VAERS Reports FN 2908

VAERS 2727645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 88,0
Geschlecht: M
Eingang: 27.12.2023
Impfdatum: 09.06.2022
Beginn: 28.10.2023
Tage bis Beginn: 506,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Aspiration COVID-19 Death Delirium Fall Hypoxia Intensive care Mental status changes Pericardial effusion Positive airway pressure therapy

Symptomtext

Patient is a 90 y.o. male with a PMH of IPF, HFpEF, AFib (Eliquis), Metastatic Prostate Cancer who presented to Hospital 10/28/2023 following an unwitnessed fall at his assisted living. He was found to have an AKI, pericardial effusion, hypoxia, AMS, and COVID-19. His hospital course was complicated by delirium and aspiration, leading to acute hypoxic respiratory failure requiring BiPAP and transfer to the ICU. Palliative Care had been following, and after goals of care conversations on 11/10/2023 the patient was transitioned to DNR-CC. Patient expired at 0107 11/12/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2723114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: FL
Alter: 86,0
Geschlecht: F
Eingang: 12.12.2023
Impfdatum: 15.08.2022
Beginn: 11.11.2023
Tage bis Beginn: 453,0
Dosis: 4
Route/Site: SYR / UN

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

Acute respiratory failure COVID-19 Gastritis Hyponatraemia Nausea Vomiting

Symptomtext

Hospitalization for Nausea/vomiting due to gastritis or COVID-19 infection, hyponatremia, acute hypoxemic respiratory failure on dates 11/11/2023- 11/13/2023. Treated with dexamethasone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Statins (HMG CoA Reductase inhibitors)
Vorherige Impfungen: -

VAERS 2689967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 03.10.2023
Impfdatum: 08.08.2022
Beginn: 15.09.2023
Tage bis Beginn: 403,0
Dosis: N/A
Route/Site: IM / LA

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

Acute respiratory failure Asthenia COVID-19 COVID-19 pneumonia Fall Nasal congestion Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

The patient was seen int he ED on 9/15/23 with nasal congestion, sore throat, and weakness for the past three days. She took a COVID test earlier that day which resulted positive. Additionally, she reported frequent falls at home. Ultimately, the patient was admitted 9/15/23 - 9/18/23 with discharge diagnoses including acute respiratory failure with hypoxia due to COVID-19 viral pneumonia, among other diagnoses. Of note, she did require supplemental oxygen, however was able to wean off during admission. The patient has received the primary COVID vaccine series and one booster.

Weitere VAERSDATA-Felder

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

VAERS 2649934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 27.06.2023
Impfdatum: 29.05.2022
Beginn: 25.11.2022
Tage bis Beginn: 180,0
Dosis: 4
Route/Site: IM / LA

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

Acute respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2647342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MN
Alter: 83,0
Geschlecht: F
Eingang: 20.06.2023
Impfdatum: 18.07.2022
Beginn: 20.04.2023
Tage bis Beginn: 276,0
Dosis: N/A
Route/Site: UN / LA

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

Acute respiratory failure Asthenia COVID-19 Hypoxia Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient has a history of dementia. She was brought to the ED by EMS on 4/20/23 for evaluation of weakness. In the ED, she was noted to initially be hypoxic requiring 2L via nasal cannula. Ultimately, the patient was admitted 4/20/23 - 5/3/23. She developed a fever overnight into 4/22. A COVID test was performed on 4/22 and resulted positive. Discharge diagnoses included acute hypoxic respiratory failure in the setting of COVID-19, among other diagnoses. She was able to be weaned to room air prior to discharge. Of note, the patient has received the primary COVID vaccine and two boosters.

Weitere VAERSDATA-Felder

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

VAERS 2632536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 16.05.2023
Impfdatum: 22.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / UN

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

Acute respiratory failure Dementia Epilepsy Hypoglycaemia Mental status changes Respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/27/2022 UNSPECIFIED DEMENTIA, UNSPECIFIED SEVERITY, WO BEHAVIORAL DISTURBANCE HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 10/27/2022 UNSPECIFIED DEMENTIA, UNSPECIFIED SEVERITY, WO BEHAVIORAL DISTURBANCE ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/27/2022 EPILEPSY, UNSPECIFIED HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 10/27/2022 EPILEPSY, UNSPECIFIED ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/27/2022 HYPOGLYCEMIA HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 10/27/2022 HYPOGLYCEMIA ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/27/2022 ALTERED MENTAL STATUS, UNSPECIFIED HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 10/27/2022 ALTERED MENTAL STATUS, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2612972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: NY
Alter: 80,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 24.09.2022
Beginn: 11.12.2022
Tage bis Beginn: 78,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Alanine aminotransferase increased Aspartate aminotransferase increased Blood creatinine increased Blood gases Blood urea increased C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Glomerular filtration rate decreased Hypertransaminasaemia Liver function test increased

Symptomtext

12/11/2022- Presents to ED, worsening SOB and cough. Afebrile. 02 mid 90's on 6L NCL (4L and cpap at HS baseline). Covid + test. CXR-b/l infiltrates . ABG 7.47/38/63/27 6L 02 via NC. Dexamethasone, hold remdesivir d/t elevated LFT's-AST 63 and ALT 66, transaminases 60's trending down. IV vanco and cefepime. Admit Acute on chronic hypoxemic respiratory failure b/l covid pna causing copd exacerbation. eGFR 27. WBC 15.8. AKI creat 2.4. BUN 87 . recently d/c 12/9 after 5 weeks stay COPD exacerbation and CAP. 12/12/-2022- cefepime d/c start meropenem. Pseudomonas. 12/19/2022-On 8L o2 via NC sat above 90's. IV decadron and meropenem. procalcitonin 0.10 and crp 1.3 d/c vanco. 12/27/2022- Transaminitis resolving, WBC 1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD on chronic 02 4L, CAD s/p CABG, AS s/p TAVR, OSA and CHF
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2607857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 31.03.2023
Impfdatum: 19.05.2022
Beginn: 17.02.2023
Tage bis Beginn: 274,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure Anaemia Ascites Aspiration pleural cavity Atelectasis Blood creatinine increased Bronchoalveolar lavage abnormal COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest tube insertion Chest tube removal Computerised tomogram abdomen abnormal Culture positive Culture urine positive Diuretic therapy

Symptomtext

Patient is a 56 y.o. female with a history of HTN, morbid obesity, DM2 c/b neuropathy, CKD, GERD, and adenocarcinoma of cecum who initially presented from facility to Hospital with worsening SOB and hypoxia in the setting of recently diagnosed COVID pneumonia. Found to be in acute hypoxic respiratory failure ultimately requiring intubation. Transferred to hospital 2/17/2023 for further management. Course complicated by MRSA pneumonia and recurrent R pleural effusion (suspected hepatic hydrothorax). Extubated 2/20/23 and urgent care consulted to assume care out of ICU on 2/21/23. Remarkable recovery and no further re-accumulation of pleural effusion with stable dose of diuretics. Discharged to SNF on room air. 1. Acute hypoxic respiratory failure: Baseline no O2 requirement. Initially due to COVID and superimposed MRSA pneumonia with right pleural effusion, ARDS. Subsequent recurrent right pleural effusion, atelectasis, shunting contributed to recurrent respiratory failure. Intubated 2/17/23, extubated 2/20/23. Worsening oxygenation 2/25/23 with rapidly re-accumulating pleural effusion as below. Resolved with repeat chest tube for effusion drainage. Diuresis as able. Room air on day of discharge. 2. Recurrent R sided pleural effusion: Hepatic hydrothorax. S/p thora 2/17/23 with transudative effusion. S/p R pigtail chest tube, removed 2/20/23. Worsening effusion again 2/25/23. S/p repeat thoracentesis with IR with 1.2L off, transudate again. Recurrent effusion noted 2/26/23 requiring chest tube placement. CT removed 3/5/23. VIR followed, poor candidate for TIPS. Hepatology following, considered OLT but also poor candidate with obesity. Started Bumex and Aldactone 3/6/23. Repeat CXR 3/9/2023 prior to discharge with minimal effusion. 3. MRSA pneumonia: s/p bronch 2/17/23 with BAL cx positive for MRSA. Completed Vancomycin course 2/24/23. 4. COVID pneumonia: dx 2/15/23 at hospital, vaccinated with primary series and booster per patient. Positive BAL 2/19/23. Remdesivir course and Decadron completed on 2/27/23. Out of isolation. 5. AKI on CKD3: likely prerenal, admit Cr 2 with baseline in 2018 of 1.5. Renal US 2/18/23 unremarkable. Appears at baseline 3/5/23. Monitor with resuming diuretics. 6. Decompensated liver cirrhosis, new diagnosis: Newly diagnosed based on CT A/P at hospital, liver with cirrhotic morphology and small ascites. Potentially NASH. AFP 1.7 on 2/17. Hepatology followed, recommended outpatient follow up for EGD and screenings, scheduled 3/22/23. Diuretics as discussed above. 7. ESBL Klebsiella UTI: UA infectious and cx 2/17/23 grew ESBL. Completed course of Ertapenem 2/21/23. 8. Sepsis: Multifactorial due to the above. Abx as above. Resolved. 9. Hypomagnesemia: Replete PRN. Scheduled daily repletion since continually low. 10. Anemia, thrombocytopenia: likely in the setting of acute illness. Hgb ~10 and plt >100, monitored and both Hb/plts remained stable. 11. NIDDM2: A1c 6.3. Held home meds. Started on basal/bolus insulin. Monitored and titrated for inpatient goal. 12. Uncontrolled HTN: Per hx, BP intermittently uncontrolled inpatient. Some home meds initially held. Amlodipine / carvedilol adjusted. Diuretics as above. 13. Neuropathy: Per hx. Continued home Lyrica renally dosed. 14. Severe obesity: Body mass index is 65+. Recommend outpatient bariatric follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 21,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2603406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 01.06.2022
Beginn: 07.03.2023
Tage bis Beginn: 279,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Anaemia of chronic disease Asthenia Blood creatinine increased COVID-19 Chest X-ray abnormal Condition aggravated Cough Death End stage renal disease Feeling cold Nausea Pulmonary congestion Refusal of treatment by patient Renal impairment SARS-CoV-2 test positive Tracheobronchitis

Symptomtext

Admit date: 3/7/2023 Expected discharge date and time: 3/17/2023 ? Admitting Physician: MD Discharge Clinician: MD PRESENTING PROBLEM: Acute renal failure (ARF) [N17.9] AKI (acute kidney injury) [N17.9] Anemia in other chronic diseases classified elsewhere [D63.8] COVID [U07.1] Hospital Course: 85-year-old with past medical history significant for CLL, CKD5, B-cell lymphoma, hyperlipidemia, DM 2, cardiomyopathy who was admitted to facility on 03/07/2023 for symptoms of weakness, cough, cold, nausea. Was noted to be in AKI CKD 5 with a creatinine of 7.86 (baseline between 4.3-5.3). Was positive for COVID-19 r. Chest x-ray showed peripheral vascular congestion without pneumonia. Patient was admitted to internal medicine with Nephrology on consult. Post admission patient was started on gentle IV fluids. Nephrology was consulted. Hemodialysis was offered to the patient but she refused. Currently on gentle IV fluids driven by Nephrology. Patient continued to remain on room air. However given severe symptoms Started on Decadron 6 mg orally daily. Was not a candidate for remdesivir with her AKI. Hospice was offered to the patient which she refused initially. Palliative following along for goals of care discussion. Ultimately patient's renal function continued to worsen. Patient was treated for tracheobronchitis as well. Patient was treated with IV fluids for renal failure worsening chronic kidney disease. Patient admitted to Facility 3/7/23 to 3/17/23 for AKI and Anemia. Patient transitioned to comfort and care and passed on 3/18.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Paroxysmal atrial fibrillation, Diabetes mellitus, type II, CLL (chronic lymphocytic leukemia), Anemia in chronic kidney disease, Essential hypertension, Left bundle branch block (LBBB), Cardiomegaly, Edema, Insomnia, GERD (gastroesophageal reflux disease), Compression fracture of lumbar spine, non-traumatic, Age-related osteoporosis with current pathological fracture, vertebra(e), initial encounter for fracture, Amaurosis fugax, B-cell lymphoma, Chronic back pain, Chronic dermatitis, Fatigue, Herpesvirus infection, Hyperlipidemia, Intervertebral disc disorders with radiculopathy, lumbar region, Thoracic region somatic dysfunction, Malignant lymphoma, lymphocytic, intermediate differentiation, Mild nonproliferative diabetic retinopathy, Osteoarthrosis Other myositis, multiple sites, Renal osteodystrophy, Trochanteric bursitis, unspecified hip, Chronic kidney disease (CKD), stage V, Thrombocytopenia, unspecified, Acute on chronic combined systolic and diastolic heart failure, Goals of care, counseling/discussion, ,Advanced directives, counseling/discussion, iventricular automatic implantable cardioverter defibrillator in situ, Intractable nausea and vomiting, Acute respiratory insufficiency, Depression, recurrent, Hyperparathyroidism, Nonischemic cardiomyopathy, Nausea, ESRD (end stage renal disease), Counseling regarding advance care planning and goals of care, SOB (shortness of breath), Acute metabolic acidosis, Acute renal failure (ARF), Hypomagnesemia, Cancer related pain
Andere Medikamente: acetaminophen (TYLENOL) 325 MG suppository, acetaminophen (TYLENOL) 500 MG tablet, amiodarone (PACERONE) 200 MG tablet, benzonatate (TESSALON) 200 MG capsule, bisacodyl (DULCOLAX) 10 MG suppository, carvedilol (COREG) 12.5 MG tablet, halope
Allergien: Adhesive Bandages MiscRash, Bactrim [Sulfamethoxazole W-trimethoprim]Nausea and Vomiting, Hydrocodone-acetaminophenNausea and Vomiting, Dizziness, LatexHives, TramadolNausea Only, IodineUnknown
Vorherige Impfungen: -

VAERS 2599655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 55,0
Geschlecht: M
Eingang: 20.03.2023
Impfdatum: 14.07.2022
Beginn: 08.01.2023
Tage bis Beginn: 178,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Anticoagulant therapy Aspiration Atelectasis Blood pressure decreased Bronchial secretion retention Bronchoscopy abnormal COVID-19 Cardio-respiratory arrest Computerised tomogram head normal Condition aggravated Corynebacterium test positive Culture positive Deep vein thrombosis Dyspnoea Echocardiogram abnormal Electroencephalogram normal Endotracheal intubation

Symptomtext

Discharge Physician: MD; Primary Care Physician: MD; Date of Admission: 1/8/2023; Discharge Date: 3/15/2023 Room Number: PRESENTING PROBLEM: Acute hypoxemic respiratory failure (HCC) [J96.01] Tracheoesophageal fistula, acquired (HCC) [J86.0] Esophageal cancer (HCC) [C15.9] Acute on chronic respiratory failure (HCC) [J96.20] Septic shock (HCC) [A41.9, R65.21] 56-year-old with a PMH of non-Hodgkin's lymphoma s/p chemotherapy and radiation 1992, hx of left bundle-branch block and complete heart block s/p pacemaker, hypertension, severe GERD, HFPEF, and squamous cell esophageal cancer s/p esophagectomy 8 months ago, stent placement 6 months ago and hospitalizations x4 for recurrent pleural effusions, pneumonia, hypoxia, and aspiration who presented to the ER 1/7/23 with shortness of breath. Patient was found to have moderate to large bilateral pleural effusions with adjacent compressive atelectasis vs pneumonia. Patient was started on azithromycin and Rocephin and was transferred to Hospital for admission. Pulmonary was consulted and recommended cont pleurX drain. Patient also tested positive for COVID-19 on 01/08/2023. GI was consulted and recommended reaching out to Surg oncology CTS as they performed his esophagectomy in April. They also recommended considering upper GI if cleared by SLP but SLP still with concerns over safe swallow making contrast intake for upper GI series risky. Surg Oncology was consulted and Interventional Pulm performed bronchoscopy on 1/11/23 and confirmed to have a tracheal defect either to the mediastinum or to the esophagus. He was kept NPO with thoracic surgery consult re: operative plan for this. (CTS) planned O.R on 1/23/23 after he was clear from respiratory isolation for COIVD. His pleuraX was drained and patient finished a course of Rocephin and azithromycin for pneumonia. Eliquis was transitioned to heparin gtt and ultimately to Lovenox bid for recent LUE dvt diagnosed in November. Patient's hospital course involved multiple surgeries including right thoracotomy, repair of TEF, cervical esophagostomy, pleural drain placements by IR, and reintubation 02/03 with subsequent open tracheostomy 02/06. Patient was given IV antibiotics that was narrowed to Linezolid per ID until 2/20 after patient was found to have Corynebacterium striatum on Respiratory culture. Hospital course was complicated with neurology consulted for left facial droop, difficulty with tongue movement, with stroke code called 02/24 for transient neurological symptom with staring and unresponsiveness. Symptoms resolved at the time when stroke code team arrived in the room. NIHSS 0. CT head imaging did not demonstrate new acute changes. Continues EEG did not demonstrate any signs of seizure activity. Otherwise, patient was in the process of prior to transferring to intensive care unit. On 02/25, it was reported that patient went to the bathroom, came back, was found grey and unresponsive per nursing staff prior to code blue being called. Code blue call 02/25, being bagged via tracheostomy tube on arrival, emergent bronchoscopy done which showed right mainstem mucous plug, aspirated with improvement in SpO2 90%. Post bronchoscopy patient's blood pressure dropped and he was started on norepinephrine, epinephrine, phenylephrine sticks given. Bedside echo demonstrate large pericardial effusion, possible signs of tamponade. After achieving hemodynamic stability patient transferred to intensive care unit. During ICU course, AHRF likely secondary to mucus plug and found to be positive for Stenotrophomonas pneumonia on respiratory/BAL cultures. Patient presented with s septic shock requiring vasopressor support, was started on IV antibiotics narrowed down to Bactrim per ID for total of at least 21 days. Patient has been having baseline tachycardia that is paced, otherwise asymptomatic. Shock overall resolve with patient successfully weaned off of vasopressor support. Patient was initially on "difficult to wean" protocol, chest physiotherapy for support, and was eventually transitioned on T-piece and tolerated without further ventilator support escalation. He was then transferred out of ICU. Prior to ICU transfer, he underwent venous doppler of LE. He was found to have a right groin pseudoaneurysm for which IR was consulted. Patient underwent guided thrombin injection on 3/7 with IR. Repeat with small residual hematoma - no patent aneurysm. Patient incidentally was found to have a pericardial effusion, which was medically managed with colchicine per Cardiology recs. There was no evidence of tamponade. 2D Echo repeated 3/8 shows increase in size of large pericardial effusion in comparison to prior echo on 2/27 - no evidence of tamponade physiology. CTS/Cardio following. No plan for intervention. Recommend conservative management with repeat Echo in 1 month to reassess. He was also noted to have elevated LFTs. Abdomen shows hepatomegaly, along with possible polyps vs sludge balls. Consulted general surgery for eval. D/w general surgery, recommending HIDA scan. HIDA Scan with no evidence of cholecystitis. GGT is elevated. Palliative care was consulted. Care conference with patient and his family to determine further goals of care and overall update was completed bedside 3/14. Family agreeable. He has not progressed to tolerating PMV and communicates with gestures and brief words written down. On file with 1st signature completed. Navigated discharge planning. He was scheduled for discharge, but patient noted to be hypotensive after resuming of home medications. Entresto discontinued with recommendations for resuming outpatient if indicated. He received IVF with resolution of hypotension. Report called to hospitalist. She accepted patient and advised okay to transfer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 66,0
Labordaten: -
Aktuelle Erkrankungen: 7/2/2022 (5 hours) Hospital Emergency Arm DVT (deep venous thromboembolism), acute, left (HCC) 6/27/2022 - 7/1/2022 (4 days) Hospital Bilateral pleural effusion Principal problem
Vorgeschichte: Complete heart block s/p pacemaker hx of Melanoma 2012 hx of LBBB (left bundle branch block) Squamous cell esophageal cancer s/p esophagectomy 4/19/22 complicated by anastomotic leak requiring stenting and subsequent erosion of the stent into the trachea resulting in TEF requiring OR 1/2023 Dysphagia with recurrent aspiration s/p J tube placement hx of DVT Anticoagulated Chronic HFpEF Thrombocytosis Normocytic anemia GERD (gastroesophageal reflux disease) Non-Hodgkin's lymphoma (HCC) Environmental allergies Hyperlipidemia CAD (coronary artery disease) Essential hypertension Hypothyroidism due to acquired atrophy of thyroid Cardiac pacemaker in situ Dilated cardiomyopathy (HCC) Nonrheumatic mitral valve regurgitation Nonrheumatic aortic valve insufficiency Malignant neoplasm of overlapping sites of esophagus (HCC) CKD (chronic kidney disease) Polycystic kidney disease Hypothyroid Esophageal cancer (HCC) S/P robot-assisted surgical procedure Unspecified severe protein-calorie malnutrition (HCC) Asplenia after surgical procedure Autosomal dominant polycystic kidney disease Recurrent pleural effusion bilateral H/O splenectomy Parapneumonic effusion Pneumothorax on left, basilar Multiple comorbid conditions Advanced care planning/counseling discussion Feeding tube dysfunction Stenotrophomonas pneumonia History of esophageal cancer Cachexia (HCC) DVT (deep venous thrombosis) (HCC) Radiation esophagitis Acute and chronic respiratory failure with hypercapnia (HCC) Pneumonia due to coronavirus disease 2019 (CODE) Bilateral paralysis of tongue Pericardial effusion Right groin pseudoaneurysm (HCC) Counseling regarding goals of care Tracheostomy status (HCC)
Andere Medikamente: Acetaminophen (TYLENOL); Albuterol (PROVENTIL); Apixaban (ELIQUIS); Colchicine (COLCRYS); Fexofenadine (ALLEGRA); Fiber supplement; Fluticasone (FLONASE); Furosemide (LASIX); Hydroxyzine (ATARAX); Levothyroxine (SYNTHROID); Melatonin; Metop
Allergien: Moxifloxacin Hcl In NaclSwelling, Angioedema
Vorherige Impfungen: -

VAERS 2582749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MA
Alter: 12,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 03.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: - / LA

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

Blood electrolytes normal Brain herniation Brain oedema Headache Sudden death Toxicologic test normal

Symptomtext

Sudden Death after a headache episode Post shows Cerebellar tonsillar and bilateral uncal herniation in the setting of "mild" cerebral edema No fever No rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sudden death
Hospital-Tage: -
Labordaten: Negative tox screen Electrolytes nl for episode
Aktuelle Erkrankungen: Hx Migraine, Depression, ADD, Asthma
Vorgeschichte: Hx Migraine, Depression, ADD, Asthma
Andere Medikamente: Sertraline, Topiramate, Ibuprofen
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2574308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 24.06.2022
Beginn: 31.12.2022
Tage bis Beginn: 190,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Angiogram pulmonary abnormal Anion gap Anticoagulant therapy Aortic valve incompetence Asthenia Atelectasis Atrial fibrillation Atrial flutter Blood culture negative Blood lactic acid normal Blood sodium decreased Bronchial wall thickening C-reactive protein increased COVID-19 COVID-19 pneumonia Cardiac failure acute

Symptomtext

Patient is a 79 y.o. female patient of MD with history of HTN, HLD, hypothyroidism, recent COVID diagnosis who presented to Hospital with weakness, fatigue, shortness of breath. Admitted to obs at hospital 12/29-12/30 for chest pain and sent home with Paxlovid. She was found to be in acute hypoxic respiratory failure which acutely worsened requiring intubation and ventilator support from 1/2?1/5. Completed course of antibiotics and diuresed for treatment of acute heart failure. Cardiology and pulmonology evaluated. Acute heart failure exacerbated by atrial fibs/flutter for which she was started on rate control and anticoagulation. Course was complicated by in-hospital delirium which is since improved. PT/OT evaluated with recommendation for SNF versus IPR placement however patient declined placement in favor of home health. Acute respiratory failure with hypoxia O2 sats in the 89-90% in the ED with tachypnea in setting of COVID infection with possibly pneumonia and CHF exacerbation. Initially required 2L NC on admission. Worsening oxygenation on day 1 of admission requiring initiation of nasal oxymizer- 13L, later further deterioration lead to intubation on 1/2/23. Extubated to NC on 1/5/23, weaned to room air on 1/6 Current O2 requirements: Room air Pulm/CC followed. Management as below Atrial fib/flutter Started 1/4/23, looked more like flutter on tele. EKG with atrial fibrillation. HR controlled (70-80). TTE 1/6/2023: EF 45+/- 5%, global hypokinesis of LV, moderate aortic regurg Resume home metoprolol, dose increased for better rate control. Eliquis started given high CHADSVASC score. Cardiology evaluated, now signed off Monitor on tele. Acute on chronic combined systolic and diastolic heart failure CTPA on 12/29 did not show any PE, showed mild scattered atelectasis and peribronchial thickening CXR on admission showed interval development of bibasilar atelectatic/consolidative changes, left greater than right; small bilateral pleural effusions; central vascular crowding/congestion. NT pro BNP of 3771 Last TTE (12/12/22) with normal LVEF, grade I diastolic dysfunction, moderately severe TR Repeat Echocardiogram here showed EF 40-45%, global hypokinesis of left ventricle, moderate AR, mild to moderate MR and TR, trivial pericardial effusion, possibly the drop in EF could be from Afib. Lasix 40 mg IV BID started, transitioned to PO lasix. Cardiology follows. Septic shock, resolved In setting of COVID-19, pneumonia Lactate of 6.4 on admission, trended down Imaging with questionable pneumonia. Procalcitonin 0.13. Urinary antigens negative. Blood culture NGTD, sputum culture NGTD. MRSA probe negative. Started on Levophed (1/2/23), weaned off on 1/3. Completed 7 day course with IV Cefepime. COVID-19 Date of onset of symptoms: 12/25 Symptoms present on admission: weakness, shortness of breath Date of covid positive test: 12/27 at home, 12/30 at hospital Vaccination status: vaccinated with first boosters, did not receive bivalent booster yet Imaging: as below with CXR showing worsening atelectasis vs pneumonia with likely volume overload, repeat CXR with worsening opacities. Oxygen requirements on admission: room air, but satting 89-90% Current oxygen requirements: ventilator (FiO2 65%, PEEP 10 cm H20). CRP 25. Medical therapy: dexamethasone course completed, Remdesivir (completed 5 day course) Consultants following: Pulmonology Anticipated special isolation end date: 1/5/23 AKI, resolved Metabolic acidosis, anion gap, resolved Metabolic acidosis likely with her AKI and lactic acidosis Normal renal function at baseline, up to 1.11 from 0.73 with bicarb of 14 on admission. AG of 23 on admission, pure anion gap due to lactic acidosis Cr and bicarb improved. Monitor renal function with diuresis. Hyponatremia, resolved Suspect due to poor oral intake, though could have component of SIADH due to viral infection. Sodium of 124 on admission, was 131 at hospital Resolved with diuresis. Hyperglycemia No prior history of diabetes, last Hgb A1c of 5.5% in 7/21, repeat A1C 5.6. Likely due to COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2565900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 23.01.2023
Impfdatum: 14.06.2022
Beginn: 15.01.2023
Tage bis Beginn: 215,0
Dosis: 4
Route/Site: IM / LA

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

Acute kidney injury Anticoagulant therapy Atrial fibrillation Blood creatinine increased Blood thyroid stimulating hormone Bradycardia COVID-19 Cerebrovascular accident Culture positive Culture urine Cystitis Differential white blood cell count Dizziness Dysuria Electrocardiogram ambulatory Facial paresis Fatigue Full blood count

Symptomtext

COVID+ 1/15/2023. Vaccination status - moderna x3 + pfizer x1 BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: MD Admission Date: 1/15/2023 Discharge Date: Jan 19, 2023 Active Hospital Problems Diagnosis Date Noted POA ? History of COVID-19 01/16/2023 Yes ? AKI (acute kidney injury) 01/16/2023 Yes ? Paroxysmal atrial fibrillation 01/16/2023 Yes ? History of stroke 01/16/2023 Yes ? OSA (obstructive sleep apnea) 03/22/2016 Yes ? HTN (hypertension) 04/09/2013 Yes ? Unspecified hypothyroidism 04/09/2013 Yes ? Stage 3b chronic kidney disease 04/09/2013 Yes DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Altered mental state [R41.82] Weakness [R53.1] Acute cystitis without hematuria [N30.00] Right sided weakness [R53.1] HOSPITAL COURSE: 89-year-old admitted on 1/15 with findings of altered mental status and transient stroke-like symptoms including right-sided facial weakness and evidence of previous stroke. Evaluation emergency room showed abnormal urine with large amount of leukocytes, and the patient reported some dysuria. Patient was placed on ceftriaxone and cultures subsequently were positive for Proteus sensitive to all. Patient received 3 days of ceftriaxone which was then discontinued. Neurology was consulted and recommended brain MRI. The patient had previously undergone MRI procedures and had difficulty with general anesthesia so the family was reluctant to repeat an MRI with general anesthesia. After extensive discussion with Neurology it was recommended that the patient consider therapeutic anticoagulation because of past history of stroke, recent episode of COVID, and known atrial fibrillation. Previously it was felt that the patient had to high fall risk to warrant therapeutic anticoagulation. After additional discussion and evaluation by Physical therapy it was felt that therapeutic anticoagulation would be reasonable to pursue. The patient's neurologic symptoms resolved. At the time of admission the patient was also noted to have acute kidney injury on top of CKD. This was treated with IV fluid rehydration and discontinuation of the patient's lisinopril. Patient's initial creatinine was 2.29, his creatinine improved to 1.9 on 1/17. Patient's baseline creatinine is between 1.3 and 1.4. The patient was started on Eliquis 2.5 mg 2 times a day on 01/17. If his renal function continues to improve the Eliquis dosage may need to be increased. Patient also noted to have bradycardia with afib with heart rate in 40s at times not on rate control medication without significant symptoms occasional report of dizziness with mobility and amlodipine further decreased . Family had previously decided against pace maker and decision not to send with heart monitor as they would not want intervention. Patient was discharged in improved condition on 1/19.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: Office visit with PCP on 6/14/22 - ASSESSMENT & PLAN: 1. Fatigue, unspecified type Complete Blood Count w/Differential Comprehensive Metabolic Panel (CMP) Thyroid Stimulating Hormone (TSH), Free T4 if indicated Urinalysis (UA) Urine Culture 2. Dizziness Complete Blood Count w/Differential Comprehensive Metabolic Panel (CMP) Thyroid Stimulating Hormone (TSH), Free T4 if indicated Urinalysis (UA) Urine Culture 3. Need for vaccination PFIZER SARS-COV-2 TRI-SUCROSE VACCINE --will order labs and UA, as well as a culture. --can consider referral to MRI of brain and neurology consultation. Will consider, but they do not want this ordered at this time. --also discussed holter monitor. They will consider, but declined at this time. --may also consider stopping amlodipine as could be side effect of medication.
Vorgeschichte: Unspecified hypothyroidism HTN (hypertension) Mixed stress and urge urinary incontinence Anxiety state, unspecified GERD (gastroesophageal reflux disease) Stage 3b chronic kidney disease Prostate cancer - s/p RRP 1992 Gout Chronic pain OSA (obstructive sleep apnea) Elevated sed rate Iron deficiency anemia Morbid obesity Ataxia Chest pain Black stools Bright red blood per rectum PVC (premature ventricular contraction) Diarrhea Bradycardia Weakness Chronic venous insufficiency Nocturnal hypoxia Obesity hypoventilation syndrome Facial droop Weakness of right lower extremity History of COVID-19 History of stoke
Andere Medikamente: Acetaminophen 1,000 mg Oral 2 times daily, 2 tablets in the morning & evening; 1 tablet in the afternoon. amLODIPine Besylate 5 mg Oral Daily Aspirin 81 mg Oral Daily with dinner busPIRone HCl 10 mg Oral 2 times daily Cannabidiol Oil 0.5 mL
Allergien: Penicillins - Hives
Vorherige Impfungen: -

VAERS 2562309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 13.07.2022
Beginn: 27.12.2022
Tage bis Beginn: 167,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Atelectasis Blood cholesterol normal Blood folate normal Blood glucose increased Blood immunoglobulin M decreased Blood potassium increased Blood sodium increased Blood thyroid stimulating hormone normal Blood triglycerides increased COVID-19 pneumonia Chest X-ray abnormal Chills Computerised tomogram head abnormal Dyspnoea Encephalopathy Enlarged cerebral perivascular spaces

Symptomtext

Patient is a 79 y.o. male patient of MD with history of CLL, Colon cancer, C-dif, GERD, HLD presented to Hospital with shortness of breath . Acute hypoxic respiratory failure Suspecting secondary to COVID-19 viral pneumonia CXR shows faint patchy opacities in left mid to lower lung zone which may correspond to some subtle atelectasis or pneumonitis. Started on Rocephin and Azithromycin for possible pneumonia however symptoms more consistent with viral etiology than bacterial especially given negative pro-cal. Urinary Ags and sputum culture negative D-dimer elevated. CTPA negative for PE but did show pulmonary HTN, patchy ground-glass infiltrates bilaterally with tiny bilateral pleural effusions. Wean O2 requirements able Home O2 eval done today- qualified for 2L Management of COVID-19 listed below Covid-19 viral pneumonia Date of onset of symptoms: 12/12/22 Symptoms present on admission: productive cough, chills, altered mental status Date of covid positive test: 12/12/22 - at home, repeat test positive Vaccination status: vaccinated Imaging: 7 faint patchy opacities in the left mid to lower lobes with some subtle atelectasis or pneumonitis Oxygen requirements on admission: 3L NC -> 4L Current oxygen requirements: 2L NC Medical therapy: Steroids x10 days. Out of time frame for Remdesivir Consultants following: None at this time Anticipated special isolation end date: TBD Albuterol, steroids x5 days, and Tessalon Perles at discharge Acute encephalopathy Suspecting secondary to hypoxia, underlying infection, and possible CVA TSH, B12, Folate all wnl Attempt to regulate sleep/wake cycle Resolved Abnormal CT CT head shows low density areas in basal ganglia compatible with lacunar infarcts and/or dilated perivascular space. Low attenuation in left external capsule/subcortical insular white matter compatible with age indeterminate ischemic changes MRI brain showed chronic microvascular angiopathic changes Neuro consulted. Recommended starting ASA Neuro checks Q4H PT/OT/ST- HHC at discharge History of CLL Patient is on Calquence BID which is non-formulary Continue Valcyclovir therapy Oncology consulted. Continue to hold Calquence/Acalabrutinib while admitted. Immunoglobulin levels shows decreased IgM of 33. Discussed with Dr. on day of discharge- does not need IVIG. Follow up with outpatient Oncologist when to resume Calquence/Acalabrutinib. Hyperkalemia K 5.9 Hyperglycemia protocol with Ca-gluconate, Albuterol, and Lokelma Monitor Hypernatremia Na 147 Resolved DM, new onset Glucose also elevated due to steroids HbA1c 6.8 Recommend lifestyle changes Defer to PCP for further management Hx of HLD Cholesterol panel: Cholesterol 194, TG 260, HDL 26, LDL 116 Recommend lifestyle changes Follow up with PCP for consideration for statin Microcytic anemia Hb 12 with MV 96.5 No signs of bleeding Iron studies + ferritin pending- defer to PCP for follow up Severe malnutrition POA Nutrition consulted GERD Continue Maalox PRN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2562215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 22.06.2022
Beginn: 20.12.2022
Tage bis Beginn: 181,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Ammonia normal Angiogram pulmonary abnormal Atelectasis Blood folate normal Blood thyroid stimulating hormone normal Bronchogram abnormal COVID-19 Chest X-ray abnormal Computerised tomogram head normal Computerised tomogram thorax abnormal Full blood count normal Haematuria Hypoxia Liver function test normal Lung consolidation Lung infiltration Lung opacity

Symptomtext

Patient is a 85 y.o. male admitted to the hospital on 12/20/2022 for AMS, hypoxia, found to have covid-19, s/p dexamethasone, also given paxlovid while here. Was unable to be weaned off oxygen, repeat chest imaging showed a new RLL consolidation c/w pneumonia, started on CAP coverage with some improvement in his oxygenation, but still requiring 1-2L NC. Discharge Diagnosis and Associated Hospital Course Acute metabolic encephalopathy - secondary to COVID-19 infection, on a background mild cognitive impairment - BMP, CBC, B12/folate, ammonia, TSH, and HFP largely unremarkable. UA negative. CT Head unremarkable - Minimize central acting medications, recommend delirium precautions - PT/OT and case management consulted, initially PT/OT recs 2-3x weekly with plan to return to ILF, however now 5x weekly, rehab on dc COVID-19 Abnormal CT imaging Acute hypoxic respiratory failure Lobar pneumonia - No clear exact symptom onset. - CTPA negative for PE, does show mild bilateral lower lobe patchy lung opacities (atelectasis vs aspiration vs infiltrates) - Mildly hypoxic, initially with sleep only, but now seems relatively persistent (rather unclear how much of COVID is contributing vs undiagnosed OSA); - Continue Decadron for 10 days or when off O2; e-consult to ID and Paxlovid completed here - Wean O2 as able for goal saturation 90-92% - CXR obtained due to increasing O2 demands 12/26, noted RLL consolidation and mild effusions, worse from prior, CT chest with RLL consolidation with air bronchograms c/w pneumonia. Started CAP coverage 12/27 - will ask ST to evaluate given location of lobar pneumonia, had ST evaluate here who recommended chopped solids, ST at rehab Thrombocytopenia, resolved - presumably from acute illness / covid, possibly alcohol abuse. PLTs nml march - monitor, so far stable Alcohol abuse: Currently drinks 6 glasses of wine per night. B12/folate unremarkable. History of PE: Secondary to COVID-19 infection in 2020. S/p IVC filter placement. Consider removal as outpatient History of SDH/SAH/IPH: S/p mechanical fall from alcohol intoxication. CT head negative here. Essential hypertension: Previously on losartan. Not currently. Dyslipidemia Coronary artery atherosclerosis: Continue statin. Not currently on ASA due to above Hypothyroidism: Continue Synthroid Major depressive disorder, recurrent, in full remission: Continue Prozac BPH: S/p greenlight therapy in 2019. Continue doxazosin, finasteride Mild cognitive impairment: Per PCP notes.Unable due to finances or higher functioning tasks. Follow-up outpatient. Hematuria: noted previously. Outpatient fu recommended

Weitere VAERSDATA-Felder

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

VAERS 2558514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 92,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 02.06.2022
Beginn: 05.01.2023
Tage bis Beginn: 217,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Blood creatinine increased Blood glucose normal Blood test abnormal Chest X-ray abnormal Computerised tomogram head abnormal Condition aggravated Confusional state Cough COVID-19 Cardiac failure acute Cardiac failure congestive Cardiorenal syndrome Cerebral ischaemia Diuretic therapy Dyspnoea Hallucination, visual

Symptomtext

Discharge Date: Jan 11, 2023 Discharge Provider: MD Primary Care Provider : MD COVID positive date 1/5/2023 PRESENTING PROBLEM: Acute on chronic respiratory failure with hypoxia HOSPITAL COURSE: 92-year-old male with past medical history of chronic diastolic heart failure, chronic respiratory failure with hypoxia on 3 L of oxygen at daytime, 4-6 L with sleep, presented with cough, dyspnea, and increasing lower extremity swelling. Patient tested positive for COVID-19 and influenza A and was also found to be on acute on chronic diastolic heart failure. Patient was admitted and was started on Tamiflu for influenza a, dexamethasone for COVID -19, and IV Lasix for CHF exacerbation. Patient initially had poor urine output on Lasix 40 mg IV 2 times a day so this was increased to 80 mg IV 2 times a day with the better urine output response. Because patient was just recently admitted for another CHF exacerbation last month, Cardiology was consulted for assistance in management and outpatient follow-up. With improvement of symptoms and decrease in weight, patient was eventually transitioned to torsemide 40 mg in the morning and 20 mg in the afternoon. This was a change from his previous regimen of Lasix 40 mg orally twice a day. Patient was discharged home on improved condition and will followed up with Cardiology as an outpatient. Patient was also discharged on potassium 40 mEq daily. BMP check in 1 week

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: Hospital note from admission at Hospital: Discharge Provider: DO Primary Care Provider at Discharge: MD Admission Date: 12/28/2022 Discharge Date: 1/2/2023 HOSPITAL COURSE: Patient is a 92-year-old male with history of chronic diastolic CHF, type 2 diabetes mellitus, atrial fibrillation, hypertension, carotid artery stenosis, OSA and gout who presented to the ED with confusion/visual hallucinations. In the emergency department, he was hypoxemic but otherwise hemodynamically stable. Blood work showed evidence of acute kidney injury with a creatinine of 2.67 and glucose of 194. CT head was negative for acute intracranial abnormalities, though did show moderate chronic microvascular ischemic white matter disease. Chest x-ray showed findings consistent with CHF. Due to his acute kidney injury, he was given 1 L of IV fluids, and was admitted to the hospital for further care. Upon admission, psychiatry was consulted due to his visual hallucinations. They recommended observation and no medical therapy for this. It was felt that hypoxemia may have contributed to his hallucinations, and these resolved within 48 hours of being hospitalized. For his acute kidney injury, he was initially felt to be dry. His diuretics were held and his renal function was monitored. His Cr remain unchanged. He developed worsening hypoxemia (3 L oxygen with activity and 6 L oxygen with sleep), and developed worsening lowe extremity edema. He had recently decreased his Lasix to 40 mg PO daily in outpatient setting. He was started on Lasix 40 mg IV twice daily with good diuresis. His Cr improved with diuresis, consistent with cardiorenal syndrome. His hypoxemia improved. He was felt stable for discharge home on 1/2/23. He was instructed to increase his Lasix back to 40 mg PO BID at discharge. He should follow-up with his PCP in 1 week. He continued to require 3 L oxygen with activity and 6 L oxygen with sleep at discharge.
Vorgeschichte: OSA (obstructive sleep apnea) Chronic respiratory failure with hypoxia Hypertension A-fib Heart failure Carotid stenosis, asymptomatic, bilateral Chronic diastolic heart failure Polymyalgia rheumatica Vitreous degeneration, left Mild nonproliferative diabetic retinopathy of both eyes without macular edema associated with type 2 diabetes mellitus Microalbuminuria due to type 2 diabetes mellitus Stage 3b chronic kidney disease AKI (acute kidney injury) Hypothyroidism Hyperlipidemia Gout Diabetes mellitus, type 2, without long-term current use of insulin Other osteoporosis Recurrent major depressive disorder, in full remission Hallucination
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG tablet amLODIPine (NORVASC) 10 MG tablet apixaban (ELIQUIS) 2.5 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet atorvastatin (LIPITOR) 20 MG tablet Calcium Carbonate-Vit D-Min (CALCIUM 1200 PO) empagliflozin
Allergien: Benazepril
Vorherige Impfungen: -

VAERS 2557548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

kritisch

Staat: OK
Alter: 18,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 20.07.2022
Beginn: 09.11.2022
Tage bis Beginn: 112,0
Dosis: N/A
Route/Site: IM / UN

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

Balance disorder Blood glucose increased Cardiomegaly Death Dyspnoea Organ failure Pain

Symptomtext

Acute and immediate onset of difficulty breathing, full body pain, unsteadiness, and death at 112 days post injection. Blood glucose of 610 at time of death, organ failure and "swollen heart" per attending ER physician. Patient has no history of diabetes or other long standing health conditions or illnesses and was in good health.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: currently investigating
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Birth Control
Allergien: none
Vorherige Impfungen: -

VAERS 2554855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 88,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 20.05.2022
Beginn: 25.12.2022
Tage bis Beginn: 219,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Angiogram cerebral normal Blood cholesterol increased COVID-19 Computerised tomogram head normal Computerised tomogram normal Computerised tomogram spine Condition aggravated Haemangioma Hypercapnia Hypoaesthesia Hypoxia Magnetic resonance imaging head normal Pain in extremity Positive airway pressure therapy Respiratory failure SARS-CoV-2 test positive Sciatica

Symptomtext

Admission Date: 12/25/2022 COVID positive Date: 12/25/2022 Admitting Diagnoses: COVID-19 Discharge Date: 1/5/2023 PRESENTING PROBLEM: Acute on chronic respiratory failure with hypoxia (HCC) HOSPITAL COURSE: With patient is a 88 year old female presented with complaints of hypoxia and hypercapnia. She was found positive for covid. She was placed on bipap. She was started on decadron and remdesevir. Her oxygenation improved and she returned to her baseline oxygenation. She completed her 10 day course of Decadron. She developed right leg pain with numbness. Stroke code was called. She was evaluated by neurology. She had CT spine , CT head, CT angio and MRI brain. IT did not show stroke. Her pain got better next day. An incidental cavernoma was identified and the patient should follow up with with Neurosurgery in the outpatient setting. Otherwise her symptoms are likely explained by sciatica exacerbated by position the in bed. In the midst of the stroke workup it was identified that the patient had high cholesterol in the OB started on Lipitor at time of discharge. The patient should follow-up with her PCP for post hospitalization evaluation. PT and OT evaluated the patient and recommended home with assist. The patient will return to her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Very severe chronic obstructive pulmonary disease (HCC) Chronic respiratory failure with hypoxia (HCC) Supplemental oxygen dependent Lung nodule Acute on chronic respiratory failure with hypoxia (HCC) COPD with acute exacerbation (HCC) OSA (obstructive sleep apnea) Acute exacerbation of chronic obstructive pulmonary disease (COPD) (HCC) Coronary artery disease Essential hypertension Exudative age-related macular degeneration, right eye, with active choroidal neovascularization (HCC) Anginal pain (HCC) GERD (gastroesophageal reflux disease) Dysphagia Gastroesophageal reflux disease, esophagitis presence not specified Arthritis Arthritis of right knee Anemia Dementia (HCC) Low back pain with sciatica Chronic back pain Hearing loss, unspecified hearing loss type, unspecified laterality Neuropathy Hypothyroidism Hyperlipidemia Anxiety Depression Osteoporosis Cognitive impairment History of tobacco abuse History of pulmonary embolism Violation of narcotic use agreement Somnolence
Andere Medikamente: albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization alendronate (FOSAMAX) 70 MG tablet amLODIPine (NORVASC) 5 MG tablet atorvastatin (LIPITOR) 40 MG tablet diclofenac sodium 1 % gel donepezil (ARICEPT) 10 MG tablet ELIQUIS 5 MG tablet fl
Allergien: Codeine Flovent [Fluticasone] Lisinopril
Vorherige Impfungen: -

VAERS 2554818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 90,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 05.08.2022
Beginn: 20.12.2022
Tage bis Beginn: 137,0
Dosis: 4
Route/Site: IM / -

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

Acute respiratory failure Arthralgia Asthenia Blood creatine phosphokinase increased COVID-19 Computerised tomogram spine Condition aggravated Confusional state Dehydration Electrocardiogram COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Computerised tomogram head normal Computerised tomogram normal Fall Fatigue SARS-CoV-2 test positive

Symptomtext

COVID+ 12/20/22. Vaccination Status - Pfizer x4 BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider: MD Admission Date: 12/20/2022 Discharge Date: 12/24/2022 Active Hospital Problems Diagnosis Date Noted POA ? Pneumonia due to COVID-19 virus 12/20/2022 Yes ? Weakness 12/20/2022 Yes ? Vascular parkinsonism 09/08/2021 Yes ? Elevated blood-pressure reading without diagnosis of hypertension 05/18/2021 Yes ? AF (paroxysmal atrial fibrillation) 02/22/2021 Yes ? Complete heart block Discharge Disposition: skilled nursing facility Active Issues Requiring Follow-up: COVID-19 pneumonia Acute hypoxic respiratory failure - oxygenation stable on 2 L nasal cannula, wean as able at rehab - continue dexamethasone 6mg daily through 12/30/22 - incentive spirometer - if no improvement would consider trial of low dose oral lasix due to hx of known EF 48%, he is not on this typically Frequent falls Acute left lateral hip pain - continue PT and OT at acute rehab - tylenol, ice, lidocaine patch for left thigh/hip pain DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Generalized weakness [R53.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 90 y.o. male with complex PMH, including prior CVA, HLD, paroxysmal A fib on Eliquis, CHB s/p pacemaker, HLD, and colon cancer who presented 12/20/22 due to weakness, fatigue, and possible fall and/or prolonged time on ground. Patient found to be COVID-19 positive. He was reportedly found down on the ground in his independent living facility and was confused. In the ED, vitals on arrival with T 37.2C, HR 60s, RR low 20s, BP 170s-190s/70s-80s, SpO2 92-94% on room air. Pt appeared dehydrated and was given 1L NS bolus, EKG with paced rhythm, Trp 24->23. CXR with cardiomegaly and retrocardiac opacities. Given use of blood thinners, ordered CT head and C spine, which were negative for any acute intracranial process, fracture or dislocation. Pacemaker was interrogated and did not show any abnormal rhythms. CK notably elevated to 2500 on admission and trended down with fluid resuscitation. Xray of left hip obtained and negative for fracture. PT evaluated recommending acute rehab. PMR evaluated initially recommending SAR but he had improvement in pain and was able to meet criteria for acute rehab. He remained on 2L NC through admission and was started on remdesivir (which he completed 4 days of) and dexamethasone which will be continued on discharge. Patient did have a fall early morning 12/23 landing on his knees. X-rays without evidence of injury however does demonstrate possible CPPD left knee. Patient without left knee pain currently so no further workup pursued. CXR repeated day before discharge continuing to show pneumonia. He was discharged to acute rehab in stable condition without new complaints. Inpt Rehab 12/24/22- 1/4/2023

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: ED 7/27/22 ? - CLINICAL IMPRESSION 1. Fall, initial encounter 2. Injury of head, initial encounter 3. General weakness ED COURSE / MEDICAL DECISION MAKING / TREATMENT PLAN: Patient arrived via EMS with a chief complaint of fall earlier today. Patient was seen and examined by myself and the attending physician in the emergency department. The patients vitals were obtained and pt was stable. We obtained a urinalysis to rule out UTI which returned as negative. In addition we obtained a CT without contrast which I examined myself and found no evidence for acute pathology. As the patient is alert and oriented x4 and appears to be at his baseline without findings on the CT, we are comfortable with the patient being discharged home. The results were discussed with the patient, questions were answered, and he expressed verbal understanding and agreement with the plan. Strict return precautions were given and patient was found to be appropriate for d/c home. Patient was instructed to follow up with their primary care doctor at next available appointment or to return to the emergency department if symptoms worsen. Patient is improved at this time and stable for discharge home. DIAGNOSTIC TESTING - CT HEAD WO CONTRAST Final Result 1. No evidence of acute intracranial pathology. Severe senescent brain changes. 2. If there are focal neurologic symptoms or concern for CT occult pathology, MRI followup is recommended
Vorgeschichte: History of CVA with residual deficit Balance disorder Complete heart block Mixed hyperlipidemia History of SCC (squamous cell carcinoma) of skin History of colon cancer in adulthood AF (paroxysmal atrial fibrillation) Long term (current) use of anticoagulants Cardiac pacemaker in situ Elevated blood-pressure reading without diagnosis of hypertension Vascular parkinsonism Localized edema
Andere Medikamente: Apixaban 5 mg Oral 2 times daily Atorvastatin Calcium 20 mg Oral Daily Cyanocobalamin 1,000 mcg Oral Daily Fluorouracil 5 % See Admin Instructions, PLEASE SEE ATTACHED FOR DETAILED DIRECTIONS hydroCHLOROthiazide 12.5 mg Oral Daily Ketoconaz
Allergien: No Known allergies
Vorherige Impfungen: -

VAERS 2544684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 28.12.2022
Impfdatum: 13.06.2022
Beginn: 09.12.2022
Tage bis Beginn: 179,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Anaemia Blood creatinine increased COVID-19 Chest X-ray abnormal Cough Diarrhoea Dyspnoea Glomerular filtration rate decreased Glycosylated haemoglobin normal Haematochezia Haemoglobin decreased Haemoptysis Hypoxia Legionella test Lung disorder Malaise

Symptomtext

Patient is a 73 y.o. male who presented from home on 12/9/2022 with 1 day history of fevers, cough, shortness of breath, malaise. He was found to be COVID-positive on admission, and requiring up to 3 L nasal cannula of oxygen. Clinical course further complicated by prerenal AKI. Acute issues resolving, renal function returned to baseline. No longer having the rest of her symptoms. Patient will follow-up with PCP in outpatient setting for ongoing management. Discharge Diagnosis and Associated Hospital Course Acute Hypoxic Respiratory Failure, resolved Community acquired pneumonia Presented with respiratory failure believed due to covid 19 with possible superimposed bacterial pneumonia -See further plan for COVID-19 below -MRSA, Legionella antigen and strep antigen negative. Sputum culture revealed moderate mixed flora -Treated with Rocephin and azithromycin with transition to oral antibiotics on discharge -Weaned off O2 and breathing comfortably, no shortness of breath or other respiratory complaints at this time. Hemoptysis resolved. COVID-19 - Presented with: Fevers, cough, shortness of breath, malaise - Symptom onset: 12/9 - Positive COVID-19: 12/9 - Vaccination status: Vaccinated with Pfizer with last dose June 2022 - CXR on admission showed patchy right upper and right lower airspace disease - Oxygen status: Previously on 2 to 3 L nasal cannula, now on room air - Decadron: Treated with steroids on arrival. Patient has been weaned off oxygen and has no further respiratory symptoms. Will not discharge with further steroid medications given concern for hyperglycemia, and since his symptoms/hypoxia have resolved - Remdesivir: Does not qualify due to eGFR <30 ml/min. -Not considered a candidate for Paxlovid due to renal function - DVT prophylaxis:Subcutaneous heparin - Serial COVID labs ordered: yes - Case Management/Social Services consulted: Yes Hemoptysis Chronic anemia Likely due to COVID-19 and CAP as well. History of lung cancer likely also contributing -Hemoptysis resolving, most recent hemoglobin is 8.7 AKI on CKD stage IV Resolving and now appears to be close to baseline. Baseline creatinine appears to be 3.0. was 3.1 on 8/26/2022 -Creatinine on admission 4.27. Likely prerenal secondary to vomiting, diarrhea, COVID-19 infection -Received IV fluid. Improved Repeat Cr 3.09. in am 12/10 -Plan to resume Lasix on discharge, continue to hold lisinopril until seen in evaluation by PCP Diarrhea Likely secondary to COVID-19, patient spouse reports blood in the stool. Per chart review, patient has a known history of internal and external hemorrhoids which is likely etiology of blood -Would follow with PCP for this issue, if any further bleeding can consider outpatient GI work-up. Essential hypertension Holding lisinopril on discharge on home medications of Norvasc 5 mg, Coreg 25 mg twice daily, Lasix -Plan to continue Lasix, hold lisinopril on discharge until seen in reevaluation by PCP Coronary artery disease -History of CABG in 2019 -Echo 5/17/2022 showed mild LVH with EF 50 to 55%, hypokinesis of the basal inferior segment, grade 2 diastolic dysfunction, and mild MR--unchanged compared to 2019. -Continue statin, aspirin, beta-blocker Diabetes type 2, insulin-dependent, with nephropathy, and neuropathy -A1c from Aug 2022 was 6.3 -Home insulin regimen includes Lantus 60 units at bedtime and NovoLog 40 units with breakfast and dinner, and then 15 units novolog with lunch. -Continue home regimen on discharge. Continue follow-up with PCP in outpatient setting for ongoing monitoring Hx of CVA -In 2009, with residual left sided deficits of upper and lower extremities -Continue aspirin and statin RLS -Continue home magnesium and Requip Peripheral vascular disease -History of lower extremity stenting. Continue previous antiplatelet regimen on discharge History of lung cancer in 2019 -Adenocarcinoma, status post radiation. -Last CT chest 5/13/2022 stable. -Continue ongoing outpatient follow-up with Dr.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2542174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 23.12.2022
Impfdatum: 28.06.2022
Beginn: 15.11.2022
Tage bis Beginn: 140,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Acute respiratory failure Blood creatinine increased Blood glucose normal Blood lactic acid Blood urea increased COVID-19 Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Cough Dyspnoea Echocardiogram Electrocardiogram normal Glycosylated haemoglobin normal Leukocytosis Lung infiltration Malaise

Symptomtext

Patient is a 61 y.o. female patient of MD with history of HTN, CAD, HFrEF, COPD who presented with dyspnea. Acute Respiratory Failure w/Hypoxia - Resolved Multifactorial, including COVID, PNA, sepsis, AECOPD Initially required 4L NC, no baseline requirement CT Chest w/RUL infiltrate Aggressive pulmonary hygiene NIPPV ordered on admission for significant WOB Pulm/CC consulted Now stable on room air Septic Shock - Resolved Present on admission: yes Etiology: PNA Criteria: tachycardia, tachypnea, fever, leukocytosis, source Evidence of end organ damage: Initial lactic acid: 1.4 WBC 28, COVID + Resp PCR, Blood/sputum culture, urine AG, MRSA probe pending Given Rocephin/Azithro in ED Current antibiotic regimen: Rocephin Vasopressors/steroids: Levo off by 11/17 Covid-19 Virus Infection Date of onset of symptoms: 11/7 Symptoms present on admission: Cough, fever, malaise Date of covid positive test: 11/7 at MC Vaccination status: vaccinated, booster x2 Imaging: CT w/RUL infiltrate Oxygen requirements on admission: 4L Current oxygen requirements: Room air Medical therapy: Decadron, Cefepime and zithromax Consultants following: Pulm Special isolation end date: 11/18 Complete 10 day course of Decadron on discharge AKI Likely pre-renal/ATN from shock vs COVID renal injury BUN/Cr 54/3.46, baseline WNL Limit nephrotoxins as able Monitor UOP, strict in/out Improving slowly; 2.54 on 11/17, 2.03 on 11/18 Monitor renal function Elevated Troponin Asymptomatic, likely demand ischemia Initial trop 39 EKG w/o acute ischemic changes Monitor on tele Negative trend; no further cardiac work up at this time COPD, w/acute exacerbation Secondary to COVID, PNA Scheduled MDI, tiotropium, Symbicort Steroids, abx as above Aggressive pulmonary hygiene Advair on discharge (based on coverage) T2DM, non-insulin dependent Chronic, controlled BG 133, A1c 6.7 Home oral agents held on admission Accuchecks and SSI ordered Due to worsening, changed to insulin drip Now with low sugars so changing back to basal bolus insulin Resume home agents on discharge HFrEF, w/o acute exacerbation NICM s/p dual chamber AICD placement Stable, clinically euvolemic ECHO 2010: EF 45-50% Holding GDMT given shock Echo with EF 41%, mild MVR and TVR Obesity BMI 33.01 Weight loss, lifestyle modification encouraged Tobacco Use Disorder Smokes 1/2 PPD >3 minutes spent counseling cessation NRT while hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 29.11.2022
Impfdatum: 24.05.2022
Beginn: 23.11.2022
Tage bis Beginn: 183,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after two vaccines; PATIENT EXPIRED ; Pfizer 4/23/22 Lot# FK9894; Pfizer 5/24/22 Lot# FN2908

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

VAERS 2504560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: OH
Alter: 84,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 19.05.2022
Beginn: 12.09.2022
Tage bis Beginn: 116,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Probable case of COVID-19, died from illness on 9/12/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Anterior nares swab collected on 09/08/2022 detected SARD-CoV-2-Antigen on 9/8/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2502934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: NY
Alter: 79,0
Geschlecht: M
Eingang: 09.11.2022
Impfdatum: 13.06.2022
Beginn: 26.08.2022
Tage bis Beginn: 74,0
Dosis: 4
Route/Site: IM / LA

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

Acute respiratory failure C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Confusional state Fall Lung opacity Pneumonia aspiration SARS-CoV-2 test positive Sepsis

Symptomtext

8/26/2022- Presents to Ed, EMS found him, had fallen. confusion. o2 sat was in 80's put on NRB. CRP-140 covid + test. CXR: bibasilar opacities which may represent atelectasis. Admit sepsis s/t to aspiration pna, covid pna. Acute hypoxic resp failure s/t COPD. Given Vanco and clindamycin. Ordered remdesivir, dexamethasone, doxy, Afebrile. cefepime, Flagyl and vanco. G Supplemental 02 HFC, 30L 90%. 8/28/2022-BC negative, taper antibiotics to ceftriaxone, Flagyl and doxy. 02 requirements down to 6L. 8/30/2022- improving, downgraded to 4L NC. Completed remdesivir. Continue ceftriaxone and doxy. VSS 9/2/2022-Tolerating room air. IV doxy and decadron continued. 9/7/2022- Tolerating 2L NC, cannot wean will need 02 at d/c. Completed remdesivir, Rocephin d/c. Continue doxy. VSS. D/C to Snf.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, MI,
Andere Medikamente: -
Allergien: ASA, Augmentin, Moxifloxacin, Roflumilast and sulfa
Vorherige Impfungen: -

VAERS 2494197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 09.06.2022
Beginn: 19.09.2022
Tage bis Beginn: 102,0
Dosis: 4
Route/Site: IM / -

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

Acute kidney injury COVID-19 Death General physical health deterioration Nodal rhythm Unresponsive to stimuli

Symptomtext

The patient was admitted to local Hospital where he was seen by PT, OT, Wound Care, dietician and Speech Therapy. Infectious Disease was consulted and the plan was to continue Ancef for 6 weeks through Nov 3rd. During the hospital course, the patient developed acute kidney injury and was evaluated by Nephrology. He also developed junctional rhythm for which Cardiology was consulted. During the hospital course, he developed COVID-19. He was treated with remdesivir and Decadron. Initially his oxygen requirements increased. Pulmonary was consulted. There was also possibility of aspiration pneumonia for which the patient's antibiotic was changed to Zosyn. His condition gradually was getting worse and the patient's family elected to proceed with do not resuscitate and do not intubate. On the evening of Oct. 21, 2022 the patient was unresponsive. Pt was made comfort cares and passed away on 10/21/2022 at 2328.

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

VAERS 2473463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 28.06.2022
Beginn: 30.09.2022
Tage bis Beginn: 94,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure C-reactive protein abnormal COVID-19 pneumonia Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Lung infiltration Oxygen saturation abnormal Procalcitonin normal

Symptomtext

Admission Date: 9/30/2022 Discharge Date: 10/5/2022 Clinical Narrative: Admitted with Covid Pneumonia/exacerbation of COPD. Doing well after Decadron/Remdesivir/MDIs/Pulmonary Hygiene/care. Home today with continued attention to symptomatic management. Please see the following problem-list oriented Hospital Course below: * Pneumonia due to COVID-19 virus Assessment & Plan Will give Decadron, vitamin- C, zinc, Pepcid and Remdesivir. Lovenox prophylaxis. Follow-up chest x-ray tomorrow morning. 10/2.... Continue IV remdesivir, Decadron, oxygen as per protocol on vitamins Saturating 97% on 1 L nasal cannula 10/3..... Chest x-ray today shows worsened or persistent filtrates however patient shows clinical improvement, she is presently on room air saturating 96% Procalcitonin is normal and CRP improved 10/5 - consistencies steady improvement during her hospital stay. Doing well. Oxygen needs back to baseline on room air. Discharge planning. Acute respiratory failure with hypoxemia Assessment & Plan Titrate oxygen to effect. Encourage prone positioning. Encourage pulmonary toilet. Bronchodilator p.r.n. Will give Lasix IV now for diuresis A result of COVID-19 pneumonia Continue treatment as above Encourage prone positioning 10/5 - continues to do well. Will finish remdesivir today. Discharge planning. Oxygen needs at baseline. On room air.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Acute respiratory failure with hypoxemia Atrial fibrillation with RVR Morbid obesity with BMI of 40.0-44.9, adult Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin D-dimer, elevated
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet allopurinol (ZYLOPRIM) 100 MG tablet apixaban (ELIQUIS) 5 MG tablet ascorbic acid (VITAMIN C) 1000 MG tablet atorvastatin (LIPITOR) 20 MG tablet baclofen (LIORESAL) 5 MG tablet bisoprolol (ZEBETA) 5 MG
Allergien: Bactrim [Sulfa Drugs
Vorherige Impfungen: -

VAERS 2452312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 85,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 05.07.2022
Beginn: 08.09.2022
Tage bis Beginn: 65,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Agitation Angiogram pulmonary abnormal Blood creatinine increased Blood lactic acid Brain natriuretic peptide increased COVID-19 Cardiogenic shock Chest pain Cholelithiasis Death Dyspnoea General physical health deterioration Haemoglobin decreased Hiatus hernia Hypotension Intensive care Positive airway pressure therapy

Symptomtext

Discharge Provider: MD Primary Care Physician at Discharge: PA-C Admission Date: 9/8/2022 PRESENTING PROBLEM: Shock HOSPITAL COURSE: Patient is a 85 year old with a past medical history Rheumatoid arthritis ( on Prednisone), HTN, Anemia, Chronic Back pain ( see the pain clinic), HFrEF (EF 20%) who presented to ED via EMS from her home with Shortness of breath and chest pain. Per documentation, she had worsening SOB and a productive cough since 9/4. Today she developed respiratory distress which prompted the call to EMS. En route, she received ASA and nitro x1. In the ED, she was found to be Covid PCR (+). CTA thorax negative for PE, new T7 compression fracture, thyroid nodules > 17 mm, Large hiatal hernia, incidental cholelithiasis. Significant labs noted: Troponins > 300, creatinine > 2, BNP 9.5K. Due to the concern for NSTEMI, the ED physician spoke with cardiology- PA-C. Due to low hemoglobin at 10g/dL, plan to hold on starting AC at this time. Due to patient's refractory hypotension, she was started on NE and transferred to ICU for management. Plan to obtain Echo. Pt continued to decompensate overnight, Epi was added for presumred cardiogenic shock, mixed venous only 50, vaso added for ongoing hypotension. Pt agitated, bipap placed, precedex started. Haldol given. Troponin rising, rpt lactic 7. Family updated and came to pt bedside, after further discussion the decision was made to place patient on comfort care and withdrawal life saving medications. Patient pronounced dead at 1743. Please see death note for additional details. Date of Death: 9/9/22 Time of Death: 5:43 PM Preliminary Cause of Death: Acute hypoxemic respiratory failure due to COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Iron deficiency anemia secondary to inadequate dietary iron intake Other specified rheumatoid arthritis, multiple sites Primary osteoarthritis involving multiple joints Encounter for long-term (current) drug use Chronic congestive heart failure, unspecified heart failure type Left bundle branch block Chronic back pain Compression fracture of thoracic vertebra Compression fracture of lumbar vertebra Anxiety with depression Drug induced constipation Advanced care planning/counseling discussion Cardiogenic shock AKI (acute kidney injury) COVID-19 Encephalopathy acute Acute respiratory failure with hypoxia Other specified anemias NSTEMI (non-ST elevated myocardial infarction) Stress hyperglycemia
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet (#10-pack) alendronate (FOSAMAX) 70 MG tablet aspirin 81 MG enteric coated tablet carvedilol (COREG) 6.25 MG tablet DULoxetine (CYMBALTA) 20 MG delayed release capsule ferrous sulfate 325 (65 Fe) MG tab
Allergien: Sulfa Drugs
Vorherige Impfungen: -

VAERS 2407043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: NH
Alter: 85,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Cerebral infarction Cerebrovascular accident Computerised tomogram head abnormal Fall

Symptomtext

Readmitted with new Left temporal lobe infarct (new stroke) after an unwitnessed fall at Skilled Care Facility

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 21,0
Labordaten: Head CT 7/12/22
Aktuelle Erkrankungen: Past Medical History: ? Benign prostatic hyperplasia ? CAD (coronary artery disease) ? Chronic kidney disease (CKD), Stage III ? Chronic obstructive pulmonary disease ? Diabetes mellitus ? Hyperlipidemia ? Hypertensive disorder Advanced dementia, CAD s/p CABG
Vorgeschichte: As noted above
Andere Medikamente: acetaminophen 650 mg Oral Every 6 hours PRN albuterol sulfate 90 mcg/actuation 2 puffs Inhalation Every 4 hours PRN amlodipine besylate 5 mg Oral Daily aspirin 81 mg Oral Daily atorvastatin calcium 40 mg Oral Every evening benzocaine/mentho
Allergien: pneumocococal vaccine - arm swelling
Vorherige Impfungen: pneumococcal vaccine - arm swelling

VAERS 2388222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 25.07.2022
Impfdatum: 23.06.2022
Beginn: 12.07.2022
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Angiogram pulmonary abnormal Atrial flutter Bladder catheterisation Blood glucose normal Brain natriuretic peptide increased COVID-19 Computerised tomogram thorax abnormal Condition aggravated Cyanosis Decreased appetite Dizziness Dyspnoea Dyspnoea exertional Dysuria Electrocardiogram abnormal Emphysema Fibrin D dimer

Symptomtext

Patient up to date on COVID vaccinations who admitted with COVID positive PCR. Provider d/c note below: "78 YO male that presented to the ED with c/o SOB and worsening dizziness. Chronic health conditions include TIA PAF orthostatic Hypotension T2DM Hypothyroid Anxiety Emphysema. Pt reports that he has been getting very SOB working harder to breathe when up moving around and getting worse dizziness. No cough. His wife reports he has been sleeping more and more through the day and now has his days and nights confused. Today he got up and poured a bowel of cereal and had to take a break before he could finish. She reports that his lips have been blue. He wears the 02 all the time at 2L when resting and has been requesting and increased both at rest and when up moving. Has had major loss of appetite. He denies chest pain, fever, cold and flu symptoms. Feet and ankles starting swelling two days ago. In the ED, CTA negative for PE but does show small bilateral pleural effusions and possible pulmonary edema. . BNP 5,001 d dimer 990 EKG is aflutter. Hgb 13.5 Glucose 156. BP has been quite high while in the ED. (HPI per NP) Hospital Course: No notes on file patient is a 78yr old male with a history of CAD, Emphysema, Anxiety, Gout, DM, PAfib, Hypothyroidism, Idiopathic hypotension, BPH who presented with SOB and dizziness. He is usually on 2L at home but in past week he has had worsening labored breathing and was found to have covid. He and wife had been vaccinated with mederna and booster. Today he is on highflow oxygen, feels much better today. Acute on Chronic Hypoxic Respiratory Failure secondary to Covid - Improving clinically on dexamethasone day#8, completed remdesivir and supplemental oxygen. This is in the setting of Emphysema and past smoking history. CT showed Mild to moderate emphysematous changes and possible superimposed interstitial lung disease. He is much improved and now on 4L NC oxygen. He is being discharged to complete dexamethasone (2 more doses for a total of 10 days) and on supplemental oxygen to follow up with PCP. Idiopathic Orthostatic hypotension - he has had a syncopal episode in the past and more recent episodes of pre-syncope. Improved on midodrine. Urinary retention with incomplete emptying - difficulty straight cath. Urology consulted - Place Foley catheter, increase tamsulosin 0.8 mg daily, trial of voiding in the next 5-7 days when medically stable, outpatient follow up."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: COVID detected PCR on 07/12/22.
Aktuelle Erkrankungen: -
Vorgeschichte: Alcohol induced fatty liver Type 2 diabetes mellitus without complication, without long-term current use of insulin (*) BMI 33.0-33.9,adult Ventricular premature depolarization Hyperlipidemia Personal history of transient ischemic attack (TIA), and cerebral infarction without residual deficits History of atrial fibrillation History of gout Lung nodule Emphysema of lung (*) Coronary artery calcification seen on CT scan History of diabetes mellitus, type II Idiopathic hypotension Generalized anxiety disorder Bilateral carotid artery stenosis Depressed mood
Andere Medikamente: Proair Amoxil Aspirin Lipitor Colcrys Drisdol Lexapro Lasix Cortef Synthroid Proamatine Mycostatin Fish oil K dur Flomax
Allergien: Zanaflex
Vorherige Impfungen: -

VAERS 2370542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MA
Alter: 86,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 24.06.2022
Beginn: 10.07.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: IM / LA

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

Death

Symptomtext

Patient has been on hospice and expired on 7/10/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Pt expired
Aktuelle Erkrankungen: Dementia, PVD, hx of Resp failure with hypoxia, CKD, trigeminal neuralgia, dysphagia, CVA, TIA
Vorgeschichte: Had been on Hospice Services since 5/20/2021
Andere Medikamente: Acetaminophen 650mg suppository every 6 hrs as needed, Xanax 2mg every 6 hours, Morphine 10mg every hours .
Allergien: choline,magnesium salicylate, codeine sulfate, Immune Globulin, Magnesium, Salicylates, Vicodin HP
Vorherige Impfungen: -

VAERS 2367913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MA
Alter: 64,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 24.06.2022
Beginn: 08.07.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: IM / LA

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

Death

Symptomtext

Patient expired. Was on hospice services prior to vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: DEMENTIA, HTN, DYSPHAGIA, PSYCHOSIS
Vorgeschichte: PATIENT ON HOSPICE SERVICES
Andere Medikamente: BACTRIM DS 1 TAB 2 X DAY; ACIDOPHILUS 1 TAB 2 X DAY; ATROPINE 1% DROPS SL FOR SECRETIONS; LORAZEPAM ; MORPHINE
Allergien: NKA
Vorherige Impfungen: -

VAERS 2320547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: MN
Alter: 71,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 09.06.2022
Beginn: 14.06.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: IM / LA

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

Pulmonary embolism

Symptomtext

Acute Pulmonary Embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, HLD, hypothyroidism, Mobitz type II AVB s/p PPM (8/2021), OSA on CPAP, vertigo, and seronegative RA (
Andere Medikamente: chlortalidone, vitamin d, levothyroxine, potassium chloride, simvastatin, melatonin
Allergien: oxycodone = itching
Vorherige Impfungen: -

VAERS 2316995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

kritisch

Staat: TX
Alter: 90,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 07.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Cardiac disorder Chest discomfort Chest pain Cough Death Dyspnoea Pyrexia

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Severe, Additional Details: Patient received vaccine on 6/7/2022 around 3pm. Patient starting experiencing coughing, fever and shortness of breath at 7:15am on 6/8/2022. Patient passed away by 8:15am from a sudden cardiac event.

Weitere VAERSDATA-Felder

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

VAERS 2591063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: WV
Alter: 57,0
Geschlecht: F
Eingang: 03.03.2023
Impfdatum: 25.07.2022
Beginn: 31.07.2022
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

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

Alanine aminotransferase normal Angiogram cerebral abnormal Anion gap Anticoagulant therapy Antiplatelet therapy Arteriogram carotid abnormal Aspartate aminotransferase normal Asthenia Bacterial test positive Basophil count normal Basophil percentage decreased Bilirubin urine Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium increased Blood chloride normal Blood creatinine normal

Symptomtext

ED note by Dr. on 7/31/22: "Patient Date of Service: 7/31/2022 Primary Care Doctor: MD Patient information was obtained from patient. History/Exam limitations: none. Chief Complaint:Vomiting HPI: Patient is a 57 y.o. female who presents to the Emergency Department with dizziness and vomiting. Patient states that she was feeling well yesterday and she was asleep in a proximally 2:00 a.m. awoke to use the restroom she states that when she got up out of bed she suddenly felt very dizzy with a spinning sensation and associated nausea vomiting. She states that she lays still the symptoms all seem to improve but that any time she moves her head she feels a sense of spinning with vomiting. She states that her mouth feels dry. She denies any fever cough chest pain shortness of breath or congestion. The nurse's triage note states that the patient wants to be checked for COVID but when I spoke with the patient she states that she does not believe that she has COVID and that she is immunized. She denies any headaches, double vision, blurry vision, chest pain, focal weakness numbness or rashes. She denies any recent head injuries. Denies any tinnitus or changes in hearing. " "Impression: Encounter Diagnoses Name Primary? ? Vertigo Yes ? Nausea and vomiting ? Elevated troponin Disposition: pending Condition on Disposition: Stable" H&P by FNP on 8/1/22: Date of Admission: 7/31/2022 Date of Service: 8/1/2022 PCP: MD Chief Complaint: dizziness HPI: Patient is a 57 y.o., female with a history of migraines, type II DM, CAD, HTN, HLD, and COPD who presented to the ED for further evaluation of dizziness and vomiting. Patient states that she was feeling like her normal self yesterday and when she went to sleep but at aproximally 2:00 a.m. she awoke to use the restroom and suddenly felt very dizzy/spinning associated nausea vomiting. She states that she lays still the symptoms all seem to improve but that any time she moves her head she feels a sense of spinning with vomiting. She admits to gneralized weakness, none unilaterally, and trouble standing/walking but denies headache, facial droop, vision changes, speech changes, recent illness, fever, chest pain, paraesthesias, abdominal pain, urinary symptoms, or diarrhea. Has hx of triple bipass a few years ago but denies hx of stroke. A CT of her brain today revealed an Asymmetric hypodensity in the left cerebellum suggesting area of evolving infarct. No acute intracranial bleed. Her lab workup is generally unremarkable apart from a trivially elevated trop of 55, no change on repeat a few hours later. UA is negative for infection. Her vertigo has improved after meclazine. NIHSS in the ED= 0. Not a candidate for tpa regardless as she is out of time window. Slightly hypertensive in the 170s, other vss. " "Assessment/Plan: Patient is a 57 y.o., female who presents with the following: 1. Acute left cerebellar infarct --vertigo improving. NIHSS=0. Out of time window to be tpa candidate regardless --confirm with MRI --CTA head and neck pending --stroke orderset initiated, neurology consulted --check updated lipid panel, pending results and further workup continue 80 mg atorvastatin and TriCor --continue daily low dose aspirin --updated echo with bubble study --pt/ot consulted as well per stroke protocol 2. hypercalcemia --check phos and PTH levels 3. Uncontrolled HTN --elevated today mostly 170s systolic --will allow for permissive HTN for now, continue home metoprolol. Will likely need additional maintenance med 4. Uncontrolled Type II DM --recent A1C 8.7 --on metformin and trajenta at home --hold oral diabetic meds for now and add ssi coverage with Humalog achs 5. Hx of CAD --s/p CABG --continue asprin statin, 6. COPD --no acute issues, continue home inhalers 7. Tobacco abuse --pt counseled on smoking cessation 10 Depression and anxiety --continue home Lexapro 11. Hx of migraines --continue home topamax. Takes maxalt at home DVT PPx: subq heparin Code Status: Full Code DNP,FNP-C" Consult note by Dr. on 8/2/22: Date of service: 8/2/2022 Chief Complaint: Dizziness, N/V Subjective: History was obtained from a review of the electronic record and discussion with the patient and family. Patient is a 57 y.o. female with PMH significant for type II DM, HTN, HLD, CAD s/p CABG who presented to the ED 7/31/22 with acute onset dizziness, N/V, admitted for left PICA territory stroke secondary to occluded left PICA. Pt states she feels the same today, denies any vomiting but still notes significant dizziness/nausea with moving her head or posture change. Her daughter is present at bedside. " " Assessment and Plan: 1) Stroke summary: 57 y/o F with PMH significant for CAD s/p CABG, HLD, HTN, type II DM and tobacco use disorder who presented to the ED 7/31 with acute onset dizziness with N/V. CT brain shows evolving left cerebellar infarction without signs of hemorrhage and CTA head and neck shows occluded left PICA as well as moderate to severe stenosis of the left vertebral artery origin as well as multiple intracranial calcified and noncalcified plaques particularly in the posterior circulation. MRI brain w/o contrast confirms left PICA territory ischemic stroke. Etiology is likely artery to artery embolus due to the left PICA occlusion. TTE with bubble was negative intracardiac shunt, EF 65%. Continue with best medical management with dual antiplatelet therapy with ASA 81 mg and Plavix 75 mg daily x 3 months, with ASA 81 mg daily to continue and high dose statin therapy with atorvastatin 80 mg qhs. She also has significant underlying vascular risk factors with tobacco use disorder and uncontrolled type II DM and will need aggressive glycemic control and smoking cessation to lower her risk factors. Stroke Etiology: Artery to artery embolus secondary to left PICA occlusion General Plan: -Normoglycemia -Normothermia Blood pressure plan: -Place pt on telemetry -BP goal: - <130/90 Medications: -Antiplatelet: ASA 81 mg and Plavix 75 mg x 3 months, then ASA 81 mg daily to continue -Statin: atorvastatin 80 mg qhs -DVT ppx: Lovenox 40 mg subq daily Imaging: - TTE- 2D echo w bubble - negative for intracardiac shunt, EF 65% - CTA head and neck - L PICA occlusion, moderate to severe stenosis left vertebral artery origin, moderate to severe stenosis right vertebral artery, multiple intracranial calcified and noncalcified plaques -MRI brain - acute left PICA territory ischemic stroke Lab work: -LDL 170 -Hemoglobin A1c - 8.7 Diet plan: - low glycemic index diabetic diet Consultants: - Physical therapy, occupational therapy Activity Level: - PT/OT Disposition: Continue to work with PT/OT, will need outpatient therapy as well. She should follow-up with Neurology clinic with myself or Dr. in 4-6 weeks for re-evaluation. Stroke Education: 1. Patient was educated that he would benefit from tight control of his vascular risk factors (LDL < 70, BP < 130/90, glycemic control A1c < 7) 2. Patient was educated to call 911 for any acute stroke symptoms (BE FAST- Balance problems, Eyes-blurry vision, double vision, Facial Droop, Arm Weakness, Speech Problems, Syncope, Seizure) 3. Medications: Patient was counseled to take Asprin 81 mg daily / Plavix 75 mg daily / Lipitor 80 mg daily 4. Patient was counseled about the need for follow-up with PCP and in neurology clinic after discharge 5. Lifestyle: Smoking cessation is vital. We counseled this patient on need to quit smoking and resources to do so. We encourage risk factor treatment and management by pt?s PMD. Patient was educated on Mediterranean diet, exercise, medication compliance Stroke Education was given verbally to the patient and family member and the teaching was effective and patient and family member in agreement with the plan."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebellar stroke
Hospital-Tage: 4,0
Labordaten: EXAM: Temperature: 36.5 ?C (97.7 ?F) Heart Rate: 62 BP (Non-Invasive): (!) 167/73 Respiratory Rate: (!) 22 SpO2: 94 % Labs: I have reviewed all lab results. Lab Results for Last 24 Hours: Results for orders placed or performed during the hospital encounter of 07/31/22 (from the past 24 hour(s)) URINALYSIS WITH MICROSCOPIC REFLEX IF INDICATED BMC/JMC ONLY Result Value Ref Range COLOR Light Yellow Light Yellow, Straw, Yellow APPEARANCE Clear Clear PH 6.0 <8.0 LEUKOCYTES Negative Negative WBCs/uL NITRITE Negative Negative PROTEIN 30 (A) Negative, 10 mg/dL GLUCOSE >=1000 (A) Negative mg/dL KETONES Negative Negative mg/dL UROBILINOGEN 0.2 <=2.0 mg/dL BILIRUBIN Negative Negative mg/dL BLOOD Negative Negative mg/dL SPECIFIC GRAVITY 1.015 <1.022 URINALYSIS, MICROSCOPIC Result Value Ref Range RBCS 0-2 0 - 2 /hpf WBCS 0-2 0 - 2 /hpf BACTERIA Slight (A) None /hpf SQUAMOUS EPITHELIAL 0-2 0 - 2 /hpf MUCOUS Slight (A) None, Light /hpf COMPREHENSIVE METABOLIC PANEL, NON-FASTING Result Value Ref Range SODIUM 140 136 - 145 mmol/L POTASSIUM 4.3 3.5 - 5.1 mmol/L CHLORIDE 105 96 - 111 mmol/L CO2 TOTAL 22 22 - 30 mmol/L ANION GAP 13 4 - 13 mmol/L BUN 11 8 - 25 mg/dL CREATININE 0.77 0.60 - 1.05 mg/dL BUN/CREA RATIO 14 6 - 22 ESTIMATED GFR 90 >=60 mL/min/BSA ALBUMIN 4.5 3.5 - 5.0 g/dL CALCIUM 11.0 (H) 8.5 - 10.0 mg/dL GLUCOSE 283 (H) 65 - 125 mg/dL ALKALINE PHOSPHATASE 75 50 - 130 U/L ALT (SGPT) 23 (H) 8 - 22 U/L AST (SGOT) 17 8 - 45 U/L BILIRUBIN TOTAL 0.4 0.3 - 1.3 mg/dL PROTEIN TOTAL 8.5 (H) 6.4 - 8.3 g/dL LIPASE Result Value Ref Range LIPASE 12 10 - 60 U/L TROPONIN-I Result Value Ref Range TROPONIN I 55 (HH) 7 - 30 ng/L CBC WITH DIFF Result Value Ref Range WBC 10.8 3.7 - 11.0 x10?3/uL RBC 5.29 (H) 3.85 - 5.22 x10?6/uL HGB 15.6 11.5 - 16.0 g/dL HCT 45.5 34.8 - 46.0 % MCV 86.0 78.0 - 100.0 fL MCH 29.5 26.0 - 32.0 pg MCHC 34.3 31.0 - 35.5 g/dL RDW-CV 12.7 11.5 - 15.5 % PLATELETS 348 150 - 400 x10?3/uL MPV 10.2 8.7 - 12.5 fL NEUTROPHIL % 85 % LYMPHOCYTE % 13 % MONOCYTE % 2 % EOSINOPHIL % 0 % BASOPHIL % 0 % NEUTROPHIL # 9.10 (H) 1.50 - 7.70 x10?3/uL LYMPHOCYTE # 1.42 1.00 - 4.80 x10?3/uL MONOCYTE # 0.24 0.20 - 1.10 x10?3/uL EOSINOPHIL # <0.10 <=0.50 x10?3/uL BASOPHIL # <0.10 <=0.20 x10?3/uL IMMATURE GRANULOCYTE % 0 0 - 1 % IMMATURE GRANULOCYTE # <0.10 <0.10 x10?3/uL POC FINGERSTICK GLUCOSE - BMC/JMC (RESULTS) Result Value Ref Range GLUCOSE, POC 254 (H) 60 - 100 mg/dl Imaging Studies: Female, 57 years old. CT BRAIN WO IV CONTRAST performed on 8/1/2022 12:56 AM. REASON FOR EXAM: vertigo RADIATION DOSE: 1307.90 TECHNIQUE: CT of the brain was performed without the use of intravenous contrast. COMPARISON: None. FINDINGS: There is asymmetric hypodensity in the left cerebellum. There is no acute intracranial hyperdense hemorrhage, midline shift , or mass effect. There is no hydrocephalus. There is no acute calvarial abnormality. A 7 mm nodule in the left temporal scalp, may represent a sebaceous cyst. There is mucosal thickening in the ethmoid air cells and sphenoid sinuses bilaterally. Atrophic mucosal thickening in the left maxillary sinus and mild mucosal thickening at the floor of the right maxillary sinus. There is partial opacification of the tip of the mastoids on the right. IMPRESSION: Asymmetric hypodensity in the left cerebellum suggesting area of evolving infarct. No acute intracranial bleed. Follow-up MRI may be obtained for further evaluation.
Aktuelle Erkrankungen: -
Vorgeschichte: Patient Active Problem List Diagnosis Date Noted ? Coronary artery disease 10/28/2019 ? Sleep apnea 07/23/2019 ? Thickened endometrium 07/11/2017 ? Asthma ? Chronic obstructive airway disease ? Arthritis ? Hyperlipidemia ? HTN (hypertension) ? Anxiety ? Depression ? Type 2 diabetes mellitus ? Esophageal reflux ? Migraines 08/14/2015 Past Medical History: Diagnosis Date ? Abnormal CT of the abdomen 01/2022 "CT scan at that time showed circumferential rectal wall thickening without stranding." ? Anxiety ? Arthritis knees, hands ? Asthma ? Back problem mid back pain occasionally, no tx helps with heating pad ? Beta blocker prescribed for left ventricular systolic dysfunction ? Blood thinned due to long-term anticoagulant use asa 81 mg ? Chronic obstructive airway disease ? Chronic pain ? Constipation ? Coronary artery disease severe, open heart bypass 2019 ? Cough chronic dry cough ? Depression ? Diabetes mellitus, type 2 ? Dyspnea on exertion ? Esophageal reflux sleeps with 3 pillows ? Graves disease Dr. following ? Headache ? HTN (hypertension) ? Hyperlipidemia ? LLQ pain intermittent ? Lung nodule 12/17/2021 Incidental calcified granuloma in the right lung. No noncalcified pulmonary nodules. ? Migraine ? Motion sickness ? Obesity ? Pneumonia due to COVID-19 virus 01/2022 admitted for 1 day. Patient states she feels back to normal now. ? Pyelonephritis ? Shortness of breath SOB with minimal exertion ? Sleep apnea 7/23/2019 ? Smoker ? Type 2 diabetes mellitus Newly dx DM Past Surgical History: Procedure Laterality Date ? ARTERIAL BYPASS SURGERY 10/15/2019 open heart surgery ? GASTROSCOPY 05/11/2017 ? HX COLONOSCOPY 7/1/16 ? HX COLONOSCOPY 10/2016 tubular adenoma ? HX DENTAL EXTRACTION ? HX HEART CATHETERIZATION 09/16/2019 ? HX INCISION AND DRAINAGE 8/1/2014 INCISION AND DRAINAGE PERINEAL ABSCESS ? HX TUBAL LIGATION 1989 ? HX WISDOM TEETH EXTRACTION
Andere Medikamente: Medications Prior to Admission Prescriptions ANORO ELLIPTA 62.5-25 mcg/actuation Inhalation Disk with Device USE 1 INHALATION ONCE A DAY aspirin (ECOTRIN) 81 mg Oral Tablet, Delayed Release (E.C.) Take 81 mg by mouth Once a day
Allergien: Allergies Allergen Reactions ? Nka [No Known Allergies]
Vorherige Impfungen: -

VAERS 2591063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: WV
Alter: 57,0
Geschlecht: F
Eingang: 03.03.2023
Impfdatum: 25.07.2022
Beginn: 31.07.2022
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / RA

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

Alanine aminotransferase normal Angiogram cerebral abnormal Anion gap Anticoagulant therapy Antiplatelet therapy Arteriogram carotid abnormal Aspartate aminotransferase normal Asthenia Bacterial test positive Basophil count normal Basophil percentage decreased Bilirubin urine Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium increased Blood chloride normal Blood creatinine normal

Symptomtext

ED note by Dr. on 7/31/22: "Patient Date of Service: 7/31/2022 Primary Care Doctor: MD Patient information was obtained from patient. History/Exam limitations: none. Chief Complaint:Vomiting HPI: Patient is a 57 y.o. female who presents to the Emergency Department with dizziness and vomiting. Patient states that she was feeling well yesterday and she was asleep in a proximally 2:00 a.m. awoke to use the restroom she states that when she got up out of bed she suddenly felt very dizzy with a spinning sensation and associated nausea vomiting. She states that she lays still the symptoms all seem to improve but that any time she moves her head she feels a sense of spinning with vomiting. She states that her mouth feels dry. She denies any fever cough chest pain shortness of breath or congestion. The nurse's triage note states that the patient wants to be checked for COVID but when I spoke with the patient she states that she does not believe that she has COVID and that she is immunized. She denies any headaches, double vision, blurry vision, chest pain, focal weakness numbness or rashes. She denies any recent head injuries. Denies any tinnitus or changes in hearing. " "Impression: Encounter Diagnoses Name Primary? ? Vertigo Yes ? Nausea and vomiting ? Elevated troponin Disposition: pending Condition on Disposition: Stable" H&P by FNP on 8/1/22: Date of Admission: 7/31/2022 Date of Service: 8/1/2022 PCP: MD Chief Complaint: dizziness HPI: Patient is a 57 y.o., female with a history of migraines, type II DM, CAD, HTN, HLD, and COPD who presented to the ED for further evaluation of dizziness and vomiting. Patient states that she was feeling like her normal self yesterday and when she went to sleep but at aproximally 2:00 a.m. she awoke to use the restroom and suddenly felt very dizzy/spinning associated nausea vomiting. She states that she lays still the symptoms all seem to improve but that any time she moves her head she feels a sense of spinning with vomiting. She admits to gneralized weakness, none unilaterally, and trouble standing/walking but denies headache, facial droop, vision changes, speech changes, recent illness, fever, chest pain, paraesthesias, abdominal pain, urinary symptoms, or diarrhea. Has hx of triple bipass a few years ago but denies hx of stroke. A CT of her brain today revealed an Asymmetric hypodensity in the left cerebellum suggesting area of evolving infarct. No acute intracranial bleed. Her lab workup is generally unremarkable apart from a trivially elevated trop of 55, no change on repeat a few hours later. UA is negative for infection. Her vertigo has improved after meclazine. NIHSS in the ED= 0. Not a candidate for tpa regardless as she is out of time window. Slightly hypertensive in the 170s, other vss. " "Assessment/Plan: Patient is a 57 y.o., female who presents with the following: 1. Acute left cerebellar infarct --vertigo improving. NIHSS=0. Out of time window to be tpa candidate regardless --confirm with MRI --CTA head and neck pending --stroke orderset initiated, neurology consulted --check updated lipid panel, pending results and further workup continue 80 mg atorvastatin and TriCor --continue daily low dose aspirin --updated echo with bubble study --pt/ot consulted as well per stroke protocol 2. hypercalcemia --check phos and PTH levels 3. Uncontrolled HTN --elevated today mostly 170s systolic --will allow for permissive HTN for now, continue home metoprolol. Will likely need additional maintenance med 4. Uncontrolled Type II DM --recent A1C 8.7 --on metformin and trajenta at home --hold oral diabetic meds for now and add ssi coverage with Humalog achs 5. Hx of CAD --s/p CABG --continue asprin statin, 6. COPD --no acute issues, continue home inhalers 7. Tobacco abuse --pt counseled on smoking cessation 10 Depression and anxiety --continue home Lexapro 11. Hx of migraines --continue home topamax. Takes maxalt at home DVT PPx: subq heparin Code Status: Full Code DNP,FNP-C" Consult note by Dr. on 8/2/22: Date of service: 8/2/2022 Chief Complaint: Dizziness, N/V Subjective: History was obtained from a review of the electronic record and discussion with the patient and family. Patient is a 57 y.o. female with PMH significant for type II DM, HTN, HLD, CAD s/p CABG who presented to the ED 7/31/22 with acute onset dizziness, N/V, admitted for left PICA territory stroke secondary to occluded left PICA. Pt states she feels the same today, denies any vomiting but still notes significant dizziness/nausea with moving her head or posture change. Her daughter is present at bedside. " " Assessment and Plan: 1) Stroke summary: 57 y/o F with PMH significant for CAD s/p CABG, HLD, HTN, type II DM and tobacco use disorder who presented to the ED 7/31 with acute onset dizziness with N/V. CT brain shows evolving left cerebellar infarction without signs of hemorrhage and CTA head and neck shows occluded left PICA as well as moderate to severe stenosis of the left vertebral artery origin as well as multiple intracranial calcified and noncalcified plaques particularly in the posterior circulation. MRI brain w/o contrast confirms left PICA territory ischemic stroke. Etiology is likely artery to artery embolus due to the left PICA occlusion. TTE with bubble was negative intracardiac shunt, EF 65%. Continue with best medical management with dual antiplatelet therapy with ASA 81 mg and Plavix 75 mg daily x 3 months, with ASA 81 mg daily to continue and high dose statin therapy with atorvastatin 80 mg qhs. She also has significant underlying vascular risk factors with tobacco use disorder and uncontrolled type II DM and will need aggressive glycemic control and smoking cessation to lower her risk factors. Stroke Etiology: Artery to artery embolus secondary to left PICA occlusion General Plan: -Normoglycemia -Normothermia Blood pressure plan: -Place pt on telemetry -BP goal: - <130/90 Medications: -Antiplatelet: ASA 81 mg and Plavix 75 mg x 3 months, then ASA 81 mg daily to continue -Statin: atorvastatin 80 mg qhs -DVT ppx: Lovenox 40 mg subq daily Imaging: - TTE- 2D echo w bubble - negative for intracardiac shunt, EF 65% - CTA head and neck - L PICA occlusion, moderate to severe stenosis left vertebral artery origin, moderate to severe stenosis right vertebral artery, multiple intracranial calcified and noncalcified plaques -MRI brain - acute left PICA territory ischemic stroke Lab work: -LDL 170 -Hemoglobin A1c - 8.7 Diet plan: - low glycemic index diabetic diet Consultants: - Physical therapy, occupational therapy Activity Level: - PT/OT Disposition: Continue to work with PT/OT, will need outpatient therapy as well. She should follow-up with Neurology clinic with myself or Dr. in 4-6 weeks for re-evaluation. Stroke Education: 1. Patient was educated that he would benefit from tight control of his vascular risk factors (LDL < 70, BP < 130/90, glycemic control A1c < 7) 2. Patient was educated to call 911 for any acute stroke symptoms (BE FAST- Balance problems, Eyes-blurry vision, double vision, Facial Droop, Arm Weakness, Speech Problems, Syncope, Seizure) 3. Medications: Patient was counseled to take Asprin 81 mg daily / Plavix 75 mg daily / Lipitor 80 mg daily 4. Patient was counseled about the need for follow-up with PCP and in neurology clinic after discharge 5. Lifestyle: Smoking cessation is vital. We counseled this patient on need to quit smoking and resources to do so. We encourage risk factor treatment and management by pt?s PMD. Patient was educated on Mediterranean diet, exercise, medication compliance Stroke Education was given verbally to the patient and family member and the teaching was effective and patient and family member in agreement with the plan."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebellar stroke
Hospital-Tage: 4,0
Labordaten: EXAM: Temperature: 36.5 ?C (97.7 ?F) Heart Rate: 62 BP (Non-Invasive): (!) 167/73 Respiratory Rate: (!) 22 SpO2: 94 % Labs: I have reviewed all lab results. Lab Results for Last 24 Hours: Results for orders placed or performed during the hospital encounter of 07/31/22 (from the past 24 hour(s)) URINALYSIS WITH MICROSCOPIC REFLEX IF INDICATED BMC/JMC ONLY Result Value Ref Range COLOR Light Yellow Light Yellow, Straw, Yellow APPEARANCE Clear Clear PH 6.0 <8.0 LEUKOCYTES Negative Negative WBCs/uL NITRITE Negative Negative PROTEIN 30 (A) Negative, 10 mg/dL GLUCOSE >=1000 (A) Negative mg/dL KETONES Negative Negative mg/dL UROBILINOGEN 0.2 <=2.0 mg/dL BILIRUBIN Negative Negative mg/dL BLOOD Negative Negative mg/dL SPECIFIC GRAVITY 1.015 <1.022 URINALYSIS, MICROSCOPIC Result Value Ref Range RBCS 0-2 0 - 2 /hpf WBCS 0-2 0 - 2 /hpf BACTERIA Slight (A) None /hpf SQUAMOUS EPITHELIAL 0-2 0 - 2 /hpf MUCOUS Slight (A) None, Light /hpf COMPREHENSIVE METABOLIC PANEL, NON-FASTING Result Value Ref Range SODIUM 140 136 - 145 mmol/L POTASSIUM 4.3 3.5 - 5.1 mmol/L CHLORIDE 105 96 - 111 mmol/L CO2 TOTAL 22 22 - 30 mmol/L ANION GAP 13 4 - 13 mmol/L BUN 11 8 - 25 mg/dL CREATININE 0.77 0.60 - 1.05 mg/dL BUN/CREA RATIO 14 6 - 22 ESTIMATED GFR 90 >=60 mL/min/BSA ALBUMIN 4.5 3.5 - 5.0 g/dL CALCIUM 11.0 (H) 8.5 - 10.0 mg/dL GLUCOSE 283 (H) 65 - 125 mg/dL ALKALINE PHOSPHATASE 75 50 - 130 U/L ALT (SGPT) 23 (H) 8 - 22 U/L AST (SGOT) 17 8 - 45 U/L BILIRUBIN TOTAL 0.4 0.3 - 1.3 mg/dL PROTEIN TOTAL 8.5 (H) 6.4 - 8.3 g/dL LIPASE Result Value Ref Range LIPASE 12 10 - 60 U/L TROPONIN-I Result Value Ref Range TROPONIN I 55 (HH) 7 - 30 ng/L CBC WITH DIFF Result Value Ref Range WBC 10.8 3.7 - 11.0 x10?3/uL RBC 5.29 (H) 3.85 - 5.22 x10?6/uL HGB 15.6 11.5 - 16.0 g/dL HCT 45.5 34.8 - 46.0 % MCV 86.0 78.0 - 100.0 fL MCH 29.5 26.0 - 32.0 pg MCHC 34.3 31.0 - 35.5 g/dL RDW-CV 12.7 11.5 - 15.5 % PLATELETS 348 150 - 400 x10?3/uL MPV 10.2 8.7 - 12.5 fL NEUTROPHIL % 85 % LYMPHOCYTE % 13 % MONOCYTE % 2 % EOSINOPHIL % 0 % BASOPHIL % 0 % NEUTROPHIL # 9.10 (H) 1.50 - 7.70 x10?3/uL LYMPHOCYTE # 1.42 1.00 - 4.80 x10?3/uL MONOCYTE # 0.24 0.20 - 1.10 x10?3/uL EOSINOPHIL # <0.10 <=0.50 x10?3/uL BASOPHIL # <0.10 <=0.20 x10?3/uL IMMATURE GRANULOCYTE % 0 0 - 1 % IMMATURE GRANULOCYTE # <0.10 <0.10 x10?3/uL POC FINGERSTICK GLUCOSE - BMC/JMC (RESULTS) Result Value Ref Range GLUCOSE, POC 254 (H) 60 - 100 mg/dl Imaging Studies: Female, 57 years old. CT BRAIN WO IV CONTRAST performed on 8/1/2022 12:56 AM. REASON FOR EXAM: vertigo RADIATION DOSE: 1307.90 TECHNIQUE: CT of the brain was performed without the use of intravenous contrast. COMPARISON: None. FINDINGS: There is asymmetric hypodensity in the left cerebellum. There is no acute intracranial hyperdense hemorrhage, midline shift , or mass effect. There is no hydrocephalus. There is no acute calvarial abnormality. A 7 mm nodule in the left temporal scalp, may represent a sebaceous cyst. There is mucosal thickening in the ethmoid air cells and sphenoid sinuses bilaterally. Atrophic mucosal thickening in the left maxillary sinus and mild mucosal thickening at the floor of the right maxillary sinus. There is partial opacification of the tip of the mastoids on the right. IMPRESSION: Asymmetric hypodensity in the left cerebellum suggesting area of evolving infarct. No acute intracranial bleed. Follow-up MRI may be obtained for further evaluation.
Aktuelle Erkrankungen: -
Vorgeschichte: Patient Active Problem List Diagnosis Date Noted ? Coronary artery disease 10/28/2019 ? Sleep apnea 07/23/2019 ? Thickened endometrium 07/11/2017 ? Asthma ? Chronic obstructive airway disease ? Arthritis ? Hyperlipidemia ? HTN (hypertension) ? Anxiety ? Depression ? Type 2 diabetes mellitus ? Esophageal reflux ? Migraines 08/14/2015 Past Medical History: Diagnosis Date ? Abnormal CT of the abdomen 01/2022 "CT scan at that time showed circumferential rectal wall thickening without stranding." ? Anxiety ? Arthritis knees, hands ? Asthma ? Back problem mid back pain occasionally, no tx helps with heating pad ? Beta blocker prescribed for left ventricular systolic dysfunction ? Blood thinned due to long-term anticoagulant use asa 81 mg ? Chronic obstructive airway disease ? Chronic pain ? Constipation ? Coronary artery disease severe, open heart bypass 2019 ? Cough chronic dry cough ? Depression ? Diabetes mellitus, type 2 ? Dyspnea on exertion ? Esophageal reflux sleeps with 3 pillows ? Graves disease Dr. following ? Headache ? HTN (hypertension) ? Hyperlipidemia ? LLQ pain intermittent ? Lung nodule 12/17/2021 Incidental calcified granuloma in the right lung. No noncalcified pulmonary nodules. ? Migraine ? Motion sickness ? Obesity ? Pneumonia due to COVID-19 virus 01/2022 admitted for 1 day. Patient states she feels back to normal now. ? Pyelonephritis ? Shortness of breath SOB with minimal exertion ? Sleep apnea 7/23/2019 ? Smoker ? Type 2 diabetes mellitus Newly dx DM Past Surgical History: Procedure Laterality Date ? ARTERIAL BYPASS SURGERY 10/15/2019 open heart surgery ? GASTROSCOPY 05/11/2017 ? HX COLONOSCOPY 7/1/16 ? HX COLONOSCOPY 10/2016 tubular adenoma ? HX DENTAL EXTRACTION ? HX HEART CATHETERIZATION 09/16/2019 ? HX INCISION AND DRAINAGE 8/1/2014 INCISION AND DRAINAGE PERINEAL ABSCESS ? HX TUBAL LIGATION 1989 ? HX WISDOM TEETH EXTRACTION
Andere Medikamente: Medications Prior to Admission Prescriptions ANORO ELLIPTA 62.5-25 mcg/actuation Inhalation Disk with Device USE 1 INHALATION ONCE A DAY aspirin (ECOTRIN) 81 mg Oral Tablet, Delayed Release (E.C.) Take 81 mg by mouth Once a day
Allergien: Allergies Allergen Reactions ? Nka [No Known Allergies]
Vorherige Impfungen: -

VAERS 2559199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: OH
Alter: 69,0
Geschlecht: M
Eingang: 12.01.2023
Impfdatum: 11.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: SYR / LA

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

Cardiac electrophysiologic study Cardiac flutter Cardiac monitoring Cardiac stress test Echocardiogram Electrocardiogram Implantable cardiac monitor insertion Magnetic resonance imaging heart Myocarditis Ventricular tachycardia

Symptomtext

Spring / summer of 2021 after first vaccine doses, started noticing occasional chest flutters. After many tests including a heart mri at facility, myocarditis was identified as possible / probable cause. Started on metoprolol 12.5 mg daily June 2022 - 3 days after receiving the 4th covid vaccine, I experienced a Ventricular Tachycardia event. An study was performed at Hospital in July 2022 and a specific reason for the VT was not identified. I had an ICM implanted and have not experienced any further cardiac events. Background I have CLL and started being treated with Acalabrutinib about the same time the initial heart flutters were felt (spring/summer 2021). Both Acalabrutinib and Covid vax are possible causes. Numerous tests - EKG, echocardiogram (hospital), heart mri and stress test. After MRI, cardiologist diagnosed as myocarditis and Rx metoprolol. In fall of 2021, I switched from Acalabrutinib into a clinical trial for an experiment BTK inhibitor LP-168. for my CLL. Dr is my oncologist and most familiar with this entire situation. In spring of 2022, I experienced some dizziness clinical trial personnel ordered a heart holster to determine if I was having any heart rhythm problems. A couple days into wearing this holster (6/13/22) , a VT event was recorded early in the morning when I was asleep. i did not notice anything. The EV event lasted 19 sec with a max heart rate of 157 and resolved itself. The VT occurred 3 days after having received the 4th Covid vax dose. Despite an study, the exact cause of the VT event has not been determined. There was no apparent permanent heart wiring issues from the study. It is not clear if the heart issues (myocarditis and VT event) were caused by the covid vax or something else. Some other factors which may be relevant: - I have a farm and am quite active outside in spring. It is possible I was experiencing some dehydration which was causing the dizziness and may have caused the VT. I try to drink lots of water but it had been purified bottled water. After discussion with my Drs, I started drinking Smart Water which has some of the essential nutrients added. When I started using Smart Water, the dizziness decreased. I am not sure if I started drinking the Smart Water before or after the VT event. - As noted, I have been taking an experimental BTK inhibitor LP-168 for my CLL. There had not been any issues with heart rhythm with this drug but to be cautious, I discontinued using it until the study could not identify any cause. My oncologist did not believe the LP-168 caused the issue and I restarted the drug. I also had an ICM implanted to monitor my heart rhythm. 6+ months later, there have not been any VT or other cardiac events recorded. - The VT event occurred at night when I was asleep. Earlier in the day, I was cleaning an area under a cracked shower pan which had become moldy. I was exposed to the mold and to an anti-mold agent. - I have sleep apnea and use a CPAP. My CPAP reports do not show any significant abnormal events on the day of the VT. - I have a lot of sinus congestion issues and routinely go to sleep with a Halls cough drop in my mouth. I don't know that I did but it is possible that I choked momentarily on the cough drop. - Throughout the night, I change sleeping positions several times - back, right side, left side. Other conditions and drugs: I am 71, obese, have several chronic conditions - OSA, high blood pressure, cholestrol. I take various medications to address the issues above. These include: Mucinex, Flonase (50 mcg), azelastine .15% nasal spray to address sinus congestion lisinopril 20 mg (blood pressure) lovastatin 20 mg (cholesterol) levothyrozine 50 mg (throid) valtrex 500 MG (shingles prevention) LP-168 100 mg (cll clinical trial med) metoprolol 25 mg (heart) sildenafil 50 mg (rarely used and don't remember using it during any of the events) I listed all of the covid vaccine doses above. Dates of each dose are as follows: Dose 1 - 2/11/21 Dose 2 - 3/4/21 Dose 3 - 10/1/21 Dose 4 - 6/10/22 (VT event occurred 3 days later) I participated in an study to determine antibodies created by the covid vax. I tested after the first 3 doses and did not record any antibodies. It is difficult to say definitively that the covid vax caused my cardiac issues but it is certainly one of the possible causes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG, echo cardiogram, heart mri, stress test, heart monitor, study
Aktuelle Erkrankungen: -
Vorgeschichte: cll, high blood pressure, cholesterol, obstructive sleep apnea, obesity, chronic sinus congestion
Andere Medikamente: Mucinex, Flonase (50 mcg), azelastine .15% nasal spray to address sinus congestion lisinopril 20 mg (blood pressure) lovastatin 20 mg (cholesterol) levothyrozine 50 mg (throid) valtrex 500 MG (shingles prevention) LP-168 100 mg (cll clinica
Allergien: none
Vorherige Impfungen: -

VAERS 2544618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: MI
Alter: 94,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 19.08.2022
Beginn: 29.11.2022
Tage bis Beginn: 102,0
Dosis: 3
Route/Site: - / -

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

Atrial fibrillation COVID-19 Cardiac failure acute Cardiac failure chronic Cardiac failure congestive Dementia Alzheimer's type Essential hypertension Facial paralysis Influenza virus test positive Left ventricular failure Respiratory syncytial virus test positive SARS-CoV-2 test positive Transient ischaemic attack Troponin increased

Symptomtext

Date of Admission: 11/29/2022 Date of Discharge: 12/5/2022 Hospital Principal Problem (Discharge Diagnoses): Acute on chronic diastolic CHF (congestive heart failure) (CMS/HCC) All Hospital Problems (Other Diagnoses): Active Hospital Problems Diagnosis o Principal Problem: Acute on chronic diastolic CHF (congestive heart failure) (CMS/HCC) o COVID o TIA (transient ischemic attack) o Facial droop o Acute on chronic CHF (NYHA class III, ACC/AHA stage C) (CMS/HCC) o New onset a-fib (CMS/HCC) o Elevated troponin o Late onset Alzheimer's disease without behavioral disturbance (CMS/HCC) o History of CVA (cerebrovascular accident) o Essential hypertension

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Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: 11/30 Covid-19, Flu, RSV -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2507207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 12.08.2022
Beginn: 12.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dysmenorrhoea Fatigue Headache Heavy menstrual bleeding Lethargy Oligomenorrhoea Thrombosis Ultrasound abdomen normal

Symptomtext

I experienced about one month I was having menstrual bleeding. My cycle did not stop completely where I had to wear pantyliners everyday. During the bleeding episodes I had severe abdominal cramping. I also had some blood clotting as well. I went in for an ultrasound 11-10-2022 and it was normal. I will have to get lab work in the next few days. I also feel very tired and lethargic at times. I also have dull headaches that come and go. I also experienced heavy menstrual cycles after my first, second and third doses that lasted about one week and periodically they would 3-4 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: 10NOV2022 Ultrasound of the abdomen; normal.
Aktuelle Erkrankungen: Asthma; Allergies
Vorgeschichte: Asthma; Allergies; Obesity
Andere Medikamente: LEXAPRO; ZYRTEC; prenatal vitamin; VICTOZA; TYLENOL; ibuprofen
Allergien: Penicillin; adhesive tape
Vorherige Impfungen: -

VAERS 2400331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: TN
Alter: 12,0
Geschlecht: M
Eingang: 03.08.2022
Impfdatum: 03.08.2022
Beginn: 03.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Immediate post-injection reaction Loss of consciousness Posture abnormal

Symptomtext

COVID-19 vaccine administered in left deltoid around 9:13 am on 8/3/2022. Less than a minute after vaccine administration, patient slouched forward, passed-out while sitting on clinical room table. He was laid down on the table. Patient came back to as was being laid down. His feet were raised. Vital signs taken at 9:15 am. Pulse oximeter 99%, pulse 60 and blood pressure 100/72. Patient given juice and had head raised. He was alert and oriented. He stated he felt better. Patient given Tdap vaccine afterward. Checked on patient 20 minutes later. Had him sit up for a bit. Retook vitals at 9:44 am. Pulse ox 99%, pulse 61 and blood pressure 102/64. Had patient get up and walk down the hall with me and another nurse behind. Patient walked steady and needed no support. He stated felt perfectly fine. He left clinic after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: -
Vorgeschichte: None
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2399055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: NY
Alter: 15,0
Geschlecht: M
Eingang: 02.08.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium

Weitere VAERSDATA-Felder

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

VAERS 2398073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 25.05.2022
Beginn: 26.07.2022
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: - / -

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

Angiogram cerebral abnormal Anticoagulant therapy Arteriogram carotid abnormal Asymptomatic COVID-19 Blood glucose increased Cerebral arteriosclerosis Cerebral artery occlusion Cerebral hypoperfusion Computerised tomogram head normal Condition aggravated Dizziness Dysarthria Echocardiogram abnormal Ejection fraction Facial paralysis Glycosylated haemoglobin increased Hypertension Ischaemic stroke

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 7/26/2022 Discharge Date: Jul 29, 2022 PRESENTING PROBLEM: Left-sided sensory deficit present [R44.9] Acute ischemic stroke (HCC) [I63.9] Stroke-like symptoms [R29.90] HOSPITAL COURSE: Patient is a 64 year old male (speaks Spanish only) with a PMH significant for HTN, HLD, prior R MCA stroke (2014) without residual deficits, left PCA stroke found on MRI 1/2021, severe stenosis of left vertebral artery on ASA & Plavix (Non-compliant), CAD, OSA, Diabetes type 2, and glaucoma that presented 7/26 with slurred speech, acute onset dizziness and lightheadedness, left facial droop concerning for acute ishcemic stroke. Initial NIHSS 8. CTH negative for acute pathology demonstrates prior strokes, CTA head/neck revealed unchanged chronic occlusion of left A2 and left P2, occlusion of V3/V4, severe stenosis of left vertebral artery with possible dissection, CT perfusion with 64 ml hypoperfusion in A2/P2 segments. TNK was administered at 1801, he was not a mechanical thrombectomy candidate as there was no noted proximal occlusion. Neurosurgery was consulted for possible CT angiogram but patient is not deemed a candidate for intervention given occlusion is chronic. MRI brain 7/27 showed a 7mm focus of restricted diffusion in the pons just to the left of midline. TTE w/ EF 48%, mild global hypokinesis, LA mildly dilated, no shunting. Initial blood glucose was 426, HbA1c of 11.3, LDL 63. Etiology secondary to intracranial atherosclerosis. Patient was started on Lipitor 80 mg daily and DAPT with ASA 81 mg daily and Plavix 75 mg daily for 90 days, followed by monotherapy of ASA 81 mg daily. Pt mildly hypertensive despite home Losartan 100 mg daily and Norvasc 10mg daily so Coreg 6.25 mg BID was added with improvement in blood pressure. Patient was evaluated by endocrinology who resumed home diabetic agents upon discharge with plans to follow up with DGMS outpatient. Pt was re-evaluated by PT/OT day of discharge who recommended disposition of home with outpatient PT/OT. He tested positive for covid during admission but remained asymptomatic. Discussed at length with patient and his wife (using hospital translation services) importance of medication and follow up compliance. Pt was also provided educational materials regarding recent hospitalization, medications, and covid. Pt verbalized understanding. Patient discharged in stable condition to home with plans for follow up with stroke clinic, neurosurgery team, and DGMS outpatient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Late effects of CVA (cerebrovascular accident) Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) Dyslipidemia, goal LDL below 70 Hypertension associated with diabetes (HCC) Erectile dysfunction Insomnia OSA (obstructive sleep apnea) Nuclear senile cataract of both eyes Moderate nonproliferative diabetic retinopathy with macular edema associated with type 2 diabetes mellitus (HCC) Glaucoma suspect of both eyes Uncontrolled type 2 diabetes mellitus with hyperglycemia (HCC) Severe uncontrolled hypertension Language barrier Medication noncompliance due to cognitive impairment H/O cardiac radiofrequency ablation Colon polyp Helicobacter pylori gastritis Adjustment disorder with depressed mood Suicidal ideation Acute ischemic stroke (HCC)
Andere Medikamente: amLODIPine (NORVASC) 10 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 80 MG tablet Blood Pressure Monitoring (BLOOD PRESSURE CUFF) MISC carvedilol (COREG) 6.25 MG tablet clopidogrel (PLAVIX) 75 MG tablet Contour Test
Allergien: None
Vorherige Impfungen: -

VAERS 2398056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: NE
Alter: 19,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 01.07.2022
Beginn: 01.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / UN

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

Blood immunoglobulin A decreased Blood immunoglobulin G normal Blood immunoglobulin M decreased CSF test normal Immunoglobulin therapy Intensive care Magnetic resonance imaging head normal Plasmapheresis Status epilepticus Thrombocytopenia Viral test negative

Symptomtext

Status epilepticus requiring multiple antiepileptics, IVIG, high-dose steroids, plasmapheresis. Afebrile. The patient is still in the ICU as of 8/1/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 31,0
Labordaten: Thrombocytopenia. Low serum IgM and IgA, Normal serum IgG. Negative autoimmune encephalitis studies (both serum and CSF). Normal CSF studies. Negative viral studies. Brain MRI without any changes compared to prior.
Aktuelle Erkrankungen: None known.
Vorgeschichte: Autoimmune encephalitis (antibody-positive, N-type calcium channel).
Andere Medikamente: Onfi, Tranxene, Valproic acid, Vimpat, Keppra, Cellcept, Zofran, Ditropan, Protonix, Dilantin, Prednisone.
Allergien: None known.
Vorherige Impfungen: -

VAERS 2379380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: DC
Alter: -
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Arthralgia Asthenia Cough Dizziness Headache Decreased appetite Dyspnoea Fatigue Heart rate increased Myalgia Nausea Heart rate Syncope

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), as dose 3 (booster), single (Lot number: FN2908), in left arm for covid-19 immunization. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN taken for diabetes mellitus; LANTUS taken for diabetes mellitus. Vaccination history included: Covid-19 vaccine (Dose: 1st, Manufacturer: Unknown), for Covid-19 immunization; Covid-19 vaccine (Dose: 2nd , Manufacturer: Unknown), for Covid-19 immunization. The following information was reported: COUGH (non-serious), outcome "not recovered", described as "I did coughy breathing"; HEART RATE INCREASED (non-serious), outcome "not recovered", described as "fast heart beat"; DIZZINESS (non-serious), outcome "not recovered"; ASTHENIA (non-serious), outcome "not recovered", described as "Weakness"; HEADACHE (non-serious), outcome "not recovered"; NAUSEA (non-serious), outcome "not recovered"; MYALGIA (non-serious), outcome "not recovered", described as "muscle pain it just goes"; ARTHRALGIA (non-serious), outcome "not recovered", described as "Joint pain". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Reported that, patient got shot yesterday (unspecified date) and need to report all the side effects. Stated that, Immediately 10 minutes after getting the shot he did cough breathing, fast heart beat, dizziness and weakness, headache, muscle pain it just goes, joint pain, nausea and it wasn't fine. Therapy details were reported as, Patient's doctor suggested, he guess to drink lots of water and wait it out, so not active treatment. Patient just doing like doctor told him waiting for everything to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: Heart rate; Result Unstructured Data: Test Result:fast heart beat; Comments: Side effects: Consumer stated, "Immediately 10 minutes after getting the shot I did coughy breathing, fast heart beat, dizziness and weakness, headache, muscle pain it just goes, joint pain, nausea and it wasn't fine."
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes
Andere Medikamente: METFORMIN; LANTUS
Allergien: -
Vorherige Impfungen: -

VAERS 2379380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

schwer

Staat: DC
Alter: -
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Asthenia Cough Dizziness Headache Decreased appetite Dyspnoea Fatigue Heart rate increased Myalgia Nausea Heart rate Syncope

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), as dose 3 (booster), single (Lot number: FN2908), in left arm for covid-19 immunization. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN taken for diabetes mellitus; LANTUS taken for diabetes mellitus. Vaccination history included: Covid-19 vaccine (Dose: 1st, Manufacturer: Unknown), for Covid-19 immunization; Covid-19 vaccine (Dose: 2nd , Manufacturer: Unknown), for Covid-19 immunization. The following information was reported: COUGH (non-serious), outcome "not recovered", described as "I did coughy breathing"; HEART RATE INCREASED (non-serious), outcome "not recovered", described as "fast heart beat"; DIZZINESS (non-serious), outcome "not recovered"; ASTHENIA (non-serious), outcome "not recovered", described as "Weakness"; HEADACHE (non-serious), outcome "not recovered"; NAUSEA (non-serious), outcome "not recovered"; MYALGIA (non-serious), outcome "not recovered", described as "muscle pain it just goes"; ARTHRALGIA (non-serious), outcome "not recovered", described as "Joint pain". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Reported that, patient got shot yesterday (unspecified date) and need to report all the side effects. Stated that, Immediately 10 minutes after getting the shot he did cough breathing, fast heart beat, dizziness and weakness, headache, muscle pain it just goes, joint pain, nausea and it wasn't fine. Therapy details were reported as, Patient's doctor suggested, he guess to drink lots of water and wait it out, so not active treatment. Patient just doing like doctor told him waiting for everything to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: Heart rate; Result Unstructured Data: Test Result:fast heart beat; Comments: Side effects: Consumer stated, "Immediately 10 minutes after getting the shot I did coughy breathing, fast heart beat, dizziness and weakness, headache, muscle pain it just goes, joint pain, nausea and it wasn't fine."
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes
Andere Medikamente: METFORMIN; LANTUS
Allergien: -
Vorherige Impfungen: -

VAERS 2388118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: IL
Alter: 17,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Syncope Vomiting

Symptomtext

After the COVID-19 vaccine, patient was feeling dizzy. She then fainted however did not lose consciousness. She was still responsive. She was immediately laid out with legs are lifted. Patient was offered water, juice, and a granola bar. Patient then vomited and felt better. She was monitored for 30 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Not applicable
Aktuelle Erkrankungen: Did not disclose any illnesses
Vorgeschichte: Did not disclose any long-standing health conditions
Andere Medikamente: Did not disclose
Allergien: Denies any allergies
Vorherige Impfungen: -

VAERS 2379386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: WA
Alter: 51,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 22.07.2022
Beginn: 22.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Loss of consciousness Swollen tongue

Symptomtext

Member lost conscience and tongue swelled. Given epi with pen and Benadryl injection. Member transport to hospital via ambulance and admitted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP 201/100 after epi, O2 94, HR 80 7/22/2022 9:30 am. Now in-patient at hospital.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: SEVERE OBESITY, BMI 40-44.9, ADULT HX OF TOBACCO USE Quit 4/2014 ELEVATED LIVER FUNCTION TEST ESSENTIAL HTN ASTHMA, UNSPECIFIED ADULT OBSTRUCTIVE SLEEP APNEA, MILD BRONCHIOLITIS DM 2 POSTABLATIVE HYPOTHYROIDISM VITAMIN D DEFICIENCY VITAMIN B12 DEFICIENCY REFLEX SYMPATHETIC DYSTROPHY. MIGRAINE HEPATOMEGALY FHX OF COLON CANCER COLON POLYP TENDINITIS OF LEFT ROTATOR CUFF OSTEOARTHRITIS OF LEFT KNEE MRSA INFECTION BILAT GLAUCOMA SUSPECT
Andere Medikamente: Outpatient Medications Albuterol (PROVENTIL/VENTOLIN) 2.5 mg /3 mL (0.083 %) Inhl Neb Soln Use 3 mL via nebulizer every 4 hours as needed for cough , shortness of breath, or wheezing Benzonatate (TESSALON PERLES) 100 mg Oral Cap Ta
Allergien: Allergies DextranAngioedema Methylprednisolone Methotrexate Atorvastatin Calcium Covid-19 Vaccine, Mrna, Bnt162b2, Lnp-s (Pfizer) Nicotine Tartrazine Class (Not Screened) Tiotropium Bromide Tramadol HclNausea and/or Vomiting Trazodone Hydrochloride Wool Fd & C No.5 (Tartrazine) Fentanyl
Vorherige Impfungen: -

VAERS 2379283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: FL
Alter: 55,0
Geschlecht: M
Eingang: 22.07.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness/Lightheadedness-Medium, Systemic: Fainting/Unresponsive-Medium.

Weitere VAERSDATA-Felder

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

VAERS 2374238

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: -
Alter: 20,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 19.07.2022
Beginn: 19.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Syncope

Symptomtext

Pt had a syncopal event w/ associated dizziness. Vitals: 115/75, 61, 18 Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: Fractures (Lumbar & Thoracic compression) femoroacetabular impingement of left hip
Andere Medikamente: Medications: None
Allergien: Allergies: None reported but pt has RX for Epi Pen
Vorherige Impfungen: -

VAERS 2374220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: OR
Alter: 50,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 06.07.2022
Beginn: 16.07.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / RA

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

Superficial vein thrombosis Ultrasound Doppler abnormal

Symptomtext

Superficial right saphenous vein thrombus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Superficial vein thrombosis
Hospital-Tage: -
Labordaten: right venous ultrasound
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Avian levonorgesterel-ethinyl estradiol 0.1-20 mg-mcg
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2374034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

schwer

Staat: KS
Alter: 37,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 09.07.2022
Beginn: 11.07.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain upper Back pain Blood test normal Computerised tomogram Computerised tomogram abdomen Computerised tomogram head Computerised tomogram pelvis Differential white blood cell count Electrocardiogram Enteritis Feeding disorder Full blood count Lipase Loss of consciousness Metabolic function test Nausea Pain Pregnancy test urine

Symptomtext

No reaction until Monday afternoon. Stomach ache, increasing in pain. By Tuesday evening @ 5pm was unbearable, I felt nauseous, blacked out. My stomach was in agony, pain began radiating up my back, so my husband took me to the ER. I had blood panels done, all returned normal. CT scan with and without dye. Doctor came and said that I was diagnosed with enteritis. I've never before had this. He said they don't know why it happened, I was perfectly healthy beforehand and I informed him that I just received my Covid vaccine on Saturday and this was listed by Pfizer as a post-authorisation adverse reaction. No doctor will confirm that it is the reason and be liable so I am unable to be exempt me from the second dose. 1 week from being in the ER and the pain has continued. I am unable to eat, I've lost 8 lbs. I can sip water. No position is comfortable, and no doctor will prescribe pain medication either. They simply say I have to wait for it to go away. 10 days from injection and no sign of the pain going away. I have another appointment with a doctor 7/20/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: CBC and Diff Comprehensive metabolic panel Lipase Urinalysis Reflex Urine Pregnancy Test Imaging: CT abdominal pelvis with contrast. CT abdomen pelvis without contrast, CT head without contrast, ECG BP 114/62 Respiration 16 Temp 97.8 Pulse 70
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sertraline 50mg
Allergien: None
Vorherige Impfungen: -

VAERS 2372015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

schwer

Staat: AZ
Alter: 31,0
Geschlecht: M
Eingang: 17.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Seizure

Symptomtext

Systemic: Seizure-Mild

Weitere VAERSDATA-Felder

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

VAERS 2370781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: CO
Alter: 74,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Syncope

Symptomtext

Per secondhand report, client collapsed a few hours after receiving vaccine. She was taken to ER by ambulance and then was released to home after being seen. Client never responded to outreach attempts.

Weitere VAERSDATA-Felder

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

VAERS 2370188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: NY
Alter: 18,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 11.07.2022
Beginn: 11.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood glucose normal Confusional state Dizziness Fall Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Shakiness-Mild, Additional Details: Patient recieved first dose of covid-19 pfizer vaccine, appeared fine, was sitting in the chair, about 2-5 minutes later patient fell over and appeared unresponsive for about 30-60 seconds, emergency was called immediately, mother and pharmacist checked to see if she was okay, she gained consciousness and was given water and soda while we waited for medics and police - patient was then taken by medics out of store - appearing okay - blood pressure and blood sugar were in normal range

Weitere VAERSDATA-Felder

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

VAERS 2367812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: NJ
Alter: 26,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 10.07.2022
Beginn: 10.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Disorientation Feeling hot Flushing Hyperhidrosis Nausea Paraesthesia Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Systemic: Nausea-Mild, Systemic: Shakiness-Mild, Systemic: Weakness-Mild, Additional Details: Pt recievd vaccine and fainted while in the observation area. Pt was not unconscious when i arrived. Pt was disoriented. Had patient lay down. Called 911. Pt stated he was warm, and nauseous. Provided patient with water. 911 came. Pt refused transport to hospital. Pt felt better. Friend came to tajke patient home. Pt again felt week and had tingling in the arms. Asked if he wanted 911 or if he wanted friend to take hime to the ER. Pt did not want 911. Stressed need to go to the ER.

Weitere VAERSDATA-Felder

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

VAERS 2367801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

schwer

Staat: MA
Alter: 14,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 09.07.2022
Beginn: 09.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Confusional state Dizziness Seizure Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Seizure-Mild, Systemic: Shakiness-Mild

Weitere VAERSDATA-Felder

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

VAERS 2366434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

schwer

Staat: OK
Alter: 24,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

passed out for a few seconds about 1 min after vaccinantion

Weitere VAERSDATA-Felder

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

VAERS 2365956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: PA
Alter: 29,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild

Weitere VAERSDATA-Felder

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

VAERS 2330132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: AZ
Alter: 55,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 07.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: IM / LA

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

Dry eye Facial pain Facial paralysis Hypoaesthesia Lacrimation increased Lymphadenopathy Pain in extremity

Symptomtext

Vaccine administered 6/7/22 Patient experience arm pain same day and next day Experienced L sided facial paralysis, numbness and pain with hearing changes L sided, Dry L eye with tearing presented 6/22/22 with L clavicular node enlargement

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: US Neck ordered for enlarged node Referred to Opthalmologist, Neurologist,
Aktuelle Erkrankungen: BEll's Palsey R-sided - 3/2022 - resolved
Vorgeschichte: Hypertension, Obesity, Hyperlipidemia, Iron Deficiency Anemia, Reactive Airway Disease, Seasonal Allergies, Vertigo, GERD, chronic headaches, Sacral fracture,
Andere Medikamente: cetirizine, rosuvastatin,lisinopril,Albuterol HFA, FLovent HFA, Flonase, Diclofenac Topical
Allergien: none
Vorherige Impfungen: -

VAERS 2322802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: NY
Alter: 17,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 08.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain upper Dizziness Malaise Presyncope Throat tightness Visual impairment

Symptomtext

Patient was given vaccine by LPN in the arm (deltoid) Apoximately 1 min after vaccine was administered, patient said she felt unwell. Throat tightness, saw "black spots", dizziness and stomach pain. Near syncopal episode. Patient was monitored for >60 minutes after near syncopal event. No signs of anaphylaxis were observed. Symptoms improved within 15-20 minutes of onset. Blood pressure prio to administration of vaccine was 115/70. Blood pressure during symptoms was 100/68. BP 90 minutes after symptom onset 115/60. Lungs remined clear, no swelling observed to the lips/face/tongue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: NO
Vorgeschichte: ADHD Anxiety
Andere Medikamente: Blisovi Fe Lexapro 20mg Adderall 10mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2318963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: AR
Alter: 16,0
Geschlecht: M
Eingang: 14.06.2022
Impfdatum: 14.06.2022
Beginn: 14.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Skin discolouration Syncope

Symptomtext

Patient had a syncope event after the meningococcal immunization. I had administered the 3rd Covid dose and did the menactra. We put him supine and obtained a set of vitals, mom went to get him a apple and juice. Vital WNL. I put a cold rag on his forehead while mom went to get something for him to eat. I stayed with him during that time. He was alert and oriented x3, his color was much better and we kept him here at the office until he knew he could stand and not feel weak. We did not administer the other two immunizations that he was going to have today.

Weitere VAERSDATA-Felder

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

VAERS 2315657

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

schwer

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 10.06.2022
Beginn: 10.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Loss of consciousness Nausea Pallor Unresponsive to stimuli

Symptomtext

Approximately 6 to 8 minutes after receiving the first dose of Pfizer COVID vaccine, patient became unresponsive for about 2-3 minutes. While on the phone with 911, patient regained consciousness. I was informed to not provide medical treatment (no medication was administered). While waiting for paramedics, patient reported nausea and lightheadedness. Patient also appeared to be pale and was excessively sweating. Emergency service arrived and evaluated the patient. Patient declined to go to the hospital.

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: No known Drug allergies
Vorherige Impfungen: -

VAERS 2722027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 07.12.2023
Impfdatum: 22.02.2022
Beginn: 03.03.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SC / RA

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

Arthritis Hypertension Laboratory test abnormal Systemic lupus erythematosus Vasculitis

Symptomtext

Developed lupus, blood pressure high, vasculitis and arthritis things I never had before, I have an evolution of more than a year and a half, started specifically after the third vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Studies related to lupus.
Aktuelle Erkrankungen: None
Vorgeschichte: None before the vaccine
Andere Medikamente: None
Allergien: NO
Vorherige Impfungen: -

VAERS 2677343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NY
Alter: 74,0
Geschlecht: F
Eingang: 28.08.2023
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Essential tremor Fatigue Feeling abnormal Tremor

Symptomtext

On 09/15/2022, I had gotten my 6th Covid vaccine booster and my yearly flu vaccine. (Details below,) Felt very tired. I went to bed and as I was sitting in bed, reading, my hands started shaking violently. It wasn't like an essential tremor. I sat there in shock, trying to control my hands, but they kept shaking for about 5 minutes. The shaking stopped, and has not returned. I'm hesitant to get a booster for Covid.

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Praegender Schweregrund: Essential tremor
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep apnea, obesity, high blood pressure & cholesterol, depression
Andere Medikamente: Gabapentin, triamterene, bupropion, sertraline, Zolpidem, D3,
Allergien: Intolerance to most statins, and lactose
Vorherige Impfungen: -

VAERS 2660804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 25.07.2023
Impfdatum: 01.07.2022
Beginn: 01.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Neck pain Paraesthesia Trigger finger

Symptomtext

Tingling sensations in lower right arm and hand; The fingers on right hand can suddenly snap shut/ Snap Finger; The pain in my neck began about 17 to 18 minutes after injection; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Jul2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 71 years, in left arm 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 Number: EN6201, Anatomical site of vaccine administration: Left arm), administration date: 10Mar2021, for COVID-19 immunization, reaction(s): "Terrible joint pain", "Muscle aches", "Headaches", "Nausea", "Terrible fatigue"; BNT162b2 (DOSE 2, SINGLE, Lot Number: ER8732, Anatomical site of vaccine administration: Left arm), administration date: 31Mar2021, for COVID-19 immunization, reaction(s): "Terrible joint pain", "Muscle aches", "Headaches", "Nausea", "Terrible fatigue"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot Number: PF2590, Anatomical site of vaccine administration: Left arm), administration date: 21Oct2021, for COVID-19 immunization, reaction(s): "Terrible joint pain", "Muscle aches", "Headaches", "Nausea", "Terrible fatigue". The following information was reported: NECK PAIN (non-serious) with onset 01Jul2022, outcome "not recovered", described as "The pain in my neck began about 17 to 18 minutes after injection"; PARAESTHESIA (non-serious), outcome "not recovered", described as "Tingling sensations in lower right arm and hand"; TRIGGER FINGER (non-serious), outcome "not recovered", described as "The fingers on right hand can suddenly snap shut ". The events "the pain in my neck began about 17 to 18 minutes after injection", "tingling sensations in lower right arm and hand" and "the fingers on right hand can suddenly snap shut " required physician office visit. Therapeutic measures were not taken as a result of neck pain, paraesthesia, trigger finger. Additional Information: When she went for the second booster, she had reported her previous reactions. The pain in her neck began about 17 to 18 minutes after injection and the reaction was much worse than the prior ones. The fingers on her right hand can suddenly snap shut and she had tingling sensations in her lower right arm and hand. While not as serious as in Jul2022 and Aug2022, she still had difficulties.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300258400 same patient/reporter, different dose/event;

Weitere VAERSDATA-Felder

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

VAERS 2633015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 17.05.2023
Impfdatum: 12.07.2022
Beginn: 07.02.2023
Tage bis Beginn: 210,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia COVID-19 Confusional state Cough Dyspnoea Metabolic encephalopathy SARS-CoV-2 test positive Sepsis

Symptomtext

The patient has a history of cholangiocarcinoma currently receiving chemotherapy. He presented to the ED on 2/6/23 with weakness, confusion, cough, and difficulty breathing. A COVID PCR test done in the ED returned positive. He was admitted to the hospital 2/6/23 - 2/9/23. Discharge diagnoses include sepsis, generalized weakness and metabolic encephalopathy secondary to COVID-19 infection, and suspect CAP, among other diagnoses. He did not require supplemental oxygen during his admission. He was started on paxlovid, however there were no indications for steroids. The patient's most recent COVID booster was administered 7/12/22.

Weitere VAERSDATA-Felder

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

VAERS 2631046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MI
Alter: 79,0
Geschlecht: F
Eingang: 12.05.2023
Impfdatum: 21.07.2022
Beginn: 05.04.2023
Tage bis Beginn: 258,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

04/05/23 presents to ED for "fatigue" "shortness of breath". PMHx of "COPD, CHF, hypertension"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 04/05/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2613002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MN
Alter: 60,0
Geschlecht: M
Eingang: 11.04.2023
Impfdatum: 08.06.2022
Beginn: 10.04.2023
Tage bis Beginn: 306,0
Dosis: 2
Route/Site: IM / LA

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

Confusional state Encephalopathy Pneumonia

Symptomtext

Pneumonia of both lungs, non-hypoxic. Encephalopathy with greater than usual confusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ? Acute kidney injury (nontraumatic) (HCC) 06/08/2020 ? Anemia ? Astigmatism ? Bipolar 1 disorder (HCC) ? Cerebral hypoxia (HCC) 04/02/2012 ? Chronic fatigue ? Complicated urinary tract infection 06/02/2020 ? Controlled type 2 diabetes mellitus, without long-term current use of insulin (HCC) ? COPD (chronic obstructive pulmonary disease) (HCC) ? Dementia (HCC) unknown etiology ? Gastric ulcer ? Gastroparesis ? GERD (gastroesophageal reflux disease) ? Hiatal hernia ? High risk medication use ? Hyperplasia of prostate without lower urinary tract symptoms (LUTS) ? Hypotension ? Hypothyroidism ? Incarcerated right inguinal hernia 09/30/2020 Added automatically from request for surgery 782735 ? Incomplete bladder emptying ? Intermittent self-catheterization of bladder 05/31/2020 ? Lung disease has a "speck" on his lung, prone to bronchitis ? Myopia ? Nocturia ? Obsessive compulsive disorder 04/02/2012 ? Organic mental disorder ? Osteopenia ? PONV (postoperative nausea and vomiting) ? Schizoaffective disorder (HCC) ? Sensorineural hearing loss of both ears ? Sensorineural hearing loss, bilateral 09/20/2019 ? Sepsis (HCC) 11/27/2020 ? Sinus tachycardia ? TBI (traumatic brain injury) ? Urinary tract infection associated with indwelling urethral catheter (HCC) 11/27/2020 ? Urinary tract infection without hematuria
Andere Medikamente: -
Allergien: Navane, metformin
Vorherige Impfungen: -

VAERS 2587851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: OK
Alter: 14,0
Geschlecht: F
Eingang: 27.02.2023
Impfdatum: 23.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Dyspnoea Headache Loss of personal independence in daily activities Myalgia Scoliosis

Symptomtext

In August 2022, after dose 3, she began to experiencing pain from Scoliosis in the muscles, headache, short of breath. She was diagnosed with Scoliosis in September 2022. She has not been able to attend school due to her symptoms. On February 10, 2023 she went to the emergency department due to a severe headache. They gave her intravenous fluids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Mild fever on the day of booster
Vorgeschichte: N/A
Andere Medikamente: Cetirizine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2561588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: WI
Alter: 80,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 16.08.2022
Beginn: 24.12.2022
Tage bis Beginn: 130,0
Dosis: 4
Route/Site: IM / RA

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

Akinesia Cardiac disorder Cardiac failure acute Chest discomfort Computerised tomogram thorax abnormal Dyspnoea Dyspnoea paroxysmal nocturnal Echocardiogram abnormal Ejection fraction decreased Hypoperfusion Ischaemia Left atrial enlargement Magnetic resonance imaging heart Mitral valve incompetence Oedema Orthopnoea Pleural effusion Pulmonary mass

Symptomtext

Patient is a 81 y.o. female who was admitted on 1/15/2023 for acute heart failure and elevated troponin. The patient reported an episode of upper chest discomfort on around 3rd week of Dec. It abated spontaneously. She did not have any recurrent symptoms until about 3 days prior to presentation when she developed progressive dyspnea and was just unable to catch her breath. She endorses orthopnea, PND and bend up knee. Denied any recurrent chest discomfort. No palpitations, presyncope or syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Echocardiogram which is in progress during the interview shows reduced EF around 35-40% with septal, anterior and apical regional wall motion abnormalities. EXAM: MR CARDIAC WITHOUT AND WITH IV CONTRAST COMPARISON: No prior cardiac MRI available at the time of dictation. Limited correlation with CT chest 01/15/2023. FINDINGS: LEFT VENTRICLE: Normal left ventricular chamber size. Normal wall thickness. Akinesis of the inferior and inferolateral wall at the mid level. Hypokinesis of the mid inferior septum. Hypokinesis apical lateral and inferior walls. LVEF = 46%. Suspected mild subepicardial edema in the mid inferior wall (series 8 image 2). Subendocardial hypoperfusion in the mid inferior and inferolateral walls extending into the apical inferior wall. Normal myocardial nulling kinetics on the cine IR. Subepicardial delayed enhancement of the mid inferior and inferolateral walls. RIGHT VENTRICLE: Normal right ventricular size, myocardial thickness, and systolic function. RVEF = 58%. No abnormal delayed myocardial enhancement. ATRIA: Left atrial enlargement. Left atrial enlargement. VALVES: Mitral regurgitation. Tricuspid regurgitation. PERICARDIUM: Normal pericardial thickness. No pericardial effusion. No abnormal pericardial enhancement. OTHER: Moderate bilateral pleural effusions, right greater than left. Small pulmonary nodule in the left upper lobe as seen on recent chest CT (series 3 image 6). Postoperative changes upper abdomen. MEASUREMENTS: Patient weight: 88 kg Patient height: 165 cm BSA: 2 m2 Series 7: LEFT VENTRICLE: LV End Diastolic Volume = 156mL; Index = 78mL/m2 LV End Systolic Volume = 85mL; Index = 42mL/m2 LV Stroke Volume = 71mL; Index = 35mL/m2 LV Ejection Fraction = 46% LV End Diastolic Mass = 99g; Index = 49g/m2 Series 7: RIGHT VENTRICLE: RV End Diastolic Volume = 112mL; Index = 56mL/m2 RV End Systolic Volume = 47mL; Index = 23mL/m2 RV Stroke Volume = 66mL; Index = 33mL/m2 RV Ejection Fraction = 58% IMPRESSION: 1. Akinesis of the mid inferior and inferolateral wall and hypokinesis of the mid inferior septum, apical inferior, and apical lateral walls. Probable subepicardial edema in the mid inferior wall. Subepicardial delayed enhancement in the mid inferior and inferolateral walls. Overall findings are most suggestive of acute myocarditis. 2. Mild subendocardial hypoperfusion in the mid inferior and inferolateral walls extending into the apical inferior wall suggesting mild subendocardial resting ischemia. 3. Mildly decreased left ventricular systolic function. LVEF = 46%. Specimen Collected: 01/17/23 14:35 CST Last Resulted: 01/17/23 15:03 CST
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2559586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 29.06.2022
Beginn: 20.07.2022
Tage bis Beginn: 21,0
Dosis: 4
Route/Site: IM / RA

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

Blood test Chest pain Dyspepsia Echocardiogram normal Electrocardiogram normal Painful respiration

Symptomtext

About three weeks after receiving the fourth dose of Pfizer, I started to experience some chest pain on the left side. This pain and aching lasted for several days. I was experiencing indigestion also. I sleep on my left side so I was thinking it could have been from that. Around August, it started to ease up and get better, but then it would come back. When I cough, sneeze or take a really deep breath it hurts. I put myself on the back burner for a while since my mother was sick. I had a doctor's appointment with my PCP in November. I was explaining about my chest pains and how I had it for a while and she was very concerned. She told me to contact a cardiologist. I had an EKG scheduled and the results were normal. I also had an ECHO performed and the results were normal on that as well. I have been prescribed medication, but I haven't taken it yet because my insurance won't cover it. My doctor prescribed a new medication, but the pharmacy is currently out of stock. I have a follow up appointment with the cardiologist in two weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG; ECHO; Blood draw
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-diabetic
Andere Medikamente: Amlodipine besylate; vitamin D3; vitamin C; B-12; magnesium chew (occasionally)
Allergien: Codeine; sulfa
Vorherige Impfungen: -

VAERS 2552113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN-2908

moderat

Staat: ID
Alter: 36,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 15.08.2022
Beginn: 16.08.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea Palpitations

Symptomtext

Patient had symptoms of shortness of breath and palpitations which lasted for 2 to 3 days initially and most of the day. He still reports some occasional intermittent symptoms

Weitere VAERSDATA-Felder

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

VAERS 2547543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 31.12.2022
Impfdatum: 06.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

Cardiac flutter Dehydration Dizziness Hunger SARS-CoV-2 test

Symptomtext

I have experienced a fluttering in my chest and some slight dizziness over the past year or so; I have experienced a fluttering in my chest and some slight dizziness over the past year or so; hunger; dehydration; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Jun2022 at 15:30 as dose 4 (booster), single (Lot number: FN2908) at the age of 66 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot Number: EN6196; , Anatomical site: Arm Left; vaccine administration Time: 12:00 AM), administration date: 02Mar2021, when the patient was 65-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE; Lot No: EN6203, Anatomical site: Arm Left; Vaccine Administration Time: 08:30 AM), administration date: 24Mar2021, when the patient was 65-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; , Lot Number: FF2590; Anatomical site: Arm Left, Vaccine Administration Time: 09:15 AM), administration date: 09Nov2021, when the patient was 65-year-old, for COVID-19 Immunization. The following information was reported: CARDIAC FLUTTER (medically significant), DIZZINESS (non-serious) all with onset 2022, outcome "unknown" and all described as "I have experienced a fluttering in my chest and some slight dizziness over the past year or so"; DEHYDRATION (non-serious) with onset 2022, outcome "unknown"; HUNGER (non-serious) with onset 2022, outcome "unknown". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (15Dec2022) Negative. Additional Information: It was reported that the patient had experienced a fluttering in chest and some slight dizziness over the past year or so, which patient had attributed to hunger and dehydration . The patient had mentioned this to doctor at yearly physical in Oct. The patient was to monitor and make a return visit should they become more prevalent. The patient did not receive other vaccines within four weeks prior to COVID vaccine. The patient had no known allergies. The patient did not receive any medications within two weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201391908 same patient/drug, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: Test Date: 20221215; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2521217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: IN
Alter: 68,0
Geschlecht: M
Eingang: 01.12.2022
Impfdatum: 19.07.2022
Beginn: 01.09.2022
Tage bis Beginn: 44,0
Dosis: 4
Route/Site: IM / UN

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

Computerised tomogram abnormal Dyspnoea Pericardial effusion Positron emission tomogram normal

Symptomtext

He started to have more and more shortness of breath. He was not able to do anything without getting short of breath. He was having breathing issues. Then we saw the doctor and they did a CAT scan. It showed he had fluid around the heart. He can't have an MRI he had a PET scan instead. The PET scan was fine. In the meantime, the doctor called to see how he was doing, and the fluid was building around his heart. The doctor said he doesn't feel like it was heart failure. The doctor didn't know what it was and where it started. The doctor said I wonder if this is happening due to the vaccine or the booster. As of right now they are running tests on him.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: PET scan; CAT scan
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis; High blood pressure
Andere Medikamente: Atorvastatin; ezetimibe; leflunomide; losartan; XARELTO
Allergien: None
Vorherige Impfungen: -

VAERS 2403002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NH
Alter: 14,0
Geschlecht: F
Eingang: 01.12.2022
Impfdatum: 01.08.2022
Beginn: 01.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure systolic decreased Cardiac stress test abnormal Dizziness Fatigue Headache Visual impairment Heart rate increased Malaise Orthostatic hypotension Postural orthostatic tachycardia syndrome

Symptomtext

Prior to August 1st, pt. was a healthy and active 14 year old girl who loved playing soccer and hockey and no had medical conditions. Pt developed sudden onset, severe POTS (postural orthostatic tachycardia syndrome)-like symptoms 10/15 minutes after receiving the Pfizer COVID vaccine on 8/1/22. Her symptoms include notable orthostatic hypotension, fatigue, and postural headache and dizziness that worsens when going from sitting to standing and persists when standing or walking. Orthostatic measurements showed that her heart rate increased by 22 bpm when going from the time to be seated position, going from 65 to 87 bpm, then increased by another 28 bpm when going from the seated to the standing position with a heart rate of 115?120 when standing. Overall her heart rate increased by 50 bpm when going from the supine to the standing position and her systolic blood pressure decreased by 22 points, with a blood pressure of 94/58 while supine and 72/55 while standing. Based on the timing of pt.'s symptoms, she has had an unusual adverse reaction from the COVID-vaccine, triggering POTS-like symptoms. At this point, it is difficult to determine whether these symptoms will subside in a timely manner, or whether the vaccine is possibly triggered in autoimmune reaction, that could potentially linger for a longer period of time. Patient had a stress test at a local Hospital where they showered a "blunted Blood pressure" (her BP was not reacting to running) and her BP suddenly tanked after a few minutes for no reason. This caused patient to feel ill and severe headache.

Weitere VAERSDATA-Felder

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

VAERS 2517874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 14.06.2021
Beginn: 23.11.2022
Tage bis Beginn: 527,0
Dosis: 3
Route/Site: - / -

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

Blood glucose increased COVID-19 Cough Dyspnoea Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

Pt has a history of type 1 diabetes, CKD, and CHF. She has increased blood sugars as well as a mild cough and shortness of breath over the past couple of days. Her family was recently diagnosed with COVID and she is also COVID positive.

Weitere VAERSDATA-Felder

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

VAERS 2489884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 07.07.2022
Beginn: 15.10.2022
Tage bis Beginn: 100,0
Dosis: 4
Route/Site: IM / -

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

Acute kidney injury Asthenia COVID-19 Chest X-ray normal Chronic kidney disease Condition aggravated Fall Haematuria Hyponatraemia Hypovolaemia SARS-CoV-2 test positive Ultrasound kidney abnormal Urine analysis normal

Symptomtext

COVID+ 10/15/22 - Vaccination status - pfizer x4 BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider at Discharge: MD Discharge disposition: MFB Condition on discharge: Stable. DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute kidney injury (HCC) [N17.9] COVID-19 virus infection [U07.1] Generalized weakness [R53.1] HOSPITAL COURSE: Is a 74-year-old gentleman with a history of AFib on Xarelto, BPH with chronic Foley catheter, insulin-dependent type 2 diabetes, hypertension, sleep apnea, iron deficiency, and bolus pemphigoid on chronic immunosuppression. He presented to the ER due to generalized weakness and recent fall at home. Patient had viral symptoms beginning on 10/08. He had recently started Bactrim, per his urologist, for possible urinary tract infection in setting of new hematuria. Initial workup in the ER revealed AKI on CKD 4, hyponatremia, and tested positive for COVID-19 on 10/15. He was admitted to Internal Medicine for workup and therapy evaluation. Regarding COVID-19 infection, chest x-ray was negative for infiltrates, so patient was treated with supportive care. He did not require supplemental oxygen. AKI and acute hypovolemic hyponatremia resolved with IV hydration. Urinalysis was negative for infection and patient was without hematuria so no further antibiotics were given. PT/OT evaluated the patient and recommended SAR. Care manager assisted with placement and patient discharged in stable condition to MFB. While inpatient he had renal US showing possible renal cysts. Instructed to follow up with PCP for repeat US in 6 months to ensure stability

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: BPH with chronic Foley; IDDM2; Anticoagulated; Immunocompromised (HCC); HTN (hypertension); Hypercholesterolemia; Cognitive and behavioral changes; Hyponatremia CKD (chronic kidney disease), stage IV (HCC); Primary hyperparathyroidism (HCC) Paroxysmal atrial fibrillation (HCC); PAT (paroxysmal atrial tachycardia) (HCC) Mild nonproliferative diabetic retinopathy of right eye without macular edema associated with type 2 diabetes mellitus (HCC); Central sleep apnea, moderate; Bullous pemphigoid; Other specified glaucoma.
Andere Medikamente: Amiodarone HCl; Atorvastatin Calcium; B Complex Vitamins; Cholecalciferol; Coenzyme Q10; Fenofibrate; Ferrous Sulfate; Insulin Aspart; Insulin Glargine; Krill Oil; Lidocaine HCl 2 % Topical; Lisinopril; Lutein,Lutein-Zeaxanthin; Metoprolol
Allergien: DoxycyclineDermatitis; Latex; Penicillins-Swelling; Tamsulosin; TorsemideOther; Victoza [Liraglutide]Other; Adhesive Tape-Other.
Vorherige Impfungen: -

VAERS 2481809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: AZ
Alter: 79,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 29.06.2022
Beginn: 09.08.2022
Tage bis Beginn: 41,0
Dosis: 4
Route/Site: SYR / LA

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

Back pain Dyspnoea Fatigue Feeling abnormal Gait disturbance Haemoglobin normal Headache Mobility decreased Post-acute COVID-19 syndrome Pyrexia Renal function test SARS-CoV-2 test positive

Symptomtext

After my second COVID-19 diagnosis, I was feeling crappy, I had a high fever of 103, I was in bed a lot. I was very tired for a while. I had trouble walking and catching my breath. I had lower back pain. I'm not sure if it was remnants of the first time in 2020, I had long COVID-19. I had a lot of headaches. My pharmacist told me that my doctor put me on PAXLOVID, but I needed to reduce dosage because of my kidney function. So, I went to my doctor for an appointment eventually and I had her test my kidney function. The first test 08/09 I had a CKD of 49 then the second test was on 08/15 the numbers were a little bit better my CKD was 52. That's all that I have right now for my kidney issues. I am now seeing a Nephrologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test positive; Kidney function test 8/9, CKD 49; Kidney Function test 8/15, CKD 52; Hemoglobin test 8/9, normal.
Aktuelle Erkrankungen: COVID-19
Vorgeschichte: Diabetic Type II; High blood pressure; Anemia
Andere Medikamente: Omeprazole; amlodipine; olmesartan; metformin; atorvastatin; hydroxyzine; famotidine; echinacea; CALTRATE; NUTRAFOL; probiotics; melatonin
Allergien: Iodine; penicillin; vancomycin; sulfa
Vorherige Impfungen: -

VAERS 2480820

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: HI
Alter: 54,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 10.06.2022
Beginn: 12.06.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / UN

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

Blood test normal Cardiac stress test normal Chest X-ray normal Chest discomfort Cough Dyspnoea Dyspnoea exertional Electrocardiogram normal Hypertension Pulmonary function test normal Throat tightness

Symptomtext

I didn't make the connection of the vaccination to difficulties I had right around the same time following the vaccination. I don't know if it is related but I suddenly began to have difficulty breathing with brisk walking, running, excessive talking (ie facilitating a meeting). It was more like a dry cough with a tightness in the back of my throat or upper chest. I could take a deep breath in but would cough upon exhale. In some instances, the coughing was so bad that I had to stop what I was doing to try to catch my breath. It sometimes occurred at night when I layed down to sleep. I contacted my doctor who did an initial series of xrays of my lungs, heart. Did a blood draw. Did an EKG. Everything was considered normal except for high blood pressure. I continued off and on for the about three months with different intensities. During that time, we did a stress test and pulmonary function test which were within normal range. Doctor prescribed Alvesco and have been taking two doses for the past month reducing to one dose. Symptoms have definitely lessened in intensity and happening with very mild and less frequent intensity. Still occurs occasionally but very mildly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: All tests described above were within normal range.
Aktuelle Erkrankungen: none
Vorgeschichte: borderline diabetes, borderline hypertension
Andere Medikamente: Ocella, Hydrochlorothiazide, Bioastin, MoveFree,
Allergien: none
Vorherige Impfungen: -

VAERS 2473377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: TX
Alter: 60,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 12.07.2022
Beginn: 25.09.2022
Tage bis Beginn: 75,0
Dosis: 4
Route/Site: IM / RA

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

Asthma Blood pressure increased COVID-19 Cough Disturbance in attention Dyspnoea Feeling abnormal Headache Lacrimation increased Pain Rhinorrhoea SARS-CoV-2 test positive Secretion discharge Taste disorder Vision blurred

Symptomtext

On 9/25/2022 at 5PM I had sniffles and it felt like an asthma attack. On 9/26/2022 morning, I started to feel really bad. I had full blown aches, mucous, cough, shortness of breath, tearing of eyes, massive headache, and brain fog. I tried to call my doctor and did not get in touch. That came back 9/28/ positive COVID-19 test. On Thursday I got in touch with my doctor. They prescribed PAXLOVID, doxycycline and prednisone. I am basically taking 2 a day of each, and that seem to have done the trick because I had 2 COVID-19, negative tests. I still have a lot of mucous, a lot of brain fog, not able to concentrate, I am starting to get some of my taste buds back. It is really triggering my asthma. I have to use my nebulizer with albuterol twice a day. It is even doing something to my eyes, I am seeing blurry, raised blood pressure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 9/28/2022, 2 COVID-19 tests, both came back positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Severe asthma; upper respiratory disease; sleep apnea
Andere Medikamente: Multivitamin complex B; complex D; complex C; complex E; PROAIR; albuterol; TRELEGY; FLONASE
Allergien: Sulfides; amoxicillin; penicillin; erythromycin; bacitracin
Vorherige Impfungen: -

VAERS 2444810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MN
Alter: 76,0
Geschlecht: M
Eingang: 14.09.2022
Impfdatum: 27.06.2022
Beginn: 14.09.2022
Tage bis Beginn: 79,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Dyspnoea

Symptomtext

Requiring hospitalization for SOB, O2 requirements and weakness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: IBS, HTN, HLD, Obesity
Andere Medikamente: -
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2433416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 03.03.2021
Beginn: 12.08.2022
Tage bis Beginn: 527,0
Dosis: 3
Route/Site: - / -

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

Asthenia COVID-19 Compression garment application Fluid intake reduced Hyperkalaemia Hyponatraemia Hypophagia Interchange of vaccine products Orthostatic hypotension SARS-CoV-2 test positive

Symptomtext

72y.o. male with orthostatic hypotension presents with generalized weakness from home. He has not been eating or drinking much at home and felt weaker. He was admitted with covid 19 as well. He declined any treatment for covid 19. He remained on room air without respiratory issues. He had hyponatremia and hyperkalemia which improved. He was followed by psychiatry as well as nephrology. He had orthostatic hypotension which improved gradually with midodrine and salt tabs as well ace wraps and cmopression stalkings. Discussed if comprssion stalkings were to tight not to wear. He did have ace bandages used as wraps aslo which helped. Patient is deemed medically stable for discharge

Weitere VAERSDATA-Felder

Praegender Schweregrund: Orthostatic hypotension
Hospital-Tage: 17,0
Labordaten: 8/12 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2422721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MT
Alter: 46,0
Geschlecht: M
Eingang: 29.08.2022
Impfdatum: 29.08.2022
Beginn: 29.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Anxiety Dyspnoea

Symptomtext

Patient had trouble breathing. Patient was given oxygen approximately 10-15 minutes after vaccine, Benadryl, Symbicort (patients own inhaler), Metoprolol (patients own) and hydroxyzine (patients own, for anxiety), O2 sats and blood pressure were monitored while patient received oxygen. Patient felt better after about 20-25 minutes after injection. Patient went home with instructions to monitor blood pressure with him home blood pressure monitor and to go to the ER if he felt worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: High blood pressure, asthma
Vorgeschichte: Patient had Covid and was in the hospital for an extended period of time.
Andere Medikamente: None known
Allergien: None
Vorherige Impfungen: -

VAERS 2422476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 21.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: UN / UN

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

Dizziness Dyspnoea Fatigue Pyrexia

Symptomtext

Fever, dizzy, fatigue, SOB.

Weitere VAERSDATA-Felder

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

VAERS 2419461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 24.08.2022
Impfdatum: 16.05.2022
Beginn: 20.06.2022
Tage bis Beginn: 35,0
Dosis: 4
Route/Site: SYR / LA

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

Blood test normal Dyspnoea Immunology test normal Nasal congestion Nasal dryness Rhinorrhoea

Symptomtext

I woke up in the middle of the night with difficulty breathing. I thought I had a stuffy nose. I used a nasal spray, but it burned. I realized my nose was really dry and not stuffy. I sound like I'm sniffling, but I'm just trying to get air up my nose during the day. Now, its day and night. I made an appointment with my doctor. They ran some tests but they all came back clear. My doctor made an appointment for me to see an ENT doctor. My nose is still the same. It hasn't changed. I can't seem to get a lot of air. I take deep breaths through my nose and exhale through my mouth to get a bit gush of oxygen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 06/09/2022 blood tests and autoimmune test normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Omeprazole DR; rosuvastatin; amlodipine; VITAFUSION women's multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2418279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: AR
Alter: 65,0
Geschlecht: M
Eingang: 23.08.2022
Impfdatum: 30.06.2022
Beginn: 18.08.2022
Tage bis Beginn: 49,0
Dosis: 3
Route/Site: - / -

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

Anaemia COVID-19 Condition aggravated Hypokalaemia Mental status changes

Symptomtext

Patient admitted with covid 19, anemia, hypokalemia and ams

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: anemia, hypokalemia
Vorgeschichte: Lung cancer, muscle atrophy, nephrotic syndrome, type 2 diabetes, hyperlipidemia, heart attack, BPH, hypertension, atherosclerosis
Andere Medikamente: Acetaminophen 650 mg po q4 hours prn, ambien 5 mg po hs, amiodarone 100 mg po daily, arava 20 mg po daily, aspirin 81 mg po daily, bisacodyl 5 mg po daily prn, carvediolo 6.25 mg po bid, ceftazidime 1 gm IM hs, cortisone topical application
Allergien: Sulfa, Flexeril, Enbrel
Vorherige Impfungen: -

VAERS 2415806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 18.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Aphasia Chest pain Cold sweat Dizziness Dyspnoea Headache Hypoaesthesia oral Pallor Paraesthesia oral Swollen tongue

Symptomtext

Patients vaccines were administered and she was asked to wait for a 15 minute observation period. She initially reported feeling light headed and like she felt she could pass out. She was pale, cold and clammy. She was also having a hard time forming words and completing a sentence. She was given water, 7 Up and ate a few peanut butter crackers and a cool pack was applied to her neck. This helped her feel a little better and she was asked to still sit and rest for a few more minutes. After about 5 minutes she started complaining that her head hurt, she was having trouble getting deep breaths, that her chest was hurting and her tongue felt numb and her lips were tingling. She was asked to focus on some breathing exercises and her feet were elevated. She was also saying if she looked up then she was dizzy and wanted to pass out so she kept her head looking straight ahead. We were not able to obtain her vitals because she could not handle the blood pressure cuff. After about 10 minutes she was not improving and continued to say her chest hurt and she could not breath. At this point a call was placed to 911 for ambulance services. They arrived within about 5 minutes and was transported to the hospital for evaluation of anxiety and possible allergic reaction due to some tongue swelling. She also mentioned she had been taken to the ED last week with similar symptoms of shortness of breath and chest pain and been given clonazepam for anxiety.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None in office but the ambulance did evaluate and transport to the hospital.
Aktuelle Erkrankungen: Recently evaluated in ED for anxiety.
Vorgeschichte: Unknown
Andere Medikamente: Clonazepam
Allergien: None Listed
Vorherige Impfungen: Patient reported mild symptoms that were similar after her first COVID vaccine that was received on 5/17/2022. No treatment was

VAERS 2410051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 12.08.2022
Impfdatum: 08.06.2022
Beginn: 05.08.2022
Tage bis Beginn: 58,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Confusional state Dizziness Dyspnoea Headache Oropharyngeal pain Pain Productive cough Pyrexia SARS-CoV-2 test positive Sinus congestion Vaccine breakthrough infection

Symptomtext

Break through infection. Sore throat, sinus congestion, productive cough, body aches, headache, dizziness, shortness of breath, fever, confusion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Positive Covid-19 antigen test card
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Keflex
Vorherige Impfungen: -

VAERS 2403325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: ND
Alter: 13,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Immediate post-injection reaction Injected limb mobility decreased Injection site pain Loss of personal independence in daily activities Pain Pain in extremity Shoulder injury related to vaccine administration

Symptomtext

Client's mother reported to staff that client's arm hurt immediately after injection. Both client and mother attested this to having just received an IM injection. Client reported that her arm continued to hurt. Client reported about 2 hours after the injection, while at home, client's arm pain continued to increase and client was reporting sharp, burning pain to her arm and shoulder and limited range of motion to the point client was unable to use her right arm for activities of daily living (ADL's). Mother gave client ibuprofen and had client ice her arm/shoulder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: 2 days after the injection on 7/14/2022, client was brought in to a clinic for continued shoulder and arm pain and limited range of motion and was seen by Dr. Client was diagnosed with SIRVA and given a 5 day course of prednisone (10 mg TID). Client's pain and range of motion only slightly improved after prednisone and client's mother messaged the doctor back on 7/20/2022. Client started physical therapy on 7/27/2022.
Aktuelle Erkrankungen: Allergies or a cold.
Vorgeschichte: Asthma
Andere Medikamente: Allegra daily Ibuprofen as needed
Allergien: Peanut/Tree Nut Environmental
Vorherige Impfungen: -

VAERS 2403035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: -
Alter: 46,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 27.07.2022
Beginn: 27.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chest discomfort Chest pain Discomfort Dizziness Electrocardiogram Headache Palpitations Screaming Troponin T

Symptomtext

Pt screamed and grabbed her chest. Vitals taken w/ 178 other vitals WNL. Pt reported chest pain and pain in the back of her head. Pt rated 10/10. Pt also reported feeling heavy and dizziness. 911 called immediately. Pt placed in wheelchari and assessed by RN. Pt transported to ED. IN ED: 46-year-old presenting for palpitations status post COVID vaccine, no evidence of anaphylaxis, complains of substernal chest pressure as well no history of ACS or recent ACS workup -history is not consistent with ACS however patient reports substernal chest pain at this time. Started 20 minutes prior to presentation discussed risk benefits of further work-up, patient preferred to have ACS work-up here in the emergency department. Differential diagnosis includes ACS, pulmonary embolism, pneumothorax, pneumonia, cardiac tamponade, esophageal rupture, pericarditis, myocarditis. 1107 My interpretation of the EKG is sinus rhythm, rate of 62, short PR interval 105, no delta wave, normal axis, no ST elevations meeting STEMI criteria. 1300 Troponin T high sensitivity: <6 Pending delta Trope. 1355 Pt will be Be signed out to oncoming ED attending Dr. pending delta Trope. Patient is a low risk chest pain if COVID-negative patient okay for discharge. Doubt ACS. Patient is now chest pain-free on my reevaluation. 1403 SIGNOUT: pending hstrop3 for DC 1403 S/o: 46F low risk chest pain, pending 2nd trop, if neg can go home 1510 Troponin T high sensitivity: <6 After re-evaluation, patient was clinically improved. Pertinent diagnostic results discussed with the patient. All questions were answered. Return precautions discussed as well as pertinent wound/injury care instructions. Utilizing shared decision making, patient will be discharged home. Patient agrees to close follow up with their primary care physician and appropriate outpatient specialist. 1510 Doubt ACS. Low risk for major adverse cardiac event, less than 1.7%. Heart score of 1. Patient informed of results and agreeable. Pt discharged home with return precautions.

Weitere VAERSDATA-Felder

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

VAERS 2401325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: PR
Alter: 32,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 21.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Burning sensation Chest X-ray normal Dyspnoea Full blood count normal Hypotension Laboratory test normal Mobility decreased Muscle spasms

Symptomtext

Cramp in the upper extremities and from the waist down. Burning sensation throughout the body. Mobility limitation and leg pain. Low pressure. 94/73 Difficulty Breathing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest X-Ray, CBC, Laboratories No altered result.
Aktuelle Erkrankungen: None
Vorgeschichte: Epilepsy, Asthma.
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2400434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 24.05.2022
Beginn: 19.07.2022
Tage bis Beginn: 56,0
Dosis: 4
Route/Site: - / -

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

Arrhythmia Asthenia Bradycardia COVID-19 Cough Electrocardiogram abnormal Extrasystoles Fatigue Headache Laboratory test normal SARS-CoV-2 test positive Sinus bradycardia

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admitting Service: Admission Date: 7/19/2022 Discharge Date: 07/21/2022 PRESENTING PROBLEM: Generalized weakness Fatigue, unspecified type HOSPITAL COURSE: Patient is a 73 y.o. female who presented with her daughter for evaluation of heart arrhythmia and generalized fatigue. . Today driving to a doctor's appointment she noted patient had dry cough and headache. At this appointment an EKG was obtained noting an abnormal rhythm with multiple skipped beats. Due to these changes she was defer to the emergency department for further testing. She was found to be COVID positive in the emergency department, vitals were stable apart from bradycardia with heart rate in 50s. Labs were mostly unremarkable. Initial concern for Mobitz type 2 but discussing with Cardiology/EP pelvis was sinus bradycardia with pauses. PT and OT evaluated the patient recommended home health, Care Management. doing well discharge home today with homecare in stable condition.

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Praegender Schweregrund: Arrhythmia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HTN (hypertension) Asthma Spondylolisthesis, grade 2 Vitamin D deficiency Adenomatous colon polyps Chondromalacia patellae of right knee Ventral hernia, unspecified, without mention of obstruction or gangrene Skin ulcer of abdominal wall (HCC) Hair loss Irregular heart rate-1st degree AV block Chronic gastritis Other malaise and fatigue Varicose veins of lower extremity with other complication Osteopenia Small bowel obstruction (HCC) Rheumatoid arteritis (HCC) Obstructive sleep apnea syndrome Chronic midline low back pain with left-sided sciatica History of metabolic disorder Language barrier affecting health care - Thrombocytopenia (HCC) Restless legs syndrome (RLS) Asymmetric SNHL (sensorineural hearing loss) Tinnitus of both ears Seasonal rhinitis Urge incontinence Thoracic or lumbosacral neuritis or radiculitis Arthritis Female pattern alopecia Seborrheic dermatitis Elevated blood pressure reading Generalized weakness
Andere Medikamente: CALCIUM PO cholecalciferol (VITAMIN D3) 50 MCG (2000 UT) capsule fexofenadine (ALLEGRA) 180 MG tablet fluticasone (FLONASE) 50 MCG/ACT nasal spray gabapentin (NEURONTIN) 800 MG tablet hydroxychloroquine (PLAQUENIL) 200 MG tablet monte
Allergien: Ace InhibitorsCough Seasonal Allergies, Unspecified
Vorherige Impfungen: -

VAERS 2397734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 31.07.2022
Impfdatum: 30.07.2022
Beginn: 31.07.2022
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: - / LA

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

Condition aggravated Migraine

Symptomtext

migraine, started about 15 -17 hours after vaccine. I have not had a migraine since the last COVID booster (moderna) in December 2021. Lasted all day.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: migraines but haven't had one since my last COVID booster in December 2021
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: COVID (moderna), 57years, 12/12/2021

VAERS 1938335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 30.07.2022
Impfdatum: 19.11.2021
Beginn: 15.07.2022
Tage bis Beginn: 238,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Fatigue Myalgia Pain Pain in extremity Diarrhoea Hyperhidrosis Nausea Paraesthesia Pyrexia

Symptomtext

BAD DIARRHEA (SCALDING DIARRHEA); SWEATING (SWEAT WAS POURING OFF HER); FEVER; PUKEY; INJECTION SITE WAS A LITTLE TOUCHY WHEN SHE LAID ON IT AT NIGHT, HAD SOME PROBLEMS SLEEPING; This spontaneous report received from a patient concerned an 81 year old female. The patient's weight was 62.6 kilograms, and height was 161 centimeters. The patient's concurrent conditions included: penicillin allergy, and vision problems (She reported that her vision has been going downhill with her age for a long time. Her eyes were going faster than her body. She had to go to the eye doctor and the machines were all germy), and other pre-existing medical conditions included: Patient reported that she used to be 125lbs but has Covid pounds. Patient reported that she was never sick and did not taken any medications. Patient reported that she does not do anything else medically except foods and takes in plenty of Zinc and Vitamin D. Patient did not have any past medical history or illness at time of vaccination with Pfizer covid-19 vaccine. The patient was previously treated with covid-19 vaccine ad26. cov2. s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1802068 and expiry: UNKNOWN) dose was not reported, 1 total, administered on 02-APR-2021 for covid-19 prophylaxis. It was unknown if patient experienced any adverse event after covid-19 vaccine ad26. cov2. s (dose number in series 1). The patient received covid-19 vaccine ad26.cov2.s (dose number in series 2) (suspension for injection, route of admin not reported, batch number: 213D21A and expiry: UNKNOWN) dose was not reported, 1 total, administered on 19-NOV-2021 for covid-19 prophylaxis. Age at time of vaccination 80 years old. Concomitant medications included ergocalciferol and zinc for used for unknown indication. It was unknown if patient experienced any adverse event after covid-19 vaccine ad26. cov2. s (dose number in series 2). The patient additionally received non-company suspect vaccine included: Pfizer Biontech Covid-19 vaccine (tozinameran) (dose number in series 3) (form of admin, and route of admin were not reported, batch number: FN2908 and expiry: UNKNOWN) dose was not reported, administered on 15-JUL-2022 in left arm for covid-19 prophylaxis. On 15-JUL-2022 11:11 , the patient had some problems sleeping because the arm she laid on. Patient did not have any pain at the injection site, but reported that it was a little touchy when she laid on it that night (dose number in series 3). On 16-JUL-2022, at around 36-48 hours after the vaccine the patient experienced sweat was pouring off her, she was pukey, sweating, figured she had a fever, so she drank plenty of water (dose number in series 3). On 17-JUL-2022 (12hrs into the sweating), she had bad diarrhea. It was a scalding diarrhea. She had to get A&D ointment. Patient reported that by the end of the third day (18-JUL-2022) it was all over and everything went away (dose number in series 3). The patient did not visit emergency room or physician office for the events. On 15-JUL-2022, the patient experienced injection site was a little touchy when she laid on it at night, had some problems sleeping. On 16-JUL-2022, the patient experienced sweating (sweat was pouring off her), fever, and pukey. On 17-JUL-2022, the patient experienced bad diarrhea (scalding diarrhea). The action taken with covid-19 vaccine ad26.cov2.s, and tozinameran was not applicable. The patient recovered from sweating (sweat was pouring off her), fever, bad diarrhea (scalding diarrhea), and pukey on 18-JUL-2022, and the outcome of injection site was a little touchy when she laid on it at night, had some problems sleeping was not reported. This report was non-serious.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Penicillin allergy; Visual disturbance (She reported that her vision has been going downhill with her age for a long time. Her eyes were going faster than her body. She had to go to the eye doctor and the machines were all germy.)
Vorgeschichte: Comments: Patient reported that she used to be 125lbs but has Covid pounds. Patient reported that she was never sick and did not taken any medications. Patient reported that she does not do anything else medically except foods and takes in plenty of Zinc and Vitamin D. Patient did not have any past medical history with Pfizer covid-19 vaccine.
Andere Medikamente: ZINC; VITAMIN D [ERGOCALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2396478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN 2908

moderat

Staat: CO
Alter: 52,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 27.07.2022
Beginn: 27.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Mobility decreased

Symptomtext

About 9 hours after getting the vaccine, my wrist started hurting like I had sprained it. I couldn't twist my wrist.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia Overweight
Andere Medikamente: Lyrica
Allergien: None
Vorherige Impfungen: -

VAERS 2395869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: FL
Alter: 51,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 15.07.2022
Beginn: 17.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / LA

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

Migraine

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 15Jul2022 at 11:00 as dose 4 (booster), single (Lot number: FN2908) at the age of 51 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "ehlers danlos syndrome" (unspecified if ongoing); "hypothyroid" (unspecified if ongoing); "seafood allergy" (unspecified if ongoing); "yellow dye" (unspecified if ongoing), notes: Yellow dye number 5. Concomitant medication(s) included: LEXAPRO; LITHIUM; SYNTHROID; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; BACLOFEN. Vaccination history included: BNT162b2 (Dose Number: 3 booster, Batch/Lot No: FN2590, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM), administration date: 22Oct2021, when the patient was 50-year-old, for Covid-19 immunization; Covid-19 vaccine (Primary immunization series completed, Manufacturer unknown.), for Covid-19 immunization. The following information was reported: MIGRAINE (non-serious) all with onset 17Jul2022 at 02:00, outcome "not recovered" and all described as "migraine headaches bilateral". The event "migraine headaches bilateral" required physician office visit. Therapeutic measures were taken as a result of headache, migraine. Additional information: Dose number 1 (Lot FN2590) given at left arm on 22Oct2021 and dose number 2 (Lot FN2908) given at Left arm on 15Jul2022. The patient did not get these side effects with first pfizer booster. Prescriptions for ubrelvy and Imitrex as treatment of adverse events.

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Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to chemicals (Yellow dye number 5); Ehlers-Danlos syndrome; Hypothyroidism; Seafood allergy
Andere Medikamente: LEXAPRO; LITHIUM; SYNTHROID; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; BACLOFEN
Allergien: -
Vorherige Impfungen: -

VAERS 2394885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 27.07.2022
Beginn: 27.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Blood pressure increased Chest pain Dizziness Headache Palpitations

Symptomtext

Pt received pfizer booster dose. during observation period 5 mins after vaccination, pt felt palpitations and dizziness. Pain 10/10 in upper/mid chest region, and in the back of her head. Pt's BP elevated 178/104 other vitals WDL. EMS called and pt was taken to ED for further evaluation.

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

VAERS 2387834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MN
Alter: 73,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 14.07.2022
Beginn: 17.07.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: SYR / RA

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

Ataxia Blood pressure increased Bundle branch block left Coordination abnormal Defect conduction intraventricular Echocardiogram abnormal Electrocardiogram abnormal Hypertension Hypotension Posture abnormal Troponin increased

Symptomtext

1. Mild ataxia ? postural imbalance/lag in coordination 2. Rising BP (from hypotension to hypertensive) 3. Rise in TROPONIN. 60, 96 4. Change in heart imaging from 7/14 echocardiogram (pre vax) to 7/19 limited echo. Interventricular delay to incomplete LBBB on ekgs Overnight ER to Observation admission. Hospital

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: See 18 above. Had echocardiogram just before vax. Ltd echo in hospital reflected changes. Troponin mildly elevated and rising. Ataxia resolved quickly; BP stabilized
Aktuelle Erkrankungen: Gyn cancer (high grade serous)
Vorgeschichte: Gyn cancer, benign arrythmias (PSVT/PAC)
Andere Medikamente: Flecainide, miralax, citrucel, vitamin D, super B complex
Allergien: Hydrocodone, sulfa, chromalyn, adhesive, cremaphor EL/pacliz
Vorherige Impfungen: -

VAERS 2379723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NE
Alter: 37,0
Geschlecht: M
Eingang: 22.07.2022
Impfdatum: 22.07.2022
Beginn: 22.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Cough Dysphagia Paraesthesia oral Throat irritation

Symptomtext

Patient complained of scratchy throat, tongue tingling , cough and difficulty swallowing 15 minutes after administering vaccine. Administered 50mg, Benadryl IM, after 15 minutes patient continued to complain of difficulty swallowing and was administered 0.3mg, Epinephrine, IM. Monitored patient for 1 hour until symptoms resolved. Patient dismissed in no apparent distress.

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Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Infected sebaceous cyst on 7/12/2022
Vorgeschichte: Asthma, chronic GERD, depression, hypercholesteremia, morbid obesity, obstructive sleep apnea, tobacco abuse
Andere Medikamente: Buproprion, citalopram, pantoprazole, testosterone
Allergien: Peanuts, hepatitis B vaccine, penicillin, tetanus toxoid
Vorherige Impfungen: 11/3/2020, Hepatitis B Vaccine, age 35

VAERS 2379270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 05.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Angiogram cerebral normal Arteriogram carotid normal Computerised tomogram head normal Condition aggravated Headache Magnetic resonance imaging head normal Multiple sclerosis relapse Muscular weakness Perfusion brain scan normal

Symptomtext

Discharge Provider: Medical Doctor Primary Care Provider: Medical Doctor Admission Date: 7/6/2022 Discharge Date: Jul 10, 2022 PRESENTING PROBLEM: Weakness; Weakness of right lower extremity HOSPITAL COURSE: 61-year-old female with a past medical history significant for multiple sclerosis who presents due to complaints of headache and right lower extremity weakness. Patient was seen by EMS. She was overall stable and had no hypoglycemia that time. She was brought into the emergency department where code stroke was called. Patient was found to have an stroke scale score 5. She went for CT scan of the head which showed no acute bleed. Neurology was consulted for further evaluation and the patient was thought to warrant admission to the hospital. Patient did undergo CT angiography of the head and neck as well as CT perfusion scan of the brain. No acute pathology was seen on CT angiogram number CT perfusion scan. Neurology recommended MRI for further evaluation. Patient was admitted to the hospital and did undergo MRI evaluation. MRI was of limited value but it did rule out acute ischemic event. All further imaging did not show any acute pathology. With no interventions, the patient did feel some symptomatic improvement in her right lower extremity weakness. However, the patient states that her symptoms seemed very reminiscent of her previous episodes of MS flare and she inquired as to the use of steroids. Discussion was had with Neurology. Neurology did agree with steroid use. Patient was prescribed methylprednisolone 1 g IV daily for 3 days. With methylprednisolone, patient's strength significantly improved in her right lower extremity. Although patient's strength is improving in her right lower extremity, she was still not back to her baseline state in regards her functional status. Patient was seen in consultation by PT/OT. She was thought to benefit from subacute rehab placement. Patient was discharged to skilled nursing facility on 07/10/2022 in stable condition.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: 6/8/2022 visit for Impetigo
Vorgeschichte: MS (multiple sclerosis) Mixed incontinence urge and stress (male)(female) Neurogenic bladder, NOS Depression Other malaise and fatigue Multiple sclerosis Parasomnia Insomnia Urgency-frequency syndrome Decreased activities of daily living (ADL) Multiple sclerosis exacerbation Lower extremity weakness Other urinary incontinence Hypothyroid Overactive bladder History of atrial fibrillation Major depressive disorder, recurrent, moderate Vitamin D deficiency COVID-19 virus infection Generalized muscle weakness Headache Nausea and vomiting Immunocompromised Acute on chronic Weakness of right lower extremity
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet baclofen (LIORESAL) 10 MG tablet gabapentin (NEURONTIN) 100 MG capsule levothyroxine (SYNTHROID) 175 MCG tablet Multiple Vitamins-Minerals (MULTIVITAMIN WOMEN 50+ PO) oxybutynin (DITROPAN) 5 MG tab
Allergien: NitrofurantoinAsthma/Shortness of Breath AmpicillinShortness of Breath AugmentinShortness of Breath CodeineHallucinations Dimethyl Fumarate Dimethyl Sulfoxide Fish Fish-derived ProductsShortness of Breath
Vorherige Impfungen: -

VAERS 2375031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: HI
Alter: 74,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 06.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Condition aggravated Injection site pain Pain Pain in extremity

Symptomtext

2 days after receiving vaccine - sore arm then next day pain worse. Excruciating sporadic shooting pain in left arm lasting from 5 to 10 minutes. No swelling or redness at shot site.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Metfromin; Syunthroid; Tribenzoe; Aspirin
Allergien: Penicillin and Compazine.
Vorherige Impfungen: -

VAERS 2374705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 19.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / LA

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

Nausea Pain in extremity Palpitations

Symptomtext

arm pain, heart palpitations, nausea,

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: rheumatoid arthritis, Sjogen's syndrome, Hashimoto's thyroid
Andere Medikamente: levoxyl, folic acid, multi-vitamin, vit d, vit c, astaxanthin, krill oil, biotin currently on Actemra (biologic, infusion administered 07-05-22) and methotrexate (injection, last administered 07-16-22)
Allergien: n/a
Vorherige Impfungen: -

VAERS 2374155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 17.06.2022
Beginn: 06.07.2022
Tage bis Beginn: 19,0
Dosis: 4
Route/Site: SYR / UN

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

COVID-19 Chest discomfort Cough Dyspnoea Malaise Nasal congestion Pyrexia SARS-CoV-2 test positive Sneezing Throat irritation

Symptomtext

Tested positive for COVID-19 on 07/06/2022. I received my 4th dose on 06/17/2022 and my COVID-19 symptoms started on 07/06/2022 in the morning, sneezing; coughing; fever 99.2; congestion of nose; scratchy throat; compression in the chest. I felt like I was having trouble breathing. My husband went to the nearest pharmacy to get some advise from the pharmacist, said to take cold medication and beeline; precede mole; I took the medication for 5 days straight regularly. When my symptoms were getting better I took it less. I am still recovering from it.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Home COVID-19 test.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; hypothyroidism
Andere Medikamente: Losartan; levothyroxine; vitamin B12; vitamin D
Allergien: Hydrocodone; latex; cats
Vorherige Impfungen: -

VAERS 2370743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 09.07.2022
Beginn: 10.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Ankylosing spondylitis Arthralgia Condition aggravated Pyrexia

Symptomtext

The next morning after vaccine, I had a fever and had severe joint pain. The next day I had a flare in the bottom of my spine, where I have Ankylosis Spondylitis. I saw my Rheumatologist yesterday (07/15/2022) and got prescription for Prednisone. I'm not sure if I'm going to take it because it makes me nauseas. Right now I'm sleeping on a heating pad as I'm still in pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Ankylosing Spondylitis; Psoriatic Arthritis; Rhumetoid Arthritis; Bipolar; Diabetic
Andere Medikamente: Seroquel; Pantoprazole Sodium; Levothyroxine; Lyrica; Tramadol HCI; Lisinopril; Jardiance; Loratadine glycopyrrolate; Eliquis; Meloxicam; Orencia - monthly infusion
Allergien: Baclosen; Demerol; Lovastatin; Macrobid; Metformin; Ranitidine; Tegretol; Topamax
Vorherige Impfungen: -

VAERS 2367704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: TX
Alter: 55,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Abdominal pain Back pain Chest pain Dizziness Headache Injection site pain Nausea Throat tightness

Symptomtext

Increased pain during injection. Post injection: headache, dizziness, nausea, chest pain, abdominal and back pain, throat closing .

Weitere VAERSDATA-Felder

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

VAERS 2367458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 15.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Condition aggravated Confusional state Culture urine positive Disorientation Electroencephalogram normal Enterococcus test positive Exposure to SARS-CoV-2 Mental status changes Metabolic encephalopathy Patient restraint SARS-CoV-2 test positive Urinary tract infection

Symptomtext

Discharge Provider: Primary Care Provider : 6/28/2022 - 7/11/2022 (13 days) Hospitals - PRESENTING PROBLEM: Acute metabolic encephalopathy HOSPITAL COURSE: Patient is an 89 year old with PMHx of CAD, CLL, CAD, Parkinson's who presented to the hospital with acute metabolic encephalopathy. Patient recently admitted for a similar event from 6/3-6/15, found to have enterococcus UTI. Extensive work up at that time including MRI, EEG, and LP were unremarkable. Patient was able to have improvement on its own as the UTI was treated. Patient was re-admitted, Urine + for UTI, growing enterococcus again. Patient also + for COVID-19, family members were sick prior to admission. Patient was very confused again, not oriented to anything. He had an EEG done which was negative. Neurology consulted, and recommended treating underlying infections. Patient required restraints early in his hospital stay. Slowly his mental status improved. He was evaluated by SLP and PT/OT who recommended subacute rehab. Patient was switched to amoxicillin to completed a 14 day course of treatment. Patient was recommended to follow up with Urology as an outpatient to evaluate his recurrent UTIs. Patient had to stay in COVID isolation until he was cleared for subacute rehab. Patient was ultimately discharged to Assisted living with home therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: Admitting Physician: Discharge Attending Physician: Primary Care Physician at Discharge: Admission Date: 6/3/2022 Discharge Date: 6/14/22 HOSPITAL COURSE: The patient is a 89 year-old M with pmh of Parkinson's disease who presented after a ground level fall. He was found by a family member and arrived to hospital via EMS. He was unsure of how he lost consciousness. At the hospital, CT scan showed small areas of hypoperfusion R temporal and R occipital lobes. A possible worsening left pca stenosis was also noted. Initial CXRs showed L rib fractures 6-8 and R rib fractures 7-8. The patient was admitted to the surgical intensive care unit. While in the SICU the patient developed episodes of altered mental status with lethargy and an extensive workup was pursued. This included an MRI brain, continuous EEG, lumbar puncture, and neurology consult. MRI was negative for abnormality, cEEG did not show any seizures or epileptiform activity, lumbar puncture was insignificant, and neurology signed off during hospitalization. The patient was found to have a UTI which was treated. Gradullay during the hospitalization, the patient's mental status gradually improved, and it was thought the patient had suffered from toxic metabolic encephalopathy with episodes of hospital delirium. Throughout his hospitalization, the patient worked with the PT/OT/and SLP teams who recommended skilled nursing facility. By 6/15 this was arranged, and the patient was medically cleared for discharge. On 6/15 the patient was discharged in stable condition. PRESENTING PROBLEM and ADMISSION DIAGNOSIS Closed fracture of multiple ribs of both sides, initial encounter [S22.43XA] Trauma [T14.90XA] Multiple rib fractures involving four or more ribs [S22.49XA] Trauma
Vorgeschichte: Dysphagia ASHD (arteriosclerotic heart disease) Nephrolithiasis GERD (gastroesophageal reflux disease) Anxiety Dyslipidemia HTN (hypertension) History of prostate cancer Erectile dysfunction of organic origin IBS (irritable bowel syndrome) Urinary urgency Family history of colon cancer Personal history of colonic polyps Bilateral carotid artery disease (HCC) Parkinsons disease (HCC) Prostate cancer (HCC) Idiopathic chronic gout without tophus Chronic total occlusion of coronary artery Occlusion and stenosis of bilateral carotid arteries Pure hypercholesterolemia, unspecified Trauma Acute metabolic encephalopathy
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet allopurinol (ZYLOPRIM) 100 MG tablet amLODIPine (NORVASC) 10 MG tablet amoxicillin (AMOXIL) 875 MG tablet aspirin (ECOTRIN LOW STRENGTH) 81 MG enteric coated tablet atropine 1 % ophthalmic solution
Allergien: AtorvastatinMyalgia Morphine SulfateOther Tadalafil
Vorherige Impfungen: -

VAERS 2356628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NJ
Alter: 61,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 19.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Body temperature increased Pyrexia Tremor

Symptomtext

I woke up and could not stop shaking. My hand was shaking so bad (almost like a Parkinson's type shake) that I could not even put a thermometer in (my hands could not stop shaking); had a fever of about 101; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 19Jun2022 at 09:00 as dose 4 (booster), single (Lot number: FN2908) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Chronic daily Migraines" (unspecified if ongoing); "Seasonal allergies" (unspecified if ongoing). Concomitant medication(s) included: GABAPENTIN; CYCLOBENZAPRINE; FROVATRIPTAN; NALTREX. Past drug history included: Levaquin, reaction(s): "Drug Allergy"; Topomax, reaction(s): "Drug Allergy". Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), Lot number: Fh8030, Vaccine Administration Date: 21Nov2021, Vaccine Administration Time: 09:00AM, Vaccine location: Arm Left), administration date: 21Nov2021, when the patient was 61-year-old, for COVID-19 immunization; Bnt162b2 (DOSE 2, Lot number: En6201,, Vaccine location: Left arm), for COVID-19 immunization; Bnt162b2 (DOSE 1, Lot number: El1284,, Vaccine location: Left arm), for COVID-19 immunization. The following information was reported: TREMOR (non-serious) with onset 20Jun2022 at 01:30, outcome "recovered", described as "I woke up and could not stop shaking. My hand was shaking so bad (almost like a Parkinson's type shake) that I could not even put a thermometer in (my hands could not stop shaking)"; PYREXIA (non-serious) with onset 20Jun2022 at 01:30, outcome "recovered", described as "had a fever of about 101". The events "i woke up and could not stop shaking. my hand was shaking so bad (almost like a parkinson's type shake) that i could not even put a thermometer in (my hands could not stop shaking)" and "had a fever of about 101" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of tremor, pyrexia. Additional information: She woke up and could not stop shaking. she hand was shaking so bad (almost like a Parkinson's type shake) that she could not even put a thermometer in (She hands could not stop shaking) she could barely keep the thermometer in She mouth because even She mouth was shaking. She had a fever of about 101 and once She took Tylenol the shaking subsided. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Test Name: temperature; Result Unstructured Data: Test Result:101; Comments: had a fever of about 101
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine; Seasonal allergy
Andere Medikamente: GABAPENTIN; CYCLOBENZAPRINE; FROVATRIPTAN; NALTREX
Allergien: -
Vorherige Impfungen: -

VAERS 2347434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: IA
Alter: 56,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Adverse reaction Chest pain Hypersensitivity Hypoaesthesia Hypoaesthesia oral

Symptomtext

Following vaccination of her covid booster, patient called the clinic and said that she had a reaction within 30 minutes of leaving the clinic and had to use her epi pen. Reported feeling arm numbness, chest pain and tongue numbness and said she had called the local emergency room that instructed her to use her epi pen. We encouraged her to follow up with her provider on her reaction. Patient stated she felt fine within an hour of vaccination and during additional follow up call on 6/29/22 , reported she still felt normal but did not go to the emergency room or doctor in person for follow up care. She did receive her regular allergy injection at her regular doctor on 6/28/22, the day following her injection with no adverse events reported. Discussed that she should talk to her provider about her reaction and that next time she receives a vaccination, in particular a covid vaccination she should check "yes" on the screening form about a history of allergic reactions that require an epi pen so that the clinic is aware and that she should be monitored for at least 30 minutes following vaccination. At the time she received her booster injection on 6/27 she had checked no on the screening form.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Carries epi pen for extreme shellfish allergy
Vorherige Impfungen: -

VAERS 2347356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fn2908

moderat

Staat: VA
Alter: 35,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 28.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Chest discomfort Crying Depression Dizziness Fear Palpitations Suicidal ideation

Symptomtext

I am experiencing Severe Depression, severe Anxiety, and Suicidal ideation. I do not have insurance so I am not able to seek help. I was in perfect mental health before taking the vaccine. Today is my 3rd day and I am very scared of what is going on with me as I am having constant suicidal thoughts and constant crying spells with no apparent reason. On the 3rd day, I am experiencing chest pressure , dizziness and palpitations. But the depression and the suicidal ideation is the major symptoms right now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: I do not have insurance and I am suffering silently!
Aktuelle Erkrankungen: N/A (In perfect health)
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Food and Medication sensitivities not allergies
Vorherige Impfungen: -

VAERS 2344885

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FN2908

moderat

Staat: SC
Alter: 64,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 27.05.2022
Beginn: 22.06.2022
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Exercise tolerance decreased Fatigue Feeling hot Lacrimation increased Myalgia Nasal congestion Nasal discomfort Paraesthesia Photophobia SARS-CoV-2 test positive Sneezing Upper-airway cough syndrome Vaccine breakthrough infection

Symptomtext

My breakthrough infection began about June 22nd with post nasal drip. I tested positive for COVID-19 on Friday. No fever. Oxygen was 99% at Urgent Care. I did not have shortness of breath. On that Friday I had biked 30 miles. On Saturday I had a cough and muscle aches and fatigued. I was unable to hike. I had lots of nasal congestion and began to sneeze a lot. Sunday my head felt hot and eyes were watery. I continued to sneeze. The light was bothering my eyes. My nose began to burn. My skin began to tingle when I touched it. I used ice packs to help. I began to take Paxlovid. My symptoms began to decrease on Monday. As of today, June 30th, I am still taking Paxlovid but I have a bad taste in my mouth and still fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Home COVID-19 nasal swab, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2336017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: FL
Alter: 50,0
Geschlecht: M
Eingang: 27.06.2022
Impfdatum: 20.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Chest pain Induration Muscle tightness

Symptomtext

Date of booster 6/20/2022 at 12:30 pm. Reports woke up on 6/21/2022 at 0500 with left mid back ache "feeling internal." Report felt tight and firm. Has been applying OTC icy hot and icing without relief. Referral to PCP or for further evaluation and work up due to symptoms not improving over the last 7 days. Continues to complain of "positional internal left back pain" without relief with OTC conservative management.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Rest, ice and heat area as needed. Biofreeze as needed. Discussed with patient referral to primary care provider or (Urgent Care setting) for further evaluation and work up as he may needs lab work, urine, diagnostic testing per that clinic provider's discretions. Discussed with patient physical exam in employee health clinic was within normal limits except positional complaints of left side thoracic aspect pain.
Aktuelle Erkrankungen: none
Vorgeschichte: HTN, DM
Andere Medikamente: Metformin, Trulicity, Rosuvastatin, Pioglitazone
Allergien: none
Vorherige Impfungen: -

VAERS 2335448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fn2908

moderat

Staat: OH
Alter: 51,0
Geschlecht: M
Eingang: 26.06.2022
Impfdatum: 25.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Condition aggravated Fatigue Tinnitus

Symptomtext

Chills fatigue, mainly very Large increase in tinnitus, happened after 2nd dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Huge increase in tinnitus which I have mildly had for years, no major hearing loss with it. It happened after the 2nd shot as well and was starting to subside a little bit after a year, until my 3rd shot. I never would have received any shots at all, ever, but it is almost a requirement for travel.
Aktuelle Erkrankungen: None
Vorgeschichte: None, unless mild tinnitus is a health condition
Andere Medikamente: Losartan
Allergien: None known
Vorherige Impfungen: 2nd covid shot 5/3/21 lot ew0172

VAERS 2332402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: OR
Alter: 76,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 21.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Atrial fibrillation Condition aggravated

Symptomtext

Patient called health clinic on 6/24/2022 to report that the evening before she went into A-fib and had to be seen by urgent care. She also was seen on 6/24/2022 by her PCP and talked with her cardiologist on 6/24/2022. She reports she had a prior history of A-fib but has been without an issue for 4 years until last evening. She is still currently in A-fib.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: CKD
Vorgeschichte: None noted at time of vaccination. On 2/24/2022 reported history of A-fib.
Andere Medikamente: -
Allergien: None noted on COVID19 screening and consent form
Vorherige Impfungen: -

VAERS 2328809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: FL
Alter: 46,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 21.06.2022
Beginn: 22.06.2022
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 Injection site erythema Injection site nodule Injection site pain Injection site swelling Injection site warmth Paraesthesia

Symptomtext

Patient reports after receiving 3rd dose (booster) to left upper extremity the injection site became painful, red, warm to touch, raised knot over injection site, pain to axilla, tingling to left fingertips. Reports pain near injection site/armpit with range of motion of left upper extremity. Reports she has taken Ibuprofen and iiced the injection site without relief. States the redness to injection site has increased in size over night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Keflex 500 mg PO TID X 7 days. Continue icing area every 2 hours for 20 minutes. Follow up in clinic on 6/27/22 at 3 pm for left injection site evaluation.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Yaz
Allergien: none
Vorherige Impfungen: -

VAERS 2327244

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NC
Alter: 20,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 15.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Chest pain Hypoaesthesia Palpitations Paraesthesia

Symptomtext

Pt states about 2 hours after vaccine was given, she developed numbness and tingling in her arm which lasted for about 2 days. Later that same afternoon, she developed chest pain with a pounding sensation in her heart. Denied tachycardia. Chest pain seemed to come and go for a few weeks. Last episode was end of last week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None - Pt had previously received Moderna dose on 04.09.21 at which time she developed itching of her tongue and flu like symptoms. Prior to the Pfizer dose, she was given Benadryl and made to wait app. 30mins prior to vaccine being given.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Eggs
Vorherige Impfungen: Moderna Covid on 04.09.21- itching of tongue

VAERS 2325567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NJ
Alter: 61,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 09.06.2022
Beginn: 10.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Dyspepsia Dysphagia Dyspnoea Extra dose administered Flushing Hyperhidrosis Injection site erythema Injection site pain Pruritus Rash Swelling Throat tightness

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: Patient reported tongue swelling, whole body rash, heartburn, difficulty breathing, and a shingles-like rash all over the body

Weitere VAERSDATA-Felder

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

VAERS 2324028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MO
Alter: 51,0
Geschlecht: F
Eingang: 19.06.2022
Impfdatum: 20.05.2022
Beginn: 20.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Back pain Blood test normal Computerised tomogram Condition aggravated Cyst Gait disturbance Gastrooesophageal reflux disease Magnetic resonance imaging Mobility decreased Pain in extremity X-ray

Symptomtext

Lower half of body (waist down) aches, like one would expect with all over body aches with the flu or like I had with the 2nd dose. Upper body was fine. This started to occur late at night about 10-12 hours after shot on Friday May 20th, 2022. Next morning, symptoms worsened but I carried on. Left home and when returning around 11:30am, had much difficulty ascending stairs as the pain in back and legs were quite noticeable. Laid down and rested. Symptoms continued to get worse and I had to lay in bed with alternating ice and heat packs to get relief. Took Tylenol. Already was on Meloxicam so did not take any more NSAIDS. Ultimately had to start taking Vicodin (I have Rx leftover from a surgery) and only got out of bed to go to the bathroom. By Wednesday, May 25th, the pain was so severe I had to be taken to the ER. X-rays, CT and MRI completed. Finding of Turkic cysts on either side of spine at S1-2. These were considered incidental findings but I was given two steroid injections that helped. While in the hospital, my acid reflux became severe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: 5/25/and5/26/22 Noted in 18 Also numerous blood tests not showing anything else wrong.
Aktuelle Erkrankungen: Seasonal allergies
Vorgeschichte: Migraine Depression Anxiety Fibromyalgia Vit D deficiency Restless leg syndrome Insomnia Obstructive sleep apnea Acid reflux
Andere Medikamente: Wellbutrin Viibryd Meloxicam Mirapex Vit D iron Vit C Omeprazole Osteo BiFlex Triple Strength Preservision AREDS2 Dulcolax Emgality
Allergien: Sulfa Gabapentin Vicryl sutures
Vorherige Impfungen: -

VAERS 2323193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: TN
Alter: 28,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 11.06.2022
Beginn: 11.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Ageusia Discomfort Headache Hypoaesthesia Paraesthesia Pyrexia

Symptomtext

She felt feverish later in the evening after receiving her vaccination, but this resolved. At approximately 2300-000 that night she had an "extreme headache" lasting approximately one hour. She took Tylenol with little relief. She states at the time of the headache, she immediately experienced numbness from her left temple to her chin that has not resolved. She continues to experience pressure, tingling, and a loss of taste on the left side only. She denies facial drooping, difficulty swallowing, changes in facial movements, or any other concerns.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Patient reports that she has not received medical care due to lack of ability to pay. We recommended that she go to the ED and provided the contact information for free or sliding scale clinics in our area.
Aktuelle Erkrankungen: Unknown. She did report that she had not experienced any symptoms in the 24 hours before vaccination.
Vorgeschichte: History of conversion disorder
Andere Medikamente: Unknown- unable to reach patient. Phone number is out of service at this time.
Allergien: Vancomycin
Vorherige Impfungen: -

VAERS 2316612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

moderat

Staat: MD
Alter: 43,0
Geschlecht: F
Eingang: 11.06.2022
Impfdatum: 06.06.2022
Beginn: 06.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Dysphagia Headache Hypertension Throat tightness

Symptomtext

Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Headache-Mild, Systemic: Hypertension-Medium

Weitere VAERSDATA-Felder

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

VAERS 2314373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MA
Alter: 18,0
Geschlecht: M
Eingang: 09.06.2022
Impfdatum: 09.06.2022
Beginn: 09.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Blindness Blood pressure decreased Chest pain Ear discomfort Hyperhidrosis

Symptomtext

Patient started to lose vision and ears were blocked about 3 minutes after receiving vaccination. Patient complained of chest pain. Patient was diaphoretic, BP dropped to 70/50s, and HR was in the 40s. Gave patient Benadryl and was immediately more aware and awake

Weitere VAERSDATA-Felder

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

VAERS 2311712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: RI
Alter: 15,0
Geschlecht: F
Eingang: 07.06.2022
Impfdatum: 07.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Dyspnoea Hyperhidrosis

Symptomtext

COVID vaccine dose booster (third vaccine) Mom present no questions at present. Epi pen on hand. Multiple allergies. No reported concerns with previous 2 doses. Pfizer 12 yo and older. 30 min. Watch 15 minute of watch;mom came out of room, patient anxious c/o SOB asking for her inhaler. She had spacer with her but no albuterol. Mom had epi pen with her. This writer (registered nurse) used auto inject through her pants to right thigh. 12:03pm 0.3mg Epi Initial Pulse ox 100% Ap120 100 % non breathing No audible wheezing +diaphoresis, hunched over, AP initially 120s at 100% Benadryl1 25 mg PO at 12:21pm Patient calming down, ice to nape of neck 130/76 AP 87 Refocused breathing with 100% non rebreather that was placed early on. Transporting no more concerns. Lungs with excellent air movement in all fields To ED for rebound monitoring. Doctors assisted in evaluation and response. Registered nurse assisted in transport, oral medication Pulse oc, registered nurse. Supervisor registered nurse, certified, on hand. To ED with registered nurse and medical doctor, with O2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ED department continued tx and assessment from this point. Will defer further tx/evaluation outside of this clinic.
Aktuelle Erkrankungen: unknown
Vorgeschichte: Mild persistent asthma without complication Allergy ALLERGIC RHINITIS NOS Nut allergy Left tibia vara Eczema OBESITY NOS Status post osteotomy
Andere Medikamente: albuterol (PROVENTIL HFA;VENTOLIN HFA) 90 mcg/actuation inhaler cetirizine (ZYRTEC) 10 MG tablet diphenhydrAMINE (BENADRYL) 25 mg capsule EPINEPHrine (EPIPEN) 0.3 mg/0.3 mL auto-injector EPINEPHrine (EPIPEN) 0.3 mg/0.3 mL auto-injector ergo
Allergien: peanuts, nuts, seasonal, dogs, cats
Vorherige Impfungen: -

VAERS 2310784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 06.06.2022
Impfdatum: 31.05.2022
Beginn: 31.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Abdominal pain upper Arthralgia Back pain Breast tenderness Dry eye Eye pain Fatigue Headache Lymphadenopathy Muscle twitching Musculoskeletal chest pain Musculoskeletal stiffness Pain in extremity Paraesthesia Peripheral swelling Pruritus Pyrexia Rash

Symptomtext

Sore right arm, increased stiffness in neck and shoulders, intermittent headache, right hand tingling (thumbs and fingers) and slight swelling of thumb and last 2 fingers on right hand, right thumb pain at base, right side stomach pain moving to just below center rib cage, left thumb pain at base, pain over left eye, fatigue, sneezing, dry eyes, swelling of left and right arm pit lymph nodes, fever in the evening of 6/1 and 6/2, sinus congestion, off and on sharp cramping in right knee the evening of 6/1, two lumps on right arm above elbow by 6/2 morning (became rashy, swollen and hot/itchy, looked like sunburn), left breast tenderness, back and leg aches. noticed muscle twitch above right elbow on 6/4. Took

Weitere VAERSDATA-Felder

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

VAERS 2305587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: NJ
Alter: 66,0
Geschlecht: M
Eingang: 01.06.2022
Impfdatum: 01.06.2022
Beginn: 01.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Epistaxis Hypertension

Symptomtext

pt wife called around 4:39pm stating that pt had received a 2nd booster for his pfizer. stated once he reached home he developed a watery nose bleed. bleed was somewhat managed by tilting his head and applying pressure on it with papertowel. pt's wife was questioning if the vaccine had anything to do with the nose bleed. upon checking in with pfizer prescriber info there was no mention of such side effect in the package insert. asked to pt to see medical attention via urgent care if the nose bleed dose not stop or he feels light headed. pt's wife states she will go to urgent care and keep us informed. pt's wife called back at 7:59pm with update. upon visit to urgent care. the pt bp was checked and it was hypertensive BP>200/100 mmHg. He was taken to ER by wife and being treated for high bloodpressure. pt will follow up with the cardiologist re: bp medications and get it re-evaluated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: PT TREATED FOR SINUS INFECTION WITH ABX/STEROID
Vorgeschichte: BLOOD PRESSURE DIABETES
Andere Medikamente: SIMVASTATIN MINOXIDIL LISINOPRIL BYSTOLIC CLARITIN FLONASE METFORMIN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2305111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: IA
Alter: 29,0
Geschlecht: F
Eingang: 01.06.2022
Impfdatum: 31.05.2022
Beginn: 31.05.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal discomfort Body temperature increased Dizziness Pain Tremor

Symptomtext

First started with full body aches and shakes, temperature went up and heart rate remains resting at around 95 beats per minute before vaccine it was 60 bpm, feeling lightheaded and dizzy with an upset stomach.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid 3 weeks prior
Vorgeschichte: None
Andere Medikamente: None
Allergien: Amoxicillin
Vorherige Impfungen: Gardasil

VAERS 2303830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MN
Alter: 54,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 31.05.2022
Beginn: 31.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Chest discomfort Cough Dyspnoea Oropharyngeal discomfort Paraesthesia

Symptomtext

Pt. arrived at the COVID vaccination mass clinic today for her 2nd Pfizer booster. Per the patient, she requested to be observed in our observation area. She was noted to have no past history of anaphylaxis, allergies to the vaccine or vaccine ingredients or any past reaction to any of her COVID vaccines. She received her booster dose at approximately 1307. When she was checked in to the observation area the patient explained to the observation nurse that she experienced chest tightness, SOB, a tickling cough and left arm tingling with her 2nd dose of Pfizer vaccine requiring 2 puffs of Albuterol. She also explained that she has a history of chest tightness with exposure to cats and exercise but has no formal asthma diagnosis and no cardiac history. Her 3rd dose of Pfizer (1st booster) occurred without incident. While in observation, at approximately 1330, she noted a repeat of some of her prior symptoms, chest tightness 2/10 on 0-10 pain scale and was noted to have a dry cough. The observation nurse gave the patient Albuterol 1 puff at 1335, repeated at 1340 and 1345. At this time I was alerted to the situation, obtained vital signs, which were stable. Patient symptoms continued to improve. 1415 symptoms were completely resolved. Nursing Assessment: Airway: Open, no visible oral/facial swelling noted, no wheezing noted per auscultation Breathing: Spontaneous, RR 18, unlabored Circulation: BP 134/84, P 79 regular, Sats 98% on RA, cap refill <2 sec, skin pink/warm/dry Disability: RASS 0, GCS 15, no deficits noted

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: unknown
Vorgeschichte: Hashimoto's Thyroiditis
Andere Medikamente: Unknown
Allergien: Amoxicillin - rash Environmental (cats) - chest tightness, cough
Vorherige Impfungen: 1/15/2021, Pfizer COVID vaccine dose 2 Lot EL1283

VAERS 2280581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

moderat

Staat: MA
Alter: 15,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 12.05.2022
Beginn: 12.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Hypoaesthesia Injection site pain Paraesthesia

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe

Weitere VAERSDATA-Felder

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

VAERS 2718021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 56,0
Geschlecht: M
Eingang: 27.11.2023
Impfdatum: 15.06.2022
Beginn: 24.11.2023
Tage bis Beginn: 527,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

Patient presented to ED with weakness and fatigue. No other symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID 19 PCR Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Epilepsy, HTN, Lupus/SLE
Andere Medikamente: -
Allergien: Penicillin, Sulfa, Cipro, Leflunomid, Cefprozil, Erythromycin, Felbamate, Infliximab, Lisinopril, Oxycodone, Carbamazepine
Vorherige Impfungen: -

VAERS 2709736

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge FN2908

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 03.11.2023
Impfdatum: 30.09.2023
Beginn: 30.09.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Asthenia Body temperature Decreased appetite Fatigue Headache Illness Influenza Malaise Nausea Pain Pyrexia SARS-CoV-2 test Sinus disorder Urticaria Vomiting

Symptomtext

Flu; Sinus literally killing me; Horrible body ache; Have no energy; Appetite have been exhausted/no appetite; Have been so sick; Threw up few times; Excruciating Headache; Nauseous; Fever 102.5/100; Not feeling great; Have been exhausted; Hives; This spontaneous case was received on 26-Oct-2023 from other non-healthcare professional (consumer) via Pfizer (reference number: US-PFIZER-INC-202300316345) and concerned a female patient of an unspecified age and gender. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient was vaccinated with Flucelvax Quadrivalent (influenza vaccine inact sag 4v; route of administration, anatomical location, dose, and indication: not reported). The batch number reported was 942309 and expiry date reported was Jun-2023. As reported, the patient did not receive flu shot in 2023. On an unspecified date, the patient was vaccinated with first dose of non-company, co-suspect COVID-19 vaccine (reported as Moderna unspecified vaccine, active ingredients not specified; dose, anatomical location, route of administration and indication: not reported). The batch number reported was 027A2119. On an unspecified date, the patient was vaccinated with second dose of non-company, co-suspect COVID-19 vaccine (reported as Moderna unspecified vaccine, active ingredients not specified; dose, anatomical location, route of administration and indication: not reported). The batch number reported was 064H21A. On an unspecified date, the patient was vaccinated with third dose of non-company, co-suspect COVID-19 vaccine (reported as Moderna unspecified vaccine, active ingredients not specified; dose, anatomical location, route of administration and indication: not reported). The batch number was not reported. On an unspecified date, the patient was vaccinated with non-company, co-suspect COVID-19 vaccine (reported as Pfizer COVID-19 vaccine, active ingredients not specified; dose, anatomical location, route of administration and indication: not reported. The batch number reported was FN2908 and expiry date reported was Sep-2022. On an unspecified date, the patient was vaccinated with non-company, co-suspect COVID-19 vaccine (reported as Pfizer COVID-19 bivalent vaccine, active ingredients not specified; dose, anatomical location, route of administration and indication: not reported. The batch number reported was GJ3274 and expiry date reported was May-2023. On 30-Sep-2023 at about 11.20 am, reported as on Saturday, the patient was vaccinated with non-company, co-suspect Comirnaty vaccine (tozinameran; anatomical location: left deltoid, dose: 0.3 ml, route of administration and indication: not reported). The batch number reported was HG4628 and expiry date reported was Nov-2023. On an unspecified date, an unknown amount of time after receiving Flucelvax Quadrivalent vaccine, and non-company co-suspect unspecified Moderna COVID-19 vaccine, the patient had rough time and experienced flu for two days. On 30-Sep-2023, an unknown amount of time after receiving Flucelvax Quadrivalent and non-company co-suspect unspecified Moderna COVID-19 vaccines, non-company co-suspect unspecified Pfizer and Pfizer bivalent COVID-19 vaccine and Comirnaty vaccine, the patient was felling so sick. The patient was nauseous and was not feeling great. The patient threw up few times, had no appetite, and have been exhausted. It was reported that sinus was literally killing the patient. At three o'clock, the patient experienced excruciating headache. At six o'clock patient experienced body ache and at eight o'clock terrible fever of 102.5. On an unspecified date in 2023, reported as 24 hours later, the patient woke up with hives. The patient still had headache. Fever was improved to 100. Patient was not throwing up, and sinus was better when patient was up right. The patient took Tylenol (paracetamol) at dose of 325 mg three times a day. On an unspecified date in 2023, reported as this morning, the patient took one Tylenol 325 mg. At the time of initial reporting, the patient was recovering from event fever. The outcome of all events flu, sinus disorder, general body pain, loss of energy, appetite lost, sickness, vomiting, headache, hives, nauseous, feeling unwell and exhaustion was not reported. The reporter did not provide a causality assessment. The event flu was considered to be medically significant by Physician within Seqiruss. Company comment: A patient of unspecified age experienced influenza an unknown amount of time after receiving the suspect product Flucelvax Quadrivalent vaccine, and non-company co-suspect unspecified Moderna COVID-19 vaccine. The patient also developed sinus disorder, general body pain, asthenia, decreased appetite, illness, vomiting, headache, urticaria, nausea, fever, malaise, and fatigue at least approximately nine months after vaccination. The patient's medical history, concomitant drugs, and diagnostic findings were not provided. Due to lack of information and unclear temporal relationship, causality for the event influenza is unassessable. For the rest of the events causality is assessed as not related, based on implausible temporal relationship.; Sender's Comments: A patient of unspecified age experienced influenza an unknown amount of time after receiving the suspect product Flucelvax Quadrivalent vaccine, and non-company co-suspect unspecified Moderna COVID-19 vaccine. The patient also developed sinus disorder, general body pain, asthenia, decreased appetite, illness, vomiting, headache, urticaria, nausea, fever, malaise, and fatigue at least approximately nine months after vaccination. The patient's medical history, concomitant drugs, and diagnostic findings were not provided. Due to lack of information and unclear temporal relationship, causality for the event influenza is unassessable. For the rest of the events causality is assessed as not related, based on implausible temporal relationship.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 2023; Test Name: Body temperature; Result Unstructured Data: 100; Test Date: 20230930; Test Name: Body temperature; Result Unstructured Data: 102.5; Test Date: 2023; Test Name: COVID test; Result Unstructured Data: No COVID
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2621121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: -
Geschlecht: M
Eingang: 25.04.2023
Impfdatum: 01.08.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Fatigue Pain in extremity Vaccination site pain

Symptomtext

fatigue; arm soreness; Injection site soreness in the arm soreness; 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 male patient received BNT162b2 (BNT162B2), in Aug2022 as dose 4 booster, single (Lot number: FN2908, Expiration Date: 14May2023) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: FATIGUE (non-serious), outcome "unknown"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "arm soreness"; VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "Injection site soreness in the arm soreness". Additional information: Caller wanted to know if the Pfizer COVID-19 Bivalent Vaccine meant the vaccine was wearing off, the shelf life for the Pfizer COVID-19 Bivalent Vaccine, if there was safety information for the Pfizer COVID-19 Bivalent Vaccine administered after its beyond use date, if the side effects he experienced with the Pfizer COVID-19 Bivalent Vaccine meant the vaccine was working and if the Pfizer COVID-19 Bivalent Vaccine is different from the Monovalent. Per agent, caller got 4 covid vaccines, primary dose, 2 boosters, and bivalent booster, all of them from Pfizer. He mentioned that he usually felt fatigue and arm soreness for a while. He wanted to know if someone else has experienced this for this long and what to do to feel better. If there was a difference in the formulation that could have caused this. He also mentioned that he didn't have any COVID-19 symptoms, but that if one could get the vaccine with a previous infection of COVID-19 in case he had the infection without being aware. He also wanted to know why sometimes the expiry was placed as 6 months and other times as 10 weeks, given that his vaccine expires on 14May2023. He also wanted to know if his side effects meant that the vaccine was working and if the fact that we're constantly needing boosters means that the vaccine is wearing off. Typically, with the other injections, a few hours later, he started feeling fatigue and then later in the evening injection site soreness in the arm soreness. Sender's Comments: Linked Report(s): US-PFIZER INC-202300163844 same patient/event, different vaccine dose;

Weitere VAERSDATA-Felder

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

VAERS 2612938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 20.07.2022
Beginn: 01.12.2022
Tage bis Beginn: 134,0
Dosis: 4
Route/Site: IM / RA

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

Asthenia COVID-19 Chest X-ray normal Chills Fall Fatigue Fibrin D dimer SARS-CoV-2 test positive Spinal fusion surgery White blood cell count decreased

Symptomtext

12/1/2022- Presents to ED, fall at rehab s/p spinal fusion surgery. C/o fatigue and chills. T-99, BP-139/94. Spo2 96% on RA. Covid + test. CXR- no infiltrates. Ordered bebtelovimab, IV ceftriaxone given in ED, IV decadron and IV remdesivir. Admit generalized weakness l/t mechanical fall Covid. WBC-7.0, D Dimer 345. 12/4/2022-WBC-3.7, continue doxy and ceftriaxone. Spo2-95% on RA. 12/6/2022- WBC-9.7, completed 5 day course remdesivir. Maintained sat of above 95% on RA. Continue deadon Po for 6 more days. Was on ceftriaxone and doxy, will take cefdinir and doxy at home. Discharge to Home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, High cholesterol,
Andere Medikamente: -
Allergien: Bacitracin and Sulfamethoxazole-trimethoprim
Vorherige Impfungen: -

VAERS 2573913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: TX
Alter: 21,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 28.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Lymph node pain Lymph node palpable Lymphadenopathy

Symptomtext

palpable swollen lymph node tender to touch, painful since after vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: Dapsone gel 7.5% topical Tazarotene .045% topical
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2570344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FN2908

mild

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 25.08.2022
Beginn: 26.08.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Skin lesion Urticaria

Symptomtext

UrticariaPruritus tiny sore Narrative: urticaria and tiny sore that isn't healing

Weitere VAERSDATA-Felder

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

VAERS 2569269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 27.01.2023
Impfdatum: 28.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia Arthralgia COVID-19 Cough Decreased appetite Diarrhoea Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I experienced a breakthrough case of COVID-19 with coughing, fever, loss of taste/smell, joint aches, diarrhea, congestion and loss of appetite.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic type 2
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2559478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OH
Alter: 77,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 27.10.2022
Beginn: 05.01.2023
Tage bis Beginn: 70,0
Dosis: 4
Route/Site: SYR / AR

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

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

The first thing in the morning I felt a slight fever and when I took my temperature it was one hundred point something so I took a home COVID-19 test and it was positive so I called my Doctor and he had me come to the parking lot of his office and gave me a nasal swap and that COVID-19 test resulted in positive. Dr suggested Paxlovid and it was prescribed by the Pharmacy and I did use the prescription with no side effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Two Covid-19 tests both positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Acid reflux; Elevated cholesterol
Andere Medikamente: Pravastatin; Pantoprazole; Famotine
Allergien: None
Vorherige Impfungen: -

VAERS 2558245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 30,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pruritus

Symptomtext

Pt stated she got side effect:skin itching on neck area for 10 days, felt fast heart beat for 2 weeks, nausea for 2 weeks after Pfizer vaccination. Pt did not seek medical care. Pt received Novavax as alternative for 2nd dose on 8/24/22. No reaction noted for Novavax at the time of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Unknown to this writer
Andere Medikamente: Unknown to this writer
Allergien: None
Vorherige Impfungen: -

VAERS 2548929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 70,0
Geschlecht: M
Eingang: 03.01.2023
Impfdatum: 28.06.2022
Beginn: 19.12.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Malaise Nausea Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 12/19/22 with symptoms of nausea, runny nose, congestion, fatigue, and cough. I was prescribed Tamiflu, and a z-pack on 12/ 21/22. I was ill for 4 to 5 days before my symptoms began to improve. I am fully recovered with no lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 12/20/22
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Hypothyroidism; High Cholesterol; Blocked Carotid Artery
Andere Medikamente: Lisinopril, Hydrochlorothiazide; Atorvastatin; Levothyroxine; Aspirin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2546943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 94,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 07.06.2022
Beginn: 29.12.2022
Tage bis Beginn: 205,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia COVID-19 Chest X-ray Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient presented to ED for generalized weakness and was found to have a fever upon admission. No clear onset date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Positive COVID 12/29/22, Chest xray 12/29/22 and 12/30/22.
Aktuelle Erkrankungen: -
Vorgeschichte: CKD, Chronic anticoagulation, pacemaker, COPD, Heart block, HTN, Oxygen dependent
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2545732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: TX
Alter: 56,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 28.06.2022
Beginn: 20.12.2022
Tage bis Beginn: 175,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Headache Pain Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

12/20/2022 tested positive on an at home COVID-19 test. No symptoms. Went to doctor. Doctor prescribed PAXLOVID and azithromycin. Had just a slight headache and a runny nose that day. 12/21 developed slight cough with body aches. 12/22 body aches, headache and runny nose stopped. Cough persists to time of reporting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 12/20/2022 tested positive on an at home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Benazepril HCTZ; montelukast sodium; loratadine; multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2539030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MI
Alter: 90,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 18.03.2021
Beginn: 25.09.2022
Tage bis Beginn: 556,0
Dosis: 4
Route/Site: - / -

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

Asthenia Blood culture Blood lactic acid COVID-19 Chest X-ray abnormal Culture urine Laboratory test Pleural effusion Pyrexia SARS-CoV-2 test positive Sepsis Troponin normal Urine abnormality Urine analysis abnormal Urostomy

Symptomtext

92y.o. male with a PMHx significant for bladder cancer, CKD (Stage 4), HTN, CAD, dementia. Pt presents to facility from SAR after patient was found to have multiple days of fever and generalized weakness. He had received tylenol with some relief, but fever persisted, according to family. Family had noticed that patient had cloudy urine in his urostomy bad and they had concern for infection. In the ED, patient was worked up for sepsis and covid-19 test was positive. He received IVF bolus, started on Vancomycin and Merrem, labs drawn and blood/urine cultures sent. Troponins were negative, Lactic acid 2.0, UA positive for bacteria, chest xray shows small pleural effusion. Upon arrival to the unit, patient had some difficulty with communication due to language barrier. He is not in acute distress, denies chest pain, shortness of breath, headache, dizziness, nausea, abdominal pain, diarrhea. Spoke with patient's son and daughter over the phone to discuss patient's home medications and history. Disposition - Pt stable for dc today home. Daughter refused home care . Pt to continue home meds except lasix. F/u with specialists

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: 4,0
Labordaten: 9/25 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2531314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: AZ
Alter: 13,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 25.07.2022
Beginn: 31.07.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

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

Rash Skin discolouration

Symptomtext

patient presented to the ED with a rash to her stomach, back, back of legs, and left arm on 7/31/22 after having recieved a Pfizer booster on 7/25/2022. No new clothes, detergent, food. Has been out in the heat. Has not had any sleepovers recently. Rash causes no itching nor pain. Its presentation is not suggestive of viral or bacterial or fungal etiology. No treatment given at that time as it was expected to resolve on its own. Patient presented to the Clinic on 8/30/2022 because the rash was still present, but was not causing any pain or itching. Provider thought it may also be related to the vaccine, as did a dermatologist on 9/1/2022. Patient was scheduled to follow up with the dermatologist on 9/15/22 but has not returned. Called the patient's mother 12/15/2022 to see if the rash had resolved. She said it has, rash is gone but there is spotty discoloration of her skin in those areas. Skin is lighter than it had been prior to the rash. Patient did not get her primary series here, but her primary series was Pfizer and no reactions were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: unknown
Vorgeschichte: None per medical record.
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2528208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CO
Alter: 57,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 29.07.2022
Beginn: 17.10.2022
Tage bis Beginn: 80,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Nasal congestion Pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had low grade fever under 100, fatigue, body ache, nasal congestion, and head congestion. I tested positive for COVID-19 at home. I talked to my doctor, and she did not prescribe me anything.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 10/17/2022, COVID-19 Test, Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin; Calcium w/ Vitamin D; Iron; Allegra; Meloxicam
Allergien: Dogs; Dust; Cats; Trees
Vorherige Impfungen: -

VAERS 2519934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 24.05.2022
Beginn: 24.08.2022
Tage bis Beginn: 92,0
Dosis: 4
Route/Site: IM / LA

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

Cough Feeling abnormal Insomnia Pain Pyrexia SARS-CoV-2 test

Symptomtext

I had a fever for a couple of days with achiness. I could not sleep, with an associated cough. I also experienced brain fog for a while.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: At home rapid COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Alendronate sodium; calcium magnesium citrate; vitamin D3; red yeast rice; woman's multivitamin; fish oil
Allergien: Bee stings
Vorherige Impfungen: -

VAERS 2515865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: HI
Alter: -
Geschlecht: F
Eingang: 24.11.2022
Impfdatum: 18.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Fatigue Pain in extremity

Symptomtext

Sore arm; fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An elderly female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Nov2021 at 10:15 as dose 3 (booster), single (Lot number: FN2908), in left arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing), notes: Other Medical History: high blood pressure; "high cholesterol" (unspecified if ongoing); "brain aneurysm" (unspecified if ongoing), notes: Other Medical History: brain aneurysm. The patient's concomitant medications were not reported. Past drug history included: Aspirin, reaction(s): "known allergies: Sensitive to aspirin", notes: known allergies: Sensitive to aspirin; Ibuprofen, reaction(s): "known allergies: Sensitive to ibuprofen", notes: known allergies: Sensitive to ibuprofen. Vaccination history included: BNT162b2 (DOSE 1, lot number: EW0153, location: Left arm), administration date: 14Apr2021, for Covid-19 immunization, reaction(s): "Sore arm", "fatigue"; BNT162b2 (DOSE 2, lot number: EW0167, location: Left arm), administration date: 05May2021, for Covid-19 immunization, reaction(s): "Sore arm", "fatigue". The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Sore arm"; FATIGUE (non-serious), outcome "unknown". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Aneurysm (Other Medical History: brain aneurysm); Blood pressure high (Other Medical History: high blood pressure); High cholesterol
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2509627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: VI
Alter: 74,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 11.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

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

Blister Eye pain Headache Herpes zoster

Symptomtext

He developed Shingles on his left scalp, left eye, and left ear. He had pain in his eye and headaches. He was given valacyclovir HCL and methylprednisolone. He has completed both of the prescriptions. He still has blisters, but the symptoms have improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Bacterial and viral infection in toe
Vorgeschichte: Kidney Disease; Hypertension; Coronary Heart Disease
Andere Medikamente: Atorvastatin; aspirin; famotidine; amlodipine; alopurinol; doxycycline hyclate
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2504625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MI
Alter: 38,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 19.01.2021
Beginn: 14.09.2022
Tage bis Beginn: 603,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

09/14/22 presents to ED for "abdominal pain". PMHx of "MVP, HOCM, GERD, depression, and hypothyroidism"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 09/15/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2504565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OH
Alter: 83,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 16.07.2022
Beginn: 15.10.2022
Tage bis Beginn: 91,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Headache Illness Myalgia Pyrexia SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

Tested positive for COVID-19, illness resulted in hospital admission. Symptoms include fever, myalgia, and headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: 2,0
Labordaten: Nasal Swab collected 10/15/2022 detected 2019 Novel Coronavirus RNA on 10/15/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: SC
Alter: 22,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 19.09.2022
Beginn: 20.09.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site rash Rash Rash erythematous Vaccination site erythema Vaccination site urticaria

Symptomtext

On 9/19 /22 - several hours after vaccination, developed itching and redness at vaccine site. On 9/20/22 noticed bumps at the injection site. On 9/21/22 noticed had a red bumpy rash over entire body. No swelling or difficulty breathing related to rash and itching. On 9/26 reported to work, and told supervisor that she was experiencing a rash. Supervisor sent employee to Occupational Health office. Employee was evaluated by Dr. Prescriptions given to employee: fexofenadine 180mg BID; prednisone 20mg BID x 3 days. No work restrictions per MD and will return for follow-up visit in 1 week. Employee states itching is better, but still has a rash over body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2461821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NV
Alter: 72,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 03.08.2022
Beginn: 07.09.2022
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal discomfort COVID-19 Cough Myalgia Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I experienced a breakthrough case of COVID-19 with heavy congestion, coughing, sore muscles and upset stomach.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: COVID-19 Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 1 Diabetes
Andere Medikamente: Insulin; Sertraline; Propranolol
Allergien: Percocet
Vorherige Impfungen: -

VAERS 2454616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 22.09.2022
Impfdatum: 13.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Hypoaesthesia Pain in extremity

Symptomtext

patient reports vaccine caused LT arm numbness and pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 22.07.2022
Beginn: 07.09.2022
Tage bis Beginn: 47,0
Dosis: 4
Route/Site: UN / UN

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

Asthenia Confusional state Fatigue

Symptomtext

fatigue, weakness, confusion

Weitere VAERSDATA-Felder

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

VAERS 2429633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 37,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 03.06.2022
Beginn: 12.08.2022
Tage bis Beginn: 70,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia COVID-19 Exposure during pregnancy Oropharyngeal pain Paranasal sinus discomfort SARS-CoV-2 test positive Sinus congestion

Symptomtext

I had my 3rd vaccination on 06/03/2022. On 08/12/2022 I started have a sore throat and I brushed it off as allergies as it was so mild. I tested 08/13/2022 COVID-19 positive. I was not put on any prescription but over the counter medication. I developed pretty bad sinus pressure and congestion and my throat was pretty painful. I lost my sense of taste and smell. This is my second pregnancy and my first child. Estimated date of birth is 11/19/2022 but my 40 week gestational period is 12/10/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 08/13/2022 COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Diabetes Type II; ADHD
Andere Medikamente: Prenatal vitamin; folic acid; ZYRTEC; amlodipine; metoprolol; metformin; insulin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2429007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 05.09.2022
Impfdatum: 20.07.2022
Beginn: 24.07.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Electromyogram Nerve conduction studies Neuralgic amyotrophy

Symptomtext

4 d after shot developed sudden onset of severe pain in left shoulder, left arm (same arm shot given in).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: ER visit referred to orthopedic surgeon. Orthopedic surgeon referred to neurologist. Neurologist performed EMG and nerve conduction study. Confirmed diagnosis as consistent with Parsonage Turner Syndrome.
Aktuelle Erkrankungen: Had +Covid-19 test (home test) on July 2nd. Was treated with Paxlovid July 3-7, 2022. Tested negative for Covid (home test) on 7/12/22.
Vorgeschichte: HTN, asthma, and osteoporosis.
Andere Medikamente: Lisinopril w/HCTZ, Raloxifene, Vit D, Albuterol inhaler and K+
Allergien: Keflex
Vorherige Impfungen: -

VAERS 2429362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Nausea Vomiting

Symptomtext

NauseaVomiting Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Employee reported having nausea and vomiting after receiving the 2nd and 3rd (booster) Covid vaccines

VAERS 2429359

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 19.07.2022
Beginn: 19.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Headache Nausea Pyrexia Vomiting

Symptomtext

Headache, Fever & NauseaVomiting Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2429357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 28.07.2022
Beginn: 28.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Headache Injection site discomfort

Symptomtext

Headache DISCOMFORT AT INJECTION SITE. Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2429356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Fatigue Headache

Symptomtext

Headache FATIGUE. Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2429334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 29.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dyspepsia Myalgia

Symptomtext

Myalgia HEARTBURN. Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2429333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 29.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Headache Nausea Vomiting

Symptomtext

Headache & NauseaVomiting Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2427616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 05.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Pain in extremity Throat irritation

Symptomtext

My arm was sore, my throat was itching, like something stocked in the back of my throat, I used a lamp, and it was a white spot, it gets bigger every time. I called my dentist because I had an issue with my teeth and she saw my throat it was recommended for me a doctor, I have an appointment for next week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Auto Immune Disorders
Andere Medikamente: Cyclobenzaprine; trazodone; hydroxyzine; oxybutynin; prazosin; pantoprazole; ziprasidone; topiramate; albuterol; ibuprofen; cetirizine; prochlorperazine; meclizine; infliximab; gabapentin; finasteride
Allergien: Pecans; walnuts; sulfa; latex
Vorherige Impfungen: Every year - Flu vaccine, fever, chills.

VAERS 2427499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OH
Alter: 79,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 25.07.2022
Beginn: 27.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Biopsy artery abnormal Blindness Giant cell arteritis Headache Impaired driving ability Pain in jaw Pyrexia Surgery Vision blurred

Symptomtext

Pt states that two days after vaccine she developed a fever. On the third day she states she developed severe jaw pain. States she went to urgent care and was given 4mg of steroids and that helped for six days but after that the jaw pain "came back with a vengeance". States since the vaccine she has developed headaches, blurry vision, and is now partially blind without possibility of reversal. On August 14th she states she went to Hospital and was transferred to a different Hospital. States she had surgery on August 15th where they did temporal artery biopsy where she was diagnosed with "Giant Cell Arteritis" and is "a rare disease". States she was given IV steroids in the hospital for 3 days and declares she was prescribed 50mg of steroids daily that she must take for 18 months. States she can no longer drive and can only get around her home. States her primary care doctor is private and her specialist is private (Rheumatology)

Weitere VAERSDATA-Felder

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

VAERS 2422734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 29.08.2022
Impfdatum: 28.07.2022
Beginn: 30.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Cellulitis Erythema Joint swelling

Symptomtext

I received pain; redness and swelling in my right wrist lasting 2 days. I was given antibiotics and felt better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: The doctors diagnosed Cellulitis.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Metoprolol
Allergien: N/A
Vorherige Impfungen: -

VAERS 2420999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: PA
Alter: 71,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 22.06.2022
Beginn: 05.07.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: IM / LA

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

Bundle branch block COVID-19 Cardiac pacemaker insertion Chest discomfort Electrocardiogram abnormal Malaise

Symptomtext

Patient given 4th vaccination of Pfizer on 6/22. On 7/5 he developed symptoms and tested positive for COVID. Soon afterwards he started having chest tightness with exertion. Was found to have alternating bundle branch block on EKG on 8/25 and sent to hospital, urgent pacemaker placed 8/26.

Weitere VAERSDATA-Felder

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

VAERS 2419512

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: HI
Alter: 63,0
Geschlecht: F
Eingang: 24.08.2022
Impfdatum: 09.06.2022
Beginn: 02.07.2022
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: IM / RA

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

Dry skin Erythema Impaired work ability Pain in extremity Pruritus Rash Skin exfoliation

Symptomtext

Pt report redness, bumps, pruritis, spreading eventually all over body, went to see Dermatologist, started approximately a month after 3rd dose booster. Arms are now dry, red and peeling. Showed bumps all over body, legs & feet. Patient said had pain in arms and legs that could not go to work. Says she is a masseuse but could not work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: undisclosed skin disorder
Vorgeschichte: -
Andere Medikamente: methotrexate, folic acid
Allergien: vancomycin, penicillin, cipro, bees, cockroach, taro
Vorherige Impfungen: -

VAERS 2418343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 38,0
Geschlecht: F
Eingang: 23.08.2022
Impfdatum: 23.08.2022
Beginn: 23.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Chest discomfort Dizziness Heart rate increased

Symptomtext

Patient started to feel dizzy about 7 minutes after vaccine administered. She then reported squeezing in the chest. Called for RN and provider help in the pharmacy. Patient O2 was 100% and blood pressure was in 120s/80s. Pulse increased to 112 at its peak. Patient reported squeezing would come and go. She thought she might faint, but never fainted. Provider decided to bring her up to clinic for an EKG and further testing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: armpit rash starting 1-2 weeks ago
Vorgeschichte: Fibromyalgia, carpal tunnel syndrome, meniere's disease, sarcoidosis of lung, asthma, vit d deficiency, vit b12 deficiency, GERD, PCO, acne, osteoarthritis, major depressive disorder, s/p laprascopic sleeve gastrectomy
Andere Medikamente: Mupirocin 2% external cream, pregabalin, celecoxib, prazosin, olanzapine, meclizine, ondansetron, lamotrigine, albuterol (as needed), duloxetine, cetirizine, oxybutynin, pantoprazole, sumatriptan, cholecalciferol, cyclobenzaprine
Allergien: no known drug allergies
Vorherige Impfungen: -

VAERS 2417585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OH
Alter: 16,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 18.08.2022
Beginn: 19.08.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Bandaemia C-reactive protein increased Cellulitis Fatigue Headache Immunisation reaction Immunodeficiency Injection site erythema Injection site pain Injection site swelling Laboratory test Leukocytosis Malaise Pyrexia Shift to the left Ultrasound scan normal Vomiting

Symptomtext

Received vaccines on 8/18. Beginning on the evening of 08/18, the patient began to experience unexpectedly severe pain in her L deltoid with associated swelling and erythema. She began to feel fatigued with malaise and a headache shortly after despite taking Tylenol Q6H for her symptoms. This continued until 08/19 when she became febrile to 101 F and experienced one episode of NBNB emesis follow dinner. The patient fevered again to 102 F on the day of admission which prompted her mother to seek care at a health care facility. She was started on IV clinda with rapid improvement within 24 hours. Difficult to say for certain if this was cellulitis vs vaccine reaction. Given her immunocompromised status we decided to be more cautious and treat as a true cellulitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: 2,0
Labordaten: Leukocytosis with left shift and bandemia, fever, elevated CRP and PCT. US showed no fluid collection.
Aktuelle Erkrankungen: -
Vorgeschichte: Evans syndrome ( ITP and hemolytic anemia d/t warm antibodies)
Andere Medikamente: Sirolimus, erythromycin, Nexplanon, desonide ointment for lips
Allergien: Amoxicillin/penicillin
Vorherige Impfungen: -

VAERS 2417303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 01.07.2022
Beginn: 27.07.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / LA

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

Cough Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I received my first Pfizer booster for COVID-19 on 7/1/2022. On the morning of 7/27/2022, I woke up with a sore throat. I have allergies, so I didn't think much of it. I just drank some lemon tea and went about my day. I had a slight headache later that day, which I didn't really give much thought to. I didn't have any other symptoms, but I was babysitting my granddaughter at the time, and she vomited at one point and felt lethargic. When my daughter returned home from a conference, I told her about it, and she suggested that we all get tested for COVID-19. On 7/28/2022, we underwent a PCR test. When I got my results back a few days later, they were positive. On 7/29/2022, I called my doctor's office and got a prescription for Paxlovid. Aside from the abovementioned symptoms, the only real issue I had with the COVID-19 was a slight cough, which lasted for maybe just a day. I took a home COVID-19 test on or about 8/2/2022, and the result was still positive. I didn't take any more tests after that. I just isolated for about 5 days, as I was directed by my doctor, and then came out of isolation and resumed my normal activities afterwards.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 7/28/2022--PCR Test--Positive Result; circa 8/2/2022--Home COVID-19 Test--Positive Result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension; Hypercholesterolemia; Asthma.
Andere Medikamente: Hydrochlorothiazide.
Allergien: Bananas; Walnuts; Pecans; Iodine.
Vorherige Impfungen: After I received the first Pfizer booster for COVID-19, I experienced pain in the left arm and left breast for about 5 days.

VAERS 2415933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: GA
Alter: 35,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 04.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site erythema Injection site pruritus Pain of skin Rash

Symptomtext

Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: scalp pain-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2415912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 19.08.2022
Impfdatum: 05.07.2022
Beginn: 05.08.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / LA

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

Blood test Colitis ischaemic Colonoscopy abnormal Computerised tomogram Diarrhoea Gastrointestinal disorder Large intestinal haemorrhage Pain Stool analysis

Symptomtext

I began to have bowel changes. I would have regular bowel movements, about once a week I would have severe pain and diarrhea. This went on for about 4 weeks. I began bleeding from my colon on August 14th. I went to the ER and was admitted to the hospital and was released yesterday. The diagnosis was Ischemic Colitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 3,0
Labordaten: Blood Panel; Stool Test; Colonoscopy; CT Scan
Aktuelle Erkrankungen: N/A
Vorgeschichte: Anemia; Interstitial Cystitis
Andere Medikamente: Lisinopril; Pravastatin; Vitamin B12; CoQ10; Fish Oil; Premarin Cream
Allergien: Cipro; Shell Fish; Pollen; Dust
Vorherige Impfungen: -

VAERS 2414810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 18.05.2022
Beginn: 03.08.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Decreased appetite Diarrhoea Head discomfort Insomnia Lethargy Paranasal sinus hypersecretion SARS-CoV-2 test positive

Symptomtext

COVID symptomatic 8/3/2022. Positive antigen test - symptoms: diarrhea, head congestion & sinus drainage causing cough, lethargic however had trouble sleeping, loss of appetite

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: antigen test at home
Aktuelle Erkrankungen: none
Vorgeschichte: rosacea
Andere Medikamente: soolantra, restasis, culturelle, fish oil, pantoprozole
Allergien: milk, sulfa drugs
Vorherige Impfungen: -

VAERS 2413540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CT
Alter: 72,0
Geschlecht: F
Eingang: 17.08.2022
Impfdatum: 17.05.2022
Beginn: 12.07.2022
Tage bis Beginn: 56,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Injection site pain SARS-CoV-2 test positive

Symptomtext

My arm hurt for about a day or so at the injection site. I test positive for COVID-19 on 07/12/2022 with a home test. I went to a clinic but they did not let me in. They contacted me while I waited in the car. I was advised I was not eligible to take Plaxlovid due to my current medication. I was referred to the hospital to receive the antibody infusion. I started feeling better in two days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: Home test for COVID-19 and it was positive 07/12/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: Vitamin D; yes
Allergien: None
Vorherige Impfungen: Yes with the senior flu shot last year. I was told they added something to the vaccine which apparently I can not take.

VAERS 2407427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NE
Alter: 10,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 09.08.2022
Beginn: 10.08.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered Pain in extremity

Symptomtext

PT came into the office for her yearly physical on 8/10/22. While in the office, they requested the Pfizer covid booster. 12+ year covid dosage (30 mcg) instead of the 5-11 yr doseage (10 mcg). What had happened is I saw her 2012 birth year and thought that she was 12. I drew up the 30 mcg dose and administered dosage. Today 8/10/22 , a day after the event, notified the provider and mom of event. Aria is feeling fine besides a really sore arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 2407333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 08.07.2022
Beginn: 09.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Chills Fatigue Headache Myalgia Pyrexia

Symptomtext

FEVER - 103, HEADACHE, MUSCLE ACHES, CHILLS, FATIGUE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Synthroid, Omneprozole, D3, calcium
Allergien: -
Vorherige Impfungen: -

VAERS 2407024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: FL
Alter: 20,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 06.08.2022
Beginn: 06.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dizziness

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Additional Details: patient felt a little dizzy and light head. we assisted him to floor, and call rescue. He began to feel better and left on his on

Weitere VAERSDATA-Felder

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

VAERS 2405456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fn2908

mild

Staat: MI
Alter: -
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 01.08.2022
Beginn: 03.08.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / LA

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

Oropharyngeal pain

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Aug2022 at 14:30 as dose 4 (booster), single (Lot number: Fn2908), in left arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing). There were no concomitant medications. Past drug history included: No. Vaccination history included: Moderna (DOSE 3, ;Lot No: Os4e4a; Anatomical location: Arm Left, Vaccine Administration Time: 02:30 PM), administration date: 24Nov2021, for Covid-19 Immunization; Covid 19 (Initial immunization completed: MANUFRACTURER UNKNOWN ), for COVID-19 immunization. The following information was reported: OROPHARYNGEAL PAIN (non-serious) with onset 03Aug2022 at 06:00, outcome "recovering", described as "Sore throat". Therapeutic measures were not taken as a result of oropharyngeal pain. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 15.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: IM / RA

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

Bacterial test negative Diarrhoea Inflammation Stool analysis abnormal

Symptomtext

A week after I received the vaccine I developed crapping, extreme diarrhea, urgency to go to the bathroom. I went to the doctor who prescribed me steroids and is currently looking into changing my medications. She ordered two different types of of stool samples to check for bacteria and inflammation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Stool samples negative for bacteria positive for severe inflammation.
Aktuelle Erkrankungen: No
Vorgeschichte: Ulcerative Colitis
Andere Medikamente: Humira; Jolessa: Pantoprazole; Zyrtec as needed; Turmeric; Multivitamin
Allergien: Mushrooms; Landol
Vorherige Impfungen: -

VAERS 2402946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 20.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Dizziness

Symptomtext

Pt reported dizziness. Vitals: 164/73, 64, 20 Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH: vertigo, HTN, Migraines w/o aura, hx of CVA, OSA, Asthma, GERD, osteoporosis, HLD, aortic valve stenosis, peripheral neuropathy, diverticulosis, glaucoma
Andere Medikamente: Medications: Topiramate 50mg Omeprazole 20mg Montelukast 10mg Ibuprofen 800mg Gabapentin 300mg Flonase Symbicort 80-4.5 Atorvastatin 40mg
Allergien: None
Vorherige Impfungen: -

VAERS 2402560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 26.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Arthralgia Diarrhoea Fatigue Pyrexia Somnolence

Symptomtext

Tiredness/fatigue; Sleepiness; Diarrhea; Joint pain; Fever; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old male patient received BNT162b2 (BNT162B2), on 26Jul2022 as dose number unknown, single (Lot number: FN2908) at the age of 67 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: FATIGUE (non-serious), outcome "unknown", described as "Tiredness/fatigue"; SOMNOLENCE (non-serious), outcome "unknown", described as "Sleepiness"; DIARRHOEA (non-serious), outcome "unknown", described as "Diarrhea"; ARTHRALGIA (non-serious), outcome "unknown", described as "Joint pain"; PYREXIA (non-serious), outcome "unknown", described as "Fever". Additional information: Consumer reported, that he was basically trying to figure out how long these side effects last. He had the COVID shot the Lot# FN2908 on the 26th of July that was Tuesday. Queried for how long these side effects last. Consumer stated, that well it was just on the side effects listed its mentioned to report the side effects and report them to the Pfizer account. Reporter stated that he got the shot on Tuesday, 4 days ago and tiredness, sleepiness, fatigue, diarrhea, joint pain, fever. Reporter stated that patient had no Medical history and not had received any other medication and had not undergone any laboratory test.

Weitere VAERSDATA-Felder

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

VAERS 2401279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: WI
Alter: 55,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 20.07.2022
Beginn: 31.07.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Chest discomfort Cough Lung neoplasm malignant Nasopharyngitis Pruritus Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

I had Cancer treatment on the 18th, COVID-19 shot on the 20th, and a pnuemonia shot on the 25th. My resistance was down and I contracted COVID-19. Started off as just mild cold symptoms- itchy ears, runny nose, coughing, scratchy throat. That started Sunday night and into Monday. I thought it was just allergies, but my boyfriend encouraged me to get tested. I called the Doctor's office and gave them my symptoms and explained that I did not want a rapid test or anything over the counter. I wanted to go to a facility, because my sister had gotten several false positives. I made an appt for a drive through facility and I drove in and got tested and 6 hours later had the positive result. They then gave me the "antiviral hotline" where I completed a self assessment survey to determine if I could receive the antivirals. I am part of a healthcare system and once I had tested positive it notified all of my doctors, like my oncologists, and GP. I was concerned about my cancer treatment and about isolation guidelines, and they were able to guide and comfort me. I started taking Paxlovid yesterday evening, Wednesday. The medicine tastes absolutely horrible, very bitter. It effects my taste buds just like my cancer treatments. Nothing helps with the taste. My throat is still itchy and my ears are itchy and I'm a little congested but not as bad as a few days ago. I have cancer in my lungs so I am always coughing but I could tell the difference between this new cough and I am still coughing a little. My breathing feels better, I had previously experienced some chest pressure, like an elephant.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: -
Vorgeschichte: Stage 3 Breast Cancer; Heart Disease; High Blood Pressure; Diabetes; COPD
Andere Medikamente: Metformin; Atorvastatin ; Azatamine; Cetirizine; Omeprazole; Losartan; Vitamin D3
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2399318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OK
Alter: 75,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 21.06.2022
Beginn: 22.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Rash

Symptomtext

The day after the shot, she got a rash on her right arm, which spread to right trunk and right thigh and buttock. I saw her July 5. Although it was fading, it was still there. I saw her again Aug 2, 2022. The rash was still producing new patches that were flaring up, lasting about a week or two and then fading again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, hypothyroidism, Chron's, wheezing
Andere Medikamente: Albuterol, Aleve, Nebivolol, Olmesartan, Levothyroxine, Tizanidine
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2399057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MD
Alter: 19,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Immediate post-injection reaction Injection site bruising Injection site erythema Injection site haemorrhage Injection site pain Injection site swelling

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Additional Details: Patient's mother reported at she saw the patient bleed at the site of injection immidiately after getting the injection. Patient later report severe pain and swelling at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2398046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 25.07.2022
Beginn: 28.07.2022
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Burning sensation Head discomfort Muscle spasms Muscle twitching Nausea Neuralgia Pain Pain in extremity Vertigo

Symptomtext

3 days after dose 2 vaccine, I started having muscle cramps in lower back and nerve pain shooting into left hip and leg. I was also nauseated possibly due to the pain. The intensity increased over the night and into the next day so I went into the walk in clinic on 7-29. They did not order any tests or labs because he felt it could be a delayed reaction to the vaccine. He prescribed a muscle relaxer but I did not take any and just took TYLENOL. On 7-30 I had to go back to the walk in clinic because I was having vertigo if I turned my head to look in any direction other than straight ahead. The doctor just did a physical workup in the office and also stated these symptoms were likely due to the vaccine. On 7-31, I had a squeezing and burning sensation in my head. Today, 8-1, I feel better but I am having muscle twitching all over. I had COVID19 back in March 2021, and 4-5 months later, I did have muscle twitching at the time and was told by a doctor that I am a long COVID19 sufferer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Ehlers Danlos Syndrome; Von Willebrand's
Andere Medikamente: Vit B12
Allergien: MACROBID; sulfa drugs; DEMEROL; tobramycin; clindamycin; cephalexin
Vorherige Impfungen: -

VAERS 2397965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: LA
Alter: 67,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 11.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Abdominal pain Appendicectomy Appendicitis Blood test abnormal Computerised tomogram abdomen abnormal Gastrointestinal oedema Laboratory test Pyrexia Sepsis

Symptomtext

On 7-12-2022, the day after dose 4 vaccine, I started having very, very bad abdominal pain. It got progressively worse with extreme pain over the course of the day. I went to the emergency room around 4pm and they ran blood tests, CT scan of abdomen and I don't remember what else. They diagnosed me with appendicitis late that night. They admitted me into the hospital and performed an appendectomy on 7-13-2022. I was discharged on the afternoon of 7-14. I was still having abdominal pain and I began running a fever up to 103.5 on that evening of 7-14. I went back to the ER that night and was readmitted back into the hospital with a diagnosis of Sepsis. I was given IV antibiotics and tylenol. I had numerous blood tests and another CT of the abdomen. I am unsure of what the results of any of these tests were. I was discharged on 7-16. I went back to the same ER "just a couple of days ago- maybe Friday 7-29?" due to abdominal cramps and temp of 100.4. They performed more blood work and another abdominal CT scan. They showed bloodwork to be abnormal. They were going to admit me but I wanted to go home and they gave me Cipro and Flagyl. I am unsure of what the final diagnosis was for 7-29-2022 visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 4,0
Labordaten: 7-12-2022 hospital multiple lab tests; CT of Abdomen showed Appendicitis; unsure of what other tests were done; 7-14-2022 Medical Center - multiple lab tests; CT of Abdomen; unsure of what other tests were done; 7-29-2022 (unsure of date) Medical Center - multiple lab tests; CT of Abdomen- result shows post operative change after recent surgery shows persistent right lower quadrant mesenteric edema remains concerning for developing abcess; unsure of what other tests were done
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Hx breast cancer; Depression; Anxiety; Hx Polymyalgic Rheumatica (PMR)
Andere Medikamente: Prednisone; Divalproex; Irbesartan; Bupropion HCL; Pepcid; Calcium with magnesium/vitd3/zinc; Vit B12; K-2 supplement; Biotin;
Allergien: Dilauded; Adhesive sensitivity;
Vorherige Impfungen: -

VAERS 2397607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 30.07.2022
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Chills Cough Decreased appetite Diarrhoea Ear pain Fatigue Lymphadenopathy Malaise Myalgia Pyrexia Renal pain

Symptomtext

cough, tiredness, fatigue, ear ache, muscle pain, chills, joint pain, fever, feeling unwell, decreased appetite, diarrhea Swollen lymph nodes. Kidney pain lower rightside of back. These side effects started on the wve of 07/26/2022 and have persisted to the time of this writing. the kidney pain started 07/28/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Ckd stage 3, major depression, GAD.
Andere Medikamente: brupropion xl 150 mg. 1x daily, mirtazamine 10 mg, 1x at night. glucosamine chondrotine, vit. d
Allergien: ciproflaxine, sulur
Vorherige Impfungen: -

VAERS 2388522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NY
Alter: 52,0
Geschlecht: M
Eingang: 30.07.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Abdominal pain Chest discomfort Dizziness Headache

Symptomtext

Headache all day everyday since vaccinated; abdominal pain for nine days following vaccination; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old male patient received BNT162b2 (BNT162B2), on 12Jul2022 at 16:30 as dose 1, single (Lot number: FN2908) at the age of 52 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Stage II Rectal Cancer 2007", start date: 2007 (unspecified if ongoing), notes: Stage II Rectal Cancer 2007; "Stage IV Rectal Cancer" (unspecified if ongoing), notes: Stage IV Rectal Cancer; "Metastasized to the Liver 2011", start date: 2011 (unspecified if ongoing), notes: Metastasized to the Liver 2011; "If COVID prior vaccination: Yes" (unspecified if ongoing). There were no concomitant medications. The following information was reported: HEADACHE (non-serious) with onset 12Jul2022 at 16:45, outcome "not recovered", described as "Headache all day everyday since vaccinated"; ABDOMINAL PAIN (non-serious) with onset 12Jul2022 at 16:45, outcome "not recovered", described as "abdominal pain for nine days following vaccination". Therapeutic measures were not taken as a result of headache, abdominal pain. Additional information: The patient did not receive any other medications in two weeks. The patient did not receive other vaccine in four weeks. The patient had no known allergies. The patient has not been tested for COVID-19 post vaccination. Device timestamp: 25Jul2022. The reporter assessed the case as non-serious with no seriousness criteria of resulting in death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating, Congenital anomaly/birth defect. AE resulted in none of the above.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Liver metastases (Metastasized to the Liver 2011); Rectal cancer stage II (Stage II Rectal Cancer 2007); Rectal cancer stage IV (Stage IV Rectal Cancer)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2388522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NY
Alter: 52,0
Geschlecht: M
Eingang: 30.07.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Chest discomfort Dizziness Headache

Symptomtext

Headache all day everyday since vaccinated; abdominal pain for nine days following vaccination; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old male patient received BNT162b2 (BNT162B2), on 12Jul2022 at 16:30 as dose 1, single (Lot number: FN2908) at the age of 52 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Stage II Rectal Cancer 2007", start date: 2007 (unspecified if ongoing), notes: Stage II Rectal Cancer 2007; "Stage IV Rectal Cancer" (unspecified if ongoing), notes: Stage IV Rectal Cancer; "Metastasized to the Liver 2011", start date: 2011 (unspecified if ongoing), notes: Metastasized to the Liver 2011; "If COVID prior vaccination: Yes" (unspecified if ongoing). There were no concomitant medications. The following information was reported: HEADACHE (non-serious) with onset 12Jul2022 at 16:45, outcome "not recovered", described as "Headache all day everyday since vaccinated"; ABDOMINAL PAIN (non-serious) with onset 12Jul2022 at 16:45, outcome "not recovered", described as "abdominal pain for nine days following vaccination". Therapeutic measures were not taken as a result of headache, abdominal pain. Additional information: The patient did not receive any other medications in two weeks. The patient did not receive other vaccine in four weeks. The patient had no known allergies. The patient has not been tested for COVID-19 post vaccination. Device timestamp: 25Jul2022. The reporter assessed the case as non-serious with no seriousness criteria of resulting in death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating, Congenital anomaly/birth defect. AE resulted in none of the above.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Liver metastases (Metastasized to the Liver 2011); Rectal cancer stage II (Stage II Rectal Cancer 2007); Rectal cancer stage IV (Stage IV Rectal Cancer)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2396414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: PA
Alter: 67,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 23.06.2022
Beginn: 21.07.2022
Tage bis Beginn: 28,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Headache Malaise Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 on 07/21/2022 with symptoms of headache, runny nose, cough, congestion, and fatigue. I was prescribed PAXLOVID on 07/22/2022. I was ill for 2 days before my symptoms began to resolve. I am fully recovered with no lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 rapid nasal swab home test was positive on 07/22/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: NORVASC; lisinopril
Allergien: N/A
Vorherige Impfungen: -

VAERS 2393249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: VA
Alter: 64,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 20.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / RA

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

Asthenia COVID-19 Chills Cough Fatigue Nasal congestion Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

From time to time I feel a stuffy nose I always do a home test on the 22nd it was negative. Fever, chills, runny nose, fatigue, weak. After going to patient first I started taking over the counter medicine for the fever on the 23rd I was so weak I couldn?t even wake up. On the 25th I stopped taking the meds. Today I have no fever, but I have runny nose, congestion and a weakness and coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home test COVID-19- Positive Urgent Care COVID-19- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure; Prostate Issues
Andere Medikamente: Allegra; Lisinopril; Flomax
Allergien: N/A
Vorherige Impfungen: -

VAERS 2393235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 20.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: SYR / RA

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

Body temperature increased COVID-19 Chills Fatigue Head discomfort Headache Nasal congestion Productive cough SARS-CoV-2 test positive Sputum discoloured Throat irritation

Symptomtext

It started out with a scratchy throat and a slight headache and that started Monday. I took a test, and it was positive. That evening I started with chills I took the Tylenol. I made contact doctor. I had a stuffy head stuffy nose, chills and bad fatigue. My temperature is down, and it had been up to 100.6. Today it is at 99.1. I am having a progressive cough and coughing out something with a yellowish tint.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: At home COVID-19 test- positive
Aktuelle Erkrankungen: Diabetes : High Blood Pressure
Vorgeschichte: Diabetes : High Blood Pressure
Andere Medikamente: Blood pressure medication; Diabetic Medication
Allergien: Allegra
Vorherige Impfungen: -

VAERS 2393125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: IN
Alter: 73,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 25.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Chills Fatigue Headache Pain Pyrexia Vaccine positive rechallenge

Symptomtext

chills, fever, aches, fatigue, headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: blood pressure, high cholesterol
Andere Medikamente: lisonpril, carvedilol. zoloft, levothyroxine, amiodarone, 7.5mg oxycodone, statin at night, vitamins
Allergien: penicillin
Vorherige Impfungen: same symptoms with previous pfizer booster

VAERS 2388069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MD
Alter: 56,0
Geschlecht: M
Eingang: 25.07.2022
Impfdatum: 22.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Asthenia Headache Hyperaesthesia Lethargy Myalgia Nausea Pyrexia

Symptomtext

High Fever, muscle pain and Joint pain throughout body, super sensitivity to touch, nausea, headache, weakness. To put this in perspective, I have had kidney stones 11 times in my life which is painful. This was worse. I contemplated going to the ER, but I did not have the money to spend. So I used tylenol, cool compresses, a hot bath with essential oils, and tried to keep hydrated with water and pedialyte. After about 24 hours I thought I was feeling a bit better. I attempted to get showered, and run a few errands. After about 2 hours, the headache returned and I had muscle and joint discomfort which was not as severe as the pain the day before. I had intermittent fever like symptons as on and of nausea. Today I am starting the day with a headache, and general lethargy. But the day is still young.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none due to finances
Aktuelle Erkrankungen: kidney stones
Vorgeschichte: psoriatice arthritis, anxiety, chronic insomnia, hsv-2,ADD, osteoarthrits
Andere Medikamente: valacyclovir, cosentyx, buproprion,trazodone,adderall, buspar
Allergien: IVP dye, tramadol, lyrica, celebrex
Vorherige Impfungen: To each dose of the COVID vaccine I have had a progressive worsening response. All were Pfizer

VAERS 2387620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 15.07.2022
Beginn: 01.07.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Diarrhoea Hyperhidrosis Injection site discomfort Insomnia Pyrexia Vomiting Weight

Symptomtext

Bad diarrhea; Sweating; she had a fever; she was pukey; She had some problems sleeping; it was a little touchy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 81-year-old female patient received BNT162b2 (BNT162B2), on 15Jul2022 at 11:11 as dose 3 (booster), single (Lot number: FN2908) at the age of 81 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "She is allergic to penicillin though." (unspecified if ongoing); "Vision has been going down hill" (unspecified if ongoing), notes: Vision has been going down hill with her age for a long time. There were no concomitant medications. Vaccination history included: coviD-19 vaccine janssen (DOSE1, SINGLE, Batch Number: 1802068), administration date: 02Apr2021, when the patient was 80-year-old, for COVID-19 immunization, reaction(s): "eyes are going faster than her body"; coviD-19 vaccine janssen (DOSE 2, SINGLE, Batch/Lot Number: 213D21A), administration date: 19Nov2021, when the patient was 80-year-old, for COVID-19 immunization, reaction(s): "eyes are going faster than her body". The following information was reported: DIARRHOEA (non-serious) with onset Jul2022, outcome "recovered" (Jul2022), described as "Bad diarrhea"; INSOMNIA (non-serious) with onset Jul2022, outcome "unknown", described as "She had some problems sleeping"; HYPERHIDROSIS (non-serious) with onset Jul2022, outcome "unknown", described as "Sweating"; INJECTION SITE DISCOMFORT (non-serious) with onset Jul2022, outcome "unknown", described as "it was a little touchy"; PYREXIA (non-serious) with onset Jul2022, outcome "unknown", described as "she had a fever"; VOMITING (non-serious) with onset Jul2022, outcome "unknown", described as "she was pukey". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of diarrhoea. Additional information: Patient was never sick and does not take any medications. She takes certain vaccines, like for tetanus, polio and Covid. She does not do anything else medically except foods. Takes in plenty of zinc and Vitamin D. No other vaccines were administered on the same date of the suspects. On 15Jul2022, after taking the vaccine for the first 12 hours she was fine. At around 36-48 hours after the vaccine there was sweat was pouring off her, she was pukey, sweating, figured she had a fever, so she drank plenty of water. The diarrhea occurred 12 hours after the sweating started, she had bad diarrhea. It was a scalding diarrhea. Patient had to get A&D ointment. By the end of the third day it was all over and everything went away. The sweating and the diarrhea was all she had from it. The events did not require visit to emergency room or physician office. There were no prior vaccinations within four weeks prior to the first administration date of the suspect vaccines. Apart from penicillin allergy patient had no medical History (including any illness at time of vaccination). Patient's family medical history relevant to the event was not provided. No relevant tests done for the events. Patient had vision problem for a long time. She had some problems sleeping because the arm she lays on was a little touchy but she did not have any pain at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Test Name: weight; Result Unstructured Data: Test Result:125 lbs; Comments: Used to be 125lbs, but has Covid pounds.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy; Vision decreased (Vision has been going down hill with her age for a long time)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2381835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: FL
Alter: 50,0
Geschlecht: F
Eingang: 23.07.2022
Impfdatum: 19.07.2022
Beginn: 19.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Flushing Hyperhidrosis Nausea

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium, Additional Details: patient heart rate, blood pressure and oxygen level within normal range. Checked by clinic nurse.

Weitere VAERSDATA-Felder

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

VAERS 2379426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NH
Alter: 53,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abnormal behaviour Affect lability Ammonia Anticonvulsant drug level Bladder scan Computerised tomogram normal Culture urine positive Electrocardiogram Fall Flight of ideas Full blood count Insomnia Irritability Logorrhoea Mental status changes Metabolic function test Tangentiality Urinary incontinence

Symptomtext

07/09 through 07/17/2022: Change of mental status: Increased irritability, intrusiveness, flight of ideas, tangential, labile, hyperverbal, disorganization and vomited x 1. 07/13/2022: Unwitnessed fall; inciting peers. 07/14/2022: Incontinent of urine, U/A negative/culture mixed mucosal flora. Bladder scan 114mL. 07/15/2022: Reduced sleep - Zero hours. 07/16/2022: Reduced sleep - 2 hours. 07/17/2022: Slept 6 hours and then maintained greater than 6 hours/night. 07/18/2022: Less elevated and less irritability.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: 07/14/2022: U/A negative. Bladder scan 114mL. 07/21/2022: Sent to emergency department: CT negative, U/A negative, CBC, CMP, urinalysis, bladder scan, ammonia, valproic acid level and ECG. No significant results.
Aktuelle Erkrankungen: Bipolar disorder, schizoaffective disorder, GERD, constipation, mixed dyslipidemia, bullets in left thigh retained from 1995.
Vorgeschichte: Bipolar disorder, schizoaffective disorder, GERD, constipation, mixed dyslipidemia, bullets in left thigh retained from 1995.
Andere Medikamente: MiraLax, Vitamin D3, Clozapine, Depakote, Zyprexa, Loratadine, Protonix, Risperdal, Colace and Multivitamin. As needed: Haldol, Maalox, Acetaminophen and Melatonin (took during time span).
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2379290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 19.07.2022
Beginn: 19.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Fatigue Flushing Hyperhidrosis Lethargy

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild, Systemic: Flushed / Sweating-Mild

Weitere VAERSDATA-Felder

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

VAERS 2347986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: PR
Alter: 66,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 01.07.2022
Beginn: 01.07.2022
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 refers, after being vaccinated while in the observation area began to feel itching (itching) in the right arm. Evaluation of vital signs is performed and the result is as follows: Oxygenation 99%, 120/80mmHg, 91 heart rate, 15 Respirations per minute, A DEXTRO test is performed with a result of 107mg/dl. According to medical order is performed administration of medication of 25mg Benadryl is left in the area of observation. A reevaluation of vital signs was performed with the result in Oxygenation in 98%, 130/80 mmHg, 77 heart rate, breaths in 16 per minute. Patient withdraws by walking alert, and oriented.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Report does not provide such information.
Vorgeschichte: Report does not provide such information.
Andere Medikamente: Report does not specify that information.
Allergien: Patient refers to being allergic to drugs such as: Sulfa, ASA, Cortisone, in addition to foods such as: mango, lactose, berry's and in addition to pollen, dust, laxatives.
Vorherige Impfungen: -

VAERS 2374997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 16.07.2022
Beginn: 16.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Rash

Symptomtext

Rash on the right hand

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: Eyelid Lesion Solitary osteochondroma
Vorgeschichte: Asthma Obesity
Andere Medikamente: Ventolin HFA Clotrimazole 1% Erythromycin 5mg/gram loratadine 10mg tablets
Allergien: No Known allergies
Vorherige Impfungen: -

VAERS 2373739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: WI
Alter: 61,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 27.05.2022
Beginn: 08.06.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: IM / -

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

Dizziness Magnetic resonance imaging head normal

Symptomtext

patient reports significant issues with dizziness post having vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: MRI of brain, no acute findings.
Aktuelle Erkrankungen: none
Vorgeschichte: BPH, lumbar disc disease, Barretts esophagus, CAD, ventricular tachycardia, non sustained, insomnia, gouty arthritis, GERD, hypertension, gilberts syndrome.
Andere Medikamente: allopurinol, tamsulosin, celebrex prn, flonase prn, eszopiclone prn, gabapentin, metoprolol, ambien, benazapril, crestor, pepcid multivitamin, allegra and aspirin.
Allergien: latex, levaquin and sulfa
Vorherige Impfungen: -

VAERS 2372036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: PA
Alter: 18,0
Geschlecht: F
Eingang: 17.07.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Injection site erythema

Symptomtext

Site: Redness at Injection Site-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2372014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NC
Alter: 46,0
Geschlecht: F
Eingang: 17.07.2022
Impfdatum: 28.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Back pain Muscle spasms Pain Pain in extremity Sciatica

Symptomtext

Systemic: SCIATICA PAIN, RADIATING FROM SPINE TO LOWER BACK PROGRESSING TO THE THIGH/CALF AREA WITH CRAMPING-Medium

Weitere VAERSDATA-Felder

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

VAERS 2371781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 11.07.2022
Beginn: 12.07.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Fatigue Lymph node pain Lymphadenopathy Pyrexia Vaccination site pain

Symptomtext

Extremely swollen gland under arms; Pain in glands; Pain in shot site/Shot arm left arm worse; slight fever; tiredness; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 11Jul2022 at 17:30 as dose 1, single (Lot number: FN2908) at the age of 63 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Coconut" (unspecified if ongoing). Concomitant medication(s) included: ATENOLOL; PREMARIN. Past drug history included: Macrotatin, reaction(s): "Allergy"; Benydryl, reaction(s): "Allergy". The following information was reported: LYMPHADENOPATHY (non-serious) with onset 12Jul2022 at 07:00, outcome "not recovered", described as "Extremely swollen gland under arms"; LYMPH NODE PAIN (non-serious) with onset 12Jul2022 at 07:00, outcome "not recovered", described as "Pain in glands"; VACCINATION SITE PAIN (non-serious) with onset 12Jul2022 at 07:00, outcome "not recovered", described as "Pain in shot site/Shot arm left arm worse"; PYREXIA (non-serious) with onset 12Jul2022 at 07:00, outcome "not recovered", described as "slight fever"; FATIGUE (non-serious) with onset 12Jul2022 at 07:00, outcome "not recovered", described as "tiredness". Therapeutic measures were not taken as a result of lymphadenopathy, lymph node pain, vaccination site pain, pyrexia, fatigue. Additional information: There were no other vaccine in four weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Food allergy
Andere Medikamente: ATENOLOL; PREMARIN
Allergien: -
Vorherige Impfungen: -

VAERS 2371666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: TX
Alter: 35,0
Geschlecht: M
Eingang: 16.07.2022
Impfdatum: 08.07.2022
Beginn: 09.07.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Chills Decreased appetite Diarrhoea Headache Myalgia Nausea Pain Pain in extremity Vomiting

Symptomtext

legs are hurting and is having body pain; muscle pain; joint pain; nauseous; legs are hurting and is having body pain; vomiting; diarrhea; lost his appetite; headaches; chill; 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 35-year-old male patient received BNT162b2 (BNT162B2), on 08Jul2022 as dose 1, single (Lot number: FN2908) at the age of 35 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: CHILLS (non-serious) with onset 09Jul2022, outcome "not recovered", described as "chill"; DIARRHOEA (non-serious) with onset 09Jul2022, outcome "unknown", described as "diarrhea"; HEADACHE (non-serious) with onset 09Jul2022, outcome "not recovered", described as "headaches"; PAIN IN EXTREMITY (non-serious) with onset 09Jul2022, outcome "not recovered", PAIN (non-serious), outcome "unknown" and all described as "legs are hurting and is having body pain"; DECREASED APPETITE (non-serious) with onset 09Jul2022, outcome "recovered", described as "lost his appetite"; VOMITING (non-serious) with onset 09Jul2022, outcome "not recovered"; MYALGIA (non-serious), outcome "unknown", described as "muscle pain"; ARTHRALGIA (non-serious), outcome "unknown", described as "joint pain"; NAUSEA (non-serious), outcome "unknown", described as "nauseous". Therapeutic measures were taken as a result of pain in extremity, pain, vomiting, diarrhoea, decreased appetite, headache, chills, myalgia, arthralgia, nausea. Additional information: Reporter had the first dose this past Friday, has been experiencing vomiting, diarrhea, leg pain b/l and loss of appetitive, and headache that hasn't gone away. Some side effects that have been reported was headache, muscle pain, joint pain, diarrhea, vomiting, nauseous. Loss of appetite was not mentioned in the reported side effects. These may not be all the possible side effects of the vaccine. Serious and unexpected side effects may occur. The possible side effects of the vaccine are still being studied in clinical trials; Persons 18 Years and Older: Systemic reactions usually lasted around 1 day. When clarifying that the reporter was calling regarding the Pfizer Covid-19 vaccine and not Paxlovid, transferring agent states that patient was actually calling from support line as previously stated. Reporter states patient was having diarrhea, headaches and chills, legs are hurting and is having body pain. Adverse Event: diarrhea, headaches and chills, pain in both legs, loss of appetite; Time of Onset: 9Jul2022.

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 2370685

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 02.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 19,0
Dosis: 4
Route/Site: IM / RA

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

Blood urine present Computerised tomogram Computerised tomogram kidney Culture urine negative Dysuria Flank pain Sinusitis

Symptomtext

Saw Dr. on 6/11 for a sinus infection. Started antibiotic. On 6/21, started burning with urination, flank pain, and blood in the urine. continued for 4 days. Urine culture negative but treated with antibiotics as a precaution. On 7/9, burning with urination again, blood in urine, and flank pain on 7/11 again for several days. Negative urine culture. Kidney/bladder CT scan done on 7/15. I will have a cystoscopy on 7/20.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Flank pain
Hospital-Tage: -
Labordaten: urine culture x2, kidney/bladder CT scan, will have a cystoscopy next week.
Aktuelle Erkrankungen: none
Vorgeschichte: fibromyalgia, asthma, functional neurological disorder, arthritis, Raynaud's, GERD
Andere Medikamente: amitriptyline, astelin, breztri, cevimeline, emgality, estradoil, famotidine, flonase, lansoprazole, ipratropium, baclofen, metoprolol, mirena, morphine, movantik, qudexy, restasis, lasix, potassium, tamsulosin, ubrelvy, calcium, magnesium,
Allergien: rocephin, bactrim, biaxin, codeine, hydrocodone, oxycodone, maxide, latex, singular, mangos, onions
Vorherige Impfungen: -

VAERS 2369510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OR
Alter: 72,0
Geschlecht: M
Eingang: 14.07.2022
Impfdatum: 12.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Pruritus Urticaria

Symptomtext

Onset of mild pruritis & urticaria over torso starting evening of 7/13. Awoke on morning of 7/14 to pronounced urticaria on torso, arms, buttocks, and upper legs with moderate pruritis. Patient had taken "an antihistamine" and "itching was better". Instructed patient to contact PCP and seek medical aid if hives continued to spread, or if additional s/sx of allergic reaction occured(swelling of lips, tongue, throat; fever; low blood pressure; etc.).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Depression, Hypertension, Restless Leg Syndrome, Insomnia, Osteoarthritis, GERD
Andere Medikamente: Venlafaxine ER, Meloxicam, Pantoprazole, Lisinopril, Ropinirole, Atorvastatin, Trazodone, Amlodipine
Allergien: None
Vorherige Impfungen: -

VAERS 2368111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 13,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Tic

Symptomtext

Patient has Tourette's Syndrome, she forgot to take her guanfacine this morning. Her grandmother brought her to get her 3 vaccine for Pfizer-BioNTech. She did not have lunch or a good night of sleep according to the grandmother and patient. After 5-10 minutes after receiving the vaccine, the patient started to feel dizzy so we brought her into the consultation room and sat the patient down. She started to blink her eyes to keep from feeling dizzy and stay awake. She had tics for a brief moment. After the tics, she said she felt better but we kept her in the room for observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Tourette's Syndrome
Vorgeschichte: Tourette's Syndrome
Andere Medikamente: Guanfacine 2 mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2367695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: AR
Alter: 69,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 26.05.2022
Beginn: 06.07.2022
Tage bis Beginn: 41,0
Dosis: 4
Route/Site: SYR / AR

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

COVID-19 Cough Headache Malaise Oropharyngeal pain SARS-CoV-2 test positive Sinusitis

Symptomtext

COVID-19 symptoms started on 07/06/2022 at night time; tested positive the same day. I had sore throat, coughing, sinus infection stuff, headache, and I had already been around some that tested positive so I went and got tested and it came up positive. I called the Doctor and he gave me prescription for 5 days and I took the last dose of it on Sunday night. I have been quarantined at home and haven't left the house. I still have a cough but not like it was and it's calmed way down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 Positive 07/06/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; high blood pressure; history of blood clots
Andere Medikamente: Xarelto; Leptopril; carisoprodol; levothyroxine; Meloxicam; Calcium.
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2366156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 07.07.2022
Beginn: 09.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / LA

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

Pain in extremity Vertigo

Symptomtext

I received my 2nd booster shot on 07/07/2022 and my adverse event on 07/09/2022 vertigo; my left arm was sore. Soreness of the arm lasted till yesterday. My vertigo is still on going. My doctor did a positional vertigo. She also told me that I have to go to see a therapist it could be could of sessions. They don't know how long its going to be there for.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: Positional Vertigo
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid arthritis
Andere Medikamente: Multivitamins; TYLENOL
Allergien: Molds; dusts
Vorherige Impfungen: -

VAERS 2363960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: WV
Alter: 83,0
Geschlecht: M
Eingang: 09.07.2022
Impfdatum: 05.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / AR

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

Anticoagulant therapy Fall Unresponsive to stimuli Vomiting

Symptomtext

Was notified by the assisted living home he was living in on 7/7/2022 that patient was found unresponsive that morning and rushed to the emergency department. Administrator states that after pt vaccine tuesday that the patient began throwing up on the next day Wednesday. During the vomit process patient had fallen going to the trash can. He states pt denied injury at this time. Pt was currently taking blood thinners during this time. He states that family refused emergency services after this fall. The next morning on 07/07/2022 staff went into his room and found him unresponsive. Administrator states the pt would not respond to sternal rub and ems was called at this time. No further information of patient status at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: unknown at this time
Aktuelle Erkrankungen: stage 3 ckd, htn, afib, anxiety, hypothyroidism, hyperlipidemia, diabetes
Vorgeschichte: same as box 11
Andere Medikamente: amlodipne 5 mg, aspirin 81mg, atenolol 25mg, docusate 100mg, donepezil 10mg, escitalopram 10mg, farxiga 10mg, ferrous sulfate 325mg, levothyroxine 50mcg, loratadine, meclizine 25mg, pravastatin 20mg, trulicity 1.5mg, vitamin d, xarelto 20mg
Allergien: nkda
Vorherige Impfungen: -

VAERS 2361295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 12,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 30.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Immediate post-injection reaction Urticaria

Symptomtext

immediate facial hives. no SOB, no signs of anaphylaxis. gave oral benadryl 25 mg and hives immediately resolved. pt stayed in clinic for 30 min and MD reassessed after that time. pt was doing well so pt cleared to leave.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: Keflex, Latex
Vorherige Impfungen: -

VAERS 2361118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN 2908

mild

Staat: MO
Alter: 59,0
Geschlecht: M
Eingang: 07.07.2022
Impfdatum: 24.05.2022
Beginn: 28.06.2022
Tage bis Beginn: 35,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Exposure to SARS-CoV-2 Malaise Pyrexia SARS-CoV-2 test positive

Symptomtext

June 28, 2022 - after likely COVID exposure, felt ill and tested positive with a home rapid covid test. Received Paxlovid 6/28/22, completed paxlovid 7/2/22. Highest fever of 100.7F was managed with tylenol until resulted in temperatures of 98.3-96.8F, Temperature was normal by 7/2/22 without tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: BiNax home covid test positive 6/28/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Rheumatoid Arthritis
Andere Medikamente: Linsinopril, Hydroxychloroquine, Atorvastatin, Allegra, Humira
Allergien: Some adhesives
Vorherige Impfungen: -

VAERS 2361101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: CT
Alter: 16,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 03.07.2022
Beginn: 03.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Site: Pain at Injection Site-Mild

Weitere VAERSDATA-Felder

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

VAERS 2359849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NC
Alter: 12,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 30.06.2022
Beginn: 01.07.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Chills Diplopia Laboratory test Magnetic resonance imaging head normal Visual impairment

Symptomtext

Patient experienced acute onset diplopia the morning after her Pfizer booster vaccine. She had chills the night preceding her vision changes. Patient was evaluated at ED. A brain MRI was normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Brain MRI, 7/2/22, Myasthenia gravis marker testing, 7/2/22.
Aktuelle Erkrankungen: Treatment for tick borne illness with doxycycline in May 2022.
Vorgeschichte: Celiac disease. Chronic fatigue.
Andere Medikamente: Melatonin
Allergien: No known drug or food allergies
Vorherige Impfungen: -

VAERS 2358142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 96,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 28.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Injection site erythema Injection site induration Injection site mass

Symptomtext

Caregiver reported client had red ring and hard lump where injection was given within 24 hours on vaccination. Site is still red but hard lump has dissipated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Dementia, HTN
Andere Medikamente: Unknown
Allergien: Iodine
Vorherige Impfungen: -

VAERS 2357862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: TN
Alter: 50,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 17.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Nasal congestion Oropharyngeal pain SARS-CoV-2 test negative SARS-CoV-2 test positive

Symptomtext

When I caught COVID-19 I had a minor sore throat, nasal congestion, and a minor cough. I am a nurse practitioner, and I thought I should take a COVID-19 test since I am around patients. The test had came back positive. My doctor prescribed paxlovid. I took the paxlovid for 2 days, and then it messed up my stomach and gave me a metallic taste in my mouth so my doctor told me to stop taking it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 6/23/2022- At Home COVID-19 Test- Negative; 6/24/2022- At Home COVID-19 Test- Negative; 6/24/2022- PCR COVID-19 Test- Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetic; Hypertension
Andere Medikamente: Losartan; Carvedilol; Amitriptyline; Metformin; Novolog; Levemir; Spironolactone
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2357226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: AL
Alter: 59,0
Geschlecht: F
Eingang: 04.07.2022
Impfdatum: 20.05.2022
Beginn: 27.06.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Headache Oropharyngeal pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

At the time of the second booster on May 20, extreme fatigue was experienced; first shingles shot was administered in the right arm on the same date. On June 27, several symptoms were observed: fever (100.4), persistent cough, fatigue, runny nose, headache, sore throat, and chest congestion. Treatment included cold and flu remedy (Alka Selzer Plus Cold and Cough).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: A positive COVID test was received - test was administered twice. on June 27. As of today, July 4, 2022, COVID test was still positive.
Aktuelle Erkrankungen: -
Vorgeschichte: asthma
Andere Medikamente: Minoxidil, tofacitinib, black cohosh, Hairfinity vitamin, Vitamin E
Allergien: Allergy to shrimp
Vorherige Impfungen: -

VAERS 2357064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: TX
Alter: 64,0
Geschlecht: F
Eingang: 04.07.2022
Impfdatum: 22.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site bruising

Symptomtext

Site: Bruising at Injection Site-Mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2356815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MA
Alter: 53,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 28.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: SYR / -

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

Chills Fatigue Flushing Headache Hyperhidrosis Influenza like illness Malaise Nausea Odynophagia Pain Pyrexia

Symptomtext

Headache, flush/fever, chills, sweating, aching, feels like swallowing knives, nasuea. Exhausted. Note: felt sicker then when I had morning sickness with twins. Truly the sickest I've ever been. Almost like an extreme flu.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Hydrochlorothiazide Lisinopril Celexa
Allergien: Latex
Vorherige Impfungen: -

VAERS 2356811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: IN
Alter: 59,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 01.07.2022
Beginn: 01.07.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SYR / RA

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

Fatigue Injection site pain Lymphadenopathy Pain Pyrexia

Symptomtext

First 24 hours (Fri - Sat): extreme fatigue; full body pain/aching; tenderness at shot area on arm; low grade fever off and on over 24 hours; swollen lymph nodes/glands under right arm and both sides of neck. Second 24 hours (Sat - Sun): extreme fatigue; full body pain/aching; tenderness at shot area on arm; swollen lymph nodes/glands under right arm and both sides of neck.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Chronic: Bronchiectasis as a primary disease; Chronic Ischemic Heart Failure; high blood pressure; high cholesterol; sinusitis; Castleman's Disease; glaucoma; ascites; inflammation issues. I am also a two-stroke survivor.
Vorgeschichte: Chronic: Bronchiectasis as a primary disease; Chronic Ischemic Heart Failure; high blood pressure; high cholesterol; sinusitis; Castleman's Disease; glaucoma; ascites; inflammation issues. I am also a two-stroke survivor.
Andere Medikamente: 1. ATORVASTATIN 40 MG TABLET 2. AMLODIPINE BESYLATE 2.5 MG 3. PANTOPRAZOLE SOD DR 40 MG TAB 4. MONTELUKAST SOD 10 MG TABLET OTC SUPPLEMENTS: 1. Vitamin D3 4000 IUs per day 2. Non-Drowsy LORATADINE 10MG 1 per day 3. B12 SUBLINGUAL 500MG (on
Allergien: steroids; sulfa-based medications; all prescription painkillers & anesthetics
Vorherige Impfungen: After 1st COVID-19 booster (02 March 2022), had swollen lymph nodes/glands under right arm (shot arm) and both sides of neck; fu

VAERS 2348501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: HI
Alter: 65,0
Geschlecht: F
Eingang: 02.07.2022
Impfdatum: 30.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Chills Headache Pain in extremity

Symptomtext

Arm sore after about 3 hrs later, chills started early evening, headache. 2nd day still slight chills occasionally, headache but better, arm soreness still present but much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: PVC
Vorgeschichte: Chronic neck pain
Andere Medikamente: Metoprolol Osteobalance supplement
Allergien: -
Vorherige Impfungen: Arm injection site soreness, Pfizer 1st booster

VAERS 2347573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CO
Alter: 14,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 01.07.2022
Beginn: 01.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness

Symptomtext

Patient was seen today at Immunization Clinic to receive immunizations; HPV #2 and Gray Top Pfizer booster. Patient with guardians. Patient emailed COVID-19 record that was received in "private". Patient observed for 15 minutes in exam room and during the time created a new COVID-19 Card to reflect all three immunizations and waited for email to retrieve COVID-19 information. Updated immunization record received and Instructed guardian of child all immunizations are up-to date and walked them out to the waiting area. During that time patient and guardians was walking passed the Immunization front desk and patient started to feel dizzy. The front desk notified me my patient was feeling dizzy. I was able to quickly go to the front desk and have the patient sit down in one of the chairs and put the patients legs up. Given patient water and a lolly pop to while sitting. Vital signs; SPO2 97% RA, BP 77/43 in right arm, Pulse 51 @ 933am. 2nd set of vitals SPO2 97% Room air: BP 71/44 right arm. Pulse: 53 @ 9:35am. Took patient into exam 12 and had her Supine position: BP: 108/60 Pulse right arm: Pulse: 75 @ 9:44am. 4th set of vitals: Fowler's position: BP 98/62 right arm Pulse: 81 @ 9:50am. 5th set of vitals: Fowler's position: BP 96/68 right are, Pulse: 84 @ 9:56am. Patient states she was feeling much better and was able to stand up without feeling dizzy. Patient and guardians were comfortable leaving to go home.

Weitere VAERSDATA-Felder

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

VAERS 2347397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: DC
Alter: 32,0
Geschlecht: M
Eingang: 01.07.2022
Impfdatum: 22.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Myalgia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I started getting symptoms of a cough. Then next I still had a cough then I felt muscle aches. Then I felt fatigues with an elevated temp with a fever of 99. I took an at home COVID-19 test that was positive. I contacted my doctor and was prescribed Paxlovid. I had a fever for 3 days and muscle aches and fatigue for 4 days. The cough and congestion is still lingering. I am still testing positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Amlodipine
Allergien: None
Vorherige Impfungen: Pfizer 2nd dose - March 2021 - dizzy, lightheaded, fatigued, chills for 1-2 days

VAERS 2347393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 08.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 8,0
Dosis: 4
Route/Site: SYR / LA

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

Abdominal discomfort Body temperature increased COVID-19 Decreased appetite Headache Nasopharyngitis Pain SARS-CoV-2 test positive Secretion discharge

Symptomtext

Starting 06/16/2022, I started getting a headache, body aches and pains, and felt like I was getting a cold but it was worsening. I had an upset stomach causing me to lose my appetite. Also, I had a mild temperature. It got worse and the next day I tested myself with an at home COVID-19 test (06/17/2022) and it was positive. I went to see the doctor on 06/18/2022 and had a test done in office and a PCR which came back positive. I was told to take any over the counter medications that I would take normally to alleviate cold symptoms. I was instructed to go to the ER if I have trouble breathing. I am feeling a little better but I am still having lots of mucous and feel like I have a bad cold. I tested negative this morning but still am experiencing symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: At-home test (06/17/2022): positive; PCR test (06/18/2022): Positive; At-home test (07/01/2022): Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; High Cholesterol
Andere Medikamente: Metformin; Lipitor; Citracal; Magnesium; Vitamin C; Vitamin D; Vitamin E; Probiotic; Ubiquinol
Allergien: None
Vorherige Impfungen: -

VAERS 2347173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: MA
Alter: 73,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Heart rate increased Nausea

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: heart rate elevated seemed to be per apple watch-Mild, Systemic: Nausea-Mild.

Weitere VAERSDATA-Felder

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

VAERS 2344800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: IA
Alter: 49,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 17.05.2022
Beginn: 24.06.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Exposure to SARS-CoV-2 Fatigue Feeling cold Myalgia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I started having muscle pain, was tired, very congested, colder than normal. I had a friend and a sister who's household tested positive. I took the home COVID-19 test since I had been around them to be safe. Once my home COVID-19 test came back positive I called the doctor and had a telehealth visit. They advised me to use TYLENOL cold and flu, to use an inhaler to help me breath. I am still testing positive but I no longer have symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: ZYRTEC; meloxicam
Allergien: Latex; codeine; mango
Vorherige Impfungen: -

VAERS 2341714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 03.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Headache Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Tenderness

Symptomtext

My arm felt a little tender after the vaccine and I was tired. On June 25 I had a sore throat, cough, bad headache, runny nose, congestion and fatigue that progressed in the next few days. I took two home test one was negative and the other one was positive COVID-19. I took CLARITIN D and TYLENOL which helped with my symptoms. On June 27 I contacted my doctor and the prescribed PAXLOVID. As of today I am feeling much better but I still have congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 test one was negative and the other was positive.
Aktuelle Erkrankungen: Spring time allergies; arthritis in my hip
Vorgeschichte: Arthritis
Andere Medikamente: Lipitor; multivitamin; vitamin D; baby aspirin; estradiol
Allergien: Amoxicillin; clindamycin
Vorherige Impfungen: -

VAERS 2338959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MA
Alter: 49,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Erythema Eye swelling Fatigue Pruritus Swelling face

Symptomtext

Employee developed extreme fatigue 3 hours after vaccine administration. Went home, fell asleep. Woke about midnight with redness, swelling to cheeks and eyes; also a generalized itch. Took Benadryl which helped. Pt has multiple food allergies and sensitivities to medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Employee presented to Occ Health clinic next morning (6/28/22); symptoms mostly resolved.
Aktuelle Erkrankungen: none
Vorgeschichte: other allergies: cloves, seasonings
Andere Medikamente: no
Allergien: percocet, epidoral, zpac
Vorherige Impfungen: Fatigue from Jansen Covid vaccine on 8/30/21; same itchiness

VAERS 2338956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: WY
Alter: 15,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 06.06.2022
Beginn: 06.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Rash Urticaria

Symptomtext

Pt's father reported that within 24 hours of first dose on 6/6/22 pt had small hive-like rashes on body, mostly between fold of arm at elbow. Pt's father stated that hydrocortisone cream was applied and claritin given. Pt recovered without any complications. Pt and pt's father denied any respiratory involvement, difficulty breathing, or rash on neck, chest, or face. Pt's father stated that hive-like rash reappeared several times throughout the last several weeks when showering and when at the lake but resolved on it's own. Unsure if related to vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2332410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 17.06.2022
Beginn: 19.06.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Atrial fibrillation Blood test Computerised tomogram Confusional state Disorientation Erythema Mental status changes Swelling face Echocardiogram Electrocardiogram Hypoaesthesia Urine analysis Vomiting

Symptomtext

Patient developed swelling in the face, confusion, disoriented to date, numbness in right arm, atrial fibulation, vomiting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: Blood work, ct scan, ekg, urinalysis, echocardiogram
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, hyperlipidemia
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2336482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 24.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dysphagia Flushing Neck pain Pressure of speech Tachypnoea

Symptomtext

1500: Pt answered immunization screening questions, received the covid vaccine, waited the recommended 15 minutes post vaccine and left the facility. 1530: Pt returned to the vaccine hub indicating that while she was driving in heavy traffic, she experienced pain to the nape of her neck and indicated that she was "swallowing hard" and felt the need to come back. Pt appeared flushed, was speaking rapidly, and tachypnea noted . Writer encouraged pt to sit in chair and focus on breathing deeply in through her nose and out through her mouth. 1535: BP 132/71, HR 92. 1540: BP 130/76, HR 88, RR 22 and unlabored. Pt given bottle of water and encouraged to continue to focus on breathing. Writer verified the allergy of garlic listed was indeed the only know allergy. Pt agreed and indicated she "takes alot of child dose of benadryl for environmental/seasonal issues". 1600: BP 127/74, HR 84, RR 18, even and unlabored. Pt states she was feeling much better. Writer informed pt to present to ED if the problem recurred and to follow up with PCP. Pt voiced understanding.

Weitere VAERSDATA-Felder

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

VAERS 2335399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 26.06.2022
Impfdatum: 22.06.2022
Beginn: 22.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Feeling hot Vaccine positive rechallenge

Symptomtext

Felt hot, dizzy - had same reaction for both prior Pfizer vaccinations

Weitere VAERSDATA-Felder

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

VAERS 2331771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OH
Alter: 47,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 23.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Erythema Flushing Pruritus Urticaria

Symptomtext

Patient C/O itching and hives to left side of face and neck, patient's left side of face appeared red and flushed compared to right side, Benadryl 25mg (E-Kit) administered immediately. Patient denied SOB, difficulty breathing, and denied having any other symptom except itching and hives. Patient declined need to seek medical care. Medical Director notified. Patient was observed for approximately 20 minutes, patient reported itching was subsiding, and she did not need additional observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: No
Vorherige Impfungen: -

VAERS 2331721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: KY
Alter: 79,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 22.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Diarrhoea Vomiting

Symptomtext

Went to bed at 11:00 pm on June 23, 2022 was awakened at 1:00 am with extreme diarrhea and vomiting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: nothing.
Vorgeschichte: Triple-bypass 17 years ago, heart condition, lots of back problems and arthritis.
Andere Medikamente: atorvastatin (40 mg. 1 daily) diclofenac sod (75 mg 2 daily) cyclobenzaprine (5 mg. 3 daily) metoprolol er succ (25 mg. 1 daily) Vitamins: 1 baby aspirin, multi-vitamin, flaxseed oil. d-3, E. fish oil, vision multi 50+, 2 tylenol 8 hr
Allergien: Just shell fish.
Vorherige Impfungen: -

VAERS 2331424

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OK
Alter: 55,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 23.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Back pain Chills Feeling hot Headache Pyrexia Toothache

Symptomtext

She got her vaccine, was OK, had no symptoms and was fine, went to bed and woke up having chills and hot. She then got a headache, her teeth are hurting, her back is aching. The headache continues and so does her teeth. She has not taken anything for the symptoms. She was running fever last night, but did not measure it. She was not able to get up to take her temperature. She did not have any symptoms from the first two vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetes, pacemaker, chronic kidney disease.
Andere Medikamente: None.
Allergien: Morphine.
Vorherige Impfungen: -

VAERS 2327416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: CA
Alter: 13,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 22.06.2022
Beginn: 22.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Dizziness Nausea Vomiting

Symptomtext

13 y/o M reported feeling anxious, lightheaded, and nauseous during post recovery. Patient then started to vomit. He reported that he was nervous for the shot. BP was taken at start (118/50) and again before discharge (108/60). SpO2 remained between 97-100. Patient felt better after emesis and water was provided and patient laid down on floor with legs elevated for another 15 minutes. Patient reported feeling completely fine after 15 minutes and left clinic with guardian.

Weitere VAERSDATA-Felder

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

VAERS 2327110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: ME
Alter: 8,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 17.06.2022
Beginn: 19.06.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Headache

Symptomtext

Headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Reactive Airway Disease
Andere Medikamente: Albuterol Sulfate 90 mcg, EpiPen 2-Pak 0.3mg as needed
Allergien: Nuts, Peanuts, Eggs
Vorherige Impfungen: -

VAERS 2326809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: MA
Alter: 17,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 16.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chills Injection site erythema Injection site pain Injection site rash Injection site swelling Injection site vesicles Pain Pruritus Rash

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Chills-Medium, Additional Details: patient noticed blisters and rash appearing at site of injection and also on the chest, it didn't get better and she decided to call the pharmacy, patient was recommended benadryl and tylenol pain relief and was also recommended to check with md

Weitere VAERSDATA-Felder

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

VAERS 2326667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: RI
Alter: 62,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 17.06.2022
Beginn: 17.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Lymphadenopathy Pain Pyrexia Swelling

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 17Jun2022 at 07:00 as dose 4 (booster), single (Lot number: FN2908) at the age of 62 years, in left arm for covid-19 immunization. The patient had no relevant medical history. Concomitant medication(s) included: METOPROLOL; HYPOTHIAZIDE. 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; Covid-19 vaccine (Dose 3 (Booster); Manufacturer unknown), for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 17Jun2022 at 22:00, outcome "not recovered", described as "Fever"; LYMPHADENOPATHY (non-serious) with onset 17Jun2022 at 22:00, outcome "not recovered", described as "swelling of lymph nodes onset within 15 hours of injection"; PAIN (non-serious) with onset 18Jun2022 at 23:30, outcome "not recovered", described as "Severe pain"; SWELLING (non-serious) with onset 18Jun2022 at 23:30, outcome "not recovered". Therapeutic measures were not taken as a result of pyrexia, lymphadenopathy, pain, swelling. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient has not been tested for COVID-19 since the vaccination. No known allergies. The patient experienced fever and swelling of lymph nodes onset within 15 hours of injection.

Weitere VAERSDATA-Felder

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

VAERS 2323940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 61,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 13.06.2022
Beginn: 14.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Injection site discomfort Injection site erythema Injection site induration Injection site pruritus Injection site swelling Injection site urticaria Injection site warmth Urticaria Vaccination site discomfort Vaccination site erythema Vaccination site pruritus Vaccination site swelling Vaccination site warmth

Symptomtext

Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Quickly spread to a welt 4inches by 3 inches and growing; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Jun2022 at 15:45 as dose 3 (booster), single (Lot number: FN2908) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Breast cancer" (unspecified if ongoing); "Known allergies: Unknown food allergy" (unspecified if ongoing), notes: Known allergies: Unknown food allergy. Concomitant medication(s) included: ANASTROZOLE. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: ER8731, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM), administration date: 15Apr2021, when the patient was 60-year-old, for COVID-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: ER2613, Vaccine Administration Time: 01:45 PM), administration date: 23Mar2021, when the patient was 60-year-old, for COVID-19 Immunization. The following information was reported: URTICARIA (non-serious) with onset 14Jun2022 at 08:00, outcome "recovering", described as "Quickly spread to a welt 4inches by 3 inches and growing"; VACCINATION SITE SWELLING (non-serious), VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE WARMTH (non-serious), VACCINATION SITE PRURITUS (non-serious), VACCINATION SITE DISCOMFORT (non-serious) all with onset 14Jun2022 at 08:00, outcome "recovering" and all described as "Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection". The events "redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection" and "quickly spread to a welt 4inches by 3 inches and growing" required physician office visit. Therapeutic measures were taken as a result of vaccination site swelling, vaccination site erythema, vaccination site warmth, vaccination site pruritus, vaccination site discomfort, urticaria. Additional information: Serious: No Seriousness criteria-Results in death: No Seriousness criteria-Life threatening: No Seriousness criteria-Caused/prolonged hospitalization: No Seriousness criteria-Disabling/Incapacitating: No Seriousness criteria-Congenital anomaly/birth defect: No. If other vaccine in four weeks: No. Other medication in 2 weeks: Centrum Silver Multivitamin for Adults 50 Plus. Ae treatment: Cold compresses, Stronger antihistamines. If COVID prior vaccination: No. If COVID tested post vaccination: No

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discomfort
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer; Food allergy (Known allergies: Unknown food allergy)
Andere Medikamente: ANASTROZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2323940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 61,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 13.06.2022
Beginn: 14.06.2022
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 discomfort Injection site erythema Injection site induration Injection site pruritus Injection site swelling Injection site urticaria Injection site warmth Urticaria Vaccination site discomfort Vaccination site erythema Vaccination site pruritus Vaccination site swelling Vaccination site warmth

Symptomtext

Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection; Quickly spread to a welt 4inches by 3 inches and growing; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Jun2022 at 15:45 as dose 3 (booster), single (Lot number: FN2908) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Breast cancer" (unspecified if ongoing); "Known allergies: Unknown food allergy" (unspecified if ongoing), notes: Known allergies: Unknown food allergy. Concomitant medication(s) included: ANASTROZOLE. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: ER8731, Location of injection: Arm Left, Vaccine Administration Time: 02:00 PM), administration date: 15Apr2021, when the patient was 60-year-old, for COVID-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: ER2613, Vaccine Administration Time: 01:45 PM), administration date: 23Mar2021, when the patient was 60-year-old, for COVID-19 Immunization. The following information was reported: URTICARIA (non-serious) with onset 14Jun2022 at 08:00, outcome "recovering", described as "Quickly spread to a welt 4inches by 3 inches and growing"; VACCINATION SITE SWELLING (non-serious), VACCINATION SITE ERYTHEMA (non-serious), VACCINATION SITE WARMTH (non-serious), VACCINATION SITE PRURITUS (non-serious), VACCINATION SITE DISCOMFORT (non-serious) all with onset 14Jun2022 at 08:00, outcome "recovering" and all described as "Redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection". The events "redness, swelling, warmth, hardness, itchiness and discomfort around the site of injection" and "quickly spread to a welt 4inches by 3 inches and growing" required physician office visit. Therapeutic measures were taken as a result of vaccination site swelling, vaccination site erythema, vaccination site warmth, vaccination site pruritus, vaccination site discomfort, urticaria. Additional information: Serious: No Seriousness criteria-Results in death: No Seriousness criteria-Life threatening: No Seriousness criteria-Caused/prolonged hospitalization: No Seriousness criteria-Disabling/Incapacitating: No Seriousness criteria-Congenital anomaly/birth defect: No. If other vaccine in four weeks: No. Other medication in 2 weeks: Centrum Silver Multivitamin for Adults 50 Plus. Ae treatment: Cold compresses, Stronger antihistamines. If COVID prior vaccination: No. If COVID tested post vaccination: No

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discomfort
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer; Food allergy (Known allergies: Unknown food allergy)
Andere Medikamente: ANASTROZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2324002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MD
Alter: 43,0
Geschlecht: M
Eingang: 19.06.2022
Impfdatum: 15.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cough Influenza like illness Malaise Pain Sputum discoloured

Symptomtext

Felt very sick like the flu even beyond 72 hours from receiving dose. Green mucus. Bad cough, body aches. Much worse reaction then after 2nd dose of vaccine.

Weitere VAERSDATA-Felder

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

VAERS 2324001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: OH
Alter: 28,0
Geschlecht: M
Eingang: 19.06.2022
Impfdatum: 18.06.2022
Beginn: 18.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Nausea Vomiting

Symptomtext

Individual experienced adverse effect after receiving a first booster dose of Pfizer after initial dose of Janssen at a public event 06/18/22. Symptoms included nausea and vomiting. We attended to him and contacted on-site medical. A squad was called as well. He declined to be transported to ER and was released after stability was established. He was able to proceed to the event without incident with his partner.

Weitere VAERSDATA-Felder

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

VAERS 2323936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MA
Alter: 39,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 15.06.2022
Beginn: 17.06.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Eye pain Eyelid pain Loss of personal independence in daily activities Neuralgia Ocular hyperaemia

Symptomtext

Eye redness, pain - one eye (left) - it feels like a neurological pain !! This is the second time I report this side effect I received the third dose (booster) June 15, 2022 and I have the same side effect ( that i reported previously) but less severe ( red eye, moderate pain on the upper lid). I had the same side effect (1 eye) after the 2nd dose (Sep 2021) and I went to an ophthalmologist (was not convinced it is a side effect - although I'm a pharmacist and I can tell with confidence that was a side effect). The pain was so severe that I couldn't even go out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: NO
Vorgeschichte: NO
Andere Medikamente: NO
Allergien: NO
Vorherige Impfungen: 2nd dose covid19 Pfizer

VAERS 2323293

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MA
Alter: 55,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 13.05.2022
Beginn: 26.05.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: SYR / RA

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

Dizziness Fatigue Feeling abnormal Nausea

Symptomtext

I have been feeling not myself since my last vaccination on 5/13/22. I have been tired, nauseous and dizzy most days since approx. one week, maybe two after vaccination #4.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Foot and heel pain. Lower back pain
Vorgeschichte: Lower back degenerative discs. Foot and heel pain. Lower back pain. Migraines.
Andere Medikamente: Estradiol, Omeprizole, VitE, VitD, Ibuprophen, Zomig
Allergien: CIPRO, Doxycycline, Cephalexin, iodine surgical wash, adhesive from bandages
Vorherige Impfungen: I had sore and swollen lymph nodes under armpit on the injection side

VAERS 2320584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: PR
Alter: 42,0
Geschlecht: M
Eingang: 15.06.2022
Impfdatum: 13.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness

Symptomtext

Patient reports feeling dizzy, patient is transported to the tx area. A: clear and maintainable, no edema B: clear lungs, no retraction, 16 breaths, sat 99% C: strong and present peripheral pulses, capillary filling minus 2sgs BP 150/80 mg Hg, pulse in 82 strong and regular D: conscious alert in place time and space E: skin, nor itching, no edema, no rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Patient reports non-diseases at the time of vaccination.
Vorgeschichte: Asthma
Andere Medikamente: Patient reports not taking medication.
Allergien: NKA
Vorherige Impfungen: -

VAERS 2317408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NC
Alter: 62,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 09.06.2022
Beginn: 09.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Feeling hot Injection site erythema Injection site rash Limb discomfort Malaise Nausea Pain in extremity Pruritus

Symptomtext

Well my arm was bothering me. It started hurting and I started feeling really achy and hot. So I checked to see if I had a fever but I did not, but I got a rash ( local rash on the injected site). It's gotten bigger and a little redder. I've been putting some cold compress to help with the pain. and I have been a little nauseas. I didn't feel well so I laid sown and put the cold compress on my and that seemed to help to take the heat away and the itchy away. I also kepted it elevated because to swell a little bit. And I took tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes, C-PAP for sleep apnea, High Blood Pressure under control
Andere Medikamente: Celexa, Wellbutrin XL, Norvasc, Threequel, Leprosil, Clonopin, Valsartan, Lantus Insulin, B12, D3, B6, B3
Allergien: Penicillin, Cipro, Levaquin, Macropain
Vorherige Impfungen: A bad reaction to a Flu vaccine about 15 years ago (2005 or 2006). Arm swelled up, it went up to my neck up to my shoulder, down

VAERS 2317243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NC
Alter: 69,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 20.05.2022
Beginn: 07.06.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Fatigue Malaise Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I exposed to COVID-19 on June 03, 2022. I had a few symptoms on June 5, 2022 but they were not major, on Monday June 6, 2022 I started feeling unwell and took a home COVID-19 Test that came back positive. I called my doctor and made an appointment to go in and confirm my test results. He prescribed Paxlovid that I started taking that day. I am feeling better despite feeling a little tired and still having a bit of congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID-19 Test
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure
Andere Medikamente: Eliquis
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2316613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: CT
Alter: 52,0
Geschlecht: F
Eingang: 11.06.2022
Impfdatum: 07.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Chest discomfort Dizziness Dysphagia Flushing Headache Hyperhidrosis Nausea Throat tightness

Symptomtext

Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Abdominal Pain-Mild, Systemic: Chest Tightness / Heaviness / Pain-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Headache-Medium, Systemic: Nausea-Mild

Weitere VAERSDATA-Felder

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

VAERS 2301874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: CT
Alter: 58,0
Geschlecht: F
Eingang: 30.05.2022
Impfdatum: 25.05.2022
Beginn: 26.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia Injection site pain Injection site swelling

Symptomtext

Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Weakness-Medium

Weitere VAERSDATA-Felder

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

VAERS 2294518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: MN
Alter: 51,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 23.05.2022
Beginn: 23.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Headache Tinnitus Vision blurred

Symptomtext

Here are the symptoms I am having: ? New Headache started afternoon of 5/23 and continues still at present ? Worsening Tinnitus started 5/23 evening and continues still at present. For background, I experienced new onset Tinnitus with my first does of Pfizer COVID Vaccination. At first it was severe and over the months lessened into a mild background bilateral tinnitus. This was reported as a VAERS to the VAERS System by the previous our Nurse, Infection Control Nurse, and Dr. Infectious Disease Physician. ? New Blurred Vision stared 7:30pm 5/24/22 and continues today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: with first pfizer

VAERS 2290021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

mild

Staat: NJ
Alter: 47,0
Geschlecht: F
Eingang: 22.05.2022
Impfdatum: 22.05.2022
Beginn: 22.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Nervousness Vision blurred

Symptomtext

Pt was nervous about getting vaccine and stated she usually cries and hates needles. 5 minutes after vaccine she stated she feels dizzy and has blurry vision. I had her sit down and gave her an instant cold pack which she applied to her forehead and neck. After a few minutes she felt better. She called her son in law to come pick her up. I asked if we can call EMS and she stated she was feeling much better and she wants to go home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: latex
Vorherige Impfungen: stated she gets a rash and fells dizzy due to her nerves

VAERS 2284816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: PR
Alter: 60,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 13.05.2022
Beginn: 14.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Cough Headache Injection site pain Oropharyngeal pain Pyrexia Rhinorrhoea

Symptomtext

I received my 2nd booster shot on 05/13/2022 my adverse event started on 05/14/2022 in the morning at 8;00AM I had headache, and pain on the left arm where I got my shot. The pain was till Sunday. On Tuesday 05/17/2022 in the night 9:00PM I had cough, fever, headache, runny nose, and sore throat. When I woke up it was worse. I went to my doctor medication azithromycin 500mg for 5 days. He also gave me Claritin for 5 days. I am still taking the medicine. Today 05/19/2022 is my second day. I feel much better. I have little headache, and runny nose the other symptoms are gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroids; breast cancer; high blood pressure; seasonal allergies
Andere Medikamente: Regular medication Synthroid; zinc; Benicar; atorvastatin
Allergien: Penicillin; Avelox; mushroom; corn
Vorherige Impfungen: COVID vaccines, flu like symptoms for 24 hours.

VAERS 2283102

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: NJ
Alter: 83,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 13.05.2022
Beginn: 14.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Chills Flushing Headache Hyperhidrosis Influenza like illness Pyrexia

Symptomtext

Systemic: Chills-Medium, Systemic: Fever-Medium, Systemic: patient states her temperature was 100.2 F-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Additional Details: Patient called 2 days after vaccination to speak to me and stated her first doses she had not experienced any side effects and wanted me to report her side effects which include fever (100.2 F), chills,and similar flu like symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2283100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

mild

Staat: FL
Alter: 78,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 13.05.2022
Beginn: 14.05.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / UN

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

Hypoaesthesia Incorrect route of product administration Injection site pain Monoplegia Movement disorder

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Pain at injection site that last 2 days and numbness-Medium, Systemic: Joint Pain-Medium, Additional Details: Patient states she is feeling paralyzed on arm that was injected and cant move 2 days after injection. Patient stated she never had any side effects with first doses and would like it reported. Patient stated vaccine was given to high up on arm.

Weitere VAERSDATA-Felder

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

VAERS 2726067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OK
Alter: 69,0
Geschlecht: M
Eingang: 20.12.2023
Impfdatum: 13.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / RA

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

Therapeutic response unexpected

Symptomtext

I had 5 Pfizer shots and after everyone of them the arthritis pain disappeared; This is a spontaneous report received from a Consumer or other non HCP. A 71-year-old male patient received BNT162b2 (BNT162B2), on 13Jul2022 as dose 3 (booster), single (Lot number: FN2908) at the age of 69 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Osteoarthritis" (unspecified if ongoing). Concomitant medication(s) included: MELOXICAM taken for osteoarthritis. Past drug history included: Aspirin for Joint pain. Vaccination history included: BNT162b2 (DOSE 1, SINGLE (Lot Number: EN5318)), administration date: 26Jan2021, for COVID-19 immunisation, reaction(s): "I had 5 Pfizer shots and after everyone of them the arthritis pain disappeared"; BNT162b2 (DOSE 2, SINGLE (Lot Number: EN6198)), administration date: 23Feb2021, for COVID-19 immunisation, reaction(s): "I had 5 Pfizer shots and after everyone of them the arthritis pain disappeared". The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "unknown", described as "I had 5 Pfizer shots and after everyone of them the arthritis pain disappeared". Additional information: The patient wanted to discuss some really unusual and positive after effects of the COVID vaccine and it has not happened once and it also happened with Moderna. The patient had horrible Osteoarthritis (Intent: History) and the pain in every joint was unbearable and the best thing the patient could do was some Aspirin. After the Pfizer shot, all the pain in all of his joints went away. It was not the first time; the patient had taken four or five shots and after each one his arthritis went away between 3 days in a week. The patient had more flexibility. The patient did not know if it added some kind of moisture into the joint or restoring it, some of it to some degree. The patient was 71-year-old and most senior citizens just kind of take their pain or no pain for granted but the patient very aware of what goes on with his body since he had been coaching forever. The patient stated that there was something here and whatever in this product, there was a piece of it that worked for arthritis that worked for both Pfizer and Moderna oddly enough.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300449913 Same patient/drug/AE, different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Therapeutic response unexpected
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Osteoarthritis
Andere Medikamente: MELOXICAM
Allergien: -
Vorherige Impfungen: -

VAERS 2715727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: AR
Alter: 76,0
Geschlecht: F
Eingang: 20.11.2023
Impfdatum: 18.07.2022
Beginn: 20.11.2023
Tage bis Beginn: 490,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19

Symptomtext

hospitalized with COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: HTN, DMII, Afib
Andere Medikamente: unknown
Allergien: hydromorphone
Vorherige Impfungen: -

VAERS 2708394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fn2908

gering

Staat: SD
Alter: 64,0
Geschlecht: F
Eingang: 01.11.2023
Impfdatum: 21.07.2022
Beginn: 21.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / RA

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

Brain fog Diplopia Disorientation Gait disturbance Weight

Symptomtext

I couldn't find my way home on a walk the block; Was not able to walk/Felt like she was walking through mud; I got double vision; brain fog; 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 65-year-old female patient received bnt162b2 (BNT162B2), on 21Jul2022 as dose 4 (booster), single (Lot number: Fn2908) at the age of 64 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Bumped on head", start date: Jul2022 (unspecified if ongoing), notes: maybe a few years ago. Concomitant medication(s) included: FLINTSTONES MULTIPLE VITAMINS [VITAMINS NOS]; VITAMINE C. Vaccination history included: bnt162b2 (1st dose, Anatomical Site of injection: Unknown, Batch/Lot number: appears to be, EJ1686), administration date: 12Mar2021, when the patient was 62-year-old, for COVID-19 immunization; bnt162b2 (2nd dose, Anatomical Site of injection: Unknown. Thinks she always gets in right arm, gets flu shots in right arm. , Batch/Lot number: EP6955), administration date: 02Apr2021, when the patient was 62-year-old, for COVID-19 immunization; bnt162b2 (3rd dose, Batch/Lot number: FE2590), administration date: 11Nov2021, when the patient was 63-year-old, for COVID-19 immunization, reaction(s): "developed brain fog". The following information was reported: DIPLOPIA (non-serious) with onset 21Jul2022, outcome "unknown", described as "I got double vision"; BRAIN FOG (non-serious) with onset 21Jul2022, outcome "recovered" (24Jul2022); DISORIENTATION (non-serious) with onset 23Jul2022, outcome "unknown", described as "I couldn't find my way home on a walk the block"; GAIT DISTURBANCE (non-serious) with onset 23Jul2022, outcome "unknown", described as "Was not able to walk/Felt like she was walking through mud". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of brain fog, disorientation, gait disturbance, diplopia. Additional information: Caller mentions that she already spoke with someone else from Medical Information department last year regarding the 3rd and 4th Pfizer COVID vaccines. Caller added, "my fourth dose, I not only got brain fog where I couldn't find my way home on a walk the block, this is like day 2 brain fog, I had it for three days, but also I got double vision on my fourth dose and that was last July." Caller stated that she really want to have a children's dose. Caller states she weighs 110 pounds, totally healthy, no medicines, 65 years, freely active, not immunocompromised. Caller states that she is going on a trip and she is not getting the vaccine as she got scared of the brain fog and the double vision. She will only receive the vaccine if it is the children's dose. Caller states when she spoke with someone from this line a year ago and was informed that "After and evaluation it is ultimately up to my health care provider's discretion." Caller states her physician would like to give her the half dose however it is against the rules. Caller would like to know if she could receive half of the dose of the COMIRNATY 2023-2024 formula. Provided that caller received 4th dose Pfizer Covid vaccine. Developed some brain fog, wasn't able to walk. Had that for 3 days. Also, had double vision last July. Weighs around 110 pounds, is extremely active, not really immunocompromised. With third dose Pfizer Covid vaccine last year, developed brain fog, that was reported. Fourth dose, where she developed brain fog and double vision, not sure if that was reported. Clarified, today is first day reporting brain fog and not being able to walk, after fourth dose Covid vaccine. Clarified, double vision occurred last Jul2022. Clarified, caller is respiratory therapist, for about 15 years, was also in nursing also. Clarified, she was never licensed as nurse, physician or pharmacist. Developed some brain fog: Got fourth dose, 21Jul2022. Started shortly after that, brain fog lasted 3 days. Would say, it started the next day, after the vaccine on 21Jul2022, it started, within 24 hours. Wasn't able to walk: Started on third day. Was going for walk, thought maybe she could walk and get rid of this, by walking around. Felt like she was walking through mud, got 3/4 way around block, just got over whelmed with brain fog. For a moment, wasn't sure where she was, looked over, could see house. Was not able to walk, would say, once she got home, didn't go anywhere. Can't say, when it was, was in fog but, knew she could function, could cook dinner, do everything she needed to do. It was peaked at that walk, then after, didn't notice anything as intense. Double vision: Clarified, this started same time as brain fog. Lasted maybe, a half a day. Is familiar with that because, she bumped head maybe a few years ago. Never had concussion before, understands what double vision is, husband is ER physician. It was vertical double vision. Horizontal double vision is more eye function. Treatment: No, is a person who does not like to take medication. Maybe the first day, if she had fever or chills, would be the only time she would take something. Maybe day 1, she may have had a little fever, may have taken something if she was having symptoms. Would have taken Advil. Indication: Didn't want to take it because, previous time, was asking for half dose, wasn't confirmed she could do half dose or, children's dose. Didn't want to take because of brain fog of third dose. Husband told her she was going to get long Covid, did not want that. Put the fear in her to get it done. Believes in vaccines, don't think she is an anti vaxxer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain fog
Hospital-Tage: -
Labordaten: Test Name: weight; Test Result: 49.9 kg
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Head injury (maybe a few years ago.)
Andere Medikamente: FLINTSTONES MULTIPLE VITAMINS [VITAMINS NOS]; VITAMINE C
Allergien: -
Vorherige Impfungen: -

VAERS 2700291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MN
Alter: 88,0
Geschlecht: F
Eingang: 23.10.2023
Impfdatum: 15.07.2022
Beginn: 30.09.2023
Tage bis Beginn: 442,0
Dosis: 4
Route/Site: IM / LA

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

Abnormal behaviour Agitation COVID-19 Fall Head injury SARS-CoV-2 test positive

Symptomtext

The patient has a history of uterine cancer and ovarian cancer. She was brought to the ED by EMS on 9/30/23 for evaluation after a fall. She was trying to use the bathroom at home, fell, and hit her head. Her husband additionally reported that he tested positive for COVID 5 days prior. A COVID PCR test resulted positive for the patient while in the ED. Ultimately, the patient was admitted 9/30/23 - 10/9/23, with discharge diagnoses including mild COVID-19 and increased agitation and behavioral disturbances secondary to acute COVID-19 infection, among other diagnoses. During admission, she remained on room air. She was not started on steroid therapy. Of note, the patient has received four doses of the Pfizer Monovalent COVID vaccine (3/1/2021; 3/22/2021; 10/15/2021; 7/15/2022).

Weitere VAERSDATA-Felder

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

VAERS 2698732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 66,0
Geschlecht: F
Eingang: 19.10.2023
Impfdatum: 01.07.2022
Beginn: 01.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / LA

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

COVID-19 Disease recurrence Drug ineffective Interchange of vaccine products Investigation SARS-CoV-2 test

Symptomtext

covid symptoms 10Oct2023/Pfizer Covid Vaccine- Tested positive for covid again; Drug ineffective/Pfizer Covid Vaccine- Tested positive for covid; COVID-19/Pfizer Covid Vaccine- Tested positive for covid; Interchange of vaccine products; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 67-year-old female patient received bnt162b2 (BNT162B2), on 01Jul2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 66 years intramuscular, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 04Jan2021 as dose 1, single (Batch/Lot number: unknown), on 03Feb2021 as dose 2, single (Lot number: 032L20H) and on 10Nov2021 as dose 3 (booster), single (Lot number: 022C21A) for covid-19 immunisation. The patient's relevant medical history included: "High cholesterol" (ongoing); "asthma", start date: Aug2022 (ongoing), notes: controlled asthma rarely need any medical intervention for this; "smoked" (unspecified if ongoing), notes: Many years ago, she smoked for 4 years when she was in early 20s. Concomitant medication(s) included: CALCIUM; ROSUVASTATIN taken for blood cholesterol increased; TYLENOL; VITAMIN C [ASCORBIC ACID]; VITAMINS NOS. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 01Jul2022, outcome "unknown"; COVID-19 (medically significant) with onset Aug2022, outcome "recovered", described as "COVID-19/Pfizer Covid Vaccine- Tested positive for covid"; DRUG INEFFECTIVE (medically significant) with onset Aug2022, outcome "recovered", described as "Drug ineffective/Pfizer Covid Vaccine- Tested positive for covid"; DISEASE RECURRENCE (medically significant) with onset 10Oct2023, outcome "unknown", described as "covid symptoms 10Oct2023/Pfizer Covid Vaccine- Tested positive for covid again". The patient underwent the following laboratory tests and procedures: oxygen: (unspecified date) 93-95 %; SARS-CoV-2 test: (Jan2021) Positive; (Aug2022) Positive; (10Oct2023) Positive. Therapeutic measures were taken as a result of disease recurrence. Clinical course: Patient received Paxlovid treatment from 11Oct2023 to 12Oct2023.; Sender's Comments: The vaccine efficacy varies from one patient to another and can be affected by different factors; however, a contributory role of the suspect vaccine BNT162B2 to drug ineffectiveness, COVID-19 and disease recurrence cannot be ruled out. Events are considered related conservatively. Case will be reassessed upon receipt of additional information.,Linked Report(s) : US-PFIZER INC-202300330660 same patient, different drug/events;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: oxygen; Result Unstructured Data: Test Result:93-95 %; Test Date: 202101; Test Name: Pfizer Covid Vaccine- Tested positive for covid again; Test Result: Positive ; Test Date: 202208; Test Name: Pfizer Covid Vaccine- Tested positive for covid again; Test Result: Positive ; Test Date: 20231010; Test Name: Pfizer Covid Vaccine- Tested positive for covid again; Test Result: Positive
Aktuelle Erkrankungen: Asthma (controlled asthma rarely need any medical intervention for this); High cholesterol
Vorgeschichte: Medical History/Concurrent Conditions: Smoker (Many years ago, she smoked for 4 years when she was in early 20s)
Andere Medikamente: CALCIUM; ROSUVASTATIN; TYLENOL; VITAMIN C [ASCORBIC ACID]; VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 2686785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 26.09.2023
Impfdatum: 06.08.2022
Beginn: 05.09.2023
Tage bis Beginn: 395,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 19Mar2021 as dose 1, single (Lot number: EP6955), in left arm, on 09Apr2021 as dose 2, single (Lot number: EW0151), in left arm, on 21Oct2021 as dose 3 (booster), single (Lot number: 30155BA), in left arm and on 06Aug2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 66 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "CFIDS" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "COPD" (unspecified if ongoing); "DDD" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing); "High cholesterol" (unspecified if ongoing); "depression" (unspecified if ongoing); "anxiety" (unspecified if ongoing); "severe sleep apnea" (unspecified if ongoing); "insomnia" (unspecified if ongoing); "chronic pain" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Choline, reaction(s): "Allergy"; Amoxicillin, reaction(s): "Allergy". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 05Sep2023, outcome "not recovered" and all described as "Treatment of COVID-19". The event "treatment of covid-19" required emergency room visit. Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid from 12Se2023 to 16Sep2023. Clinical course: Patient got COVID from her Caregiver and was exposed to it on 07Sep2023 (as reported) before this new and 5th vaccination was made available to her on 12Sep2023! So, instead of being proactive and making this latest vaccination available sooner, now they are getting sick and having to be reactive! Called (Withheld) three times to be checked out and to ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Chronic fatigue syndrome; Chronic pain; COPD; Degenerative disc disease; Depression; Fibromyalgia; High cholesterol; Hypothyroidism; Insomnia; Sleep apnea
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2686779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: 61,0
Geschlecht: M
Eingang: 26.09.2023
Impfdatum: 28.05.2022
Beginn: 09.09.2023
Tage bis Beginn: 469,0
Dosis: 4
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old male patient received bnt162b2 (BNT162B2), on 23Mar2021 at 11:30 as dose 2, single (Lot number: EP7534), in right arm, on 08Oct2021 at 13:15 as dose 3 (booster), single (Lot number: 301358A), in right arm and on 28May2022 at 13:15 as dose 4 (booster), single (Lot number: FN2908) at the age of 61 years, in right arm for covid-19 immunisation; covid-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "CLL - leukemia" (unspecified if ongoing); "malignant melanoma" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 09Sep2023 at 21:00, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: From 11Sep2023 to 16Sep2023 patient Paxlovid as treatment of COVID-19. The patient had fever, headaches, body aches, nausea, lung congestion heavy, intense fatigue, light sensitivity, sneezing, coughing, brain fog.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic lymphocytic leukemia; Malignant melanoma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2686769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 26.09.2023
Impfdatum: 01.09.2022
Beginn: 01.09.2023
Tage bis Beginn: 365,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), on 01Sep2022 as dose 5 (booster), single (Lot number: FN2908) at the age of 58 years, in left arm for covid-19 immunisation; covid-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Auto immune disease, undetermined" (unspecified if ongoing); "asthma" (unspecified if ongoing); "blood clotting disorder" (unspecified if ongoing); "chronic pain" (unspecified if ongoing); "known allergies: Yes" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Patient was on treatment with Paxlovid from 12Sep2023 to 16Sep2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300308115 Same patient, different drug and different event (Paxlovid case);

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Asthma; Autoimmune disorder; Chronic pain; Clotting disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2664902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 02.08.2023
Impfdatum: 24.06.2022
Beginn: 22.08.2022
Tage bis Beginn: 59,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 4 vaccines Pfizer 4/2/21 lot# ER8730; Pfizer 4/3/21 lot# Ew0162; Pfizer 11/24/21 lot# FJ1620; Pfizer 6/24/22 lot# FN2908

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Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2664151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 01.08.2023
Impfdatum: 02.06.2022
Beginn: 13.02.2023
Tage bis Beginn: 256,0
Dosis: 3
Route/Site: IM / RA

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

Angina unstable

Symptomtext

UNSTABLE ANGINA

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

VAERS 2649056

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 28,0
Geschlecht: F
Eingang: 24.06.2023
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / RA

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

Alopecia Computerised tomogram Interchange of vaccine products

Symptomtext

Minor hair loss; dose1, dose 2, dose 3: Moderna Dose 4: Comirnaty; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 29-year-old female patient received BNT162b2 (BNT162B2), on 15Jul2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 28 years intramuscular, in right arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure", start date: 15Oct2012 (ongoing), notes: Pertinent details: None; "Acute Psychosis" (unspecified if ongoing); "Altered mental status" (unspecified if ongoing); "Hallucinations" (unspecified if ongoing), notes: X 3 days. There were no concomitant medications. Vaccination history included: moderna (Dose: 1, Lot 046A21A), administration date: 24Mar2021, when the patient was 27-year-old, for COVID-19 immunization; moderna (Dose: 2, Lot 046A21A), administration date: 28Apr2021, when the patient was 27-year-old, for COVID-19 immunization; moderna (Dose: 3, Lot# 033F21A, Expiry date: 02Feb2022), administration date: 17Nov2021, when the patient was 28-year-old, for COVID-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 15Jul2022, outcome "unknown", described as "dose1, dose 2, dose 3: Moderna Dose 4: Comirnaty"; ALOPECIA (non-serious), outcome "unknown", described as "Minor hair loss". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: It was reported that patient did not received prior Vaccinations. Booster dose due to a weakened immune system. No specific relevant test for thromboembolic events with thrombocytopenia. Patient had first 3 Moderna vaccines without incident. Patient had minor hair loss after Pfizer vaccine on 15Jul2022. Technique was CT images acquired through the Head without contrast. Multiplanar reconstructions were performed. All CT scans are performed using dose optimization techniques as appropriate to the exam being performed. These techniques include automatic exposure control and/or standardized protocols utilizing dose matching according to exam type and patient size.; Sender's Comments: Linked Report(s) : US-PFIZER INC-PV202300098133 same reporter/patient/vaccine, different dose/AE.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: Test Name: CT head; Result Unstructured Data: Test Result:Abnormal
Aktuelle Erkrankungen: Blood pressure high (Pertinent details: None)
Vorgeschichte: Medical History/Concurrent Conditions: Acute psychosis; Hallucinations (X 3 days.); Mental disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2647195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 20.06.2023
Impfdatum: 10.06.2022
Beginn: 17.02.2023
Tage bis Beginn: 252,0
Dosis: 4
Route/Site: SYR / AR

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

Asthenia Blood test Bowel movement irregularity Computerised tomogram Decreased appetite Pancreatic carcinoma Ultrasound scan

Symptomtext

In the few weeks before my Urgent care center visit I had lost strength, had irregular bowell movements and loss of appetite. I was put on Miralax at the Urgent care center visit. I had all the side effects with no benefits so I discontinued use after two and one half weeks. I met with my PCP on 20MAR2023 I was given a blood profile, ultrasound and a CT scan. Pancreatic cancer was diagnosed.

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Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: 20MAR2023 CT scan, blood profile and an Ultraound. Diagnosis was Pancreatic cancer.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2633629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 25,0
Geschlecht: F
Eingang: 18.05.2023
Impfdatum: 01.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: - / -

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

Immunisation reaction

Symptomtext

Adverse effect of other vaccines and biological substances, initial encounter on 2022-06-07.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Immunisation reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Viremia NOS
Vorgeschichte: -
Andere Medikamente: IBUPROFEN 100 MG/5ML ORAL SUSP
Allergien: -
Vorherige Impfungen: -

VAERS 2631958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 40,0
Geschlecht: F
Eingang: 15.05.2023
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Discontinued product administered No adverse event

Symptomtext

Vaccine was give after we were aware of new vaccine recommendation. Pt had no reaction to the vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Discontinued product administered
Hospital-Tage: -
Labordaten: None done
Aktuelle Erkrankungen: Type 2 DM
Vorgeschichte: Type 2 DM
Andere Medikamente: Zlpidem Tritate, Buspirone, clonazepam, divalproxex, Emgality, hydroxyzine, levonorgestrel, lisinopril, lybalvi, norethindrone, phentermine, promethazine, quetiapine, ropinirole, sumatriptan, topiramate, trulicity, wellburtin
Allergien: Ondansetron, Dihydroergotamine, metoclopramide, Prochlorperazine
Vorherige Impfungen: -

VAERS 2625697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 22.08.2022
Beginn: 21.12.2022
Tage bis Beginn: 121,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 4 vaccines Moderna 2/20/21 Lot# 023M20A; Moderna 3/16/21 Lot# 002B21A; Moderna 11/12/21 Lot# 034F21A; Pfizer 8/22/22 Lot# FN2908

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2623136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 32,0
Geschlecht: M
Eingang: 28.04.2023
Impfdatum: 27.05.2022
Beginn: 29.05.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Adverse event

Symptomtext

Adverse effect of other vaccines and biological substances, initial encounter on 2022-05-29.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Onychomycosis; Obesity NOS; Other seasonal allergic rhinitis; Encounter for adult health check-up NOS; Encounter for screening for other viral diseases; Body mass index [BMI] 40.0-44.9, adult
Vorgeschichte: -
Andere Medikamente: FLUTICASONE PROPIONATE 50 MCG/ACT NASAL SUSP
Allergien: -
Vorherige Impfungen: -

VAERS 2617165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 82,0
Geschlecht: M
Eingang: 19.04.2023
Impfdatum: -
Beginn: 08.07.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Factor VIII inhibition

Symptomtext

Developed a factor VIII inhibitor; This is a spontaneous report received from a contactable reporter(s) (Nurse). An 82-year-old male patient received BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FN2908) at the age of 82 years for covid-19 immunisation. The patient's relevant medical history included: "MI with stent" (unspecified if ongoing); "CKD" (unspecified if ongoing); "gout" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "MI with stent" (unspecified if ongoing), notes: MI with stent. Concomitant medication(s) included: ALLOPURINOL; NORVASC; LIPITOR; JARDIANCE; COZAAR; METOPROLOL; OXYBUTIN. Vaccination history included: Bnt162b2 (product=COVID 19, brand=Pfizer, brand unknown=False, is bivalent=False, lot number=EW0161, lot unknown=False, administrator route=Intramuscular, dose number=1), for Covid-19 immunization; Bnt16b2 (product=Pfizer, Other vaccine same date lot number=EW0172, dose number=2), for Covid-19 immunization; Bnt16b2 (product=Pfizer, Other vaccine same date lot number=FE3594, dose number=3), for Covid-19 immunization. The following information was reported: FACTOR VIII INHIBITION (hospitalization, medically significant, life threatening) with onset 08Jul2022, outcome "recovering", described as "Developed a factor VIII inhibitor". The patient was hospitalized for factor viii inhibition (hospitalization duration: 14 day(s)). The event "developed a factor viii inhibitor" required physician office visit and emergency room visit. Therapeutic measures were taken as a result of factor viii inhibition. Clinical course: The patient did not receive any other vaccine in four weeks. The patient did not have COVID prior vaccination. The patient was not tested COVID post vaccination. The patient had none known allergies. Other vaccine same date dose number=4. Adverse event resulted in: [Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event)]. Adverse event treatment: FEIBA, DDAVP, Advate, high dose steroids IV.; Sender's Comments: Based on the information provided, a causal relationship between suspect drug BNT162b2 and the reported event Factor VIII inhibition cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Factor VIII inhibition
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Chronic kidney disease; Gout; Myocardial infarction; Stent placement (MI with stent)
Andere Medikamente: ALLOPURINOL; NORVASC; LIPITOR; JARDIANCE; COZAAR; METOPROLOL; OXYBUTIN
Allergien: -
Vorherige Impfungen: -

VAERS 2600178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 51,0
Geschlecht: F
Eingang: 21.03.2023
Impfdatum: 20.06.2022
Beginn: 20.03.2023
Tage bis Beginn: 273,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

covid vaccine breakthrough case dose 1 Pfizer 6/2/21 EW0172

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ 3/20/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2598621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 66,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine administered 1 day BUD refrigerated. Pfizer contacted and advised dose be repeated. Pt contacted and advised to repeat dose, patient verbalized understanding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2596229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 06.07.2022
Beginn: 18.08.2022
Tage bis Beginn: 43,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 4/1/21 Lot# Ew0150; Pfizer 4/2/21 Lot# Ew0172; Pfizer 7/6/22 Lot# FN2908

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2594633

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 17.01.2023
Beginn: 07.03.2023
Tage bis Beginn: 49,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Fall SARS-CoV-2 test positive Subdural haematoma

Symptomtext

Hospitalization following a fall and subdural hematoma; no COVID sx noted

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 1,0
Labordaten: SARS-CoV-2 PCR test was positive on admission
Aktuelle Erkrankungen: -
Vorgeschichte: DMII, MGUS, Obesity, HTN, LVH, SLE, anemia, AFib/flutter, ESRD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2593151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 26.07.2022
Beginn: 12.02.2023
Tage bis Beginn: 201,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 4 vaccines Moderna 2/9/21 Lot# 015M20A; Moderna 3/9/21 Lot# 032M20A; Moderna 8/20/21 Lot# 007B21A; Pfizer 7/26/22 Lot# FN2908

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2590386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 02.03.2023
Impfdatum: 25.07.2022
Beginn: 28.07.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 2/22/22 LOt# FJ6369; Pfizer 3/17/22 LOt# FK9894; Pfizer 7/25/22 Lot# FN2908;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2589975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 02.03.2023
Impfdatum: 02.08.2022
Beginn: 08.02.2023
Tage bis Beginn: 190,0
Dosis: 4
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Pfizer covid vaccine: positive for covid with fever; Pfizer covid vaccine: positive for covid with fever; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 78-year-old male patient received BNT162b2 (BNT162B2), on 11Feb2021 as dose 1, single (Lot number: EL9269, Expiration Date: 31May2021), on 04Mar2021 as dose 2, single (Lot number: EN6198, Expiration Date: 30Jun2021), on 11Nov2021 as dose 3 (booster), single (Batch/Lot number: unknown) and on 02Aug2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 77 years for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (ongoing), notes: high blood pressure diagnosed about 5 years ago; "covid", start date: 06Nov2020 (unspecified if ongoing), notes: Covid (prior to vaccination) & then covid was not detected on 03Dec2020. No symptoms. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 08Feb2023, outcome "not recovered" and all described as "Pfizer covid vaccine: positive for covid with fever". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (08Feb2023) positive, notes: positive for covid; (Feb2023) positive, notes: tested for covid three days in a row; (Feb2023) positive, notes: tested positive for covid three days in a row; (Feb2023) positive, notes: tested positive for covid three days in a row. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: It was reported that dose 3 lot number - 320308D or 320308P, last letter might be a D (he was looking on vaccine record card).Started Paxlovid on day 1 of covid positive test, clarified started Paxlovid on 08Feb2023. Completed treatment (all 30 pills).He was prescribed Paxlovid when he had a fever, with his initial covid illness, he ran a fever for a day and a half and then cleared up. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300082945 Same patient, different product, different event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230208; Test Name: covid test; Test Result: Positive ; Comments: positive for covid; Test Date: 202302; Test Name: covid test; Test Result: Positive ; Comments: tested for covid three days in a row; Test Date: 202302; Test Name: covid test; Test Result: Positive ; Comments: tested positive for covid three days in a row; Test Date: 202302; Test Name: covid test; Test Result: Positive ; Comments: tested positive for covid three days in a row
Aktuelle Erkrankungen: Blood pressure high (high blood pressure diagnosed about 5 years ago)
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Covid (prior to vaccination) & then covid was not detected on 03Dec2020. No symptoms.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2588567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 28.02.2023
Impfdatum: 09.08.2022
Beginn: 13.12.2022
Tage bis Beginn: 126,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 4 vaccines Pfizer 10/5/21 Lot# 30155BA; Pfizer 10/26/21 Lot# FF2590' Pfizer 4/5/22 Lot# FK9895; Pfizer 8/9/22 Lot# FN2908

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2587883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: KY
Alter: 89,0
Geschlecht: F
Eingang: 27.02.2023
Impfdatum: 02.03.2021
Beginn: 01.02.2023
Tage bis Beginn: 701,0
Dosis: 3
Route/Site: IM / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient COVID positive after completing vaccine series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID + on 2/26/23
Aktuelle Erkrankungen: -
Vorgeschichte: CKD, DM, diverticulitis, HTN
Andere Medikamente: -
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2586919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 12,0
Geschlecht: U
Eingang: 24.02.2023
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was inadvertently administered 1 day after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 13,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine was inadvertently administered 1 day after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 91,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was inadvertently administered 1 day after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 29,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was inadvertently administered 1 day after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FN2908

gering

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was inadvertently administered 1 days after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 57,0
Geschlecht: M
Eingang: 24.02.2023
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was inadvertently administered 1 day after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: non
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 78,0
Geschlecht: M
Eingang: 24.02.2023
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine was inadvertently administered 5 days after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 55,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Product administration error Product use issue

Symptomtext

Vaccine was inadvertently administered 5 days after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administration error
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 21,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product administration error Product use issue

Symptomtext

Vaccine was inadvertently administered 5 days after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administration error
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unk
Vorgeschichte: unk
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2586863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 64,0
Geschlecht: F
Eingang: 24.02.2023
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine was inadvertently administered 5 days after the BUD of refrigerated vaccine. Pfizer was contacted and their recommendation was for the dose to be repeated, CDC appendix D. Vaccine administration errors and deviations guidance was also followed Patient was contacted and advised to return for another dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none reported
Vorgeschichte: not reported
Andere Medikamente: unknown
Allergien: denied
Vorherige Impfungen: -

VAERS 2583373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 17.02.2023
Impfdatum: 02.08.2022
Beginn: 17.02.2023
Tage bis Beginn: 199,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

COVID vaccine breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID positive test 2/16/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 66,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 16.08.2022
Beginn: 26.09.2022
Tage bis Beginn: 41,0
Dosis: 4
Route/Site: IM / LA

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

Alopecia

Symptomtext

I was brushing my hair and noticed a lot of hair coming out. At first, I thought it was normal. Then I noticed my hair was thinning from brushing so much hair out. I really noticed more shedding towards the end of October 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: COVID-19
Vorgeschichte: Back pain
Andere Medikamente: Rosuvastatin; hydrochlorothiazide; duloxetine; clonazepam; levothyroxine; potassium chloride; tizanidine; hydrocodone; vitamin B-12; vitamin C; vitamin E; biotin; vitamin D-3; fer sulfate
Allergien: Penicillin; sulfa
Vorherige Impfungen: -

VAERS 2495406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 13.02.2023
Impfdatum: 03.06.2022
Beginn: 03.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Expired product administered No adverse event Product storage error

Symptomtext

No adverse event, vaccine may have been expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 13.02.2023
Impfdatum: 03.06.2022
Beginn: 03.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event Product storage error

Symptomtext

No adverse event, vaccine may have been expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2578998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Unevaluable event

Symptomtext

No adverse event, vaccine may have been expired

Weitere VAERSDATA-Felder

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

VAERS 2578971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 09.02.2023
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Expired product administered No adverse event

Symptomtext

No adverse event, vaccine may have been expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2578047

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 08.02.2023
Impfdatum: 16.06.2022
Beginn: 03.02.2023
Tage bis Beginn: 232,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

COVID vaccine breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive COVID test on 2/3/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2577976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NM
Alter: 81,0
Geschlecht: M
Eingang: 08.02.2023
Impfdatum: 09.08.2022
Beginn: 20.01.2023
Tage bis Beginn: 164,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Feeling abnormal SARS-CoV-2 test positive

Symptomtext

I was feeling a little out of it and I had surgery coming up. As a precautionary measure, I took a home test and I was positive. I was unsure of if it was a valid test because the liquid in the vile was not at the level described in the instructions. Because of that, I went to the urgent care and got another test and it came back positive. For treatment, I called my PCP Monday morning and let him know that I was positive for COVID-19. He prescribed Paxlovid just in case. I took that and I had no other symptoms. I just sat and waited until the necessary time frame and retested and came back negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 20JAN2023 At Home COVID-19 Test - Positive; 20JAN2023 COVID-19 Test at Urgent Care - Positive; 25JAN2023 At Home COVID-19 Test - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; High cholesterol; History of Blood clots
Andere Medikamente: Atorvastatin; Levothyroxine; Lansoprazole; Amlodipine Besylate; Flomax; Finasteride; Low Dose Aspirin; Vitamin D3; Vitamin C; Multivitamin; Eliquis; Tylenol Arthritis
Allergien: None
Vorherige Impfungen: -

VAERS 2577256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 18.07.2022
Beginn: 18.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

No adverse event

Symptomtext

No adverse event, vaccine may have been expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2577177

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 07.02.2023
Impfdatum: 01.01.2001
Beginn: 01.09.2022
Tage bis Beginn: 7.913,0
Dosis: UNK
Route/Site: - / -

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

Product storage error

Symptomtext

Advised by the local authority that Pfizer Covid Vaccine adminstered was stable based on Manufacturer but was not stored based on EUA guidelines and deemed not viable. Reached out to the patients effected via phone and sent the required letter to offer revaccination. 13 Patients were effected by this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 15.06.2022
Beginn: 15.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Expired product administered No adverse event

Symptomtext

No adverse event, vaccine may have been expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576518

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 25.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Expired product administered No adverse event

Symptomtext

No adverse events, vaccine may have been expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Expired product administered No adverse event

Symptomtext

No Adverse effects, vaccine may have been expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576494

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 01.08.2022
Beginn: 01.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Expired product administered No adverse event

Symptomtext

No adverse event, vaccine may have been expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2574684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MO
Alter: 15,0
Geschlecht: F
Eingang: 03.02.2023
Impfdatum: 09.06.2022
Beginn: 31.01.2023
Tage bis Beginn: 236,0
Dosis: 3
Route/Site: OT / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Tested Positive for Covid-19 after vaccination.; Tested Positive for Covid-19 after vaccination.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. A 16-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27May2021 as dose 1, single (Lot number: EN6207), in left arm, on 16Jun2021 as dose 2, single (Lot number: EN6207), in left arm and on 09Jun2022 as dose 3 (booster), single (Lot number: FN2908) at the age of 15 years, in left arm, all intramuscular for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 31Jan2023 at 07:00, outcome "recovering" and all described as "Tested Positive for Covid-19 after vaccination.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (31Jan2023) Positive, notes: nasal swab. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical course: The patient has no covid prior vaccination and no other vaccine in four weeks. The patient has no known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230131; Test Name: Nasal Swab; Test Result: Positive ; Comments: nasal swab
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2568575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: IN
Alter: 77,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 27.07.2022
Beginn: 30.08.2022
Tage bis Beginn: 34,0
Dosis: 4
Route/Site: SYR / LA

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

Eye inflammation Ocular hyperaemia Swelling

Symptomtext

The red first appeared in my left eye and the white part was bloody red so I called my eye doctor and he said to get LUMIFY and it would only help for a half a day and the red would come back so when that didn't really help I went to see the doctor who said it was not an infection but an inflammation and he prescribed a steroid which I took for three weeks but the whites in my eyes were not bloody red but still red, he told me I would always probably have the red tint in my eyes due to the swollen capillaries due to the swelling and the way they stay until today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye inflammation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Acid Reflux; Incontinence; Precancerous skin lesions; Macular degeneration
Andere Medikamente: Amlodipine; benazepril; imipramine HCL; metoprolol; FLONASE; pantoprazole; macular protect complete AREDS 2 ; RESTASIS; VIACTIV ONE MD krill oil; cholestyramine; cholesterol 360; CORICIDIN HBT cold and flu; estradiol; REFRESH liquid gel
Allergien: FLAGYL
Vorherige Impfungen: -

VAERS 2568283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 15.06.2022
Beginn: 07.10.2022
Tage bis Beginn: 114,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Interchange of vaccine products Vaccination failure

Symptomtext

COVID-19; COVID-19; Dose Number 5; Moderna; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 15Jun2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 53 years for covid-19 immunisation; BNT162b2 (BNT162B2), on 12Mar2021 as dose 1, single (Lot number: EN6195), on 09Apr2021 as dose 2, single (Lot number: 0153) and on 30Nov2021 as dose 3 (booster), single (Lot number: FF2593) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 07Oct2022 at 08:15 as dose 5 (booster) single (Lot number: 053D224), in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 07Oct2022, outcome "unknown", described as "Dose Number 5; Moderna"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jan2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: No other medication was taken in 2 weeks. Patient received Paxlovid Treatment from Jan2023 till Jan2023. Patient did not had Known allergies and no medical history was reported. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2564962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: FL
Alter: 53,0
Geschlecht: F
Eingang: 21.01.2023
Impfdatum: 21.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; 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 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 04Jun2021 as dose 1, single (Lot number: BW0168), in left arm, on 14Aug2021 as dose 2, single (Lot number: EW 0168), in left arm, on 09Dec2021 as dose 3 (booster), single (Lot number: FJ8757), in left arm and on 21Jul2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 53 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin. Concomitant medication(s) included: LOSARTAN taken for hypertension, start date: 01Jun2016; VENTOLIN [SALBUTAMOL] taken for inhalation therapy, start date: 01Jun2016. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Blood pressure high; Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: LOSARTAN; VENTOLIN [SALBUTAMOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2564953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 21.01.2023
Impfdatum: 13.08.2022
Beginn: 14.08.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Breast swelling Capsular contracture associated with breast implant Device breakage Investigation

Symptomtext

breast implant on right side was ruptured; swelling in axillary and breast; capsular contracture; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Aug2022 as dose 3 (booster), single (Lot number: FN2908) at the age of 54 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: T3/T4 SUPPORT; ASPIRIN (E.C.); VITAMIN C [ASCORBIC ACID]. Past drug history included: Demerol, reaction(s): "Known allergies: demerol", notes: Known allergies: demerol. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: FA7484, Location of injection: Arm Right), administration date: 29Jul2021, when the patient was 53-year-old, for COVID-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: FC3181, Location of injection: Arm Right), administration date: 21Aug2021, when the patient was 53-year-old, for COVID-19 immunization, reaction(s): "swelling in axillary and breast"; Sudafed (Known allergies: sudafed), reaction(s): "Known allergies: sudafed"; Augmenting (Known allergies: augmenting), reaction(s): "Known allergies: augmenting". The following information was reported: DEVICE BREAKAGE (medically significant) with onset 14Aug2022, outcome "not recovered", described as "breast implant on right side was ruptured"; CAPSULAR CONTRACTURE ASSOCIATED WITH BREAST IMPLANT (medically significant) with onset 14Aug2022, outcome "not recovered", described as "capsular contracture"; BREAST SWELLING (medically significant) with onset 14Aug2022, outcome "not recovered", described as "swelling in axillary and breast". The events "breast implant on right side was ruptured", "swelling in axillary and breast" and "capsular contracture" required physician office visit. The patient underwent the following laboratory tests and procedures: testing: Unknown results. Therapeutic measures were not taken as a result of device breakage, breast swelling, capsular contracture associated with breast implant. Clinical course: Reported as, Had significant swelling in axillary and breast. After booster, swelling in breast did not subside. Went to physician, sent for testing - breast implant on right side ( all 3 shots on right arm) was ruptured with capsular contracture. Other medical history - factor 5 (as reported). Unknown if patient experienced COVID-19 prior to vaccination. Patient was not tested for COVID-19 post vaccination. Patient did not received other vaccine within four weeks of COVID vaccine.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine cannot be excluded for the reported events of Device breakage, Breast swelling and Capsular contracture due to temporal relationship. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast swelling
Hospital-Tage: -
Labordaten: Test Name: testing; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: T3/T4 SUPPORT; ASPIRIN (E.C.); VITAMIN C [ASCORBIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2564111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WI
Alter: 70,0
Geschlecht: M
Eingang: 20.01.2023
Impfdatum: 23.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Drug ineffective SARS-CoV-2 test Suspected COVID-19

Symptomtext

if covid tested post vaccination Yes; if covid tested post vaccination Yes; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old male patient received BNT162b2 (BNT162B2), on 19Apr2021 as dose 1, single (Lot number: Ew0169), on 18Jun2021 as dose 2, single (Lot number: Ew0187), on 25Oct2021 as dose 3 (booster), single (Lot number: Fe3590) and on 23Jun2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 70 years for covid-19 immunisation. The patient's relevant medical history included: "High cholesterol" (unspecified if ongoing), notes: High cholesterol at that time only, minor other unrelated health concerns; "known allergies: New stings" (unspecified if ongoing), notes: known allergies: New stings. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant), outcome "unknown" and all described as "if covid tested post vaccination Yes". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: unknown result, notes: COVID test type post vaccination: Nasal Swab. Clinical Information: if COVID prior vaccination was Yes. if COVID tested post vaccination was Yes. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Drug ineffective
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Result Unstructured Data: Test Result:unknown result; Comments: COVID test type post vaccination: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to sting (known allergies: New stings); High cholesterol (High cholesterol at that time only, minor other unrelated health concerns)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 38,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

Patient received pfizer primary #1 on 7/19/22 and received moderna bivalent 11/22/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: Migraine without status migrainosus, not intractable Subconjunctival hemorrhage Symptomatic bradycardia Tricuspid valve insufficiency
Andere Medikamente: IUD paraguard
Allergien: no
Vorherige Impfungen: -

VAERS 2553647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 90,0
Geschlecht: F
Eingang: 08.01.2023
Impfdatum: 12.07.2022
Beginn: 04.01.2023
Tage bis Beginn: 176,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

COVID vaccine breakthrough case All Moderna dose 1 1/18/21 027L20A dose 2 2/15/21 011M20A dose 3 11/19/21 067F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ 1/4/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 45,0
Geschlecht: F
Eingang: 08.01.2023
Impfdatum: 05.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

No adverse event

Symptomtext

no adverse reaction

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: Ulcerative colitis
Andere Medikamente: Humira Probiotic Vit D3
Allergien: Penicillin Codeine
Vorherige Impfungen: -

VAERS 2552453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WI
Alter: 8,0
Geschlecht: M
Eingang: 06.01.2023
Impfdatum: 28.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Product administered to patient of inappropriate age

Symptomtext

Given the wrong vaccine for his age

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2551422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 05.01.2023
Impfdatum: 15.06.2022
Beginn: 15.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Patient received vaccine that was stored post incorrectly post puncture of vial (up to 28 days)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2552171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 11,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 30.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

No adverse event

Symptomtext

0 signs or symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 2552156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 6,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 30.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

No adverse event

Symptomtext

None 0 signs or symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 2540149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: AZ
Alter: 62,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 27.06.2022
Beginn: 01.12.2022
Tage bis Beginn: 157,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Apr2021 as dose 1, single (Lot number: ER8733), in left arm, on 21Apr2021 as dose 2, single (Lot number: EW0161), in left arm, on 09Dec2021 as dose 3 (booster), single (Lot number: 3300ba), in left arm and on 27Jun2022 at 13:15 as dose 4 (booster), single (Lot number: FN2908) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "copd" (unspecified if ongoing); "hypothyroid" (unspecified if ongoing), notes: hypothyroid; "Gerd" (unspecified if ongoing); "IBS-D" (unspecified if ongoing), notes: IBS-D; "Osteoarthritis" (unspecified if ongoing); "Elhers Danlos Syndrome" (unspecified if ongoing); "Depression" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "PTSD" (unspecified if ongoing), notes: PTSD. The patient's concomitant medications were not reported. Past drug history included: Vicodin, reaction(s): "known allergies: vicodin", notes: known allergies: vicodin; Codeine, reaction(s): "known allergies: codeine", notes: known allergies: codeine. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: It is unknown whether other medication was received in 2 weeks. Patient received treatment for COVID-19 with Paxlovid from 06Dec2022 to 11Dec2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; COPD; Depression; Ehlers-Danlos syndrome; GERD; Hypothyroidism (hypothyroid); Irritable bowel syndrome (IBS-D); Osteoarthritis; Post-traumatic stress disorder (PTSD)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2539335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 48,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 19.07.2022
Beginn: 18.12.2022
Tage bis Beginn: 152,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

COVID vaccine breakthrough case Dose 1 Moderna 4/27/21 047A21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID+ 12/18/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2539078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 05.04.2021
Beginn: 02.10.2022
Tage bis Beginn: 545,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Anaemia COVID-19 Cardiac flutter Chest X-ray normal Computerised tomogram head normal Electrocardiogram abnormal Mental status changes SARS-CoV-2 test positive Supraventricular extrasystoles Troponin normal

Symptomtext

61y.o. female with PMH of Asthma, Carotid artery occlusion, CVA with left hemiparesis (06/13/2020), DM type 2, Fatty liver, HTN (hypertension) who presented to EC on 10/2/2022 with AMS. It is thought that possible pt was given her mother's medications by mistake, causing the AMS. Pt was also diagnosed with COVID 2 days PTA. Labs noted acute kidney injury, chronic anemia, and positive covid testing. Head CT was negative for acute findings. Chest x-ray was negative for pneumonia. Troponin was negative. ECG appeared abnormal with question of PACs versus possible flutter waves. She was not hypoxic.She was seen by ID, no indication for antiviral or steroid at this time/ remains on room air. Mentation is at baseline.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute kidney injury
Hospital-Tage: -
Labordaten: 10/2 SARS-CoV-2 -COVID-19 by NAA, Micro - detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2537899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 76,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine vial stored longer than recommended time post puncture (28 days)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2537888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 20.12.2022
Impfdatum: 30.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine vial was stored at longer than recommended time post puncture (28 days)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2535310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: KY
Alter: 54,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 01.04.2021
Beginn: 12.12.2022
Tage bis Beginn: 620,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient COVID positive after completing vaccine series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic kidney disease, diabetes, GERD, bilateral BKA,
Andere Medikamente: -
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2535200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 01.06.2022
Beginn: 01.07.2022
Tage bis Beginn: 30,0
Dosis: 4
Route/Site: IM / UN

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

Asthenia Computerised tomogram head normal Computerised tomogram neck Magnetic resonance imaging head Vertigo Vestibular function test normal

Symptomtext

Severe and debilitating vertigo that lasted until 09/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: MRI Head-07/22. Negative CT Head w/o IV, CT Neck - 08/22. Negative Vestibular tests no at neurological center- negative
Aktuelle Erkrankungen: Hashimotos disease and carcinoid tumors of stomach controlled by scopes
Vorgeschichte: Same as above
Andere Medikamente: Synthroid, lisinoprol, fluoxetine,, multivitamin, vitamin D and E, cynocloban injection, Zyrtec, flonase. I also started a Keto diet 05/22 and was taking keto activate powder and keto vitals electrolyte powder.
Allergien: Penicillin and sulfa
Vorherige Impfungen: -

VAERS 2528981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 77,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 19.10.2022
Beginn: 03.12.2022
Tage bis Beginn: 45,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Vaccine breakthrough infection

Symptomtext

Fully vaccinated. COVID infection breakthrough

Weitere VAERSDATA-Felder

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

VAERS 2525426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 56,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 16.06.2022
Beginn: 05.12.2022
Tage bis Beginn: 172,0
Dosis: 2
Route/Site: - / -

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

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

Symptomtext

covid vaccine breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ 12/5/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2524197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MN
Alter: 67,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 05.08.2022
Beginn: 06.12.2022
Tage bis Beginn: 123,0
Dosis: UNK
Route/Site: - / -

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

Asymptomatic COVID-19

Symptomtext

Asymptomatic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2523106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 65,0
Geschlecht: U
Eingang: 05.12.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

admin pfizer instead of Moderna in error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2523105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MN
Alter: 14,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 02.12.2022
Beginn: 02.12.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient given vaccine that expired 10/31/2022 on 12/2/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2523071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MN
Alter: 15,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 01.12.2022
Beginn: 01.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient received expired vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2522927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: MA
Alter: 41,0
Geschlecht: M
Eingang: 05.12.2022
Impfdatum: 04.06.2022
Beginn: 30.08.2022
Tage bis Beginn: 87,0
Dosis: 4
Route/Site: IM / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Contracted COVID-19 - tested positive around 8/30/22 almost 3 months from last booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home test 8/30/22.
Aktuelle Erkrankungen: none
Vorgeschichte: glioma (in remission)
Andere Medikamente: bupropion, depakote ER, famotidine, zinc, vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 2628788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: RI
Alter: 67,0
Geschlecht: M
Eingang: 01.12.2022
Impfdatum: 27.05.2022
Beginn: 15.09.2022
Tage bis Beginn: 111,0
Dosis: UNK
Route/Site: SYR / AR

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

NOTHING AS A RESULT OF SHOT. I WAS ADVISED BY FACILITY TO REPORT TESTING POSITIVE FOR COVID ON 9-15-22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: TESTED POSITIVE FOR COVID 09-15-22
Aktuelle Erkrankungen: -
Vorgeschichte: Degenerative disc disease; Right & left sacroiliac joints degeneration; Failed Back Surgery Syndrome; Fibro Myalgia; High blood pressure; High cholesterol; Hypothyroidism; Migraines; Leg Muscle Disease; Sleep apnea; Spinal stenosis; Systemic Exertion Intolerance Disease; Tinnitus; Vertigo
Andere Medikamente: Divalproex ER 250mg; Flomax 0.4mg; Flonais 50 mcg; Gabapentin 800mg; Levothyroxine 50mcg; Lipitor 80 mg; Meciizine 25mg; Medical Marijuana; Metoprolo succinate ER 25mg; Morphine Sulfate ER 30mg; Omeprazole 40 mg; oxycodone 10-325mg; Prometh
Allergien: -
Vorherige Impfungen: -

VAERS 2518096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 09.08.2022
Beginn: 25.11.2022
Tage bis Beginn: 108,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Vaccine breakthrough infection

Symptomtext

vaccinated and boosted. COVID breakthrough infection

Weitere VAERSDATA-Felder

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

VAERS 2503316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: IA
Alter: 25,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 04.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine expired on 10/31/22, dose administered to patient on 11/4/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2503311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: IA
Alter: 30,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 03.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine expired on 10/31/22, dose administered to patient on 11/3/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2503305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: IA
Alter: 29,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 03.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Vaccine expired on 10/31/22, dose administered to patient on 11/3/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2496771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

No adverse event Product storage error

Symptomtext

Vaccine vial store for longer than recommended post puncture of vial (potentially up to 28 days) no adverse reaction

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2496636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 56,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 01.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Expiration date for the vial was 10/31/2022. Vaccine administered on 11/1/2022. Vaccine was stored in the Ultra Low Temp Freezer up until the vial was thawed and administered on 11/1/2022. I called the manufacturer (Pfizer) for guidance as per CDC instruction on the website and am awaiting further instruction. No adverse effects reported by patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2496496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 02.11.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

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

Expired product administered

Symptomtext

Pfizer COVID 19 Vaccine was administered to 2 patients after the beyond use date. Medical Associates Director of Clinical Services and Vaccine Coordinator are working with Agency to reconcile the errors and provide appropriate follow upto affected patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: RI
Alter: 67,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 22.07.2022
Beginn: 22.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event Product storage error

Symptomtext

Vaccine stored in the practice longer than the manufacturer's recommended time (6 hours past first puncture of vial) Vaccine was potentially stored for 28 days in the practice. Patient suffered no adverse effects, no illness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Niacin
Vorherige Impfungen: -

VAERS 2495166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OK
Alter: 31,0
Geschlecht: M
Eingang: 01.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Given 2nd dose Pfizer FN2908 on 11/1/22. The lot number had expired on 10/31/22. Reports no adverse reactions

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2494005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MN
Alter: 66,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: -
Beginn: 29.10.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

Asymptomatic

Weitere VAERSDATA-Felder

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

VAERS 2489517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: HI
Alter: 52,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 19.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 52-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Jan2021 at 09:00 as dose 1, single (Lot number: EL1283), in left arm, on 06Feb2021 at 10:00 as dose 2, single (Lot number: EL9264), in left arm, on 04Oct2021 at 12:00 as dose 3 (booster), single (Lot number: 30145BA), in left arm and on 19Jun2022 at 15:00 as dose 4 (booster), single (Lot number: FN2908) at the age of 52 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 12Sep2022 at 20:00 as dose 5 (booster), single (Lot number: AS7148B), in left arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing), notes: Other medical history: High blood pressure; "Known allergies: NSAIDs" (unspecified if ongoing), notes: Known allergies: NSAIDs; "Known allergies: dye" (unspecified if ongoing), notes: Known allergies: dye. Concomitant medication(s) included: SERTRALINE, start date: 03Dec2018, stop date: 21Oct2022; AMLODIPINE, start date: 01Jan2019, stop date: 21Oct2022. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: indication=Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19.; Sender's Comments: Based on the available information in the case, an association between the reported events and bnt162b2 cannot be ruled out. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to NSAIDs (Known allergies: NSAIDs); Blood pressure high (Other medical history: High blood pressure); Hair dye sensitivity (Known allergies: dye)
Andere Medikamente: SERTRALINE; AMLODIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 2487149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 05.08.2022
Beginn: 08.10.2022
Tage bis Beginn: 64,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after three vaccines Pfizer 3/23/21 Lot# EN6207; Pfizer 4/13/21 Lot# EW0150; Pfizer 8/5/22 Lot# FN2908

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2483717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: -
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Pfizer / BioNTech - Dose Number: 4 ... Moderna - Dose Number: 3; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Jul2022 as dose 4 (booster), single (Lot number: FN2908) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 04Mar2021 as dose 1, single (Lot number: 030A21A), on 03Mar2021 as dose 2, single (Lot number: 019B21A) and on 09Nov2021 as dose 3 (booster), single (Lot number: 071F21) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies : Steroids" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN POTASSIUM; SIMVASTATIN; HYDROCHLOROTHIAZIDE. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 06Jul2022, outcome "unknown", described as "Pfizer / BioNTech - Dose Number: 4 ... Moderna - Dose Number: 3"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received Paxlovid from 06Oct2022 to 10Oct2022 as covid-19 treatment. Other medication in 2 weeks included losartan potassium, simvastatin and hydrochlorothiazide.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy
Andere Medikamente: LOSARTAN POTASSIUM; SIMVASTATIN; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2479660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: NJ
Alter: 70,0
Geschlecht: M
Eingang: 16.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2479647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: NJ
Alter: 69,0
Geschlecht: M
Eingang: 16.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2478597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 04.06.2022
Beginn: 06.06.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / AR

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

Aphthous ulcer Chapped lips Skin exfoliation

Symptomtext

My lips became very chapped, skin would be flaking off, and remains that way to this day. I started having canker sores inside my mouth. That have backed off a little, but my lips stay chapped. They have me taking hydrocortisone ointment twice a week. There really isn't anything they could give me for the canker sores.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Aphthous ulcer
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Central Sensitization; Fibromyalgia
Andere Medikamente: Multivitamin; calcium with vitamin D3; vitamin D3; TYLENOL; tramadol
Allergien: N/A
Vorherige Impfungen: -

VAERS 2478457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 13.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient given incorrect product. Administered Monovalent instead of Bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2478443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 12,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 05.10.2022
Beginn: 05.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / UN

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

Incorrect product formulation administered

Symptomtext

CLIENT RECEIVED PRIMARY SERIES PFIZER AS A BOOSTER DOSE. LATER A DUPLICATE RECORD WAS DISCOVERED AND SHOWED THE CLIENT RECEIVED 3 PREVIOUS DOSES OF MODERNA BETWEEN 10YO-11YO WHICH WAS NOT APPROVED FOR THAT AGE GROUP. THE PFIZER DOSE ADMINISTERED SHOUL'DVE BEEN THE BIVALENT BOOSTER NOT THE REGULAR PRIMARY SERIES GRAY-CAP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: NO ILLNESS REPORTED
Vorgeschichte: NO CHRONIC CONDITIONS REPORTED
Andere Medikamente: NONE REPORTED
Allergien: NO ALLERGIES REPORTED
Vorherige Impfungen: -

VAERS 2478426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OR
Alter: 20,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 08.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was given monovalent Pfizer instead of bivalent Pfizer by MA mistake. no adverse reaction was reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2478333

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 43,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 03.10.2022
Beginn: 03.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Patient was given Covid vaccine 28 days after the beyond use date. Patient reports no side effects to vaccine administration. Pfizer has been notified. Patient has been notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension, GERD, anxiety
Andere Medikamente: Lisinopril, Buspar, Prilosec
Allergien: none
Vorherige Impfungen: -

VAERS 2478329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 20,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 27.09.2022
Beginn: 27.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Patient was given first dose of Covid Pfizer vaccine 21 days past the beyond use date. Pfizer was contacted about it. Patient was contacted. Patient report no side effects following administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: Patient
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2478093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 10.06.2022
Beginn: 11.10.2022
Tage bis Beginn: 123,0
Dosis: 4
Route/Site: - / -

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

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

Symptomtext

COVID vaccine breakthrough case. Pfizer 1/27/21 EL3247, 2/17/21 EM9810, and boosted 9/28/21 EW0169 and 6/10/22 FN2908

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive COVID test on 10/11/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2477944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: OH
Alter: 81,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 13.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

As of now, no adverse drug reactions, but the patient was supposed to get the bivalent covid vaccine and was administered the original gray vial pfizer

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: latex allergy
Vorherige Impfungen: -

VAERS 2477938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: OH
Alter: 82,0
Geschlecht: M
Eingang: 13.10.2022
Impfdatum: 13.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

As of now, no adverse drug reactions, but the patient was supposed to get the bivalent covid vaccine and was administered the original gray vial pfizer

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: nka
Vorherige Impfungen: -

VAERS 2477247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TN
Alter: 15,0
Geschlecht: F
Eingang: 13.10.2022
Impfdatum: 18.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Pfizer monovalent vaccine ordered by provider and administered by nursing staff when patient presented fro office visit on 8/18/22. Almost two months later, on 10/13/22, parents were in our office and brought in documentation that patient had received 2 prior Pfizer Covid vaccines, on 6/30/22 and 7/30/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2477140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TN
Alter: 65,0
Geschlecht: M
Eingang: 13.10.2022
Impfdatum: 12.10.2022
Beginn: 12.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

The patient was scheduled to receive a Pfizer bivalent dose and he received a monovalent dose. The vaccine given was also expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: none
Vorherige Impfungen: -

VAERS 2473737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 29,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer booster instead of the bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2473733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 78,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer vaccine instead of the bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Penicillin, Sulfa
Vorherige Impfungen: -

VAERS 2473728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer booster instead of the bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2473721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 73,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer booster instead of the bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Latex, Amoxicillin
Vorherige Impfungen: -

VAERS 2473717

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer booster instead of the bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2473713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 86,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer booster instead of bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2473707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer booster instead of the bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2473691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 76,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer vaccine instead of the bivalent booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2473687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 34,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Gave standard pfizer vaccine instead of the bivalent dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: -
Andere Medikamente: n/a
Allergien: NKA
Vorherige Impfungen: -

VAERS 2473677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 72,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 07.10.2022
Beginn: 07.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Gave standard pfizer instead of pfizer bivalent vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: type 2 diabetes with diabetic neuropathy, insomnia, rosacea, vitamin d deficiency, BPH with obstruction, essential hypertension, chronic shoulder pain
Andere Medikamente: -
Allergien: zolpidem, pregabalin, Propofol, carbamazepine analogs, gabapentin, tramadol, tapentadol
Vorherige Impfungen: -

VAERS 2473575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: 69,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

VACCINE GIVEN AFTER BYOND USE DATE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2473139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ME
Alter: 64,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 13.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia

Symptomtext

Selective loss of taste and smell noticed 10 days after first covid vaccine. I can no longer taste certain foods. Tastes that are present are diminished. No improvement after 18 months. One week after the fourth shot, I lost the taste of more foods. This additional loss continues after 2 months. To my knowledge, I have never had Covid-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ageusia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Cymbalta, Flonase
Allergien: Almonds, Filberts, various pollen
Vorherige Impfungen: -

VAERS 2471450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fn2908

gering

Staat: NH
Alter: 71,0
Geschlecht: M
Eingang: 06.10.2022
Impfdatum: 01.02.2021
Beginn: 02.05.2021
Tage bis Beginn: 90,0
Dosis: UNK
Route/Site: - / -

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

Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: No
Andere Medikamente: Metoprolol; Losarten; clopedigrel; clorthaladone; atorvastatin; low dose aspirin, vitamin D; vitamin B.
Allergien: NA
Vorherige Impfungen: -

VAERS 2469857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 76,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 05.10.2022
Beginn: 05.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

The RN selected the Pfizer primary vaccine vial instead of the Pfizer bivalent vaccine vial and administered 0.3 ml dose to the patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: Niacin
Vorherige Impfungen: -

VAERS 2469846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 50,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 05.10.2022
Beginn: 05.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

The RN selected the Pfizer primary vaccine vial instead of the Pfizer Bivalent vaccine vial and administered a 0.3 ml dose to the patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: Bees
Vorherige Impfungen: -

VAERS 2467186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: KY
Alter: 14,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 03.10.2022
Beginn: 03.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was given Pfizer Monovalent injection for injection #3 (booster) rather than Pfizer Bivalent booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None. No adverse reactions.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Zoloft 50 mg Tablet Albuterol Sulfate 90 mcg Zyrtec 10 mg Tablet
Allergien: -
Vorherige Impfungen: -

VAERS 2464568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: 76,0
Geschlecht: M
Eingang: 29.09.2022
Impfdatum: 28.09.2022
Beginn: 28.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was given Pfizer Covid monwalent vaccine instead of Pfizer Covid bi-valent vaccine for booster dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 28.09.2022
Beginn: 28.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: - / LA

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

Wrong product administered

Symptomtext

Patient was given Pfizer Covid monovalent vaccine instead of Pfizer Covid bi-valent vaccine for booster dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2464559

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FN2908

gering

Staat: NY
Alter: 28,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 28.09.2022
Beginn: 28.09.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was given Pfizer Covid monovalent vaccine instead of Pfizer Covid bi-valent vaccine for booster dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2463460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: -
Geschlecht: U
Eingang: 28.09.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Monovalent vaccine was given to patient instead of the Bi- Valent all patients were notified and had no adverse reaction noted and instructed they are eligible for the Bi- valent 2months after they received the Monovalent. Moderna Monovalent was given to one patient on each of these days: 9/8/22, 9/9/22, and 9/14/22. Pfizer Monovalent was given to one patient on each of these days 9/6/22, 9/9/22, 9/12/22, 9/13/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2462780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CT
Alter: 59,0
Geschlecht: M
Eingang: 28.09.2022
Impfdatum: 28.05.2022
Beginn: 22.09.2022
Tage bis Beginn: 117,0
Dosis: 4
Route/Site: OT / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Breakthrough COVID-19 Infection; Breakthrough COVID-19 Infection; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 60-year-old male patient received BNT162b2 (BNT162B2), on 22Mar2021 as dose 1, single (Lot number: EP6955), on 12Apr2021 as dose 2, single (Lot number: EP6955), on 12Dec2021 as dose 3 (booster), single (Lot number: 33130BA) and on 28May2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 59 years, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "High Blood Pressure" (unspecified if ongoing), notes: High Blood Pressure; "High Cholesterol" (unspecified if ongoing); "Pre-Diabetes" (unspecified if ongoing); "Rosacea" (unspecified if ongoing); "tree nut allergy" (unspecified if ongoing), notes: tree nut allergy. Concomitant medication(s) included: LEVOTHYROXINE; ROSUVASTATIN; FARXIGA; ORACEA [DOXYCYCLINE]; OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 22Sep2022, outcome "recovering" and all described as "Breakthrough COVID-19 Infection". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (24Sep2022) Positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of covid-19. Clinical course: No other vaccine in four weeks. No covid prior vaccination. No follow up attempts possible. No further information is required.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220924; Test Name: COVID-19 Antigen Rapid Test; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts (tree nut allergy); Blood pressure high (High Blood Pressure); High cholesterol; Pre-diabetes; Rosacea
Andere Medikamente: LEVOTHYROXINE; ROSUVASTATIN; FARXIGA; ORACEA [DOXYCYCLINE]; OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2461991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WI
Alter: 46,0
Geschlecht: M
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

None

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2461985

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WI
Alter: 71,0
Geschlecht: M
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

None

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2460372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 38,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 12.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Monovalent COVID-19 Vaccine was administered as a booster shot instead of a bilavent. Patient did not have any adverse events or outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: depression, anorexia, Pre DM
Vorgeschichte: Same as above
Andere Medikamente: lisinopril naproxen cyclobenzaprine olanzapine fluoxetine
Allergien: nkda
Vorherige Impfungen: -

VAERS 2460365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 28,0
Geschlecht: U
Eingang: 23.09.2022
Impfdatum: 06.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Monovalent COVID-19 vaccine was administered as a booster shot instead of abivalent. Patient did not having an adverse event or outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2460364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 37,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 06.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

monovalent COVID-19 vaccine was administered as a booster shot instead of a bivalent. Patient did not have an adverse event or outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2460363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 36,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 06.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

monovalent COVID-19 vaccine was administered as a booster shot instead of a bivalent. Patient did not have any adverse events or outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2460362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 63,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 12.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

monovalent COVID-19 vaccine was administered as a booster shot instead of a bivalent. Patient did not have any adverse events or outcome

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: COPD, hyperlipidemia,
Vorgeschichte: Same as above
Andere Medikamente: Flonase Allergy Relief ProAir HFA ipratropium 0.5 mg-albuterol 3 mg (2.5 mg base)/3 mL nebulization soln naproxen
Allergien: nkda
Vorherige Impfungen: -

VAERS 2460358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 61,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 07.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered No adverse event

Symptomtext

Monovalent COVID-19 vaccine was administered as a booster shot instead of a bivalent. Patient did not have any adverse events or outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Diabetes, HTN, COPD, Hypothyroidism, GAD, GERD PVD, Depression
Vorgeschichte: Same as above
Andere Medikamente: fluticasone propionate; GABAPENTIN; BUSPIRONE HYDROCHLORIDE; ProAir HFA; clopidogrel; METFORMIN HYDROCHLORIDE; OXYBUTYNIN CHLORIDE; BUPROPION HYDROCHLORIDE ER (SR); OMEPRAZOLE; LEVOTHYROXINE SODIUM; HYDROCHLOROTHIAZIDE; clotrimazole; montel
Allergien: Estrogens
Vorherige Impfungen: -

VAERS 2459979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 62,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 09.09.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Monovalent COVID-19 vaccine was administered as a booster shot instead of a bivalent. Patient did not have any adverse events or outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: Diabetes, HTN, Hyperlipidemia
Vorgeschichte: Same as above
Andere Medikamente: Farxiga lisinopril metformin allopurinol atorvastatin glimperide
Allergien: none
Vorherige Impfungen: -

VAERS 2454689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 18,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 06.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was leaving the country the next day(Sept 7th) and stated he HAD to have a covid booster. I did not have any Bivalent vaccine in house and so gave him Pfizer grey cap that just the day before had been given as a booster dose but apparently could no longer be given as such. He did not have any adverse reactions. His parents were notified that he should receive a bivalent dose of covid vaccine 2 months after he received this dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2454659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OR
Alter: 35,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 22.09.2022
Beginn: 22.09.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

None - Vaccine expired on 09/05/2022 so it was subpotent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2454648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OR
Alter: 41,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

None - The vaccine was expired on 9/5/2022 so the vaccine was subpotent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 2454453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 45,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 18.09.2022
Beginn: 18.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2453731

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 23,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 08.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient given booster dose of Pfizer monovalent after policy changed on 9-3-22 when bivalent was not yet available. No adverse reaction or complaints reported by patient. Will update when bivalent is in stock.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Amitriptyline, flexeril, hydroxyzine, metformin, omeprazole
Allergien: -
Vorherige Impfungen: -

VAERS 2453710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 39,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 07.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient given booster dose of Pfizer monovalent after policy changed on 9-3-22 when bivalent was not yet available. No adverse reaction or complaints reported by patient. Will update when bivalent is in stock.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: levothyroxine
Allergien: -
Vorherige Impfungen: -

VAERS 2453692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 32,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 06.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient given booster dose of Pfizer monovalent after policy changed on 9-3-22 when bivalent was not yet available. No adverse reaction or complaints reported by patient. Will update when bivalent is in stock.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: proair, montelukast
Allergien: -
Vorherige Impfungen: -

VAERS 2453689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 40,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 06.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient given booster dose of Pfizer monovalent after policy changed on 9-3-22 when bivalent was not yet available. No adverse reaction or complaints reported by patient. Will update when bivalent is in stock.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: 18,0
Geschlecht: M
Eingang: 20.09.2022
Impfdatum: 19.08.2022
Beginn: 19.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Pt received first Moderna COVID vaccine on 1/14/22 and never received the second. When in the office for a WCC on 8/19/22, we administered Pfizer COVID vaccine for what was the second vaccine in the primary series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperopia
Andere Medikamente: None
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2452159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: 19,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 30.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Inappropriate schedule of product administration Interchange of vaccine products

Symptomtext

Pt started COVID Vaccine series with Moderna on 6/15/22. Pt never went and received a second Moderna dose. When pt was in the office for a physical, we gave a Pfizer dose as the second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Optic Disc Cupping, bilateral Myopia, bilateral
Andere Medikamente: None
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2452126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ID
Alter: 16,0
Geschlecht: M
Eingang: 20.09.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Patient was not given Pfizer-Biotech Bivalent as booster as required by regulatory authority.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: NONE
Vorgeschichte: -
Andere Medikamente: NONE
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2451202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 92,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 27.05.2022
Beginn: 19.09.2022
Tage bis Beginn: 115,0
Dosis: 4
Route/Site: - / -

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

Unevaluable event

Symptomtext

Fully vaccinated boosted twice

Weitere VAERSDATA-Felder

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

VAERS 2451199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OR
Alter: -
Geschlecht: U
Eingang: 19.09.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

2 Staff member's used monovalent Pfizer vaccine thinking it was Bivalent Vaccine and administered doses to a total of 4 patients between 09/16/2022 and 09/19/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2451181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: ME
Alter: 43,0
Geschlecht: F
Eingang: 19.09.2022
Impfdatum: 15.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

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

Product storage error

Symptomtext

Vaccine had been stored at temperatures 35-45 degrees Fahrenheit for greater than 10 weeks prior to being discarded. Discard date was 9/2

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 18.05.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 69-year-old male patient received BNT162b2 (BNT162B2), on 24Jan2021 at 13:00 as dose 1, single (Batch/Lot number: unknown), in left arm, on 14Feb2021 at 13:00 as dose 2, single (Lot number: FL9267), in left arm, on 01Oct2021 at 14:00 as dose 3 (booster), single (Lot number: 31035BA), in left arm and on 18May2022 at 15:00 as dose 4 (booster), single (Lot number: FN2908) at the age of 69 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Milk protein A" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: At Home test became strongly positive after fading to almost gone; Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical summary: Other medication in 2 weeks was None. Patient took Paxlovid, starting 31Aug2022 and Treatment stop date was 04Sep2022 for treatment of COVID-19. Adverse event was also reported as at home test became strongly positive after fading to almost gone on 10Sep2022 at 9:00 AM. It was unknown if patient recovered with no treatment. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive ; Comments: At Home test became strongly positive after fading to almost gone.; Test Name: COVID-19 test; Test Result: Positive ; Comments: Treatment of COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Milk allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2450281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 64,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 19.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Interchange of vaccine products; 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 64-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 19Jul2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 64 years, in right arm for covid-19 immunisation; elasomeran (COVID-19 VACCINE MODERNA), on 19Feb2021 at 15:00 as dose 1, single (Lot number: 006M20A), in left arm, on 19Mar2021 as dose 2, single (Lot number: 003AZIA), in left arm and on 06Dec2021 as dose 3 (booster), single (Lot number: 030H21B), in left arm for covid-19 immunisation. The patient's relevant medical history included: "no" (unspecified if ongoing), notes: Other medical history: no. Concomitant medication(s) included: CITALOPRAM; OMEPRAZOLE. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Covid-19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Report about covid treatment was yes. Patient received other medication in 2weeks. anti viral details as product: COVID 19 Treatment, brand: PAXLOVID, treatment start date: 01Sep2022, treatment stop date: 06Sep2022, indication: Treatment of COVID-19. No Known allergies. No Other medical history.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID -19 virus test; Test Result: Positive ; Comments: Covid-19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: no, Comment: Other medical history: no
Andere Medikamente: CITALOPRAM; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2450167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 01.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received BNT162b2 (BNT162B2), on 04Feb2021 as dose 1, single (Lot number: EN5318), in left arm, on 21Feb2021 as dose 2, single (Lot number: EN6201), in right arm, in Aug2021 as dose 3 (booster), single (Lot number: EW0182), in left arm and on 01Jun2022 as dose 4 (booster), single (Lot number: FN2908) at the age of 72 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Paxlovid", start date: 01Sep2022, stop date: 06Sep2022, notes: Stopped. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Covid-19 treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive ; Comments: Covid-19 treatment
Aktuelle Erkrankungen: COVID-19 treatment (Stopped)
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2447911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 74,0
Geschlecht: M
Eingang: 16.09.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was meant to receive the Pfizer bivalent vaccine, but in turn received the Pfizer monovalent vaccine. Pfizer drug safety report reference number issued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Uknown
Vorgeschichte: Chronic lung disease
Andere Medikamente: Unable to determine
Allergien: Quinolones
Vorherige Impfungen: -

VAERS 2447903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered Wrong product administered

Symptomtext

Patient received the Pfizer monovalent vaccine, but was meant and expecting the Pfizer bivalent vaccine. Pfizer drug safety report reference number.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Hypertension
Andere Medikamente: Unable to determine
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2447901

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge FN2908

gering

Staat: OH
Alter: 56,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Patient received the Pfizer monovalent vaccine when she was meant to receive the Pfizer bivalent vaccine. Pfizer drug safety report reference number: D3VH0R6L

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unable to determine
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2447893

UNKNOWN MANUFACTURER · COVID19 (COVID19 (UNKNOWN)) · Charge FN2908

gering

Staat: OH
Alter: 59,0
Geschlecht: M
Eingang: 16.09.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Patient was meant to receive the Pfizer bivalent booster but received the monovalent by mistake. Pfizer drug safety report reference number D3VH0R6L

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Ulcerative colitis, osteoarthritis, pancreatic insufficiency
Andere Medikamente: Unable to determine at the time
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2447876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OH
Alter: 53,0
Geschlecht: M
Eingang: 16.09.2022
Impfdatum: 15.09.2022
Beginn: 15.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Patient was meant to receive the Pfizer bivalent booster, but instead received the pfizer monovalent vaccine. Pfizer drug safety report reference number: D3VH0R6L

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Crohn's Disease
Andere Medikamente: Unable to determine full medication profile.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2447851

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 14.09.2022
Beginn: 14.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Interchange of vaccine products

Symptomtext

COVID-19 mRNA Pfizer gray top monovalent dose ordered, dispensed, and administered. Upon later review, noticed patient had already received 3 mRNA vaccine doses previously and should have received a bivalent booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2444693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: AZ
Alter: 16,0
Geschlecht: M
Eingang: 14.09.2022
Impfdatum: 07.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Patient received first dose on 09/07/2022 and received a second dose on 09/13/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 2442901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MN
Alter: 65,0
Geschlecht: M
Eingang: 13.09.2022
Impfdatum: 26.05.2022
Beginn: 10.09.2022
Tage bis Beginn: 107,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19

Symptomtext

Patient developed COVID-19 post vaccinations.

Weitere VAERSDATA-Felder

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

VAERS 2440035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Pt has no reactions, but received monovalent vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2439913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MN
Alter: 85,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 22.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. An 85-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jan2021 at 17:30 as dose 1, single (Lot number: EC9201), in left arm, on 18Feb2021 at 17:15 as dose 2, single (Lot number: EN6201), in left arm, on 30Sep2021 at 13:30 as dose 3 (booster), single (Lot number: FC3184), in left arm and on 22Jun2022 at 11:30 as dose 4 (booster), single (Lot number: FN2908) at the age of 85 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "migraines" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "Known allergies: NSAIDs" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: COVID 19 Treatment; (unspecified date) Negative, notes: Rebound positive 8 days after negative. Treated with Paxlovid; (07Sep2022) Positive, notes: Rebound positive 8 days after negative. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: It was unknown if the patient received other medication in 2weeks. Patient received Paxlovid for treatment of COVID-19 from 24Aug2022 to 29Aug2022. On 07Sep2022, at11:30 AM patient had Rebound positive 8 days after negative. Treated with Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Name: COVID-19 test; Test Result: Negative ; Comments: Rebound positive 8 days after negative. Treated with Paxlovid.; Test Date: 20220907; Test Name: COVID-19 test; Test Result: Positive ; Comments: Rebound positive 8 days after negative.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to NSAIDs; High cholesterol; Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 44,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 31.08.2022
Beginn: 31.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Expired product administered

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 31.08.2022
Beginn: 31.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Expired product administered Product storage error

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 61,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 30.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Expired product administered

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 75,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 30.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Expired product administered

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 72,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 30.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Expired product administered

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to regulatory authority, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 29.08.2022
Beginn: 29.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Expired product administered

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 52,0
Geschlecht: M
Eingang: 09.09.2022
Impfdatum: 29.08.2022
Beginn: 29.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / UN

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

Expired product administered

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 76,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 26.08.2022
Beginn: 26.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / UN

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

Expired product administered

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 89,0
Geschlecht: M
Eingang: 09.09.2022
Impfdatum: 25.08.2022
Beginn: 25.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / UN

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

Expired product administered Product storage error

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 63,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 23.08.2022
Beginn: 23.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

Expired product administered Product storage error

Symptomtext

Vaccine was received from our Pharmacy on 6/9/22, vaccine expired in 10 weeks due to refrigeration storage which would have been 8/18. Patient received vaccine after expiration date. Spoke to CDC, they advise patient to be revaccinated for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2436276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: KY
Alter: 5,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 09.09.2022
Beginn: 09.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LL

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

Incorrect dose administered

Symptomtext

patient was given Pfizer COVID vaccine for age 12 years and older instead of for age 5 years to 11 years. was given 0.2 ml

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2431063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WA
Alter: 50,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incident Details: Per a local clinic provider's email sent out on 9/1/22-"the monovalent mRNA COVID-19 vaccines are not authorized as booster doses for individuals 12 years of age and older. Any patients that are currently scheduled to receive a booster should wait until we have the bivalent booster on hand." The patient, was seen in office on 9/2/22 and received a booster dose of the monovalent mRNA COVID-19 vaccine (pfizer) by *** in error as patients are now only supposed to receive the bivalent booster per Dr.'s email. Pt was due for booster at the time they received it, however the bivalent booster was not yet stocked at the pharmacy. Possible Cause: Possible cause of the incident is that an email was sent out regarding the discontinuation of monovalent covid boosters until the pharmacy receives the bivalent booster doses. This was overlooked by management and staff, as previous changes to clinic processes is usually discussed in a meeting. Also ?monovalent? and ?bivalent? are new terms that have not previously been used when discussing booster vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2431062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WA
Alter: 53,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incident Details: Per a clinic provider's email sent out on 9/1/22- "the monovalent mRNA COVID-19 vaccines are not authorized as booster doses for individuals 12 years of age and older. Any patients that are currently scheduled to receive a booster should wait until we have the bivalent booster on hand." The patient was seen in office on 9/2/22 and received a booster dose of the monovalent mRNA COVID-19 vaccine (Pfizer) by *** in error as patients are now only supposed to receive the bivalent booster per Drs. email. Patient was due for booster at the time they received it, however the bivalent booster was not yet stocked. Possible Cause: Possible cause of the incident is that an email was sent out regarding the discontinuation of monovalent Covid boosters until Private receives the bivalent booster doses. This was overlooked by management and staff, as previous changes to clinic processes is usually discussed in a meeting. Also "monovalent" and "bivalent" are new terms that have not previously been used when discussing booster vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2431060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WA
Alter: 56,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Per a clinic provider's email sent on 9/1/2022: "The monovalent mRNA COVID-19 vaccines are not authorized as booster doses for individuals 12 years of age and older. Any patients currently scheduled to receive a booster should wait until we have the bivalent booster on hand." The patient, seen in office on 9/2/2022, received a booster dose of the monovalent mRNA COVID-19 vaccine (Pfizer). This was in error as patients are now only supposed to receive the bivalent booster per email. Patient due for booster at the time they received it, however the bivalent booster was not yet stocked. Possible cause of the incident is that an email was sent out regarding the discontinuation of monovalent COVID-19 boosters until receipt of the bivalent booster doses. This was overlooked, as previous changes to clinic processes is usually discussed in a meeting. Also 'monovalent' and 'bivalent' are new terms that have not previously been used when discussing booster vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2431048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WA
Alter: 26,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incident Details: Per an email sent out on 9/1/22 from a Clinic provider-"the monovalent mRNA COVID-19 vaccines are not authorized as booster doses for individuals 12 years of age and older. Any patients that are currently scheduled to receive a booster should wait until we have the bivalent booster on hand." The patient, was seen in office on 9/2/22 and received a booster dose of the monovalent mRNA COVID-19 vaccine (pfizer) by staff in error as patients are now only supposed to receive the bivalent booster per Dr. email. Pt was due for booster at the time they received it, however the bivlalent booster was not yet stocked at clinic. Possible Cause: Possible cause of the incident is that an email was sent out regarding the discontinuation of monovalent covid boosters until clinic receives the bivalent booster doses. This was overlooked by management and staff, as previous changes to clinic processes is usually discussed in a meeting. Also ?monovalent? and ?bivalent? are new terms that have not previously been used when discussing booster vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2431021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 96,0
Geschlecht: M
Eingang: 07.09.2022
Impfdatum: 12.03.2021
Beginn: 05.08.2022
Tage bis Beginn: 511,0
Dosis: 4
Route/Site: - / -

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

Asymptomatic COVID-19 C-reactive protein increased COVID-19 Computerised tomogram head normal Fall Fibrin D dimer increased Full blood count normal Head injury Inflammatory marker increased Metabolic function test normal SARS-CoV-2 test positive Troponin normal

Symptomtext

97y.o. male with history of dementia, anemia, L1 compression fracture, urinary retention, and atrial fibrillation. He was brought in yesterday after he had fallen outside and hit his head on the concrete, unsure if any LOC. CT head was negative for any acute process. Labs including CBC, BMP, and troponin were all unremarkable. He was found to be positive for COVID but was saturating well on room air and otherwise asymptomatic. Inflammatory markers were checked, he did have elevated CRP and d-dimer. Patient deemed medically stable for discharge by physician. Hospital accepted patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: 16,0
Labordaten: 8/5 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2428177

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CA
Alter: 57,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered Incorrect product formulation administered

Symptomtext

Patient given Pfizer monovalent vaccine for the 4th dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Type 2 diabetes
Vorgeschichte: DM, dyslipidemia
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2428176

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Pt given 4th dose of pfizer monovalent vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Hemiplegia and hemiparesis following cerebral infarction affecting left non-dominant side (HCC-CMS) [I69.354]
Vorgeschichte: Carotid body tumor (HCC-CMS) Hemiplegia and hemiparesis following cerebral infarction affecting left non-dominant side (HCC-CMS) Essential hypertension Mixed hyperlipidemia Morbid obesity due to excess calories (HCC-CMS) Prediabetes BMI 31.0-31.9,adult Acute pain of left knee Noncompliance with diet and medication regimen Illiteracy and low-level literacy Osteoarthritis of multiple joints Noncompliance with diagnostic test Complicated grief History of stroke Acute stroke due to ischemia (HCC-CMS) Adjustment disorderCarotid body tumor (HCC-CMS) Hemiplegia and hemiparesis following cerebral infarction affecting left non-dominant side (HCC-CMS) Essential hypertension Mixed hyperlipidemia Morbid obesity due to excess calories (HCC-CMS) Prediabetes BMI 31.0-31.9,adult Acute pain of left knee Noncompliance with diet and medication regimen Illiteracy and low-level literacy Osteoarthritis of multiple joints Noncompliance with diagnostic test Complicated grief History of stroke Acute stroke due to ischemia (HCC-CMS) Adjustment disorder
Andere Medikamente: atorvastatin (LIPITOR) 80 mg tablet diclofenac sodium (VOLTAREN) 1 % gel lisinopriL 10 mg tablet naproxen (NAPROSYN) 500 mg tablet LORazepam (ATIVAN) 0.5 mg tab
Allergien: knda
Vorherige Impfungen: -

VAERS 2427978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

pt given pfizer monovalent booster dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic pain bilateral wrists, Hypothyroidism
Andere Medikamente: fluticasone propionate (FLONASE) 50 mcg/actuation nasal spray diphenhydrAMINE HCL (BENADRYL) 25 mg capsule ibuprofen 600 mg tablet meclizine (ANTIVERT) 25 mg tablet
Allergien: knda
Vorherige Impfungen: -

VAERS 2427976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CA
Alter: 30,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient given Pfizer monovalent for the first booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Polycystic ovarian syndrome
Andere Medikamente: Klonopin, Zoloft, Aldactone
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2427974

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 02.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Pt given 4th booster dose of Pfizer monovalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Morbid obesity,
Vorgeschichte: CPOD,, Obesity, DM11,Cirhhosis of liver ,splenomegaly ,obstructive sleep apnea,
Andere Medikamente: benzonatate (TESSALON) 100 mg capsule montelukast (SINGULAIR) 10 mg tablet omeprazole (PRILOSEC) 20 mg DR capsule diclofenac sodium (VOLTAREN) 1 % gel fluticasone propionate (FLONASE) 50 mcg/actuation nasal spray polyethylene glycol 3350 17
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2427959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

3RD dose of Pfizer monovalent given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: GERD, Elevated cholesterol., ST elevation
Andere Medikamente: atorvastatin (LIPITOR) 40 mg tablet metoprolol tartrate (LOPRESSOR) 25 mg tablet fluticasone propionate (FLONASE) 50 mcg/actuation nasal spray baclofen (LIORESAL) 10 mg tablet traMADoL (ULTRAM) 50 mg tablet famotidine (PEPCID) 20 mg tablet
Allergien: Ibuprofen,Naprosyn
Vorherige Impfungen: -

VAERS 2427954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: CA
Alter: 24,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / -

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

Exposure during pregnancy Incorrect product formulation administered

Symptomtext

3RD Dose of Pfizer monovalent vaccine given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Exposure during pregnancy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Gestational Diabetes, FE deficiency anemia
Vorgeschichte: None
Andere Medikamente: Novolog Insulin u/100, Lantus, Fe Sulfate, DSS
Allergien: NONE
Vorherige Impfungen: -

VAERS 2427944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 02.09.2022
Beginn: 02.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

3rd dose of Pfizer monovalent given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control
Allergien: None
Vorherige Impfungen: -

VAERS 2426693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: WI
Alter: 85,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 08.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Extra dose administered Memory impairment

Symptomtext

Patient was seen in clinic on 6/8/22. Patient's chart showed that he was due for the 2nd COVID booster even after querying the local Immunization Registry. Patient was asked if he wanted the COVID vaccine, he said yes so it was given. Clinic later received an update from patient's daughter via database that patient already ready received his 2nd COVID booster on 5/9/2022 at another healthcare facility. Patient's daughter reported uploading the vaccine via database. Per report filed, patient has some memory issues, but attends appointments alone and does not have an activated online chart. When chart was reviewed the following day (6/9/22), the vaccine from 5/9/2022 was available. Of note, at times there have been delays when querying the local Immunization Record (sometimes up to 5 minutes or at times it errors out). Due to potential system error and patient's memory concerns, he ended up receiving a total of 5 doses of the vaccine vs 4. Patient denied any current symptoms and provider is aware.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Atrial fibrillation, BPH, CAD, cluster headaches, elevated fasting glucose, CKD, osteoarthritis, GERD, HTN, peripheral neuropathy, vitamin D deficiency, ,oxed hyperlipidemia, tremor
Andere Medikamente: aspirin, atenolol, atorvastatin, cephalexin, flonase, loratadine, lutein, magnesium oxide, glucosamine, multivitamin, potassium chloride, tamsulosin, vitamin D, warfarin
Allergien: celecoxib
Vorherige Impfungen: -

VAERS 2426686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: NJ
Alter: 17,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 18.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Extra dose administered

Symptomtext

4th covid vaccine giving by mistake. guardian/ patients forgot their covid card. 4rth vaccine giving instead of 3rd . immunization record not up to date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2426680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 14,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 18.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / -

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

Extra dose administered

Symptomtext

4th COVID-19 vaccine giving by mistake. Patient didn't have records with her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2426649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 14,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 01.09.2022
Beginn: 01.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Gave Covid booster after time of 12 hour expiration period

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2425326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 31.08.2022
Impfdatum: 03.06.2022
Beginn: 22.08.2022
Tage bis Beginn: 80,0
Dosis: 4
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

pt tested positive for COVID on 08/22/2022

Weitere VAERSDATA-Felder

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

VAERS 2423502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 59,0
Geschlecht: M
Eingang: 29.08.2022
Impfdatum: 22.07.2022
Beginn: 01.08.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: SYR / LA

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

Burning sensation

Symptomtext

After my 4th dose I started getting this burning sensation in my both the feet. It's intermittent burning sensation . I haven't had this issue before the 4th shot. I haven't made any changes in my diet to think that that might have been the root cause.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Burning sensation
Hospital-Tage: -
Labordaten: I haven't got any tests done in the lab
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: On the morning of 7/22/2022 I took one capsule of natures own's "RAW Probiotics for Men 50 and Wiser"
Allergien: Not known
Vorherige Impfungen: -

VAERS 2422807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 55,0
Geschlecht: F
Eingang: 29.08.2022
Impfdatum: 19.08.2022
Beginn: 19.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient received vaccine that was beyond it's use date of 7/22/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Chronic conditions only
Vorgeschichte: Allergic Rhinitis, Night sweats, Chronic Kidney Disease, Stress incontinence, History of MVA, Paresthesia, Headache, Neck Pain, Shoulder Pain / bilateral, Vaginal itching, BMI over 40, Tobacco Abuse, Restrictive lung disease, Obstructive sleep apnea, Cough, Essential Hypertension, Supraventricular tachycardia, Triscupid valve insufficiency, Chronic diastolic heart failure, Chronic Right Heart failure, Cirrhosis, Ascites, Elevated Alkaline phosphatase, Abnormal LFTs, Gastric Antral Vascular Ectasia with hemorrhage, Dyspepsia, Hiatal Hernia, Hyperlipidemia, Tubular Adenoma of Colon, Erythrocytosis, Restless leg syndrome, Lymphedema arm, Adhesive capsulitis - left, Fatigue
Andere Medikamente: Furosemide, Spironolactone, Immodium, Tums, Icy Hot, Salonpas-Hot, Ventolin, Claritin, Fluticasone, Albuterol, Atorvastatin, Valacyclovir, Glimepiride, Ozempic, Vitamin D3, Vitamin B-12, Metoproll, Escitalopram, Plexus, Prilosec, Melatonin
Allergien: Shingrix Vaccine, Amoxicillin, Penicillin, Sulfa, Formoterol, Jardiance, Doxycycline, Latex, Adhesive, Scopolamine, Bedesonide, Metformin, Symbicort, Cephalexin
Vorherige Impfungen: Shingrex - unknown date , localized swelling, redness

VAERS 2422472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: WY
Alter: 59,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 27.08.2022
Beginn: 27.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

We administered a Pfizer vaccine that expired the day previously, 8/26/22. I notified the patient and they did not report any adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: None
Vorherige Impfungen: -

VAERS 2422181

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: SC
Alter: 60,0
Geschlecht: F
Eingang: 27.08.2022
Impfdatum: 16.05.2022
Beginn: 01.08.2022
Tage bis Beginn: 77,0
Dosis: 4
Route/Site: - / RA

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

COVID-19 Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Mar2021 at 13:00 as dose 1, single (Lot number: EN6204), in right arm, on 30Mar2021 at 13:00 as dose 2, single (Lot number: EN6198), in right arm, on 28Oct2021 at 13:00 as dose 3 (booster), single (Lot number: FE3590), in right arm and on 16May2022 at 13:00 as dose 4 (booster), single (Lot number: FN2908) at the age of 60 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient did not take any other medications/products within 2 weeks of starting COVID-19 treatment. The patient previously received a COVID-19 Vaccine. The patient reported Known allergies: No, other medical history: None.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None Known allergies: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2421051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 12,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 18.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient given vaccine that was beyond it's use date of 7/22/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Dyspnea on Exertion, Allergic Rhinitis, Snoring, Twitching, Headaches, Enuresis/Noctunal
Andere Medikamente: Azelastine
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2421041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 14.07.2022
Beginn: 26.08.2022
Tage bis Beginn: 43,0
Dosis: 4
Route/Site: - / -

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

Unevaluable event

Symptomtext

Fully vaccinated and boosted twice

Weitere VAERSDATA-Felder

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

VAERS 2421033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 56,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 18.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient received vaccine that was beyond it's use date of 7/22/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Management of chronic conditions
Vorgeschichte: Prediabetes, Impaired Renal Function, Restless Leg Syndrome, Myofascial Pain Syndrome, Paroxysmal Atrial Fibrillation, Post surgical dumping syndrome, Obstructive Sleep Apnea, Depression/Anxiety, Obesity, CHF, Cardiomyopathy, Allergic Asthma, GERD, Fatigue
Andere Medikamente: Advair Diskus, Spironolactone, Trazodone, Paroxetine, Fluticasone, Albuterol, Buspirone, Gabapentin, Metoprolol, Allegra allergy, NAC, Prevacid, Slow-Mag, Acarbose, Enestro, Amlodipine, Zarfirlucast, Farxiga,
Allergien: Tamiflu, Fish, Peanuts, Lisinopril, Statins, Codeine, Iodine, Prilosec
Vorherige Impfungen: -

VAERS 2421022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 59,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 17.08.2022
Beginn: 17.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

Given vaccine that was beyond it's use date of 7/22/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Parasthesias, Tachycardia, Generalized Anxiety Disorder, IBS, Endometriosis, Multinodular Thyroid Goiter, Posterior Vitreous Detachment - right, Tinnitis, Raynauds,
Andere Medikamente: Clindamycin, Metamucil, Multivitamin
Allergien: Adhesive Tape, Danocrin, Magnesium, Pollen, Pantoprazole, Sulfa, Cipro, Amoxicillin, Latex, Bactrim, CT dye, Monistat, Cyclobenzaprine,
Vorherige Impfungen: -

VAERS 2421010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 64,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 17.08.2022
Beginn: 17.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient was given a vaccine that was beyond it's use date of 7/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Hypertension
Vorgeschichte: Osteoarthritis, Elevated PSA, Hyperlipidemia, Degenerative Disc disease C6-7
Andere Medikamente: Valsartan, Vit B-12
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2420873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 17,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 10.08.2022
Beginn: 10.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Given vaccine with a BUD of 7/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, Allergic Rhinitis, Menometrorrhagia
Andere Medikamente: Proair, Xulane, Zyrtec
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2420820

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fn2908

gering

Staat: NC
Alter: 31,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 07.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: SYR / LA

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

Blood test normal Exposure during pregnancy Foetal heart rate abnormal Foetal hypokinesia Laboratory test normal Stillbirth

Symptomtext

I was 32 weeks when I got my 2nd booster. Completely healthy pregnancy. I was due October 2. The baby stopped moving 1-2 days after the shot was given. I went to the dr and was told there was no heartbeat. I delivered my stillborn a few days later- she weighed 5 pounds 3 oz. this was my first pregnancy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test normal
Hospital-Tage: 2,0
Labordaten: All scheduled labs and tests that are routine for pregnancy had all come back normal. Further testing was done for bloodwork to look for reason or infections- everything came back normal.
Aktuelle Erkrankungen: No illnesses
Vorgeschichte: None. I was 32 weeks pregnant when I got my 2nd Covid booster (Pfizer) as recommended by my OBGYN. I had a healthy pregnancy so far, everything was normal and going according to plan. 2 days after I received the booster, the baby wasn?t moving. I found out the next day that there was no heartbeat.
Andere Medikamente: Iron pill and prenatals.
Allergien: No allergies
Vorherige Impfungen: -

VAERS 2420113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 73,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 08.08.2022
Beginn: 08.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Product use issue

Symptomtext

Vaccine given with BUD of 7/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product use issue
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Type II diabetes
Vorgeschichte: Type II diabetes, peripheral neuropathy, COPD, hypertension, hyperlipidemia, macular degeneration - right, venous insufficiency, mild sleep apnea, decreased hearing, ED, psoriasis, obesity
Andere Medikamente: Farxiga, Metoprolol, Levemir, Incruse Ellipta, Magnesium oxide, Losartan, Torsemide, Glimepiride, Pravastatin, Amlodipine, Vitamin D3, Aspirin
Allergien: Actos, Metformin, Lisinopril, Lipitor
Vorherige Impfungen: -

VAERS 2420107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 15,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 05.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Received vaccine with a BUD of 7/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2420106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PA
Alter: 19,0
Geschlecht: F
Eingang: 25.08.2022
Impfdatum: 19.08.2022
Beginn: 19.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Expired product administered No adverse event

Symptomtext

Vaccine administered after expired. Dispensed from pharmacy 8/18/2022; given 8/19/2022. No symptoms reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Epilepsy, migraines
Andere Medikamente: Zonisamide, Escitalopram, Brivaracetam, Fludrocortisone, Folic acid
Allergien: Penicillin, Lidocaine, bee venom, Latex
Vorherige Impfungen: -

VAERS 2420105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 67,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 03.08.2022
Beginn: 03.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient received a vaccine with a BUD of 7/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: -
Vorgeschichte: Prostate cancer, hyperlipidemia, dyspepsia, ED, hearing loss, tobacco abuse, alcohol abuse, exertional shortness of breath
Andere Medikamente: Omeprazole, HCTZ, Diclofenac, Atorvastatin, Viagra, Aspirin, Proair, Lupron, Calcium carbonate
Allergien: Beestings
Vorherige Impfungen: -

VAERS 2420100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 24,0
Geschlecht: F
Eingang: 25.08.2022
Impfdatum: 03.08.2022
Beginn: 03.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine given beyond-use-date of 7/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Decreased hearing in right ear
Vorgeschichte: None
Andere Medikamente: Dasetta, Flonase
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2420038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 18,0
Geschlecht: F
Eingang: 25.08.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Vaccine given beyond-use-date of 7/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Cystic acne, mild asthma
Andere Medikamente: ProAir, Azelaic cream, Doxycycline, Medroxyprogesterone
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2420028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: VT
Alter: 57,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 01.08.2022
Beginn: 01.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Patient given vaccine past it's BUD of 7/22/2022 - no know reaction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Obesity, COPD
Vorgeschichte: COPD, Obesity, Hyperlipidemia, Hypertension, Dyspepsia, Schizoaffective Disorder
Andere Medikamente: Propranolol, Losartan, Chlortimazole Cream, Aspirin, Invega Sustena, Tylenol, Risperdol
Allergien: Percocet, Welbutrin, Haldol
Vorherige Impfungen: -

VAERS 2419956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MN
Alter: 11,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 08.08.2022
Beginn: 08.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

The patient did not have an adverse health event. The wrong dose of covid vaccine was given to the patient with no harm caused towards the patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: N/A
Allergien: None
Vorherige Impfungen: -

VAERS 2419043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fn2908

gering

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 24.08.2022
Impfdatum: 03.08.2022
Beginn: 12.08.2022
Tage bis Beginn: 9,0
Dosis: 4
Route/Site: IM / RA

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

Cardiac disorder Confusional state Transient global amnesia

Symptomtext

Systemic: Cardiac Disorder (diagnosed by MD)-Medium, Systemic: Confusion-Severe, Systemic: transglobal amnesia-Severe

Weitere VAERSDATA-Felder

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

VAERS 2418441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 18,0
Geschlecht: M
Eingang: 23.08.2022
Impfdatum: 23.08.2022
Beginn: 23.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

COVID VACCINE GIVING 2 WEEKS BEFORE ACTUAL TIME. 6 MONTHS APART 3RD VACCINE FROM 2ND INSTEAD OF 8 WEEKS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2418237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: SC
Alter: 55,0
Geschlecht: F
Eingang: 23.08.2022
Impfdatum: 25.07.2022
Beginn: 19.08.2022
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Patient administered vaccine that was past it's BUD of 7/22/2022 - No known adverse effects

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Right foot pain
Vorgeschichte: Right mid-foot amputation, Depression
Andere Medikamente: Cetirizine, Gabapentin, Bupropion, Pantoprazole, Lido Patch
Allergien: PCN, Effexor, Zoloft, Simvastatin
Vorherige Impfungen: -

VAERS 2418227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PR
Alter: 57,0
Geschlecht: M
Eingang: 23.08.2022
Impfdatum: 22.05.2022
Beginn: 22.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Administration error: Patient is vaccinated with second Pfizer booster before completing his four months of indication between the first booster and his second booster. We proceed to inform the patient and Dr. in charge of the vaccination clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes
Andere Medikamente: Metformin 850 MG.
Allergien: None
Vorherige Impfungen: -

VAERS 2418222

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PR
Alter: 49,0
Geschlecht: M
Eingang: 23.08.2022
Impfdatum: 25.05.2022
Beginn: 25.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Product administered to patient of inappropriate age

Symptomtext

Administration error 2nd booster of the Pfizer BioNTech vaccine is administered to a patient who does not meet the recommended age to receive the 2nd booster. Patient evaluated vital signs Pulso-84, SPO2- 97%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Thyroid; Hypertension
Andere Medikamente: Unknown
Allergien: No allergies at the time of vaccination.
Vorherige Impfungen: -

VAERS 2414669

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge FN2908

gering

Staat: TN
Alter: 18,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 17.08.2022
Beginn: 17.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Immediate post-injection reaction Incoherent Muscle twitching Pallor

Symptomtext

Immediately upon 2nd injection patient became pale and incoherent also making seizure like twitches. Code green was paged and Nurse practitioner arrived to assess patient. 911 was also notified and an ambulance was dispatched. Upon assessment from the NP patient was becoming more coherent and vitals stabling with a BP pf 102/60. Patient was provided crackers and water. EMS arrived but patient refused transport. Patient also requested HPV vaccine to be given after incident and was told by NP that was acceptable. Patient was laid down on exam table and given HPV vaccine while EMS present. Patient tolerated HPV vaccine without difficulty.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Immediate post-injection reaction
Hospital-Tage: -
Labordaten: refused transport by EMS
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported
Andere Medikamente: none reported
Allergien: none reported
Vorherige Impfungen: -

VAERS 2413459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 17.08.2022
Impfdatum: 16.08.2022
Beginn: 16.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered

Symptomtext

Pfizer Covid 19 vaccine vial opened 08/15/2022 @ 8:28am and expired 08/15/2022 @ 8:28 pm On 08/16/2022 The Clinical Staff administered 0.3 cc of the expired Pfizer Covid vaccine @ 10:08am Patient informed and is currently doing well However vaccine dose invalid and will need to be repeated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Creatinine Supplement
Allergien: NKDA No Known food allergies
Vorherige Impfungen: -

VAERS 2412881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: SC
Alter: 42,0
Geschlecht: F
Eingang: 16.08.2022
Impfdatum: 21.07.2022
Beginn: 30.07.2022
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Herpes zoster

Symptomtext

Shingles to right upper chest, shoulder, ear and neck Treated with Valtrex, Lyrica, calamine and silvadene cream.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Ulcerative colitis/crohns disease
Andere Medikamente: Infliximab
Allergien: None
Vorherige Impfungen: -

VAERS 2411228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: IN
Alter: 16,0
Geschlecht: M
Eingang: 15.08.2022
Impfdatum: 02.08.2022
Beginn: 12.08.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / -

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

Eye haemorrhage Ophthalmological examination abnormal

Symptomtext

Patient woke up 10 days after vaccines with what appeared to be bleeding in the white part of the far corner of left eye. Patient already had appointment with his pediatrician. MD told parents "He probably scratched eye in his sleep." On the next day, patient woke up with the same symptom on the right eye. Mother took patient to see his eye doctor. Patient examined and cleared from having scratches/anything that could have caused this. Optometrist advised patient's mother to file an adverse report for vaccines received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye haemorrhage
Hospital-Tage: -
Labordaten: 08/13/2022 eye exam.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Concerta, Sertraline, protein shakes
Allergien: N/A
Vorherige Impfungen: -

VAERS 2411153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: AK
Alter: 17,0
Geschlecht: F
Eingang: 15.08.2022
Impfdatum: 11.08.2022
Beginn: 11.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

At time of vaccine administration and per the completed CDC pre-vaccination checklist, family states that patient had only 2 prior doses of Pfizer COVID-19 vaccine. After vaccine administration it was discovered that per our vaccine registry that patients record showed 3 prior doses (last dose on 12/30/21). Family is adamant that this vaccine dose was not received as patient left prior to vaccine admin, but after following up with vaccinating facility this pharmacy stated that it is not possible for them to have this documentation if the patient didn't receive the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: cough on exercise, multiple benign melanocytic nevi
Andere Medikamente: albuterol sulfate HFA 90 mcg/actuation, nitrofurantoin monohydrate/macrocrytsals 100 mg capsule, phenazopyridine 200 mg tablet
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2411148

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: AK
Alter: 15,0
Geschlecht: F
Eingang: 15.08.2022
Impfdatum: 11.08.2022
Beginn: 11.08.2002
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

At time of vaccine administration and per the completed CDC pre-vaccination checklist, family states that patient had only 2 prior doses of Pfizer COVID-19 vaccine. After vaccine administration it was discovered that per our vaccine registry that patients record showed 3 prior doses (last dose on 1/9/22). Family is adamant that this vaccine dose was not received.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Irregular mestruation
Andere Medikamente: Zyrtec
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2410022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NY
Alter: 18,0
Geschlecht: M
Eingang: 12.08.2022
Impfdatum: 05.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Inappropriate schedule of product administration

Symptomtext

Pt came in for a Well Child Check up, determined to be healthy with no medical issues. Ordered by provider for a COVID booster and it was administered. Pt had a COVID booster on 1/24/22, so was not due for a COVID Booster at the time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2408431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: -
Alter: 83,0
Geschlecht: U
Eingang: 11.08.2022
Impfdatum: 12.07.2022
Beginn: 28.07.2022
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19

Symptomtext

HOSPITALIZED WITH COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2407287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: OK
Alter: 16,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 08.08.2022
Beginn: 10.08.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

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

Symptomtext

Breakthrough case COVID-19 after fully vaccinated with 3 doses of Pfizer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 Abbott ID NOW/PCR positive on 8/10/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2407259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 18,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

First booster. Given 0.2ml instead of 0.3ml

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2407250

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 68,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

Second booster. Given 0.2ml instead of 0.3ml

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2407249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 79,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Second Booster. Given 0.2ml instead of 0.3ml

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2407246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 93,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Second booster. Given 0.2ml instead of 0.3ml

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2407243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 86,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Second booster dose. Given 0.2ml instead of 0.3ml

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2407240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 70,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Second booster dose. Given 0.2ml instead of 0.3ml

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2407232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: NJ
Alter: 61,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

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

Incorrect dose administered

Symptomtext

First booster dose. Received 0.2ml instead of 0.3ml of Pfizer

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MA
Alter: 22,0
Geschlecht: M
Eingang: 08.08.2022
Impfdatum: 08.08.2022
Beginn: 08.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Pfizer dose #2 administered sooner than recommended schedule.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2404423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 11,0
Geschlecht: M
Eingang: 08.08.2022
Impfdatum: 08.08.2022
Beginn: 08.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Vaccine administered in higher dose than recommended in the 12-year-old and up formulation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2404399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 08.08.2022
Beginn: 08.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

The covid vaccine vial was opened on August 5, 2022 and should have been disposed of after 12 hours. Instead it was given to a patient on August 8, 2022. It was refrigerated the whole time. The patient had no symptoms or signs. Our pharmacy is also reaching out to the manufacturer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 DM
Andere Medikamente: Meloxicam, Fluoxetine, calcium, Jardiance, Lipitor, Metformin, Nicotinamide, Tylenol, Vitamin D3, Vitamin E oil, Aloe vera gel
Allergien: Augmentin
Vorherige Impfungen: -

VAERS 2404061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: CO
Alter: 46,0
Geschlecht: F
Eingang: 07.08.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

None. Patient was given the 4th dose and she is only 46 yo

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None noted
Vorgeschichte: None noted
Andere Medikamente: Daily ASA
Allergien: Yes, but not noted
Vorherige Impfungen: -

VAERS 2404060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CO
Alter: 45,0
Geschlecht: M
Eingang: 07.08.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient had no reaction. He was given his 4th dose and he is under 50 yo

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None known
Andere Medikamente: None
Allergien: Cats
Vorherige Impfungen: -

VAERS 2403489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CA
Alter: 2,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 01.08.2022
Beginn: 01.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LL

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

Product administered to patient of inappropriate age Wrong product administered

Symptomtext

The patient by error received the coronavirus 19 Pfizer vaccine for the age 12 years and above instead of the appropriate for his age.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2402544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: CO
Alter: -
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 01.06.2022
Beginn: 01.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Alopecia Neoplasm progression Neutrophil count Neutrophil count decreased Platelet count Platelet count decreased Positron emission tomogram Red blood cell count Red blood cell count decreased

Symptomtext

she has metastatic breast cancer that has spread to a lot of places an for the past 9 months; red blood cell count were low; her neutrophils were low; platelets were low; her hair was coming out a little bit at a time (2-3 hairs would come out if she ran it through her fingers)/hair loss; 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 73-year-old female patient received BNT162b2 (BNT162B2), on 27Jan2021 as dose 1, single (Lot number: EN5318), in left arm, on 24Feb2021 as dose 2, single (Lot number: EN6203), in left arm, on 18Aug2021 as dose 3 (booster), single (Lot number: EW0187), in left arm and on 01Jun2022 as dose 4 (booster), single (Lot number: FN2908), in left arm for covid-19 immunisation; palbociclib (IBRANCE), first regimen at 125 mg and second regimen since Jul2022 (ongoing) at 100 mg for breast cancer female. The patient's relevant medical history included: "right mastectomy" (unspecified if ongoing), notes: right mastectomy. Concomitant medication(s) included: FULVESTRANT as unk, monthly (injection once a month injection). Vaccination history included: evusheld (No NDC Lot or expiration date), administration date: 30Mar2022, when the patient was 73-year-old, for Immunization. The following information was reported: ALOPECIA (non-serious) with onset Jun2022, outcome "not recovered", described as "her hair was coming out a little bit at a time (2-3 hairs would come out if she ran it through her fingers)/hair loss"; NEOPLASM PROGRESSION (non-serious), outcome "unknown", described as "she has metastatic breast cancer that has spread to a lot of places an for the past 9 months"; RED BLOOD CELL COUNT DECREASED (non-serious), outcome "unknown", described as "red blood cell count were low"; NEUTROPHIL COUNT DECREASED (non-serious), outcome "unknown", described as "her neutrophils were low"; PLATELET COUNT DECREASED (non-serious), outcome "unknown", described as "platelets were low". Relevant laboratory tests and procedures are available in the appropriate section. The action taken for palbociclib was dosage reduced. Additional Information: She had been on Ibrance 125mg for about 9 months. It was working great on all of her cancer. She has had very few side effects. Recently, she started with her hair coming out a little at a time. Like individual hairs, like 2-3 hairs would come out when she combs her hair or runs her fingers through her hair. Now they had reduced her to Ibrance 100mg because she had problems with her blood. She was perplexed and doctors were not concerned. They were curious as to why it was starting so late with the hair loss. She wanted to know if it was normal for it to start so late. She wanted to know if we had any information if it would start falling out a lot since it's started to come out now. Caller stated she was also on Fulvestrant. She had been vaccinated with 2 boosters of the Pfizer COVID19 vaccine and was not sure if it may be due to the vaccines as well. She had regular IV for 3 years and understands what it's like to had alopecia. When she had regular chemotherapy, her hair started coming off and she buzzed it off. With the Ibrance it was coming out a few strands at a time. Caller asked, Is it normal for it to start so late? Does that mean a lot of it will start falling out? Caller said that she does not want to see it come out and will just buzz her head if that was what was going to happen. She had both of her Pfizer vaccines and booster and does not know if there was any relationship with this and her Ibrance. She had no bad effects from the Covid shots, it was great. Weight was 245lbs because of prednisone. She had been on it for 5 years. She previously weighed 130lbs when she started Prednisone and said that she put on the weight of a entire person. NO NDC, lot, or expiration. The prednisone was in a pharmacy vial. She had seen 2 Oncologists. Dr. info was populated in the formal field. Hair was coming out which started the last week of Jun2022. It was 1-2 strands that come out all day long. It was not coming out in big clumps. She knows that hair loss was a side effect, but she thought it would be sooner than now. Even her doctor's thought it would happen sooner than this. Patint took Ibrance for 21 days, then they let your blood regenerate. The 1st time it occurred was a month ago. Her white count was critically low, and her red blood cell count and her neutrophils were low. They did not want her to restart the Ibrance and stayed off of it 14 days instead of 7. She came back to the office to get another blood test and her blood levels were the same and the doctor told her to stay off another 7 days. She came back for another blood test and her levels were all back to low. They had her restart Ibrance 125mg even though it was low. She took it for 21 days and her white counts were critically low, red blood cells and neutrophils were low, and her platelets were low which was new. They told her to come back in a week for more blood tests. There was still a problem and nothing was critical, but they were all low as of this past Thursday and they told her to restart, but at the Ibrance 100mg dose. She was going back this Wednesday to see how things were doing. Her PET scan was showing Ibrance was doing very well and keeping the cancer from spreading. Her cancer had not gone away, but it was not spreading. She had some new cancer a couple of months and that was not spreading because of Ibrance. She was on something else prior to this and was on regular chemotherapy for 3 years prior to that. In addition to her covid-19 shots she was given a shot of Evusheld. No NDC Lot or expiration date. 30Mar2022 it was received. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: Test Name: neutrophil; Result Unstructured Data: Test Result:Low; Test Name: platelet; Result Unstructured Data: Test Result:Low; Test Name: PET scan; Result Unstructured Data: Test Result:showing Ibrance is doing very well; Comments: showing Ibrance is doing very well and keeping the cancer from spreading; Test Name: Red blood cell count; Result Unstructured Data: Test Result:Low
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Mastectomy (right mastectomy)
Andere Medikamente: FULVESTRANT; IBRANCE
Allergien: -
Vorherige Impfungen: -

VAERS 2395217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: AZ
Alter: -
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 19.07.2022
Beginn: 19.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Expired product administered Feeling hot Poor quality product administered Product quality issue

Symptomtext

states she is hot; had been a mishandling of vaccine she received; had been a mishandling of vaccine she received; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) f The reporter is the patient. A 51-year-old female patient received BNT162b2 (BNT162B2), on 19Jul2022 as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Disabled" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization series completed but unknown manufacturer), for Covid-19 Immunization. The following information was reported: POOR QUALITY PRODUCT ADMINISTERED (non-serious) with onset 19Jul2022, outcome "unknown", PRODUCT QUALITY ISSUE (non-serious), outcome "unknown" and all described as "had been a mishandling of vaccine she received"; FEELING HOT (non-serious), outcome "unknown", described as "states she is hot". Additional information: The patient was calling about the Pfizer COVID 19 vaccine. The patient stated she received her booster dose on19Jul2022. She then received a call on Sunday 31Jul2022 where she got her dose asking her how she was feeling and that there had been a mishandling of the vaccine at the pharmacy, but no other details were given. She wanted to make a report about that she has called the pharmacy back and they won't give her any details about what the mishandling was, if it was a temperature excursion or whatever. The patient was told that the pharmacy did call into Pfizer and today was Tuesday already and the patient just called in a little while ago saying that they did not hear back from Pfizer and so the patient was kind of freaking out because she did not know what the mishandling was. She did not know if the vaccine was good or proper because if they mishandled it, that told her that there might be something wrong, she might be protected, but she might not be protected, and she lived with her father. Her father is 80 years old and the last thing she needed was for him to get him sick and get her family sick. She has called back and the pharmacy told her they were waiting to hear from Pfizer to tell her more details about her dose mishandling. She was asking if there was anything that can be done or any information about this. The patient stated she was disabled and had been stuck in her house because she didn't know what to do. The patient states she was hot, she lives in (withheld) and didn't know if that was why she was hot or if she was just nervous and that was why she was hot. She was very frustrated, not at Pfizer but just with this whole situation. She stated they referred her to a web site and to Pfizer. The patient was appreciative for any help that can be given her. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Disability
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2401412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: TX
Alter: 12,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 01.08.2022
Beginn: 01.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

Booster dose given too soon

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: Pes planus and Pes planus
Andere Medikamente: ibuprofen as needed
Allergien: penicillin and ampicillin
Vorherige Impfungen: -

VAERS 2401280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: KY
Alter: 12,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 04.08.2022
Beginn: 04.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Expired product administered No adverse event

Symptomtext

Patient had no adverse reaction in office, patient received an expired vaccine. Vial expired 7/27/2022 injection given 8/4/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: KNA
Vorherige Impfungen: -

VAERS 2401261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: TX
Alter: 18,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Expired product administered

Symptomtext

Vaccine was administered four days after expiration date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2401258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: TX
Alter: 14,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Expired product administered

Symptomtext

Vaccine was administered four days after expiration date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2401255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 12,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Expired product administered

Symptomtext

Vaccine was administered four days after expiration date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2401251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 17,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Expired product administered

Symptomtext

Vaccine administered four days after expiration date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2401247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: TX
Alter: 17,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 02.08.2022
Beginn: 02.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Expired product administered

Symptomtext

Was administered four days after expiration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2401182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: PR
Alter: 59,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 21.07.2022
Beginn: 21.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

The vaccine was administered after a high temperature event reported according to the thermometer. Patient did not present any symptoms out of the ordinary. The experience was similar to his third dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2401180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

gering

Staat: PR
Alter: 67,0
Geschlecht: M
Eingang: 04.08.2022
Impfdatum: 21.07.2022
Beginn: 21.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Product storage error

Symptomtext

The vaccine was administered after a high temperature event reported according to the thermometer. Patient did not present any symptoms out of the ordinary. The experience was similar to his third dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2400517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: PR
Alter: 65,0
Geschlecht: M
Eingang: 03.08.2022
Impfdatum: 20.07.2022
Beginn: 01.07.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

Patient was vaccinated after an out of range temperature event (High temperature).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2399139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FN2908

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Staat: MN
Alter: 17,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 01.08.2022
Beginn: 01.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient/parent disclosed 2 previous vaccines, but not a 3rd. Our system said she was due for booster. Queried database, and no immediate response, so administered booster. After administration, database responded with information indicating that she had already gotten her booster in 12/2021. Is not eligible for 2nd booster, but received it at this visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -