appointment with GI is in 2 weeks. Patient has had previous GI scopes. Patient had an EGD and colonoscopy in Feb 2021 that only showed duodenitis. Of note, family had COVID start of July, ended quarantine more than 2 weeks ago. Family tested positive, patient was assumed positive (not tested due to agitation), had sneezing/coughing. Family did have diarrhea as one of their symptoms. Patient's diarrhea does predate family's symptoms. Patient has a long psychiatry related history. Patient has had multiple psych admissions at facility. Patient has been previously taken olanzapine, valproic acid, clonidine and risperidone. Per mother, they follow with Dr. who 1 month ago began a med washout as none of the medications have been helping. Mother says that currently, she administers medical grade THC solution that she gets from a dispensary that is mixed in juice and given twice a day. Further chart review shows that patient was seen in 03/10/2021 for a similar presentation of worsening behavior. At the time, patient received an extensive work-up that included a dental examination, rheumatology and neurology consultation for autoimmune encephalitis and psychiatry consult who had started the patient on some of his previous anti-psychiatry medications. Per the note, it appears that the diagnosis most favored was that this behavior was most consistent with early pubertal changes. Patient is a 13y.o. male with PMH of cerebral palsy, ARID1B-related (Coffin-Siris) syndrome-spectrum neurodevelopmental disorder, developmental delay, agitation/self-injurious behavior requiring protective helmet, encopresis with constipation and overflow incontinence of stool, aerophagia, and hx of GI perforation in 2020 who presented with worsening agitation, self-injurious behavior and mother's concern that this was secondary to abdominal pain. Patient was going to go to camp today, but mother was too concerned about his behavior and so brought him to the ED. Mother says that patient has worsening agitation and self-injurious behavior (crying excessively, banging head on items, hitting mother, etcc..) in the past that has been a sign of abdominal pain. She say that these behaviors have increased recently. Per mother, patient is nonverbal and has not been able to demonstrate abdominal tenderness in the past. Mother says that his last BM was early yesterday (08/07/2022). She says that he typically has a lot of flatulence, but has not had much recently. She states that his appetite has been decreased for the last 6 weeks. Patient has a long history of encopresis with constipation and overflow incontinence of stool. He typically will use a diaper, however can sometimes sit on the toilet with assistance by his caretaker. Mother says that a few months ago, although previously he would produce occassional hard pebble balls, he was now experiencing explosive diarrhea. Mother says that she cut down his bowel regimen, stopping colace, and decreasing dulcolax to 15 from 30, while continuing Miralax. Diarrhea is brown/yellow in color. Patient was last seen by GI on 04/15/2022. There they recommended use of milk of mag, periactin, Levsin, speaking with a GI dietitian and trial of pecid. Currently patient is not taking of any of those medications. An abdomen XR on that same date, did show moderate gaseous distention. Their next appointment with GI is in 2 weeks. Patient has had previous GI scopes. Patient had an EGD and colonoscopy in Feb 2021 that only showed duodenitis. Of note, family had COVID start of July, ended quarantine more than 2 weeks ago. Family tested positive, patient was assumed positive (not tested due to agitation), had sneezing/coughing. Family did have diarrhea as one of their symptoms. Patient's diarrhea does predate family's symptoms. Patient has a long psychiatry related history. Patient has had multiple psych admissions. Patient has been previously taken olanzapine, valproic acid, clonidine and risperidone. Per mother, they follow with Dr. who 1 month ago began a med washout as none of the medications have been helping. Mother says that currently, she administers medical grade THC solution that she gets from a dispensary that is mixed in juice and given twice a day. Further chart review shows that patient was seen in 03/10/2021 for a similar presentation of worsening behavior. At the time, patient received an extensive work-up that included a dental examination, rheumatology and neurology consultation for autoimmune encephalitis and psychiatry consult who had started the patient on some of his previous anti-psychiatry medications. Per the note, it appears that the diagnosis most favored was that this behavior was most consistent with behavioral changes due to early pubertal changes. During his hospital admission, Pt was started on Zyprexa and we noticed a decrease it the number of aggressive outburst. He was also evaluated by GI and had upper endoscopy that showed mild duodenitis therefore patient was started on Lansoprazole. Patient also had stool culture which returned negative. He was also started on Levsin and home bowel regimen was restarted. Patient was also evaluated by surgery who recommended a CT abdomen with PO and IV contrast. After discussion with anaesthesilogy and GI team and due to patient needed to be intubated for imaging decision was made to hold of on any additional imaging. Patient follows with GI clinic and as an appointment scheduled for next Friday. Since we do not have a GI motility clinic, it was advised that mother establish care there. Mother in agreement with plan.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 8/7 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2431001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 03.02.2021
Beginn: 03.08.2022
Tage bis Beginn: 546,0
Dosis: 3
Route/Site: - / -

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

Anticoagulant therapy Atrial fibrillation Blood thyroid stimulating hormone decreased COVID-19 Cardioversion Chest X-ray normal Cold sweat Dizziness Electrocardiogram abnormal Feeling hot Gastrointestinal disorder Heart rate increased Hyperhidrosis Hypotension Nausea SARS-CoV-2 test positive Thyroxine free normal Vomiting

Symptomtext

65-year-old woman with history of provoked right lower extremity DVT status post right total knee arthroplasty, HTN, anemia, hypocalcemia who comes to the emergency department due to dizziness, nausea and vomiting. Started 5 hours before presentation to the ER, she was at store, having episodes of diaphoresis, feeling hot, clammy and top of GI symptoms. Upon presentation to the ER, she was found to have new onset atrial fibrillation with RVR, heart rate as high as 134, blood pressure as low as 84/53 on the night of presentation. Received fluid bolus. She was found to be COVID-positive, vaccinated and posted with 1 booster. Chest x-ray without acute abnormalities, EKG was reviewed A. fib with RVR, without acute ischemic changes. Initially started on amiodarone drip which was later discontinued. TSH was 0.3 with normal free T4. Patient converted to normal sinus rhythm, started initially on heparin which was transitioned to Eliquis, hydrochlorothiazide and losartan were discontinued, started on Toprol 12.5 mg twice daily with good heart rate control. Unable to obtain echocardiogram inpatient due to COVID-positive status, okay per cardiology to do an echocardiogram as an outpatient. Instructed to follow-up with PCP to repeat thyroid function test in 4-6 weeks to rule out hyperthyroidism as an inciting etiology for her atrial fibrillation. Endocrinology follow-up added in AVS. Evaluated by ID did not require treatment for COVID during this admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: 2,0
Labordaten: 8/3 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 30.07.2022
Impfdatum: 07.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Condition aggravated Elbow operation Inflammation Platelet rich plasma therapy

Symptomtext

After five days, I experienced severe inflammation in both elbows; even though, I was being treated for tendonitis in both elbows. I had a TENIX surgery, PRP plus physical therapy done on my left elbow in May 2021. The surgery was a success and my elbow felt like new. When I received the third shot (booster), the inflammation came back with a vengeance. In fact, the inflammation never subsided over the months and the doctor needed to do another PRP on my left arm to bring the inflammation down. My right arm was also affected. I had a TENIX elbow surgery on my right elbow in April 2022 as well as PRP plus physical therapy. I am doing great and I refuse to receive any more vaccines. If I had not gotten that last booster, I would not have had to go through another PRP procedure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: NONE-
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, GERD, chronic tendonitis in both elbows due to adverse reaction to statins,
Andere Medikamente: Synthroid, Nexium, Gabapentin, Allegra in morning; Vitamin E, Vitamin D, Co-Q 10, Omega 3 Fish Oil, Silymarin, Homocysteine Resist capsule, Pro DHA Memory capsule, and Nortriptyline in the evening
Allergien: Pencillin, Cipro, all Statins
Vorherige Impfungen: -

VAERS 2379107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: WI
Alter: 56,0
Geschlecht: M
Eingang: 22.07.2022
Impfdatum: 19.01.2022
Beginn: 22.05.2022
Tage bis Beginn: 123,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Dyspnoea Fatigue Feeling cold Feeling hot Hypersomnia Lethargy Nasal congestion Oropharyngeal pain Pain in extremity SARS-CoV-2 test positive

Symptomtext

I felt an sore arm and lethargic after the vaccine for a two days. On my 05/22/2022 tested positive for COVID-19 with the home test. My symptoms where I had a sore throat, stuffy head, difficulty breathing, didn't run a fever, my arms and legs where freezing but my head felt very hot. I also felt very fatigued and slept a lot. My breathing got worse so I went to an urgent care center. They gave me a steroid which helped for a few days. After that tampered off I got worse again. I went back to the doctor and they prescribed another steroid which helped again. The biggest complaint now is fatigue. I am sleeping 10-12 hours a night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Home test for COVID-19 and it was positive on 05/22/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid arthritis, asthma; high blood pressure
Andere Medikamente: Advair; Pregabalin; Truvada; Losartan; Simvastatin; Trazodone; Incruse ellipta inhaler; Pramipexole; Leflunomide; Enbrel; Allegra; Aspirin; Fluticasone
Allergien: Fentanyl; Versed; Latex
Vorherige Impfungen: -

VAERS 2371477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: AR
Alter: 82,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 29.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Dyspnoea Mass Pruritus Rash Urticaria

Symptomtext

bumps and welts are getting worse and are now on her head and all over the side of her body/ A few days after receiving booster dose Pfizer Vaccine started breaking out; bumps and welts are getting worse and are now on her head and all over the side of her body; Itches so bad can't stand it/ itching of these bumps and welts; Sometimes have trouble breathing; Has knots on head/ Sometimes the knots are half as big as an egg yolk; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. An 83-year-old female patient received BNT162b2 (BNT162B2), on 29Dec2021 as dose 3 (booster), single (Lot number: FE3594) at the age of 82 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1,SINGLE; lot number : 8737 or 8727; Route of administration: left arm), administration date: 20May2021, when the patient was 81-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2,SINGLE; lot number :EWO162 or EW0162; Route of administration: left arm), administration date: 08Jun2021, when the patient was 81-year-old, for COVID-19 Immunization. The following information was reported: RASH (non-serious), outcome "not recovered", described as "bumps and welts are getting worse and are now on her head and all over the side of her body/ A few days after receiving booster dose Pfizer Vaccine started breaking out"; URTICARIA (non-serious), outcome "not recovered", described as "bumps and welts are getting worse and are now on her head and all over the side of her body"; PRURITUS (non-serious), outcome "not recovered", described as "Itches so bad can't stand it/ itching of these bumps and welts"; DYSPNOEA (non-serious), outcome "not recovered", described as "Sometimes have trouble breathing"; MASS (non-serious), outcome "not recovered", described as "Has knots on head/ Sometimes the knots are half as big as an egg yolk". The events "bumps and welts are getting worse and are now on her head and all over the side of her body/ a few days after receiving booster dose pfizer vaccine started breaking out", "bumps and welts are getting worse and are now on her head and all over the side of her body", "itches so bad can't stand it/ itching of these bumps and welts", "sometimes have trouble breathing" and "has knots on head/ sometimes the knots are half as big as an egg yolk" required physician office visit. Therapeutic measures were taken as a result of rash, urticaria, pruritus, dyspnoea, mass. Additional information: Caller stated that a few days after receiving the vaccine developed large bumps and welts that come and go and she still has them. Caller stated that the bumps and welts are getting worse and are now on head and all over the side of her body. Caller stated that the 1st and 2nd Pfizer Covid19 vaccines did not bother her. Comes up kind of like in bumps and started spreading big whelps covering hand. Itches so bad can't stand it. Has knots on head, big knows. Caller stated had seen a dermatologist and allergy doctor who prescribed her for steroids and creams but the bumps and welts have not gone away. Zyrtec and Claritin was given to take twice a day. Zyrtec(NDC/UPC: Unknown, does not see on bottle; lot number: WJ49274; expiration: Feb2025, product strength and count size dispensed: 10mg, 60 tablets); Claritin (Bottle is so small and is blind, lot number: 2CEL9768 NDC: Unknown, Expiration: Nov2023, product strength and count size dispensed:10mg, 30 count). The patient received steroid shot and didn't' do any good either. Also used Benadryl to rub on. Zyrtec and Claritin are just not getting the break out. When go out to water flowers, before done out of breathe have to come back in house, thought it effected lungs. Started in the last week noticing having trouble breathing and was about the same. There were no other vaccinations within four weeks prior to the first administration date of the suspect vaccine. There were no AE(s) following prior vaccinations. There were no relevant tests.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to chemicals (Does not have Iodine NDC/lot/expiration because was more than 30 years ago); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2364597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CO
Alter: 23,0
Geschlecht: M
Eingang: 11.07.2022
Impfdatum: 07.01.2022
Beginn: 15.06.2022
Tage bis Beginn: 159,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chest pain Cough Fatigue Heart rate increased Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection Vision blurred

Symptomtext

This is a breakthrough case. I tested positive COVID-19. My symptoms were coughing, fatigue, difficulty focusing, sore throat congestion, fever, elevated heart rate, and chest pain from coughing. The doctor recommend PAXLOVID due to my chronic lung condition. Severe symptoms lasted for a day, but the cough lingered for a couple of weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Lung Collapse
Andere Medikamente: CLARITIN
Allergien: Peanuts; chicken
Vorherige Impfungen: -

VAERS 2344724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IA
Alter: 59,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 22.12.2021
Beginn: 17.01.2022
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: IM / -

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

Angiogram pulmonary abnormal Blood gases Blood pH decreased COVID-19 Chest X-ray normal Chills Computerised tomogram thorax Decreased appetite Dyspnoea Exposure to SARS-CoV-2 Fibrin D dimer increased Hypoxia Inappropriate schedule of product administration Influenza A virus test negative Influenza B virus test Lung disorder PCO2 increased Pneumonia

Symptomtext

Pfizer Dose 1 12/22/21 (FE3594) COVID Positive 1/18/22 1/18/22: 60-year-old female with COPD not on home oxygen, obstructive sleep apnea noncompliant with CPAP, hypertension, anxiety/depression, tobacco abuse, cocaine use presented with shortness of breath. Reportedly called EMS for shortness of breath noted to be wheezing placed on 2 L oxygen for hypoxia. Patient reports she was having fever , chills and has decreased appetite. Denies any muscle aches or joint pain, reportedly had exposure to COVID positive contact. Patient denies any illicit drug use at this time. Patient is a febrile and hemodynamically stable. VBG showed pH 7.32 with pCO2 70, influenza A and B negative, COVID-19 PCR is pending unremarkable WBC count. Chest x-ray is unremarkable for acute abnormalities. Mild elevation of D-dimer, CT chest PE protocol is pending. 1/21/22: 60-year-old woman who presented with complaints of fever, chills, shortness of breath of few days duration. She was found to be hypoxic on presentation requiring initiation of supplemental oxygen. CT pulmonary angiogram was negative for pulmonary embolism but demonstrated bilateral airspace disease compatible with pneumonia. COVID-19 PCR was subsequently positive, she was started on IV steroids and remdesivir as she met criteria for treatment in the presence of hypoxia. Clinical response was favorable with gradual improvement in cough, shortness of breath and wheezing. Oxygen walk for home determination was done prior to discharge, she did not meet criteria for home oxygen. She has been discharged in stable medical condition to continue outpatient follow-up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD OSA HTN anxiety depression tobacco abuse cocaine use
Andere Medikamente: albuterol 2 puffs Q4h PRN alprazolam 0.5 mg PO TID PRN Symbicort 2 puffs inh BID citalopram 40 mg PO QD furosemide 40 mg PO QD lisinopril 10 mg PO QD mirtazapine 15 mg PO HS omeprazole 40 mg PO QD sucralfate 1 gm PO ACHS
Allergien: Augmentin - hives Bactrim - rash codeine - nausea, GI upset dicyclomine - hives latex - rash oxycodone - nauesa, irritability, anger silvadene - unknown
Vorherige Impfungen: -

VAERS 2325649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: SD
Alter: 54,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 17.12.2021
Beginn: 18.04.2022
Tage bis Beginn: 122,0
Dosis: 3
Route/Site: IM / AR

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

Aphasia Arthralgia Balance disorder COVID-19 Chest pain Cough Dizziness Fatigue Feeling abnormal Headache Hypersomnia Malaise Memory impairment Mobility decreased Mood altered Oropharyngeal pain SARS-CoV-2 test positive Vertigo

Symptomtext

I was given the flu shot and the vaccine in the same day. I received one in each arm. The covid vaccine was Pfizer as listed above. I started feeling sick on the 18 of April. Fatigue headaches joint pain chest pain -doctors said it could e from coughing so much cough unsure about the sore throat I had the oh i am getting sick feeling. I took a at home test and it was negative. So I was scheduled to have a colonoscopy done and I called to check to see what I needed to do anything before coming in. The night before I had to call and cancel because I felt so bad.. I called my Dr and she told me to wait a few days to retest. That Tuesday and Wednesday I felt horrible and sleep most of the day. I felt very dizzy and off balanced like I had vertigo. Thursday morning when I got up I took another at home COVID test and the results came in really fast this time and it was positive. I called my Dr again and she schedules me to come in and have an infusion that Friday. I went that Friday to the infusion center and before the infusion I had a PCR Test were Positive the system had a H in there which stands for High Level.. My balance was still off so I had to use a wheelchair. I felt a little better but I could tell I was starting to recover. I had the worst brain fog and it was so bad that I lost my phone while it was in my hand. I also found everything very funny. I spent a lot of time in bed until the 29 and that surprised me because I thought the infusion would make me feel better sooner. The first of May I could tell the recovery process had started but it was very slow. It took another 2 weeks before I started to feel normal. I was still having memory issues and I cant characterize it very well ....I lose words mid sentence and even full conversations just go blank. These things drive me up a wall. I also have issues putting things in the right order like I cant remember when I did something but I know I did it. The memory issues are slowly getting better but they are still here.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: COPD anxiety Asthma ADHD Bipolar disorder Chronic Pain Gerd IBS Insomnia Sleep apnea low testosterone in females Obesity Osteopenia Pelvic Floor dysfunction in female PTSD vitamin d deficiency
Andere Medikamente: Acetaminophen Albuterol Vitamin C Progastrin Cyclobenzaprine Desbenlafaxine Succinate Estradiol Probiotics Eszopiclone Lamotrigine Levocetirizine Lorazetam Methylphenidate Montelukast Omeprazole prucalopride Multi Vitamin Multi
Allergien: Ondansetron Doxycycline Tree pollin Nickle Peanuts Corn Potatoes Wheat
Vorherige Impfungen: -

VAERS 2325624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 27.02.2021
Beginn: 28.02.2022
Tage bis Beginn: 366,0
Dosis: 3
Route/Site: SYR / RA

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

Cardiac pacemaker insertion Headache Mobility decreased Musculoskeletal stiffness Pain

Symptomtext

The next day after my 3rd dose vaccination I experienced the following symptoms: Severe headache, Body aches, Stiffness on my back and neck. It was very difficult to move because of the pain. I did not take anything for treatment because I don't want it to trigger something. I stayed in bed for the rest of the day and then the next day I was feeling so much better. The pain was gone and I was back to my normal self.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma, Seasonal Allergies
Andere Medikamente: Iron, Vitamin D, Baby Aspirin, Atorvastatin, Multivitamins
Allergien: N/A
Vorherige Impfungen: -

VAERS 2318861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: FL
Alter: 63,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 13.12.2021
Beginn: 09.05.2022
Tage bis Beginn: 147,0
Dosis: 3
Route/Site: IM / LA

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

Blood test abnormal COVID-19 Cough Diarrhoea Fatigue Headache Hepatic enzyme increased Impaired work ability Malaise Middle insomnia Mobility decreased Neck pain Paranasal sinus hypersecretion Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sleep disorder Vibratory sense increased

Symptomtext

I experienced a headache at 03:00AM and I couldn't go back to sleep. The headache pain was concentrated in the back of my head and neck. I did take Excedrin migraine. It took some of the edge off but the headache was still. By 09:00AM I did have bouts of diarrhea. I took Imodium and that helped the diarrhea. I went to bed that night at about 07:00PM, but I had woken up in the middle of the night with the headache again. I took my temp and it was 98.8. but the walls felt like I was vibrating. I took an oral temp 103.3. I went to urgent care and I was prescribed Paxlovid. For the next 5-6 days I was so fatigue and sick feeling I couldn't even lift my head. The following week I went back to work and I was wearing a mask. When I came home I had a 101 temp. I had a fever for the next 3 days. I was taking Tylenol and Ibuprofen. I did go back to the doctor for my annual bloodwork and they found that my liver enzymes are high. I was told to stop taking the Tylenol and my blood pressure medication. As of today, I still have a cough, congestion and sinus drainage.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 05/10/2022: COVID-19: Positive 05/23/2022: Bloodwork: Elevated Liver Enzymes
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma, Allergies, High Blood Pressure
Andere Medikamente: Atorvastatin, Vitamin C, Metoprolol
Allergien: Sulfur ( like eyedrops) , Latex
Vorherige Impfungen: Flu Vaccine: Red arm for 3 days.

VAERS 2308396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 19.04.2021
Beginn: 25.04.2022
Tage bis Beginn: 371,0
Dosis: 3
Route/Site: IM / UN

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

COVID-19 Chest pain Dysarthria Dyspnoea Headache Hemiparesis Hypotonia SARS-CoV-2 test positive

Symptomtext

Pt brought in by EMS 4/24 having weakness on the left side and his speech was a little bit slurred. Denied any chest pain, palpitations, or shortness of breath. Pt COVID positive 4/25 denies any new symptoms besides mild headache. 4/28 pt denies any pain. Left arm and leg are noted to be flaccid. Pt remains A/Ox4. Appetite moderate. 4/29 pt stable, reported weakness, shortness of breath or chest pain. Left arm and leg continued to be flaccid. Pt c/o headache and medicated x2 with tylenol. 4/30 L side flaccid but pt is able to assist with repositioning. Pt continues to have daily headaches but denies any photophobia or neck stiffness. Discharged 4/30.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 7,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Elevated blood pressure reading, Elevated blood pressure reading Skin lesion of left arm Tobacco abuse CVA (cerebral vascular accident) Acute CVA (cerebrovascular accident) Stroke
Andere Medikamente: acetaminophen (TYLENOL) 325 MG PO Tab, acetaminophen (TYLENOL) 325 MG PO Tab aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 20 MG PO Tab atorvastatin (LIPITOR) 40 MG PO Tab clopidogrel (PLAVIX) 75 MG PO Tab heparin 5,000 UNITS/ML INJ Solu
Allergien: None
Vorherige Impfungen: -

VAERS 2294472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3594

moderat

Staat: -
Alter: 26,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 16.12.2021
Beginn: 19.05.2022
Tage bis Beginn: 154,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest pain Influenza virus test SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID after booster. Patient admitted with chest pain and hospitalized 5 days. Vaccine times 2 and booster. COVID positive after booster 12/16/2022. First dose 3/4/2022 EN 6198. Second dose 3/25/2021 ER 8730 and booster 12/16/2022 FE 3594

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Coronavirus/flu PCR detected 5/19/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2284774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: AS
Alter: 39,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 04.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: SYR / LA

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

Dry skin Erythema Headache Hypoaesthesia Immunisation reaction Impaired work ability Lip swelling Neck pain Paraesthesia Pruritus Rash Rash erythematous Rash pruritic Rash vesicular Skin discolouration Skin exfoliation Skin weeping Stevens-Johnson syndrome

Symptomtext

A severe headache and neck pain started on 1/14/22 that would not go away. It lasted continuously for two weeks and finally on 1/28/22 I went to the ER with only partial relief from IV infusion of three different meds. Headache later subsided. Then on 4/8/22 I started with itching and I noticed that I had whole-body rash (patchy red). It was unbearable and I went to the ER on 4/14/22. They gave me IV benedryl and steroid cream and prednisone. This only partially helped with the itching. Then, my upper legs started turning into a purple rash. On 4/24/22 I went to the ER again because I woke up with a swollen tongue and lip and the rash started blistering on my hands and feet and genitalia and was EXTREMELY itchy. I was admitted into the Hospital at that time (4/24/22) due to swelling of my lips and tongue and was also experiencing numbness/tinglling in my hands and feet. As an inpatient I received more IV medications for the above and also the itching and the rash and blistering. The swelling was reduced however, I experienced little relief of the ithcing/blistering and was discharged a day and a half later to continue meds at home (Steroids, benedry, claritin, gabapentin). They also gave me a prescription or an EPI pen. The redness subsided days later, however the blistering still continued and actually turned into weeping blisters on my hands and feet. I was then seen by a dermatologist who diagnosed me with SJS (Steven-Johnson-Syndrome) and "Covid toe". She advised my to NOT GET ANY MORE VACCINES. I was to continue my medication regime and "let it run its course". My hands became much worse with blisters and became a concern in doing my job at work, so I then made an appointment with a Wound/burn physician. She basically told me the same thing - it has to run its course. Another follow-up appointment is on the horizon. To this day, my hands and feet have now blistered and are dry and peeling. (I can't even clock into work with my finger pads because the biometrics can read my fingers!) The numbness continues in my hands and feet, which I was advised to follow up with a Neuologist and will.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: See above
Aktuelle Erkrankungen: no
Vorgeschichte: Chronic migraines
Andere Medikamente: Botox injections, Lipitor
Allergien: no
Vorherige Impfungen: -

VAERS 2277576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: PA
Alter: 80,0
Geschlecht: F
Eingang: 14.05.2022
Impfdatum: 11.12.2021
Beginn: 01.04.2022
Tage bis Beginn: 111,0
Dosis: 3
Route/Site: - / -

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

Condition aggravated Diarrhoea Drug ineffective Nasopharyngitis SARS-CoV-2 test SARS-CoV-2 test positive

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 80-year-old female patient received BNT162b2 (BNT162B2), on 13Apr2021 as dose 1, single (Lot number: ER8731), on 04May2021 as dose 2, single (Lot number: EW0167) and on 11Dec2021 as dose 3 (booster), single (Lot number: FE3594) at the age of 80 years for Covid-19 immunisation. The patient's relevant medical history included: "Back problems has had for years" (ongoing), notes: Caller states she has issues with her back, has had them for years; "Fibromyalgia" (ongoing), notes: Fibromyalgia has had for years. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), SARS-COV-2 TEST POSITIVE (medically significant) all with onset Apr2022, outcome "unknown" and all described as "tested positive"; CONDITION AGGRAVATED (non-serious), outcome "unknown", described as "symptoms were worse"; DIARRHOEA (non-serious), outcome "unknown", described as "diarrhea"; NASOPHARYNGITIS (non-serious), outcome "unknown", described as "cold". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Apr2022) Positive, notes: she tested and tested positive. Therapeutic measures were taken as a result of sars-cov-2 test positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 202204; Test Name: Covid; Test Result: Positive; Comments: she tested and tested positive.
Aktuelle Erkrankungen: Back discomfort (Caller states she has issues with her back, has had them for years); Fibromyalgia (Fibromyalgia has had for years)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 24.03.2021
Beginn: 09.05.2022
Tage bis Beginn: 411,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Chest discomfort Chest pain Electrocardiogram ST segment elevation Electrocardiogram T wave abnormal Electrocardiogram abnormal SARS-CoV-2 test positive Troponin increased

Symptomtext

47 year old male admitted with chest pain, elevated troponin, found to be Covid 19 positive. Pt denies any health hx, he follows with a PCP yearly he reports. Pt developed exertional chest pain which began 30 minutes prior to arriving to the ED overnight. he had EKG initially showing acute ST elevation in leads V1-V2, lateral leads with Q wave and ST/T wave changes. Initial troponin 71,2, 1845 . Pt denies any hx of previous MI, stroke or DM2. he reports he works as a software engineer. Pt reports some mild midsternal chest pressure this AM. he denies SOB, edema, orthopnea. INPATIENT AT THIS TIME.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2266015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NH
Alter: 36,0
Geschlecht: F
Eingang: 06.05.2022
Impfdatum: 11.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Diarrhoea Dyspnoea exertional Fatigue Fear Insomnia Malaise Mobility decreased Oropharyngeal pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sinus congestion Sleep disorder Sneezing Speech disorder Vomiting

Symptomtext

COVID-19 symptoms started on 01/01/2022, tested positive on 01/03/2022. Saturday I started feeling the sore throat but I had a negative test. 01/02/22 I had a negative test, but 01/03/22 early morning is when I woke up at 3 AM with vomiting, diarrhea, fever of 99.6, and sore throat, and that is when I had a positive COVID-19 test. After that, it was just a lot of congestion, runny nose, sneeze, couldn't sleep, and very tired. 01/05/22 I got a bit scared because I could barely talk and couldn't get out of bed but it was just that day. After that it was just the fatigue and congestion. I noted a lot of fatigue and sinus congestion from 01/04/22-01/11/22. I called my PCP and let them know and they said to stay put. Since then, I've just felt my breathing takes a little bit more out of me just going upstairs but that could be me working remotely and not being active.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: COVID-19 Positive 01/03/22
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 2248011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NC
Alter: 36,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Blood test normal Dysstasia Mobility decreased

Symptomtext

I could not move for a day and half. I could not stand or get off the bed. This lasted for about a day and half. I been having joint pain in shoulders, hip, wrist, ankles, and knees and has been going on since Dec 30th. I went to an Ortho specialist about this. They did blood work, normal results. They are referring me to a rheumatologist. I have an appointment in June.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Bloodwork
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Bipolar II; Anxiety; Depression; Migraines
Andere Medikamente: Claritin; Omeprazole; Inhaler; Albuterol; Protocone; Aver inhaler; Santorin; Seroquel
Allergien: Latex
Vorherige Impfungen: -

VAERS 2238091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: TX
Alter: 33,0
Geschlecht: F
Eingang: 16.04.2022
Impfdatum: 13.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: - / RA

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

Chest pain Echocardiogram Electrocardiogram Exposure during pregnancy Extrasystoles Ultrasound scan Umbilical cord abnormality

Symptomtext

A week to two weeks after getting the first dose of vaccine, my heart started skipping beats. Chest pains followed. I am pregnant and was during time of vaccine. The blood flow from the umbilical cord to the fetus was compromised.

Weitere VAERSDATA-Felder

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

VAERS 2231370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: VA
Alter: 29,0
Geschlecht: M
Eingang: 13.04.2022
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Angiogram pulmonary normal Antinuclear antibody negative Blood glucose Blood iron Blood lactate dehydrogenase Blood testosterone Blood uric acid normal Borrelia test negative Brain natriuretic peptide normal Burning sensation C-reactive protein decreased Cardiac stress test Chest discomfort Cognitive disorder Computerised tomogram head normal Depression Electrocardiogram normal Electromyogram normal

Symptomtext

Events:tachycardia, chest discomfort, heart palpitations, tinnitus, paresthesia (numbness, tingling, pins and needles)(head/face, neck, arm, leg, and foot), burning sensations, internal tremors/vibrations, muscle spasms, neurocognitive disorder, headaches/migraines, severe anxiety/depression, insomnia, and jaw pain. Treatment: Prednisone, Gabapentin, Cymbalta

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Lab results: 01/05/22 - Positive D-Dimer, Negative BNP; 01/10/22 - Negative ANA Screen, CBC, CMP, Negative D-Dimer, Negative Lyme, Negative SED Rate, Normal Uric Acid; 01/20/22 - CBC, CMP. 02/14/22 - Negative D-Dimer, B-12, Testosterone. 03/15/22 - CMP, OmegaCheck, Glucose, Iron and TIBC, B-12, Testosterone, Luteinizing Hormone, B-6, Vitamin D, CLow C-Reactive Protein, Cardiac; B1, LDH. Imaging Results: 01/06/22 - Negative CTA Chest WW C-PULM, Negative VASC Venous Doppler - BLE; 01/10/22 - Negative CT Head Brain WO IV Con; 01/14/22 Negative MRI Cervical, Negative MRI brain; 02/21/22 - Nonspecific MR Lumbar Spine without contract; 3/11/22 - Negative foot/ankle X-ray Other: 01/07/22 - normal EKG; 01/24/22 - cardio stress test - average with PVCs. 01/13/22 - EMG - no clincial neuropathy. no clinical myelopathy
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2227691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 17.12.2021
Beginn: 12.02.2022
Tage bis Beginn: 57,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Dialysis Dyspnoea Hypervolaemia SARS-CoV-2 test positive

Symptomtext

Narrative: Positive covid test in fully vaccinated patient admitted for SOB 2/2 volume overload due to missed dialysis

Weitere VAERSDATA-Felder

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

VAERS 2223225

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 68,0
Geschlecht: M
Eingang: 08.04.2022
Impfdatum: 19.03.2021
Beginn: 27.11.2021
Tage bis Beginn: 253,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 pneumonia Hypoxia Skin ulcer Toxicity to various agents

Symptomtext

Janssen (J&J) COVID vaccine received on 03/19/2021, Pfizer COVID vaccine received on 12/22/2021 after the recorded adverse event Hospitalization on 11/28/2021 and discharged on12/2/2021. Diagnosis: COVID 19 pneumonia, Coumadin toxicity, Hypoxia, Chronic ulcer of leg, Treatment: Hospitalization, Decadron, Remdesivir, Supplemental O2, Wound care, cardiology consult

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2219813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 29,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 18.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Condition aggravated Hyperacusis Photophobia

Symptomtext

lights and sounds mildly affected me/After that dose, lights as well as sound started to get worse for me; lights and sounds mildly affected me/After that dose, lights as well as sound started to get worse for me; lights and sounds mildly affected me/After that dose, lights as well as sound started to get worse for me; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 29-year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 18Jan2022 10:30 (Lot number: FE3594) at the age of 29 years as dose 1, single for COVID-19 immunization. Relevant medical history included: "Epilepsy" (unspecified if ongoing); "Covid-19", start date: Sep2021 (unspecified if ongoing); "Since then lights and sounds mildly affected me" (unspecified if ongoing), notes: but not enough to hinder my day to day routine. The patient had no known allergies. Concomitant medication included: DILANTIN [PHENYTOIN]. The following information was reported: PHOTOPHOBIA (disability), HYPERACUSIS (disability), CONDITION AGGRAVATED (disability), outcome "unknown" and all described as "lights and sounds mildly affected me/After that dose, lights as well as sound started to get worse for me". Patient reported that, "I was positive for COVID-19 in the end of Sep2021. Since then lights and sounds mildly affected me but not enough to hinder my day to day routine. I received my first dose of Pfizer in Jan2022. After that dose, lights as well as sound started to get worse for me however I was still able to work out and go to work as usual." The patient was not tested for COVID, post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Epilepsy; Light sensitivity to eye (but not enough to hinder my day to day routine); Sound sensitivity increased (but not enough to hinder my day to day routine)
Andere Medikamente: DILANTIN [PHENYTOIN]
Allergien: -
Vorherige Impfungen: -

VAERS 2200801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 29,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 08.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

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

Acoustic stimulation tests abnormal Blood test normal Condition aggravated Deafness unilateral Dizziness Dizziness postural Drug level decreased Ear discomfort Headache Hyperacusis Migraine Motion sickness Impaired driving ability Impaired work ability Laboratory test normal Loss of personal independence in daily activities Nausea Ophthalmological examination normal

Symptomtext

vertigo attack; migraine; constant headache; a constant dizziness that worsens with sounds, lights and especially motion; a constant dizziness that worsens with sounds, lights and especially motion; a constant dizziness that worsens with sounds, lights and especially motion; dizzy/light headed/a constant dizziness that worsens with sounds, lights and especially motion; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Feb2022 16:45 (Lot number: FE3594) at the age of 29 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Epilepsy" (unspecified if ongoing); "COVID 19", start date: Sep2021 (unspecified if ongoing). Concomitant medication(s) included: DILANTIN [PHENYTOIN]. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; lot number:FE3594; administration time: 10:30AM; anatomical location: Left arm), administration date: 18Jan2022, when the patient was 29 years old, for COVID-19 immunization, reaction(s): "lights and sounds mildly affected me", "lights and sounds mildly affected me". The following information was reported: DIZZINESS (disability) with onset 10Feb2022 22:30, outcome "not recovered", described as "dizzy/light headed/a constant dizziness that worsens with sounds, lights and especially motion"; VERTIGO (disability) with onset 15Feb2022, outcome "not recovered", described as "vertigo attack"; MIGRAINE (disability) with onset 15Feb2022, outcome "not recovered", described as "migraine"; HEADACHE (disability) with onset 15Feb2022, outcome "not recovered", described as "constant headache"; PHOTOSENSITIVITY REACTION (disability), HYPERACUSIS (disability), MOTION SICKNESS (disability) all with onset 10Feb2022 22:30, outcome "not recovered" and all described as "a constant dizziness that worsens with sounds, lights and especially motion". The events "dizzy/light headed/a constant dizziness that worsens with sounds, lights and especially motion", "vertigo attack", "migraine", "constant headache", "a constant dizziness that worsens with sounds, lights and especially motion", "a constant dizziness that worsens with sounds, lights and especially motion" and "a constant dizziness that worsens with sounds, lights and especially motion" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (Sep2021) positive. Therapeutic measures were taken as a result of dizziness, vertigo, migraine, headache, photosensitivity reaction, hyperacusis, motion sickness which includes migraine medication and steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 202109; Test Name: positive for COVID-19; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Epilepsy
Andere Medikamente: DILANTIN [PHENYTOIN]
Allergien: -
Vorherige Impfungen: -

VAERS 2200801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 29,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 08.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Acoustic stimulation tests abnormal Blood test normal Condition aggravated Deafness unilateral Dizziness Dizziness postural Drug level decreased Ear discomfort Headache Hyperacusis Migraine Motion sickness Impaired driving ability Impaired work ability Laboratory test normal Loss of personal independence in daily activities Nausea Ophthalmological examination normal

Symptomtext

vertigo attack; migraine; constant headache; a constant dizziness that worsens with sounds, lights and especially motion; a constant dizziness that worsens with sounds, lights and especially motion; a constant dizziness that worsens with sounds, lights and especially motion; dizzy/light headed/a constant dizziness that worsens with sounds, lights and especially motion; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Feb2022 16:45 (Lot number: FE3594) at the age of 29 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Epilepsy" (unspecified if ongoing); "COVID 19", start date: Sep2021 (unspecified if ongoing). Concomitant medication(s) included: DILANTIN [PHENYTOIN]. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; lot number:FE3594; administration time: 10:30AM; anatomical location: Left arm), administration date: 18Jan2022, when the patient was 29 years old, for COVID-19 immunization, reaction(s): "lights and sounds mildly affected me", "lights and sounds mildly affected me". The following information was reported: DIZZINESS (disability) with onset 10Feb2022 22:30, outcome "not recovered", described as "dizzy/light headed/a constant dizziness that worsens with sounds, lights and especially motion"; VERTIGO (disability) with onset 15Feb2022, outcome "not recovered", described as "vertigo attack"; MIGRAINE (disability) with onset 15Feb2022, outcome "not recovered", described as "migraine"; HEADACHE (disability) with onset 15Feb2022, outcome "not recovered", described as "constant headache"; PHOTOSENSITIVITY REACTION (disability), HYPERACUSIS (disability), MOTION SICKNESS (disability) all with onset 10Feb2022 22:30, outcome "not recovered" and all described as "a constant dizziness that worsens with sounds, lights and especially motion". The events "dizzy/light headed/a constant dizziness that worsens with sounds, lights and especially motion", "vertigo attack", "migraine", "constant headache", "a constant dizziness that worsens with sounds, lights and especially motion", "a constant dizziness that worsens with sounds, lights and especially motion" and "a constant dizziness that worsens with sounds, lights and especially motion" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (Sep2021) positive. Therapeutic measures were taken as a result of dizziness, vertigo, migraine, headache, photosensitivity reaction, hyperacusis, motion sickness which includes migraine medication and steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Date: 202109; Test Name: positive for COVID-19; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Epilepsy
Andere Medikamente: DILANTIN [PHENYTOIN]
Allergien: -
Vorherige Impfungen: -

VAERS 2215950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 03.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / RA

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

Blood pressure measurement Computerised tomogram Electrocardiogram ambulatory Palpitations Ventricular extrasystoles

Symptomtext

About a week after the booster I started having heart palpitations. I went to my PCP and they detected PVC and sent me to the cardiologist. I wore a heart monitor for over a week and started taking a medication for my blood pressure- Lisinopril.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: CT Scan, Heart Monitor was worn for about a week.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Trintellix; Wellbutrin Flonase; Alprazolam; Zyrtec; Xyzal; Melatonin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2206548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 12,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Headache Paraesthesia

Symptomtext

She had a really bad headache, so I gave her 1 Ibuprofen and then she started complaining that she felt like pins and needles were sticking her all over her body. I was told it was not vaccine related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2201802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: AL
Alter: 24,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 21.12.2021
Beginn: 18.03.2022
Tage bis Beginn: 87,0
Dosis: 2
Route/Site: SYR / LA

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

Anaemia Autoimmune disorder Bacterial infection Chest pain Condition aggravated Cough Dizziness Dyspnoea Dysstasia Fatigue Fear Gait disturbance Headache Heart rate increased Hypomenorrhoea Illness Laboratory test abnormal Oropharyngeal pain

Symptomtext

I contracted COVID in October 2021 prior to vaccine. It started off having a sore throat and my partner was sick for a period of time, and it just hit me harder. It started off with a lot of congestion and drainage down my throat. Couldn't get enough air in, coughing, chest congestion, left like there was stuff in my lungs. A lot of fatigue. I can't walk or stand for more than 5 minutes which means I had to sit up at the urgent care for 2 hours and felt like I was going to pass out. Also had a fever, chest pain, felt like I was going to pass out. HR resting was 140, when I would stand it would shoot up to 170. That's been scary. Diagnosed me with acute respiratory infection with risk of morbidity without treatment. Labs showed a bacterial infection. Abnormalities in my labs showed a bacterial infection as well. I'm mildly anemic after the health event and I was told that at the ER. I do also have this very bad tremor ever since the health event started. Headaches form. I was sick and on top of that, it caused an autoimmune flare up and both of those together caused an ER visit and it's the sickest I've ever been. Almost as if every time I get sick, it turns into COVID-19 symptoms. I've had an autoimmune disease my whole life and I've noticed that change in symptoms every time I get sick. My heart rate has been fairly consistently high. It's always over 120, which my doctors are aware of, but it's concerning. Ever since I got the vaccine as well, my periods have been significantly lighter. Was on antibiotics, was told it was bacterial, other doctor said it was viral, and that it was a flare up of COVID symptoms. I was given IV fluids at ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Lab results - bacterial infection, COVID test came back negative, X-ray - Doctor indicated that the x-ray was "not too bad yet"
Aktuelle Erkrankungen: PMDD - on period during the time
Vorgeschichte: Autoimmune Disease - in process of diagnosis, In process of diagnosis for POTS, Dissociative Identity Disorder (DID), PTSD, Arthritis, Chronic Migraines
Andere Medikamente: Yaz Birth control, Duloxetine 60mg, Prazosin 2mg, Adderall XR 20mg, Metoprolol 100mg, Magnesium 250mg 1xdaily, Vitamin B12 3,000mcg
Allergien: Penicillin, Latuda, Lactose Intolerance, Gluten Sensitivity, Antipsychotics - bad reactions
Vorherige Impfungen: 1st COVID Pfizer - 04/08/2021 - Autoimmune flare up, but not as bad as this recent health event

VAERS 2201419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: WI
Alter: 61,0
Geschlecht: M
Eingang: 28.03.2022
Impfdatum: 10.01.2022
Beginn: 06.02.2022
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia Visual impairment

Symptomtext

Patient presented to ED for vision problems and paresthesia within 6 weeks of receiving the COVID-19 vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2201079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 28.03.2022
Impfdatum: 17.12.2021
Beginn: 02.03.2022
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Chest pain

Symptomtext

Started after about 2 months after my third dose have chest pain. Also various roving joint pain, in my one knee and ankle and wrist. This is similar to what I had when I had an outbreak of Sarcoidosis, except not as severe. I am referring to the joint pain. I am hoping this goes away or I will visit my Doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I have not gone to the Doctor yet for this.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertention Hypothyroid Endometrosis Lichen Schelosis Sarcoidosis autoimmune disease
Andere Medikamente: Multi vitamin Centrum
Allergien: Amoxicillin Iodine Celebrex
Vorherige Impfungen: -

VAERS 2162835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: LA
Alter: 28,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Mobility decreased Pain in extremity Paraesthesia SARS-CoV-2 test

Symptomtext

My arm was extremely sore / has continued to feel sore; I have felt more soreness down my arm and fingers; slow to move; tingling sensation; This is a spontaneous report received from 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 17Dec2021 13:00 (Lot number: FE3594) at the age of 28 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Previous Dose Details: , Previous Dose Product=COVID 19, Prev Dose Brand=Pfizer, Prev Dose Brand Unknown=False, Prev Dose Lot Number=EW0217, Prev Dose Lot Unknown=False, Prev Dose Administration Date=09Jun2021, Prev Dose Dose Number=2, Prev Dose Vaccine Location=Left Arm), administration date: 09Jun2021, when the patient was 28 years old, for Covid-19 immunization; Bnt162b2 (Prev Dose Product=COVID 19, Prev Dose Brand=Pfizer, Prev Dose Brand Unknown=False, Prev Dose Lot Number=EW0168, Prev Dose Lot Unknown=False, Prev Dose Administration Date=11May2021, Prev Dose Number=1, Prev Dose Vaccine Location=Left Arm), administration date: 11May2021, when the patient was 28 years old, for Covid-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 17Dec2021, outcome "not recovered", described as "My arm was extremely sore / has continued to feel sore"; PAIN IN EXTREMITY (non-serious) with onset 17Dec2021, outcome "not recovered", described as "I have felt more soreness down my arm and fingers"; MOBILITY DECREASED (non-serious) with onset 17Dec2021, outcome "not recovered", described as "slow to move"; PARAESTHESIA (non-serious) with onset 17Dec2021, outcome "not recovered", described as "tingling sensation". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, pain in extremity, mobility decreased, paraesthesia. Additional information: The patient received a Pfizer booster in (city withheld) at (pharmacy name withheld) at (address withheld).Her arm was extremely sore following the shot and has continued to feel sore. Recently, she had felt more soreness down my arm and fingers. Her arms and fingers have felt sore, slow to move, and at times a tingling sensation. She called the (pharmacy name withheld) and they recommended reported it to you all. The patient did not have any known allergies. The patient did not receive any other medications in two weeks. The facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. 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. Since the vaccination, the patient has been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20220303; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2162835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: LA
Alter: 28,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Mobility decreased Pain in extremity Paraesthesia SARS-CoV-2 test

Symptomtext

My arm was extremely sore / has continued to feel sore; I have felt more soreness down my arm and fingers; slow to move; tingling sensation; This is a spontaneous report received from 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 17Dec2021 13:00 (Lot number: FE3594) at the age of 28 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Previous Dose Details: , Previous Dose Product=COVID 19, Prev Dose Brand=Pfizer, Prev Dose Brand Unknown=False, Prev Dose Lot Number=EW0217, Prev Dose Lot Unknown=False, Prev Dose Administration Date=09Jun2021, Prev Dose Dose Number=2, Prev Dose Vaccine Location=Left Arm), administration date: 09Jun2021, when the patient was 28 years old, for Covid-19 immunization; Bnt162b2 (Prev Dose Product=COVID 19, Prev Dose Brand=Pfizer, Prev Dose Brand Unknown=False, Prev Dose Lot Number=EW0168, Prev Dose Lot Unknown=False, Prev Dose Administration Date=11May2021, Prev Dose Number=1, Prev Dose Vaccine Location=Left Arm), administration date: 11May2021, when the patient was 28 years old, for Covid-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 17Dec2021, outcome "not recovered", described as "My arm was extremely sore / has continued to feel sore"; PAIN IN EXTREMITY (non-serious) with onset 17Dec2021, outcome "not recovered", described as "I have felt more soreness down my arm and fingers"; MOBILITY DECREASED (non-serious) with onset 17Dec2021, outcome "not recovered", described as "slow to move"; PARAESTHESIA (non-serious) with onset 17Dec2021, outcome "not recovered", described as "tingling sensation". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain in extremity, pain in extremity, mobility decreased, paraesthesia. Additional information: The patient received a Pfizer booster in (city withheld) at (pharmacy name withheld) at (address withheld).Her arm was extremely sore following the shot and has continued to feel sore. Recently, she had felt more soreness down my arm and fingers. Her arms and fingers have felt sore, slow to move, and at times a tingling sensation. She called the (pharmacy name withheld) and they recommended reported it to you all. The patient did not have any known allergies. The patient did not receive any other medications in two weeks. The facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. 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. Since the vaccination, the patient has been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20220303; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2198739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: ND
Alter: 23,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 30.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

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

Autonomic nervous system imbalance Blood smear test Blood test Differential white blood cell count Dizziness Dyspnoea Echocardiogram Electrocardiogram Fatigue Feeling abnormal Full blood count Metabolic function test Palpitations Panic disorder Postural orthostatic tachycardia syndrome Tachycardia Vertigo Visual impairment

Symptomtext

Began having symptoms of disautonomia 5 days post vaccine. Symptoms included: dizziness, vertigo, SOB, heart palpitations, tachycardia, tachycardia upon standing, panic episodes, feeling faint, slow visual processing, visual "floaters", fatigue, brain fog. Has gotten progressively worse since then, and was recently diagnosed with postural orthostatic tachycardia syndrome and was advised to report to CDC by primary care doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG 12-lead: 2/21/22 Blood smear review: 2/21/22 CBC with differential: 2/21/22 Comprehensive metabolic panel: 2/21/22 Echocardiogram: 3/4/22 TSH blood test: 3/18/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2198315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3594

moderat

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 04.02.2022
Beginn: 19.02.2022
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: - / LA

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

Anxiety Chest discomfort Dyspnoea Headache Hypertension Malaise Nausea Palpitations SARS-CoV-2 test Tremor

Symptomtext

Tremors; headache; heart palpitations; shortness of breath; chest tightness; nausea; anxiety; high blood pressure; feeling unwell and doomed; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 48 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 04Feb2022 12:00 (Lot number: FE 3594) at the age of 48 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Latex" (unspecified if ongoing); "Penicillin" (unspecified if ongoing). Concomitant medication(s) included: PREDNISONE [PREDNISONE ACETATE]. The following information was reported: TREMOR (non-serious) with onset 19Feb2022, outcome "not recovered", described as "Tremors"; HEADACHE (non-serious) with onset 19Feb2022, outcome "not recovered", described as "headache"; PALPITATIONS (non-serious) with onset 19Feb2022, outcome "not recovered", described as "heart palpitations"; DYSPNOEA (non-serious) with onset 19Feb2022, outcome "not recovered", described as "shortness of breath"; CHEST DISCOMFORT (non-serious) with onset 19Feb2022, outcome "not recovered", described as "chest tightness"; NAUSEA (non-serious) with onset 19Feb2022, outcome "not recovered", described as "nausea"; ANXIETY (non-serious) with onset 19Feb2022, outcome "not recovered", described as "anxiety"; HYPERTENSION (non-serious) with onset 19Feb2022, outcome "not recovered", described as "high blood pressure"; MALAISE (non-serious) with onset 19Feb2022, outcome "not recovered", described as "feeling unwell and doomed". The events "tremors", "headache", "heart palpitations", "shortness of breath", "chest tightness", "nausea", "anxiety", "high blood pressure" and "feeling unwell and doomed" 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 not taken as a result of tremor, headache, palpitations, dyspnoea, chest discomfort, nausea, anxiety, hypertension, malaise. Additional Information: No other vaccine in four weeks. Covid prior to vaccination and covid tested post vaccination. Pfizer have permission to contact the reporter about this event. Pfizer have permission to contact your/the patient's healthcare provider about this report. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20220225; Test Name: COVID-19 TEST; Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab; Test Date: 20220307; Test Name: COVID-19 TEST; Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Latex allergy; Penicillin allergy.
Andere Medikamente: PREDNISONE [PREDNISONE ACETATE].
Allergien: -
Vorherige Impfungen: -

VAERS 2109603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: AL
Alter: 37,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 12.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Paraesthesia

Symptomtext

Parasthesias in arms and legs; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 37 year-old female patient (not pregnant) received BNT162b2 (BNT162B2), administered in arm right, administration date 12Feb2022 11:00 (Lot number: FE3594) at the age of 37 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ASPIRIN (E.C.); TAMSULOSIN; VITAMIN B12 & FOLIC ACID. Past drug history included: Levaquin, reaction(s): "Drug Allergy". The following information was reported: PARAESTHESIA (non-serious) with onset 12Feb2022 16:00, outcome "not recovered", described as "Parasthesias in arms and legs". Therapeutic measures were not taken as a result of paraesthesia. Additional Information: The patient did not have other vaccine in four weeks. The patient did not have covid prior vaccination. The patient did not have covid tested post vaccination. No follow-up attempts are possible. 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.
Andere Medikamente: ASPIRIN (E.C.); TAMSULOSIN; VITAMIN B12 & FOLIC ACID.
Allergien: -
Vorherige Impfungen: -

VAERS 2109603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: AL
Alter: 37,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 12.02.2022
Beginn: 12.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Paraesthesia

Symptomtext

Parasthesias in arms and legs; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 37 year-old female patient (not pregnant) received BNT162b2 (BNT162B2), administered in arm right, administration date 12Feb2022 11:00 (Lot number: FE3594) at the age of 37 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ASPIRIN (E.C.); TAMSULOSIN; VITAMIN B12 & FOLIC ACID. Past drug history included: Levaquin, reaction(s): "Drug Allergy". The following information was reported: PARAESTHESIA (non-serious) with onset 12Feb2022 16:00, outcome "not recovered", described as "Parasthesias in arms and legs". Therapeutic measures were not taken as a result of paraesthesia. Additional Information: The patient did not have other vaccine in four weeks. The patient did not have covid prior vaccination. The patient did not have covid tested post vaccination. No follow-up attempts are possible. 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.
Andere Medikamente: ASPIRIN (E.C.); TAMSULOSIN; VITAMIN B12 & FOLIC ACID.
Allergien: -
Vorherige Impfungen: -

VAERS 2182526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MT
Alter: 64,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Autonomic nervous system imbalance Bone pain Chest discomfort Chest pain Chills Condition aggravated Dyspnoea Erythema Injection site erythema Insomnia Myalgia Nausea Peripheral swelling Vomiting

Symptomtext

Redness in right arm, below site of injection, began to turn red at about 15 minutes after the vaccine injection was administered. Took 20mg of Prednisone orally at this point (and had premedicated with 50mg of Benadryl prior to injection). Vital Signs remained within normal limits and I was allowed to leave the clinic with the instructions to continue taking the Prednisone until the prescribe doses doses were completed. During the next 72 hours there was a progression of the same symptoms as I experienced with the first dose, except that there was not the cytokine storm coma like effect; instead, there was no ability to sleep at all. There was a lot of bone and muscle pain, difficulty breathing, swelling and redness of the right arm that extended under the armpit area and over to the sternum, chest pain and pressure in the area of the carotid artery systems, and wild swings of dysautonomia, chills, nausea, and vomiting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Mast Cell Activation Disorder, Fibromuscular Dysplasia of Internal Carotid Arteries with Dysautonomia, Possible Ehlers-Danlos, Metabolic Disorder
Andere Medikamente: Aspirin, Cabergoline, Cetirizine Hcl, Cimetidine, Cromolyn Sodium Nasal Solution, Cyancobalamin, Cytomel, Diphenhydramine, Ephinephrine, Femring, Furosemide, Ketotifen, Levalbuterol Tartrate HFA, Metformin Hcl, Metformin Hcl ER, Nitroglycer
Allergien: Codeine, Iodine Contrast Media (IVP Dye), Iron Sucrose, Latex Sensitivity, Multiple Food Allergies
Vorherige Impfungen: Cytokine Storm type coma with first Pfizer Vaccine

VAERS 2162896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MN
Alter: 35,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 18.02.2022
Beginn: 25.02.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Condition aggravated Gastrooesophageal reflux disease Headache Hypoaesthesia Skin discolouration

Symptomtext

I had left side chest pain and reflux. Numbness down the left arm. Midcalf numbness and purpling of my foot through my ankle and all my toes. My doctor recommended to monitor it. By the morning it improved and I still just had the reflux and minor headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Lupus and Connective Tissue Disease, Asthma and Arthritis
Andere Medikamente: None
Allergien: Steroids, Fentanyl, Opioids
Vorherige Impfungen: Just chest pain and numbness in my extremities in the two previous Pfizer COVID vaccines.

VAERS 2151485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: VA
Alter: 52,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 18.10.2021
Beginn: 18.10.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Acoustic stimulation tests abnormal Condition aggravated Magnetic resonance imaging Tinnitus

Symptomtext

The tinnitus, eye aches, nausea and vertigo from the earlier vaccines had simmered down. By the time I got this vaccine I was only suffering the eye pain and the tinnitus (which was getting better). As soon as I got this vaccine the tinnitus began again with an uproar and hasn?t abated much.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: MRI, hearing test
Aktuelle Erkrankungen: I had been suffering vertigo, nausea, and tinnitus from the last 2 vaccines. I also suffered eye pain. It was like a musculature pain.
Vorgeschichte: I?ve suffered optic neuritis in the past.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Flu vaccine makes me achy for a day

VAERS 2148668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MT
Alter: 27,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 18.12.2021
Beginn: 25.02.2022
Tage bis Beginn: 69,0
Dosis: 2
Route/Site: SYR / LA

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

Anxiety Dizziness Dyspnoea Fear Feeling hot Hyperhidrosis Nausea Palpitations Panic attack Tremor

Symptomtext

Severe anxiety and panic attacks beginning approximately two months after the second dose of the Pfizer vaccine. Around February 21st, 2022, I started to experience severe anxiety (that I've never experienced before) with symptoms of excessive worry, sweating / hot all over, dizziness, heart racing, shakiness, and fear of not being able to go back to feeling "normal." On February 25th, 2022, the anxiety heightened almost escalating to a panic attack but did not, although severe anxiety was still experienced. On the night of February 27th, 2022, a panic attack struck with intense fear (sense of impending doom), sweating / hot all over, heart racing, dizziness, shakiness, nausea, and difficulty breathing. I did not seek medical attention at the moment of the panic attack but rather worked to calm myself down (panic attack lasted approximately 2 hours). I did, however, schedule an appointment with a psychiatrist the week prior to the panic attack due to the excessive anxiety. The appointment is scheduled for Tuesday, March 1st, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D, Fioricet as needed for headache
Allergien: None
Vorherige Impfungen: -

VAERS 2148398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 14.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Arthralgia Blood test COVID-19 Discomfort Full blood count Hypertension Nasopharyngitis Peripheral swelling Rash SARS-CoV-2 test negative SARS-CoV-2 test positive Swelling face Thyroid function test

Symptomtext

began 3 days after vaccination: face swelling with rash, swelling of right hand, very cold, high blood pressure (160/100); saw staff (my nurse practitioner) on 21Jan2022 regarding the symptoms. I tested positive for Covid19; went back to doctor on 24 Feb due to on-going discomfort and same rash in face appeared and right hand is still swollen; joints hurts; BP continues to be 160/100.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: rechecked for Covid19 (negative); checked for pericarditis - negative; potential issue with kidney; blood was drawn on 25 Feb 2022 and waiting for results with focus on kidney function (hepatic panel), thyroid function, CBC, etc
Aktuelle Erkrankungen: Possibly had Covid19 when vaccination was administered. Tested positive for Covid19 on 21 Jan 2022
Vorgeschichte: None.
Andere Medikamente: Claritin
Allergien: None.
Vorherige Impfungen: -

VAERS 2131095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NC
Alter: 75,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Cardiac flutter Cardiac monitoring abnormal Sleep disorder Supraventricular tachycardia

Symptomtext

I experienced fluttering in my chest woke me up in the middle of that Friday night. On that Monday contacted my doctor went was given a monitor to wear for 3 days. After the results was referred to a Cardiologist diagnosed with Supraventricular tachycardia (SVT). i was advised to continue to monitor as of right now there short can be long. I'm keeping a diary of the episodes last recorded was on February 17, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: -
Labordaten: Monitor
Aktuelle Erkrankungen: No
Vorgeschichte: Arthritis, Migraine
Andere Medikamente: Ibandronate
Allergien: Levaquin, Tetracycline
Vorherige Impfungen: Pfizer Dose 1,2 (stiffness of joints), Shingles vaccine 2 or 3 years ago exp stiffness of joints and headaches on and off lasted

VAERS 2127970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3594

moderat

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 28.01.2022
Beginn: 31.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: OT / RA

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

Chest pain Cough Dyspnoea Feeling abnormal Headache Muscle spasms Pain Pain in extremity SARS-CoV-2 test Swelling

Symptomtext

Swelling of the supraclavicular region/little bit swelling in the neck; shortness of breath/cannot breathe; cough; chest pain; headache; cramping in the arm where I received the vaccine; pain; I feel really bad; I have pain in my arm, the side that I received the vaccine; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), intramuscular, administered in arm right, administration date 28Jan2022 14:45 (Lot number: Fe3594) at the age of 38 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Asthma overcome in adolescence" (unspecified if ongoing). The patient was not pregnant at time of vaccination. The patient had no known allergies. The patient was not diagnosed with COVID-19 prior to vaccination. Concomitant medication(s) included: FLU taken for influenza immunisation, administration date 16Jan2022. Vaccination history included: BNT162B2 (Dose Number: 2, Batch/Lot No: Cr8731, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 08May2021, when the patient was 37 years old, for COVID-19 immunisation; BNT162B2 (Dose Number: 1, Batch/Lot No: Ew0162, Location of injection: Arm Right, Vaccine Administration Time: 01:00 PM), administration date: 18Apr2021, when the patient was 37 years old, for COVID-19 immunisation. The following information was reported: SWELLING (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "Swelling of the supraclavicular region/little bit swelling in the neck"; DYSPNOEA (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "shortness of breath/cannot breathe"; COUGH (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "cough"; CHEST PAIN (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "chest pain"; HEADACHE (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "headache"; MUSCLE SPASMS (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "cramping in the arm where I received the vaccine"; PAIN (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "pain"; FEELING ABNORMAL (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "I feel really bad"; PAIN IN EXTREMITY (prolonged hospitalization) with onset 31Jan2022 04:00, outcome "not recovered", described as "I have pain in my arm, the side that I received the vaccine". The patient underwent the following laboratory tests and procedures: SARS-COV-2 test: (06Feb2022) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of swelling, dyspnoea, cough, chest pain, headache, muscle spasms, pain, feeling abnormal, pain in extremity. The patient took Tylenol and drunk hot water with Lemon and Honey and Garlic capsules (Kyolic) number 103 formula as treatment for the events.; Sender's Comments: There is a reasonable possibility based on known safety profile and plausible temporal association that the events are related to the suspected vaccine. 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: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 20220206; Test Name: Quickvue at home; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2112011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3594

moderat

Staat: WY
Alter: 56,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 01.01.2022
Beginn: 02.02.2022
Tage bis Beginn: 32,0
Dosis: 2
Route/Site: SYR / RA

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

Blood test Impaired work ability Migraine Nasopharyngitis SARS-CoV-2 test negative

Symptomtext

Started with head cold for 1 week, missed 2 days of work. Which now has led to 6 days of a migraine headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Blood work, covid test negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None, healty male prior to vaccine
Andere Medikamente: Zero, was a healthy male at the time of vaccination.
Allergien: None
Vorherige Impfungen: -

VAERS 2108790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MS
Alter: 40,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 21.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: - / LA

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

Condition aggravated Electrocardiogram Feeling abnormal Sinus rhythm Ventricular extrasystoles

Symptomtext

felt bad for 36 hours after second dose, she felt similar on the booster dose; I began experiencing intermittent PVC's [premature ventricular contractions] that have been progressively getting worse; I began experiencing intermittent PVC's [premature ventricular contractions] that have been progressively getting worse; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 40 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21Dec2021 16:00 (Lot number: FE3594, Expiration Date: 28Feb2022) at the age of 40 years as dose 3 (booster), 0.3 ml single for covid-19 immunisation. Relevant medical history included: "headaches" (unspecified if ongoing); "body aches" (unspecified if ongoing), notes: body aches; "horrible, terrible heartburn" (unspecified if ongoing), notes: horrible, terrible heartburn; "She had PVCs before but never this bad" (unspecified if ongoing). Concomitant medication(s) included: TYLENOL taken for headache, pain; NEXIUM [ESOMEPRAZOLE SODIUM] taken for dyspepsia. Vaccination history included: Bnt162b2 (Dose 01, Lot: EN6199, Expiration: nknown), administration date: 10Mar2021, when the patient was 39 years old, for COVID-19 immunization, reaction(s): "First two doses made her arm kind of sore"; Bnt162b2 (Dose 02, Lot: EP7533, Expiration: unknown), administration date: 20Apr2021, when the patient was 40 years old, for COVID-19 immunization, reaction(s): "felt bad for 36 hours after second dose", "First two doses made her arm kind of sore". The following information was reported: CONDITION AGGRAVATED (non-serious), VENTRICULAR EXTRASYSTOLES (non-serious) all with onset Jan2022, outcome "not recovered" and all described as "I began experiencing intermittent PVC's [premature ventricular contractions] that have been progressively getting worse"; FEELING ABNORMAL (non-serious), outcome "unknown", described as "felt bad for 36 hours after second dose, she felt similar on the booster dose". The events "i began experiencing intermittent pvc's [premature ventricular contractions] that have been progressively getting worse", "i began experiencing intermittent pvc's [premature ventricular contractions] that have been progressively getting worse" and "felt bad for 36 hours after second dose, she felt similar on the booster dose" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: On 3-4/Jan2022 I began experiencing intermittent PVC's [premature ventricular contractions] that have been progressively getting worse. I been to the doctor and everything came back normal. She had an appointment with cardiologist next week (on 02Feb2022). It was reported that a review of the Prescribing Information for the Pfizer-BioNTech COVID-19 vaccine for 12 years and older formulation (purple cap) did not find information regarding premature ventricular contractions (PVC's). As the Prescribing Information does not include all adverse reactions that have been reported or that may occur, please consult with your doctor/healthcare provider about what you have experienced/are experiencing. Because your doctor/healthcare provider was most familiar with your medical condition, clinical history, how your treatment has been conducted and any relevant information to your specific case, your doctor/healthcare provider is in the best position to advise you about the appropriate action to take. In regards to heart conditions, myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the lining outside the heart) have occurred in some people who have received Comirnaty (COVID-19 Vaccine, mRNA) or the Pfizer-BioNTech COVID-19 Vaccine. In most of these people, symptoms began within a few days following receipt of the second dose of vaccine. The chance of having this occur was very low. According to the withheld Centers for Disease Control and Prevention (or CDC), reports of myocarditis and pericarditis were rare given the number of doses administered. Patients have typically quickly improved with treatment and rest. The patient taking covid 19 vaccine (Verbatim) as prevention, did not want to catch covid. She went to the doctor and had an EKG, or ECG, nothing abnormal was seen and sinus rhythm was normal. She caught the PVCs on her apple watch, and she showed the doctor that it was kind of adding an extra beat. They have gotten progressively worse over last two weeks. Prior vaccinations (within 4 weeks) was none. . Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: EKG, or ECG; Result Unstructured Data: Test Result:nothing abnormal was seen; Comments: EKG, or ECG, nothing abnormal was seen; Test Name: sinus rhythm; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: General body pain (body aches); Headache; Heartburn (horrible, terrible heartburn); Premature ventricular contractions
Andere Medikamente: TYLENOL; NEXIUM [ESOMEPRAZOLE SODIUM]
Allergien: -
Vorherige Impfungen: -

VAERS 2105928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 11.02.2022
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

COVID-19 Condition aggravated Dizziness Dry skin Dysgeusia Erythema Hypersensitivity Injection site pruritus Injection site reaction Pain Pain in extremity Pruritus Skin warm Urticaria

Symptomtext

I became light headed and dizzy this happened with every Covid vaccination. But for the Booster I felt a metallic taste in my mouth at the same time I got light headed, about 5-10 minutes after the injection. By the next day my arm was sore and a red welt formed at the injection site. The welt got bigger about 2-3 inches, warm, hurting and itchy. It remained that way for 2 weeks as did the metallic taste. I contracted Covid 2 weeks after the Booster and the injection site became very itchy and my skin became very dry. The itching subsided 3 weeks later but the dryness has remained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Spoke with my Doctor and she stated it's very rare to have these symptoms. The reaction to the shot could be due to my sensitive skin and just an allergic reaction. I also get a very warm and red welt after a flu injection, which I haven't had in 3 years.
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis, Spondylilethesis, Fibromyalgia
Andere Medikamente: Flovent, ProAir, Zyrtec, Montelukast, HCTZ, Multi-Vitamin, Iron supplement, Omega 3, Magnesium 500mg
Allergien: Penicillin, lactose intolerant and Gluten sensitive. Have sensitive skin.
Vorherige Impfungen: -

VAERS 2104758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MN
Alter: 32,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 09.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Injection site erythema Injection site induration Injection site warmth Paraesthesia

Symptomtext

hardness and redness x 3 1/2 cm in diameter at site; left arm numbness; describes as feels like I slept on it wrong and it fell asleep; redness developed pencil eraser size 6 hours after injection. Took po tylenol prior to bed; woke up in morning 2/10/22 with 2 cm diameter redness and numbness; continued to take tylenol; pm of 2/10/22 applied ice; 2/11/22 woke up with redness 3.5 cm diameter; warm to touch and hard; will continue tylenol and ice; if no improvement will see provider 2/14/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: premature ovarian failure diabetes
Andere Medikamente: tylenol
Allergien: seafood, shellfish, eggs, mushrooms, celery, coconut ibuprofen amoxicillin
Vorherige Impfungen: -

VAERS 2102778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: FL
Alter: -
Geschlecht: U
Eingang: 10.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Essential tremor Grip strength decreased Laboratory test Loss of personal independence in daily activities Magnetic resonance imaging Neurological examination Tremor

Symptomtext

I have developed Essential Tremors (ET) because of the vaccines. This was diagnosed by my neurologist with appropriate tests. I did not have these prior to the vaccines, and every time I got another vaccine it got worse and worse. There is no cure for ET, I have to live with this the rest of my life. I have trouble doing everything in life as I shake like crazy whenever I use a muscle. I am not even able to hold a glass or mug without spilling or dropping it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Essential tremor
Hospital-Tage: -
Labordaten: Neurology visit with exam/tests 9/29/2021, MRI 10/3/2021, follow-up Neurology visit 10/29/2022 and 2/3/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2102546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OR
Alter: 59,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Dizziness Dyspnoea Influenza like illness Injection site pain Pyrexia Rhinorrhoea

Symptomtext

2 days of significant weakness and medium flu-like symptoms (dizziness, sniffling, mild fever/chills, mild shortness-of-breath); worst reaction of the 3 shots in Covid vaccine series. Relieved after 2 days of bedrest. Minor pain at injection site for about 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None needed.
Aktuelle Erkrankungen: No acute illnesses
Vorgeschichte: Chronic hypothyroidism, chronic mild hypertension, borderline high cholesterol
Andere Medikamente: Levothyroxine 0.075mg, Lisinopril 10mg, Atorvastatin 20mg, Pramipexole 0.125mg, Aspirin 81mg chewable, Estradiol 3mg daily, Spironolactone 50mg,
Allergien: None
Vorherige Impfungen: Very mild weakness for 1 day following Pfizer Covid vaccine #2 April 24, 2021

VAERS 2098632

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MD
Alter: 43,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 13.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Immediate post-injection reaction Mobility decreased Pain in extremity Pruritus Rash Urticaria

Symptomtext

Patient complained of itching and hives occurring a couple of days after vaccination over entire body. A rash had developed near neck on the shoulder. Her left arm was in pain immediately after receiving vaccination. It is difficult to move the left arm in any direction. The patient took Tylenol for 3 days after the injection and was still experiencing pain in her arm. The patient started taking Benadryl a week after itching and hives. She takes Benadryl once a day. It helps but the itching and hives comes back the next day. This is a daily occurrence for the patient and has not received any relief. The patient said there were no issues with the first two vaccinations. Patient has no known allergies

Weitere VAERSDATA-Felder

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

VAERS 2098509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: PR
Alter: 29,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dyspnoea Tachycardia Tracheal obstruction Tremor

Symptomtext

Female patient reported respiratory difficulty and that her trachea was blocked, tremor and tachycardia. Vitals taken, O2 administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Iodine; Ginger; Crustaceans
Vorherige Impfungen: -

VAERS 2092930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: LA
Alter: 43,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 13.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Blood immunoglobulin G Chills Differential white blood cell count Fatigue Full blood count Headache Herpes zoster Hot flush Metabolic function test Migraine Night sweats Ocular discomfort

Symptomtext

Migraine Headache, Pressure behind the left eye, Stabbing headache, Weakness, Fatigue, Hot Flashes, Chills, Night Sweats, Shingles

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: V Zoster IgG, CBC with Auto Differential, Comprehensive Metabolic Panel
Aktuelle Erkrankungen: Laryngitis
Vorgeschichte: None
Andere Medikamente: Vitamins and Vitamin C
Allergien: None
Vorherige Impfungen: -

VAERS 2091453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 28.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Blood pressure increased Cardiac flutter Chest pain Dyspnoea Fatigue Headache Memory impairment Pain Palpitations Pyrexia

Symptomtext

Headache, body aches, and low grade fever 2-3 days Fatigue still on-going, but most severe 1-3 weeks Heart palpitations/fluttering, chest pain, shortness of breath, elevated blood pressure, worse when laying down still on-going, but improving Memory issues, forgetfulness, repeating things still on-going

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: None
Vorgeschichte: Heartburn/acid reflux Anxiety/Depression Allergies Polycystic Ovarian Syndrome Premenstrual Dysphoric Disorder
Andere Medikamente: Zantac Sertraline Iron supplements Flonase
Allergien: N/A
Vorherige Impfungen: -

VAERS 2088198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: UT
Alter: 73,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 28.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Body temperature increased Dehydration Eye discharge Herpes simplex Malaise Ocular hyperaemia Oral herpes Oropharyngeal pain Pain Pain in extremity Pain in jaw Productive cough

Symptomtext

The first two vaccines resulted in sore are for a few days. The 3rd vaccine caused 36 hours of 102.4 - 103 temperature with malaise and body aches. On day 5 following the vaccine, I developed 3 cold sores on my lower lip, with elevated temperature, mucus in both eyes, and body aches from the herpes simples outbreak. On day 7 - January 4th, following the 3rd vaccine I traveled to visit with family. On day 9 - January 13, I had a nurse home visit for several days, very sore throat, productive cough, 102 temperature, malaise and dehydration. On day 16th - January 20, I broke out with 3 more cold sores that are still noticeable February 4th. Right jaw pain, and blood shot eyes with mucus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Celiac Disease
Andere Medikamente: CA, C, Magnesium, Vitamin D, TG100, Saw Palmetto,
Allergien: Celiac Disease
Vorherige Impfungen: -

VAERS 2082580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: WA
Alter: 58,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 13.02.2021
Beginn: 29.01.2022
Tage bis Beginn: 350,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

Patient was admitted to Hospital on 1/29/22 for COVID pneumonia. This is considered a breakthrough case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2079413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 27,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 13.12.2021
Beginn: 18.01.2022
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Condition aggravated Diabetic ketoacidosis Hyperglycaemia Hypertension Hypophagia Nausea SARS-CoV-2 test positive Type 1 diabetes mellitus Vomiting

Symptomtext

Hospitalized (1.22.22 - 1.30.22); COVID-19 positive (1.18.22); Fully vaccinated PLUS booster Admission Date: 1/22/2022 Discharge Date: 01/30/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: DKA, type 1, not at goal (HCC) [E10.10] Type 1 diabetes mellitus with hyperglycemia (HCC) [E10.65] Intractable vomiting with nausea, unspecified vomiting type [R11.2] COVID-19 [U07.1] HOSPITAL COURSE: 27-year-old female with history of diabetes mellitus and gastroparesis presented to Community Hospital with complaints of intractable nausea and vomiting. She had been tested on January 18 and was found to be COVID positive. She was managing at home until worsening nausea and vomiting led to her presentation at the hospital. During her hospital stay she had persistence of her nausea and vomiting and only very gradually was able to show signs of improvement. Multiple times she was on IV insulin due to little to no oral intake. She gradually did show signs of improvement with use of antiemetics and by the day of discharge felt that she was able to manage reasonably well at home. She was discharged under usual anti nausea medication as well as her usual insulin dosing. She number required significant treatment for her COVID infection. She did not need steroids or other intervention. She had high blood pressures during hospital stay and was started on oral lisinopril 5 mg daily at discharge. She is instructed to follow up with her primary care provider within the week post discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Gastroparesis Type 1 diabetes mellitus with hyperglycemia (HCC) Marijuana smoker, continuous Depression GAD (generalized anxiety disorder) PTSD (post-traumatic stress disorder) DKA, type 1, not at goal (HCC) Hypertension associated with diabetes (HCC)
Andere Medikamente: busPIRone (BUSPAR) 10 MG tablet insulin glargine (LANTUS SOLOSTAR) 100 UNIT/ML pen-injector insulin lispro (HUMALOG KWIKPEN) 100 UNIT/ML pen-injector lisinopril (PRINIVIL,ZESTRIL) 5 MG tablet medroxyPROGESTERone (DEPO-PROVERA) 150 MG/ML SUS
Allergien: CefiximeHives, Rash MetoclopramideOther Tegaderm MiscRash AdhesiveRash LatexRash
Vorherige Impfungen: -

VAERS 2075833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 19.12.2021
Beginn: 21.01.2022
Tage bis Beginn: 33,0
Dosis: 3
Route/Site: UN / UN

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

Alanine aminotransferase normal Anion gap Aspartate aminotransferase normal Basophil percentage Blood albumin decreased Blood alkaline phosphatase normal Blood bicarbonate increased Blood bilirubin normal Blood calcium decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood magnesium normal Blood phosphorus normal Blood potassium normal Blood sodium normal Blood urea normal Brain natriuretic peptide increased

Symptomtext

Discharged. This is a 73 y.o. year old patient who was admitted on 1/24/2022 with PMH of recently diagnosed AML on treatment with cycle 1 of Vidaza/venetoclax, COPD, HTN, HLD, and hypothyroidism who presented to the ED after discovering low oxygen saturation at her office appointment. Patient was known to be positive for COVID, having tested positive on 1/21. She had also noted weight gain of 11 pounds with swelling in bilateral legs. Patient was placed on oxygen and started of a 10-day course of dexamethasone and 5-day course of remdesivir. BNP was elevated at 1659 with negative troponins and bilateral LE dopplers negative for DVT. Patient was started on PRN lasix with good urine output. Patient was noted on telemetry to have a bundle branch block, which was confirmed on EKG. Cardiology was consulted and started patient on lasix 20mg BID with plans for outpatient stress test. Limited echo on 1/26 showed an EF of 65% with mild-moderate mitral regurgitation. On 1/28, patient was noted to have an asymptomatic 5-beat run of non-sustained V-tach. Cardiology was notified and started patient on metoprolol with plans for a 14-day ziopatch at discharge. Patient experienced good diuresis with above lasix and was able to be weaned down to 1-2L per NC. Patient was still desaturating to the 80s without oxygen, and thus home oxygen arranged per respiratory. PT/OT followed during stay, and home services were recommended. Patient accepted to organization. Prior to discharge today, patient doing well on 1L NC and has completed 5 days of remdesivir. Care discussed with doctor and patient deemed stable for discharge. Patient and daughter are agreeable - she is feeling overall improved with no new or worsening ROS. Home oxygen and services arranged. Ziopatch to be placed at discharge and cardiology follow-up arranged. Daily weights and diet/fluid restrictions discussed. All new medications discussed in detail with patient and her daughter. Patient will plan to follow up in our office as below. Patient's discharge medication plan were discussed as per below and new prescriptions were sent to patient's requested pharmacy prior to discharge as per generated list below. Patient is aware to call our office should further questions or concerns arise following this discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ventricular tachycardia
Hospital-Tage: 4,0
Labordaten: USV Venous Lower Extremity Duplex Bilateral Resulted: 01/24/22 2331 Order Status: Completed Updated: 01/24/22 2333 Narrative: EXAMINATION: Complete Right and Left Lower Extremity Venous Duplex Doppler Ultrasound EXAM DATE: 1/24/2022 10:55 PM 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: Bilateral lower extremity edema 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: The common femoral vein waveforms are abnormally pulsatile. This finding may be seen with elevated central venous pressure from heart failure, tricuspid valve regurgitation, pulmonary hypertension, or right heart dysfunction. Additional Findings: None. _____________________ Impression: There is no deep venous thrombosis in the visualized deep veins of the right or left lower extremity. Reflected cardiac pulsations are present in the common femoral vein waveforms. This finding may be seen with elevated central venous pressure from heart failure, tricuspid valve regurgitation, pulmonary hypertension, and elevated right heart pressures or dysfunction. DR CHEST SINGLE VIEW Resulted: 01/24/22 1313 Order Status: Completed Updated: 01/24/22 1315 Narrative: EXAMINATION: Single View Chest EXAM DATE: 1/24/2022 1:03 PM TECHNIQUE: Single view chest INDICATION: cough, covid 19 COMPARISON: January 19, 2022 ENCOUNTER: Not applicable _________________________ FINDINGS: A tunneled central line is present with tip Rector over the midsuperior vena cava. The mediastinum and pulmonary vasculature are normal. Streaky airspace disease is demonstrated within the right lower lung as well as the left central and left lower lung. This has progressed since the previous study January 19, 2022. No pleural effusion or pneumothorax is present. _________________________ Impression: Progressing airspace disease is present since the previous exam Result Value Ref Range Status Sodium Level 138 134 - 146 mmol/L Final Potassium Level 4.5 3.4 - 5.0 mmol/L Final Chloride 101 98 - 112 mmol/L Final HCO3 32 (H) 21 - 29 mmol/L Final Anion Gap 5 (L) 9 - 18 mmol/L Final Glucose Level 98 70 - 99 mg/dL Final Blood Urea Nitrogen 20 8 - 20 mg/dL Final Creatinine 0.95 0.50 - 1.10 mg/dL Final MDRD eGFR 58 (L) >=60 mL/min/1.73 m2 Final CG eCrCl 44 mL/min/1.73 m2 Final Calcium Level Total 8.8 8.6 - 10.4 mg/dL Final Protein Total 5.5 (L) 6.0 - 8.0 g/dL Final Albumin Level 2.9 (L) 3.5 - 5.0 g/dL Final Bilirubin Total 0.3 0.2 - 1.0 mg/dL Final Alkaline Phosphatase 44 35 - 104 IU/L Final Alanine Aminotransferase 14 10 - 40 IU/L Final Aspartate Aminotransferase 24 10 - 40 IU/L Final Complete Blood Count w/Differential Status: Abnormal Result Value Ref Range Status White Blood Cell 2.38 (L) 4.00 - 10.80 x10*3/uL Final Red Blood Cell 2.41 (L) 4.20 - 5.40 x10*6/uL Final Hemoglobin 8.3 (L) 12.0 - 16.0 g/dL Final Hematocrit 25.3 (L) 37.0 - 47.0 % Final Mean Cell Volume 105.0 (H) 80.0 - 100.0 fL Final Mean Cell Hemoglobin 34.4 (H) 27.0 - 33.0 pg Final Mean Cell Hemoglobin Concentration 32.8 32.0 - 37.0 g/dL Final Red Cell Diameter Width 22.5 (H) 11.0 - 16.0 % Final NRBC Absolute Count 0.02 (H) 0.00 - 0.01 x10*3/uL Final NRBC Automated 0.8 (H) 0.0 - 0.1 %WBC Final Platelet 248 140 - 400 x10*3/uL Final Mean Platelet Volume 11.7 (H) 7.4 - 11 fL Final Neutrophil Absolute Count 0.94 (L) 1.80 - 7.80 x10*3/uL Final Magnesium, Blood Level Status: Normal Result Value Ref Range Status Magnesium Level 1.7 1.6 - 2.5 mg/dL Final Phosphorus, Blood Level Status: Normal Result Value Ref Range Status Phosphorus Level 3.7 2.5 - 4.5 mg/dL Final Manual Differential ADD ON Status: Abnormal Result Value Ref Range Status Segmented Neutrophils Manual 32 (L) 35 - 80 % Final Lymphocytes Manual 63 (H) 20 - 50 % Final Monocytes Manual 4 2 - 12 % Final Eosinophil Manual 0 0 - 6 % Final Basophils Manual 1 0 - 2 % Final RBC Morphology Normal Final Platelet Estimate Normal Final
Aktuelle Erkrankungen: 11/12/2021- Chronic fatigue, unspecified
Vorgeschichte: Acute myeloid leukemia not having achieved remission
Andere Medikamente: acetaminophen (TYLENOL) 650 MG tablet acyclovir (ZOVIRAX) 400 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler allopurinol (ZYLOPRIM) 300 MG tablet dexamethasone (DECADRON) 6 MG tablet Docusate
Allergien: Codeine- Hallucinations, Other Sulfa Drugs- Other, Myalgia, Joint Pain
Vorherige Impfungen: -

VAERS 2021099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

moderat

Staat: FL
Alter: 24,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 07.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Lymphadenopathy Paraesthesia Muscle swelling Muscle tightness Myalgia Pain in extremity Peripheral swelling Oedema peripheral

Symptomtext

painful shooting down to her thumb/forearm is sore; under left armpit swollen; left bicep is swollen; muscles in inner bicep feels tight; muscles in inner bicep feels tight, and kind of painful; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jan2022 (Lot number: FE359Y) at the age of 24 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: NEXPLANON taken for contraception (ongoing). Vaccination history included: Bnt162b2 (Dose 1, single, Lot: EN6199), administration date: 08Mar2021, when the patient was 23 years old, for COVID-19 Immunization; Bnt162b2 (Dose 2, single, Lot: EN6208), administration date: 29Mar2021, when the patient was 23 years old, for COVID-19 Immunization. The following information was reported: PERIPHERAL SWELLING (non-serious) with onset 08Jan2022, outcome "not recovered", described as "under left armpit swollen"; MUSCLE SWELLING (non-serious) with onset 08Jan2022, outcome "not recovered", described as "left bicep is swollen"; MUSCLE TIGHTNESS (non-serious) with onset 08Jan2022, outcome "not recovered", described as "muscles in inner bicep feels tight"; MYALGIA (non-serious) with onset 08Jan2022, outcome "not recovered", described as "muscles in inner bicep feels tight, and kind of painful"; PAIN IN EXTREMITY (non-serious) with onset 09Jan2022, outcome "not recovered", described as "painful shooting down to her thumb/forearm is sore". Therapeutic measures were taken as a result of peripheral swelling, muscle swelling, muscle tightness, myalgia, pain in extremity. Additional information: Concomitant Product Nexplanon: has been in for three years. No past history, patient got the Pfizer booster vaccine on Friday. Patient called pharmacist and was having an adverse reaction. Any advice for what she can do. Advised to consult with HCP. Clarified the reaction was under armpit was really swollen and bicep was swollen, forearm was sore. The muscle in inner bicep feels tight, and kind of painful. If she raises her arm, it was a painful shooting down to her thumb. This was all in the left arm where she received the booster vaccine. These symptoms aside from the pain and shooting pain, started on Saturday 08Jan2022. The pain and shooting pain started yesterday and was continuing today, the day of reporting. Treatment included taking over the counter Advil and Tylenol. The patient has a birth control implant in her left arm called Nexplanon. Additional vaccines administered on same date of the Pfizer suspect were none. The adverse events did not require a visit to emergency room, physician Office. Prior Vaccinations (within 4 weeks) were none. Events following prior vaccinations were none. Patients Medical History was reported as none. Family Medical History Relevant to adverse events was reported as no. Relevant Tests: none. Follow-Up: 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: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: NEXPLANON
Allergien: -
Vorherige Impfungen: -

VAERS 2065854

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3594

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort Amylase increased Asthenia Computerised tomogram abdomen abnormal Hypoaesthesia Lipase increased Musculoskeletal stiffness Myalgia Pain in extremity Pancreatitis Paraesthesia Somnolence Vision blurred

Symptomtext

Blurred Vision, weakness, sleepy, tingling head, arms and legs. Numbness of limbs at night, increased muscle pain more in the legs, legs stiffness. Stomach discomfort with a later diagnosis of pancreatitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 1/21/22-LYPASE 5,303; AMYLASE 488; ABDOMINAL CT 24/JANUARY/2022- DX. PACREATITIS
Aktuelle Erkrankungen: HBP, FIBROMYALGIA, RADICULOPATHY, THYROID NODULE
Vorgeschichte: HBP, FIBROMYALGIA, RADICULOPATHY, THYROID NODULE
Andere Medikamente: Losartan 25mg, Hydrochlorothiazide
Allergien: Parafon Forte, Migralam, Demerol
Vorherige Impfungen: -

VAERS 2065355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 14.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / -

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

Mobility decreased

Symptomtext

patient said his temperature was 92 degrees and could not get out of bed

Weitere VAERSDATA-Felder

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

VAERS 2062685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: KS
Alter: 31,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 20.12.2021
Beginn: 21.01.2022
Tage bis Beginn: 32,0
Dosis: UNK
Route/Site: SYR / RA

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

Alanine aminotransferase Anion gap increased Asthenia Blood pressure increased Blood test Chest X-ray normal Computerised tomogram normal Dizziness Dysstasia Electrocardiogram normal Fatigue Feeling abnormal Fine motor skill dysfunction Gait disturbance Hypertension Loss of personal independence in daily activities Speech disorder Urine analysis normal

Symptomtext

Friday 1/21: fatigue, weakness, brain fog. Difficulty completing everyday tasks. Saturday 1/22: Weakness, fatigue, brain fog. Sunday 1/23: Weakness, brain fog, dizziness, high blood pressure (172/120), difficulty standing up, walking, talking, and using hands. No treatment, no known cause

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: All 1/23: CT scan: normal EKG: normal Urine: normal Chest x-ray: normal BP: high, 155/100 before leaving for hospital, 172/120 at ED. Blood: anion gap high (15mmol/L), Alanine Aminotransferase low (10U/L)
Aktuelle Erkrankungen: A cold of some sort (not covid, not strep) in early December: sneezing, coughing, headache, fatigue Accidental gluten-ingestion early December
Vorgeschichte: Non-Celiac Gluten Sensitivity Depression PTSD
Andere Medikamente: Prenatal vitamins 3 times a week (I am breastfeeding)
Allergien: Non-Celiac gluten sensitivity Allergic to sensodyne toothpaste
Vorherige Impfungen: -

VAERS 2057372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: PA
Alter: 39,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Blood pressure measurement Headache Heart rate Heart rate increased Hypertension Immunisation

Symptomtext

Elevated heart rate; High blood pressure with a headache; High blood pressure with a headache; Dose received: 3; This is a spontaneous report from a contactable reporter (other healthcare professional). The reporter is the patient. A 39-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 14Jan2022 at 12:00 (Lot number: FE3594) at the age of 39 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Sulfonamide allergy" (unspecified if ongoing), notes: Known allergies: Sulfa. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EL0140; Route of administration: unspecified), for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: EL3246; Route of administration: unspecified), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 14Jan2022 at 12:00, outcome "unknown", described as "Dose received: 3"; HEART RATE INCREASED (non-serious) with onset 15Jan2022, outcome "not recovered", described as "Elevated heart rate"; HYPERTENSION (non-serious), HEADACHE (non-serious) all with onset 15Jan2022, outcome "not recovered", and all described as "High blood pressure with a headache". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of heart rate increased, hypertension and headache. Additional information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20220115; Test Name: Blood pressure; Result Unstructured Data: Test Result:High blood pressure; Test Date: 20220115; Test Name: Heart rate; Result Unstructured Data: Test Result:Elevated heart rate
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy (Known allergies: Sulfa)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057346

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MS
Alter: 74,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 13.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Asthenia Bronchitis Chest discomfort Cough Dizziness Feeling abnormal Headache Heart rate Heart rate irregular Illness Immunisation Pain Pain in extremity Palpitations Tremor

Symptomtext

Pain; Tightness in chest; having pounding and an irregular heartbeat/she could feel it pounding outside of her body; Booster; severe headache; trembling all over; weakness; Dizziness; having pounding and an irregular heartbeat/booster brought it back to a high level; had a weird feeling; she was so sick; it is like if you are coming down with bronchitis; later on a cough loosens; pain is all over caller's legs, arms, and torso and is persisting; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team. The reporter is the patient. A 74 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 13Jan2022 10:08 (Lot number: FE3594) at the age of 74 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetes", start date: 2014 (ongoing); "Immunocompromised" (ongoing); "She has had irregular heartbeat intermittently in the past but it was not serious" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (First dose, lot: EL3249, Route of administration: left arm), administration date: 20Jan2021, when the patient was 73 years old, for COVID-19 Immunization, reaction(s): "did not have any reaction at all"; Bnt162b2 (Second dose, lot: EL9267, Route of administration: left or right arm, doesn't remember which arm), administration date: 10Feb2021, when the patient was 73 years old, for COVID-19 Immunization, reaction(s): "did not have any reaction at all". The following information was reported: IMMUNISATION (medically significant) with onset 13Jan2022 10:08, outcome "unknown", described as "Booster"; HEADACHE (disability) with onset 13Jan2022, outcome "recovered" (14Jan2022), described as "severe headache"; TREMOR (medically significant) with onset 13Jan2022, outcome "recovering", described as "trembling all over"; ASTHENIA (disability) with onset 13Jan2022, outcome "not recovered", described as "weakness"; PAIN (medically significant) with onset 13Jan2022 11:00, outcome "not recovered", described as "Pain"; CHEST DISCOMFORT (medically significant) with onset 13Jan2022 11:00, outcome "recovering", described as "Tightness in chest"; DIZZINESS (disability) with onset 13Jan2022, outcome "recovered" (14Jan2022), described as "Dizziness"; HEART RATE IRREGULAR (medically significant) with onset 13Jan2022, outcome "recovering", described as "having pounding and an irregular heartbeat/booster brought it back to a high level"; PALPITATIONS (medically significant) with onset 13Jan2022 11:00, outcome "recovering", described as "having pounding and an irregular heartbeat/she could feel it pounding outside of her body"; FEELING ABNORMAL (non-serious) with onset 13Jan2022, outcome "unknown", described as "had a weird feeling"; ILLNESS (non-serious) with onset 13Jan2022, outcome "recovering", described as "she was so sick"; BRONCHITIS (non-serious) with onset Jan2022, outcome "unknown", described as "it is like if you are coming down with bronchitis"; COUGH (non-serious) with onset Jan2022, outcome "unknown", described as "later on a cough loosens"; PAIN IN EXTREMITY (non-serious) with onset Jan2022, outcome "not recovered", described as "pain is all over caller's legs, arms, and torso and is persisting". The events "having pounding and an irregular heartbeat/booster brought it back to a high level" and "having pounding and an irregular heartbeat/she could feel it pounding outside of her body" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: heart rate: (13Jan2021) irregular. Clinical Course: The caller reported that her and her husband had the first two Pfizer Covid vaccines, and they were fine. They got the Pfizer booster dose yesterday and they had severe reactions that were terrible, and they still have some residual left today. She was shocked after receiving it because the first two were fine. She stated she has diabetes and was immunocompromised. Due to heart conditions, she was having pounding and an irregular heartbeat. She stated she does not have a heart condition and the vaccine did this to her. She has had irregular heartbeat intermittently in the past, but it was not serious. The booster brought it back to a high level where she could feel it pounding outside of her body. She stated her husbands temperature was higher yesterday and he was very sick also. She stated she went to the ER yesterday but so many people were in there and she was so sick that she could not sit up, so she left to go home and get in bed and did not get seen. She stated she wished she had been seen. She stated it is a little better today. The caller states the Pfizer Comirnaty Covid Vaccine effected the callers nervous system. The caller was trembling all over, heart pounding, severe headache, weakness, and dizziness. The caller was trembling all over. The caller received the booster dose Pfizer Comirnaty Covid Vaccine at 1030 on 13Jan2022 and had a weird feeling 10 or 15 minutes later and at about 1100 on 13Jan2022 the caller had everything, pain, tightness in chest, heart pounding. Heart pounding: The caller could feel heart beating. The caller had irregular beats. The caller clarifies everything advanced and was not all at once, advanced as it got later in the day on 13Jan2022. Caller clarifies severe headache, weakness and dizziness all started on 13Jan2022. Everything the patient had occur began on 13Jan2022.trembling all over: The caller states the trembling all over is still occurring slightly but is not as bad. heart pounding: The caller states the heart pounding continued on until the caller went to sleep at 2200. The heart pounding went away today, 14Jan2022. asks if caller recovered completely or with lasting effects from heart pounding and the caller replies, the caller can still feel heart beating, do not usually feel heartbeat, can still feel somewhat. severe headache: When the caller awoke this morning, 14Jan2022 the severe headache was gone. The caller went to sleep on 13Jan2022 with the headache. The caller has recovered completely. weakness: The caller still has weakness, and it is persisting. dizziness: When the caller awoke this morning, 14Jan2022 the dizziness was gone, and the caller recovered completely. pain: The pain was all over caller legs, arms, and torso and is persisting. tightness in chest: The tightness in chest is still going on. The caller would like to explain that it is like if you are coming down with bronchitis and have a tightness in chest and later on a cough loosens. The tightness in chest is improving. irregular beats: The caller has a stethoscope because the caller was nurse, but the caller has not checked the irregular beats this morning, 14Jan2022 and cannot really say if still ongoing. Seriousness criteria: irregular beats: The caller thought irregular beats was serious, could have been myocarditis is what caller is thinking. No other vaccinations within four weeks prior to the first administration date of the suspect vaccine and no AE(s) following prior vaccinations.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events cannot be totally excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Test Date: 20210113; Test Name: Heart rate; Result Unstructured Data: Test Result:Irregular
Aktuelle Erkrankungen: Diabetes; Immunocompromised
Vorgeschichte: Medical History/Concurrent Conditions: Heartbeats irregular
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2036070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 03.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Arthralgia Condition aggravated Feeling abnormal Headache Product preparation issue Immunisation Poor quality product administered Product preparation error

Symptomtext

mild headache; booster; the vaccine, that they gave me was inactivated because it had been diluted in sterile water instead on normal saline; the vaccine, that they gave me was inactivated because it had been diluted in sterile water instead on normal saline; Shoulder pain; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 43 year-old female patient received bnt162b2 (BNT162B2), administration date 03Jan2022 08:40 (Lot number: FE3594) at the age of 43 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Type 1 diabetes" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE; LANTUS; HUMALOG. Vaccination history included: Bnt162b2 (Dose:1, have the same shoulder pain that I experienced with the first two vaccine), administration date: 21Dec2020, when the patient was 41 years old, for COVID-19 Immunization, reaction(s): "shoulder pain"; Bnt162b2 (Dose:2, have the same shoulder pain that I experienced with the first two vaccine), administration date: 18Jan2021, when the patient was 42 years old, for COVID-19 Immunization, reaction(s): "shoulder pain". The following information was reported: IMMUNISATION (non-serious) with onset 03Jan2022 08:40, outcome "unknown", described as "booster"; PRODUCT PREPARATION ERROR (non-serious), POOR QUALITY PRODUCT ADMINISTERED (non-serious) all with onset 03Jan2022, outcome "unknown" and all described as "the vaccine, that they gave me was inactivated because it had been diluted in sterile water instead on normal saline"; HEADACHE (non-serious) with onset 04Jan2022, outcome "unknown", described as "mild headache"; ARTHRALGIA (non-serious) with onset Jan2022, outcome "unknown", described as "Shoulder pain". Additional Information: The patient stated that she did not receive any vaccination within 4 weeks of the booster COVID-19 Vaccine. No investigation assessment. Consumer (Physician) stated, "I have a question. I am a physician who practices in withheld and I went in yesterday for my booster vaccine and that one fine then I got a call back from the person who had administered it, a nurse practitioner saying that the pharmacy had contacted them. Stating them, that the vaccine, that they gave me was inactivated because it had been diluted in sterile water instead on normal saline and they ask me to come back and re boost and they said, I could to do it to the same day and I declined because I wanted to see if I develop symptoms and I did not have a lot of familiarity with this happening and so, I guess I just wanted to know if diluting with in sterile water versus normal saline truly inactivate the vaccine or is it just a suboptimal vaccine. No treatments. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type 1 diabetes mellitus
Andere Medikamente: LEVOTHYROXINE; LANTUS; HUMALOG
Allergien: -
Vorherige Impfungen: -

VAERS 2036070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 03.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Condition aggravated Feeling abnormal Headache Product preparation issue Immunisation Poor quality product administered Product preparation error

Symptomtext

mild headache; booster; the vaccine, that they gave me was inactivated because it had been diluted in sterile water instead on normal saline; the vaccine, that they gave me was inactivated because it had been diluted in sterile water instead on normal saline; Shoulder pain; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 43 year-old female patient received bnt162b2 (BNT162B2), administration date 03Jan2022 08:40 (Lot number: FE3594) at the age of 43 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Type 1 diabetes" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE; LANTUS; HUMALOG. Vaccination history included: Bnt162b2 (Dose:1, have the same shoulder pain that I experienced with the first two vaccine), administration date: 21Dec2020, when the patient was 41 years old, for COVID-19 Immunization, reaction(s): "shoulder pain"; Bnt162b2 (Dose:2, have the same shoulder pain that I experienced with the first two vaccine), administration date: 18Jan2021, when the patient was 42 years old, for COVID-19 Immunization, reaction(s): "shoulder pain". The following information was reported: IMMUNISATION (non-serious) with onset 03Jan2022 08:40, outcome "unknown", described as "booster"; PRODUCT PREPARATION ERROR (non-serious), POOR QUALITY PRODUCT ADMINISTERED (non-serious) all with onset 03Jan2022, outcome "unknown" and all described as "the vaccine, that they gave me was inactivated because it had been diluted in sterile water instead on normal saline"; HEADACHE (non-serious) with onset 04Jan2022, outcome "unknown", described as "mild headache"; ARTHRALGIA (non-serious) with onset Jan2022, outcome "unknown", described as "Shoulder pain". Additional Information: The patient stated that she did not receive any vaccination within 4 weeks of the booster COVID-19 Vaccine. No investigation assessment. Consumer (Physician) stated, "I have a question. I am a physician who practices in withheld and I went in yesterday for my booster vaccine and that one fine then I got a call back from the person who had administered it, a nurse practitioner saying that the pharmacy had contacted them. Stating them, that the vaccine, that they gave me was inactivated because it had been diluted in sterile water instead on normal saline and they ask me to come back and re boost and they said, I could to do it to the same day and I declined because I wanted to see if I develop symptoms and I did not have a lot of familiarity with this happening and so, I guess I just wanted to know if diluting with in sterile water versus normal saline truly inactivate the vaccine or is it just a suboptimal vaccine. No treatments. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type 1 diabetes mellitus
Andere Medikamente: LEVOTHYROXINE; LANTUS; HUMALOG
Allergien: -
Vorherige Impfungen: -

VAERS 2055528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OR
Alter: 41,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Diarrhoea Dyspnoea Headache Hot flush Hyperhidrosis Pain

Symptomtext

(She started with Moderna) That evening she had hot flashes, started sweating, diarrhea, and a headache. She had body aches overnight which developed into joint pain. She still had symptoms today although they have improved some. (the diarrhea had stopped). She also was short of breath this morning. She has no fever although she started Tylenol for the pain yesterday and continued it today. I advised her to seek medical attention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unkown
Vorgeschichte: Unknown
Andere Medikamente: Lexapro and Prazosin
Allergien: Latex
Vorherige Impfungen: -

VAERS 2054790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 14,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 17.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / -

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

Chest X-ray normal Chest pain Echocardiogram normal Electrocardiogram abnormal Laboratory test normal Troponin increased

Symptomtext

Patient presented to hospital with chest pain that began the morning of 1/20/2022. He recently received his COVID-19 booster vaccine 1/17/2022. EKG was performed in the ER, showed changes concerning for myocarditis. A chest x-ray was performed and did not show any pathology. An ECHO was also obtained and showed adequate cardiac function. Basic labs that were drawn were mostly within normal limits, other than a high troponin level of 9,913 ng/L. The patient was given ibuprofen 400mg Q6H and was monitored overnight.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: EKG with changes concerning for myocarditis. Troponin >9000.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1975464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 48,0
Geschlecht: F
Eingang: 21.01.2022
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

Anxiety Erythema Pruritus Urticaria Asthma Chest discomfort Condition aggravated Feeling hot Flushing

Symptomtext

Itching, all over redness, flushing .severe itching, feeling hot, hives..given 25mg Benadryl by EMT..felt better..but had some chest tightness after and needed to use my rescue inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cold, viral with negative Covid test.
Vorgeschichte: Asthma; DM Type 2; Depression; Anxiety Fibromyalgia; OA.
Andere Medikamente: Topirimate; Montelukast sodium; Lyrica; Pantoprazole; Loratadine; Duloxetine HCL DR; Cyproheptadine ; Atorvastatin; Trazodone; Budesonide Nasal Spray;Saline Nasal Spray; Vitamin C 250mg; Vitamin D3;Women's Multi vitamin; CBD .
Allergien: Keflex Anaphylaxis; Tomatoes moderate allergy; My Dr has my other allergy that possibly caused Cdiff.
Vorherige Impfungen: -

VAERS 2053235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NM
Alter: 42,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chest pain Dyspnoea Hypoaesthesia

Symptomtext

ABOUT 20 MINUTES AFTER ADMINISTRATION OF VACCINE, PATIENT LEFT ARM AND LEG SIZED AND WENT NUMB. SHE ALSO EXPERIENCE SHORTNESS OF BREATH AND CHEST TIGHTNESS/PAIN, AND REQUIRED OXYGE BEFORE PARAMEDICA ARRIVED ON SCENE. PATIENT WAS TAKEN BY AMBULANCE TO THE HOSPITAL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: DIABETES
Vorgeschichte: LONG TERM SIDE EFFECTS FROM COVID
Andere Medikamente: PIOGLITIZONE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2051192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IN
Alter: 31,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 20.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Inflammation Injection site pain Lymphadenopathy Pain Pharyngeal paraesthesia Swelling

Symptomtext

Left arm pain at site Very swollen Lymph nodes, caused inflammation and circulation in left arm Could not hold arm up to stop pain, could not have it down at a normal position without pain Pain was more like build up pressure Took Several days to one week to go down Happened about 12 hours after injection (I did have weird tingling in my throat when I was waiting after the injection was done during my second shot) Seen by doctor, given prescription strength Aleve for swelling and pain It took almost 48-72 hours to feel back to normal and able to function without pain. I could not wear a bra or anything tight or restricting during the time. Extreme tiredness and exhaustion during that time. Booster shot I had same thing happen with arm and lymph nodes, except it did not happen for 48 hours after injection. I had tiredness for the first 24 hours after booster, then swelling kicked in.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: Physical examination was conducted
Aktuelle Erkrankungen: Allergies
Vorgeschichte: Raspatory Allergies IBS PMDD Chronic GERD
Andere Medikamente: I was also doing allergy shots at the time under the care of Dr.. I was a couple months into the 35 week treatment. I am now in the maintenance stage of the shots. I had the same reaction with my booster. ketotifen 0.025% ophthalmic solut
Allergien: Albuterol Sulfate- hives and issues bleeding Tree Nuts- itching in mouth and throat Penicillin Molds
Vorherige Impfungen: -

VAERS 2048055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 42,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 13.12.2021
Beginn: 11.01.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Cough Dyspnoea Nausea SARS-CoV-2 test positive

Symptomtext

cough, short of breath, nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: + COVID test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2046268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

moderat

Staat: FL
Alter: 41,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 09.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Joint injury Limb injury Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 2043391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 86,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 12.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: UN / UN

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

COVID-19 Dyspnoea Hypoxia SARS-CoV-2 test positive

Symptomtext

CHIEF COMPLAINT: Pt tested covid+ 2 days ago. Pt reports room air spo2 88 at home. 84 on room air at triage. Pt denies CP, c/o sob. Spo2 to 90 on 6lpm. HISTORY OF PRESENT ILLNESS: Patient is a 53-year-old male with past medical history significant for hyperlipidemia who presents emergency room with complaints of hypoxia. Patient reports he has been experiencing symptoms for 11 days, tested positive for COVID 2 days ago. States when he was discharged from here he was given a pulse ox to monitor his symptoms at home. States today his oxygen was 88 consistently and he could not bring it up with his breathing exercises. States he does not feel very short of breath but noticed that and thought he should come in. He denies any fever, chills, chest pain, nausea, vomiting, diarrhea, weakness or fatigue. Patient is not currently on any medications for the COVID. Denies any history of asthma, COPD, or seasonal allergies. Patient is not a smoker. Patient has not been vaccinated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Hyperlipidemia
Andere Medikamente: Unknown
Allergien: N/A
Vorherige Impfungen: -

VAERS 2042425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CO
Alter: 24,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 02.01.2022
Beginn: 02.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Dyspnoea Immunisation Pain SARS-CoV-2 test Urticaria

Symptomtext

Hives on arms and legs; Sever Shortness of Breath; Body aches; booster; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 24 year-old female patient (unknown if pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 02Jan2022 05:15 (Lot number: FE3594) at the age of 24 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 (Dose Number: 2, Batch/Lot No: EW0172, Location of injection: Arm Right, Vaccine Administration Time: 09:15 AM), administration date: 29Apr2021, when the patient was 23 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8737, Location of injection: Arm Right, Vaccine Administration Time: 09:45 AM), administration date: 06Apr2021, when the patient was 23 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 02Jan2022 05:15, outcome "unknown", described as "booster"; DYSPNOEA (non-serious) with onset 02Jan2022 17:15, outcome "recovered" (03Jan2022 17:15), described as "Sever Shortness of Breath"; PAIN (non-serious) with onset 02Jan2022 17:15, outcome "recovered" (03Jan2022 17:15), described as "Body aches"; URTICARIA (non-serious) with onset 03Jan2022 05:15, outcome "recovering", described as "Hives on arms and legs". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of dyspnoea, pain. Therapeutic measures were taken as a result of urticaria. Additional information: Patient did not received any other vaccine in four weeks and no other medications in two weeks. Sever shortness of breath and body aches 12 hours after booster lasting 24 hours. Hives on arms and legs 24 hours after booster, only relieved with benydryl. No covid prior vaccination. No known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: PCr; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2039219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: PA
Alter: 50,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 05.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Abdominal pain Abdominal pain upper Appetite disorder EGFR status assay Formication Full blood count normal Gastrointestinal inflammation Liver function test normal Metabolic function test Muscle tightness Neurological examination Oropharyngeal discomfort Paraesthesia Platelet count normal Sleep disorder

Symptomtext

(1/7) 2 days after vaccination, onset of paresthesia like symptoms such as tingling and crawling throughout body, most significant at inner right thigh, right foot at toes, right bicep and forearm, under right eye. Also notable at abdomen. Subsided 4 days after vax with occasional flare-ups. Doctor recommended follow-up with Neurology. (1/9) 4 days after vaccine, abdominal pain accompanied with burning sensation at abdominals. Pain bursts at upper abdominal - upper right to center abdominal. Progressed to worsen 5 days after vax, impacting sleep and diet. Awaken from sharp pains at upper abdominal area. Persistent pain after eating at upper abs - center. Inflammation and tightness at entire abdominal area throughout the day. Much worse at night. Discomfort along digestive track including throat. (1/13) GI doctor diagnosed epigastric pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: CBC W/Auto Diff & PLT, BMP W/EGFR, Liver Hepatic Function Panel - All negative, Neurology - TBD.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Multivitamin
Allergien: -
Vorherige Impfungen: -

VAERS 2038073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NJ
Alter: 34,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Adverse drug reaction Asthma Chest discomfort Condition aggravated Contusion Dyspnoea Dyspnoea exertional Fine motor skill dysfunction Hypoaesthesia Muscular weakness Pain Paraesthesia Sensory loss Tenderness Tremor

Symptomtext

Within 3 hours of receiving the injection on 12/16/2021, I felt "pins and needles" from fingers to shoulder in the vaccinated arm. This briefly extended upwards to include the side of my neck, jaw and cheek on this same side. Although the ?pins and needles? dissipated after 2 hours, I developed numbness from elbow to fingertips, generalized weakness in my wrist and hand, finger tremors and a loss of sensation with impaired fine motor control. A tender area in the middle of my forearm felt bruised, and although the skin in that area showed no difference in color or temperature, I felt a sharp shooting pain whenever the area was touched. I believe these symptoms were neuropathy. By 12/19/2021, the neuropathy disappeared with the exception of the forearm bruise/shooting pain, but I then began to experience chest tightness and shortness of breath which increased in response to minimal exertion and worsened at night. By 12/20/2021, I recognized these symptoms as the same that I had suffered when I had mild childhood asthma (from around age 4 to 19) and had needed to use a rescue inhaler. However, for the past 15 years my asthma has been completely resolved, and prior to the Pfizer vaccine I was a healthy, active, physically fit 34-year-old who enjoyed hiking, aerobics, dancing, etc. without any breathing issues. On 12/20/2021, I had a doctor visit which resulted in a diagnosis "shortness of breath" and "adverse effect of vaccines and biological substances", caused by the Pfizer vaccine, and a prescription for an Albuterol rescue inhaler. I used this rescue inhaler for a week but my breathing difficulties did not improve at all. On 12/27/2021, I had another doctor visit with a pulmonologist who diagnosed me with moderate adult asthma and prescribed Advair Diskus. I began taking Advair that day but by 1/10/2022 I was still suffering from asthma. A second visit with the pulmonologist resulted in a prescription for Trelegy Ellipta, a stronger inhaler for asthma. To this day I am still experiencing asthma that was caused by the first dose of the Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2038006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3594

moderat

Staat: -
Alter: 32,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Eye pain Migraine Photophobia

Symptomtext

12hrs or so after booster was administered, I developed a migraine, strong sensitivity to light, and eye pain when moving my eyes to the far left/right/up/down. The migraine went away within another 12hrs, but the eye pain persisted. It is currently 3 days later and it has gradually lessened, but not resolved. I was not aware that this could be a side effect and have never experienced such a thing after any vaccine, ever in my life, so am reporting it here.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Nickel, kiwi
Vorherige Impfungen: -

VAERS 2037796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: AL
Alter: 46,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 27.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / UN

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

Condition aggravated Oedema peripheral

Symptomtext

Patient had worsening of lower extremity edema 4-5 days after his vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, DM Type 2
Andere Medikamente: Alive multivitamin, protein shakes, Mega-men's multivitamin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2037651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 17,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 09.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Asthenia Burning sensation Feeling abnormal Feeling cold Hypersomnia Immunisation Moaning Movement disorder Muscle discomfort Pain Pyrexia SARS-CoV-2 test Speech disorder Tremor

Symptomtext

shaking with fever this morning/ really bad fevers/ she had a really high fever; shaking with fever this morning; her muscles were so bad; she couldn't move her body or yell at her mother; she couldn't move her body or yell at her mother; moaning in pain; burning hot; she felt so cold even though she already had two blankets on her; her daughter was weak; moaning in pain; she was lost; received her booster dose of the Pfizer COVID Vaccine; doesn't wake up or only wakes up when mother wakes her and gives her water; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 17 year-old female patient received bnt162b2 (BNT162B2), administration date 09Jan2022 (Lot number: FE3594) at the age of 17 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "pseudo seizures" (unspecified if ongoing), notes: she has a history of pseudo seizures. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, LOT: EW0168, Dosage text: injected in her right arm), administration date: 11May2021, when the patient was 17 years old, for COVID-19 Immunization, reaction(s): "Covid-19", "vaccination failure"; Bnt162b2 (Dose 2, LOT: EW0187), administration date: 01Jun2021, when the patient was 17 years old, for COVID-19 Immunization, reaction(s): "Covid-19", "vaccination failure". The following information was reported: HYPERSOMNIA (non-serious) with onset Jan2022, outcome "recovering", described as "doesn't wake up or only wakes up when mother wakes her and gives her water"; PYREXIA (non-serious) with onset 10Jan2022, outcome "recovering", described as "shaking with fever this morning/ really bad fevers/ she had a really high fever"; TREMOR (non-serious) with onset 10Jan2022, outcome "recovering", described as "shaking with fever this morning"; MUSCLE DISCOMFORT (non-serious) with onset 10Jan2022, outcome "recovering", described as "her muscles were so bad"; MOVEMENT DISORDER (non-serious), SPEECH DISORDER (non-serious) all with onset 10Jan2022, outcome "recovering" and all described as "she couldn't move her body or yell at her mother"; MOANING (non-serious), PAIN (non-serious) all with onset 10Jan2022, outcome "recovering" and all described as "moaning in pain"; BURNING SENSATION (non-serious) with onset 10Jan2022, outcome "recovering", described as "burning hot"; FEELING COLD (non-serious) with onset 10Jan2022, outcome "recovering", described as "she felt so cold even though she already had two blankets on her"; ASTHENIA (non-serious) with onset 10Jan2022, outcome "recovering", described as "her daughter was weak"; FEELING ABNORMAL (non-serious) with onset 10Jan2022, outcome "recovering", described as "she was lost"; IMMUNISATION (non-serious) with onset 09Jan2022, outcome "unknown", described as "received her booster dose of the Pfizer COVID Vaccine". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of hypersomnia, pyrexia, tremor, muscle discomfort, movement disorder, speech disorder, moaning, burning sensation, feeling cold, asthenia, pain, feeling abnormal. Additional information: The patient received her booster dose of Pfizer COVID-19 vaccine on 09Jan2022, 9 days after her COVID-19 diagnosis. It was mentioned that yesterday, the patient was fine and had no symptoms, and received the booster dose as advised by the doctor. The reporter thought that the patient should wait 30 days after getting diagnosed with COVID-19 to be able to get the vaccine shot. In the morning of 10Jan2022, the patient was shaking with really high fever, and could not move or even yell at her mother. The patient was burning hot and was so cold even though the patient already had 2 covers of blanket. The patient was literally shaking and was moaning in pain, was lost and was weak. On Jan2022, the patient does not want to wake up and only wakes up when she wanted to drink water. The patient had a history of pseudo-seizures and the patient's mother initially thought that the patient was having an episode but turned out not. It was also reported that the patient's muscles were so bad. The patient's mother was assuming that the booster dose was given too soon but the doctor gave the go signal to do it. The patient's mother was asking what to do and if the booster dose was given too early. The patient received treatment of two Extra Strength Tylenol 500mg as treatment for the events. The patient took two in one time and they were extra strength gel capsules. The patient's symptoms got better and they have been giving the patient a lot of water. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20220101; Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID-19 PCR test; Test Date: 20220101; Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID-19 rapid test; Test Date: 20220109; Test Name: COVID-19 test; Test Result: Negative ; Comments: COVID-19 PCR test; Test Date: 20220109; Test Name: COVID-19 test; Test Result: Negative ; Comments: COVID-19 rapid test
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Seizures (she has a history of pseudo seizures.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2035879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 37,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Abdominal pain upper Headache Migraine Nausea Vomiting

Symptomtext

Later that night and for a week now, I've thrown up and felt nauseated and or had stomach pain. I also had/have headaches and migraines all week. I didn't not have a stomach ache at the time of injection. I also was given a flu shot as well in the left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None, but I have contacted my doctor by message.
Aktuelle Erkrankungen: Sinus infection Upper respiratory virus
Vorgeschichte: IC, anxiety and carpal tunnel in both wrists
Andere Medikamente: Escitalopram 30mg Loratadine 10mg Flonase nasal spray Elderberry with zinc and vitamin C gummy Vitamin D3 gummy Biotin gummy Herbal tea cold care Tylenol
Allergien: Food dyes Bleach Prednisone Certain surgical cleaners Possibly lime/strawberry high acidic fruits
Vorherige Impfungen: -

VAERS 2035543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: VA
Alter: 23,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 11.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Blood creatinine increased Condition aggravated Dyspepsia Face oedema Flank pain Hypertension Nausea Vomiting

Symptomtext

Facial edema, heartburn, nausea and vomiting beginning the morning after the vaccine. Progressively worsened for 3 days until I visited the emergency department and was admitted for acute kidney injury, flank pain, and intractable vomiting with nausea on 12/14. Creatinine was 2.1 at time of admission. Treatment included intravenous saline for the AKI, ondansetron for the nausea, and oxycodone for pain management. I was discharged on 12/17 with a creatinine of 1.6. On 12/18 I visited the emergency department once again with severe hypertension (BP 191/110). I was treated for the hypertension and discharged the same evening.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: Elevated creatinine: 2.1mg/dL on 12/15 Severe hypertension: BP 191/110
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Benadryl
Allergien: -
Vorherige Impfungen: Facial edema and lupus-like symptoms (malar rash, joint pain) following second dose of Moderna Covid-19 vaccine on January 31. S

VAERS 2035517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MS
Alter: 56,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Diarrhoea Feeling abnormal Headache Pain in extremity Palpitations Paraesthesia

Symptomtext

30 minutes after vaccine started feeling bad, headache, tingling in the head, heart was racing and diarrhea. Symptoms lasted all day. Arm hurt for 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: stomach virus a week prior
Vorgeschichte: hypertension, pre diabetic
Andere Medikamente: lisinopril 5mg
Allergien: pollen, pets
Vorherige Impfungen: -

VAERS 2028696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IN
Alter: 25,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

PATIENT REPORTED NUMBNESS/TINGLING SENSATION ON LEFT SIDE OF FACE ABOUT 2 HOURS AFTER VACCINATION. PATIENT FEELS EFFECTS GETTING BETTER 4 HOURS AFTER VACCINATION.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: NONE.
Aktuelle Erkrankungen: NONE.
Vorgeschichte: NONE.
Andere Medikamente: NONE NOTED ON FILE.
Allergien: NONE.
Vorherige Impfungen: -

VAERS 2025943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 29,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 20.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / RA

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

Blood test normal Chest X-ray Chest pain Dizziness Dyspnoea Electrocardiogram Fatigue Fibrin D dimer Full blood count Headache Heart rate abnormal Human chorionic gonadotropin Hypertension Influenza virus test Metabolic function test Musculoskeletal pain Nausea Pain

Symptomtext

12/20/21 got the first dose. 12/29/21 started having chest pain, shortness of breath, pain radiating between shoulder blades, heart rate was bouncing between low 40's and upper 180's, headaches, dizziness, and nausea. 12/31/21 contacted cardiologist due to persistent symptoms and was told to take a Covid test, negative. 1/3/22 contacted cardiologist again due to symptoms not resolving, was told to monitor at home. 1/7/22 cardiologist advised to call PCP to start a work up for a clot. PCP then advised I go to the ER. Went to the ER and was started on IV fluids, had blood work drawn, urine analysis, EKG and an X-Ray. They stated the blood work did not indicate a clot and I was discharged home. 1/10/22 I contacted PCP again for continued chest pain, shortness of breath, exhaustion, racing heart rate, high blood pressure, and pain between my shoulders. Was advised that this may be indicative of a vaccine reaction but he was unsure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 1/7/22 Chest X-Ray, CBC, Troponin, D-Dimer, Urine Analysis, CMP, HCG, Covid/Flu/RSV, and EKG. 1L IV fluids.
Aktuelle Erkrankungen: Fibromyalgia
Vorgeschichte: Fibromyalgia
Andere Medikamente: Tramadol, Savella, Metoprolol, Lunesta
Allergien: N/A
Vorherige Impfungen: -

VAERS 2025905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: AZ
Alter: 45,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 24.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dizziness Dyspnoea Echocardiogram Electrocardiogram Feeling hot Laboratory test normal Palpitations

Symptomtext

Patient reported lightheadedness at the time of vaccination. I did not notice any signs of shortness of breath at the time of vaccination. Today, 1-11-22, he reported that he had an instantaneous warm sensation in his heart and a feeling of heaviness in his chest. He said that since the time he was vaccinated, he has been experiencing palpitations and shortness of breath. A week prior to 1-10-22, patient went to cardiologist. The cardiologist ran an echocardiogram and an EKG. Labs were normal. Patient was admitted to hospital last night, 1-10-22, hospitalist examined patient for myocarditis and patient's heart is healthy and normal. Patient is convinced that he may have developed myocarditis after vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: A week prior to 1-10-22 patient had an echocardiogram and EKG done at cardiologist's office. 1-10-22, patient was seen at the hospital in the evening for an EKG.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 2025203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain Chills Discomfort Dizziness Feeling abnormal Neck pain Neuralgia Pain in extremity Paraesthesia Spinal pain

Symptomtext

Upon getting the vaccine I had the same reaction had I got from receiving the 1st and 2nd dose which was dizziness so I thought noting of it. Then when I got home within a half hour I felt a chill down my spine. I had a shiver go down my spine that felt weird. I had some neck and back pain that felt like spinal pressure. That continued throughout the day on and off. I felt better than I did the first couple of weeks. The pain came and went. I felt discomfort more on some days than other days. Close to the first 5 or 6 days I had felt it the worse. I still feel the lower neck and upper back pain. I also had pain and tingling in my legs. I see an acupuncture to try to help with the pain. When I seen my neurologist they said my immune system started attacking healthy cells and then that affected my nerves. They said that that caused pressure on the nerves. The neurologist said they think I will make a full recovery, but if I don't fell better by next week then I could start getting steriod treatments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Endometriosis
Andere Medikamente: Omega 3 Turmeric Viviscal Ashwangda Iron Vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 2025124

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IN
Alter: 51,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 06.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Mobility decreased Pain in extremity X-ray

Symptomtext

Severe internal arm pain. Reduced mobility in left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: X-ray 01/10/2022. Referred for MRI.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: -
Vorherige Impfungen: -

VAERS 2025006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Hypertension Lip discolouration

Symptomtext

Patient received her 1st Pfizer booster shot and started experiencing anxiety and reported high blood pressure in observation. Vital signs were as follows: 142/90 blood pressure, heart rate 65, respirations 15, SPO2 97%. She did not report any other symptoms at this time. Taken to ambulance truck via paramedics. Next set of vital signs: 190/109 blood pressure, heart rate 63, respirations 18, SPO2 96%. Per patient daughter, she does not have history of high blood pressure. Patient did not look to be in distress, shortness of breath or any chest pain. She had slight discoloring of lips, but talking without distress. Next set of vital signs: 173/86 blood pressure, heart rate 65, respirations 18, SPO2 97%. Educated by patient still sitting without distress and talking to paramedics and her daughter. Next set of vital signs: 164/86 blood pressure, heart rate 65, respirations 18, SPO2 97%. On back of paramedics paper, safety officer listed when family should take her to the ER based on vital signs, if feeling shortness of breath, chest pain or difficulty breathing. Next set of vital signs were: 154/90 blood pressure, heart rate 61, respirations 18, SPO2 97%. Cleared by safety officer to go home and rest over the weekend. Patient left site without any symptoms and feeling safe to go home. Safety officer called patient's daughter on 1/11/2022 to check up on patient and was told family took patient to the ER over the weekend for blood pressure 130/90 but told to go home. She has a PCP appointment this week and will take list of vital signs to MD for review.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Hypothyroidism, not a new diagnosis
Vorgeschichte: None reported by patient or family
Andere Medikamente: None reported by patient
Allergien: Ibuprofen, Benadryl
Vorherige Impfungen: -

VAERS 2023704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IN
Alter: 42,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Axillary pain Breast pain Chest pain Fatigue Headache Muscle spasms Pain in extremity Palpitations Tenderness

Symptomtext

Same day: headache, fatigue, localized arm tenderness Next day: headache, more fatigue, arm pain, sharp pain in left arm pit, heart palpitations, spasm in left chest with pain that wrapped from sternum, under left breast to near shoulder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None. Monitored symptoms due to holiday weekend. Symptoms improved by 80% within 3-4 days.
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety
Andere Medikamente: Seasonale Trazodone Clonazepam Phentermine Bupropion
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2002340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

moderat

Staat: MI
Alter: 55,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dysphagia Dyspnoea Fatigue Hot flush Palpitations Erythema Feeling abnormal Flushing Rash Pruritus Rash erythematous Skin warm Tongue disorder

Symptomtext

Flush, itchy, difficulty swallowing, palpitations, mild dyspnea, fatigue on exertion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Emergency room
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, Iron deficiency, Multinodular goiter,
Andere Medikamente: None
Allergien: Iodinated contrast media, keflex, penicillins, shellfish derived, tree nut
Vorherige Impfungen: -

VAERS 2020856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: WI
Alter: 65,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Paraesthesia oral

Symptomtext

Patient experienced tingling lips 1 hours after first Pfizer injection. Followed up with patient and PCP - Patient took Benadryl and was ok 1 hour after.

Weitere VAERSDATA-Felder

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

VAERS 2019960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 45,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Disturbance in attention Dizziness Dyspnoea Headache Insomnia Nausea Palpitations Vaccine positive rechallenge

Symptomtext

For three weeks, I experienced racing heart, dizziness, nausea, shortness of breath, headaches, trouble focusing and difficulties sleeping. I experienced the same symptoms with the first dose, but with lesser intensity (symptoms went away within a week or so). My primary care suggested over-the-counter medication to help with sleep and to go to urgent care/ER if my heartrate became unbearable. I stayed home and took life tasks extremely slow.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Wheat, dairy and eggs. Adverse reaction to injections such as Novocain.
Vorherige Impfungen: -

VAERS 2019696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MA
Alter: 32,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 12.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / RA

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

Adverse reaction Blister Blood test normal Dyspnoea Electrocardiogram normal Erythema Pain Pain in extremity Palpitations Pruritus Rash

Symptomtext

Covid vaccine 1: rash, blisters, redness, itchy and painful toes 4 days post vaccine. These lasted 2.5 weeks. Treatment: steroid cream prescription, hydrocortisone cream, NSAIDS. No relief. Went away on its own. Heart palpitations: 1 day post vaccine. No treatment. Went away on their own after a few weeks. Covid vaccine 2: same symptoms as above. Covid toes last 3.5 weeks, non receptive to medications. Much worse adverse reaction than first vaccine. Heart palpitations persisted for 2-3 months. Covid booster: same reactions as above. Onsight of covid toes started within 24 hours and are present today 1/9/2022 (booster on 12/10/2021) with no signs of relief an are worse than previous times. Heart palpitations are re-occurring every 2-3 days that take my breathe away. Palpitations are more frequent and tracked manually when occurred due to consistency and pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG for palpitations, blood panel pre-vaccine (1/2021) and post vaccine 1 and 2 and booster done 1/2022. Unremarkable. Normal blood work/panel.
Aktuelle Erkrankungen: NA
Vorgeschichte: NA.
Andere Medikamente: NA - no medications, vitamins, supplements etc.
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2018512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Body temperature Chills Headache Hyperhidrosis Immunisation Myalgia Pyrexia Tremor

Symptomtext

High fever; chills; shaking; headache; muscle aches; sweating; dose received: 3; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Dec2021 (Lot number: FE3594) at the age of 38 years as dose 3 (booster), 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: EL3247, brand=Pfizer), administration date: 09Mar2021, when the patient was 38 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EL3247, brand=Pfizer), administration date: 30Mar2021, when the patient was 38 years old, for Covid-19 immunization. The following information was reported IMMUNISATION (non-serious) with onset 20Dec2021, outcome unknown, described as dose received 3; PYREXIA (non-serious) with onset 21Dec2021, outcome recovered (2021); CHILLS (non-serious) with onset 21Dec2021, outcome recovered (2021); TREMOR (non-serious) with onset 21Dec2021, outcome recovered (2021); HEADACHE (non-serious) with onset 21Dec2021, outcome recovered (2021); MYALGIA (non-serious) with onset 21Dec2021, outcome recovered (2021); HYPERHIDROSIS (non-serious) with onset 21Dec2021, outcome recovered (2021). Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, chills, tremor, headache, myalgia, and hyperhidrosis. The patient did not receive any other vaccines in four weeks. Covid prior vaccination and covid tested post vaccination was reported as no. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Date: 20211221; Test Name: fever; Result Unstructured Data: Test Result: High.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1997329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: RI
Alter: -
Geschlecht: U
Eingang: 08.01.2022
Impfdatum: 16.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / UN

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

Condition aggravated Dysgeusia Immunisation Pruritus

Symptomtext

booster; Today it actually seems to be getting worse; had a "metal taste" in my mouth; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (005570). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administration date 16Dec2021 17:30 (Batch/Lot number: unknown) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Unknown Dose, MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021 17:30, outcome "unknown", described as "booster"; DYSGEUSIA (non-serious) with onset Dec2021, outcome "not recovered", described as "had a "metal taste" in my mouth"; CONDITION AGGRAVATED (non-serious) with onset 16Dec2021, outcome "not recovered", described as "Today it actually seems to be getting worse". The lot number for bnt162b2 was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

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

VAERS 2647054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: VA
Alter: 12,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Palpitations

Symptomtext

Pt experienced heart palpitations after 30 mins from vaccination. Pt examined by Dr. and advise to take 200-400mg of ibuprofen. Also advised to limit activity for today. Pt vitals @ 1501 124/78 77 bpm @ 1511 124/76 81 bpm and @ 1528 114/74 86 bpm. Pt by 1530 felt well and went home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Citrus food allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IA
Alter: 43,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood pressure increased Dyspnoea Oxygen therapy Throat tightness Urticaria

Symptomtext

a little over 2 hours after receiving 2nd COVID vaccine, patient reported feeling like her throat was closing in on her and short of breath. , also developed hives around her neck. patient also developed elevated blood pressures of 160/100 and 180/100, EMT was called and patient taken to ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: vitals overall stable except blood pressure elevated, patient on 4 liters of oxygen
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Albuterol inhaler, alprazolam, vitamin c, buspirone, fiber-caps, cyclobenzaprine, dicyclomine, depo-provera, multivitamin, paroxetine, trazodone
Allergien: Sulfa
Vorherige Impfungen: flu vaccibne

VAERS 2014309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 16,0
Geschlecht: M
Eingang: 07.01.2022
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

Paraesthesia Swelling face

Symptomtext

Patient c/o face tingling. Face swelled significantly. He ended up in the ER. He received Iv steroids and Benadryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Focalin
Allergien: NKA
Vorherige Impfungen: -

VAERS 2012975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: WA
Alter: 38,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Abdominal pain Arthralgia Balance disorder Cough Decreased appetite Discomfort Dizziness Fatigue Headache Myalgia Nausea Pain Palpitations

Symptomtext

Approximately 6 hours after the vaccine injection, symptoms began and then progressed over the next 24 hours: extreme fatigue, headache, body pain (muscles/joints), specifically aching/uncomfortable feelings in my left breast, left arm pit, left side of abdomen and left buttocks, cough (dry/tight), nausea and abdominal cramps, poor appetite, heart palpitations, dizziness, poor balance, achiness behind sternum. 8 days later some symptoms have lessened the following continues: Fatigue is still present, cough (dry/tight), left breast/chest achiness, dull ache behind sternum, mild heart palpitations, occasional nausea and occasional headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Provider notified. No appt or tests were ordered.
Aktuelle Erkrankungen: None. Recovering from Covid-19 (July 2021) illness and recovering from worsened symptoms from 1st Pfizer Vaccine dose.
Vorgeschichte: None
Andere Medikamente: Vitamin C, Vitamin D, Zinc, Colace (as needed), Prenatal Vitamin, Melatonin (new started nightly 12/21/2021), Albuterol (as needed)
Allergien: Clindamycin (c. difficile) and clotrimazole (chest rash)
Vorherige Impfungen: -

VAERS 2011019

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain

Symptomtext

Pt got booster dose on 01/05/2022 at 3 pm. She called today at 4:30 pm complained chest pain and tightness

Weitere VAERSDATA-Felder

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

VAERS 2010745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 27,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test Chest discomfort Chest pain Dyspnoea Laboratory test Spirometry

Symptomtext

Chest pain, tightness in chest, and trouble breathing all through the day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Cardiogram - 1/3/22 Bloodwork - 1/3/22 Spirometry - 1/3/22
Aktuelle Erkrankungen: Asthma - This was controlled and I only used my inhaler every few months.
Vorgeschichte: None
Andere Medikamente: Prescriptions: Truvada Herbal remedies: Apple cider vinegar (1 table spoon), bigelow benefits stress tea (rose blossoms, chamomile, hibiscus, tulsi leaves, licorice root, passionflower, skullcap, natural rose and raspberry flavors, rose hi
Allergien: Morton; causes asthma attacks.
Vorherige Impfungen: -

VAERS 2010066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 38,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood pressure increased Chest pain Physical examination

Symptomtext

Chest/heart pain - stabbing lasting seconds multiple times per day Increased blood pressure I've had low blood pressure my entire life. After the vaccine my blood pressure moved from 93/49 and 86/62 in May 2021 to 136/82 in Jan 2022 following the Pfizer vaccine. Patient has lifetime of low blood pressure. Patient also reports chest pain. For 2.5 weeks following vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Physical exam Jan 2022
Aktuelle Erkrankungen: -
Vorgeschichte: Auto immune Chiari malformation
Andere Medikamente: COQ10 INTRAMAX DHEA Metal free Spray Pregnenolone 150 Vitamin D-K
Allergien: -
Vorherige Impfungen: -

VAERS 2006420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 20,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Condition aggravated Headache Nausea Pain Pyrexia Vomiting

Symptomtext

Extreme chills, head and aches, 101.3 fever, nausea. vomiting. Lasted about 15 hours. Gave tylenol for fever which helped. Visited the ER because of the vomiting and was advised to hydrate and take tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: The second dose of the original covid vaccine (pfizer) at age 20, 5/12/21. Had the similar symptoms without the nausea and vomi

VAERS 2001843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CO
Alter: 57,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 13.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain

Symptomtext

Woke up in the middle of the night with strong chest pain. Considered going to the ER, but the pain subsided within about 10 minutes. No issues since then.

Weitere VAERSDATA-Felder

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

VAERS 2001055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: SC
Alter: 43,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Blood pressure systolic increased Dizziness Dyspnoea Rash Rash erythematous Urticaria

Symptomtext

She was at pharmacy had her 3rd Pfizer booster 3 days ago. She denies problems with the first 2 doses She got her booster and was walking around shopping, and within 15 min she got dizzy. Her dizziness got worse in an hour later. She went home and ate dinner, then 30 min later she felt even worse with severe dizziness and sob, but no angioedema. She called EMS and her Systolic BP was 200s. She got epinephrine and benadryl IV. The EMT noted that she had a bright red rash on her chest. By the time she arrived to the hospital she was feeling better. Arrived to hospital at 1720 with VS: Temp 98.1, HR 110, Resp 18, BP 177/99, O2 98 She was observed in the ED and was feeling better with improving urticarial rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Allergic Rhinitis HTN Bipolar. Prior surgeries: C3-5 diskectomy R lumpectomy 2/2 breast cancer Hysterectomy R hip replacement. She was hospitalized in the past (R hip). Gastroesophageal reflux.
Andere Medikamente: 1 Aleve 220 Mg Caplet SIG: As needed 2 Amlodipine-valsartan 5-320 Mg SIG: nightly 3 Benadryl Allergy 25 Mg Ultratb SIG: As needed 4 Carvedilol 25 Mg Tablet SIG: twice daily 5 Claritin 10 Mg Tablet SIG: daily (alternate with zyrtec) 6 E
Allergien: amoxicillin trihydrate, azithromycin, Betalactams, COVID-19 (SARS-CoV-2) vaccine, Ad26 (Sputnik), erythromycin base, Fish Containing Products, Macrolide Antibiotics, nut - unspecified, Penicillins
Vorherige Impfungen: -

VAERS 1999830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: GA
Alter: 38,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Discomfort Exposure during pregnancy Fatigue Headache Hypertension Pain in extremity Paranasal sinus discomfort Pyrexia SARS-CoV-2 test positive

Symptomtext

It started the first night as a sinus pressure sand Saturday more arm pain, I also had fatigue and low grade fever. On Sunday was the headache and arm pressure. I didn't see my doctor, I just dealt with it. I am now in the hospital due to high blood pressure and I'm pregnant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Covid-19 test, results positive.
Aktuelle Erkrankungen: Nausea and heartburn
Vorgeschichte: Asthma, anxiety, depression, IBS, thyroid, Breast Fibroadenomas, scoliosis.
Andere Medikamente: Prenatal Vitamins, Iron 18MG, Zofran 4MG, Prevacid 20MG 1 daily, Pulmicort inhaler 180MG, baby aspirin 81MG 1 daily.
Allergien: N?A
Vorherige Impfungen: -

VAERS 1999324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 32,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac flutter Chest discomfort Chest pain Dyspnoea Palpitations

Symptomtext

Heart fluttering/palpitations within a couple of hours after second dose. Tightness/pain in chest, mostly left side/center, difficulty breathing/shortness of breath consistent two days following the second dose but got better on the third day. Took Tylenol but did not notice a difference.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Brain aneurysm.
Andere Medikamente: Effexor 75Mg 1x day.
Allergien: -
Vorherige Impfungen: -

VAERS 1998960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: VA
Alter: 38,0
Geschlecht: F
Eingang: 03.01.2022
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: ja Erholt: ja

Hyperventilation Injection site erythema Injection site pain Injection site reaction Myalgia Palpitations Urticaria Vertigo

Symptomtext

heart palpitations, heavy breathing, muscle aches, vertigo, red welt/severe pain at injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: birth control
Allergien: none
Vorherige Impfungen: -

VAERS 1998831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: PA
Alter: 36,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Chest pain Computerised tomogram Dyspnoea Electrocardiogram Fibrin D dimer Heart rate increased Hypertension Lymphadenopathy Pain Pain in extremity Pruritus Urine analysis Urticaria

Symptomtext

I had symptoms the same day as booster and I started to itch, I itching on my scalp and my belly. I had welts on my chest areas. I took a cool shower and took two Benadryl. I went to sleep. I woke up the next morning my cheeks started to get hot and I started to itch more. Wednesday my lymph nodes started to swell in my armpits. I started to have pain. I went to an urgent care. They told me it was normal reaction to the vaccine. I did have high blood pressure. The next day I decided to get sleep. I started to have shortness of breath and my chest was hurting. I went to the ER and my pulse and blood pressure was high. They decided to do a EKG and a urine test. They did a D-dimer to check for blood clot. They also did a CT scan. They did not find a blood clot. Yesterday I started to feel less pain in my arm and my lymph nodes started to go down. I can start to feel a significant difference in my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, CT Scan, Urine Test, D-dimer.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Seasonal Allergies; Dermographia; Clinical Depression; Anxiety
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Previous Pfizer Vaccines (cheeks warm).

VAERS 1998021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NJ
Alter: 70,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Condition aggravated Feeling abnormal Injection site rash Interchange of vaccine products Sensory disturbance

Symptomtext

Upon receiving the Pfizer booster, I had the same reaction which occurred with Moderna vaccine #1 and #2. after 5 minutes I had an unusual sensation in my mouth and throat. I reported this to the staff and all vitals were checked and found to be good. I continued to feel bad, however, I waited for 30 minutes and then headed home. I did so, because this was the third time I had the reaction and I assumed I would make it home. Before leaving, a nurse advised me to take Benedryl as soon as I got home. Just as occurred the previous 2 times, on the ride home I felt worse in my face, eyes and neck. 1 hour after taking the Benadryl, the symptoms subsided and I felt appreciably better. I also had a a mild rash at the injection sight for 2 days, whereas with Moderna, it was hives on the injection arm for 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Chronic undifferentiated connective tissue disease; hypertention; hypothyroidism
Vorgeschichte: Chronic undifferentiated connective tissue disease; hypertention; hypothyroidism
Andere Medikamente: Chlorphen-12 mg allergy pill; plaquenil 200 mg. OD; Cytomel 35 mg. OD, Vitamin B6 50 mg; Ester C 500 mg.
Allergien: Allergy to Augmentin
Vorherige Impfungen: Covid vaccine Moderna

VAERS 1996694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 61,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / -

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

Insomnia Mobility decreased Nodule Pain

Symptomtext

My left arm had big knots in it and I can hardly move it. The pain is so bad that I'm taking massive amounts of Tylenol, ibuprofen, Aleve, and aspirin trying to make it tolerable. I'm also using bengay. I cannot sleep very much for the pain. I'm someone that pain is never an issue. I can put up with most pain and just wait it out, but not this. I've used ice and heat both trying to get some relief, nothing is helping. I don't know what to do at this point. They keep saying it will get better, but it's been over 2 weeks and getting worst each day!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: seizures
Andere Medikamente: Vimpat, Briviact, vitamin D, Metformin
Allergien: doxycycline
Vorherige Impfungen: -

VAERS 1996136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 29.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

C-reactive protein increased Chest discomfort Chest pain Electrocardiogram abnormal Full blood count abnormal Lymphocyte count decreased Troponin I normal

Symptomtext

Chest pain, 4/10 "tight"; started upon waking up the morning of 12/31 - between 36-48hrs post injection. VS stable - normal oxygen and HR no murmurs on exam no reproducible pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG found incidental abnormalities (RSR'), but no sign of heart strain or myocarditis Labs done - Troponin I was normal (<12), CRP slightly elevated at 13, CBC normal except for low absolute lymphocyte count
Aktuelle Erkrankungen: None
Vorgeschichte: h/o rolandic seizures as young child
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1992447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

moderat

Staat: NC
Alter: 32,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Flushing Hyperhidrosis Hypertension Hypoaesthesia Nausea Pruritus Rash Tachycardia

Symptomtext

Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypertension-Severe, Systemic: Nausea-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tachycardia-Mild

Weitere VAERSDATA-Felder

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

VAERS 1992443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

moderat

Staat: CA
Alter: 14,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Tremor

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Shakiness-Mild

Weitere VAERSDATA-Felder

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

VAERS 1983166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Back pain Chills Fatigue Feeling abnormal Hyperhidrosis Illness Interchange of vaccine products Laboratory test normal Mobility decreased Pain Pyrexia Tremor

Symptomtext

12/21/21 11 PM - shaking, chills and sweats, followed by achiness that got worse throughout the night. I took Tylenol, which didn't do much. I had a fever, though I don't know how high, as I was too sick to get out of bed. I was completely incapacitated with severe aches for about 12 hours. After that, I still was not able to function for another 24 hours because I felt so poorly and fatigued. 12/24/21 Developed very sharp and sudden pain on my right side, under the ribcage in front and the back. I went to the ER, where tests did not show anything. Within 6 hours, the pain became intermittent, and finally ended on 12/26 21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: My first two covid shots were Moderna. This booster was Pfizer
Aktuelle Erkrankungen: none
Vorgeschichte: Osteoarthritis GERD
Andere Medikamente: Omeprazole, oxycodone, losartin, sertraline, trazodone, melatonin
Allergien: penicillin, neosporin, polysporin, bacitracin, plastic tape, plastic bandages
Vorherige Impfungen: 2nd Covid shot, Moderna, on 04/20/2021. Very severe aching, chills, fever, nausea, vomiting. Terrible 12 hours, and then the int

VAERS 1982100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: TN
Alter: 70,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 21.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Arrhythmia Asthenia Blood pressure increased Dizziness Electrocardiogram Heart rate increased Myalgia Tremor

Symptomtext

No adverse event at the time of injection, except normal muscle soreness. Early in the morning of 25 December, three and a half days after the injection, at approximately 06:00 hours, just prior to the event, I had experienced some arrhythmia, which usually signals low electrolyte levels; so I took one potassium pill (Klor-Con M20, 1500 mg). immediately after taking the potassium, I began trembling and feeling weak. Suddenly, and without warning, I began shaking violently, and my blood pressure and pulse began to rise rapidly, getting faster and faster, accompanied by severe lightheadedness, as if I were about to lose consciousness. There was no chest pain. I fought the urge to pass out and managed, with difficulty, to call 911 on my mobile phone. By the time the EMTs arrived, the feeling that I was going to pass out had abated somewhat, and my thoughts were not as cloudy, but I was still shaky and weak. I managed to go outside when the ambulance arrived and walk to the ambulance that was parked at the curb. The EMTs took me into the ambulance, where they took my blood pressure (BP) and heart rate (pulse), and did an EKG. My initial BP was, I think, around 197/99, and my pulse was, if I recall correctly, around 125 (slower than it was when the episode began). The EKG was normal. By the time they took my BP, Pulse, and EKG, everything was dropping. When my pulse rate dropped to 90, and my BP had stabilized, they asked if I wanted to go to the hospital to have them examine me, and I said no. After the EMTs left, and I sat down in my home, and I began to feel better. I monitored my blood pressure and pulse. My BP steadily dropped and leveled off at 137/77, with a pulse rate of 79 bpm (beats per minute). At 07:30 hours, I took my regularly scheduled dose of Hydralazine (vasodilator). By 08:30 hours, my BP had dropped to and leveled off at 124/75, with a pulse rate of 72 bpm. My BP remained at 124/75 after the event ended. I am not sure if the event was an adverse effect of the Pfizer COVID-19 vaccine; but I think it was, because I have never had such an event happen to me before. It seems to have caused a depletion of potassium; because after the potassium began to get into my blood stream, the symptoms began to abate. By the time I took the dose of Hydralazine, the symptoms had disappeared, and I felt calm and relaxed. As I said at the beginning of this narrative, there was never any chest pain at all. It was not a heart attack or other heart event, except for the dangerously fast pulse. Today I had another attack of weakness, but my pulse did not exceed 90-95 beats per minute; and the symptoms abated a few minutes after eating two bananas and the potassium from them began to get into my system. The reason why I cannot say for sure that it is caused by the COVID-19 vaccine is because I have a tendency to not eat right at times, and I don't consume enough foods high in electrolytes to keep my electrolytes optimized. When my electrolytes get low, I am usually warned by a couple of arrhythmias, at which point I either eat foods high in electrolytes, like potato, sweet potato, or banana; or I'll take a Klor-con M20 potassium pill. Either of those solutions will begin to act within 20-30 minutes, and will raise my potassium level and stop any symptoms. I also take a magnesium supplement, plus a multivitamin with magnesium, Vitamin A, and B complex. For the two days prior to the event, I had not eaten much, just one meal a day for the two days prior to the event. Whether the low electrolytes was brought on by the vaccine or was just the result of not consuming enough electrolytes, I am not certain. What I am certain of is that I have NEVER had such a severe episode until after I received the Pfizer booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Blood Pressure, Pulse rate, EKG.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure; had Quadruple bypass February 2019.
Andere Medikamente: Armour Thyroid, Amlodipine Besylate, Aspirin (low-dose), Hydralazine (BID); Klor-con M20 Potassium (1500 mg qd) as needed; Magnesium (400 mg qd, as needed); Vitamin D3; MK-7 (Vitamin K2) (100 mcg, qd); One-a-Day Men's 50+ Multivitamin (qd)
Allergien: Cortisone; Iodinated Contrast Medium for CT scan; Benadryl; Raw Celery (not allergic to cooked celery); coriander seeds; Hay fever.
Vorherige Impfungen: -

VAERS 1981034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3594

moderat

Staat: GA
Alter: 16,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Asthenia Dyspnoea Pain in extremity Palpitations

Symptomtext

Within 5 minutes of receiving shot and seated in waiting area patient said his heart began to race and pain was in his upper arm and shoulders. He felt weak. He started trying to catch his breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Nurses on site checked his heart rate and BP. Gave him bottle water. Taken to urgent care where he was continually monitored. Experienced more pain in upper arm.
Aktuelle Erkrankungen: None
Vorgeschichte: Autism/ADHD, asthma, low WBC
Andere Medikamente: None
Allergien: Sulfa, strawberry, raw nuts
Vorherige Impfungen: 4 years old DTap or MMR had a limp after. It's been so long I can't remember. His behavior and moods changed after.

VAERS 1979384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 24.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / -

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

Dizziness Dyspnoea Paraesthesia

Symptomtext

PATIETN FELT DISSNIEY AFTER THE BOOSTER PFIZER DOSE LIGHT HEADED HAD TROBLE BREATHING AND TINGLING IN HIS HANDS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: TOOK HIM TO THE ER VITALS WERE LOW
Aktuelle Erkrankungen: NNE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1976723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CO
Alter: 29,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site paraesthesia Nerve injury Paraesthesia Vertigo

Symptomtext

I started feeling tingling in the arm at vaccination point. Then both arms and legs had the tingling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: I went to the emergency on 12/17/2021. Treatment plan- Doctor thought nerve was irritated. Recommended Tylenol and Meloxicam. No test ran, but scheduled for 12/28/2021 Also, I went to Urgent Care today 12/23/2021 due to symptoms of Vertigo and tingling. Treatment plan-Recommended an MRI No test ran
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Prenatal Vitamins, Meloxicam 15mg 1xday
Allergien: Penicillin, Latex and Ibuprofen
Vorherige Impfungen: Dose 2 - Fever

VAERS 1974725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 23.12.2021
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

Asthma Chest discomfort Chills Condition aggravated Dyspnoea Headache Impaired work ability Lymphadenopathy Pain Pulmonary pain Pyrexia Wheezing

Symptomtext

She got her vaccine, started to have chills and a slight headache but not bad. A few hours later throughout the evening had a low grade fever. Around 8:00 AM had trouble breathing, wheezing, low grade fever and asthma. When she gets sick with her asthma the first thing that happens that her lungs hurt, and hurts when she breaths and tightness. This lasted for the entire day with shortness of breath. She called her doctor and he said to use the inhaler every 3-4 hours, and she did some nebulizer treatments at home. She took them every 4 hours the entire day and started to feel better around 4:00 PM. Her lungs did not hurt anymore and had some relief, but still had some wheezing, and is much improved from yesterday. She called her pulmonologist several times, and her PCP, Dr. trying to get a telehealth apt with her. Her pulmonologist wanted her to go to the ER but with her symptoms and her autoimmune disease she decided to go to the UR but was a 3 hour wait and had to wait in her car so she went home and continued to take her breathing treatments. The treatments started to improve her symptoms and by 10:00 PM she was feeling like herself again and was able to sleep last night. She did have some trouble at 5:00 AM and had to give herself another breathing treatment. Did call her doctor to see if she should take the steroids that she had, but continued with the breathing treatments and is improving. She has some swollen lymph nodes underneath her left arm where she got the vaccine, which she feels is an autoimmune response, but it is something new and painful. She does have an appointment to see her doctor on Monday to make sure that everything is OK. She is a teacher and she has missed 2 days of work due to this response to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No.
Aktuelle Erkrankungen: 2 weeks before she had asthma issues and was given Azithromycin.
Vorgeschichte: Asthma, undifferentiated connective tissue disease.
Andere Medikamente: Advair discus, Spiriva, Albuterol ProAir, Montelukast.
Allergien: Walnuts, Almonds, Pecans. Amoxicillin.
Vorherige Impfungen: -

VAERS 1974352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Dyspnoea Immunisation Pain Pyrexia

Symptomtext

Shortness of breath; Fever; Body aches; Dose received: 3; This is a spontaneous report from a contactable reporter (consumer or other non HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 15Dec2021 (Lot number: FE3594) at the age of 31 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Clear cell renal cell carcinoma" (unspecified if ongoing), notes: Clear cell renal cell carcinoma surgery and "Carcinoma excision" (unspecified if ongoing), notes: Clear cell renal cell carcinoma surgery. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Lot number: EW0161, Anatomical location: Left arm), administration date: 10Apr2021, when the patient was 31 years old, and Bnt162b2 (DOSE 1, SINGLE, Lot number: ER2613, Anatomical location: Left arm), administration date: 20Mar2021, when the patient was 31 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021, outcome "unknown", described as "Dose received: 3"; DYSPNOEA (non-serious) with onset 16Dec2021 at 01:00, outcome "recovering", described as "Shortness of breath"; PYREXIA (non-serious) with onset 16Dec2021 at 01:00, outcome "recovering", described as "Fever"; PAIN (non-serious) with onset 16Dec2021 at 01:00, outcome "recovering", described as "Body aches". Therapeutic measures were not taken as a result of dyspnoea, pyrexia and pain. Additional information: It was unknown whether the patient had any known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Carcinoma excision (Clear cell renal cell carcinoma surgery); Clear cell renal cell carcinoma (Clear cell renal cell carcinoma surgery)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1967642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Haemorrhage Paraesthesia Pruritus Urticaria Hypersensitivity Rash

Symptomtext

"Allergic type of reaction " Internal tingling throughout body, escalated, continued over for 6 days to extreme itchy, hives, rashes all over body, internally and externally. Head, scalp, ears, neck, eyes, arms, feet, hands, abdomen, chest, breasts, back, legs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: General Doctors appointment, Specialist - allergist appointment benadryl, claritin, prednisone,
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Crab, Sea Bass, Dust, Seasonal, Cats
Vorherige Impfungen: -

VAERS 1971479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 43,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Hyperhidrosis Hypotension Lethargy Nausea Paraesthesia Vomiting

Symptomtext

Patient became lethargic but responsive after injection of Pfizer. Patient stating she had a tingling sensation throughout her body. Had nausea and vomiting and diaphoretic. Was taken to cot to lay down and vital signs taken, noticed to be hypotensive.

Weitere VAERSDATA-Felder

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

VAERS 1970972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Hypotension Malaise

Symptomtext

Patient recieved booster and complained of not feeling well. Her blood pressure was low and she was placed in Trendelburg position and hydrated. Patient stated this is common post vaccines and blood work.

Weitere VAERSDATA-Felder

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

VAERS 1968131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NJ
Alter: 36,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Abdominal pain upper Chills Dyspnoea Headache Nausea Pyrexia

Symptomtext

Symtoms: Fever, Chills, Nausea, Headache, Difficulty breathing, severe stomach cramps that feel like severe period cramps. This is 2nd day I am experiencing the symptoms and am really concerned

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: penicilin
Vorherige Impfungen: flu shot

VAERS 1967436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 21.12.2021
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: ja Erholt: nein

Hypoaesthesia oral Oropharyngeal discomfort Paraesthesia oral Pharyngeal paraesthesia Throat irritation

Symptomtext

Patient had numbness of tongue and throat itchiness and tingling. Vitals were taken and additional observation was given without relief. Patient was transferred to ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: Vitals
Aktuelle Erkrankungen: -
Vorgeschichte: atypical neuralgia, shingles
Andere Medikamente: capsaicin, gabapentin, ibuprofen, lidocaine, nortriptyline, pregabalin, loratadine, zoster vaccine, psyllium
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1967396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IN
Alter: 37,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Condition aggravated Fatigue Injection site discomfort Injection site erythema Injection site mass Injection site pain Injection site swelling Limb discomfort Lymphadenopathy Pain Pain in extremity Peripheral swelling Pyrexia Vaccine positive rechallenge

Symptomtext

When I woke up on 12/18/2021 (the day after my booster), I felt very fatigued. As the day went on I developed a very low-grade fever that lasted about 12-14 hours. I had developed a very large, red, swollen lump at the injection site (maybe 3" in diameter) that was very sore to the touch. As the day went on the discomfort at my injection site migrated into my arm and underarm area. The lymph node in my under arm area on my left side also felt swollen. I noticed that I lost some strength in my left arm due to the pain/swelling. Approximately 24 hours after my booster I did experience some body aches (mostly in my left arm and left side of my body). By 12/19/2021 most of the symptoms had subsided and the only remaining side effect was (and continues to be at the time of this submission) discomfort/pain at the injection site and my underarm area. It has decreased in intensity, but it still there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: ibuprofen PM (as needed), Zantac 360 (as needed), Tums (as needed), Tylenol (as needed)
Allergien: None known
Vorherige Impfungen: I had similar side effects (but to a worse degree) with my second Covid 19 vaccination (also Pfizer). I typically have pain/lump

VAERS 1966289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 20,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 16.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / UN

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

Chest pain Troponin increased

Symptomtext

CP with elevated troponin >37,000 being admitted to cardiology team at a local HCF troponin 37,315

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1963855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 32,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / -

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

Chest discomfort Chest pain Dyspnoea

Symptomtext

Shortness of breath, chest pain, chest pressure, Each episode would last for a few hours after activity or pressure on chest.

Weitere VAERSDATA-Felder

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

VAERS 1963742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 56,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Paraesthesia

Symptomtext

Paresthesia in right leg from calf to tips of toes. Went to Emergency Room of the Hospital. No treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: blepharitis, dry eye
Andere Medikamente: none
Allergien: Ampicillin
Vorherige Impfungen: Hearing loss after 2nd dose of Pfizer vaccine administered 5/6/2021. Age at time:56 years.

VAERS 1963227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: VT
Alter: 41,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Cardiac flutter Dizziness Dyspnoea Heart rate increased

Symptomtext

Shortness of breath, rapid heart beat, fluttering heart, mild dizziness. Symptoms seem to be diminishing.

Weitere VAERSDATA-Felder

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

VAERS 1962842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 18.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Burning sensation Condition aggravated Fatigue Fungal infection Headache Myalgia Nausea Pyrexia Urinary tract disorder Urinary tract infection

Symptomtext

Symptoms of UTI and/or yeast infection came back! All of a sudden after spending a day in bed with fever, fatigue, muscle aches, mild headache and nausea. These symptoms were not unexpected or concerning but the burning sensation of a UTI or some other sort of genitourinary problem was strong and shocking. I know these reactions are considered rare so I thought I should add my experience to the reporting. I am currently attempting to self-treat with cranberry, vitamin C, and probiotics (topically-used yogurt). If the symptoms don't clear up in a day or two I will contact my physician.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None yet.
Aktuelle Erkrankungen: I was treated for a UTI successfully, I thought, using antibiotics. I finished those antibiotics a week ago and had not obvious signs of a UTI since.
Vorgeschichte: UTIs and yeast infections have been recurrent since menopause.
Andere Medikamente: Losarton, Xiao Yao Wan
Allergien: Penicillin, Benadryl
Vorherige Impfungen: -

VAERS 1962175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OR
Alter: 37,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 15.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Adverse reaction Blood test Condition aggravated Fatigue Haematuria IgA nephropathy Pain Pyrexia Urine analysis

Symptomtext

After having expected side effects for the first 36 hours, I experienced gross hematuria, increasing body aches, fatigue, fever of 100 degrees. Symptoms were consistent with an IGA Nephropathy flare up. I also experienced a more mild flare up after my second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Urine and blood work was taken the morning of the December 17th after I realized I was having a flare up. Still waiting on results.
Aktuelle Erkrankungen: -
Vorgeschichte: Suspected IGA Nephropathy (No biopsy yet).
Andere Medikamente: Linsinopril 2.5mg/day
Allergien: -
Vorherige Impfungen: 2nd dose of Pfizer-Biontech

VAERS 1962073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OR
Alter: 17,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Chest pain Neck pain Pain

Symptomtext

2nd night after vaccine. Over night Chest pain radiated to neck and left shoulder pain level 5 of 10 - hurts more laying down. Hurts when moved. Hurts when inhaled. Hurts worse when bending forward then inhaling. Hurts more with exertion. This morning pain level 4 of 10. Relieved this morning by taking Pepcid and Tylenol to pain level of 2 then 0. She has no prior history of anything like this. If this reoccurs, worsens or does not improves with Tylenol and Pepcid we will take her to emergency room per what our family physician suggested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None yet.
Aktuelle Erkrankungen: No
Vorgeschichte: None
Andere Medikamente: Claritin daily. Birth Control tablet daily
Allergien: NKA
Vorherige Impfungen: -

VAERS 1955717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: VA
Alter: 51,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Acute cardiac event Angioedema Blood test Dysphonia Electrocardiogram Complement factor C4 Dysphagia Glossodynia Increased upper airway secretion Hypersensitivity Speech disorder Swollen tongue Throat clearing Sinus tachycardia Tongue discomfort Tryptase

Symptomtext

Allergic Reaction (Angioedema of the airway) My tongue got big I had trouble speaking, tongue hurt, Hoarse voice, clearing my throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus tachycardia
Hospital-Tage: -
Labordaten: ECG 12 Lead. Was given Benadryl which through me into a cardiac event, was given Epinephrine, and famotidine, methylprednisolone sodium succinate. Blood tests were performed.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Synthroid 88 MCG
Allergien: Demerol, Morphine, Benadryl
Vorherige Impfungen: -

VAERS 1955717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: VA
Alter: 51,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Acute cardiac event Angioedema Blood test Dysphonia Electrocardiogram Complement factor C4 Dysphagia Glossodynia Increased upper airway secretion Hypersensitivity Speech disorder Swollen tongue Throat clearing Sinus tachycardia Tongue discomfort Tryptase

Symptomtext

Allergic Reaction (Angioedema of the airway) My tongue got big I had trouble speaking, tongue hurt, Hoarse voice, clearing my throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus tachycardia
Hospital-Tage: -
Labordaten: ECG 12 Lead. Was given Benadryl which through me into a cardiac event, was given Epinephrine, and famotidine, methylprednisolone sodium succinate. Blood tests were performed.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Synthroid 88 MCG
Allergien: Demerol, Morphine, Benadryl
Vorherige Impfungen: -

VAERS 1959349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3594

moderat

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Asthenia Condition aggravated Decreased appetite Dizziness Ear pain Fatigue Headache Lymphadenopathy Myalgia Tinnitus

Symptomtext

Swollen lymph nodes in left armpit Crushing continuous headache since then Extreme exhaustion Ear pain Loss of appetite Much worsened tinnitus Mild intermittent dizziness Joint/muscle pain and weakness (whole body)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Migraine
Vorgeschichte: Migraine Chronic fatigue syndrome Hypochromic microcytic anemia
Andere Medikamente: Modafinil Lunesta Thyroid
Allergien: Sulfa
Vorherige Impfungen: Pfizer-first dose- age 49-similar side effects

VAERS 1958816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: PA
Alter: 36,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure increased Chills Dyspnoea Headache Immediate post-injection reaction Palpitations Sensation of foreign body Skin warm Tachycardia Throat tightness

Symptomtext

Patient had an immediate headache, chills, pounding heart, tachycardia. B/P was elevated at 150/94, HR of 124. Pulse ox was good at 100% on room air. Patient then became warm, started taking off blanket, patient felt like something was stuck in her throat and like it was harder to breathe. Said throat felt like it was closing. 911 called and 0.3 mg Epinephrine given. Patient transferred to local hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Pollen Otherwise, unknown
Vorherige Impfungen: -

VAERS 1955806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Headache Myalgia Tremor

Symptomtext

Severe chills, whole body shaking for over an hour, muscle soreness, headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Atorvastatin, Celebrex, Metoprolol, Potassium, Magnesium, Vit D3
Allergien: -
Vorherige Impfungen: -

VAERS 1952948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

moderat

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Headache Hypoaesthesia Nausea

Symptomtext

chest pain, headache , nausea, jaw numbness

Weitere VAERSDATA-Felder

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

VAERS 1952649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Blood glucose normal Chest pain Dyspnoea

Symptomtext

Patient complained of chest pain within 15 minutes of vaccination, pain level 3/10. Heavy breathing. Called mgr/charge nurse. Advised to call paramedics. Pt did not appear to be in distress. Paramedics arrived within 10 minutes. Were not able to get BP because pt reportedly has low BP and difficult to measure. HR=97 Bloodsugar=163 Paramedics took over. Pt refused transport to ER. (Pt is not alone, has 2 people living with her)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Paramedics did assessment of BP, HR and Blood sugar
Aktuelle Erkrankungen: diabetes claimed to have heart disease but not sure what it is
Vorgeschichte: heart condition (unsure of what) diabetes rheumatoid arthritis
Andere Medikamente: insulin, rheumatoid arthritis meds, antidepressants (unsure of which)
Allergien: patient said no
Vorherige Impfungen: -

VAERS 1951860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: KY
Alter: 32,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Pain Pain in extremity Paraesthesia

Symptomtext

Pt returned back to the clinic about 25 minutes after recieving her vaccine complaining of left leg pain that was throbbing and radiating down the back of her leg down to her calf and that her right arm was going to sleep and fingers tingling. Pt denied any chest pain, difficulty breathing or tingling of lower extremity. I assess the patient first by checking Blood pressure in right arm which was 110/67. Pulses in bilaterall lower extremities were hard to palpate but were equally 1+ in PT and DP locations. I instructed patient to call a family member to come and pick her up after confirming she was stable enough at this time. Family came to pick her up and took her belongings where i had already gave them an update over the phone that she would be coming over to be assessed. I walked patient to front door and assisted her into the car. She went to ER down the road to be assessed.

Weitere VAERSDATA-Felder

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

VAERS 1951550

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: UT
Alter: 63,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Chest pain

Symptomtext

Approximately one and one half hour after my injection, I experienced moderate chest pains that lasted approximately 3 - 5 minutes. I have never had chest pains prior to this event. The chest pains subsided and they have not recurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1951538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IA
Alter: 42,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Headache Migraine

Symptomtext

No history of migraine headaches. The day following the shot he started with headache that sounds very muscle contraction-like but by 3 days later had a severe migraine headache that resulted in treatment at a walk-in clinic and then emergency room the following day. Now headache free 1 week later

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Depression
Andere Medikamente: Tramadol
Allergien: None
Vorherige Impfungen: -

VAERS 1951275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IN
Alter: 77,0
Geschlecht: F
Eingang: 15.12.2021
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: unbekannt Erholt: nein

Chest X-ray Cough Dyspnoea Immediate post-injection reaction Oropharyngeal pain SARS-CoV-2 test Sneezing

Symptomtext

Immediately had sore throat, sneezing, cough, shortness of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Quidel Sofia 2 SARS Antigen FIA Nasal swab Chest x ray oredered
Aktuelle Erkrankungen: none
Vorgeschichte: COPD, CAD,OSA,HTN, Gout, Dyslipidemia, Hypothyroidism, Anemia chronic, post menopausal
Andere Medikamente: acyclovir, allopurinol, aspirin, atorvastatin, vitamin d3, flonase nasal spray, hydrodiuril, duoneb, xalatan, levothyroxine, meclizine, olmasartan, fish oil
Allergien: losartan, oxybutynin chloride, irbesartan,
Vorherige Impfungen: -

VAERS 1948424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 14.12.2021
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: ja Erholt: nein

Blood pressure increased Dizziness Pharyngeal paraesthesia Throat tightness

Symptomtext

Patient felt lightheaded after first couple minutes of observation, vitals were normal, after 30 min, patient reported tingling in her throat and closing sensation, blood pressure was increased. Patient never lost consciousness, EMS was called to continue treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pharyngeal paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1945110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 24,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chest pain Computerised tomogram thorax Throat irritation

Symptomtext

Chest pain and a feeling "in her throat".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Pulse ox 99% HR 109 at highest averaging 98 Chest CTA, unlabored, no wheezing. Benadryl 25 mg provided, with relief of symptoms. patient called 2 hours after event indicated resolution of all chest pain, and "feeling in her throat". she denied any SOB, n/v, or any further symptoms.
Aktuelle Erkrankungen: none
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1943141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Bladder dysfunction Dysstasia Mobility decreased

Symptomtext

Started feeling weak at bedtime- woke up- could not move my legs- lost bladder function- had no ability to help myself entire day on 12/12- was able to stand with assistance around 9pm- still very weak in 12/13- when I had 2nd dose- lost function in right leg- took 12 hours before it worked- did not go to Dr or ER- Wanted to wait and see what happened

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Ms, psoriasis, psoriatic arthritis
Vorgeschichte: See above
Andere Medikamente: Ocrevus Infusion q 6 no, Skyrizi injection q 12 wks, Lyrica, dalfampridine, D3, Mg, zinc, backofen
Allergien: None
Vorherige Impfungen: Pfizer- COVID 19

VAERS 1942769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: OH
Alter: 20,0
Geschlecht: F
Eingang: 12.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Headache Nausea Paraesthesia Vomiting

Symptomtext

PATIENT FELT TINGLING IN THE ARM AND HAD A HEADACHE AFTER THE SHOT. PATIENT FELT NAUSEATED AND VOMITTED.

Weitere VAERSDATA-Felder

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

VAERS 1942592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 12.12.2021
Impfdatum: 10.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymphadenopathy Musculoskeletal chest pain Pain in extremity

Symptomtext

Pain in arm and left chest wall with under arm swelling and swollen lymph nodes on morning vaccine + 1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal chest pain
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: N/a
Andere Medikamente: None
Allergien: Ceftin, Ceclor, sensitivity to Latex, some environmental allergies
Vorherige Impfungen: -

VAERS 1942304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: IN
Alter: 92,0
Geschlecht: M
Eingang: 11.12.2021
Impfdatum: 10.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Blood glucose normal Bradycardia Drooling Hyperhidrosis Hypotension Muscular weakness Peripheral coldness Posture abnormal Staring Unresponsive to stimuli

Symptomtext

4:30pm Resident found slouched in chair drooling. Resident was assessed. Resident was found to have no strength to left arm and unable to answer questions or to focus staring straight ahead. Resident was hypotensive and bradycardia BP- 56/32, HR 51. Blood glucose was checked and was 133. Resident was cool to the touch and diaphoretic. 911 was called. Resident taken to local ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: CHRONIC OBSTRUCTIVE PULMONARY DISEASE, UNSPECIFIED, CEREBRAL INFARCTION, UNSPECIFIED, UNSPECIFIED CONVULSIONS, PERMANENT ATRIAL FIBRILLATION, CHRONIC COMBINED SYSTOLIC (CONGESTIVE) AND DIASTOLIC (CONGESTIVE) HEART FAILUREHYPERTENSIVE CHRONIC KIDNEY DISEASE WITH STAGE 1 THROUGH STAGE 4 CHRONIC KIDNEY DISEASE, OR UNSPECIFIED CHRONIC KIDNEY DISEASE, GASTRO-ESOPHAGEAL REFLUX DISEASE WITHOUT ESOPHAGITIS
Andere Medikamente: traMADol HCl Tablet 50 MG, Aspirin Tablet 325 MG, Acetaminophen Tablet, Vitamin B12 Tablet 500 MCG (Cyanocobalamin), Clopidogrel Bisulfate Tablet 75 MG, Atorvastatin Calcium Tablet 40 MG, Magnesium Oxide Tablet 400 MG, levETIRAcetam Tablet
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1937027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

moderat

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 07.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Cardiac flutter Chest pain Heart rate increased Palpitations

Symptomtext

Feelings of having a fast-beating, fluttering, or pounding heart. Starting 12/9/2021. Sudden chest pain happen randomly. According to the public information, this could be the symptom of heart inflammation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: I took 2 tablets Tylenol at 12/8/2021(one 9AM one 11PM), to reduce the fever symptom by getting the Pfizer vaccine.
Allergien: no
Vorherige Impfungen: -

VAERS 1996936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 10.07.2023
Impfdatum: 17.12.2021
Beginn: 28.04.2022
Tage bis Beginn: 132,0
Dosis: 3
Route/Site: - / LA

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

Burning sensation Fatigue Headache Immunisation Vaccination site urticaria Hypothyroidism Obstructive sleep apnoea syndrome Transient ischaemic attack

Symptomtext

G45.9 TRANSIENT CEREBRAL ISCHEMIA 4/28/2023 HYPOTHYROIDISM G47.33 OBSTRUCTIVE SLEEP APNEA 4/28/2023 HYPOTHYROIDISM

Weitere VAERSDATA-Felder

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

VAERS 2613955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 11.04.2022
Beginn: 13.09.2022
Tage bis Beginn: 155,0
Dosis: 4
Route/Site: IM / UN

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

COVID-19 Ear infection Exposure to SARS-CoV-2 Feeling abnormal Influenza virus test Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Streptococcus test

Symptomtext

I woke up with fever and sore throat, generally ickyness; I went to the doctor because my husband has tested positive 2 days before, and they tested for strep throat, flu, covid-19 and I was positive for Covid-19 and I had an ear infection, he prescribed medicine as well and PAXLOVID for the COVID-19. I took it for 7 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 11SEPT2022 COVID-19 test negative; 12SEPT2022 COVID-19 test negative; 13SEPt2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: LO LOESTRIN; omega 3; zinc; biotin; fiber supplement; calcium; vitamin D3; ZYRTEC
Allergien: Penicillin; mold algae's; animal hair; tree nuts.
Vorherige Impfungen: -

VAERS 2606578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MN
Alter: 62,0
Geschlecht: F
Eingang: 30.03.2023
Impfdatum: 26.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain lower Blood test abnormal Computerised tomogram abdomen abnormal Hepatic cyst Lymphadenopathy Staphylococcal infection

Symptomtext

following day lower belly pains started. see medical tests and I relate this issue directly to the vaxx. Pain, blood tests revield staff infection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: 5,0
Labordaten: CT ABD PELVIS W IV -3.7CM CYST IN left hepatic lobe. Few enlarged left iliac lymph nodes. Abnormal findings. Follow up MRI on Monday Feb.,20th 2022
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: hydrochlorothiazide & Citalopram
Allergien: NONE
Vorherige Impfungen: -

VAERS 2597762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: FL
Alter: 63,0
Geschlecht: M
Eingang: 16.03.2023
Impfdatum: 14.12.2021
Beginn: 02.03.2023
Tage bis Beginn: 443,0
Dosis: 3
Route/Site: IM / -

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

Abdominal pain COVID-19 SARS-CoV-2 test positive

Symptomtext

Hospitalization: 2/22/2023 - 3/4/2023 (10 days) Presentation to the ED: abd pain COVID + date: 3/2/2023 Treatment: Zosyn Discharge to: home. EP7534 3/19/2021 ER8735 4/9/2021 FE3594 12/14/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: AFIB, CKD3, CAD, DM, HTN, OBESITY
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2554618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NJ
Alter: 14,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 07.01.2022
Beginn: 01.09.2022
Tage bis Beginn: 237,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Echocardiogram normal Gait inability Juvenile idiopathic arthritis Limb operation Magnetic resonance imaging abnormal Peripheral swelling X-ray

Symptomtext

He was having pain in all his joints. We took him to the doctor for X-rays and he was admitted to the hospital for surgery on his left middle finger. It was so swollen they were concerned about the integrity of his finger. He continues to have issue with his lower extremity joint. He was diagnosed with Juvenile Idiopathic Arthritis. He was hospitalized for about two weeks unable to walk. He was prescribed prednisone, PROTONIX, NAPROSYN, and HUMIRA. He is doing better since starting HUMIRA. He still has issues, but he is able to deal with it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: 12,0
Labordaten: 16DEC2023 MRI Juvenile Idiopathic Arthritis; 31OCT2022 Echocardiogram normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: ADHD; Depression
Andere Medikamente: TEGRETOL; INTUNIV; PROZAC; CONCERTA; DEPLIN; MELATONIN; MULTIVITAMIN; VITAMIN D; vitamin B12; ATARAX
Allergien: Indomethacin
Vorherige Impfungen: -

VAERS 2552652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 30.12.2021
Beginn: 26.11.2022
Tage bis Beginn: 331,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain Acute kidney injury Antipsychotic drug level increased Blood sodium normal COVID-19 Clostridium test negative Computerised tomogram abdomen abnormal Computerised tomogram thorax abnormal Diarrhoea Electrocardiogram QT prolonged Enterocolitis Fluid intake restriction Gallbladder disorder Gastrointestinal disorder Hydrocholecystis Hyponatraemia Ileus Inappropriate antidiuretic hormone secretion

Symptomtext

Patient is a 41 y.o. female patient of Physician No with history of schizoaffective disorder, bipolar disorder and obsessive-compulsive disorder presented to a local Medical Center with diarrhea, found to have acute enterocolitis, hyponatremia and psychosis. Course complicated by Covid 19, AKI and complex discharge planning. Awaiting SNF placement Acute enterocolitis Ileus...resolved With loose stools which have persisted during stay CT abd/pelv on admission with multiple fluid-filled small bowel and colonic loops, nonspecific finding which can be seen with acute enterocolitis CT PE 12/4 concerning for mechanical obstruction Surgery consulted, more consistent with ileus than obstruction Etiology of symptoms believed to be enteritis from covid, appears less likely pancreatitis or acute cholecystitis Stopped clozapine while ileus/obstruction is a concern, has been resumed and generally tolerating Cont regular diet, cont supportive care C-Diff negative, Having daily BMs Metabolic acidosis...resolved Persistent non gap acidosis Started PO bicarb -- continue Possible RTA from Lithium but has not been present in the past Nephrology assessed, ok to cont lithium at lower dose BMP stable 12/16 Hyponatremia....resolved SIADH Pt drinking large amounts of water prior to admission and constantly requesting during admission ADH dependent, probable SIADH, polydipsia may contribute Is on SSRI Cont 2L fluid restriction, given severe thirst would not decrease Cont sodium bicarb on discharge Nephrology assessed, Na upto 141, can liberalize Fluid restriction per nephrology 12/14 Schizoaffective disorder Bipolar disorder Patient presented from a HCF; admitted there for acute psychosis Per BH -no longer meeting inpatient criteria. Stable to DC per BH perspective, Discontinued No AMA Safest disposition is to have her sister pick her up to take her home. Monitoring patient's pill sorter at least weekly would be recommended as well as assisting with making sure she is seeing her outpatient clinic regularly Will need continued clozapine dose titration as opt likely Currently on 150 mg QHS F/u with with Dr at office Covid-19 Virus Infection Date of onset of symptoms: 11/28/2022 Symptoms present on admission: diarrhea Date of covid positive test: 11/29/2022 Vaccination status: unvaccinated Oxygen requirements on admission: RA Current oxygen requirements: RA Special isolation end date: 12/9/2022 Elevated lithium level Lithium elevated at 1.6 on admission, improved to 1.0 Resumed lithium at 450 BID Li level 1.3 (12/3) -- > repeat on 12/5 1.1 Reduce lithium to 300 nightly Gallbladder distention Seen incidentally on CT abd/pelvis on 11/27 Has generalized abd pain, not specifically worse in RUQ LFTs wnl, US with hydropic gallbladder, sludge Discussed with surgery, do not think acute cholecystitis, can follow up for possible chronic issue Elevated lipase Lipase 564 on admission, due to enterocolitis Patient denies abdominal pain, only has diarrhea which is improving CT abd/pelv with unremarkable pancreas Uncertain if pancreatitis contributed, tolerating diet w/o post prandial pain Prolonged QT Qt mildly prolonged BH aware, not able to eliminate all Qt prolonging agents from her psych regimen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 21,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2544559

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 19,0
Geschlecht: M
Eingang: 28.12.2022
Impfdatum: 18.06.2021
Beginn: 23.12.2022
Tage bis Beginn: 553,0
Dosis: 3
Route/Site: IM / -

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

Acute kidney injury Alpha 1 foetoprotein normal Back pain Blood parathyroid hormone normal Blood smear test abnormal Blood thyroid stimulating hormone normal Bone scan abnormal C-reactive protein normal COVID-19 Carbohydrate antigen 19-9 Carcinoembryonic antigen normal Full blood count abnormal Human chorionic gonadotropin negative Leukocytosis Magnetic resonance cholangiopancreatography Magnetic resonance imaging spinal Magnetic resonance imaging thoracic abnormal Metabolic function test normal

Symptomtext

COVID+ 12/23/22. Vaccination status - pfizer x3 BRIEF OVERVIEW: Discharge Provider: PRIVATE MD Primary Care Provider at Discharge: PRIVATE MD Admission Date: 12/23/2022 Discharge Date: 12/24/2022 DISCHARGE DIAGNOSES 1. Vitamin D deficiency 2. Pathologic compression fracture of T6-8 3. COVID -19 4. Leukocytosis - resolved 5. AKI DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: Patient is a 21 y.o. male with no significant past medical history who presented to emergency department on 12/23 with sudden and significant back pain that woke him up at 3:00 a.m. notably, there was no inciting events. He denied recent trauma of any kind as well as prior pain. He does not play any sports. He has not had any recent flu-like symptoms. He denied bowel or bladder incontinence.In the ED his VSS, his CMP returned wnl no protein gap, crp normal, ESR 14, blood cultures drawn, CBC with WBC 19, he was given 1L NS, toradol for back pain. COVID returns positive. He was asymptomatic. He had tenderness to his thoracic spine and weakness of upper extremities. He underwent MRI whole spine, which showed subacute fractures of T6-T8 with <50 vertebral height loss T6, 50% or greater at T7 and T8. Degenerative changes of spine. Neurology and ortho spine consulted in ED and recommended inpatient admission for work up. Further workup is as follows. CT with contrast demonstrated prior mentioned subacute compression fractures of T6-8, as well as hypodensity of the pancreatic head. MRI with MRCP to evaluate this was unremarkable. A scrotal ultrasound demonstrated a small epidermal cyst with no concern for mass. A full bone scan demonstrated only the above-mentioned fractures with no other suspicious for lytic lesions. Initially his complete blood count demonstrated leukocytosis, however, this did resolve after admission. Peripheral smear demonstrated reactive leukocytosis with a left shift. Beta HCG, AFP, CEA CA19-9 were negative. PTH and TSH were normal. Vitamin-D was 9, representing severe deficiency. He was started on 50,000 IU vitamin D weekly, and his painwas well controlled with acetaminophen and a lidocaine patch. NSAID's were avoided during hospitalization due to AKI after contrast. He was given a small bolus of fluids and recommended to follow up with PCP for further monitoring. Ortho Spine was consulted be noted that he did not need a brace, and gave him 10lb lifting restrictions until follow up in the clinic in 2 weeks. Hematology on consulted and recommenced outpatient follow up. He was discharged on 12/24 with instructions to follow up with PCP, Heme/onc, and othro. He was educated on his activity restrictions and instructed to continue the vitamin D, and tylenol/lidocaine and ibuprofen for pain. He, and his parents, were in agreement with the plan and had no questions or concerns at the time of discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: none
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2541968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 68,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 21.12.2021
Beginn: 30.10.2022
Tage bis Beginn: 313,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 Cough Malaise Pain in extremity SARS-CoV-2 test positive

Symptomtext

After receiving the vaccine, I had a sore arm for a day. On 10/28/2022, I went on a trip with some friends. On 10/30/2022, I began to feel sick. My cough was just not getting any better, so I went to my doctor, and I tested positive for COVID-19 on 11/14/2022. I did not receive a prescription, but it was recommended that I isolate for five more days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 14NOV2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis; Diabetic
Andere Medikamente: Vitamin D3; vitamin C; cod liver oil
Allergien: Pineapple
Vorherige Impfungen: -

VAERS 2535350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: FL
Alter: 43,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 14.12.2021
Beginn: 17.10.2022
Tage bis Beginn: 307,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Chills Cough Headache Impaired work ability Nasal congestion Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Wheezing

Symptomtext

I had fever, chills, body aches, headache, nasal congestion, sore throat, coughing, and wheezing. I was off work for around four days. I was treated with TYLENOL, BREO inhaler and prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 at home test result was positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: PROVIGIL; URSODIOL; BREO
Allergien: None
Vorherige Impfungen: -

VAERS 2512929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: PA
Alter: 17,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 18.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Injection site erythema Injection site swelling Pruritus

Symptomtext

Red and swollen at injection site. Itching by 11/21/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Minocycline (acne), L-norest/eth (birth control), Fiber gummies and daily vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2482139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 80,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 14.12.2021
Beginn: 10.10.2022
Tage bis Beginn: 300,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Asymptomatic bacteriuria COVID-19 Diarrhoea SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 2/26/21 (lot # EN6198), 3/26/21 (lot # EP6955), and 12/14/21 (lot # FE3594). On 10/10/22, patient admitted to our inpatient med/surg unit with generalized severe weakness, asymptomatic bacteruria, and diarrhea (all secondary to COVID19 infection). Patient was discharged home on 10/12/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 2,0
Labordaten: COVID status positive 10/10/22.
Aktuelle Erkrankungen: -
Vorgeschichte: history of type 2 diabetes, coronary artery disease, paroxysmal atrial fibrillation, hypertension, diastolic congestive heart failure, restless leg syndrome, and hypercholesterolemia
Andere Medikamente: amlodipine, atorvastatin, carbidopa/levodopa, carvedilol, fluticasone/vilanterol inh, furosemide, glipizide, insulin nph, losartan, pramipexole, spironolactone
Allergien: metformin
Vorherige Impfungen: -

VAERS 2467056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 18,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 30.09.2022
Beginn: 01.10.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Burning sensation Headache Neck pain

Symptomtext

Brief headache when standing up from bent over position (like when I am touching my toes, then stand up). The headache is a burning feeling that lasts a few seconds and radiates from the left-top of my head, down to the lower-left are of my head. It lasts for a few seconds. Pain in left ankle, left wrist, left neck muscle. All these pains are on the left side, which is the same side where I got the shot (left arm). I never had these pains on previous shots. Also, previous shots didn't make me feel bad, but this bivalent shot

Weitere VAERSDATA-Felder

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

VAERS 2450548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 63,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 07.01.2022
Beginn: 14.09.2022
Tage bis Beginn: 250,0
Dosis: 3
Route/Site: SYR / AR

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

Burning sensation Rash erythematous Rash pruritic

Symptomtext

In my 63 yrs I had never been allergic to an antibiotic. Within th past 3 months I have had an allergic reaction to 2 different ones. The most recent being reaction to Amoxicillan. Red, itchy, burning rash all over my body requiring 2 trips to urgent care facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: -
Vorgeschichte: arthritis
Andere Medikamente: -
Allergien: none at time of vaccination
Vorherige Impfungen: -

VAERS 2431141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MN
Alter: 53,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 19.03.2021
Beginn: 28.07.2022
Tage bis Beginn: 496,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

WEAKNESS AND FATIGUE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 4,0
Labordaten: POSITIVE COVID TEST 7/28/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Albuterol, Conc: 2.5 Mg/3 Ml, (Proventil, Ventolin) Inhl Nebulizer Solut Aspirin 81 Mg Oral Enteric Coated Tablet Benzocaine 20 % Mm Liquid Bisacodyl (Dulcolax) 10 Mg Rectal Supp Suppository Carbamide Peroxide 6.5% (Debrox) 6.5 % Otic (Ear) Solution Cholecalciferol, Vitamin D3, 1,250 Mcg (50,000 Unit) Oral Capsule Esomeprazole Magnesium (Nexium) 40 Mg Oral Delayed Release Capsule Famotidine (Pepcid) 10 Mg Oral Tablet Ibuprofen 600 Mg Oral Tablet Lidocaine 5% (Lidoderm) Top Patch Linaclotide 145 Mcg Oral Capsule Loratadine-pseudoephedrine 5-120 Mg Oral Tab Sr 12Hr Methylphenidate Hcl (Ritalin) 20 Mg Oral Tablet Mirabegron (Myrbetriq) 25 Mg Oral Extended Release Tablet 24 Hr Modafinil (Provigil) 200 Mg Oral Tablet Ondansetron (Zofran) 8 Mg Oral Tablet Ondansetron (Zofran) 8 Mg Oral Tablet Oxycodone, Immediate Release, (Roxicodone) 5 Mg Oral Tablet Oxygen Inhl Gas Peg 400-propylene Glycol (Systane Gel) 0.4-0.3 % Opht Drpg Polyethylene Glycol (Miralax) 17 Gram Oral Packet Senna-docusate (Senna-s) 8.6-50 Mg Oral Tablet Simethicone 125 Mg Oral Chewable Tablet Testosterone 20.25 Mg/1.25 Gram (1.62 %) Td Gel Zinc Sulfate 50 Mg Zinc (220 Mg) Oral Cap
Andere Medikamente: Albuterol, Conc: 2.5 Mg/3 Ml, (Proventil, Ventolin) Inhl Nebulizer Solut Aspirin 81 Mg Oral Enteric Coated Tablet Benzocaine 20 % Mm Liquid Bisacodyl (Dulcolax) 10 Mg Rectal Supp Suppository Carbamide Peroxide 6.5% (Debro
Allergien: LATEX
Vorherige Impfungen: -

VAERS 2415967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NJ
Alter: 71,0
Geschlecht: M
Eingang: 19.08.2022
Impfdatum: 26.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Injection site erythema Pain Pain in extremity Pyrexia

Symptomtext

Ackey fever 101.5, very tired big red circle around injection site about 3dia. 5 days 6 day still fever but was not to tired I got out of bed. day 7 I was fine but still had the red circle and arm sore. 3 days later the red was gone and the soreness was less and then went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: high blood pressure and lower back pain
Vorgeschichte: high blood pressure and lower back pain
Andere Medikamente: enalapril 5mg 1xday, gabapentin 600mg 2xdays, French maritime pine bark extract, folic aid, turmeric curcumin, l-arginine, areds 2, Osteo bi-flex, Centrum silver 50+, ubiquinol qh-absorb, tadalafil, diphenhydramine hci 25mg, melatonin
Allergien: penicillin, oranges, tomatoes, chocolate, salt, ragweed
Vorherige Impfungen: -

VAERS 2404722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MA
Alter: 51,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 14.12.2021
Beginn: 15.02.2022
Tage bis Beginn: 63,0
Dosis: 3
Route/Site: IM / UN

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

Amenorrhoea Blood test Chronic spontaneous urticaria

Symptomtext

***First Issue*** Eight months after receiving my booster, I came down with CSU-Chronic Spontaneous Urticaria. After primaries treatment of antihistamine didn?t work primary referred me to Dr. Went through blood workup, medical history and any possible contributing factors. After weeks of being on mega high doses of antihistamine with no relief, Dr started me on Xoliar. After 4 months of injections hives finally subsided. ***Second Issue*** After first Pfizer injection, didn?t have menstrual cycle for 3 months After second Pfizer injection, didn?t have menstrual cycle for 4 months After Pfizer booster injection, didn?t have menstrual cycle for 8 months

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chronic spontaneous urticaria
Hospital-Tage: -
Labordaten: Blood work 4/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Depression/anxiety Hypothyroidism
Andere Medikamente: Trazodone, Nortriptyline, Lamotrigine, Effexor, Levothyroxine, Adderall, Pregabalin, Iron, Multivitamin and Calcium citrate
Allergien: Erythromycin, Flagyl and Bactrum
Vorherige Impfungen: -

VAERS 1958884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Interchange of vaccine products Rash Throat irritation Urticaria

Symptomtext

Hives and scratchy throat. Unknown time course and severity. Pt later had Moderna Booster. No reaction noted at that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Recently on ABX Septra 800-160 BID for unknown infection
Vorgeschichte: PMH: Obesity, neck mass, sialadenitis, DM2, Fatty liver, GERD, HLD, HTN
Andere Medikamente: Medications: None known except Septra DS BID x 7 days starting 12/7/21
Allergien: Allergies: PCN (anaphylaxis), Shellfish(anaphylaxis), Codeine, Metformin
Vorherige Impfungen: -

VAERS 1958884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Interchange of vaccine products Rash Throat irritation Urticaria

Symptomtext

Hives and scratchy throat. Unknown time course and severity. Pt later had Moderna Booster. No reaction noted at that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Recently on ABX Septra 800-160 BID for unknown infection
Vorgeschichte: PMH: Obesity, neck mass, sialadenitis, DM2, Fatty liver, GERD, HLD, HTN
Andere Medikamente: Medications: None known except Septra DS BID x 7 days starting 12/7/21
Allergien: Allergies: PCN (anaphylaxis), Shellfish(anaphylaxis), Codeine, Metformin
Vorherige Impfungen: -

VAERS 2379236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 15.12.2021
Beginn: 20.07.2022
Tage bis Beginn: 217,0
Dosis: 3
Route/Site: UN / UN

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

Chills Cough Myalgia Oropharyngeal pain

Symptomtext

chills, sore throat, cough, myalgias

Weitere VAERSDATA-Felder

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

VAERS 2372772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 29,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 13.01.2022
Beginn: 04.07.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Fatigue SARS-CoV-2 test positive Sinus disorder Vaccine breakthrough infection

Symptomtext

Breakthrough case. Vaccinated 1/13/2022, tested positive on 07/04/2022. Started feeling really exhausted and sinus's were more severe. Haven't fully recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID test.
Aktuelle Erkrankungen: 2 months before vaccine, had a really bad chest cold.
Vorgeschichte: Asthma; severe allergies
Andere Medikamente: Fluticasone; Albuterol HSA Inhaler; Ibuprofen as needed; Allegra; Benadryl; Multivitamin; Vitamin D3; Probiotic; Fish Oil
Allergien: Protean, Propylene Glycol; Nickel; Cobalt; Thiuram mix
Vorherige Impfungen: -

VAERS 2332157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: GA
Alter: 48,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 22.12.2021
Beginn: 07.06.2022
Tage bis Beginn: 167,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Chest discomfort Cough Ear pain Fatigue Headache Laryngitis Malaise Nasopharyngitis Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Sneezing Speech disorder Throat irritation

Symptomtext

On 6/7/2022, I woke up with sore throat, headache, sneezing, and runny nose. I took Tylenol, but the headache persisted. My throat also became scratchy and sore, and I had trouble talking. On 6/8/2022, I had the same symptoms, but I thought that I was just getting a cold. Later that afternoon, I took an at-home test for COVID, and the result was negative. I was very fatigued, but I had just returned from a plane trip, and I thought that might have been the cause. On 6/9/2022 and 6/10/2022, I continued to have the same symptoms, but I also felt like I was getting laryngitis. On 6/10/2022, my headache was gone, but I still had sneezing, runny nose, coughing, and fatigue. The sore throat was getting better, but I began to feel a tightness in my upper chest. I was taking DayQuil, NyQuil, and Robitussin. The symptoms improved with the OTC medications, but they were still present. Around 4 PM that day, I took 2 at-home tests for COVID, and the result was positive both times. I went to an urgent care clinic for further confirmation, and they confirmed that I indeed had COVID. My oxygen level was fine. They gave me benzonatate tablets (200mg). They also offered me an antiviral, but they said that it probably wouldn't help, as I had had symptoms for too long, so I declined. They sent me home and advised me to take care of myself and call them if there were any changes. From 6/10/2022 until 6/18/2022, I isolated from my husband and child at home. I slept and took both OTC medications (Tylenol, DayQuil, Robitussin) and the benzonatate tablets. On 6/14/2022, I noticed I had lost my senses of taste and smell. My other symptoms gradually resolved. On 6/16/2022 and 6/17/2022, I had left inner ear pain. On 6/17/2022, I gradually began to regain my taste and smell. On 6/18/2022, I tested negative and came out of isolation. Since then, I have felt pretty much normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Multiple sclerosis.
Andere Medikamente: Multivitamin, Avonex.
Allergien: Sulfa drugs, Bactrim.
Vorherige Impfungen: -

VAERS 2327602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: GA
Alter: 32,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 21.12.2021
Beginn: 14.06.2022
Tage bis Beginn: 175,0
Dosis: 3
Route/Site: SYR / RA

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

Aphasia Ear discomfort Head discomfort Influenza like illness Lethargy Malaise Oropharyngeal discomfort Pain Pyrexia SARS-CoV-2 test Sinusitis

Symptomtext

On June 14, 2022 he felt like he had a sinus infection. He had congestion in his head, and his ears was bothering him. He felt pressure in his throat. On June 15th his covid symptoms started to get worse. He is still currently sick. He felt like he was having the flu. He was achy and hurting. He had a bad fever on the first night. He took some Tylenol, Advil, and decongestion medicine for it. He had been drinking lot of fluids. He couldn't hardly talk, and he felt lethargic. Today he said he is feeling a lot better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Covid Test- (6/14/2022)
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma, Migraines
Andere Medikamente: Omeprazole, an Anti-Depressant, HFA Ventolin Inhaler
Allergien: Cats, Dogs, Seasonal Allergies, slightly allergic to Latex
Vorherige Impfungen: -

VAERS 2327159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WI
Alter: 23,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 21.12.2021
Beginn: 11.06.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Diarrhoea Ear infection Ear pain Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive Sinus pain

Symptomtext

I woke up with a sore throat, sinus pain, nasal congestion. Over the next couple of days those symptoms got worse and I developed ear pain, a cough, and diarrhea. I went to the doctor on 6/13/2022 because I thought I may have had a sinus and ear infection. I was tested for COVID-19 and it came back positive. I also had an ear infection. I was given antibiotics for my ear infection and instructed to take MUCINEX DM, and TYLENOL as needed. My symptoms lasted for about 9 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: COVID-19 test- positive.
Aktuelle Erkrankungen: Sinus Infection
Vorgeschichte: None
Andere Medikamente: Women's multivitamin; birth control pills; ZYRTEC
Allergien: Dust; pollen; grass
Vorherige Impfungen: -

VAERS 2327103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 83,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 26.01.2021
Beginn: 26.01.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Pain Pain in extremity

Symptomtext

Patient states that she is having soreness in left arm that started with the first dose of Pfizer in Jan 2021. She also received second dose in left arm and second dose seemed to make pain worse. Rates pain 7/10 when using arm but does not bother her at rest. Received third dose in right arm and is also experiencing pain in that arm since dose. Rates pain 4/10. Has not tried anything to relieve the pain at this time but is going to try "muscle rub." States pain seems to be getting worse rather than better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none known
Vorgeschichte: cholesterol
Andere Medikamente: vitamin d, vitamin b, multivitamin, aspirin 81 mg
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2325497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 20.12.2021
Beginn: 09.06.2022
Tage bis Beginn: 171,0
Dosis: 3
Route/Site: SYR / LA

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

Blood pressure increased COVID-19 Cough Dizziness Fatigue Oropharyngeal pain Otorrhoea Paranasal sinus hypersecretion Productive cough Pulmonary congestion Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On June 18, 2022 I noticed that I was having dizziness and drainage from my ears and sinuses. My symptoms started to get worse. I started coughing with chest congestion. June 14th my symptoms were getting better, but I contacted my doctor. I was referred to a clinic. I had a fever of 100.5 degrees, congestion, sore throat, coughing, and my blood pressure was slightly elevated. I had no shortness of breath, diarrhea, or vomiting. I was recommended to do an immunotherapy treatment. I received the bebtelovimab infusion in my home on June 16th at 6:30PM. Since then my symptoms have been getting better. I still have an occasional cough, and sometimes it contains mucus. I still have a little bit of fatigue. I was prescribed a cough pill called benzonatate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Covid Test- negative (6/12/2022) At-Home Covid Test- positive (6/13/2022)
Aktuelle Erkrankungen: none
Vorgeschichte: High Blood Pressure
Andere Medikamente: Amlodipine Desolate, Multivitamin, Vitamin D3, Ultimate Iron.
Allergien: Codeine, Softshell Fish, Lisinopril
Vorherige Impfungen: DDP- It caused me to have temporary paralysis in my right leg when I was a child in the 1970s.

VAERS 2319110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Axillary pain Lymphadenopathy Neck mass Oedema peripheral Tenderness Ultrasound scan abnormal

Symptomtext

Severe swelling in left armpit region the next day. Painful and very tender. Several days later I noticed a swollen lymph node on the left side of my neck. The armpit region swelling reduced after about 5 days. Pain subsided. There is minimal swelling present there to this day. My neck still has an enlarged lymph node (6 cm diameter) today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Ultrasound left in underarmpit region show as normal. Ultrasound on left neck shows mass, with no vasculature.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Birth control Fe
Allergien: No
Vorherige Impfungen: -

VAERS 2318786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 72,0
Geschlecht: M
Eingang: 14.06.2022
Impfdatum: 04.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: SYR / RA

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

Blood glucose increased Blood pressure increased Blood test Dizziness Feeling abnormal Laboratory test abnormal Type 2 diabetes mellitus Urine analysis

Symptomtext

I received my 2nd dose on 01/04/2022 and my adverse event started on 01/25/2022 at around 12:00 I was at the store and I was walking around, I started feeling weird. I was feeling dizzy, I felt like I was out of place. I went home straight and tried to take nap because previous day I went to the gym so I thought it may be it's because of it. After 10 days I got really dizzy and I went to the emergency room. They did all kinds of test and told me everything was up like my blood pressure as well as my glucose was up. After the reports they told me I have severe case of Diabetics type 2. I never had any health problems before I was surprised to know this. In the ER they gave me 2 bags of IV. They prescribed me 20 units of insulin 2x a day and metformin 1000 micrograms 2x a day, and cholesterol medicine 1 a day in the morning. Now I have to take medication for rest of my life. I was in the ER for 4 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Blood test, urine test.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2317313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 33,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Breast pain

Symptomtext

I experienced a pain in my right breast and armpit

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic fatigue syndrome
Andere Medikamente: -
Allergien: Cephalexin
Vorherige Impfungen: -

VAERS 2317145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 10.01.2022
Beginn: 11.02.2022
Tage bis Beginn: 32,0
Dosis: 3
Route/Site: IM / LA

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

Cold urticaria

Symptomtext

Have since been diagnosed with cold urticaria. Break out in hives from exposure to cold. It is ongoining. Instructed to take antihistimines and avoid cold exposure (weather, surfaces, food, etc.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cold urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: recieved the flu shot at the same time as the covid booster
Allergien: -
Vorherige Impfungen: -

VAERS 2294125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MO
Alter: 25,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 18.12.2021
Beginn: 13.05.2022
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: - / LA

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

COVID-19 Cough Drug ineffective Oropharyngeal pain SARS-CoV-2 test

Symptomtext

I tested positive/ I have tested positive on 16May and 17May; I tested positive/ I have tested positive on 16May and 17May; sore throat; cough; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 26-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Dec2021 as dose 3 (booster), single (Lot number: FE3594) at the age of 25 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Tree nuts, reaction(s): "Allergy". Vaccination history included: Covid-19 vaccine (Primary immunization series complete. Manufacturer unknown), for Covid-19 immunization. The following information was reported: COUGH (non-serious) with onset 13May2022 at 14:00, outcome "not recovered"; OROPHARYNGEAL PAIN (non-serious) with onset 13May2022 at 14:00, outcome "not recovered", described as "sore throat"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "I tested positive/ I have tested positive on 16May and 17May". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (08May2022) Negative, notes: testing negative on May 8th, and recovering from my symptoms I tested positive again on May 13th; (13May2022) Positive, notes: testing negative on May 8th, and recovering from my symptoms I tested positive again on May 13th; (16May2022) Positive, notes: Since then I have tested positive on May 16th and May 17th; (17May2022) Positive, notes: Since then I have tested positive on May 16th and May 17th. Therapeutic measures were taken as a result of drug ineffective, covid-19. Therapeutic measures were not taken as a result of oropharyngeal pain, cough. Clinical information: Paxlovid treatment started on 02May2022 till 07May2022 for COVID-19. After taking the Paxlovid, testing negative on 8May, and recovering from her symptoms she tested positive again on 13May and started having a sore throat and cough again on 12May. On 14May she had almost no symptoms besides a minor cough. Since then she had tested positive on 16May and 17May. No other medication in 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Test Date: 20220508; Test Name: COVID; Test Result: Negative ; Comments: testing negative on May 8th, and recovering from my symptoms I tested positive again on May 13th; Test Date: 20220513; Test Name: COVID; Test Result: Positive ; Comments: testing negative on May 8th, and recovering from my symptoms I tested positive again on May 13th; Test Date: 20220516; Test Name: COVID; Test Result: Positive ; Comments: Since then I have tested positive on May 16th and May 17th.; Test Date: 20220517; Test Name: COVID; Test Result: Positive ; Comments: Since then I have tested positive on May 16th and May 17th.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2280473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: PA
Alter: 84,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 11.12.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

COVID-19 Diarrhoea Drug ineffective Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

her husband tested and he was also positive; her husband tested and he was also positive; cold; diarrhea; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). An 84-year-old male patient received BNT162b2 (BNT162B2), on 13Apr2021 as dose 1, single (Lot number: ER8731), on 04May2021 as dose 2, single (Lot number: EW0167) and on 11Dec2021 as dose 3 (booster), single (Lot number: FE3594) at the age of 84 years for covid-19 immunisation. The patient's relevant medical history included: "Stage 4 Kidney Disease has had for years" (ongoing), notes: Continuing: True, Comments: Stage 4 Kidney Disease has had for years; "Diabetes has had for years" (ongoing), notes: Continuing: True, Comments: Diabetes has had for years. 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 "her husband tested and he was also positive"; NASOPHARYNGITIS (non-serious), outcome "unknown", described as "cold"; DIARRHOEA (non-serious), outcome "unknown", described as "diarrhea". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test positive: Positive, notes: tested positive for Covid. Clinical Course: Caller states that she and her husband are in their 80s, states they had Covid at the same time and they took the Paxlovid at the same time and after a couple weeks after that we both started getting severe muscle aches at the same time. Caller wants to know if this from the medication. Caller states the she thinks it is so odd that they both got the muscle aches at exactly the same time. Started Paxlovid on 09Apr2022, ended the treatment on 13Apr2022. States she documented the muscle aches began on 29Apr2022. States they started in the lower back and now they are down into her legs, states it even hurts to get out of bed and getting into the bed is severe and to stand and try to take the first step when she gets out of bed it is severe, states she did get a muscle relaxer prescribed by Dr. (Name withheld) called for a muscle relaxer, states that has not worked, manufacturer is unknown, product was dispensed in a pharmacy vial from pharmacy, NDC LOT and expiration date are unknown, dosage: 500mg tablets, 1 tablet by mouth every six hours as needed, has been trying this since 06May2022 until now and it has not worked. Caller states she has issues with her back, has had them for years and these muscle aches have exacerbated her back issues, this patient is confirmed a female, as documented correctly by the call handler. A clone case was filed for the husband.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Name: Covid; Test Result: Positive ; Comments: tested positive for Covid
Aktuelle Erkrankungen: Chronic kidney disease stage 4 (Continuing: True Comments: Stage 4 Kidney Disease has had for years); Diabetes (Continuing: True Comments: Diabetes has had for years)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2278554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MN
Alter: 38,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 30.12.2021
Beginn: 15.01.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cold sweat Disturbance in attention Fatigue Headache Hot flush Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Somnolence

Symptomtext

01/15/2022 I woke up and felt like I had not slept, I had extreme fatigue, body aches, headache, feverish, alternating hot flashes and cold sweats. Mainly the fatigue and body aches were the main symptoms. I took a home COVID test which was positive. This lasted for a week to 10 days. I then took a couple of more home COVID tests that were negative. I had trouble concentrating for a while after the other symptoms subsided. I started feeling fatigued again last month and felt similar as I did before with COVID. I had body aches and fatigue which lasted a few days. I also have congestion which could be allergies. I am waiting for the results of a COVID PCR test. I now feel 100% again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID tests, negative and positive tests.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Mirtazapine; Buspar; omeprazole; vitamin B complex; vitamin B3
Allergien: None
Vorherige Impfungen: -

VAERS 2278381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 45,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 17.12.2021
Beginn: 01.05.2022
Tage bis Beginn: 135,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Cough Diarrhoea Fatigue Lower respiratory tract congestion Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Upper respiratory tract congestion

Symptomtext

When I caught Covid I had body aches, fever, coughing, sore throat, congestion in my head and chest, fatigue and a little diarrhea. I took OTC cough medicine, sinus decongestion, ibuprofen, and I rested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: At home Covid test negative (5/4/2022). Covid test positive (5/5/2022).
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia; Arthritis; Diverticulitis; Degenerative Disc Disease; HS
Andere Medikamente: Ibuprofen 2400mg; celecoxib 2xday; spironolactone; rifampin; clindamycin; vitamin D 50mg 2xday; multivitamin
Allergien: Slight strawberry allergy
Vorherige Impfungen: Covid vaccine 1st and 2nd dose, I had a reaction where my tongue swelled up. (4/24/2021) & (5/15/2021).

VAERS 2268818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WI
Alter: 85,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 11.01.2022
Beginn: 09.05.2022
Tage bis Beginn: 118,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia COVID-19 Conjunctivitis Cough Feeling abnormal Malaise Myalgia Productive cough Pyrexia Rhinorrhoea SARS-CoV-2 test positive Sinus congestion Sputum discoloured

Symptomtext

Patient began feeling ill approximately the 25th of April. Was tested positive for COVID-19 04/26/2022 via home test. Treated outpatient with Paxlovid which she completed. Felt slightly better after that however shortly after began again feeling worse with increasing cough, weakness, myalgias. Has had fevers at home as well. Admits to some sinus congestion. Has had some drainage from her nose and conjunctivitis. Cough is productive of yellow and green sputum. Has pain but only with coughing. No pleuritic pain or other chest pain. Denies abdominal pain or changes in bowel or bladder. No lower extremity swelling out of the ordinary. Has not required oxygen.

Weitere VAERSDATA-Felder

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

VAERS 2267890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NH
Alter: 47,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 12.12.2021
Beginn: 30.04.2022
Tage bis Beginn: 139,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID-19 on 04/30/2022. I started with a mild sore throat and had it for a couple of days. I was with friends and one of them called and said that they had COVID-19. So, that's when I went and got tested and it was positive. I have a cough, fatigue, running nose and congestion. My symptoms was very mild and lasted for about 6 days. My doctor prescribed Paxlovid 5 days pack. I still have a little fatigue but I am feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 home test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Vitamin D 500mg Iron 20mg Zyrtec 10mg Prozac 10mg Vitamin C 500mg
Allergien: Tree Nuts
Vorherige Impfungen: -

VAERS 2261948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: MA
Alter: 43,0
Geschlecht: M
Eingang: 03.05.2022
Impfdatum: 14.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Hypoaesthesia Inflammation Pain

Symptomtext

After I got the booster shot, the next day from my elbow it feels like I hit my funny bone, it's numb all the time. If I push hard on the funny bone the pain goes all the way down to my left hand. Even picking up a cup of coffee hard I feel the pain at the joint. It feels like it got inflamed and is a constant throbbing pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: no
Vorgeschichte: diabetes type 2
Andere Medikamente: Synjardy XR, IC Lisinopril 10mg tablet
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2258150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: AZ
Alter: -
Geschlecht: U
Eingang: 29.04.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Decreased appetite Fatigue Headache Illness Pain Pyrexia

Symptomtext

Very sick with reaction to all three Covid vaccines; fever; body aches; fatigue; loss of appetite; HA; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 61-year-old patient received BNT162b2 (BNT162B2), as dose 1, single (Lot number: FE3594), in right arm and on 30Apr2021 at 14:00 as dose 2, single (Lot number: EW0172), in right arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Covid-19", start date: Nov2020 (unspecified if ongoing), notes: Had Covid Nov2020 no other illness since; "Hypothyroidism" (ongoing). Concomitant medication(s) included: ASPIRIN 81 oral, start date: 2019 (ongoing); SYNTHROID taken for hypothyroidism, start date: 2017 (ongoing). The following information was reported: ILLNESS (non-serious), outcome "unknown", described as "Very sick with reaction to all three Covid vaccines"; PYREXIA (non-serious), outcome "unknown", described as "fever"; PAIN (non-serious), outcome "unknown", described as "body aches"; FATIGUE (non-serious), outcome "unknown"; DECREASED APPETITE (non-serious), outcome "unknown", described as "loss of appetite"; HEADACHE (non-serious), outcome "unknown", described as "HA". No follow up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hypothyroidism
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Had Covid Nov2020 no other illness since)
Andere Medikamente: ASPIRIN 81; SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 2254591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: KY
Alter: 58,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 13.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Urticaria

Symptomtext

Before the 3rd shot they gave me a steroid and Benadryl and the hives weren't as bad, but they lasted for about 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Breast Cancer
Vorgeschichte: Von Willebrand; Rheumatoid Arthritis;Breast Cancer
Andere Medikamente: Alprazolam Baclofen Celebrex Cranberry Folic Acid Gabapentin Nexium Rinvoq Vitamin D Letrozole Oxybutynin
Allergien: Bee's; Blood Thinners
Vorherige Impfungen: I broke out in hives after a Hepatitis B vaccine years ago.

VAERS 2241183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IL
Alter: 65,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 30.12.2021
Beginn: 11.01.2022
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / LA

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

Erythema Pruritus Rash Skin exfoliation

Symptomtext

Skin rash with redness, scaling, itching in multiple locations (arms, back, legs, etc.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Visual inspection
Aktuelle Erkrankungen: None
Vorgeschichte: GERD, benign prostatic hyperplasia, Environmental allergies (pollen, pet dander)
Andere Medikamente: Omeprazole, dustasteride, Tamsulosin, Atorvastatin, azelastine, famotadine, multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2240786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: FL
Alter: 60,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Fall Fatigue Malaise Pain in extremity Pyrexia Vertigo Vision blurred

Symptomtext

After the booster, I have been dizzy and I have been falling a lot. I also have vertigo often. I have also been having blurry vision today. I was sick for 3 1/2 days with a fever, chills, fatigue and a sore arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None at this time. I'm getting them done soon.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism; Osteoarthritis; Asthma
Andere Medikamente: Synthroid; Meloxicam; Singulair; B-12 Complex; Vitamin D3; Magnesium; Claritin
Allergien: Cipro; Latex; Anesthesia; Environmental Allergies; Gluten; Soy; Dairy; Citrus Foods
Vorherige Impfungen: -

VAERS 2225876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 11.04.2022
Impfdatum: 19.12.2021
Beginn: 29.01.2022
Tage bis Beginn: 41,0
Dosis: 3
Route/Site: - / -

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

Encephalopathy Pain in extremity

Symptomtext

ED/Hospitalization within 6 weeks of receiving COVID vaccination. ED visit 1/23/22 for right calf pain. Hospitalization 1/29/22 for Acute encephalopathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2220147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 29.12.2021
Beginn: 30.03.2022
Tage bis Beginn: 91,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Decreased appetite Fatigue Nasal congestion Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Somnolence

Symptomtext

I developed symptoms of runny/stuffy nose, sore throat. Then I was tired and fatigued. On April 1 I had a positive COVID-19 test. I slept 20 hours a day, lose of appetite, exhaustion, and coughing. I feel it could have been worse if not vaccinated. I called my doctor and they advised me to isolate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Positive COVID-19 test.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; OTC Allergy medicine
Allergien: Gluten
Vorherige Impfungen: -

VAERS 2216006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 05.04.2022
Impfdatum: 23.02.2022
Beginn: 28.02.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: SYR / RA

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

Anxiety Decreased appetite Ear pain Insomnia Nervous system disorder Panic attack Tinnitus

Symptomtext

Severe tinnitus developed after booster shot. It's been over a month now and my entire nervous system is shot. I can't sleep, loss of appetite, ear pain, anxiety, panic attacks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: 4/4/22- Audiology exam revealed no extreme hearing loss but ENT Doctor diagnosed with Tinnitus and said it's likely permanent?? I have never had this before in my entire life nor any health issues whatsoever aside from slightly high cholesterol.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Ampicillan
Vorherige Impfungen: -

VAERS 2214896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: PR
Alter: 35,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 18.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Mechanical urticaria Physical examination Urticaria

Symptomtext

Generalized urticaria that later evolved into dermographism. From the start date to the date of this report the patient has to take a 10mg ZYRTEC every 24 hours because otherwise the symptoms return.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Physical exam
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Multivitamins.
Allergien: None
Vorherige Impfungen: -

VAERS 2213958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NE
Alter: 71,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 31.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Cataract operation Computerised tomogram Fatigue Oxygen saturation decreased Pulmonary fibrosis Scan with contrast Ultrasound scan Visual impairment

Symptomtext

Vaccine in March and then it was spring and I discovered that I couldn't mow my yard - had to stop and rest. Probably all smoking related. I went to cardiologist for heart check and had an ultrasound to check my circulation check. Pulmonologist said I was breathing at 70%. At end of the summer I had to have CT scan because they thought I had a blood clot on my lungs. Scarring on my lungs and they said was to Covid scarring- but I never tested positive. Couldn't get a pair of glasses to work - I continued to have issues with vision. Cataract surgery in January 2022. August Pulmonologist August Cardiologist

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: CT Scan with contrast, Blood work
Aktuelle Erkrankungen: None
Vorgeschichte: COPD, Emphysema
Andere Medikamente: Levothyroxine, Rosuvastatin, Calcium, Vitamin C, NyQuil
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2209361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NV
Alter: 73,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain Injection site swelling

Symptomtext

I got my Pfizer booster on the afternoon of 12/15/2021. In the early hours of the following morning, I woke up to pain and extreme swelling at the injection site. The swelling gradually got worse until it reached the size of a tennis ball. The swelling remained afterwards, but the pain finally subsided about 2 weeks later. In saw my PCP, in January 2022, because the swelling was still present. He immediately knew what it was and used medical terminology when diagnosing the issue, but I don't remember the name of the condition. He recommended that I apply ice to the area, which I did. At the time of this writing, the swelling still remains, though it is improving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Type I Diabetes; COPD.
Andere Medikamente: Insulin; Metoprolol; Furosemide; Losartan; Aspirin (81mg).
Allergien: Sulfa drugs; Penicillin.
Vorherige Impfungen: -

VAERS 2209148

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 31.03.2022
Impfdatum: 28.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Laboratory test abnormal Liver function test increased Pain in extremity

Symptomtext

I started getting symptoms that came on quickly with joint pain that started in shoulders. Either one side or the other but never both sides at once. The pain would go to my elbows and hands. It felt like a fracture. I went to my PCP and had lab work. This was an usual symptom for me. The lab work indicated that my HMH and liver functions were elevated. I am still in the process of follow up testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Lab tests.
Aktuelle Erkrankungen: -
Vorgeschichte: Narcolepsy; Bilateral knee replacement; Osteoarthritis
Andere Medikamente: Concerta; Claritin; Multivitamins
Allergien: Sulfa; Omnicef
Vorherige Impfungen: -

VAERS 2206939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OR
Alter: 40,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 14.12.2021
Beginn: 26.03.2022
Tage bis Beginn: 102,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Dysphonia Fatigue Irritability Lymph node pain Nasal congestion Oropharyngeal pain Paranasal sinus discomfort Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sinus pain Sneezing

Symptomtext

I began with to be hoarse March 26th and slept normal. But then the next day I woke up with a sore throat. A bit of stuffiness, but that is kind of typical for me because it is always dry here. As it progressed my throat began to more sore and some sinus pressure beginning. That evening it started to become more severe congestion. What was notable that day and the next day, I sneezed a few times. My lymph nodes on both sides are still tender today. As the days followed my throat began to feel better but all other symptoms fluctuated. Nasal draining from both sides now, before it was only one side. It has been tough to blow my nose due to congestion. (I have had surgery for deviated septum). As of today I have been feeling pretty better. Monday and Tuesday I was fatigued and irritable and had lots of sinus pain and pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID 19 test, nose swab, positive for COVID 19 rapid.
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine headaches: ADHD
Andere Medikamente: Prefer to keep this information private.
Allergien: None
Vorherige Impfungen: -

VAERS 2198287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WI
Alter: 73,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / -

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

Fatigue Pain in extremity Tenderness

Symptomtext

Very tired; I slept all day the day after receiving shot; The booster made my arm quite achey and tendor for about a week; The booster made my arm quite achey and tendor for about a week; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm, administration date 21Dec2021 (Lot number: FE3594) at the age of 73 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "thyroid function decreased" (ongoing), notes: thyroid function decreased; "mild high cholesterol" (ongoing), notes: mild high cholesterol. Concomitant medication(s) included: LEVOTHYROXIN taken for hypothyroidism (ongoing); ATORVASTATIN taken for blood cholesterol increased (ongoing). Vaccination history included: Bnt162b2 (Dose:1, Anatomical site of injection: arm, route of administration: intramuscular, Batch/lot number: EN6202, Vey tired), administration date: 27Feb2021, when the patient was 72 years old, for COVID-19 Immunization, reaction(s): "Tired", "Dizzy", "Afraid", "Slept all day"; Bnt162b2 (Dose:2, Anatomical site of injection: arm, route of administration: intramuscular, Batch/lot number:ER2613, Slept all day), administration date: 20Mar2021, when the patient was 72 years old, for COVID-19 Immunization, reaction(s): "Slept all day", "Tired". The following information was reported: FATIGUE (non-serious), outcome "unknown", described as "Very tired"; FATIGUE (non-serious) with onset 22Dec2021, outcome "unknown", described as "I slept all day the day after receiving shot"; PAIN IN EXTREMITY (non-serious), TENDERNESS (non-serious), outcome "recovered" and all described as "The booster made my arm quite achey and tendor for about a week". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: High cholesterol (mild high cholesterol); Thyroid function decreased (thyroid function decreased)
Vorgeschichte: -
Andere Medikamente: LEVOTHYROXIN; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2188964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CT
Alter: -
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 22.12.2021
Beginn: 07.01.2022
Tage bis Beginn: 16,0
Dosis: UNK
Route/Site: - / -

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

Angiogram Blood test Computerised tomogram Dizziness Electroencephalogram Headache Magnetic resonance imaging Pain assessment

Symptomtext

Light headedness; Headache/stabbing pain at the front of her head near her temples; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 17 year-old female patient received bnt162b2 (BNT162B2), administration date 22Dec2021 (Lot number: FE3594) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose: Unknown, MANUFACTURER UNKNOWN), for Covid-19 immunization. The following information was reported: DIZZINESS (non-serious) with onset 07Jan2022, outcome "not recovered", described as "Light headedness"; HEADACHE (non-serious) with onset 07Jan2022, outcome "not recovered", described as "Headache/stabbing pain at the front of her head near her temples". The events "light headedness" and "headache/stabbing pain at the front of her head near her temples" were evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache. Additional Information: It was reported that, her 17-year-old daughter received the Pfizer Covid19 Booster shot on 22Dec2021, 2 weeks later her daughter developed headache, light headedness which is intermittent at the beginning then progressed to constant headache. It described as stabbing pain at the front of her head near her temples. it only improves slightly for few hours and then it will go back to intense pain. It was also stated, they were seen 2 neurologists, they were in the emergency room twice, they had multiple testing done. Upon follow-up (16Feb2022) Updated information Included: Reporter address, Lab Test, Dosage Regimens (Lot Number), Event onset Date. It was reported that, it started 7Jan2022 and by 27Jan2022 has not left. States she has had CT, MRI and MRA and just did last night an overnight EEG that they don't have the results for. She relays the pain is the front of her head near her temples and it was a stabbing pain. States it was a 4 when she takes some meloxicam medication and a couple hours later is back to a 7 or 8. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Name: MRA; Result Unstructured Data: Test Result:Unknown results; Comments: More information available (Y/N): No; Test Name: Multiple testing; Result Unstructured Data: Test Result:Unknown results; Test Name: CT; Result Unstructured Data: Test Result:Unknown results; Comments: More information available (Y/N): No; Test Name: overnight EEG; Result Unstructured Data: Test Result:Unknown results; Comments: More information available (Y/N): No; Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Comments: More information available (Y/N): No; Test Date: 2022; Test Name: pain; Result Unstructured Data: Test Result:4; Comments: when she takes some meloxicam medication and a couple hours later is back to a 7 or 8
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2188906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MN
Alter: 42,0
Geschlecht: F
Eingang: 19.03.2022
Impfdatum: 18.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Arthralgia

Symptomtext

have the same shoulder pain that I experienced with the first two vaccine, very similar; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 42 year-old female patient received bnt162b2 (BNT162B2), administration date 18Jan2021 (Lot number: FE3594) at the age of 42 years as dose 2, single and administration date 21Dec2020 (Batch/Lot number: unknown) as dose 1, single for covid-19 immunisation. Relevant medical history included: "Type 1 diabetes" (unspecified if ongoing), notes: Verbatim: Type 1 diabetes. The patient's concomitant medications were not reported. The following information was reported: ARTHRALGIA (non-serious), outcome "unknown", described as "have the same shoulder pain that I experienced with the first two vaccine, very similar". Additional information: Consumer was informed about Pfizer. Consumer was informed about Information department. Consumer was provided with Information department contact information. When probed if patient has received the Pfizer COVID-19 Booster Shot: Consumer stated, "Correct." Consumer stated, "I have the Lot number." Consumer stated, "I would not be surprised. It is definitely noticeable shoulder pain so it lead me to believe that I got something." Laboratory tests were none. Investigation Assessment: No No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected. Follow-up (17Feb2022): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type 1 diabetes mellitus (Verbatim: Type 1 diabetes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2187697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 48,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 23.03.2021
Beginn: 31.03.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Diarrhoea Dizziness Fatigue Flushing Injection site discomfort Injection site erythema Injection site rash Injection site swelling Injection site warmth Interchange of vaccine products Malaise Nausea SARS-CoV-2 test negative

Symptomtext

Initially on March 31 (one week after the vaccine) I had some redness around the injection site but that resolved within a few days. Then on April 3rd (11 days following the COVID vaccine), I felt very sick. I had chills, nausea, felt very fatigued. Later that day I was feeling very flushed and had diarrhea and felt like I was going to pass out. This happened throughout the afternoon. Symptoms improved by that evening. The following day I had similar symptoms but they were more mild. I had no measured fever at home during this time. My symptoms completely resolved by 4/5/21. On 4/6/21 a new rash started on my left arm around the injection site. It was very warm to touch, uncomfortable but not painful. Red area is increasing in size and it is raised around the edges. No fevers or chills. I went to the doctor on 4/6 for my symptoms. She prescribed Cephalaxin (Keflex) and ordered a Covid test for me, which was negative. This description was taken mainly from that after-visit summary.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Covid test on 4/6/2021 was negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid, wellbutrin, omeprazole, acyclovir
Allergien: None
Vorherige Impfungen: -

VAERS 2183792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IL
Alter: 40,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 13.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: - / LA

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

Vaccination site erythema Vaccination site pain Vaccination site pruritus Vaccination site swelling Vaccination site warmth

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient.A 40 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Jan2022 (Lot number: FE3594) at the age of 40 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "asthma" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION SITE SWELLING (non-serious) with onset 19Jan2022, outcome "not recovered", described as "hump at injection site"; VACCINATION SITE WARMTH (non-serious) with onset 19Jan2022, outcome "not recovered", described as "injection site very warm to touch"; VACCINATION SITE PRURITUS (non-serious) with onset 19Jan2022, outcome "not recovered", described as "injection site very itchy down to the mid arm"; VACCINATION SITE ERYTHEMA (non-serious) with onset 19Jan2022, outcome "not recovered", described as "injection site red"; VACCINATION SITE PAIN (non-serious) with onset 19Jan2022, outcome "not recovered", described as "injection site tenderness pain". Therapeutic measures were not taken as a result of vaccination site swelling, vaccination site warmth, vaccination site pruritus, vaccination site erythema, vaccination site pain. Additional information: The patient was not received any other vaccines within 4 weeks prior to the COVID vaccine. Event reported as hump at injection site, site very warm to touch very itchy down to the mid arm red tenderness pain. Prior to vaccination, the patient was not diagnosed with COVID- 19. Since the vaccination, the patient was not tested for COVID-19.No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2183770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: GA
Alter: 70,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 10.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Decreased appetite Feeling abnormal Gastric disorder Lethargy Lymphadenopathy Peripheral swelling Pyrexia SARS-CoV-2 test Swelling of eyelid Toothache X-ray

Symptomtext

her lymph nodes were a little swollen on that side of her face; Lethargy; brain fog; felt like somebody punched her in the stomach; right eyelid was drooping almost over her eye/the eyelid being swollen; little fever; tooth started hurting/tooth ache; both of her hands were a little swollen; had no appetite; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70 year-old female patient received bnt162b2 (BNT162B2), administration date 10Jan2022 15:00 (Lot number: FE3594) at the age of 70 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Blood pressure high" (unspecified if ongoing), notes: Verbatim: Blood pressure high; "cysts in her breast", start date: Dec2019 (unspecified if ongoing); "tumors and cysts in her breasts and leg" (unspecified if ongoing); "tumors and cysts in her breasts and leg" (unspecified if ongoing). Concomitant medication(s) included: VALSARTAN taken for hypertension. Past drug history included: Losartan, reaction(s): "cysts"; Losartan, reaction(s): "tumors". Vaccination history included: Bnt162b2 (Dose:1, She says her vaccine card is handwritten and all they have for the first dose is EL and then she can't read this writing, maybe it says 9263 but it could be EL9243. Caller says she thinks it says EL9263), administration date: 06Feb2021, when the patient was 69 years old, for COVID-19 immunization, reaction(s): "Covid", "sick", "brain fog"; Bnt162b2 (Dose:2, Lot: EL6004), administration date: 09Mar2021, when the patient was 69 years old, for COVID-19 immunization, reaction(s): "Covid", "sick", "brain fog". The following information was reported: SWELLING OF EYELID (non-serious) with onset 10Jan2022 17:00, outcome "recovered", described as "right eyelid was drooping almost over her eye/the eyelid being swollen"; PYREXIA (non-serious) with onset 10Jan2022, outcome "recovered", described as "little fever"; TOOTHACHE (non-serious) with onset 10Jan2022, outcome "not recovered", described as "tooth started hurting/tooth ache"; PERIPHERAL SWELLING (non-serious) with onset Jan2022, outcome "recovered", described as "both of her hands were a little swollen"; LETHARGY (non-serious) with onset 11Jan2022, outcome "recovered", described as "Lethargy"; FEELING ABNORMAL (non-serious) with onset 11Jan2022, outcome "recovered", described as "brain fog"; GASTRIC DISORDER (non-serious) with onset 11Jan2022, outcome "recovered", described as "felt like somebody punched her in the stomach"; DECREASED APPETITE (non-serious) with onset Jan2022, outcome "recovered", described as "had no appetite"; LYMPHADENOPATHY (non-serious), outcome "recovered", described as "her lymph nodes were a little swollen on that side of her face". The event "tooth started hurting/tooth ache" was 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 pyrexia, gastric disorder. Additional information: Consumer calling about the Pfizer COVID-19 vaccine booster that she had Monday 10Jan2022 at 03:00PM because she wanted to report side effects. She says by 05:00PM that day her right eyelid was drooping almost over her eye, and then she had a little fever Monday night, but then her tooth started hurting. She says both of her hands were a little swollen, and then on Tuesday she had lethargy and brain fog and felt like somebody had punched her in the stomach, which no one has ever done that to her before but that's what it felt like. She says she had no appetite, and the toothache got worse. Caller says she called because the pharmacist she talked to said report her side effects to her doctor but they are not in the office, she doesn't know. She says by Thursday morning everything had gone away except the toothache, so she went to the dentist yesterday because she didn't know if the tooth was abscessed or broken, but the dentist found nothing, and thought that maybe the eyelid being swollen affected the joint in front of ear, and her lymph nodes were a little swollen on that side of her face. She says they thought maybe she had been clenching her teeth since she had the booster, so they filed down her tooth once they found out which one it was by tapping on it, and it still aches. Caller says there was no treatment done initially for the tooth ache. She says she went to the dentist yesterday who took about 6-7 x-rays and couldn't figure out which tooth it was, then ended up tapping on it to find it, and filed it down a bit thinking if she was gritting her teeth or something this would help. She says there is a long holiday weekend coming up so she didn't want to find herself having a dentist emergency during that. Caller says she looked up drooping eyelids and vaccination and did research online of several other things like edemas, Guillan-Barre and Bell's palsy, but knew it was not Bell's palsy, thought that does happen. Caller says for treatment she put a warm wash cloth over the eyelid. Caller says this was not better until Wednesday morning. She clarifies that she got the COVID-19 shot at 03:00PM on Monday, then by 05:00PM the eyelid was drooping and looked like it was filled with water. Caller says that her little fever got better after it started on Tuesday. She says that her treatment was not until Tuesday afternoon, due to having high blood pressure she is careful what she takes, so she finally took two regular strength Tylenol tablets, which she doesn't know that dosage. Caller says the brain fog and lethargy are gone. She says that feeling like she was punched in the stomach treatment was that she didn't eat and she drank water with a bit of lemon. She says she didn't know if she was going to throw up. She says she had cereal for supper, which she has done maybe 5 times in her life. Caller says that she got her COVID-19 vaccine doses in Feb and Mar last year, and then they were in a vehicle with their daughter after she came back from a conference on a Saturday night in Jul, then by Tuesday her husband and her got sick with COVID, they had COVID during Jul and Aug. She clarifies they had COVID last summer in Jul, at the end of Jul into the beginning of Aug and they were sick three weeks, and had brain fog for two months. She says she and her husband got sick within a couple hours of each other, and when they went to get tested, he tested positive and she was negative. She says the only thing they figured out was that she must have been a couple hours behind him and did not have enough when she tested positive. She says they were running fevers and had aches. She clarifies they did the COVID test in Aug, the COVID test done in the nose, whatever that is. She says treatment for the COVID-19 was offered to her husband, the infusion, because he has autoimmune disease. She says because she tested negative and didn't feel like going back to be tested again the next day, she didn't get offered any treatment, She says her husband didn't take the test, clarified to infusion, because he would have to go to the hospital for that and he didn't want to expose anyone or go anywhere. She says they recovered from COVID, and she was back to normal until Monday when she took the booster dose. Caller says she takes one high blood pressure medication, Valsartan, which she takes every morning, then clarifies it is not relevant to the COVID vaccine side effects. She says she was on Losartan for years until they said it causes cysts and tumors, and since then she was changed to Valsartan and they found tumors and cysts in her breasts and leg. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Test Date: 202108; Test Name: COVID-19 virus test; Test Result: Negative ; Test Name: X-ray; Result Unstructured Data: Test Result:Unknown result; Comments: went to the dentist yesterday who took about 6-7 x-rays and couldn't figure out which tooth it was
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure increased (Verbatim: Blood pressure high); Breast cyst; Cyst; Tumor
Andere Medikamente: VALSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2181977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IL
Alter: 18,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 03.01.2022
Beginn: 06.02.2022
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: - / LA

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

Back pain X-ray

Symptomtext

Severe lower back pain, felt like lower back inflamed and warm to touch; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 19 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Jan2022 (Lot number: FE3594, Expiration Date: Feb2022) at the age of 18 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), administration date 03Jan2022 (Batch/Lot number: unknown) as dose number unknown, single. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Vaccine Name: First Covid Vaccine, Lot Number / Expiry Date: ER8730, Route, Anatomical Location: left arm, No. of Previous Doses: No, Date: 30Mar2021), administration date: 30Mar2021, when the patient was 18 years old, for Covid-19 immunization; Bnt162b2 (Vaccine Name: Second Covid Vaccine, Lot Number / Expiry Date: ER8730, Route, Anatomical Location: left arm , No. of Previous Doses: one, Date: 20Apr2021), administration date: 20Apr2021, when the patient was 18 years old, for Covid-19 immunization. The following information was reported: BACK PAIN (non-serious) with onset 06Feb2022, outcome "recovering", described as "Severe lower back pain, felt like lower back inflamed and warm to touch". The event "severe lower back pain, felt like lower back inflamed and warm to touch" was evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. No follow-up attempts are possible. No further information is expected. Additional Information: The reporter wondered if a symptom could be possibly evaluated to see if its a side effect of the Pfizer booster vaccine. Recently she was boosted about a month ago and she began to experience severe lower back pain a few days later and it had not gone away even with chiropractic therapy. She highly believe that this was a symptom of the booster, she asked her chiropractor about it and he found it unusual because she was young and did not engage in heavy work. She reported that she is a healthy person, she got a physical and blood work and x-rays and it was all good. She reported as soon as she got the booster dose she had a lot of back pain but it has toned down. She went to a chiropractor and they said it could be from the vaccine. She reported that her lower back is inflamed. Follow-up (16Feb2022): This is a spontaneous follow-up report received from a contactable consumer. This 18-year-old female consumer (patient) reported that: Updated information included Ethnicity, Dosage regimens, vaccine information, vaccine facility information, HCP information, patient information, lab test, outcome of the event, onset date, Co-suspect drug. She reported that after booster, and later in report, She reported that she had her yearly Flu shot on a Flu vaccine on that same day and the same visit as getting her Covid vaccine, booster. She reported that probably 3 days after her vaccination on 03Jan2022 she experienced severe lower back pain, felt like lower back inflamed and warm to touch. She reported that she had an X-Ray, and was told by the doctor that nothing abnormal was noted. She reported that she was told that her spine was not straight. She reported that she wondered if the combination of the Covid shot and Flu shot caused her issues. Follow-up (16Feb2022): This is a spontaneous follow-up report from a contactable consumer. This consumer reported that: Updated Information included: Phone number format updated in patient tab, Dose description updated in products tab. Follow-Up (22Feb2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Test Name: X-ray; Result Unstructured Data: Test Result:Normal; Comments: Caller states she had an X-Ray, and was told by the doctor that nothing abnormal was noted.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2181809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 42,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Chills Pyrexia Vaccination site swelling Vaccination site warmth

Symptomtext

swelling at injection shot 3" in diameter and hot to the touch; swelling at injection shot 3" in diameter and hot to the touch; chills; fever; 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 23Dec2021 14:30 (Lot number: FE3594) at the age of 42 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Covid" (unspecified if ongoing), notes: if covid prior vaccination: Yes. The patient's concomitant medications were not reported. The following information was reported: VACCINATION SITE SWELLING (non-serious), VACCINATION SITE WARMTH (non-serious) all with onset 23Dec2021, outcome "not recovered" and all described as "swelling at injection shot 3" in diameter and hot to the touch"; CHILLS (non-serious) with onset 23Dec2021, outcome "not recovered", described as "chills"; PYREXIA (non-serious) with onset 23Dec2021, outcome "not recovered", described as "fever". Therapeutic measures were not taken as a result of vaccination site swelling, vaccination site warmth, chills, pyrexia. Additional information:Did the patient receive any other vaccines within 4 weeks prior to the COVID vaccine: No. List of any other medications the patient received within 2 weeks of vaccination: N/A. Since the vaccination, has the patient been tested for COVID-19?: No. known allergies: NKA. other medical history: N/A No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2179371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 12,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Body temperature Headache Pyrexia SARS-CoV-2 test

Symptomtext

headache; fever was high and it was 103.2 degrees; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team and product quality group for a Pfizer sponsored program. The reporter is the parent. A 12 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Dec2021 11:30 (Lot number: FE3594) at the age of 12 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (1st dose, lot FH8027, patient's card has no expiry dates or NDC numbers written on it.), administration date: 28Nov2021, when the patient was 12 years old, for Covid-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 19Dec2021, outcome "recovered" (20Dec2021), described as "headache"; PYREXIA (non-serious) with onset 19Dec2021, outcome "recovered" (20Dec2021), described as "fever was high and it was 103.2 degrees". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of headache, pyrexia. Additional information: After 12 hours of getting the vaccine reporter son had fever and headache which are resolved already. Her son was tested on Monday 20Dec2021 and he was positive in the PCR test. Per caller, her son have had subsequent PCR test that were all negative within the last 3 days. Reporter was looking for studies or information on patients who were tested positive 24 hours after receiving the vaccine. The report related to a study or programme. states he has a HCP calling to report an adverse event for her own 12 year old son and the patient got his 2nd dose of the Pfizer Covid vaccine on Sunday 19Dec2021 and they are going on vacation and she got the patient tested on Monday 20Dec2021 and he was not a big kid and she wanted to get him the Pfizer COVID Vaccine for 12 year old so he got it and then 12 hours later he had the side effects of fever and headache and that was within a couple of hours of having the vaccine 2nd dose; states they are going on vacation and are supposed to leave and the patient had a PCR test and he wass the only person to test positive for the PCR test. Reporter states she did subsequent PCR tests on the patient and they were all negative in the last three days; states she has searched to see if there are any studies done of people having positive tests within 24 hours of getting the vaccine and the vaccine causing positives but she does not know; states the Regulatory Authority has the patient on a no fly list and she is seeking information about this. Transferring agent states the caller said she does not know how to get the patient off the list and the patient does not have covid anymore. Reporter verified the information provided by the transferring agent and states she will do whatever it takes to get her help with the Regulatory Authority and the patient was tested to go on a trip and he was vaccinated the day before with the Pfizer Covid vaccine and she searched and searched and is asking if there are any studies done with the PCR coming up positive within 24 hours timeframe of receiving the Pfizer Covid vaccine. Reporter states she knows theoretically this can't happen and there is no live virus in the vaccine but she does not know and there are no studies. Reporter states they did the PCR test because they are going on vacation and her entire family were all negative for the PCR test except for the patient; states the patient never had symptoms of anything and did an at home test on Wednesday before and did an at home test that was negative just because this is so rampant and then she has gotten him three PCR tests in the past 24 hours and they have all been negative; states she did research to see about this and she believes in science and they are not giving live vaccine and the vaccine can't give you covid but it is all so new and so is the testing and there is not information and it had to be something if you do have a reaction and can the reaction cause the test to be positive. Reporter asks if people who get fevers have they all been tested 24 hours after the Pfizer Covid vaccine with a PCR test. Vaccination facility type was school. 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): Reporter states the patient had the 1st dose of the Pfizer Covid vaccine on 28Nov2021 with lot FH8027, had the 2nd dose on 19Dec2021 with lot FE3594 and the patient's card has no expiry dates or NDC numbers written on it. Additional Vaccines Administered on Same Date of the Pfizer Suspect was none. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine reported as none. Patient's Medical History (including any illness at time of vaccination) was none. Family Medical History Relevant to AE(s) reported as none. States she gave the patient Tylenol and the fever and headache resolved and the Tylenol was administered after the vaccination. States the patient's fever and headache began literally 12 hours later after his 2nd dose of the Pfizer Covid vaccine and she checked his temperature and it was 103 degrees so she gave him Tylenol and he had no fever by morning and he had a headache that Monday and with the Tylenol it resolved completely. Reporter states for seriousness criteria for the patient's reported events, his fever was high and it was 103.2 degrees and she is not one who worries so she would say this is not serious for the fever, headache and positive PCR test. Reporter asks if all people that have reactions are tested and do the tests come back positive because of the reactions and she knows the vaccine can't give covid but she is desperate and looking for a way. States she is looking for something from Pfizer that says this could be reportable and that it has been seen before so she can submit it and he has had negative test results and it could be from the Pfizer covid vaccine that he tested positive so he can be taken off the list. Description of complaint: Vaccine Supplemental Form completed in additional context. States her own 12 year old son and the patient got his 2nd dose of the Pfizer Covid vaccine on Sunday 19Dec2021 and they are going on vacation and she got the patient tested on Monday 20Dec2021 and he is not a big kid but is 70 pounds and she wanted to get him the Pfizer COVID Vaccine for 12 year olds so he got it and then 12 hours later he had the side effects of fever and headache and that was within a couple of hours of having the vaccine 2nd dose; states they are going on vacation and are supposed to leave and the patient had a PCR test and he is the only person to test positive for the PCR test. Reporter states she did subsequent PCR tests on the patient and they were all negative in the last three days; states she has searched to see if there are any studies done of people having positive tests within 24 hours of getting the vaccine and the vaccine causing positives but she does not know; states the Regulatory Authority has the patient on a no fly list and she is seeking information about this. Transferring agent states the reporter said she does not know how to get the patient off the list and the patient does not have covid anymore. States the patient never had symptoms of anything and did an at home test on Wednesday before and did an at home test that was negative just because this is so rampant and then she has gotten him three PCR tests in the past 24 hours and they have all been negative; states she did research to see about this and she believes in science and they are not giving live vaccine and the vaccine can't give you covid but it is all so new and so is the testing and there is not information and it had to be something if you do have a reaction and can the reaction cause the test to be positive. Caller asks if people who get fevers have they all been tested 24 hours after the Pfizer Covid vaccine with a PCR test. Reporter an HCP Calling about an Adverse Event so he has gotten her 12-year-old his second vaccine on Sunday and was going on a vacation and I got him tested on Monday. he's not a big kid he's 70 pounds but they wanted to get the 12-year-old vaccine and then 12 hours later the side effects he had fever, headache, and then within a couple of hours he get better. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the Pfizer-BioNTech Covid-19 Vaccine Injectable lot FE3594 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FE3594, fill lot FF2555, and the bulk formulated drug product lot EY0909. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. ID of Previously Completed Inv: 6666659 and Link (Previously Investigated CR): 6666477. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: Fever; Result Unstructured Data: Test Result:103.2; Comments: degrees; Test Date: 202112; Test Name: PCR; Test Result: Negative ; Comments: three PCR tests in the past 24 hours; Test Date: 20211220; Test Name: PCR; Test Result: Positive
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 2176764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 24,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Body temperature Breast pain Injection site joint pain Injection site pain Joint dislocation Ligament pain Pain in extremity Pyrexia

Symptomtext

joint ligament pain on my shoulder at the injection shot site; almost it feels kind of dislocated; rest on the injection arm too; then on my elbow; along with the fever of 100.2 Fahrenheit.; like ligament pain on my shoulder; at the injection site; my right breast almost; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24 year-old female patient received bnt162b2 (BNT162B2), administration date 21Dec2021 (Lot number: FE3594) at the age of 24 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE-1, LOT number of ER8733 , expiration date as 31Jul2021), administration date: 30Mar2021, for Covid-19 immunization; Bnt162b2 (DOSE-2, LOT number of EW0162 , expiration date as 31Jul2021), administration date: 20Apr2021, for Covid-19 immunization. The following information was reported: INJECTION SITE JOINT PAIN (non-serious) with onset 22Dec2021, outcome "not recovered", described as "joint ligament pain on my shoulder at the injection shot site"; JOINT DISLOCATION (non-serious) with onset 22Dec2021, outcome "not recovered", described as "almost it feels kind of dislocated"; PAIN IN EXTREMITY (non-serious) with onset 22Dec2021, outcome "not recovered", described as "rest on the injection arm too"; ARTHRALGIA (non-serious) with onset 22Dec2021, outcome "not recovered", described as "then on my elbow"; PYREXIA (non-serious) with onset 22Dec2021, outcome "not recovered", described as "along with the fever of 100.2 Fahrenheit."; LIGAMENT PAIN (non-serious) with onset 22Dec2021, outcome "not recovered", described as "like ligament pain on my shoulder"; INJECTION SITE PAIN (non-serious) with onset 22Dec2021, outcome "not recovered", described as "at the injection site"; BREAST PAIN (non-serious) with onset 22Dec2021, outcome "not recovered", described as "my right breast almost". Relevant laboratory tests and procedures are available in the appropriate section. Consumer stated, she wanted to report a side effect and got from my Pfizer booster shot that, the patient received yesterday. It was almost like a joint ligament pain on her shoulder at the injection shot site and then on her elbow and rest on the injection arm too, almost it feels kind of dislocated. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:Increase; Comments: fever of 100.2 Fahrenheit
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2162505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WI
Alter: 53,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 27.12.2021
Beginn: 19.01.2022
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: IM / RA

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

Angiogram cerebral normal Arteriogram carotid normal Arthralgia CSF culture CSF oligoclonal band absent Computerised tomogram head normal Gait disturbance Hemiplegia Hypoaesthesia Impaired work ability Lumbar puncture Magnetic resonance imaging head normal Magnetic resonance imaging spinal abnormal Movement disorder Muscular weakness Musculoskeletal disorder Neck pain Scan with contrast normal

Symptomtext

Patient had shoulder and neck pain that progressed to bilateral arm weakness the next day. Within hours, patient had bilateral upper and lower extremity numbness and left arm and leg weakness. She felt the strength in the right upper and lower extremities was strong and normal. She was seen in the ED that day because she was dragging her left foot/leg and couldn't use her left hand. She was admitted into the hospital with an abnormal C spine MRI. Within 24 hours, she had complete left sided paralysis with bilateral upper and lower extremities numbness. She received 5 days of 1,000 mg solumedrol. She slowly saw improvement in movement to the arm and then leg during her 8 day hospital stay. She was discharged on day 8 with a wheel chair. She is learning to walk again with the help of home PT and OT. She has been out of work for 6 weeks now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: 8,0
Labordaten: 1/19/2021: CT head negative, CT angio head and neck with contrast negative, MRI brain without contrast negative, MRI C spine without contrast shows abnormal signal at C6-C7 concerning for demyelinating plaque or mild traverse myelitis. 1/20/2021: MRI T and L spine with and without contrast, negative for spinal cord enhancement or abnormalities 1/21/2021: LP, CSF culture, viral panel, RPR, and oligoclonal bands negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, hyperlipidemia, osteoarthritis
Andere Medikamente: Atenolol, Atorvastatin, Meloxicam, Tramadol, Benadryl
Allergien: None
Vorherige Impfungen: -

VAERS 2155363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IL
Alter: 34,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 14.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RL

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

Incorrect route of product administration Injection site erythema Injection site mass Urticaria

Symptomtext

1/14/22 Pfizer COVID-19 vaccine administered in right thigh due to lack of upper extremities. No reaction during observation time after administration of vaccine, stayed with patient for 30 minutes due to extensive allergy list and possible immunocompromising illness. 2/09/22 I returned to the patient's home to administer the second dose of Pfizer COVID-19 vaccine, patient advised me that she had a "reaction" 3 days later. Upon discussion she described a local reaction at the injection site, Knot under skin with some redness. She also stated that 2 days following this reaction she had hives all over her body. We discussed consulting her physician before administering the 2nd dose. Hives had resolved at the time of my visit, patient stated they resolved within 48 hours of appearance. Patient is scheduled with a new physician in one week. RN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Presently being tested for Lupus and other auto immune disorders.
Vorgeschichte: Congenital birth defect of upper extremities.
Andere Medikamente: Unknown
Allergien: Citrus, Bismuth Subsalicylate, Morphine, Sulfa, PCN, and Iodine
Vorherige Impfungen: -

VAERS 2151169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 29,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 25.02.2022
Beginn: 26.02.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Chills Fatigue Headache Pyrexia Vaccination site lymphadenopathy Vaccination site pain

Symptomtext

Fever, Headache, Chills, Fatigue, Lymphadenopathy Pain in the area of the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hashimoto's thyroiditis; PCOS.
Andere Medikamente: Levothyroxine; Vitamin D3.
Allergien: -
Vorherige Impfungen: -

VAERS 2147292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 48,0
Geschlecht: F
Eingang: 27.02.2022
Impfdatum: 22.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / LA

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

Angiopathy Bone disorder Computerised tomogram Inflammation Pain SARS-CoV-2 test

Symptomtext

inflammatory reaction to old Juvederm facial filler; the inflammation caused vascular dilation and throbbing, pain; the inflammation caused vascular dilation and throbbing, pain; Possible compromise to bony structure of lower face; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 48 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 22Dec2021 21:30 (Lot number: FE3594) at the age of 48 years as dose 3 (booster), single, administered in arm left, administration date 04May2021 16:45 (Lot number: EW0175) as dose 2, single and administered in arm left, administration date 13Apr2021 15:45 (Lot number: ER8731) as dose 1, single for covid-19 immunisation. Relevant medical history included: "old Juvederm facial filler", start date: Jun2018 (unspecified if ongoing), notes: old Juvederm facial filler, known allergies: No. There were no concomitant medications. The following information was reported: INFLAMMATION (disability) with onset Jan2022, outcome "not recovered", described as "inflammatory reaction to old Juvederm facial filler"; ANGIOPATHY (disability), PAIN (disability) all with onset Jan2022, outcome "not recovered" and all described as "the inflammation caused vascular dilation and throbbing, pain"; BONE DISORDER (disability) with onset Jan2022, outcome "not recovered", described as "Possible compromise to bony structure of lower face". The events "inflammatory reaction to old juvederm facial filler", "the inflammation caused vascular dilation and throbbing, pain", "the inflammation caused vascular dilation and throbbing, pain" and "possible compromise to bony structure of lower face" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: computerised tomogram: (08Feb2022) unknown; sars-cov-2 test: (08Feb2022) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of inflammation, angiopathy, pain, bone disorder. Clinical course: The patient was not diagnosed with Prior to vaccination COVID-19, Since the vaccination, the patient has been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. treatment received for the adverse event Medrol dose pack, doxycycline, CT facial scan, ASA. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Test Date: 20220208; Test Name: CT facial scan; Result Unstructured Data: Test Result:Unknown; Test Date: 20220208; Test Name: Abbott home test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Dermal filler injection (old Juvederm facial filler known allergies: No)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NM
Alter: 71,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 14.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: OT / RA

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

Erythema Laboratory test Pruritus

Symptomtext

2 days after getting the booster, she woke up and was bright red on her abdomen and her arms. She reports that there continues to be some redness around her waist and a little under her arms,.; neck itches; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200194293 .A 71 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 14Jan2022 (Lot number: FE3594) at the age of 71 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "rheumatoid arthritis" (unspecified if ongoing). Concomitant medication(s) included: PREDNISONE. Past drug history included: Lidocaine for neck itches; Lidocaine for Generalized erythema. Vaccination history included: Covid-19 vaccine (Dose 1 single, Manufacturer: Unknown), administration date: 20Apr2021, when the patient was 70 years old, for COVID-19 immunization; Covid-19 vaccine (Dose 2 single, Manufacturer: Unknown), administration date: 26May2021, when the patient was 71 years old, for COVID-19 immunization. The following information was reported: ERYTHEMA (non-serious) with onset 16Jan2022, outcome "recovering", described as "2 days after getting the booster, she woke up and was bright red on her abdomen and her arms. She reports that there continues to be some redness around her waist and a little under her arms,."; PRURITUS (non-serious) with onset 16Jan2022, outcome "recovering", described as "neck itches". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of erythema, pruritus. Additional information included: Customer Verbatim: She had the Covid booster on 14Jan. On 16Jan she became red throughout her entire trunk and down her arms. It has cleared somewhat but she was still red and itchy/ she turned red, bright red and she had this kind of allergic reaction before to Lidocaine but this was definitely a skin allergic reaction, my whole abdomen from her neck all the way down to the groin area and my arms down to my elbows turned red and she still have it, it has been over two weeks, it still itch, it was still red not as red as it was but it hasn't gone away completely. So, she wonder if you have heard of this happening, she had read about it and it has happened but she did not know if there was anything she can do except to wait it out." Expiration date: Consumer stated, "It doesn't have an expiration date on it she did not know, they didn't put that on the card that they gave me information on." Other medical conditions and other medications: Consumer stated, "She have rheumatoid arthritis right now she was not taking anything for it, she was waiting to start a new medication but they wanted her to wait because for a while she was on Prednisone and they didn't want her to start the new medication until she got off the Prednisone which she was. Lab tests: Consumer stated, "The last lab test she had was at the end of December. Consumer stated, "She was still having the redness and itching, Consumer stated, "They have got a little better. Treatment for adverse events: Consumer stated, "she took Benadryl."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: Lab test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Rheumatoid arthritis
Andere Medikamente: PREDNISONE
Allergien: -
Vorherige Impfungen: -

VAERS 2054276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NM
Alter: 71,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 14.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / RA

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

Erythema Laboratory test Pruritus

Symptomtext

2 days after getting the booster, she woke up and was bright red on her abdomen and her arms. She reports that there continues to be some redness around her waist and a little under her arms,.; neck itches; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200194293 .A 71 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 14Jan2022 (Lot number: FE3594) at the age of 71 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "rheumatoid arthritis" (unspecified if ongoing). Concomitant medication(s) included: PREDNISONE. Past drug history included: Lidocaine for neck itches; Lidocaine for Generalized erythema. Vaccination history included: Covid-19 vaccine (Dose 1 single, Manufacturer: Unknown), administration date: 20Apr2021, when the patient was 70 years old, for COVID-19 immunization; Covid-19 vaccine (Dose 2 single, Manufacturer: Unknown), administration date: 26May2021, when the patient was 71 years old, for COVID-19 immunization. The following information was reported: ERYTHEMA (non-serious) with onset 16Jan2022, outcome "recovering", described as "2 days after getting the booster, she woke up and was bright red on her abdomen and her arms. She reports that there continues to be some redness around her waist and a little under her arms,."; PRURITUS (non-serious) with onset 16Jan2022, outcome "recovering", described as "neck itches". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of erythema, pruritus. Additional information included: Customer Verbatim: She had the Covid booster on 14Jan. On 16Jan she became red throughout her entire trunk and down her arms. It has cleared somewhat but she was still red and itchy/ she turned red, bright red and she had this kind of allergic reaction before to Lidocaine but this was definitely a skin allergic reaction, my whole abdomen from her neck all the way down to the groin area and my arms down to my elbows turned red and she still have it, it has been over two weeks, it still itch, it was still red not as red as it was but it hasn't gone away completely. So, she wonder if you have heard of this happening, she had read about it and it has happened but she did not know if there was anything she can do except to wait it out." Expiration date: Consumer stated, "It doesn't have an expiration date on it she did not know, they didn't put that on the card that they gave me information on." Other medical conditions and other medications: Consumer stated, "She have rheumatoid arthritis right now she was not taking anything for it, she was waiting to start a new medication but they wanted her to wait because for a while she was on Prednisone and they didn't want her to start the new medication until she got off the Prednisone which she was. Lab tests: Consumer stated, "The last lab test she had was at the end of December. Consumer stated, "She was still having the redness and itching, Consumer stated, "They have got a little better. Treatment for adverse events: Consumer stated, "she took Benadryl."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: Lab test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Rheumatoid arthritis
Andere Medikamente: PREDNISONE
Allergien: -
Vorherige Impfungen: -

VAERS 2140040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 05.01.2022
Beginn: 19.02.2022
Tage bis Beginn: 45,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia COVID-19 Diarrhoea Inappropriate schedule of product administration

Symptomtext

Patient presented to ED complaining of generalized weakness and diarrhea. PMH of obesity, DVT/PE on chronic anticoagulation with rivaroxaban, CKD stage III, COVID-19. Patient was diagnosed with COVID-19 on 01/28/22 and states that her symptoms have progressively worsened. Previously vaccinated and boosted with Pfizer on 2/6/21, 2/21/21, and 1/5/22. Admitted to facility on 2/19/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2138589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 25.02.2022
Impfdatum: 31.01.2022
Beginn: 01.02.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Biopsy Blister Blood test Chest X-ray Erythema Pruritus Rash Rash erythematous Urine analysis Urticaria

Symptomtext

Within 13 hours, I broke out in full body hives and red bumps covering the majority of my body with the exception of my feet and face. For the past 24 days, I have itched from head to toe. I have developed blisters on the back of my leg. Multiple times a day, I break out in a severe case of hives redness and red bumps and itching that is uncontrollable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: A full panel of bloodwork and urinalysis. Also a chest x-ray (done the second week of January). January 23: deep tissue biopsy as well as a traditional biopsy.
Aktuelle Erkrankungen: COVID-19 one month prior
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2123356

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FE3594

mild

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 29.12.2021
Beginn: 07.01.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: - / AR

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

Contusion Dermatitis atopic Insomnia Pruritus Rash Urticaria

Symptomtext

In early January I was experiencing a rash with severe itching and bruising with loss of sleep due to symptoms which I thought was an exacerbation of my atopic dermatitis. I completed a 10 day Prednisone tape on top of treatment with topical Triamcinilone, Atarax, Xyzal. I was able to see a dermatologist on February 14th after continued issues without resolution of symptoms and was instead diagnosed with Urticaria. Because this issue is different from my already diagnosed illness and realizing the timeframe in which it started I thought it should be reported just in case there is an association with my booster dose of Moderna Vaccine. I am not being treated with Triamcinilone topical, Atarax, Triple doses of Cetirizine and a 21 day slow Prednisone taper.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Atopic Dermatitis
Andere Medikamente: Xyzal Multivitamin
Allergien: Morphine allergy
Vorherige Impfungen: -

VAERS 2116254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: VA
Alter: 15,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Injection site pruritus

Symptomtext

On 1/19/22 I RN vaccinated patient. (DOB 12/20/2006) with Pfizer Covid-19 vaccine. After a few minutes patient scratched the injection area. Her mother came to me and said the patient felt a little itchy and asked for some medication to relieve that. I looked at the area and saw that it was a little red most likely from her scratching but there was no skin bumps present. I apply hydrocortisone 1% on the affected skin area and gave her 10 ml of diphenhydramine 12.5mg/5ml. After about 5 minutes the patient said she felt better. I recommended her mother to buy Benadryl (diphenhydramine) 25 mg capsules just in case. I asked her to let the pharmacy know if the condition got worse. Her mother never contacted the pharmacy. When she brought the patient for her second Pfizer vaccination on 12/09/2006, she mentioned to the pharmacist who did the second vaccination about the event. I was advised to file the report. I called the mother today 2/16/22 to find out about that day. She said there was no issue after they left and she never gave her the Benadryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2113040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 15.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Blood test Neuralgia Peripheral swelling

Symptomtext

On the 18th she started getting swelling in both legs. She had nerve pain and swelling in both hands. The swelling in her legs became indented. By mid Jan 2022 the swelling in her legs got a little bit better but she developed pain in both shoulders, elbows and knees. She has seen her pcp and a medical naturalist doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: yes blood work
Aktuelle Erkrankungen: no
Vorgeschichte: IBS and hypothyroidism
Andere Medikamente: estradiol, progesterone, levothyroxine, np thyroid
Allergien: no
Vorherige Impfungen: -

VAERS 2109137

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IL
Alter: 63,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 07.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Lymphadenopathy Neck pain Urticaria

Symptomtext

Hives on chest and arms; Swollen lymph nodes in neck, both still evident one month after last vaccine; Soreness on back of neck and both shoulders making arm movement painful; Soreness on back of neck and both shoulders making arm movement painful; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 07Jan2022 at 09:30 (Lot number: FE3594) at the age of 63 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication included: MULTIVITAMIN, CLARITIN and IBUPROFEN. Past drug history included: Amoxicillin, reaction: "Drug allergy", notes: Known allergies: Amoxicillin. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EN6202; Anatomical site: Right arm; Administration time: 10:00), administration date: 26Feb2021, when the patient was 62 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: ENG207; Anatomical site: Left arm; Administration time: 10:00), administration date: 17Mar2021, when the patient was 62 years old, for COVID-19 immunisation. The following information was reported: URTICARIA (non-serious) with onset 13Jan2022 at 06:15, outcome "not recovered", described as "Hives on chest and arms"; LYMPHADENOPATHY (non-serious) with onset 13Jan2022 at 06:15, outcome "not recovered", described as "Swollen lymph nodes in neck, both still evident one month after last vaccine"; NECK PAIN (non-serious), ARTHRALGIA (non-serious) all with onset 13Jan2022 at 06:15, outcome "not recovered", and all described as "Soreness on back of neck and both shoulders making arm movement painful". The events "Hives on chest and arms", "Swollen lymph nodes in neck, both still evident one month after last vaccine" and "Soreness on back of neck and both shoulders making arm movement painful" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of urticaria, lymphadenopathy, neck pain and arthralgia. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CLARITIN [LORATADINE]; IBUPROFEN
Allergien: -
Vorherige Impfungen: -

VAERS 2109093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MA
Alter: 43,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 26.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Back pain Musculoskeletal pain Neck pain Pain

Symptomtext

After a few more days the pain spread into the left side of my neck/ Over the course of the next couple weeks, the pain spread across both shoulders & completely around my neck; Now a full month after receiving the booster the pain occasionally radiates down my back & into my shoulder blades; Now a full month after receiving the booster the pain occasionally radiates down my back & into my shoulder blades; Two days after receiving the booster shot on 12/26/21 I started to have sharp pains in my left shoulder above the injection location/ Over the course of the next couple weeks, the pain spread across both shoulders & completely around my neck; The sharp pains were sporadic, but the overall pain would not go away; This is a spontaneous report received from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 43-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 26Dec2021 at 12:30 (Lot number: FE3594) at the age of 43 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: ER8736, Anatomical Location: Left arm, Route of Administration: Unspecified, Time of Administration: 11:45), administration date: 01May2021, when the patient was 42 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EW0168, Anatomical Location: Left arm, Route of Administration: Unspecified, Time of Administration: 12:00), administration date: 24May2021, when the patient was 42 years old, for COVID-19 immunisation. The following information was reported: ARTHRALGIA (non-serious) with onset 28Dec2021 at 12:00, outcome "not recovered", described as "Two days after receiving the booster shot on 12/26/21 I started to have sharp pains in my left shoulder above the injection location/ Over the course of the next couple weeks, the pain spread across both shoulders & completely around my neck"; PAIN (non-serious) with onset 28Dec2021 at 12:00, outcome "not recovered", described as "The sharp pains were sporadic, but the overall pain would not go away"; NECK PAIN (non-serious), outcome "not recovered", described as "After a few more days the pain spread into the left side of my neck/ Over the course of the next couple weeks, the pain spread across both shoulders & completely around my neck"; BACK PAIN (non-serious), MUSCULOSKELETAL PAIN (non-serious) all with onset 26Jan2022, outcome "not recovered", and all described as "Now a full month after receiving the booster the pain occasionally radiates down my back & into my shoulder blades". The events "Two days after receiving the booster shot on 12/26/21 I started to have sharp pains in my left shoulder above the injection location/ Over the course of the next couple weeks, the pain spread across both shoulders & completely around my neck", "The sharp pains were sporadic, but the overall pain would not go away", "After a few more days the pain spread into the left side of my neck/ Over the course of the next couple weeks, the pain spread across both shoulders & completely around my neck" and "Now a full month after receiving the booster the pain occasionally radiates down my back & into my shoulder blades" were evaluated at the physician office visit. Therapeutic measures were taken as a result of arthralgia, pain, neck pain, back pain and musculoskeletal pain. Additional Information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. It was reported that on 03Feb2022 (reported as today), patient saw his general practitioner who recommended him to see an orthopedic doctor and also issued a prescription for anti-inflammatory medication. He also instructed him that he need to notify Pfizer of this issue. Treatment included unspecified anti-inflammatory medication for arthralgia, pain, neck pain, back pain and musculoskeletal pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
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 2108772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: -
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 17.01.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / LA

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

Arthritis Diarrhoea Erythema Headache

Symptomtext

Diarrhea; Erythema; Cephalea; Arthritis; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP and Other HCP) from medical information team. The reporter is the patient. A 29 year-old female patient received bnt162b2 (BNT162B2), administered in deltoid left, administration date 17Jan2022 19:15 (Lot number: FE3594) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1 manufacturer unknown), for COVID-19 Immunization; Covid-19 vaccine (Dose 2 manufacturer unknown), for COVID-19 Immunization. The following information was reported: DIARRHOEA (non-serious), outcome "unknown", described as "Diarrhea"; ERYTHEMA (non-serious), outcome "unknown", described as "Erythema"; HEADACHE (non-serious), outcome "unknown", described as "Cephalea"; ARTHRITIS (non-serious), outcome "unknown", described as "Arthritis". Therapeutic measures were not taken as a result of diarrhoea, erythema, headache, arthritis. 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: -
Allergien: -
Vorherige Impfungen: -

VAERS 2105893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 90,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 27.12.2021
Beginn: 09.02.2022
Tage bis Beginn: 44,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal wall haematoma COVID-19 Malaise SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer COVID vaccine on 5/21/21 (lot # EW0183), 6/11/21 (lot # EW0191), and 12/27/21 (lot # FE3594). On 2/9/22, patient admitted to our inpatient facility with left rectus sheath hematoma, spontaneous in a patient who is anticoagulated with apixaban, and COVID19 infection (incidental, minimally symptomatic). As of today (2/11/22), patient is still admitted in the med/surg unit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: 2,0
Labordaten: COVID status positive 2/9/22.
Aktuelle Erkrankungen: -
Vorgeschichte: atrial fibrillation (on anticoagulation), heart disease, hyperlipidemia, hypertension, CAD, arthritis, memory loss
Andere Medikamente: apixaban, atorvastatin, diltiazem sr, metoprolol xl, mvi w/minerals, omega-3/fish oil
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2102785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: AK
Alter: 18,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 09.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Eye pain Headache Nausea Photophobia Speech disorder Thinking abnormal

Symptomtext

Patient developed intense headache 20-30 minutes after vaccination. Patient felt dizzy and nauseated. Patient lost ability to speak and think within one hour of vaccination. Patient developed an intense right eye pain, and became sensitive to light.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2101832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: VA
Alter: 28,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 06.01.2021
Beginn: 13.01.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: SYR / RA

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

Benign neoplasm of thyroid gland Computerised tomogram abnormal Diagnostic aspiration Injection site nodule Nodule Pain in extremity Thyroid mass Ultrasound thyroid abnormal

Symptomtext

That day had the sore arm, then 4 days later got a big knot where the vx was given. Following week ( 01/21/2022)/ is when she noticed the nodule on her throat. Called Dr that morning and was advised to get a Thyroid ultrasound, results: Prominent left thyroid nodule was 3.5 cm was dominating left lobe. Then had a CT scan with contrast to further confirm diagnosis and to see if it was pressing into her voice box. Said both tests finding were moderately suspicious and ordered fine needle aspiration biopsy. Results: A benign Focular nodule and it was categorized Bethesda category. Then had me follow up with an Endocrinologist, but is having to wait until 3/1/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site nodule
Hospital-Tage: -
Labordaten: CT and Ultrasound
Aktuelle Erkrankungen: None
Vorgeschichte: Acid Reflux
Andere Medikamente: Nexium, IUD in place
Allergien: None
Vorherige Impfungen: -

VAERS 2096277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: NY
Alter: 58,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 28.12.2021
Beginn: 14.01.2022
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: SYR / 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: iritis of the eye
Andere Medikamente: finasteride, tadalafil, dextroamp, vitamin c, multi vitain, fish oil
Allergien: -
Vorherige Impfungen: -

VAERS 2096262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IL
Alter: 46,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 10.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / -

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

Acoustic stimulation tests Cough Fatigue Feeling cold Rhinorrhoea Tinnitus

Symptomtext

On 12/11/2021 the following day after having the 3rd Phizer booster shot I started having extreme tiredness, runny nose, cough and was very cold for no reason. The following evening/morning of 12/12/2021 at around 3:30 am I was woken with a loud ringing in my ears. Louder in my left ear than the right but very loud in both. It has been nonstop 24/7 ringing since then. Over the last 8.5 weeks it has gone down from time to time but varies and always comes up. It has left my right ear from time to time and I have had the tone change but there is always ringing and sometimes a hiss and cricket sound. The sound sometimes sounds like it is in my left ear and middle of my head, or right and left ears, or right, middle and left, and sometimes just the left. On average is has been in both ears more often than not but recently mostly the left. The volume sometimes goes down but always varies and can go back to the loudness I've experienced since this started. I went to Medical Immediate Care on 12/23/201 and saw Dr. I informed him of the tinnitus started a day a half after the booster. He checked me and stated that I had congestion and prescribed me Claritin D, Flonase, and 20mg of Prednisone for 5 days starting the 3rd day after the other 2 medications. He stated that there have been other reports of complications after taking the Covid vaccine but there is no information on when I may get over my symptoms. He gave me a referral to an ENT for an immediate follow up. I saw the ENT, on 12/28/21. A separate audiologist gave me a hearing exam and stated my hearing is within the normal range. She stated that my ears were clear and there was no sign of congestion or problems with my ears and that the hearing test showed a slight difference in my left ear than right but not significant and not the cause of the tinnitus. She checked my mouth, neck, head and ears. She found nothing with those checks. She stated my ears are healthy with no congestion or ETD. She stated that there are other patients also having issues after Covid vaccines. She stated there is no cure and couldn't tell me if or when the tinnitus will get better as the data regarding the Covid vaccines is too new and incomplete. She gave me a follow up to the ENT MD specialist there at Northwestern but the closest appointment I could schedule is 5/23/2022. She also suggested trying white noise and sound masking for relief along with a referral for accupuncture as she stated it has been helpful for some to deal with ongoing tinnitus. It is 2/08/2022 and it has been 8 weeks and 3 days since the tinnitus started 1.5 days after getting the Pfizer covid booster shot on 12/10/2021. The tinnitus has been nonstop in my left ear sometimes in my right. It has lessened at times but has not gone and sometimes is as loud as the first night. It seems to increase and decrease in volume randomly. This has greatly affected my health, wellbeing, and quality of life. I am hoping it is going down overall over time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: I had a slight cough and runny nose that lasted about 2 weeks. About a week after that was over I got the 3rd Phizer booster shot.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Zyrtec D; Benadryl.
Vorherige Impfungen: -

VAERS 2020701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: PR
Alter: 18,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Pallor

Symptomtext

Patient waits in line to sign up for observation and reports feeling dizzy. Patient is left under continuous observation with dizziness. Staff was notified and the patient is taken to the Treatment area where she looks pale and is placed in anti-shock position and is evaluated. Reassessed patient refers to feeling well and recovered her color, patient does not want transport refers to feeling well.

Weitere VAERSDATA-Felder

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

VAERS 2093584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 33,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Oedema peripheral Pain

Symptomtext

About 12 hours after receiving the booster shot, I woke up in the middle of the night with sharp pain on my left side under my arm. It was very swollen and painful for 1 week and improved slightly at that point but still too painful to put any pressure on that side or lay on that side for another 3 weeks. I started taking Benadryl to try to help but the pain continued for about 7 weeks after the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Extremely swollen and painful lymph nodes under left arm (same arm as I received the shot). This was very painful for the first week after the shot and the pain continued but slowly improved over the following 6 weeks
Andere Medikamente: Lo-loestrin birth control, restasis, fish oil, NAC, Lysine, feverfew, magnesium, vitamin D
Allergien: Sulfa, latex, polymyxin, nexium
Vorherige Impfungen: Rapid heart rate after the HPV vaccine

VAERS 2092505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MN
Alter: 40,0
Geschlecht: F
Eingang: 07.02.2022
Impfdatum: 02.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Axillary pain Breast pain Injection site pain Injection site rash Injection site warmth Rash

Symptomtext

COVID arm - large hot bumps on my arm at injection site as well as under arm in arm pit and breast area accompanied by significant pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: I have not gone in as after research and a call to a local clinic there is nothing that can be done except to watch for symptoms to drastically worsen.
Aktuelle Erkrankungen: NA.
Vorgeschichte: NA.
Andere Medikamente: N/A.
Allergien: Penicillin.
Vorherige Impfungen: same side effects from dose 2 of Pfizer Vaccine back in August 2021.

VAERS 2091169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 53,0
Geschlecht: F
Eingang: 05.02.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Alopecia Anosmia Body temperature Chills Decreased appetite Fatigue Hypoaesthesia Movement disorder Muscle atrophy Muscle fatigue Muscular weakness Nausea Neuropathy peripheral Pain Pain in extremity Pyrexia Somnolence Vertigo

Symptomtext

Left arm pain and unable to move; Total weakness in extremities; Blurred vision; vertigo; Numbness in fingers, toes and legs; Numbness in fingers, toes and legs; Numbness in fingers, toes and legs; Slept for 72 hours without waking up until a welfare check by neighbors; muscle fatigue; hair loss; disuse muscle atrophy; Extreme fatigue; Left arm pain and unable to move; no appetite; vomiting; nausea; Chills; Fever 101.4; Neuropathy; body aches; loss of smell/can't smell anything, not even bad cat litter; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): US-PFIZER INC-202200121795. A 54 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Jan2022 18:00 (Lot number: FE3594) at the age of 53 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "nerve injury" (unspecified if ongoing), notes: I've had nerve injury to left arm. Before I could ask for the other arm, he already jabbed me.; "Known allergies: PCN" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Flu vaccine, reaction(s): "Known allergies: Flu vaccine".The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. .The patient did not received any other medications within 2 weeks of vaccination.Prior to vaccination, the patient was not diagnosed with COVID-19.Since the vaccination, the patient has not been tested for COVID-19.The following information was reported: NEUROPATHY PERIPHERAL (disability, medically significant) with onset 05Jan2022 22:15, outcome "not recovered", described as "Neuropathy"; PYREXIA (disability) with onset 05Jan2022 22:15, outcome "recovered" (13Jan2022), described as "Fever 101.4"; CHILLS (disability) with onset 05Jan2022 22:15, outcome "recovered" (20Jan2022), described as "Chills"; NAUSEA (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "nausea"; VOMITING (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "vomiting"; PAIN (disability) with onset 05Jan2022 22:15, outcome "recovered" (20Jan2022), described as "body aches"; ANOSMIA (disability) with onset 05Jan2022 18:00, outcome "not recovered", described as "loss of smell/can't smell anything, not even bad cat litter"; PAIN IN EXTREMITY (disability), MOVEMENT DISORDER (disability) all with onset 05Jan2022 22:15, outcome "recovered" (09Jan2022) and all described as "Left arm pain and unable to move"; MUSCULAR WEAKNESS (disability) with onset 05Jan2022 22:15, outcome "recovered" (Jan2022), described as "Total weakness in extremities"; VISION BLURRED (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "Blurred vision"; VERTIGO (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "vertigo"; HYPOAESTHESIA (disability), HYPOAESTHESIA (disability), HYPOAESTHESIA (disability) all with onset 05Jan2022 22:15, outcome "not recovered" and all described as "Numbness in fingers, toes and legs"; FATIGUE (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "Extreme fatigue"; SOMNOLENCE (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "Slept for 72 hours without waking up until a welfare check by neighbors"; DECREASED APPETITE (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "no appetite"; MUSCLE FATIGUE (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "muscle fatigue"; ALOPECIA (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "hair loss"; MUSCLE ATROPHY (disability) with onset 05Jan2022 22:15, outcome "not recovered", described as "disuse muscle atrophy".Clinical course: Fever 101.4 for 7 days. Chills, nausea, vomiting, body aches all for 14 days loss of smell immediately. Left arm pain and unable to move 3 days. Total weakness in extremities 3 weeks. Blurred vision and vertigo still. Numbness in fingers, toes and legs still. Continue vomiting and nausea, can't smell anything, not even bad cat litter. Extreme fatigue. Slept for 72 hours without waking up until awelfare check by neighbors. I keep retyping this info. Before I'm kicked out of the system Nausea, vomiting, chills fever over 101.4 times two weeks and I have documentation via camera dates and time, loss of smell, no appetite, muscle fatigue, Neuropathy, hair loss, left arm pain, with disuse muscle atrophy. The patient underwent the following laboratory tests and procedures: body temperature: (05Jan2022) 101.4. It was unknown if therapeutic measures were taken as a result of neuropathy peripheral, pyrexia, chills, nausea, vomiting, pain, anosmia, pain in extremity, movement disorder, muscular weakness, vision blurred, vertigo, hypoaesthesia, hypoaesthesia, hypoaesthesia, fatigue, somnolence, decreased appetite, muscle fatigue, alopecia, muscle atrophy. No follow up attempt needed, No follow up information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220105; Test Name: Fever; Result Unstructured Data: Test Result:101.4
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Nerve injury (I've had nerve injury to left arm. Before I could ask for the other arm, he already jabbed me.); Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2085402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 23.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / UN

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

Biopsy skin Granulomatous dermatitis Injection site reaction Laboratory test

Symptomtext

Development of persistent granulomatous dermatitis at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site reaction
Hospital-Tage: -
Labordaten: Skin biopsy and tissue culture 1/27/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Rosacea, hypothyroidism
Andere Medikamente: levothyroxine, hydrochlorothiazide, Toviaz, alpraxolam, lisinopril, doxycycline, azelaic acid, omeprazole
Allergien: None
Vorherige Impfungen: -

VAERS 2080269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: KS
Alter: 17,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 21.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: SYR / RA

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

Abdominal pain upper Appendicectomy Appendicitis Computerised tomogram abnormal

Symptomtext

Pt. experienced severe stomach pain on January 12 , 2022 which led to a trip to the Emergency Room. A cat scan was performed and acute appendicitis was diagnosed. His appendix was then removed by Doctor. It was his second trip to the emergency room as pt. had a cat scan in August 2021 for stomach pain. His first two Covid 19 pfizer BioNtech vaccinations occurred on April 3, 2021 and April 24, 2021, respectively. It must be noted his older brother who had the same Pfizer vaccinations on the same dates and schedule, had severe stomach issues (also August 2021) and after a cat scan was performed, had emergency surgery to remove his appendix for acute appendicitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: 1,0
Labordaten: Cat Scan performed at Emergency room.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Celiac
Andere Medikamente: growth hormone - Norditropine
Allergien: wheat, tree nuts and peanuts, dairy.
Vorherige Impfungen: Severe Stomach Pain in August 2021 after April 201 Pfizer vaccinations

VAERS 2079070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MD
Alter: 54,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 14.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

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

Headache Neck pain Pain

Symptomtext

I'm having pain in the lower rear of my head and upper back of my neck. Pain worsens during sleep. Almost not able to roll over at night because the pain is so bad. This has been going on since 12/21/2021 which is 1 week after the vaccination. This has occurred every night since 12/21/2021. Rear of my head and upper back of my neck are also sore during the day but not as bad as during the night. When I drive, it is hard for me to turn my head to the left or to the right. I have to turn my whole body to see to the left and to see to the right.

Weitere VAERSDATA-Felder

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

VAERS 2078779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / -

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

Erythema Pruritus Swollen tongue Urticaria

Symptomtext

My reaction was within 15mins with hives , itching and redness over my body. And tongue swelling. I took Benadryl as soon as I started itching do to I was familiar of my reactions of latex and keFlix. Then I follow up with my primary doctor as well as the Pharmacy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: No test was done but primary doctor saw my skin
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: KeFlix and Latex
Vorherige Impfungen: -

VAERS 2074998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 07.06.2021
Beginn: 11.08.2021
Tage bis Beginn: 65,0
Dosis: 3
Route/Site: SYR / LA

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

Cyst Cyst removal Mass Pain

Symptomtext

1st Dose of vaccine 06/07/21 2nd Dose of vaccination 6/28/21 Started noticing a small lump under my left arm mentioned to Dr and she referred me to a dermatologist on 8/11/2021 3rd Dose of vaccination 12/29/2021 left arm. started noticing the lump getting bigger then it started hurting. 1/24/2022 Saw a dermatologist due to severe pain and a noticeably much larger lump. Diagnosed with a cyst and scheduled for removal. Placed on medication but no change until removal 1/29/2022- Removed cyst awaiting Biopsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 1st Dose of vaccine 06/07/21 2nd Dose of vaccination 6/28/21 Started noticing a small lump under my left arm mentioned to Dr and she referred me to a dermatologist on 8/11/2021 3rd Dose of vaccination 12/29/2021 left arm. started noticing the lump getting bigger then it started hurting. 1/24/2022 Saw a dermatologist due to severe pain and a noticeably much larger lump. Diagnosed with a cyst and scheduled for removal. Placed on medication but no change until removal 1/29/2022- Removed cyst, awaiting Biopsy
Aktuelle Erkrankungen: possible Diabetes
Vorgeschichte: Diabetes
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2074983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: KY
Alter: 31,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 27.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Burning sensation Cough Fatigue Hypersomnia Oropharyngeal pain Pain Pruritus Pyrexia

Symptomtext

Had a Non-severe Allergic Reaction to the first vaccine (Pfizer, lot:EN6205), in March. Delayed 2nd shot, because we were unsure of what outcome could be (no data was present, about reactions to 2nd shots yet)... Before receiving the 2nd shot I took one Benedryl Tablet.. About an 1 to an hour and a half later, after the shot, I started to get an itching/burning sensation, went home took another Benedryl and proceeded to sleep through the rest of the day. The next day I ended up with body aches and a sore throat and coughing.. the day after that added a mild grade fever and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: Unknown
Vorherige Impfungen: 1st Covid shot (Pfizer, Lot:EN6205) non severe allergic reaction (itching/burning, hives and chest tightness) occurred 45mins af

VAERS 2071656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IA
Alter: 17,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 27.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Arthralgia Chills Dizziness Immediate post-injection reaction Pain Pyrexia

Symptomtext

Light Headed immediately after vaccination, within a few hours afterward joint pain, body aches, chills and low grade fever

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Gluten Sensitivity
Andere Medikamente: Women's Multi Vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2068896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 53,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 07.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Arthritis bacterial Aspiration joint abnormal Atrial fibrillation Blood culture positive Culture urine positive Fatigue Headache Myalgia Nausea Purulence Staphylococcus test positive Vomiting

Symptomtext

Patient initially called office with HA, myalgia and muscle pain. The patient presented to hospital on 1/17/2022 with a chief complaint of nausea, vomiting, fatigue, muscle aches, bilateral shoulder pain Septic joint in bilateral shoulders. Left shoulder had purulence on aspiration. Shoulders thought to be septic from seeding. Also new onset A. fib with RVR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: 5,0
Labordaten: Blood culture positive for MSSA, Joint aspiration bilateral shoulders culture positive MSSA, urine positive MSSA
Aktuelle Erkrankungen: -
Vorgeschichte: Kidney transplant recipient HTN obesity ESRD Gout ADD IgA neuropathy
Andere Medikamente: APAP 650mg q 6 PRN allopurinol 100mg daily Adderall 30mg BID cinacalcet 30mg BID Flexeril 10 mg TID Neurontin 300mg qHS Mag-ox 400mg daily lopressor 100mg BID myfortic 540mg BID Prilosec 40mg BID oxycodone 10mg q4hrs PRN Prograf 1.5mg BID
Allergien: PCN lisinopril
Vorherige Impfungen: -

VAERS 2068542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: GA
Alter: 53,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 05.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

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

Headache Memory impairment

Symptomtext

Headaches daily. Upper/top and foward on head. Short term memory getting worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: Body aches and chills.

VAERS 2065871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: KY
Alter: 77,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 17.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Diarrhoea Exposure to SARS-CoV-2 Hypophagia

Symptomtext

Recent COVID exposure in his house. Yesterday started feeling weak. He has had intermittent diarrhea and poor p.o. intake.

Weitere VAERSDATA-Felder

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

VAERS 2065573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CO
Alter: 43,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 20.01.2022
Beginn: 22.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac flutter Chest discomfort Fatigue Pain

Symptomtext

She had upper chest discomfort. She stated she had tense pressure in her chest just lingering there. Her heart felt fluttery which went away. Body aches and became tired. The body aches did subside.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: `no
Allergien: no
Vorherige Impfungen: -

VAERS 2062650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Lymph node pain Lymphadenopathy Pyrexia

Symptomtext

fatigue; fever up to 103 F; left axillary lymph nodes were very sore and swollen for 5 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Pfizer Covid 19; age 48; 1-19-2021; fever

VAERS 2061865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Chills Headache

Symptomtext

severe headache; chills/chills are getting worse; This is a spontaneous report received from contactable reporter (Consumer or other non-HCP) from medical information team. The reporter is patient's husband. An 89-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm, administration date 10Jan2022 10:00 (Lot number: FE3594) at the age of 89 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "Multiple myeloma", start date: 2020 (unspecified if ongoing), notes: Caller says this was diagnosed about two years ago.; "Lung cancer", start date: 2010 (unspecified if ongoing), notes: Caller says this was diagnosed 12 years ago.; "hard of hearing" (ongoing). There were no concomitant medications. The following information was reported: HEADACHE (non-serious) with onset 10Jan2022 11:00, outcome "not recovered", described as "severe headache"; CHILLS (non-serious) with onset 10Jan2022, outcome "not recovered", described as "chills/chills are getting worse". Therapeutic measures were taken as a result of headache, chills included paracetamol (TYLENOL). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Hard of hearing.
Vorgeschichte: Medical History/Concurrent Conditions: Lung cancer (Caller says this was diagnosed 12 years ago.); Multiple myeloma (Caller says this was diagnosed about two years ago.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE 3594

mild

Staat: FL
Alter: 59,0
Geschlecht: M
Eingang: 23.01.2022
Impfdatum: 15.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / LA

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

Arthralgia Musculoskeletal discomfort Pain

Symptomtext

Shoulder pain made worse by cold weather. Pt has no trouble rotating the arm, but his shoulder is painful, uncomfortable doing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none yet.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: -
Allergien: N/A
Vorherige Impfungen: -

VAERS 2516637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 07.01.2022
Beginn: 06.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Diarrhoea Headache Pain in extremity Vitreous floaters

Symptomtext

Headache, Diarrhea, seeing floaters in left eye; sore arm Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2057373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 18,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 15.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Immunisation Vaccination site pain

Symptomtext

Dose number: 3; Arm pain at the site of injection; This is a spontaneous report received from a contactable reporter (consumer or other non-HCP). A 18-year-old female patient received bnt162b2 (BNT162B2), administration date 15Jan2022 (Lot number: FE3594) at the age of 18 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19? : Yes. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EW0171, Route of administration: unspecified), for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE, Lot Number: UNKNOWN, Route of administration: unspecified), for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 15Jan2022, outcome "unknown", described as "Dose number: 3"; VACCINATION SITE PAIN (non-serious) with onset 15Jan2022, outcome "recovering", described as "Arm pain at the site of injection". Therapeutic measures were not taken as a result of vaccination site pain. Additional information: Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19? :Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

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

Chills Immunisation Pain Vaccination site pain

Symptomtext

Mild Injection site pain; chills; body aches; Dose number=3; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 47 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 05Jan2022 17:00 (Lot number: FE3594) at the age of 47 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies: Penicillin family of antibiotics" (unspecified if ongoing). Concomitant medication(s) included: SERTRALINE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EN6207), administration date: 26Apr2021, when the patient was 46 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN5318), administration date: 05Apr2021, when the patient was 46 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022 17:00, outcome "unknown", described as "Dose number=3"; VACCINATION SITE PAIN (non-serious) with onset 06Jan2022 07:00, outcome "not recovered", described as "Mild Injection site pain"; CHILLS (non-serious) with onset 06Jan2022 07:00, outcome "not recovered", described as "chills"; PAIN (non-serious) with onset 06Jan2022 07:00, outcome "not recovered", described as "body aches". Therapeutic measures were not taken as a result of vaccination site pain, chills, pain. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente: SERTRALINE
Allergien: -
Vorherige Impfungen: -

VAERS 2057034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 37,0
Geschlecht: M
Eingang: 22.01.2022
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: ja Erholt: nein

Back pain Biopsy Blood testosterone Body temperature Chest X-ray Computerised tomogram Computerised tomogram abdomen Feeling abnormal Gait inability Immobile Immunisation Lumbar puncture Magnetic resonance imaging Muscle strain Pain SARS-CoV-2 test Spinal deformity Swelling

Symptomtext

booster; arm was immobilized; pain; bad pain in back; Swollen back; body felt torn; can't walk; body messed up; Back curls up; This is a spontaneous report received from contactable reporter (Consumer). A 37-year-old male patient received bnt162b2 (BNT162B2), administration date 13Dec2021 (Lot number: FE3594) at the age of 37 years as dose 2 (booster), single for covid-19 immunisation. Relevant medical history included: "Covid-19 illness in 2006/had some kind of corona virus or sars type illness", start date: 2006 (not ongoing), notes: Covid-19 illness in 2006/had some kind of corona virus or sars type illness; "Allergic to psychological Drugs" (ongoing); "Allergic to psychological Drugs: Seizures" (unspecified if ongoing); "Smoker" (ongoing), notes: smoke 3-4 cigarettes per day; "Non-Alcohol user" (ongoing); "Fever" (ongoing), notes: patient was ill at the time of vaccination; "Body ache" (ongoing), notes: patient was ill at the time of vaccination; "Headache" (unspecified if ongoing), notes: patient was ill at the time of vaccination. Concomitant medications included: SEROQUEL, start date: 2002; METHADONE, start date: 2009. Vaccination history included: Covid-19 vaccine ad26.cov2. s (dose 1; batch number: 1805022 at 12:00 on left arm), administration date: 22Mar2021, when the patient was 37 years old, for prophylactic vaccination, reaction(s): "inappropriate route of administration", "Kidney failure", "Blood clot in the leg", "Liver infection", "Staph infection in spine that eating away bone marrow", "Kidney Infection / Kidney Inflammation", "Discitis", "can't move/ barely get out of bed/bedridden in hospital/cannot move legs/cant walk/ not been able to walk at all/ unable to walk", "severe back pain", "blood clot in the femoral artery", "infection in the arm that spread to the hips/infection in disc of the back", "confirmed COVID-19 Infection", "calcification in cerebral artery", "confirmed inflammation", "bottom part of body weighing down", "oversized artery", "Lungs filled with fluid", "Appendix messed up", "Gall Bladder messed up", "Pancreatic pain", "Abdominal swelling", "losing weight", "Loss appetite", "pain to left and right flank area", "left side of body numb/ both hands numb and cold", "Low testosterone", "leg and feet pain worsening/chronic pain", "vein inside left hip is protruding and bulging", "Loss of voice", "gasteritis in back"; Flu vaccine, reaction(s): "got nauseated once". The following information was reported: IMMUNISATION (medically significant) with onset 13Dec2021, outcome "unknown", described as "booster"; IMMOBILE (medically significant) with onset 13Dec2021, outcome "not recovered", described as "arm was immobilized"; PAIN (non-serious) with onset 13Dec2021, outcome "unknown", described as "pain"; BACK PAIN (non-serious) with onset 13Dec2021, outcome "not recovered", described as "bad pain in back"; SWELLING (non-serious) with onset 13Dec2021, outcome "unknown", described as "Swollen back"; MUSCLE STRAIN (non-serious) with onset 13Dec2021, outcome "unknown", described as "body felt torn"; GAIT INABILITY (non-serious) with onset 13Dec2021, outcome "not recovered", described as "can't walk"; FEELING ABNORMAL (non-serious) with onset 13Dec2021, outcome "unknown", described as "body messed up"; SPINAL DEFORMITY (non-serious) with onset 13Dec2021, outcome "unknown", described as "Back curls up". The event "bad pain in back" was evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: biopsy: (unspecified date) unknown results, notes: Classification: unk; (04Jun2021) results awaiting, notes: Classification: unk; blood testosterone: (unspecified date) low, notes: Classification: unk; body temperature: (23Mar2021) 102 Fahrenheit, notes: Classification: unk; chest x-ray: (unspecified date) unknown results, notes: Classification: unk; computerised tomogram: (unspecified date) unknown results, notes: Classification: unk; computerised tomogram abdomen: (unspecified date) clear, notes: Classification: unk; lumbar puncture: (unspecified date) unknown results, notes: Classification: unk; (03Jun2021) results not mentioned, notes: Classification: unk; magnetic resonance imaging: (unspecified date) staph infection, notes: Classification: unk; (unspecified date) unknown results, notes: Classification: unk; sars-cov-2 test: (unspecified date) positive; ultrasound scan: (unspecified date) unknown results, notes: Classification: unk. Additional information: on 13Dec2021, the patient was experiencing similar symptoms like the first time when he received the Covid-19 vaccine ad26. cov2 (Janssen). Following vaccination with BNT162 (13Dec2021), the patient experienced pain, body felt torn, back curled up, body was messed up, arm was immobilized, can't walk, bad pain in back and swollen back (dose number in series 2). Company (Janssen) Remarks: These events are considered unassessable. The events have a compatible/ suggestive temporal relationship, are unlabeled, and have unknown scientific plausibility. There is no information on any other factors potentially associated with the events. These events are labeled per RA and are therefore considered potentially related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Test Name: Biopsy; Result Unstructured Data: Test Result:Unknown results; Comments: Classification: unk; Test Date: 20210604; Test Name: Biopsy; Result Unstructured Data: Test Result:results awaiting; Comments: Classification: unk; Test Name: Testosterone; Result Unstructured Data: Test Result:low; Comments: Classification: unk; Test Date: 20210323; Test Name: body temperature; Result Unstructured Data: Test Result:102 Fahrenheit; Comments: Classification: unk; Test Name: chest x-ray; Result Unstructured Data: Test Result:Unknown results; Comments: Classification: unk; Test Name: CAT Scan; Result Unstructured Data: Test Result:Unknown results; Comments: Classification: unk; Test Name: CT abdominal; Result Unstructured Data: Test Result:clear; Comments: Classification: unk; Test Name: lumbar puncture; Result Unstructured Data: Test Result:Unknown results; Comments: Classification: unk; Test Date: 20210603; Test Name: lumbar puncture; Result Unstructured Data: Test Result:results not mentioned; Comments: Classification: unk; Test Name: MRI; Result Unstructured Data: Test Result:staph infection; Comments: Classification: unk; Test Name: MRI; Result Unstructured Data: Test Result:Unknown results; Comments: Classification: unk; Test Name: covid-19 test; Test Result: Positive ; Test Name: ultrasound; Result Unstructured Data: Test Result:Unknown results; Comments: Classification: unk
Aktuelle Erkrankungen: Abstains from alcohol; Drug allergy; Fever (patient was ill at the time of vaccination); Generalized aching (patient was ill at the time of vaccination); Smoker (smoke 3-4 cigarettes per day)
Vorgeschichte: Medical History/Concurrent Conditions: Headache (patient was ill at the time of vaccination); SARS-CoV-1 infection (Covid-19 illness in 2006/had some kind of corona virus or sars type illness); Seizures
Andere Medikamente: SEROQUEL; METHADONE
Allergien: -
Vorherige Impfungen: -

VAERS 2057008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MA
Alter: 45,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 18.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Body temperature Body temperature increased Chills Hot flush Immunisation Menstruation delayed Night sweats Pain Pain in extremity

Symptomtext

Dose received: 3; sore arm; temp 101; body aches; chills; night sweats; hot flashes; my period is always on time and started 5 days late; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 45 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 18Dec2021 05:00 (Lot number: FE3594) at the age of 45 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "known allergies: shell fish" (unspecified if ongoing), notes: known allergies: shell fish; "known allergies:cow dairy milk" (unspecified if ongoing), notes: known allergies: cow dairy milk; "known allergies: gluten" (unspecified if ongoing), notes: known allergies: gluten. Concomitant medication(s) included: SYNTHROID; LIOTHYRONIN; CALCIUM. Vaccination history included: Bnt162b2 (dose number=1,, lot number=EW0158,, vaccine location=Left arm, Shots 1 & 2 only gave me sore arm), administration date: 12Apr2021, when the patient was 44 years old, for Covid-19 Immunization, reaction(s): "Sore arm"; Bnt162b2 (dose number=2,, lot number=EW0173,, vaccine location=Left arm, Shots 1 & 2 only gave me sore arm), administration date: 01May2021, when the patient was 44 years old, for Covid-19 Immunization, reaction(s): "Sore arm". The following information was reported: IMMUNISATION (non-serious) with onset 18Dec2021 05:00, outcome "unknown", described as "Dose received: 3"; PAIN IN EXTREMITY (non-serious) with onset 18Dec2021, outcome "recovered" (Dec2021), described as "sore arm"; BODY TEMPERATURE INCREASED (non-serious) with onset 18Dec2021, outcome "recovered" (Dec2021), described as "temp 101"; PAIN (non-serious) with onset 18Dec2021, outcome "recovered" (Dec2021), described as "body aches"; CHILLS (non-serious) with onset 18Dec2021, outcome "recovered" (Dec2021), described as "chills"; MENSTRUATION DELAYED (non-serious) with onset Dec2021, outcome "unknown", described as "my period is always on time and started 5 days late"; NIGHT SWEATS (non-serious) with onset 18Dec2021, outcome "unknown", described as "night sweats"; HOT FLUSH (non-serious) with onset 18Dec2021, outcome "unknown", described as "hot flashes". The events "sore arm", "temp 101", "body aches", "chills", "my period is always on time and started 5 days late", "night sweats" and "hot flashes" were 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 pain in extremity, body temperature increased, pain, chills, menstruation delayed, night sweats, hot flush. Additional information; 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. 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: Chills
Hospital-Tage: -
Labordaten: Test Date: 20211218; Test Name: Temp; Result Unstructured Data: Test Result:101
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to cow's milk (known allergies: cow dairy milk); Gluten sensitivity (known allergies: gluten); Shellfish allergy (known allergies: shell fish)
Andere Medikamente: SYNTHROID; LIOTHYRONIN; CALCIUM
Allergien: -
Vorherige Impfungen: -

VAERS 2057007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Headache Immunisation Poor quality product administered Product preparation error Thinking abnormal Vaccination site pain

Symptomtext

Booster; mistakenly used sterile water for injection instead of sterile sodium chloride as the diluent for Comirnaty or the Pfizer-BioNTech COVID-19 vaccine; mistakenly used sterile water for injection instead of sterile sodium chloride as the diluent for Comirnaty or the Pfizer-BioNTech COVID-19 vaccine; Headache; brain fog; Mild soreness at the injection site; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from medical information team. A 43 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Jan2022 (Lot number: FE3594, Expiration Date: 03Jan2022) at the age of 43 years as dose 3 (booster) 0.3ml, single for covid-19 immunisation. Relevant medical history included: "Type 1 diabetes mellitus" (ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (First dose , Lot: EL0140, Expiration: Unknown, Expiry Date of Covid-19 Vaccine: 03Jan2022), administration date: 21Dec2020, when the patient was 42 years old, for COVID-19 Immunization; Bnt162b2 (Second dose: 18Jan2021, Lot: Unknown, Expiration: Unknown, Expiry Date of Covid-19 Vaccine: 03Jan2022), administration date: 18Jan2021, when the patient was 42 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 03Jan2022, outcome "unknown", described as "Booster"; PRODUCT PREPARATION ERROR (non-serious), POOR QUALITY PRODUCT ADMINISTERED (non-serious) all with onset 03Jan2022, outcome "unknown" and all described as "mistakenly used sterile water for injection instead of sterile sodium chloride as the diluent for Comirnaty or the Pfizer-BioNTech COVID-19 vaccine"; HEADACHE (non-serious) with onset 03Jan2022, outcome "unknown", described as "Headache"; THINKING ABNORMAL (non-serious) with onset 03Jan2022, outcome "unknown", described as "brain fog"; VACCINATION SITE PAIN (non-serious) with onset 03Jan2022, outcome "unknown", described as "Mild soreness at the injection site". Additional information: It was reported that the Nurse Practitioner calling on behalf of her Pharmacist that mistakenly used sterile water for injection instead of sterile sodium chloride as the diluent for Comirnaty or the Pfizer-BioNTech COVID-19 vaccine. 2 doses of the vaccine were administered as the Booster dose for a 43 and 37-year old female patient. Can I use the vaccine? If already used to vaccinate individuals, does this count as a valid dose? Pfizer has not tested the effects of using sterile water for injection as the diluent for Comirnaty or any of the Pfizer-BioNTech COVID-19 Vaccine formulations that require dilution (ie, purple or orange cap). The diluted vaccine using sterile water for injection as the diluent should be appropriately discarded and not used for vaccination. If the vaccine that was diluted with sterile water for injection was inadvertently administered to individuals, a definitive statement on the quality and usability of the vaccine diluted in water cannot be made. The vaccine has not been tested with sterile water for injection as the diluent. Pfizer is unable to definitively state if the vaccine dose is valid or invalid. However, the CDC states the following: & quot; Contact the manufacturer for information on the stability of the vaccine. If the manufacturer does not have information to support the stability of the vaccine, repeat the dose immediately (no minimum interval). & quot; Source: ACIP Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200011184 Same reporter/ drug/ event for different patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Type 1 diabetes mellitus
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054148

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NJ
Alter: 46,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Abortion spontaneous Acoustic stimulation tests Deafness unilateral Ear discomfort Exposure during pregnancy Headache Hypoacusis

Symptomtext

On December 17, I received my first Pfizer vaccine at the local Hospital. About two hours after the shot, I started with a terrible headache. The headache lasted about three days. On the third day I had a telehealth visit and the Doctor told me that he thought that I had a sinus infection and prescribed antibiotics for 5 days. Later that day I also had a miscarriage. I saw my GYN that week who confirmed my miscarriage. I finished the antibiotics on Dec 25. On December 26 felt like I had just got off plane, my ears felt clogged and I had a hard time hearing. On Dec 27 I called my primary physician told them everything that happened and they prescribed a steroid pack. The feeling did not go away and got worse in my opinion. On Jan 10 went to ENT explained the above and they scheduled a hearing test. I received hearing test on Jan 12, which showed a dramatic loss of hearing in my right ear. That same day I received a steroid shot in my ear. To date the hearing fluctuates. The doctor believes a virus attacked nerve in ear. On Jan 26 I will receive another hearing test and another steroid injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid Disease, RA, GI issues
Andere Medikamente: Levothyroxine 25MCG, Montelukast 10,
Allergien: Tree fruit and Iodine
Vorherige Impfungen: -

VAERS 2053891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: PA
Alter: 36,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal discomfort Abdominal distension Abdominal pain Diarrhoea Nausea

Symptomtext

I had the vaccine, within 14 hours, had liquid diarrhea, then had diarrhea about 5 x day for 2 days, then abdominal discomfort, then severe abdominal pain, nausea, abdominal bloating for 4 days. By 1 week then pain has subsided about 75%, appetite is still only 50%, and slight abdominal discomfort.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: tylenol, multivitamin
Allergien: augmentin, aleve, lactose intolerant, sensitive to eggs
Vorherige Impfungen: 1st pfizer vaccine, had horrible memory issues x 2.5 weeks, age 36

VAERS 2051344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 18.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Breast pain Fatigue Lymphadenopathy Pyrexia

Symptomtext

Fever for several days. Swollen lymph nodes in the armpit where the booster was given. Breast hurts. Fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: Fever.

VAERS 2051079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: FL
Alter: 81,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 31.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Muscle spasms Myalgia Rash

Symptomtext

SEVERE LEG CRAMPS/MUSCLE PAIN, CHILLS, TRUNK RASH

Weitere VAERSDATA-Felder

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

VAERS 2050321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WI
Alter: 59,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Urticaria

Symptomtext

Hives; booster; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 16Dec2021 15:00 (Lot number: FE3594) at the age of 59 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. Past drug history included: None, notes: Known allergies: None, Other medical history: None. Vaccination history included: Bnt162b2 (DOSE 2, SINGLE, Prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand unknown: False, Prev dose lot number: EW0172, Prev dose lot unknown: False, Prev dose administration date: 29Apr2021 , Prev dose number: 2, Prev dose vaccine location: Right arm), administration date: 29Apr2021, when the patient was 58 years old, for Covid-19 immunization; Bnt162b2 (DOSE 1, SINGLE, Prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand unknown: False, Prev dose lot number: EW0158, Prev dose lot unknown: False, Prev dose administration date: 08Apr2021 , Prev dose number: 1 , Prev dose vaccine location: Right arm), administration date: 08Apr2021, when the patient was 58 years old, for Covid-19 immunization.The following information was reported: IMMUNISATION (non-serious) with onset 16Dec2021 15:00, outcome "unknown", described as "booster"; URTICARIA (non-serious) with onset 20Dec2021, outcome "recovered" (2021), described as "Hives". Therapeutic measures were taken as a result of immunisation, urticaria. Additional information: The patient did not receive any other vaccines within 4 weeks. Treatment was received in response to the adverse events. The patient was not diagnosed with COVID-19 prior to vaccination and Since the vaccination, patient was not tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: Known allergies: None Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2048091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: VA
Alter: 41,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness Headache Lip swelling Pain

Symptomtext

Severe body aches, head aches, light headed, swollen lips

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sumatriptan
Allergien: None
Vorherige Impfungen: -

VAERS 2047906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 44,0
Geschlecht: F
Eingang: 19.01.2022
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: nein

Headache Product preparation error

Symptomtext

Patient was given 0.3 ml of undiluted Pfizer vaccine. Patient was in observation for 15 minutes per protocol and was not observed to have any undue affects. Patient contacted that day, but was not responding to phone calls, so voice message was left to have her call the pharmacy. She returned the phone call in the morning and was informed of the error. I asked how she was feeling, her response was that she was suffering from a severe headache and that the error obviously was the cause of that symptom.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: At this time none needed
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None known
Allergien: None
Vorherige Impfungen: -

VAERS 2045780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: GA
Alter: 31,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Immediate post-injection reaction Injection site pain Musculoskeletal discomfort

Symptomtext

Site: Pain at Injection Site-Mild, Additional Details: discomfort in shoulder lasting weeks after injection, but felt immediately at injection time that something was wrong. discomfort doesn't limit range of motion, no tingling or numbness. dr advised him it might take several weeks or mothns to go away. no further follow up at this time.

Weitere VAERSDATA-Felder

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

VAERS 2045459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MN
Alter: 15,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 08.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Visual impairment

Symptomtext

Systemic: Dizziness/Lightheadedness-Mild, Systemic: Visual Changes/Disturbances-Medium, Additional Details: O2 SAT 99.9; unable to obtain BP in both arms. She was unable to see for about 3-5 minutes. We elevated her legs and provided water. Patient was with family and appeared to improve shortly after reaction. She started walking around with family. Patient stated normal "ok" when they left the pharmacy.

Weitere VAERSDATA-Felder

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

VAERS 2042861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 53,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Hypoaesthesia Neck pain Pain

Symptomtext

Patient complains of radiating pain to shoulder and neck for about a month and arm numbness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril
Allergien: none
Vorherige Impfungen: -

VAERS 2039850

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: NC
Alter: 16,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 27.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Full blood count normal Henoch-Schonlein purpura Metabolic function test Petechiae Rash Urine analysis normal

Symptomtext

Petechial rash of lower extremities started on 01/03/2022. On 01/10/2022 rash was almost completely gone. Follow up on 01/13/2022, rash was no longer present. Only other symptom was slight fatigue. Normal CBC with diff, normal UA and normal BP. Diagnosed with henoch-schonlein purpura.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 1/06/2022: CBC w/ diff, CMP, UA (all normal) 01/13/2022: UA (normal)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Hyroxyzine 25mg, Guanfacine HCl 2mg ER 1po QD
Allergien: Amoxicillin: swollen eyes
Vorherige Impfungen: -

VAERS 2039122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 13,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Fatigue

Symptomtext

extreme fatigue for 24 hours

Weitere VAERSDATA-Felder

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

VAERS 2038423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: FL
Alter: 77,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 27.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / LA

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

Rash

Symptomtext

Patient reported a rash in her body that is been getting worse since the beginning of the year. The rash is now in her whole body. She saw a dermatologist on 1/14/22 that prescribed oral steroids and topical steroid. She was advised by dermatologist to come back in 2 weeks if no improvement. The rash is still present as of 1/15/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: nothing reported by patient
Vorgeschichte: nothing reported by the patient
Andere Medikamente: unknown
Allergien: cephalosporin/penicillin/ environmental allergies
Vorherige Impfungen: -

VAERS 2038221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 62,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Chills Fatigue Headache Injection site erythema Injection site pain Injection site pruritus Injection site swelling Myalgia

Symptomtext

Chills, muscle and joint pain, headache, fatigue, redness/swelling/itching/pain at injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, high cholesterol
Andere Medikamente: Amlodipine 5mg/day, Claritin 10mg/day, rosuvastatin 5mg 3x/wk, aspirin 81mg/day, mvi daily, vitamin d, vitamin c, co q 10, zinc, magnesium and turmeric
Allergien: Flu vaccine, beta blockers, codeine
Vorherige Impfungen: Flu vaccine

VAERS 2024375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TN
Alter: 31,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Cough Fatigue Feeling abnormal Immunisation Nasal congestion COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

cough; congestion; brain fog; exhaustion; booster; 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), administration date 15Dec2021 13:00 (Lot number: FE3594) at the age of 31 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 2, Prev dose brand: Pfizer, Lot no= EP6955), administration date: 26Mar2021, when the patient was 30 years old, for COVID-19 immunization; Bnt162b2 (Dose: 1, Prev dose brand: Pfizer, Lot no= EL3248), administration date: 05Mar2021, when the patient was 30 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 15Dec2021 13:00, outcome "unknown", described as "booster"; COUGH (non-serious) with onset 29Dec2021, outcome "recovered", described as "cough"; NASAL CONGESTION (non-serious) with onset 29Dec2021, outcome "recovered", described as "congestion"; FEELING ABNORMAL (non-serious) with onset 29Dec2021, outcome "recovered", described as "brain fog"; FATIGUE (non-serious) with onset 29Dec2021, outcome "recovered", described as "exhaustion". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of cough, nasal congestion, feeling abnormal, fatigue. Additional Information: The patient did not have other vaccine in four weeks. The patient had symptoms of cough, congestion, brain fog, and general exhaustion for a period of about 7 - 10 days. The patient did not have covid prior to vaccination. The patient had covid tested post vaccination. The patient do not have known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20211229; Test Name: COVID Test; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2035290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MN
Alter: 24,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Swelling

Symptomtext

Severe swelling of left armpit, coupled with pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2014626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 29,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Rash

Symptomtext

After vaccination I developed a painful rash that is bilateral, under my arms and on my flanks.; This is a spontaneous report from a contactable reporter (nurse). The reporter is the patient. A 29-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 04Jan2022 (Lot number: FE3594) at the age of 29 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "None". The patient did not receive any concomitant medications. The following information was reported: RASH (non-serious) with onset 04Jan2022 at 21:30, outcome "not recovered", described as "After vaccination I developed a painful rash that is bilateral, under my arms and on my flanks". Therapeutic measures were not taken as a result of rash. Additional information: The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
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 2014626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 29,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Rash

Symptomtext

After vaccination I developed a painful rash that is bilateral, under my arms and on my flanks.; This is a spontaneous report from a contactable reporter (nurse). The reporter is the patient. A 29-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 04Jan2022 (Lot number: FE3594) at the age of 29 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "None". The patient did not receive any concomitant medications. The following information was reported: RASH (non-serious) with onset 04Jan2022 at 21:30, outcome "not recovered", described as "After vaccination I developed a painful rash that is bilateral, under my arms and on my flanks". Therapeutic measures were not taken as a result of rash. Additional information: The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
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 2033036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Injection site swelling Pyrexia

Symptomtext

Patient experiencing fever and swollen in injection site area. Patient is taking tylenol to help with symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site swelling
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: nka
Vorherige Impfungen: -

VAERS 2032355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OK
Alter: 74,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Pain Pyrexia

Symptomtext

Patient started running a fever at 9am. Joint pain all over her body started last night at 9pm as well. Patient woke up at 3am and was in pain from the shot. Started taking tylenol and ibuprofen to help ease the pain and fever. She received 2 doses of Moderna and opted for Pfizer as the booster shot. Patient called the pharmacy at 445pm to report she was still having joint pain and fever. Fever got up to 102 degrees at 2pm. Fever came down some. She is not able to get in to see her Primary care doc at this time.

Weitere VAERSDATA-Felder

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

VAERS 2032151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 62,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Malaise Pyrexia

Symptomtext

Low grade fever, chills, malaise started the afternoon following my booster. Treated with ibuprofen, fluids, rest. Mostly resolved by the second morning after the injection,.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: hypertension
Andere Medikamente: Bystolic, Rosuvastatin, "Relief Factor"
Allergien: None
Vorherige Impfungen: -

VAERS 2031765

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MT
Alter: 15,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Eczema Erythema Pain Pruritus Rash Swelling

Symptomtext

Pt received Pfizzer vaccine dose #1 in left deltoid on 01/11/22 at 9:30 AM. On 01/12/22 at 8:00 PM Pt and her mother noticed a rash on her left arm that mom described as being like eczema. Mom states, "she has eczema and the rash is like eczema". States that it is reddened and bumpy in patches on her arm. States that the patches of bumps are swollen, painful and itchy. States that patient has a few bumps on her right arm. Mom has given Pt Benadryl and put a barrier cream over the rash. Mom states that she will call patient's provider if rash or swelling worsens.

Weitere VAERSDATA-Felder

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

VAERS 2031552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: PA
Alter: 25,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 14.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Back pain Blood test Electrocardiogram Pain Pain in extremity Ultrasound scan

Symptomtext

A few days after I got the shot, I started to experience very sharp throbbing pains in both of my legs. This pain then continued to other areas of my body (I was having throbbing pains in my wrists, ankles, and lower back) Very scary. My doctor said that I should not still be experiencing side effects this many days out from getting the vaccine, and advised me to go to the ER. The pain has still not fully gone away, as I still will get random throbbing pains from time to time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Ultrasound on my legs to check for clots Blood tests EKG test to check my heart
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control
Allergien: None
Vorherige Impfungen: -

VAERS 2029047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 58,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 03.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

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

Dizziness Headache Lymphadenopathy Nausea

Symptomtext

Swollen Lymph Node under right armpit noticed 3 days after injection. Headache with dizziness and nausea beginning 7 days following injection. Lasting so far for 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Left Branch Bundle Block
Andere Medikamente: Lisinopril, Metoprolol, Acyclovir, Dupixent
Allergien: None
Vorherige Impfungen: -

VAERS 2027909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: PR
Alter: 12,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Peripheral coldness

Symptomtext

Patient in immunization area felt dizzy and weak. The patient was taken to the Treatment area in a wheelchair. The patient was moved to the stretcher where the lower extremities were raised and she was covered because she is cold to the touch. The patient is evaluated and consulted by Doctor. She leaves her under observation for 30 minutes. At 4:03 Doctor was consulted again, and she authorized the discharge of the patient wish states she felt good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2027657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: SC
Alter: -
Geschlecht: U
Eingang: 12.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Immunisation Lymphadenopathy Musculoskeletal stiffness Pain in extremity Vaccination site pain

Symptomtext

just lightly feels like my glands are swollen under my left arm; booster; the arm was sore; it was really sore and stiff; soreness in the injection area; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 05Jan2022 (Lot number: FE3594, Expiration Date: Feb2022) as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 1, MANUFACTURER UNKNOWN), for COVID-19 immunization; Covid-19 vaccine (Dose 2, MANUFACTURER UNKNOWN), for Covid-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 05Jan2022, outcome "unknown", described as "booster"; PAIN IN EXTREMITY (non-serious) with onset 05Jan2022, outcome "recovered" (Jan2022), described as "the arm was sore"; MUSCULOSKELETAL STIFFNESS (non-serious) with onset 05Jan2022, outcome "unknown", described as "it was really sore and stiff"; VACCINATION SITE PAIN (non-serious) with onset 05Jan2022, outcome "unknown", described as "soreness in the injection area"; LYMPHADENOPATHY (non-serious) with onset 06Jan2022, outcome "unknown", described as "just lightly feels like my glands are swollen under my left arm". Additional information: Reporter seriousness for The arm was sore but that went away so, last night it was really sore and stiff so, I had soreness in the injection area which was the left arm, just lightly feels like my glands are swollen under my left arm was Unspecified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2027597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: VA
Alter: 43,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Blepharospasm Headache Pyrexia

Symptomtext

Fever over 101.5 and severe headache for 48hrs. About 16hrs after the vaccine my left eye began to twitch. The twitch will come and go. But occurs more than if is not occurring. The twitch is still occurring at this time on 1/12/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2027415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 79,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 22.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Immunisation Rash Urticaria

Symptomtext

Hives on back; Booster; The rash went away in about four days.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 79 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 22Dec2021 11:50 (Lot number: FE3594, Expiration Date: 28Feb2022) at the age of 79 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Prostate cancer" (unspecified if ongoing), notes: caller doesn't remember the exact date of prostate cancer diagnosis but knows occurred at age 59.; "Kidney Cancer" (unspecified if ongoing), notes: The caller states the kidney cancer was approximately 10 years ago, the caller is guessing; "Prostate Removal" (unspecified if ongoing), notes: The prostate was removed when the caller was age 59 and the caller is 79 years now.; "Kidney removal" (unspecified if ongoing), notes: kidney removal was four years ago.; "Reoccurrence of Prostate Cancer" (unspecified if ongoing), notes: underwent 6.5 weeks of radiation, this occurred about 10 years ago. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose:1, lot: EL9265, Expiration: 31May2021, Route of administration: right arm on upper part of arm, Time the Vaccination Was Given: First dose: 1030 or 1100), administration date: 27Jan2021, when the patient was 78 years old, for COVID-19 Immunization; Bnt162b2 (Dose:2, lot: EN6201, Expiration: 30Jun2021 , Route of administration: right arm, Time the Vaccination Was Given:second dose: 1030 or 1100), administration date: 17Feb2021, when the patient was 78 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021 11:50, outcome "unknown", described as "Booster"; URTICARIA (non-serious) with onset 23Dec2021, outcome "recovered" (27Dec2021), described as "Hives on back"; RASH (non-serious) with onset Dec2021, outcome "not recovered", described as "The rash went away in about four days.". Therapeutic measures were taken as a result of urticaria, rash. Additional information: The caller is a consumer who was with caller's wife at a vaccination site today. The caller received Adult Pfizer Covid 19 Vaccine because the caller was a health risk at the caller's age and the number of things the caller has. The caller had kidney removed, several operations and prostate removed. The caller had enough things and had cancer three different times. The caller had a reoccurrence of prostate cancer and underwent 6.5 weeks of radiation, this occurred about 10 years ago. The caller received the booster dose Adult Pfizer Covid 19 Vaccine one week ago, on 22Dec2021. While at the vaccination site with caller's wife today, 29Dec2021, the caller mentioned to the vaccination site that the caller had a reaction after receiving the booster dose Adult Pfizer Covid 19 Vaccine. The caller had hives on back about one day after receiving the booster dose Adult Pfizer Covid 19 Vaccine. The caller clarifies the hives began on 23Dec2021, the day after the caller received the booster dose Adult Pfizer Covid 19 Vaccine. The rash went away in about four days. The caller's wife applied Benadryl to the caller's hives. The hives were on the caller's back just below the neck on the shoulder side of where the caller received the booster dose Adult Pfizer Covid 19 Vaccine. Agent asks caller if caller recovered complete from rash or with lasting effects and the caller state, there was just a small area of 10 to 12 rashes together. Adverse event did not resulted in Emergency room or physician office visit. Route of administration: right shoulder blade on right side, not blade itself, but where normally get vaccines. Additional Vaccines Administered on Same Date of the Pfizer Suspect If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect: 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): no. Adverse events following prior vaccination: No. Other products and investigation Assessment was reported as No. Relevant test: None. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Kidney cancer (The caller states the kidney cancer was approximately 10 years ago, the caller is guessing); Nephrectomy (kidney removal was four years ago.); Prostate cancer (caller doesn't remember the exact date of prostate cancer diagnosis but knows occurred at age 59.); Prostate cancer recurrent (underwent 6.5 weeks of radiation, this occurred about 10 years ago.); Prostatectomy (The prostate was removed when the caller was age 59 and the caller is 79 years now.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2025460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 08.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Chest discomfort Lymphadenopathy Mass Pain Pain in extremity Skin warm

Symptomtext

Two days after booster lump in left side of neck with mild pain. Two days 8 hours after booster swollen armpits, warm to touch with mild pain, Two days 12 hours mild shooting like sensation in left leg and arm. Arm and leg pain is not consistent but frequent. Mild chest discomfort again not consistent but comes and goes. Waiting for doctor to call me at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None yet
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure stabilized with medication
Andere Medikamente: Lorazepam 1mg 2x day Bupropion HCL SR 150mg 1x day Lisinopril 20mg 1x day Ibuprofen
Allergien: No
Vorherige Impfungen: -

VAERS 2024925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: LA
Alter: 57,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Cough Fatigue Injection site pain Pain Pyrexia

Symptomtext

Dry cough Tiredness Fever up to 103 body aches Arm soreness at injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: high blood pressure
Andere Medikamente: Rosuvastatin Amlodipine
Allergien: no
Vorherige Impfungen: -

VAERS 2024654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Gait disturbance Neck pain Pain in extremity

Symptomtext

Back of neck started hurting within the 15 mins she had to sit after taking the vaccine. She was told she could go home and take Tylenol. The next damn she stated the pain grew increasingly from her hip to the back of her knees all on the left side. She can barely walk without holding on to something.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: -
Vorgeschichte: diabetic and high blood pressure, anemic
Andere Medikamente: metformin 500mg, lisinopril 5mg, ferrous sulfate 325mg, glipizide 5mg
Allergien: no
Vorherige Impfungen: -

VAERS 2021404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: VA
Alter: 20,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Headache

Symptomtext

Right sided temporal headache that started roughly 1 hour post vaccination, waxed/waned over the next 2 days

Weitere VAERSDATA-Felder

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

VAERS 2020723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: LA
Alter: 59,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 07.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Axillary pain Oedema peripheral

Symptomtext

severe Axillary swelling and pain over 12 hours worsening over 72 hours started on aspirin and cold compresses

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: Ultrasound pending to see if fluid filled or lymphadenopthay
Aktuelle Erkrankungen: none
Vorgeschichte: headaches/anxiety/GERD/arthritis
Andere Medikamente: -
Allergien: imitrex biaxin
Vorherige Impfungen: -

VAERS 2020721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 39,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Ear pain Fatigue Headache Oropharyngeal pain Pain in extremity

Symptomtext

Fatigue, headache, sore throat, ear ache in right ear only, soreness of arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Eye drops
Vorherige Impfungen: Covid pfizer

VAERS 2020516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: SC
Alter: 39,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 07.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Bone pain Fatigue Lymphadenopathy Myalgia

Symptomtext

Bone pain/myalgias, fatigue, ipsilateral axillary & supraclavicular lymphadenopathy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bone pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Nothing but chronic diseases
Vorgeschichte: Microscopic lymphocytic colitis Ehlers Danslo syndrome Asthma Anxiety/depression/ADHD
Andere Medikamente: Wellbutrin Adderall Effexor Tumeric with Boswellia Elavil
Allergien: Sulfa Claritin Viberzi
Vorherige Impfungen: -

VAERS 2019789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OR
Alter: 52,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 07.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia Musculoskeletal stiffness

Symptomtext

Fairly severe joint pain and muscle stiffness experienced for approximately 5 hours at 24 hours after injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: A--symptomatic HIV, obstructive sleep apnea, Alcohol use disorder, Tobacco use disorder
Andere Medikamente: Descovy, Tivicay, DEPADE/Naltrexone, Gabapentin/Neurontin, Fexofenadine, Vitamin D, Multi-vitamin.
Allergien: Sulfamethoxazole-Trimethoprim, Efavirenz, Sulfa (Sulfonamide Antibiotics)
Vorherige Impfungen: -

VAERS 2019429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CO
Alter: 88,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 22.12.2021
Beginn: 07.01.2022
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Malaise Pain Sleep disorder

Symptomtext

This is the 2nd event-(first occurred with my 2nd shot). Turned over in bed at dawn, a sack of concrete flopped over in my chest, lots of pain, didn't move, went back to sleep, pain was at a point where I was debating taking Tylenol, didn't dare move, went back to sleep, awoke about noon and the pain was almost gone. (The first episode lasted 7 full days. and occurred 7 days after the shot). Today the 8th I feel a little sick but no pain, a dull ache here and there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Never went to a doctor, let it run its coarse.
Aktuelle Erkrankungen: none
Vorgeschichte: Mild COPD from 60 years of smoking. Been "clean" from tobacco for 4 years. Not even a cold for the last 15 years.
Andere Medikamente: metoprolol tartrate- 25 mg. twice/day; Atorvastatin 40 mg once/day
Allergien: none that I know of.
Vorherige Impfungen: My 2nd dose of Pfizer COVID- BioNtechen6204 - 06/2021 3/04/21- MyoC. started 7days after shot, lasted 7 full days.

VAERS 2019370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 13,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Body temperature increased Headache Lymph node pain Pain in extremity Rhinorrhoea

Symptomtext

1/7: temp of 100, runny nose, sore arm and lymph node under armpit, headache 1/8: temp 99.6, headache, sore arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 1 diabetes
Andere Medikamente: Insulin
Allergien: None
Vorherige Impfungen: -

VAERS 1977150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: -
Geschlecht: U
Eingang: 08.01.2022
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Myalgia Tinnitus

Symptomtext

Booster; extremely loud ringing in my ears; muscle aches; fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administration date 22Dec2021 (Batch/Lot number: unknown) as dose 3 (booster), 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, reaction(s): "no adverse effect"; Bnt162b2 (DOSE 2, SINGLE), for Covid-19 immunization, reaction(s): "no adverse effect". The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021, outcome "unknown", described as "Booster"; TINNITUS (non-serious) with onset 22Dec2021, outcome "not recovered", described as "extremely loud ringing in my ears"; MYALGIA (non-serious) with onset 22Dec2021, outcome "unknown", described as "muscle aches"; FATIGUE (non-serious) with onset 22Dec2021, outcome "unknown", described as "fatigue". The event "extremely loud ringing in my ears" was evaluated at the physician office visit. As the patient reported: the patient received the covid booster mid-day last Wednesday. Later that day had extremely loud ringing in my ears (tinnitus) along with muscle aches and fatigue. The patient had no side effects with the first two shots. Felt somewhat better two days later but the tinnitus is awful. Zero improvement. The patient called doctor and was told people were having the tinnitus issue. However, when the patient asked if they would be reporting it to the CDC, they said No. Clearly this IS a side effect and consumers need this info. 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: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2015079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: NV
Alter: 29,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure increased Dizziness

Symptomtext

Adverse reaction following vaccine. About 5 minutes after vaccination, patient flagged me from observation area, stating that he felt some sudden onset dizziness. He asked for some water & consented to monitoring of vital signs. Blood pressure was elevated, at 144/93; pulse 126; o2 sat 96%. Monitoring of vitals continued at 5 minute intervals for approximately 15 more minutes. Blood pressure remained elevated. Pulse gradually came down to 107. O2 remained good at 98%. Patient declined EMS call, and left once he was feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: vitals monitored as listed above
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: none known
Allergien: none known
Vorherige Impfungen: -

VAERS 2011408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 21.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Pain in extremity

Symptomtext

Patient started having sore arm and numbing of the thumb on 12/31

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Aspirin and losartan
Allergien: none
Vorherige Impfungen: -

VAERS 2010497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: AK
Alter: 49,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 04.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Axillary pain Oedema peripheral

Symptomtext

The day after vaccination, my left armpit became mildly sore. By day 2 (post-vaccine), still moderately sore and developed a diffuse moderate puffiness/edema in the anterior axilla.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: I just had a non-COVID-19 cold (tested negative twice on rapid at-home test), and was on the mend from that when I got vaccinated.
Vorgeschichte: Lyme disease, Babesia co-infection.
Andere Medikamente: Progesterone (topical); Colesevelam; Armour thyroid
Allergien: None
Vorherige Impfungen: -

VAERS 2010184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 73,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 22.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Abdominal pain Back pain Perineal pain Pollakiuria Urticaria

Symptomtext

began frequent urination, urticaria, mild burning in peri area began on 12/24/2021, and still is experiencing it - began drinking cranberry juice to relieve symptoms - did not visit medical provider , lower back pain, lower abdominal cramps began on 12/25/2021 and lasted for week

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Heart murmer
Vorgeschichte: HBP, High cholesterol, low thyroid
Andere Medikamente: Synthroid q am vitafusion calcium q day Baby Aspirin q am Lisinopril 10 mg q am Rosuvastatin 10 mg q pm Ensure q am
Allergien: Seasonal allergies Animal allergies Corn chocolate
Vorherige Impfungen: -

VAERS 2010111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Cough Pharyngeal swelling Rash Wheezing

Symptomtext

Patient was receiving her Pfizer COVID19 vaccine. Pre-medicated with bendadryl 25mg PO given mild allergic reaction to first dose. Pt began having throat swelling, wheezing, and coughing 30 minutes after receiving vaccine. Took another Benadryl 50 mg and Prednisone 20 mg with no relief. Taken to ER where rash began as well. Given epinephrine 0.3mg IM, racemic epinephrine inhalation, famotidine 20mg PO, methylprednisolone 125mg IM. History of multiple allergies. Discharged from ED with follow-up with primary care.

Weitere VAERSDATA-Felder

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

VAERS 2006458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Ear pain Injection site reaction Respiratory tract congestion Sensory disturbance Tinnitus Vertigo

Symptomtext

About an hour after booster vaccination I felt a sensation of something spreading underneath the skin from the injection site up to the shoulder, up the neck and under the arm a bit and then Ringing in the ear started 1 hour after booster vaccination and have had it for the 13 days since. Still have it. Also some congestion and pain in the ear. Some vertigo the first 3 days as well.

Weitere VAERSDATA-Felder

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

VAERS 2002396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 41,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 31.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: ID / RA

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

Axillary pain Chills Discomfort Oedema peripheral Pain in extremity Sleep disorder

Symptomtext

Saturday after I went to bed, the pain in my arm woke me up, followed by bouts of the chills. When I got out of bed Sunday morning I didnt notice the swelling right away, just the pain. Got up to shower around 11am to help with the pain and that's when I noticed the swelling in right armpit, size bigger then a golf ball, pain and discomfort 6/10. Went to the walk-in immediately as this has never happened to me before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: No test/labs done.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxin, phentermin, metformin, multivitamin, vitamin D.
Allergien: Penicillin, toredol
Vorherige Impfungen: -

VAERS 2000459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 46,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 01.01.2022
Beginn: 02.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymph node pain Lymphadenopathy Skin warm

Symptomtext

PATIENT DESCRIBES A LUMP UNDER HER ARMPIT OF THE LEFT ARM A DAY AFTER SHE RECEIVED THE SHOT, SHE REPORTS IT AS VERY PAINFUL AND HOT TO TOUCH

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: ASTHMA
Vorgeschichte: ASTHMA
Andere Medikamente: UNKNOWN
Allergien: ASPIRIN
Vorherige Impfungen: -

VAERS 2000455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 03.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pruritus

Symptomtext

Patient was given shot and began to itch within 5 minutes. Looked at the skin, did not seem to have any hives. Asked patient to sit down, gave 25mg of liquid diphenhydramine. After patient sat down, waited for another 30 minutes to see if resolution of itching. Said the itching stopped. Warned patient to watch for any difficulties in breathing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None on file that we knew of
Vorgeschichte: None reported
Andere Medikamente: None on file
Allergien: None on file, said wasn't allergic to anything
Vorherige Impfungen: -

VAERS 2000287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 52,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 31.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Chills Feeling cold Oral herpes Pain in extremity Pyrexia

Symptomtext

Fever 102 Cold sore where one was never located previously Cold chills Sore arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Ulcerative colitis
Andere Medikamente: None
Allergien: Mesalamine
Vorherige Impfungen: -

VAERS 1999851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 28.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Deafness Dizziness Headache Tinnitus Vertigo

Symptomtext

Hearing loss, tinnitus, dizziness, vertigo, headache

Weitere VAERSDATA-Felder

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

VAERS 1999599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 39,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 24.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Hypoaesthesia Muscle tightness Pain

Symptomtext

Waiting it out to see if symptoms completely go away in time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: No further testing has been done.
Aktuelle Erkrankungen: No
Vorgeschichte: Yes. Took the Covid shot which felt like a bumble bee sting then shooting pain down forarm after a few minutes and hand muscles tightened. My ring finger, pinky and side of the arm numb and tingling for four days. Side of hand/palm and two fingers still feel slight tighten to this day. I went to doctor checkup and all he could say do next Covid shot in the opposite arm to see if get the same side effects again. He suggested maybe the shot hit a nerve and where I received the shot,
Andere Medikamente: Tricor prescription is taken in the morning.
Allergien: No
Vorherige Impfungen: -

VAERS 1999433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 35,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 02.01.2022
Beginn: 02.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Headache Injection site rash Memory impairment Nausea Rash macular

Symptomtext

Starting 1/2/22 (day of vaccination) patient reported to spouse a headache and nausea/upset stomach. On 1/3/22 spouse called the pharmacy around noon to report patient called him at work to come home, he had a rash at injection site, nausea, and was having memory problems and does not remember things. When spouse got home, patient told him he didn't know how he got where he was and didn't remember who people were. Spouse reports rash was red blotches limited to the area near the injection. Denied any swelling of lips, tongue, throat, or trouble breathing. Spouse was advised to call the patient's physician for evaluation and guidance, but they are currently out of town. Then spouse was advised to take patient to urgent care as the memory issues are not expected and very concerning and need to be evaluated by a doctor.

Weitere VAERSDATA-Felder

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

VAERS 1999198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 62,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Headache

Symptomtext

Patient has been experiencing lightheadedness and headaches since 12/22/2021. He received vaccine on 12/21/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: High blood pressure Diabetes
Andere Medikamente: Blood pressure meds Heart meds Diabetes meds Spivriva (Couldn't get names of meds, caller was breaking up really bad.)
Allergien: NONE
Vorherige Impfungen: -

VAERS 1997290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: FL
Alter: 33,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Back pain Chills Cold sweat Decreased appetite Fatigue Feeling cold Feeling hot Headache Myalgia Nausea Pain in extremity Vomiting

Symptomtext

12/28 - got chills two hours after. Took two Tylenol 12/29 - woke up with muscle pain focused in my back and legs but it traveled. Very fatigued. Constant headache. Loss of appetite. Felt very cold in the morning. Took two Tylenol every 6 hours and used a heating pad. 12/30 - Constant headache and reduced appetite. Took two Tylenol every 6 hours. Nausea came in waves. That night around 9:30 pm got very nauseous, bad headache and cold sweats. 12/31 - bad headache and took migraine medicine that afternoon. It helped some but headache was still there. Very tired. Not hungry. 1/1 - Around 12:30 a.m. got very nauseous and threw up. Bad headache. Laid down with a heating pad. As the day has progressed, I still have a headache but not as bad. Still fatigued. Nausea and feeling hot comes in waves.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes Insipidus
Andere Medikamente: Birth control (Junel), migraine medicine as needed
Allergien: Food - peanuts, tree nuts, coconut
Vorherige Impfungen: -

VAERS 1997274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: FL
Alter: 65,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 01.01.2022
Beginn: 01.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chills Diarrhoea Dizziness Fatigue Headache Nausea Pain Vomiting

Symptomtext

Headache, dizziness, fatigue, extreme nausea, vomiting, diarrhea, body aches, chills - symptoms intensified 12/29/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Na
Aktuelle Erkrankungen: Na
Vorgeschichte: Hypertension Acute intermittent porphyria
Andere Medikamente: Carvidol Lisinopril
Allergien: Na
Vorherige Impfungen: -

VAERS 1997253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: SD
Alter: 59,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Insomnia Pain

Symptomtext

BODY ACHES, CHILLS,HEADACHE, TEMPERATURE OF 100. STARTING AT 4AM ON THE 12/31/21 AND STILL HAVE THESE SYMPTOMS AT PRESENT WHICH IS 1/1/2022 AT 12NOON. TOOK ADVIL , EXCEDRIN, EVERY 4 HOURS, FLUIDS, UNABLE TO SLEEP BECAUSE OF SYMPTOMS, EVEN WITH ADVIL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: None
Vorgeschichte: bronchiectasis , history of pulmonary MAC
Andere Medikamente: None
Allergien: minocycline and oxycodone
Vorherige Impfungen: -

VAERS 1996981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 26.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Immunisation Lymph node pain Lymphadenopathy

Symptomtext

Swollen lymph nodes in left armpit causing significant level of pain; Swollen lymph nodes in left armpit causing significant level of pain; Dose number 3; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 46-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 26Dec2021 at 15:00 (Lot number: FE3594) at the age of 46 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "None", notes: Other medical history: none; Known allergies: no. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Anatomical location: left arm; Lot number: EP7534; Administration time: 17:00), administration date: 23Mar2021, when the patient was 45 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Anatomical location: left arm; Lot number: EW0150; Administration time: 17:00), administration date: 13Apr2021, when the patient was 45 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 26Dec2021 at 15:00, outcome "unknown", described as "Dose number 3"; LYMPHADENOPATHY (non-serious), LYMPH NODE PAIN (non-serious) all with onset 27Dec2021, outcome "recovering", and all described as "Swollen lymph nodes in left armpit causing significant level of pain". Therapeutic measures were not taken as a result of lymphadenopathy and lymph node pain. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Pain occurred two days after the booster shot, pain continued on day 3 somewhat reduced. 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
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
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1995616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 32,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 22.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Body temperature Chills Immunisation Pyrexia Somnolence Vomiting

Symptomtext

Dose received: 3; Chills; Fever of 101.9; Vomiting; Can't stay awake; This is a spontaneous report from non-contactable reporter (Consumer or other non HCP). The reporter is the patient. A 32-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 22Dec2021 at 14:30 (Lot number: FE3594) at the age of 32 years as dose 3 (booster), single for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot Number: EW0162, Anatomical location: Left arm), administration date: 13Apr2021, when the patient was 31 years old, and Bnt162b2 (DOSE 2, SINGLE, Lot Number: EW0172, Anatomical location: Left arm), administration date: 04May2021, when the patient was 31 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 22Dec2021 at 14:30, outcome "unknown", described as "Dose received: 3"; CHILLS (non-serious) with onset an unknown date in Dec2021, outcome "recovering", described as "Chills"; PYREXIA (non-serious) with onset an unknown date in Dec2021, outcome "recovering", described as "Fever of 101.9"; VOMITING (non-serious) with onset an unknown date in Dec2021, outcome "recovering", described as "Vomiting"; SOMNOLENCE (non-serious) with onset an unknown date in Dec2021, outcome "recovering", described as "Can't stay awake". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of chills, pyrexia, vomiting and somnolence. Additional Information: The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: Body temperature; Result Unstructured Data: Test Result:101.9
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1995562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WA
Alter: 49,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Immunisation Product use issue Vaccination site erythema Vaccination site pain Vaccination site swelling

Symptomtext

Injection site pain; injection site redness; injection site swelling; mild fatigue; dose_received: 3; product use for unapproved combination; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from a sales representative. The reporter is the patient. A 49 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 17Dec2021 10:45 (Lot number: FE3594) at the age of 49 years as dose 3 (booster), single for covid-19 immunisation; influenza vaccine inact split 4v (FLUARIX QUADRIVALENT), administered in arm right, administration date 17Dec2021 (Batch/Lot number: unknown) as dose 1, 0.5 ml single for immunisation. Relevant medical history included: "known_allergies:latex" (unspecified if ongoing), notes: known allergies: latex. Concomitant medication(s) included: SPIRONOLACTONE; LEVOTHYROXINE; ZYTREC; TYLENOL. Past drug history included: Wellbutrin, reaction(s): "known allergies: Wellbutrin", notes: known allergies: Wellbutrin; Benadryl, reaction(s): "known allergies: Benadryl", notes: known allergies: Benadryl. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0187, Location of injection: Left Arm, Vaccine Administration Time: 06:00 PM), administration date: 24May2021, when the patient was 49 years old, for COVID-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EW0176, Location of injection: Left Arm, Vaccine Administration Time: 04:00 PM), administration date: 03May2021, when the patient was 49 years old, for COVID-19 Immunization. The following information was reported: IMMUNISATION (non-serious) with onset 17Dec2021 10:45, outcome "unknown", described as "dose_received: 3"; VACCINATION SITE PAIN (non-serious) with onset 18Dec2021 00:30, outcome "recovering", described as "Injection site pain"; VACCINATION SITE ERYTHEMA (non-serious) with onset 18Dec2021 00:30, outcome "recovering", described as "injection site redness"; VACCINATION SITE SWELLING (non-serious) with onset 18Dec2021 00:30, outcome "recovering", described as "injection site swelling"; FATIGUE (non-serious) with onset 18Dec2021 00:30, outcome "recovering", described as "mild fatigue"; PRODUCT USE ISSUE (non-serious) with onset 17Dec2021, outcome "unknown", described as "product use for unapproved combination". Therapeutic measures were not taken as a result of vaccination site pain, vaccination site erythema, vaccination site swelling, fatigue. Additional information: if other vaccine in four weeks: No if covid prior vaccination: No if covid tested post vaccination: No No follow-up attempts are possible. No information is required.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Latex allergy (known allergies: latex)
Andere Medikamente: SPIRONOLACTONE; LEVOTHYROXINE; ZYTREC; TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1995320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CT
Alter: 17,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Fatigue Immunisation

Symptomtext

Extreme fatigue; Dose 3 (Booster); This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 17 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 14Dec2021 14:30 (Lot number: FE3594) at the age of 17 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: ADVIL [IBUPROFEN]. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EP6955, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 14Apr2021, when the patient was 16 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EP6955, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 24Mar2021, when the patient was 16 years old, for COVID-19 immunization. The following information was reported: FATIGUE (non-serious) with onset 15Dec2021 07:00, outcome "recovering", described as "Extreme fatigue"; IMMUNISATION (non-serious) with onset 14Dec2021 14:30, outcome "unknown", described as "Dose 3 (Booster)". Therapeutic measures were not taken as a result of fatigue. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. List of any other medications the patient received within 2 weeks of vaccination: Advil. Reported event was extreme fatigue. 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. Follow-up attempts are completed. No further information is expected.

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, Comment: other medical history: No Known allergies: No
Andere Medikamente: ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 1995282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: PA
Alter: 17,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LA

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

Computerised tomogram head Headache Immunisation Pain in jaw Photosensitivity reaction

Symptomtext

Started with headache within 24 hrs of/HA all over/ Throbbing and sharp; some sensitivity to light; sore in jaw; booster; This is a spontaneous report received from a non-contactable reporter(s) (Other healthcare professional: Nurse). The reporter is the parent. A 17 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 09Dec2021 13:15 (Lot number: FE3594) at the age of 17 years as DOSE 3 (BOOSTER), SINGLE for covid-19 immunisation. Relevant medical history included: "Anxiety" (unspecified if ongoing); "known allergies: environmental allergies" (unspecified if ongoing); "known allergies: seasonal allergies" (unspecified if ongoing); "Cramps" (unspecified if ongoing). 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. Since the vaccination, the patient has been tested for COVID-19. Concomitant medication(s) included: ADVIL [IBUPROFEN], 200 mg, as needed, orally, taken for muscle spasms; CETRIZINE, 10 mg, 1x/day, orally; SERTRALINE, 12.5 mg, 1x/day, orally. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8736, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 24Apr2021, when the patient was 16 years old, for COVID-19 immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0183, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 15May2021, when the patient was 16 years old, for COVID-19 immunization. The following information was reported: IMMUNISATION (medically significant) with onset 09Dec2021 13:15, outcome "unknown", described as "booster"; HEADACHE (medically significant) with onset 10Dec2021, outcome "not recovered", described as "Started with headache within 24 hrs of/HA all over/ Throbbing and sharp"; PHOTOSENSITIVITY REACTION (non-serious) with onset 10Dec2021, outcome "unknown", described as "some sensitivity to light"; PAIN IN JAW (non-serious) with onset 10Dec2021, outcome "unknown", described as "sore in jaw". The events "started with headache within 24 hrs of/ha all over/ throbbing and sharp", "some sensitivity to light" and "sore in jaw" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: computerised tomogram head: (Dec2021) unknown results. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: CT of head; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Cramps; Environmental allergy; Seasonal allergy
Andere Medikamente: ADVIL [IBUPROFEN]; CETRIZINE; SERTRALINE
Allergien: -
Vorherige Impfungen: -

VAERS 1995261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IL
Alter: 39,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 09.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Body temperature Chills Fatigue Insomnia Pyrexia

Symptomtext

not been able to sleep/can't sleep at all; my brain is very tired; Chills; Fever/High fever; 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 09Dec2021 16:30 (Lot number: FE3594) at the age of 39 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, Lot:30125BA , Location: My right arm), administration date: 18Nov2021, when the patient was 39 years old, for COVID-19 immunisation, reaction(s): "high fever", "feel tired". The following information was reported: PYREXIA (non-serious) with onset Dec2021, outcome "unknown", described as "Fever/High fever"; INSOMNIA (non-serious) with onset 09Dec2021, outcome "unknown", described as "not been able to sleep/can't sleep at all"; FATIGUE (non-serious) with onset Dec2021, outcome "unknown", described as "my brain is very tired"; CHILLS (non-serious) with onset Dec2021, outcome "unknown", described as "Chills". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, chills. Therapeutic measures were not taken as a result of insomnia. Additional information: Caller stated she received first dose of Pfizer COVD vaccination on 18Nov2021, and second dose on 09Dec2021, she called to report her experience after second dose: "I got the second dose of Pfizer COVID vaccine on Thursday 09Dec2021, and I am calling because since that day I have not been able to sleep at all, I have had insomnia, and the thing is that I am not sleepy, my brain is very tired, but I am not sleepy and I am very alert. I have not been able to (sleep) close even one eye since that day... I was going crazy, I did not know what to do, the thing is that I used to sleep well but this happened from the second dose, the first one did not cause me anything like this, and I have been going crazy I can't find out what to do. I told my husband about this and he did search online, and he says yes, there have been cases of people suffering from insomnia after (vaccination)". Consumer stated, "Because I had my second dose last Thursday on the 9th and since then I haven't been able to sleep at all. I don't know if that's something to do with the vaccine because I was fine, that day after I had the second vaccine, I had the reaction like the first one, I had like the high fever and feel tired but they last maybe like two days but 'being' able to sleep it was since that day like I can't sleep at all, I don't know what else to do." Patient took only Tylenol (treatment) and Motrin (treatment) because had high fever and chills. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 202112; Test Name: temperature; Result Unstructured Data: Test Result:high fever
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: WI
Alter: 12,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Injection site erythema Injection site pain Pyrexia

Symptomtext

LOW GRADE FEVER, SORENESS, AND REDNESS AT INJECTION SITE CONSISTENT WITH NORMAL COVID VACCINATION SIDE EFFECTS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: NONE AT THIS TIME
Aktuelle Erkrankungen: NONE KNOWN
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1992283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 21,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 28.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Chills Headache Nausea Pain Pyrexia

Symptomtext

Fever was 99.8 when I woke up then. Spike to 100.9. Dropped to 98.6 then back up at 99.9 . Body chills Body aches Weak Nauseous Headache Took Tylenol every six hours which was 4times of a dose of 2pills . Drank lots of fluids. And rested all day . Next day body aches temp was 99.4

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: Heart murmur
Andere Medikamente: Sprintec birth control
Allergien: N/a
Vorherige Impfungen: Covid 19 dose 2

VAERS 1991891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: MI
Alter: 20,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 19.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Rash Urticaria

Symptomtext

Systemic: Allergic: Rash Generalized-Mild, Additional Details: Patient reported hives that did not itch

Weitere VAERSDATA-Felder

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

VAERS 1989870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: PA
Alter: 20,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 27.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Pain Skin warm Swelling

Symptomtext

red half dollar sized circle painful and warm and raised

Weitere VAERSDATA-Felder

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

VAERS 1989838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 14,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Fatigue Myalgia Product administered to patient of inappropriate age Pyrexia

Symptomtext

Patient's parent made an appointment online for booster shot for patient. It was missed at screening by pharmacist that the patient is 14 years old. In the vaccine room, I assumed it was already screened by the pharmacist and I administered the vaccine. I contacted the clinic to let him know the situation. I contacted the patient's pediatrician to inform them and also informed the patient's parents. The only adverse effects likely to happen is muscle soreness and the common side effects reported from the vaccine (chills, fever, fatigue, etc). facility will take care of any medical bills if there is any.

Weitere VAERSDATA-Felder

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

VAERS 1989420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: FL
Alter: 19,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness

Symptomtext

PATIENT RECEIVED HER 3RD DOSE OF PFIZER. PATIENT WAS SITTING IN OBSERVATION AND 5 MINUTES INTO OBSERVATION SHE REPORTS FEELING LIGHTHEADED AND DIZZY. RN ADVISED HER TO LAY ON THE FLOOR WITH HER FEET ELEVATED. PATIENT REPORTS DIZZINESS GETTING BETTER WHEN LYING DOWN AND FEET ELEVATED. VITALS WHEN LYING DOWN INITIALLY WAS 108/65, HR 66, 99% O2, 5 MIN LATER VITALS WERE 105/65, HR 65 99% O2. PATIENT REPORTS HER LAST MEAL WAS 2 PM. AFTER ABOUT 10 MINUTES HER DIZZINESS SUBSIDED AND SHE WAS ABLE TO SIT UP SLOWLY. VITALS AT THIS TIME WERE 120/89, HR 75. SHE WAS GIVEN A SNACK TO EAT AND COLD BEVERAGE. PATIENT REPORTS FEELING MUCH BETTER AT THIS TIME. SHE ALSO REPORTS NOT TAKING HER LEXAPRO PRIOR TO COMING IN TO GET HER VACCINE. MOM STATES SHE HAS A PHOBIA OF NEEDLES WHICH WAS NEVER MENTIONED UP UNTIL THIS EVENT. PATIENT COMPLETED HER OBSERVATION PERIOD AND WAS ABLE TO INDEPENDENTLY AMBULATE OUT OF THE FACILITY WITH NO ACUTE ISSUES; SHE WAS STABLE AT THIS TIME.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none
Vorgeschichte: PMHx - asthma - anxiety - seasonal allergies
Andere Medikamente: LEXAPRO 10 MG QDAY
Allergien: SHELLFISH SEASONAL ALLERGIES
Vorherige Impfungen: -

VAERS 1989201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: SD
Alter: 39,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Maternal exposure during breast feeding Pain Pyrexia Suppressed lactation

Symptomtext

I experienced body aches, chills, headache, fever and my breast milk supply completely stopped.

Weitere VAERSDATA-Felder

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

VAERS 1988970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 12,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 21.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

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

Swelling face Urticaria

Symptomtext

Developed hives and facial swelling 3 days after vaccination, worsened over the course of the next 24+ hours.

Weitere VAERSDATA-Felder

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

VAERS 1988957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MT
Alter: 34,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 15.12.2021
Beginn: 15.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Fatigue Heart rate increased Insomnia Myoclonus Nightmare

Symptomtext

insomnia. Hypnic Jerks. Can't get to sleep, very tired, try to sleep and jerk awake with increased heart rate -nightmares the first few days when actually slept. Can only get a couple hours a night. Have tried, Benedryl, Nyquil, Melatonin. Contacted provider tried Trazodone, now using Melatonin and xanax to sleep. ONLY way to get any sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1988915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 15,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Feeling hot Head discomfort Nausea Pallor Visual impairment

Symptomtext

Nauseated, light headed, hot, seeing "spots", felt very warm, and became pale, complained of "pressure in head" within 10 minutes of receiving vaccine. Patient did not eat before vaccination. Patient placed in supine position and observed for 40 minutes and patient recovered from symptoms within 5 minutes of being laid down. Patient given granola bar and water. No complaints of shortness of breath or other untoward symptoms noted. Patient felt "normal" after 40 minutes of observation. Mom told to call back with any issues. Provider and RN observed patient for recovery

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: BP 106/70
Aktuelle Erkrankungen: NONE
Vorgeschichte: Asthmas, Seasonal Allergies
Andere Medikamente: Flovent HFA 110 mcg 2 puff's daily , Fexofenadine 180 mg daily, albueterol 90 mcg 1-4 puffs prn q4 as needed.
Allergien: NONE
Vorherige Impfungen: -

VAERS 1988894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: AZ
Alter: 32,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Back pain Blood urine present Exposure during pregnancy Fatigue Kidney infection Pyrexia Urinary tract infection

Symptomtext

Back pain, blood in urine, fatigue, felt feverish (no fever). Urgent care indicated UTI and kidney infection and provided 7days of antibiotics. 4 weeks pregnant, estimated delivery date 8/30/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sinus infection
Vorgeschichte: N/A
Andere Medikamente: Prenatal vitamins
Allergien: Latex, kiwi
Vorherige Impfungen: UTI and kidney infection requiring antibiotics following both initial COVID vaccine shots. 12/18/2020, 01/20/2021.

VAERS 1988706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Contusion Erythema Induration Mass Pain Pruritus Swelling

Symptomtext

extreme soreness, swelling into a hard, red lump with some bruising, and extreme itchiness. It is now 10 days later, and the bruising is faint, no soreness, but the itchiness is still there.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: hormone replacement for menopause, various vitamins
Allergien: codeine, latex
Vorherige Impfungen: -

VAERS 2524978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 47,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 22.12.2021
Beginn: 19.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Dizziness Pruritus Rhinorrhoea

Symptomtext

Dizziness RUNNY NOSE, RIGHT EAR ITCHY

Weitere VAERSDATA-Felder

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

VAERS 1984895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3594

mild

Staat: MN
Alter: 44,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Chest discomfort Cough Pruritus

Symptomtext

Tight chest, cough, itchy neck about 30 mins after shot. Took 25mg Benadryl and symptoms were mostly alleviated within 40mins. Took another 25mg Benadryl and symptoms went away in about 30mins

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No illness for 2 weeks prior to vaccination. Did have a non-covid winter cold started 11/29 and ended 12/11
Vorgeschichte: None
Andere Medikamente: Citalopram - 40mg Cetirizine hydrochloride -10mg D3 - 125mg C - 500mg Ferrous sulfate iron - 325mg Calcium - 600mg
Allergien: Montelukast
Vorherige Impfungen: -

VAERS 1984894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 66,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Vomiting

Symptomtext

HAS BEEN VOMITTING SINCE MORNING

Weitere VAERSDATA-Felder

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

VAERS 1982459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OK
Alter: 53,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 22.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Urticaria

Symptomtext

Hives starting on day 2 in the evening and every subsequent evening - now on 4th evening. Am taking 2 Benadryl nightly. cortisone cream, and cold compress.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Ibuprofen, prn
Allergien: No allergies; sensitive to MSG
Vorherige Impfungen: -

VAERS 1982084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MO
Alter: 53,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Ear pain Vision blurred

Symptomtext

Blurry vision, pain in ears

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Covid-19 Vaccine (Pfizer-BioNTech)

VAERS 1982080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 13.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site swelling Injection site warmth

Symptomtext

Pt. called to report a localized raised area around injection site. Pt. denied shortness of breath, fever, loss of feeling. Area is warm to touch, but the rest of the arm shows no signs of swelling, warm to touch, or discoloration. Pt. instructed to seek medical attention if symptoms worsen. Pt. verbalized understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site swelling
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1982045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MD
Alter: 44,0
Geschlecht: F
Eingang: 27.12.2021
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

Joint swelling Lymphadenopathy Pain in extremity

Symptomtext

Pt stated that she had had swollen lymph node near clavicular bone and feels pain in left arm that has lasted almost a week. Pt is also complaining of swollen joints and pain on her left arm not relieved by ibuprofen 400mg per day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1982026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: TX
Alter: 27,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 11.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Glossodynia Mouth ulceration Noninfective gingivitis Pain

Symptomtext

Inflammation of gums and ulcers/sores on gums, tongue, and top lip. Sores were not near teeth (mostly attached gingivae if I'm reading diagrams correctly) I noticed a single small ulcer prior to receiving vaccine so I am not certain it is related to the vaccination, but following vaccine administration, many (10+) ulcers developed, with 2 larger than 0.5 cm. There was also inflammation of the gum tissue and a couple sore spots on my tongue. The condition worsened from 12/12 to approximately 12/19 and plateaued at that point. I tried gargling with salt water and applying drops of oregano oil to relieve pain, but the sores did not improve On 12/22, I went to a periodontist who chemically cauterized some of the ulcers and prescribed an antibacterial mouthwash to use twice per day. He also recommended stress reduction and sleep. He thought it could be an immune response to a latent virus (I believe he described it similar to a cold sore, but a different virus) brought on by psychological and physical stress. The cauterization relieved ~75% of the pain within an hour of treatment. The pain was 95% improved by 12/24. As of today (12/27/2021), there is no pain and the ulcers are healing, but there is still some redness/inflammation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Visual inspection by periodontist, 12/22
Aktuelle Erkrankungen: None
Vorgeschichte: Possible interstitial cystitis Possible small intestinal bacteria overgrowth or IBS
Andere Medikamente: Alyacen (oral contraceptive) Valium (oral pill administered vaginally as needed) CBD/THC tincture (10 mg of each per day as needed) Atrantil (2 pills, 3x per day) Aloe Vera (3 pills, 2x per day) Magnesium glycinate (2 pills per day) calcium
Allergien: None
Vorherige Impfungen: -

VAERS 1982007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 90,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood glucose increased Dizziness Fall Headache

Symptomtext

Registration #11997006. Patient is a 90 year old elderly female. She came to the vaccination site for her Pfizer COVID-19 booster vaccine. Prior to having her vaccine she was in waiting area near the quiet room. When she went to sit down she felt dizzy and sat at the edge of the chair causing her to lose her balance and fall on the floor on her buttocks. No head trauma and no other body areas were hurt during the fall. Personnel was nearby which assisted in helping her get up and proceeded to sit her in a wheelchair. When MD arrived with supervisor patient was alert and oriented. No loss of consciousness. EMT arrived at the scene shortly thereafter. Patient was warm and well perfused, equal pulses. She informed us she has type 2 diabetes and is hypertensive. She is treated with Metformin and Losartan. Patient was complaining of a headache scale 3-4. She denied nausea, no abdominal pain and no weakness. Her initial BP was 152/60 and improved to 134/68 ten minutes later. Fingerstick glucose was abnormal, above standard limits read as 234 mg/dL. She had eaten an hour before. The patient was offered water which she took only a few sips and did not want more. Throughout the observation period, Patient was alert and oriented at all times. No worsening of the headache. She later received her Pfizer booster vaccine and was observed for an additional 15 minutes. She tolerated the vaccine well and there were no adverse events from the vaccine. She was taken in the wheelchair to her car. She was able to walk a few steps to the passenger side of the car assisted by Aqueduct vaccination site personnel and her daughter who proceeded to place her seat belt on and later drove away. Patient was offered a ride to the hospital via ambulance for further evaluation but she refused. Patient and her daughter were advised by the EMT and doctor to go to the nearest ER if she had worsening headache or any new symptoms such as vomiting, change in behavior, change in speech or became disoriented. Recommended to give acetaminophen for pain at home if needed. Was also advised to recheck glucose at home and if above 200 mg/dL to check for urine ketones. If ketones present was asked to go to nearest ER for further evaluation and treatment. If glucose still elevated and no urine ketones to contact her primary care provider or go to the ER for further assistance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Type 2 diabetes and hypertension
Vorgeschichte: Type 2 diabetes and hypertension
Andere Medikamente: Metformin, Losartan
Allergien: None.
Vorherige Impfungen: -

VAERS 1981903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MD
Alter: 18,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 12.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Lethargy Lymph node pain Lymphadenopathy

Symptomtext

Swelling and pain in lymph glands surrounding shot arm. Heading is continuing and has affected affect and has extreme lethargy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: none performed
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Patella Alta, GERD, gi issues
Andere Medikamente: singular 10 mg qd , Xyzal qd, Yaz Birth Control Pills, Symbacort inhaler, MVI,
Allergien: Lactose intolerant, onions and garlic are harsh on digestion
Vorherige Impfungen: -

VAERS 1981882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: OK
Alter: 44,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Blood test Computerised tomogram Electrocardiogram Facial pain Mass Neck pain Pain

Symptomtext

The day after receiving my booster, I noticed/felt a lump under my right collar bone. I looked in the mirror and noticed it was very visible. It was squishy and painful to touch. It is still painful today. It runs through my shoulder, up my neck to my ear and my face. I was up at 2:30AM today in pain and I haven't been able to go back to sleep. I went to Hospital ER and they provided me with Mobic (which I cannot take) and Toradol. I was told that I can use voltarin gel until my follow up appointment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: I had blood work completed, a CT and an EKG. They diagnosed it as generalized swelling
Aktuelle Erkrankungen: I was not experiencing any illness
Vorgeschichte: I have Lyme Disease and Ulcerative Colitis
Andere Medikamente: I was taking Zoloft; Zyprexa; Abilify; Adderall; Xanax; Xanax ER; Buspirone; Myrbetriq and Xarelto
Allergien: I am allergic to Penicillin; Phenergan and Sulfa
Vorherige Impfungen: My second dose of Pfizer

VAERS 1981657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NJ
Alter: 60,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Fatigue Injection site pain Nasopharyngitis Oropharyngeal pain Pain SARS-CoV-2 test negative

Symptomtext

Pain at injection site followed by body aches, sore throat, chills, fatigue, cold like symptoms. I still have some symptoms today. Took an at home Covid test, negative results. Had the same reaction after 1st dose of Covid vaccine but these symptoms are lasting much longer from the booster. Due to holidays it has been impossible to obtain a Covid test at a facility or be seen at an Urgent Care facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home Covid Test, negative results
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: Penicllin
Vorherige Impfungen: See above explanation

VAERS 1981244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 26.12.2021
Impfdatum: 24.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Inflammation Pain in extremity Peripheral swelling

Symptomtext

Patient got Pfizer covid 19 booster shot at our pharmacy Friday 12/24/21. He came this morning & complained that he started to have pain & felt there's "a little ball" under right arm (injection site) and inflammation since last night 12/25/21. Pt took 2 of Tylenol 500mg yesterday but not helping much. I recommended patient to see MD to have it examined for more details and take Ibuprofen OTC today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1980953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 65,0
Geschlecht: M
Eingang: 25.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Headache Nausea

Symptomtext

Fell asleep almost a hour after getting home and woke up with terrible headache and kept the headache next day. Nausea 2nd day. Took aspirin (6)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lisinopril 10 mg Rosuvastatin 20mg Isosorbide Mono Er 30mg Bayer Low dose aspirin
Allergien: Aleive
Vorherige Impfungen: -

VAERS 1980824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CT
Alter: 46,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Fatigue Immunisation Interchange of vaccine products Myalgia Nasopharyngitis Pain Pyrexia Vomiting

Symptomtext

Vomiting for 48 hours starting 24 after vaccination received; Fever; Cold; Muscle aches; Fatigue; Pain continuing; Dose 1 and 2: Moderna; booster dose: Pfizer; Dose number: 3; This is a spontaneous report from 2 contactable reporters, consumer (patient) and consumer (Pfizer employee). A 46-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in right arm, administration date 16Dec2021 (Lot number: FE3594) at the age of 46 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Penicillin allergy" (unspecified if ongoing), notes: Known allergies: Penicillin. Concomitant medications were not reported. Vaccination history included: Moderna covid-19 vaccine (DOSE 1, SINGLE, Lot number: 006B21A, Anatomical site: Right arm, Route of administration: Intramuscular), administration date: 02Apr2021, when the patient was 45 years old, for COVID-19 immunisation and Moderna covid-19 vaccine (DOSE 2, SINGLE, Lot number: 039B21A, Anatomical site: Right arm, Route of administration: Intramuscular), administration date: 30Apr2021, when the patient was 45 years old, for COVID-19 immunisation. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 16Dec2021, outcome "unknown", described as "Dose 1 and 2: Moderna; booster dose: Pfizer"; IMMUNISATION (non-serious) with onset 16Dec2021, outcome "unknown", described as "Dose number: 3"; VOMITING (non-serious) with onset 17Dec2021, outcome "recovered with sequelae" (19Dec2021), described as "Vomiting for 48 hours starting 24 after vaccination received"; PYREXIA (non-serious) with onset 17Dec2021, outcome "recovered with sequelae" (an unknown date in Dec2021), described as "Fever"; NASOPHARYNGITIS (non-serious) with onset 17Dec2021, outcome "recovered with sequelae" (an unknown date in Dec2021), described as "Cold"; MYALGIA (non-serious) with onset 17Dec2021, outcome "recovered with sequelae" (an unknown date in Dec2021), described as "Muscle aches"; FATIGUE (non-serious) with onset 17Dec2021, outcome "recovered with sequelae" (an unknown date in Dec2021), described as "Fatigue"; PAIN (non-serious) with onset 17Dec2021, outcome "not recovered", described as "Pain continuing". Therapeutic measures were taken as a result of vomiting, pyrexia, nasopharyngitis, myalgia, fatigue and pain. Additional information: Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Since the vaccination, the patient had not been tested for COVID-19. It was reported that muscle aches lasted longer. The events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Treatment for events included Tylenol and Advil.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1980762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MD
Alter: 34,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Disturbance in attention Fatigue Immunisation Lymph node pain Lymphadenopathy Musculoskeletal stiffness Neck pain Pain in extremity Pain in jaw SARS-CoV-2 test Toothache

Symptomtext

arm soreness; fatigue; about 16-20 hours later neck, jaw, and teeth pain started and is still present as of the current time; my neck was stiff and my jaw hurt; teeth pain; My lymph nodes in my neck area were very swollen and sore; My lymph nodes in my neck area were very swollen and sore; my neck was stiff and my jaw hurt; difficulty focusing on other things; 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 34-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 08Dec2021 14:00 (Lot number: FE3594) at the age of 34 years as dose 3 (booster), single for covid-19 immunization. The patient had no relevant medical history. Concomitant medication(s) included: VITAMIN C [ASCORBIC ACID]; VITAMIN D [VITAMIN D NOS]. Vaccination history included: Bnt162b2 (dose 1, single, Batch/Lot No: EW0158, Location of injection: Arm Right, Vaccine Administration Time: 11:00 AM), administration date: 12Apr2021, when the patient was 34 years old, for Covid-19 immunization; Bnt162b2 (dose 2, single, Batch/Lot No: EW0175, Location of injection: Arm Left, Vaccine Administration Time: 10:45 AM), administration date: 03May2021, when the patient was 34 years old, for Covid-19 immunization. The following information was reported: IMMUNISATION (non-serious) with onset 08Dec2021 14:00, outcome "unknown", described as "dose number 3"; PAIN IN EXTREMITY (non-serious) with onset 09Dec2021 02:00, outcome "not recovered", described as "arm soreness"; FATIGUE (non-serious) with onset 09Dec2021 02:00, outcome "not recovered", described as "fatigue"; NECK PAIN (non-serious) with onset 09Dec2021 02:00, outcome "not recovered", described as "about 16-20 hours later neck, jaw, and teeth pain started and is still present as of the current time"; PAIN IN JAW (non-serious), MUSCULOSKELETAL STIFFNESS (non-serious) all with onset 09Dec2021 02:00, outcome "not recovered" and all described as "my neck was stiff and my jaw hurt"; TOOTHACHE (non-serious) with onset 09Dec2021 02:00, outcome "not recovered", described as "teeth pain"; LYMPH NODE PAIN (non-serious), LYMPHADENOPATHY (non-serious) all with onset 09Dec2021 02:00, outcome "not recovered" and all described as "My lymph nodes in my neck area were very swollen and sore"; DISTURBANCE IN ATTENTION (non-serious) with onset 09Dec2021 02:00, outcome "not recovered", described as "difficulty focusing on other things". Relevant laboratory tests and procedures are available in the appropriate section. It was unknown if therapeutic measures were taken as a result of pain in extremity, fatigue, neck pain, pain in jaw, toothache, lymph node pain, lymphadenopathy, musculoskeletal stiffness, disturbance in attention. Additional information: At first patient had regular symptoms at first (arm soreness and fatigue), then about 16-20 hours later neck, jaw, and teeth pain started and is still present as of the current time- 80 hours after the initial booster was administered. The pain was quite severe on Friday afternoon, 09Dec. All her teeth were throbbing, and it hurt to bite down. Lymph nodes in my neck area were very swollen and sore, and my neck was stiff and my jaw hurt. The neck, jaw, and teeth pain was mild this morning (Saturday, 11Dec) but then started increasing in intensity this evening around 7pm to the point that patient had difficulty focusing on other things. She went through phases where all her teeth ached, and at other times just a couple teeth hurt in her right lower jaw. The pain ranges from mild to more severe in intensity. This type of tooth and jaw pain was unusual for her, and none of these symptoms occurred for either the 1st or 2nd doses. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient had no allergies. She was tested for covid post vaccination and was not diagnosed with COVID-19 prior to vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20210813; Test Name: PCR; Test Result: Negative ; 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: VITAMIN C [ASCORBIC ACID]; VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1979987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IA
Alter: 62,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia COVID-19 Muscle spasms Pain in extremity Therapy non-responder

Symptomtext

Meds not working. Acute pain spasms in left shoulder, left arm, left hand, left leg and left foot that lasted 2 hours. I had to take an extra dose of medicine. I have to take extra meds since current medication not working as well. I also had a similar experience with 2nd vaccine but not as severe. Additionally, I was diagnosed with COVID-19 three days after this last shot (12/20/2021).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Parkinson's disease
Andere Medikamente: Carbidopa/Levodopa; Carbidopa/Levodopa ER; Entacapone; Probiotic
Allergien: None
Vorherige Impfungen: 2nd Pfizer vaccine; 04/22/2021; similar but not as severe.

VAERS 1979545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Lymphadenopathy Pain

Symptomtext

Swollen arm pit. Feels sore like a bruise when I touch it. It feels soft and very swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1979412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 36,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Dry skin Fatigue Skin warm

Symptomtext

Attendee received second dose Pfizer vaccine at 16:05 in the Left arm. Lot# FE3594. Attendee was directed to observation area. At 16:20 voiced complaints of dizziness and fatigue. Attendee's skin was warm and dry. Attendee's respirations were not tachypneic or dyspneic. Attendee assisted to the cot to lie down, legs elevated. Water given. HR: 75 BP: 100/80 RR: 18 O2Sat%: 99 Temp: 98.5 16:35 - Attendee stated she felt better. Attendee refused to have anyone called to the site to pick her up. HR: 80 BP: 100/79 RR: 18 O2Sat%: 99 16:55 -No voiced complaints- skin warm and dry. HR: 76 BP: 104/80 RR: 18 O2Sat%: 99 Additional information for Item 18: 16:55 - Care Practitioner educated on home discharge/adverse reaction instructions and attendee was discharged to home. Attendee did not have any reported escalation of symptoms and was able to walk out of clinic independently. Attendee was retained for a longer observation time to make sure that it was safe for them to leave.

Weitere VAERSDATA-Felder

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

VAERS 1979353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: FL
Alter: 48,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site erythema Injection site pruritus Injection site swelling Pruritus

Symptomtext

Site: Itching at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Itch Generalized-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1979172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 52,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 22.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Myalgia

Symptomtext

Achy muscles - lasted about 20 hours; shivering - lasted about 6 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: COVID vaccine #2 same symptoms & duration

VAERS 1975519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness

Symptomtext

Patient approached EMS table,claims of feeling of dizziness,a few minutes after his receiving 1st dose vaccination.Sat the patient at the private area for further assesment.Patient claims,was anxious and did not eat anything in the morning.Just an episode of dizzyness,no other symptoms.was given a bottle of water,vitals was done.Alert and oriented,no pain,no shorness of breath.Oxygen saturation 98%,vitals signs within normal limits,ambulatory.After a few minutes,he felt better no more dizziness.Wants to go home and get some rest.Was not driving has a friend waiting outside.Signed PCR refusal of transportation to the hospital.I did not get what name vaccine he got,but said has to come back again for second dose.

Weitere VAERSDATA-Felder

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

VAERS 1975366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: PA
Alter: 19,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 23.12.2021
Beginn: 23.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness

Symptomtext

Pt felt dizzy after administering the vaccine. Pt did not eat or drink all day. Pt was given water

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: nka
Vorherige Impfungen: -

VAERS 1975201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: VA
Alter: 39,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 16.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Pharyngeal swelling Rash macular Sensation of foreign body Urticaria

Symptomtext

Hives. Some as big dots scattered around chest; others in clusters on both sides of torso; started around 5pm after shot. Also felt throat enlarged (ie when yawned felt blocked/not as clear). As days went on, more appeared. Hives are still there a week later (went to Medical center Monday Dec 20)--and have become more--especially small spots all over stomach and back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: none.
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: Dairy (food)
Vorherige Impfungen: -

VAERS 1974786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 42,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: UN / LA

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

Ear pain Headache Interchange of vaccine products Musculoskeletal stiffness Neck pain Oedema peripheral Oral pain Pain

Symptomtext

Around 24hrs after the Pfizer booster shot in my LEFT shoulder, I started to experience neck pain mostly on the RIGHT side of my neck, and slightly to the back. The pain increases in intensity greatly when I tilt my head to the left. It becomes TOO painful when I tilt it to the left and back. I cannot go very far when I do this. Also, when I open my mouth wide to yawn it also causes pain the area. This pain can radiate slightly up behind my ear on the right side of my skull and above my ear on the right side of my skull. My doctor recommended alleve and lidocaine patch to rule out a stiff neck. I tried that 48hrs after symptom onset, it did not help. 6 days later my symptoms have NOT improved. The pain is still there and maybe on a scale of 1-10 it is perhaps one number higher. I can tell that there's an issue when my head is in a neutral position. It feels like a slight stiffness, but no pain in that neutral position. However, when I tilt my head to the left, my pain it is about a 5 on the pain scale and if I tilt it to the left and back I would say it gets into 7-8 territory, which I have not tested beyond that. My internet sleuthing found that the closest description fitting my symptoms appeared to be "acute thyroiditis," although it is unclear if this diagnosis is correct. I have an appointment to see a general physician on the Monday, 27th of December, 2021. I received my initial of Moderna on March 18th, 2021... received a 2nd dose April 15th, 2021. I had a breakthrough infection of COVID end of July/beginning of August 2021. The adverse event was after my Pfizer booster on December 17th, 2021. After the Moderna vaccine I did NOT have similar symptoms. I had side effects in line with flu like symptoms after the first shot (but I don't completely recall exactly how severe). 24hrs after After my 2nd Moderna shot I had 24hrs of flu symptoms, fever 101-2F, chills, muscle pain and weakness. After this 3rd dose Pfizer booster shot, I have had NO flu like symptoms. The only symptoms have been the been the neck and head pain described above and a very mild swelling under the left armpit. The severe neck pain is what concerns me and how long these symptoms have lasted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Finesteride 1.3 mg/day
Allergien: None
Vorherige Impfungen: -

VAERS 1974675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pruritus Rash

Symptomtext

Patient developed rash/itching to back. Received Benadryl 25mg po with good effect. Discharged in stable condition.

Weitere VAERSDATA-Felder

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

VAERS 1974114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 34,0
Geschlecht: F
Eingang: 23.12.2021
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: nein

Rash Rash macular

Symptomtext

I received the booster on Tuesday, December 21, 2021. I woke up Wednesday to from red spots on my right and left arm. I also noticed one on my left hip. As of now, they do not hurt or itch.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Smart Pants Organic Women's Multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 1972658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: VA
Alter: 36,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 19.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Erythema Pruritus Urticaria

Symptomtext

patient stated he was red and itchy and starting to devolpe hives. I advised him to take some benadryl and contact his md

Weitere VAERSDATA-Felder

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

VAERS 1971691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 17,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 15.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / RA

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

Arthralgia COVID-19 Cold sweat Confusional state Contusion Cough Fatigue Feeling abnormal Feeling cold Feeling hot Headache Irritability Myalgia Nasal congestion Pyrexia SARS-CoV-2 test positive Throat clearing Throat irritation

Symptomtext

(Weds) At first it was a bad headache and mild to moderate fatigue, then arm feeling bruised the next morning (Thus) and by the evening of that day joint and muscle aches in addition to moderate fatigue and irritability. (Fri) The morning after that he experienced continued muscle aches and pains, fatigue and increased irritability. (Sat) Next day throat irritation began. By the evening of that day he also began feeling a bit warm, exhibited mild brain fog and confusion (I usually only associate w him being sick) and he felt cold and clammy to me tho he said he felt a bit warm. At some point in the middle of the night he awoke with a stuffed nose, scratchy throat & almost cough clearing throat feeling and at almost a fever temp (our normal body temp sits at 97.4 so, 99.5 temps are like fevers for my son and I (sweating, etc). He was also having rambling disjunctive commentary. I gave him some NyQuil and sent him back to bed. (Sun) in the morning he also developed a strong unproductive deep cough but the fever was gone, as his confusion. At this point I began searching for an at home COVID test kit. We found and used one on Monday and it showed positive (symptoms all except for cough and irritability begin to disappear). Several other students at his school also confirmed being COVID positive over the wknd, initially thinking it was just the initial effects of taking a booster shot.

Weitere VAERSDATA-Felder

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

VAERS 1971428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration Pain in extremity

Symptomtext

Pt was given 3 pfizer booster 2 months early. Denies any adverse side effects. States he only had a sore arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Booster was given 2 month early -. Pt was notified that he received the medications early.. Denies any side effect at this time 12/22/21) other than a sore arm.
Vorgeschichte: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NH
Alter: 24,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness

Symptomtext

She started feeling dizzy around 3:25pm while sitting in a chair. She did not want to go to ER. She wanted some water, so I gave her a bottle of water. she was so hungry. Hew mother who came with her had a snack bar and sandwich. she ate them and started feeling better. She left for home around 4pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: cat hair, dust, wasp bites
Vorherige Impfungen: -

VAERS 1971179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 31,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Oedema peripheral

Symptomtext

Woke up morning after vaccine with under left arm in armpit area swollen and painful. Swelling and pain have been present for two days as of now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1970952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: IN
Alter: 41,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Headache Injection site pain Pain

Symptomtext

Pain at injection site, armpit pain, headache, body aches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Levothyroxine, atenolol
Allergien: Erythromycin
Vorherige Impfungen: Pfizer Covid-19.

VAERS 1967726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: AZ
Alter: 13,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Vomiting

Symptomtext

10 minutes after vaccine administration the patient started feeling faint and vomiting repeatedly. The patient remained conscious the whole time. no other symptoms were observed. the parents called 911 after 10 minutes of vomiting. The patient was taken out the store by the paramedics.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: unknown
Allergien: no
Vorherige Impfungen: -

VAERS 1964475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fe3594

mild

Staat: AL
Alter: 12,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Rash macular

Symptomtext

Patient's opposite arm became red and splotchy within ten minutes and his face started to get red. I gave him 10ml of benadryl and had them stay for another 10 minutes for observation. Recommended to continue the benadryl at home if needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: na
Vorgeschichte: na
Andere Medikamente: na
Allergien: penicillin (breaks out)
Vorherige Impfungen: -

VAERS 1964041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: NY
Alter: 28,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 17.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Injection site erythema Injection site pain Injection site pruritus Injection site swelling

Symptomtext

Patient reported swelling/redness at injection site that was itchy. Patient also reported pain at injection site. Advised patient to be seen by a physician in order to evaluate next course of therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: No medical attention sought-to-date. Advised patient to be evaluated by a physician on 12/20/2021.
Aktuelle Erkrankungen: No other illnesses
Vorgeschichte: No known conditions
Andere Medikamente: No known medications
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1963944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: VA
Alter: 49,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Urticaria

Symptomtext

Hives all over the body. Taking Zyrtec and Claritin

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Zyrtec, Claritin
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1963882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fe3594

mild

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 17.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Eye movement disorder Hypotonia Malaise Muscle spasms Vomiting

Symptomtext

Patient was in waiting chair post vaccination approximately 2 minutes post vaccination she expressed feeling unwell, pharmacist immediately went to check, pharmacist observed patient eyes roll back and body go limp, patient had some muscle spasms lasting about 15 seconds and then came to and vomited, patient was observed extra time and given water, advised to contact pcp, denied ambulance, patient was contacted later on no repeat incidence

Weitere VAERSDATA-Felder

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

VAERS 1963745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 15.12.2021
Beginn: 16.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Constipation Dizziness Feeding disorder Headache Nausea Pyrexia SARS-CoV-2 test negative Vertigo Vomiting

Symptomtext

Felt icky for first 2 days. Fever of 100.3; next 2 days. Chills, intestinal distress, headache, nausea, vomit (small amount), not eating, dizzy and vertigo; 5th day. 99.7 fever, some appetite, intestinal distress and no stool for 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Negative COVID-19 test on 4 day in morning at pharmacy.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Tylenol; Sulfa
Vorherige Impfungen: -

VAERS 1963706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FE3594

mild

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Headache Injection site pruritus Injection site swelling

Symptomtext

Severe headache for 48 hours and swollen , itchy on injected area

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Prenatal vitamins
Allergien: No
Vorherige Impfungen: -