VAERS Reports FP7135

VAERS 2698965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: MD
Alter: 75,0
Geschlecht: F
Eingang: 19.10.2023
Impfdatum: 08.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: IM / LA

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

Death

Symptomtext

NONE PATIENT RECEIVED PREVIOUS VACCINATION PRIOR TO ADMISSION TO NURSING HOME. SHE RECIVED PFIZER , WHICH WAS HER NUMBER TWO BOOSTER ON 6-8-22 ADMINISTERD BY PHARMACIST PATIENT WAS RECEIVING HOSPICE CARE SERVICES WHEN SHE EXPIRED 6-20-22. SHE DID NOT EXPERIENCE ANY ADVERSE EFFECTS FROM THE PFIZER COVID VACCINE ON 6-8-22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: DEMENTIA WITHOUT BEHAVIORAL DISTURBANCE, TYPE TWO DIABETES
Vorgeschichte: CVA, MODERATE PROTEIN CALORIE MALNUTRITION, HYPOTHROIDSM, OBSTRUCTIVE AND REFLUX UROPATHY, HYPERENTION CHRONIC KIDNEY DISEASE, STAGE 3, ANXIETY DISORDER, MAJOR DEPRESSIVE DISORDER, GERD, INSOMIA, SECONDARY MALIGNANT NEOPLASM LEFT LUNG. PERSONAL HISTORY OF OTHER MALIGNANT NEOPLASM OF KIDNEY
Andere Medikamente: AMLODIPINE,MELATONIN, LANTUS INSULIN,ASPIRIN,MELATONIN,BENAZEPRIL HCL, CYMBALTA, NORVASC, GLIPIZIDE, VENTOLIN HFA, PROTONIX, TYLENOL, ATORVASTATIN CALCIUM, LIPITOR
Allergien: CUCUMBER, CRANBERRY JUICE, PENTAZOCINE, CODEINE, DYE, RED ORANGE, TALWIN NX
Vorherige Impfungen: -

VAERS 2696131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fp7135

kritisch

Staat: -
Alter: 88,0
Geschlecht: F
Eingang: 14.10.2023
Impfdatum: 13.07.2022
Beginn: 20.09.2023
Tage bis Beginn: 434,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Aortic valve incompetence Blood sodium decreased Blood thyroid stimulating hormone normal Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Dyspnoea Echocardiogram abnormal Ejection fraction normal Essential hypertension Hypervolaemia Hyponatraemia Hypothyroidism Hypotonia Hypoxia Inappropriate antidiuretic hormone secretion Respiratory symptom

Symptomtext

Patient is a 89 y.o. female with history of COPD, CKD IV (with history of 1986 renal transplant) who presented from home (lives with daughter) on 9/20/2023 with shortness of breath and hypoxemia in the setting of COVID-19. Course complicated by hypotonic, hyponatremia possibly in setting of COVID. Nephrology followed, s/p 2 doses tolvaptan and with fluid restriction. She is medically stable for discharge home. Home healthcare was declined. Acute respiratory failure with hypoxemia, resolved COVID-19 pneumonia - Positive COVID-19: 9/20 at ED - Vaccination status: Vaccinated with Moderna with last dose 2023 - Decadron: Yes. End date 9/28 on discharge - Remdesivir: Yes. end date 9/24 - E consult ID, appreciate recs; no need for home oxygen on discharge; stop decadron on discharge Hypotonic Hyponatremia - in light of COVID infection and respiratory symptoms above; there does remain concern for SIADH - On admit, Na 123 with nadir of 114 (9/22/23), improving; s/p tolvaptan 9/23 and 9/24; Urine osm pending, urine Na mildly elevated, more consitent with SIADH; TSH wnl; low pre-test concern for cortisol deficiency given labs and pressures - Nephrology followed; will discharge with fluid restriction(1.2L), TID NaCl tablets, and increased home lasix to 40mg PO; daughter was aware of changes and agreeable to this management Acute on Chronic HFpEF - History of HFpEF with previous hospitalization in 4/2023 for volume overload. - 12/2022 limited Echo wih EF 65%, mild AS, mild-mod AR, and mild TR; Admit BNP 41.6 K (31.5 K, 1 month prior) - resume home lasix as noted above Presumed COPD History of tobacco abuse - Presumed COPD during last admission but no formal PFTs found. Has been following up with respiratory therapy in outpatient setting per the daughter. - Continue home inhalers on discharge; recommend formal PFTs Hypothyroidism - Daughter confirms that patient takes 50 mcg of levothyroxine, but takes 2 tabs on Sundays. - Continue home synthroid History of CVA - Continue aspirin. No acute symptoms at this time. CKD stage IV History of renal transplant 1986 History of interstitial nephritis - Continue home suppression therapy for now. Continue to follow renal function. Nephrology consulted as above Hypertension, essential - Continue home medications as hemodynamics allow - Renal team added Norvasc daily. She is on Coreg 6.25 mg bid longer term; continue both on dischargeaseline creat 2, stable

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2667036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 07.08.2023
Impfdatum: 04.06.2022
Beginn: 16.07.2023
Tage bis Beginn: 407,0
Dosis: 4
Route/Site: - / -

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

Acute respiratory failure Alcohol abuse Asthma Blood bicarbonate decreased COVID-19 Chest X-ray abnormal Condition aggravated Hyponatraemia Hypophagia Influenza like illness Lung opacity Metabolic acidosis Pyrexia Rash SARS-CoV-2 test positive Sepsis Tachycardia

Symptomtext

Patient is a 61 y.o. male patient of, MD with history of anemia, Asthma, COPD, Gout, Cocaine use, HTN presented to Medical Center with flu like symptoms . Sepsis-POA, resolved Possible CAP Covid-19 pulmonary infection Acute asthma exacerbation Acute hypoxic respiratory failure/ Date of onset of symptoms: ~7/15 P/w fever, tachycardia Date of covid positive test: 7/17 Vaccination status: vaccinated Imaging: CXR bibasilar opacities Oxygen requirements on admission: RA Current oxygen requirements: RA Medical therapy: steroids; Levaquin; initiated on remdesivir and already on steroid Consultants following: ID E-consult Anticipated special isolation end date: 7/27 Overall improving Finished steroid course and remdesivir with improvement Finish 7 days of Levaquin Hyponatremia Could be due to decreased oral intake Encourage solute intake Dry lung strategy Monitor DC IV fluid Improved Mild anion gap metabolic acidosis Bicarb 15, etiology? Resolved HTN Cont home Norvasc BP stable Skin rash Over both ankles x1 week Pt attributes them to friction due to tight shoes Psoriatic look clinically Outpt f/up ETOH abuse Drinks 'plenty of beer' but denies heavy drinking or dependence Was at facility earlier

Weitere VAERSDATA-Felder

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

VAERS 2662095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 27.07.2023
Impfdatum: 03.08.2022
Beginn: 27.10.2022
Tage bis Beginn: 85,0
Dosis: 3
Route/Site: IM / RA

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

Acute respiratory failure Chronic respiratory failure Hypoxia Respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE CHRONIC RESPIRATORY FAILURE CHRONIC HYPOXEMIC RESPIRATORY FAILURE ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2646311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 16.06.2023
Impfdatum: 09.06.2022
Beginn: 02.11.2022
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: IM / LA

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

Acute myocardial infarction Hypotension

Symptomtext

ACUTE NON ST ELEVATION MI HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2645933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 15.06.2023
Impfdatum: 07.07.2022
Beginn: 17.01.2023
Tage bis Beginn: 194,0
Dosis: 4
Route/Site: IM / RA

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

Atrial fibrillation Benign prostatic hyperplasia Bradycardia Lower urinary tract symptoms Pulmonary embolism

Symptomtext

ACUTE PULMONARY EMBOLISM 5/2/2023 BPH W LOWER URINARY TRACT SYMPTOMS ACUTE PULMONARY EMBOLISM 5/2/2023 HX OF ALCOHOL USE DISORDER ACUTE PULMONARY EMBOLISM 5/2/2023 ATRIAL FIBRILLATION, UNSPECIFIED BRADYCARDIA

Weitere VAERSDATA-Felder

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

VAERS 2644018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 12.06.2023
Impfdatum: 18.07.2022
Beginn: 10.01.2023
Tage bis Beginn: 176,0
Dosis: 4
Route/Site: IM / LA

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

Acute respiratory failure Chronic respiratory failure Hypoxia Respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE CHRONIC HYPOXEMIC RESPIRATORY FAILURE HYPOXEMIA

Weitere VAERSDATA-Felder

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

VAERS 2636232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 24.05.2023
Impfdatum: 18.08.2022
Beginn: 01.11.2022
Tage bis Beginn: 75,0
Dosis: 3
Route/Site: IM / LA

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

Acid-base balance disorder mixed Acute respiratory failure Aortic valve stenosis Hypercapnia Hypoxia Respiratory failure

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE 11/1/2022 AORTIC VALVE STENOSIS ACUTE ON CHRONIC RESPIRATORY FAILURE 12/17/2022 AORTIC VALVE STENOSIS ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 12/31/2022 AORTIC VALVE STENOSIS HYPOXEMIA 12/31/2022 AORTIC VALVE STENOSIS ACUTE HYPOXEMIC RESPIRATORY FAILURE 11/1/2022 MIXED ACID BASE BALANCE DISORDER W HYPERCAPNIA ACUTE ON CHRONIC RESPIRATORY FAILURE 12/17/2022 MIXED ACID BASE BALANCE DISORDER W HYPERCAPNIA ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE 12/31/2022 MIXED ACID BASE BALANCE DISORDER W HYPERCAPNIA HYPOXEMIA 12/31/2022 MIXED ACID BASE BALANCE DISORDER W HYPERCAPNIA

Weitere VAERSDATA-Felder

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

VAERS 2634166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 19.05.2023
Impfdatum: 26.08.2022
Beginn: 22.11.2022
Tage bis Beginn: 88,0
Dosis: 5
Route/Site: IM / RA

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

Acute respiratory failure Cardiac arrest

Symptomtext

ACUTE RESPIRATORY FAILURE 11/25/2022 CARDIAC ARREST DUE TO UNDERLYING NONCARDIAC CONDITION

Weitere VAERSDATA-Felder

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

VAERS 2609973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: MN
Alter: 78,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: 16.06.2022
Beginn: 22.12.2022
Tage bis Beginn: 189,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia COVID-19 Cerebrovascular accident Confusional state Cough Rhinorrhoea SARS-CoV-2 test positive Treatment noncompliance

Symptomtext

Patient was brought to the ED by EMS on 12/22/22 for increased confusion over the past two days. Additionally, her husband reported she has had weakness, a cough and runny nose, and tested positive for COVID several days ago (12/19/22). Additional COVID-19 PCR test performed in the ED also resulted positive. Patient admitted 12/22/22 - 12/24/22 for COVID-19 infection; she was provided supportive treatment. Of note, initial work-up was noticeable for subacute vs chronic right occipital CVA but the provider states this does not appear correlated with presenting symptoms. The provider states it is suspected that the CVA is from medication non-adherence. Patient felt symptomatically better on 12/24 and wished to go home, and so was discharged.

Weitere VAERSDATA-Felder

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

VAERS 2584448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: -
Alter: 56,0
Geschlecht: M
Eingang: 20.02.2023
Impfdatum: 09.07.2022
Beginn: 15.01.2023
Tage bis Beginn: 190,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Asthenia Blood creatinine increased COVID-19 Cellulitis Chest X-ray abnormal Chills Cough Dizziness Fatigue Glomerular filtration rate decreased Hepatorenal syndrome Hypoxia Infusion Intensive care Malaise Paracentesis Pleural effusion

Symptomtext

Patient is a 56 y.o. male patient of DO with history of alcoholic liver cirrhosis, alcohol withdrawal, gastric varices status post banding, iron deficiency anemia, presented on 1/15/2023 with weakness, lightheadedness, fever/chills was admitted to the ICU for septic shock on 1/16/2023 initially requiring pressors. HMS consulted by MD for transfer of care from ICU to intermediate unit. IR re-consulted for paracentesis today; had 8750 cc of fluid drained. 75g of albumin infusion given Discharge Diagnoses: Sepsis due to R LE cellulitis Unclear etiology, likely septic shock from RLE cellulitis Or suspected hepatorenal syndrome/COVID infection VSS, BP improved, AF, on 2L NC. AAOX3 Required levophed on adm 1/16, quickly taken off On Midodrine 15 mg TID and octreotide 100 mcg TID VIR c/s for paracentesis 1/17 and removal of 9 liters, no SBP. 100g of albumin given Had repeat paracentesis today with removal of 8750L; 75g of albumin infusion given ID on board; received IV Ancef and completed 7 days of therapy AKI-improved Adm Cr: 1.4>1.2.GFR:58>70.(Baseline Cr: 0.7-0.9, GFR: >90) Probable cause(s): suspected hepatorenal syndrome/sepsis Avoid nephrotoxic agents including NSAIDs Lasix and aldactone restarted 01/20 Nephrology on board; recommendation appreciated Covid-19 Virus Infection Date of onset of symptoms: on adm (1/16) Symptoms present on admission: cough and generalized fatigue on adm (1/16) Date of covid positive test: 1/15/23 Vaccination status: vaccinated Imaging: CXR (1/15/23) Moderate-sized right-sided pleural effusion appears increased. Oxygen requirements on admission: RA Current oxygen requirements: RA Medical therapy: Dexamethasone and remdesivir started due to hypoxia, which has resolved Consultants following: N/A Anticipated special isolation end date: 1/25/23 ID on board, complete 10 days of Dexa. Remdesivir completed Alcoholic Liver cirrhosis w/ ascites Alcohol abuse MELD NA 21 on 1/17/23 Seen by Hepatology 10/14/22 --rec torsemide 20 mg TID. Noncompliant, patient continues to use alcohol on a weekly basis Overdue for Surveillance EGD (last EGD: 5/2021 S/P banding) Diagnostic paracentesis 1/15/23 (-) SBP or culture growth Therapeutic paracentesis 1/17/23 S/P 9L and 1/23/23 8750L removed. Albumin given after each session as described above Counseled to quit ETOH use; Lim it acetaminophen < 2 g daily F/u RUQ US w/ dopplers-Cirrhotic liver morphology no masses, Splenomegaly. AFP at 1.3 GI consulted, cont midodrine, 2gm diet Follow up GI as OP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 06.08.2022
Beginn: 01.11.2022
Tage bis Beginn: 87,0
Dosis: 4
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation Back pain Blister Blood test normal Computerised tomogram abnormal Echocardiogram abnormal Electrocardiogram Gait disturbance Heart rate increased Intervertebral disc degeneration Intervertebral disc operation Intervertebral disc protrusion Magnetic resonance imaging abnormal Mobility decreased Musculoskeletal pain Neuralgia Peripheral swelling

Symptomtext

In November of 2022, I developed back pain if I stood still for more than ten minutes. If I stood still for more than ten minutes, I would get a sciatica type pain starting in my left buttock. The pain would go away instantly as soon as I started moving. I could do all other activities, even running. The pain continued for several weeks. I called my doctor who performed an x-ray and prescribed physical therapy. The x-ray showed degenerative disc disease in my lumbar. I did physical therapy twice. The day after my second physical therapy, I was doing my stretches and exercises at home. However, the next morning, I couldn't move. I couldn't lay down or walk more than a few steps. All I could do was sit in a leaning forward position. On 12/25/2022, I went to the emergency room where they did an MRI which showed a disc protrusion on L5 and S1. It was hitting the L5 nerve which was most likely causing my pain. There were a couple of discs above that were bulging as well, but it was the disc protrusion that was most severe. They prescribed a six-day course of steroids which didn't do anything. They also prescribed a muscle relaxer which also didn't help. They then started me on a ten-day steroid pack. I went back to the emergency room on 1/12/2023 because the pain had gotten so bad that I couldn't even take a few steps. They were trying to manage the pain with oxycodone, PERCOCET, and TYLENOL. The only thing that ended up working was morphine, so they put me on a morphine pump. Because my only symptoms were pain, I was not a candidate for emergency surgery, I had to wait until 01/03/2023. In the meantime, my legs became very swollen due to not being able to move. My legs started to blister, and I developed large blisters on the top of my feet. I was finally able to go in for surgery, but they were worried about the blisters, so they lanced them. However, they filled up again, so they had to open them up and I had open wounds on my legs. They addressed that and took me to surgery. They did a laminotomy on L4 and L5 as well as a microdiscectomy and a fusion on L5 and S1. At the same time, when I was in the hospital on 01/12/2023, I was in atrial fibrillation, so they are trying to manage that. They were able to get my heart rate down which was up to 150 beats a minute or higher. They couldn't get me out of atrial fibrillation, but they were able to treat my heart rate with metoprolol. After surgery, the atrial fibrillation went away for a few days but came back with RVR. It didn't last long, but they were concerned I might be getting blood clots. They did a CT scan with dye and found that I did have blood clots which were already in my lungs. I had pulmonary embolism in both lungs, but I was asymptomatic. I was not having difficulty breathing or anything which the doctors found unusual. They put me on blood thinners and kept me in the hospital for observation. The atrial fibrillation went away again so they released me from the hospital on 01/31/2023 and prescribed LOVENOX injections. They are going to switch me to an ELIQUIS prescription, and I have multiple follow ups with varying doctors.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 20,0
Labordaten: 22DEC2022 X-ray, Degenerative Disk Disease diagnosis; 27DEC2022 MRI, Disc Protrusion found; 12JAN2023 Blood tests, nothing abnormal found; 13JAN2023 MRI no significant change; EKG, result unknown; 16JAN 2023 Echocardiogram, nothing abnormal found; CT Scan, surgery preparation; 23JAN2022 X-Ray, results unknown; CT scan with dye, surgery preparation; 26JAN2023 EKG, results unknown; X-Ray, results unknown; CT scan with dye, Pulmonary Embolism; 26JAN2023 Echocardiogram, Blood Clots; 27JAN2023 Echocardiogram, Blood Clots; 25JAN2023 Blood tests, results unknown
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Hypertension; Varicose Veins
Andere Medikamente: Metoprolol; hydrochlorothiazide; amlodipine; losartan; fish oil; ZYRTEC; QVAR
Allergien: None
Vorherige Impfungen: -

VAERS 2567786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: PA
Alter: 81,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 03.06.2022
Beginn: 10.06.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

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

Cerebrovascular accident

Symptomtext

Patient had a mild stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 2,0
Labordaten: not available to us
Aktuelle Erkrankungen: n/a
Vorgeschichte: hypertension
Andere Medikamente: Lisinopril-HCTZ 20-12.5
Allergien: nka
Vorherige Impfungen: -

VAERS 2543545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 27.12.2022
Impfdatum: 18.07.2022
Beginn: 25.12.2022
Tage bis Beginn: 160,0
Dosis: 4
Route/Site: - / -

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

Acute myocardial infarction Asthenia Atrial fibrillation COVID-19 Confusional state Cough Fatigue Gait disturbance SARS-CoV-2 test positive

Symptomtext

Pt has a history of hypertension and hemorrhagic stroke with mild residual expressive aphasia. He presents with generalized weakness, gait unsteadiness, and confusion for one week. He has increased fatigue and a nonproductive cough. Pt is admitted with new onset Afib, NSTEMI, and is found to be COVID positive.

Weitere VAERSDATA-Felder

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

VAERS 2469958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: CO
Alter: 68,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 01.10.2022
Beginn: 01.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Blood thyroid stimulating hormone COVID-19 Chills Cough Dyspnoea Exposure to SARS-CoV-2 Fatigue Full blood count Hepatic enzyme Lethargy Metabolic function test Oxygen saturation SARS-CoV-2 test positive

Symptomtext

a 68 year-old male who presented to the Emergency Department with complaints of difficulty breathing and shortness of breath associated with oxygen saturation levels of 86% as measured with his home pulse oximeter. He reports that his wife is COVID-19 positive and he too resulted positive 3 days previously with use of a home COVID-19 test kit. In addition to breathing problems he endorses recent onset of lethargy and fatigue, cough, and chills. He has a complex medical history notable for receipt of a liver transplant in 2019, asthma, type 2 diabetes, osteoarthritis, obstructive sleep apnea night, hypothyroidism, and hypertension. This patient received a COVID-19 bivalent vaccine booster on the day of symptom onset. He was admitted to hospital for acute hypoxemic respiratory failure. He is currently in isolation on supplemental oxygen. He is being treated with dexamethasone 6 mg daily for an anticipated duration of 10 days, remdesivir 200 mg IV once followed by remdesivir 100 mg IV daily for 4 days, antitussive and as-needed analgesic medication, as well as his usual immunosuppressant and other maintenance medicines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: Metabolic panel Complete blood count Tacrolimus concentration Oxygen saturation Thyroid stimulation hormone level Liver enzyme COVID-19 RNA
Aktuelle Erkrankungen: -
Vorgeschichte: Liver transplant Hyperlipidemia Hypertension Type 2 diabetes Obstructive sleep apnea Benign prostatic hypertrophy
Andere Medikamente: Tacrolimus; Atorvastatin Diclofenac gel Insulin Glargine Insulin Lispro Pantoprazole Losartan Levothyroxine Tamsulosin
Allergien: Indomethacin Prazosin Ondansetron
Vorherige Impfungen: -

VAERS 2446317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: MI
Alter: 34,0
Geschlecht: F
Eingang: 15.09.2022
Impfdatum: 24.08.2022
Beginn: 04.09.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Bacteraemia Blood glucose COVID-19 pneumonia Central venous catheterisation Diabetic ketoacidosis Dyspnoea Fatigue Intensive care Malaise Musculoskeletal chest pain Pneumonia Pneumonia bacterial Sepsis Sputum culture positive Staphylococcal bacteraemia Staphylococcus test positive Superinfection

Symptomtext

Discharge Provider : MD Primary Care Provider: MD Admission Date: 9/4/2022 Discharge Date: Sep 13, 2022 PRESENTING PROBLEM: Severe sepsis Diabetic ketoacidosis without coma associated with type 2 diabetes mellitus Community acquired pneumonia of right lower lobe of lung COVID-19 Bacteremia HOSPITAL COURSE: 34 year old female w/PMH including T2DM, severe persistent asthma with no baseline oxygen needs, OSA, obesity, presenting with worsening dyspnea, fatigue, general malaise, and right-sided chest wall pain. Initial workup revealed acute hypoxemic respiratory failure secondary to COVID-19 pneumonia, superimposed bacterial PNA, and DKA. She was started on IV insulin, given steroids in the ED, and admitted to the ICU for further management. While in the ICU, her oxygen requirements improved but she was found to have MRSA bacteremia. Vancomycin was started and ID were consulted. Once the patient was taken off of EndoTool and switched to basal bolus insulin she was transferred to the medical floor. Sputum culture was positive for MRSA and therefore she was being treated for pneumonia secondary to MRSA. Infectious Disease gave final recommendation with continuous vancomycin infusion for a total of 4 weeks. Home oxygen eval showed that the patient needs 2 liters of nasal cannula continuous which was arranged for her. PICC line was placed prior to discharge. Of note few days prior to discharge, the patient glucose level was dropping the for her and Lantus was decreased as well as her pre meal insulin. Endocrinology was following and adjusted her bolus insulin and provided recommendations on discharge. The patient was discharged home in a stable condition with home health care and discharge instructions provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 diabetes mellitus with hyperglycemia Anxiety Hyperlipidemia Class 3 severe obesity due to excess calories with serious comorbidity and body mass index (BMI) of 45.0 to 49.9 in adult Depression Mild obstructive sleep apnea Microalbuminuria Severe persistent asthma without complication Encounter for annual wellness exam in Medicare patient Chronic cough Moderate persistent asthma without complication Seasonal allergic rhinitis, unspecified trigger MRSA bacteremia Pneumonia of right lung due to methicillin resistant Staphylococcus aureus (MRSA) COVID-19 Acute respiratory failure with hypoxia
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 20 MG tablet azelastine (ASTELIN) 0.1 % nasal spray blood glucose test strips busPIRone (BUSPAR) 10 M
Allergien: Motrin [Ibuprofen]Hallucinations
Vorherige Impfungen: -

VAERS 2425253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 31.08.2022
Impfdatum: 29.03.2021
Beginn: 26.08.2022
Tage bis Beginn: 515,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure COVID-19 Hypoxia Interchange of vaccine products

Symptomtext

Pt arrives severely hypoxic from a residential facility and is not normally on oxygen. Pt admitted with acute respiratory failure with hypoxia and COVID-19.

Weitere VAERSDATA-Felder

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

VAERS 2416776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: GA
Alter: 68,0
Geschlecht: M
Eingang: 20.08.2022
Impfdatum: 02.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / -

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

Cerebrovascular accident Neurological symptom

Symptomtext

Stroke like symptoms two days after vacation, dx stroke one week later

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: diabetic, gout, HTN,
Andere Medikamente: Lisinopril HCTZ, metformin, Gabapentin, alopurinol, vitamin, glipizide,
Allergien: -
Vorherige Impfungen: -

VAERS 2370635

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: MD
Alter: 73,0
Geschlecht: M
Eingang: 15.07.2022
Impfdatum: 23.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Death

Symptomtext

Nursing home reported that patient passed away on 7/5/22.

Weitere VAERSDATA-Felder

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

VAERS 2332381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 23.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Patient passed away at a nursing facility listed above one day after receiving Pfizer booster. Public Health notified on the day VAERS submitted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CHF CKD- on HD, AVF Paraplegia HTN Complicated surgical history
Andere Medikamente: Unknown
Allergien: -
Vorherige Impfungen: -

VAERS 2331669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

kritisch

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 16.06.2022
Beginn: 18.06.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory failure Asthenia Blood glucose increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Dyspnoea exertional Glycosylated haemoglobin increased Hyperglycaemia Hypervolaemia Hypoxia Lung opacity Respiratory failure SARS-CoV-2 test positive

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 6/18/2022 Discharge Date: Jun 21, 2022 PRESENTING PROBLEM: Hypoxia HOSPITAL COURSE: Patient is a 73-year-old woman with a history of grade 1 diastolic dysfunction, systolic heart failure with most recent ejection fraction of 28%, type 2 diabetes, CKD stage 3, stage III squamous cell carcinoma of the right upper lobe of the lung status post radiation , DVT and PE, seizure disorder, coronary artery disease, hypertension presented to emergency department due to shortness of breath and generalized weakness. Was admitted to internal medicine service due to acute hypoxic respiratory failure she required 2-4 L of supplemental oxygen via nasal cannula at the time of arrival. Film array was positive for COVID. Her hypoxic respiratory failure most likely was secondary to COVID pneumonia. Chest x-ray showed diffuse interstitial opacity more prominent in the right upper lobe mostly due to fluid overload. Patient was started on Decadron. Her symptoms significantly improved and she was able to be weaned off to room air. She takes 20 mg of Lasix orally every other day at home which was changed to Lasix 20 every day due to fluid overload. overall patient improved significantly and was transferred to a SAR facility. patient's blood sugars were elevated but her last a1c was 7.2% and steroids would not be continued at discharge given her lack of hypoxemia so this degree of hyperglycemia was expected to resolve spontaneously. at the time of discharge patient was in good spirits with no objections to be sent out. she still had a cough and some shortness of breath on exertion. she was 89% with ambulation and was sent with oxygen and instructions for the facility to wean; she was not sent ou ton steroids but her lasix was increased and she was told to discuss this with her PCP as the need for the increased lasix was likely temporary. all questions and concerns addressed, all meds and follow-ups reviewed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hx of CVA (cerebrovascular accident) hx of DVT of lower extremity (deep venous thrombosis), right; 2000 hx of Pulmonary embolism IDDM2, poorly controlled Moderate protein-calorie malnutrition Thrombocytosis Epilepsy seizure, nonconvulsive, generalized Essential hypertension, benign Rhinitis, allergic Chronic kidney disease, stage III Dyslipidemia OSA (obstructive sleep apnea) Other and combined forms of senile cataract Hypermetropia Cardiomyopathy, nonischemic Renal lesion Osteopenia Rubral tremor Vaccination not carried out because of patient refusal Incomplete bladder emptying Gout Memory loss Complex renal cyst Chronic cough Tubular adenoma of colon Opacity of lung on imaging study Healthcare maintenance Lung mass Malignant neoplasm of upper lobe of right lung Severe sepsis Right leg pain Cardiac arrest Foot pain, bilateral Altered mental status, unspecified altered mental status type Lethargy Confusion Type 2 diabetes mellitus with diabetic nephropathy Epistaxis Acute encephalopathy Chronic deep vein thrombosis (DVT) of both lower extremities Near syncope Fever Hypoxia
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet allopurinol (ZYLOPRIM) 100 MG tablet apixaban (ELIQUIS) 5 MG tablet calcium carbonate (TUMS) 1000 MG chewable tablet carvedilol (COREG) 6.25 MG tablet cholecalciferol (VITAMIN D3) 50 MCG (2000 UT)
Allergien: Augmentin [Penicillins] Nsaids
Vorherige Impfungen: -

VAERS 2662716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: -
Alter: 69,0
Geschlecht: F
Eingang: 28.07.2023
Impfdatum: 20.07.2022
Beginn: 27.09.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: IM / LA

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

Ischaemic stroke Symptom recurrence

Symptomtext

ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 3/16/2023 & 1/21/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2660807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: NC
Alter: 59,0
Geschlecht: F
Eingang: 25.07.2023
Impfdatum: 22.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / -

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

Blood glucose increased Hyperhidrosis SARS-CoV-2 test Syncope

Symptomtext

Fainting day after vaccine; Sweating; High blood sugar; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient received BNT162b2 (BNT162B2), on 22Jun2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 59 years intramuscular, in arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma", start date: 01Jan1987 (ongoing); "Diabetes", start date: 01Jan2017 (ongoing); "Bipolar Disorder", start date: 01Jan2019 (ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, Site and Route of injection: arm, Route of administration: Intramuscular, Batch/Lot number: EL32646), administration date: 14Jan2021, when the patient was 58-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, Site and Route of injection: arm, Route of administration: Intramuscular, Batch/Lot number: FL9264), administration date: 05Feb2021, when the patient was 58-year-old, for COVID-19 immunization; BNT162b2 (DOSE 3, Site and Route of injection: arm, Route of administration: Intramuscular, Batch/Lot number: FE3592), administration date: 27Aug2021, when the patient was 59-year-old, for COVID-19 immunization. The following information was reported: SYNCOPE (medically significant) with onset 23Jun2022, outcome "recovered", described as "Fainting day after vaccine"; BLOOD GLUCOSE INCREASED (non-serious) with onset 23Jun2022, outcome "recovered", described as "High blood sugar"; HYPERHIDROSIS (non-serious) with onset 23Jun2022, outcome "recovered", described as "Sweating". The events "fainting day after vaccine", "sweating" and "high blood sugar" required emergency room visit. Patient went to ER, kept for observation. The patient underwent the following laboratory tests and procedures: Blood glucose increased: (unspecified date) High; SARS-CoV-2 test: (Jun2021) Positive. Therapeutic measures were not taken as a result of syncope, hyperhidrosis, blood glucose increased.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: Blood Sugar; Result Unstructured Data: Test Result:High; Test Date: 202106; Test Name: COVID-19 Test; Test Result: Positive
Aktuelle Erkrankungen: Asthma; Bipolar disorder; Diabetes
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2647937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: -
Alter: 25,0
Geschlecht: F
Eingang: 21.06.2023
Impfdatum: 27.07.2022
Beginn: 18.04.2023
Tage bis Beginn: 265,0
Dosis: 3
Route/Site: IM / LA

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

Bell's palsy Foetal hypokinesia Pregnancy Third trimester pregnancy

Symptomtext

RIGHT BELLS PALSY 4/17/2023 DECREASED FETAL MOVEMENT, THIRD TRIMESTER, SINGLETON/UNSPECIFIED FETUS

Weitere VAERSDATA-Felder

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

VAERS 2617786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 19.04.2023
Impfdatum: 07.07.2022
Beginn: 07.08.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / LA

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

Ischaemic stroke Lacunar stroke

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

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

VAERS 2533533

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 21.06.2022
Beginn: 21.11.2022
Tage bis Beginn: 153,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia COVID-19 Condition aggravated Cough Dysphemia Dyspnoea Fatigue Feeling abnormal Illness Muscle spasms Pain SARS-CoV-2 test positive Sinusitis Syncope Throat irritation Vision blurred Visual impairment

Symptomtext

I received the second Pfizer booster for COVID-19 on 6/21/2022. On the night of 11/22/2022, I had been dealing with sinusitis for a while, but I suddenly also had body aches, severe cough, severe fatigue, and shortness of breath. Not only that, but I actually started stuttering! I felt like I had hit a wall, like all my systems had just crashed and I couldn't function. I have dealt with sinusitis for years, but I had never had those symptoms before, so I knew something was different. I didn't think I had COVID-19, though, because I was fully vaccinated. Not only that, but my husband wasn't sick, so whatever I had, he hadn't caught. I doubled up on TYLENOL and alternated it with MOTRIN, drank extra fluids, did sinus washes, took DELSYM cough syrup, and quarantined from my family during the November holiday. I also took 120mg of OTC pseudoephedrine. The medicines helped with the active, individual symptoms, but the cough persisted. I had a doctor's appointment on 11/28/2022 to get my ears examined. All of my symptoms had resolved by then, but I still had the cough. At the doctor's office, I had to fill out a questionnaire asking if I had had certain symptoms of COVID-19. When I saw the list of symptoms, I thought that maybe I should be tested for COVID-19. On the way home from the clinic, I went to a county testing site, and the following day I received the news that I had tested positive for COVID-19. On 11/29/2022, I had a telehealth visit with a doctor. The doctor prescribed a QVAR inhaler, an albuterol inhaler, benzonatate, and TESSALON PERLES. The combination of the QVAR inhaler and the TESSALON PERLES really helped my cough, because trying to take a deep breath would cause me to have a coughing spasm. The QVAR inhaler helped with the breathing, and the TESSALON PERLES helped numb my throat to the point that any irritation to the area would not trigger coughing. The stuttering I mentioned earlier accompanied the shortness of breath I experienced with the illness. At the time of this writing, I still have some brain fog, and I will sometimes stutter a bit if I lose my train of thought, but those symptoms are now less pronounced than they were when I was sick. I have also noticed changes in my vision. During my illness, I didn't bother putting on my glasses, because my eyesight was the least of my worries at that point. After my 14-day isolation was over, though, I was able to notice better the vision changes that I had experienced. I experienced what could be described as a delayed effect in my vision; it's sort of like watching a TV show and there being a break or delay in a scene. I resumed wearing my glasses. I had a brand-new pair with an up-to-date prescription. When I put them on, though, things were out-of-focus. The prescription was no longer accurate. Not only have I dealt with changes in my eyesight and occasional stuttering since my illness, but I also had episodes of syncope on a daily basis from 11/21/2022 until 11/27/2022. I didn't automatically associate this with COVID-19, though, because my doctor had recently doubled my blood pressure medicine. I don't know if the syncope was caused by the COVID-19 or a change in the medication dosage, but ever since my doctor switched back to the original dosage and I got over COVID-19, I haven't had any more episodes. At the time of this writing, I am still dealing with vision changes, and I now have a scheduled follow-up appointment with my eye doctor in the near future. When I had the body aches that were caused by the COVID-19, my knees were among the areas affected. The all-over body aches eventually receded, but I continued to have pronounced pain in both knees. It feels like there is a painful squeeze enveloping the entire kneecap area and the area just above the knee. Kneeling and bending cause the pain, and I did not have this issue before I got COVID-19. I use the BIOFREEZE roll-on on my knees at night, and it works well enough for me to get to sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: 11/28/2022 PCR test positive result.
Aktuelle Erkrankungen: None.
Vorgeschichte: Type II Diabetes; Hypertension; High Cholesterol; Fluctuation Between Overweight and Obesity; Chronic Sinusitis; Back Pain.
Andere Medikamente: Metformin; losartan; bupropion; vitamin D3; vitamin B12; metoprolol; trospium chloride; atorvastatin; magnesium; topiramate; gabapentin.
Allergien: Lanolin.
Vorherige Impfungen: With each of my COVID-19 vaccines and boosters, I had swelling, tenderness, and heat in the lymph nodes of the axilla of the arm

VAERS 2523732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: AL
Alter: 68,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 05.08.2022
Beginn: 08.08.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: - / LA

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

Antinuclear antibody Back pain Computerised tomogram abdomen Differential white blood cell count Full blood count Blood test Computerised tomogram Gait inability Groin pain Gait disturbance Injected limb mobility decreased Injection site pain Loss of personal independence in daily activities Investigation Magnetic resonance imaging Monoplegia Movement disorder Mobility decreased

Symptomtext

. Extreme difficulty getting in and out of tub and showering. Dressing couldn't lift arms over head.; lower left groin area with severe itching/itching lower left leg ankle; Extreme pain in upper arm; then paralysis; unable to move legs up; Started with pain in lower left groin area; bad pain in my buttocks; bad pain in my thighs; bad pain in my back; Unable to lift arms up; hard "knots" in deltoids both arms.; When I could move, had to use a cane to assist with mobility.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Aug2022 at 16:30 as dose 4 (booster), single (Lot number: FP7135) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High BP" (unspecified if ongoing); "High Cholesterol" (unspecified if ongoing); "Type II Diabetes" (unspecified if ongoing); "Diverticulosis" (unspecified if ongoing); "Bone Spur in Neck" (unspecified if ongoing); "Freckle in Left Eye" (unspecified if ongoing); "Cataracts" (unspecified if ongoing); "Eczema" (unspecified if ongoing); "Molds" (unspecified if ongoing); "she diagnosed with covid" (unspecified if ongoing); "Age-Related Macular Degeneration" (unspecified if ongoing); "Discs Issues in Lower Back" (unspecified if ongoing); "Bermuda Grass" (unspecified if ongoing); "Nickel" (unspecified if ongoing); "p-Phenylenediamine (in black hair dyes)" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN POTASSIUM; HCTZ; ACETAZOLAMIDE; NIFEDIPINE; ATORVASTATIN; LEVOCETIRIZINE; TYLENOL EXTRA STRENGTH taken for pain; TYLENOL ARTHRITIS PAIN taken for arthritis, pain; ADVIL LIQUI GELS taken for pain; CENTRUM GENDER +50; VITAMIN D3; FISH OIL; COQ-10; METAMUCIL CITRON; FLUTICASONE PROPIONATE; AZELASTINE. Past drug history included: Ultram for Ultram makes me nauseated, reaction(s): "Known allergies: Ultram". Vaccination history included: BNT162b2 (Prev dose product= COVID 19, Prev dose brand=Pfizer Covid-19 Vaccine, Prev dose brand unknown= False, Is bivalent=False, Prev dose lot number=FE3590, Prev dose lot unknown= False, Prev dose administration date= 15Nov2021, Prev dose administration time=01:00 PM, Prev dose dose number= 3, Prev dose vaccine location= Left arm), administration date: 15Nov2021, when the patient was 68-year-old, for Covid-19 immunization; BNT162b2 (Prev dose product= COVID 19, Prev dose brand= Pfizer Covid-19 Vaccine, Prev dose brand unknown= False, Is bivalent=False, Prev dose lot number= EN6208, Prev dose lot unknown= False, Prev dose administration date= 15Mar2021, Prev dose administration time=02:45 PM, Prev dose dose number= 2, Prev dose vaccine location= Left arm), administration date: 15Mar2021, when the patient was 67-year-old, for Covid-19 immunization; BNT162b2 (Prev dose product= COVID 19, Prev dose brand= Pfizer Covid-19 Vaccine, Prev dose brand unknown= False, Is bivalent=False, Prev dose lot number= EN6200, Prev dose lot unknown= False, Prev dose administration date= 22Feb2021, Prev dose administration time=01:45 PM, Prev dose dose number= 1, Prev dose vaccine location= Left arm), administration date: 22Feb2021, when the patient was 67-year-old, for COVID-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 08Aug2022, outcome "recovered", described as "Extreme pain in upper arm"; GROIN PAIN (non-serious) with onset 08Aug2022, outcome "recovered", described as "Started with pain in lower left groin area"; MOVEMENT DISORDER (non-serious) with onset 08Aug2022, outcome "recovered", described as "Unable to lift arms up"; GAIT INABILITY (non-serious) with onset 08Aug2022, outcome "recovered", described as "When I could move, had to use a cane to assist with mobility."; BACK PAIN (non-serious) with onset 08Aug2022, outcome "recovered", described as "bad pain in my back"; MUSCULOSKELETAL PAIN (non-serious) with onset 08Aug2022, outcome "recovered", described as "bad pain in my buttocks"; PAIN IN EXTREMITY (non-serious) with onset 08Aug2022, outcome "recovered", described as "bad pain in my thighs"; NODULE (non-serious) with onset 08Aug2022, outcome "recovered", described as "hard "knots" in deltoids both arms."; PRURITUS (non-serious) with onset 08Aug2022, outcome "recovered", described as "lower left groin area with severe itching/itching lower left leg ankle"; PARALYSIS (medically significant) with onset 08Aug2022, outcome "recovered", described as "then paralysis"; MONOPLEGIA (medically significant) with onset 08Aug2022, outcome "recovered", described as "unable to move legs up"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "unknown", described as ". Extreme difficulty getting in and out of tub and showering. Dressing couldn't lift arms over head.". The events "then paralysis", "unable to move legs up", "started with pain in lower left groin area", "bad pain in my buttocks", "bad pain in my thighs", "bad pain in my back", "unable to lift arms up", "hard "knots" in deltoids both arms.", "when i could move, had to use a cane to assist with mobility.", "lower left groin area with severe itching/itching lower left leg ankle" and "extreme pain in upper arm" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: (unspecified date) Unknown Results; Computerised tomogram: (unspecified date) Unknown Results; Referral: (unspecified date) Unknown Results; Magnetic resonance imaging: (unspecified date) Unknown Results; SARS-CoV-2 test: (06Nov2022) Negative, notes: Nasal Swab; (30Nov2022) Negative, notes: Nasal Swab; X-ray: (unspecified date) Unknown Results. Therapeutic measures were taken as a result of paralysis, monoplegia, groin pain, musculoskeletal pain, pain in extremity, back pain, movement disorder, nodule, gait inability, pruritus, pain in extremity. Clinical information: No other vaccine in four weeks. Patient received other products as well. Started with pain in lower left groin area with severe itching (no rash); then paralysis -unable to: raise my body up, roll to either side, move legs up. Excruciating pain in my left groin area with really bad pain in my buttocks, thighs, back. Later pain in right groin area and same type itching lower left leg ankle area with no rash. When I could finally move, unable to lift up legs to climb stairs, extreme difficulty getting in and out of tub, showering and putting on clothes. Unable to lift arms up over head to comb hair or reach for objects. Extreme pain in upper arm (left and right) with hard "knots" in deltoids both arms. When I could move, had to use a cane to assist with mobility. Concomitant, Medicinal Product Name as Reported by the Primary Source: Preservision Eye Vitamin, Dosage text: Takes 2 daily and Elderberry gummy 100mg; 2 gummies daily. Went online yesterday and filled out the information online to report an adverse event and underneath the drugs she was taking 2 weeks prior to the vaccination, it wouldn't let her list out all of her medications. She started to list them but couldn't list them all. Wants to add those medications to her original report. Patient Details: She is 69 now because she has since had a birthday, but she was 68 when the adverse event happened. There were a lot of things that happened to her. She took vaccine on 05Aug2022 and late Friday evening she started the beginning of the side effects. Thinks the side effects are due to the vaccine and started on that following Monday. Got an itch in her lower left portion of her groin area and started hurting in her groin area. Couldn't get the itch to stop even when she scratched. Pain started in left groin area. No rash present and that was on the 08Aug2022. Went on that week. Itching would stop and start. Saturday night after 08Aug2022, she started experiencing paralysis. Was in the bed asleep at night, and woke up at night, couldn't move couldn't raise her body up, couldn't roll, couldn't raise legs up, had excruciating pain in left groin and buttocks thighs and back. Finally subsided. Happened that Saturday and Sunday night. Went to her provider after that. Didn't go to emergency room. Was hurting bad enough to call 911. She thought about it but didn't. Waited until Monday and went to see her provider. Did X-rays and stuff. After that, several weeks passed and it started up again. Hurting in groin, hurting in left and right groin area. Has stairs in her house and couldn't lift legs to climb stairs. Extreme difficulty getting in and out of tub and showering. Dressing couldn't lift arms over head. Extreme pain in both arms in deltoid area. Muscles would get hard in both arms and when she could move around, she had to use a cane. Was a series of this going on for several week. Started 08Aug2022 and was referred to an ortho doctor. Went to two different doctors and finally went away. Didn't put any dates with it. All of this has been reported. Made one big paragraph of it and made it as thorough and brief as she could, but its all in there. The medications was the only area that concerned her because she wanted Pfizer to know everything she took and it wouldn't let her take the rest of the medications. She reported her cat scans, xrays, MRI, blood tests, and referrals. The previous report asked her prior to vaccination was she diagnosed with covid, and she said, no. Asked if she had been tested for covid, she said yes, but they were all home tests and she did them herself. She takes pictures of each home test she does, so she had the dates for those and was able to report that as well. Medications was the only area she wasn't able to fully report on. Doesn't wish to add anything else. If Pfizer wants anymore information, they can reach out and talk to her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: Test Name: blood tests; Result Unstructured Data: Test Result:Unknown Results; Test Name: cat scans; Result Unstructured Data: Test Result:Unknown Results; Test Name: Referral; Result Unstructured Data: Test Result:Unknown Results; Test Name: MRI; Result Unstructured Data: Test Result:Unknown Results; Test Date: 20221106; Test Name: Clinitest Rapid Covid-19 Antigen Self Test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20221130; Test Name: Clinitest Rapid Covid-19 Antigen Self Test; Test Result: Negative ; Comments: Nasal Swab; Test Name: xrays; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Age-related macular degeneration; Allergy to chemicals; Allergy to metals; Allergy to molds; Allergy to plants; Blood pressure high; Bone spur; Cataracts; COVID-19; Diverticulosis; Eczema; Freckles; High cholesterol; Lumbar disc disease; Type II diabetes mellitus
Andere Medikamente: LOSARTAN POTASSIUM; HCTZ; ACETAZOLAMIDE; NIFEDIPINE; ATORVASTATIN; LEVOCETIRIZINE; TYLENOL EXTRA STRENGTH; TYLENOL ARTHRITIS PAIN; ADVIL LIQUI GELS; CENTRUM GENDER +50; VITAMIN D3; FISH OIL; COQ-10; METAMUCIL CITRON; FLUTICASONE PROPIONATE;
Allergien: -
Vorherige Impfungen: -

VAERS 2523732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: AL
Alter: 68,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 05.08.2022
Beginn: 08.08.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / RA

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

Antinuclear antibody Back pain Computerised tomogram abdomen Differential white blood cell count Full blood count Blood test Computerised tomogram Gait inability Groin pain Gait disturbance Injected limb mobility decreased Injection site pain Loss of personal independence in daily activities Investigation Magnetic resonance imaging Monoplegia Movement disorder Mobility decreased

Symptomtext

. Extreme difficulty getting in and out of tub and showering. Dressing couldn't lift arms over head.; lower left groin area with severe itching/itching lower left leg ankle; Extreme pain in upper arm; then paralysis; unable to move legs up; Started with pain in lower left groin area; bad pain in my buttocks; bad pain in my thighs; bad pain in my back; Unable to lift arms up; hard "knots" in deltoids both arms.; When I could move, had to use a cane to assist with mobility.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Aug2022 at 16:30 as dose 4 (booster), single (Lot number: FP7135) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High BP" (unspecified if ongoing); "High Cholesterol" (unspecified if ongoing); "Type II Diabetes" (unspecified if ongoing); "Diverticulosis" (unspecified if ongoing); "Bone Spur in Neck" (unspecified if ongoing); "Freckle in Left Eye" (unspecified if ongoing); "Cataracts" (unspecified if ongoing); "Eczema" (unspecified if ongoing); "Molds" (unspecified if ongoing); "she diagnosed with covid" (unspecified if ongoing); "Age-Related Macular Degeneration" (unspecified if ongoing); "Discs Issues in Lower Back" (unspecified if ongoing); "Bermuda Grass" (unspecified if ongoing); "Nickel" (unspecified if ongoing); "p-Phenylenediamine (in black hair dyes)" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN POTASSIUM; HCTZ; ACETAZOLAMIDE; NIFEDIPINE; ATORVASTATIN; LEVOCETIRIZINE; TYLENOL EXTRA STRENGTH taken for pain; TYLENOL ARTHRITIS PAIN taken for arthritis, pain; ADVIL LIQUI GELS taken for pain; CENTRUM GENDER +50; VITAMIN D3; FISH OIL; COQ-10; METAMUCIL CITRON; FLUTICASONE PROPIONATE; AZELASTINE. Past drug history included: Ultram for Ultram makes me nauseated, reaction(s): "Known allergies: Ultram". Vaccination history included: BNT162b2 (Prev dose product= COVID 19, Prev dose brand=Pfizer Covid-19 Vaccine, Prev dose brand unknown= False, Is bivalent=False, Prev dose lot number=FE3590, Prev dose lot unknown= False, Prev dose administration date= 15Nov2021, Prev dose administration time=01:00 PM, Prev dose dose number= 3, Prev dose vaccine location= Left arm), administration date: 15Nov2021, when the patient was 68-year-old, for Covid-19 immunization; BNT162b2 (Prev dose product= COVID 19, Prev dose brand= Pfizer Covid-19 Vaccine, Prev dose brand unknown= False, Is bivalent=False, Prev dose lot number= EN6208, Prev dose lot unknown= False, Prev dose administration date= 15Mar2021, Prev dose administration time=02:45 PM, Prev dose dose number= 2, Prev dose vaccine location= Left arm), administration date: 15Mar2021, when the patient was 67-year-old, for Covid-19 immunization; BNT162b2 (Prev dose product= COVID 19, Prev dose brand= Pfizer Covid-19 Vaccine, Prev dose brand unknown= False, Is bivalent=False, Prev dose lot number= EN6200, Prev dose lot unknown= False, Prev dose administration date= 22Feb2021, Prev dose administration time=01:45 PM, Prev dose dose number= 1, Prev dose vaccine location= Left arm), administration date: 22Feb2021, when the patient was 67-year-old, for COVID-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 08Aug2022, outcome "recovered", described as "Extreme pain in upper arm"; GROIN PAIN (non-serious) with onset 08Aug2022, outcome "recovered", described as "Started with pain in lower left groin area"; MOVEMENT DISORDER (non-serious) with onset 08Aug2022, outcome "recovered", described as "Unable to lift arms up"; GAIT INABILITY (non-serious) with onset 08Aug2022, outcome "recovered", described as "When I could move, had to use a cane to assist with mobility."; BACK PAIN (non-serious) with onset 08Aug2022, outcome "recovered", described as "bad pain in my back"; MUSCULOSKELETAL PAIN (non-serious) with onset 08Aug2022, outcome "recovered", described as "bad pain in my buttocks"; PAIN IN EXTREMITY (non-serious) with onset 08Aug2022, outcome "recovered", described as "bad pain in my thighs"; NODULE (non-serious) with onset 08Aug2022, outcome "recovered", described as "hard "knots" in deltoids both arms."; PRURITUS (non-serious) with onset 08Aug2022, outcome "recovered", described as "lower left groin area with severe itching/itching lower left leg ankle"; PARALYSIS (medically significant) with onset 08Aug2022, outcome "recovered", described as "then paralysis"; MONOPLEGIA (medically significant) with onset 08Aug2022, outcome "recovered", described as "unable to move legs up"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "unknown", described as ". Extreme difficulty getting in and out of tub and showering. Dressing couldn't lift arms over head.". The events "then paralysis", "unable to move legs up", "started with pain in lower left groin area", "bad pain in my buttocks", "bad pain in my thighs", "bad pain in my back", "unable to lift arms up", "hard "knots" in deltoids both arms.", "when i could move, had to use a cane to assist with mobility.", "lower left groin area with severe itching/itching lower left leg ankle" and "extreme pain in upper arm" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: (unspecified date) Unknown Results; Computerised tomogram: (unspecified date) Unknown Results; Referral: (unspecified date) Unknown Results; Magnetic resonance imaging: (unspecified date) Unknown Results; SARS-CoV-2 test: (06Nov2022) Negative, notes: Nasal Swab; (30Nov2022) Negative, notes: Nasal Swab; X-ray: (unspecified date) Unknown Results. Therapeutic measures were taken as a result of paralysis, monoplegia, groin pain, musculoskeletal pain, pain in extremity, back pain, movement disorder, nodule, gait inability, pruritus, pain in extremity. Clinical information: No other vaccine in four weeks. Patient received other products as well. Started with pain in lower left groin area with severe itching (no rash); then paralysis -unable to: raise my body up, roll to either side, move legs up. Excruciating pain in my left groin area with really bad pain in my buttocks, thighs, back. Later pain in right groin area and same type itching lower left leg ankle area with no rash. When I could finally move, unable to lift up legs to climb stairs, extreme difficulty getting in and out of tub, showering and putting on clothes. Unable to lift arms up over head to comb hair or reach for objects. Extreme pain in upper arm (left and right) with hard "knots" in deltoids both arms. When I could move, had to use a cane to assist with mobility. Concomitant, Medicinal Product Name as Reported by the Primary Source: Preservision Eye Vitamin, Dosage text: Takes 2 daily and Elderberry gummy 100mg; 2 gummies daily. Went online yesterday and filled out the information online to report an adverse event and underneath the drugs she was taking 2 weeks prior to the vaccination, it wouldn't let her list out all of her medications. She started to list them but couldn't list them all. Wants to add those medications to her original report. Patient Details: She is 69 now because she has since had a birthday, but she was 68 when the adverse event happened. There were a lot of things that happened to her. She took vaccine on 05Aug2022 and late Friday evening she started the beginning of the side effects. Thinks the side effects are due to the vaccine and started on that following Monday. Got an itch in her lower left portion of her groin area and started hurting in her groin area. Couldn't get the itch to stop even when she scratched. Pain started in left groin area. No rash present and that was on the 08Aug2022. Went on that week. Itching would stop and start. Saturday night after 08Aug2022, she started experiencing paralysis. Was in the bed asleep at night, and woke up at night, couldn't move couldn't raise her body up, couldn't roll, couldn't raise legs up, had excruciating pain in left groin and buttocks thighs and back. Finally subsided. Happened that Saturday and Sunday night. Went to her provider after that. Didn't go to emergency room. Was hurting bad enough to call 911. She thought about it but didn't. Waited until Monday and went to see her provider. Did X-rays and stuff. After that, several weeks passed and it started up again. Hurting in groin, hurting in left and right groin area. Has stairs in her house and couldn't lift legs to climb stairs. Extreme difficulty getting in and out of tub and showering. Dressing couldn't lift arms over head. Extreme pain in both arms in deltoid area. Muscles would get hard in both arms and when she could move around, she had to use a cane. Was a series of this going on for several week. Started 08Aug2022 and was referred to an ortho doctor. Went to two different doctors and finally went away. Didn't put any dates with it. All of this has been reported. Made one big paragraph of it and made it as thorough and brief as she could, but its all in there. The medications was the only area that concerned her because she wanted Pfizer to know everything she took and it wouldn't let her take the rest of the medications. She reported her cat scans, xrays, MRI, blood tests, and referrals. The previous report asked her prior to vaccination was she diagnosed with covid, and she said, no. Asked if she had been tested for covid, she said yes, but they were all home tests and she did them herself. She takes pictures of each home test she does, so she had the dates for those and was able to report that as well. Medications was the only area she wasn't able to fully report on. Doesn't wish to add anything else. If Pfizer wants anymore information, they can reach out and talk to her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: Test Name: blood tests; Result Unstructured Data: Test Result:Unknown Results; Test Name: cat scans; Result Unstructured Data: Test Result:Unknown Results; Test Name: Referral; Result Unstructured Data: Test Result:Unknown Results; Test Name: MRI; Result Unstructured Data: Test Result:Unknown Results; Test Date: 20221106; Test Name: Clinitest Rapid Covid-19 Antigen Self Test; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20221130; Test Name: Clinitest Rapid Covid-19 Antigen Self Test; Test Result: Negative ; Comments: Nasal Swab; Test Name: xrays; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Age-related macular degeneration; Allergy to chemicals; Allergy to metals; Allergy to molds; Allergy to plants; Blood pressure high; Bone spur; Cataracts; COVID-19; Diverticulosis; Eczema; Freckles; High cholesterol; Lumbar disc disease; Type II diabetes mellitus
Andere Medikamente: LOSARTAN POTASSIUM; HCTZ; ACETAZOLAMIDE; NIFEDIPINE; ATORVASTATIN; LEVOCETIRIZINE; TYLENOL EXTRA STRENGTH; TYLENOL ARTHRITIS PAIN; ADVIL LIQUI GELS; CENTRUM GENDER +50; VITAMIN D3; FISH OIL; COQ-10; METAMUCIL CITRON; FLUTICASONE PROPIONATE;
Allergien: -
Vorherige Impfungen: -

VAERS 2515330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: MI
Alter: 48,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 11.07.2022
Beginn: 17.11.2022
Tage bis Beginn: 129,0
Dosis: 3
Route/Site: UN / UN

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

Aortic arteriosclerosis Arteriosclerosis coronary artery Atelectasis Bronchial atresia Bronchial secretion retention Bronchiectasis Bronchostenosis COVID-19 Chest X-ray abnormal Chest discomfort Computerised tomogram thorax abnormal Condition aggravated Cough Diaphragmatic disorder Diaphragmatic hernia Dizziness Dyspnoea Endoscopy normal

Symptomtext

Patient is a 49-year-old male with PMH significant for type 2 diabetes, hypertension, history of stroke presents to the hospital 11/17 with complaints of dyspnea, chest tightness, an episode of lightheadedness/presyncope, intermittently diaphoretic and ongoing ?gurgling noises? in LUQ of his abdomen since his surgery in January. In ER he was noted to be COVID positive, chest x-ray unremarkable except for air-fluid level in the left upper quadrant, labs significant for microcytic anemia. Patient was given 1 unit PRBC for hemoglobin 6.7 and admitted for further management. Patient denied any melena, hematochezia or hematemesis. Patient was noted to have symptomatic microcytic iron deficiency anemia with suspected low-grade chronic GI blood loss. Hemoglobin remained stable after PRBC, 7.2 at discharge. Patient did receive 3 doses of Ferrlecit and will need further IV dosing as outpatient through his PCP. Recommended him to take daily oral iron as well. GI was consulted but given covid status, without any active bleed, EGD/colonoscopy was not felt to be urgent and will need to be scheduled within the next 2 weeks. PCP can also consider CT abdomen/pelvis if EGD/colonoscopy are negative. Patient was given empiric Protonix. Patient complained of gurgling noises in LUQ, intermittently since his surgery January 2022, more notable after a meal. CT thorax was obtained, showed large left diaphragmatic hernia with diaphragmatic defect measuring 69 mm in maximum diameter and contain 50% of the stomach. Offered patient to have General surgery evaluate him here, however patient wanted to discharge in follow-up as outpatient. Patient also stated that he does not want to see his previous surgeon again he felt that the surgeon was disinterested in his care. Give him contact details for surgeon (was on-call for today) and requested patient to call office to arrange appointment. Patient was also noted to have scattered pulmonary nodules (largest 13 mm, previously 7 mm) that needs to be followed up with a repeat CT in 3-6 months. (This was notified to him after he was discharged, on the phone) --- Chart reviewed History of left-sided loculated pleural effusion/empyema--05/04/2021 Thoracentesis, followed by left thoracotomy with total decortication of the left lung 5/7/2021. Subsequently in 09/2021, patient was noted to have a new eventration of stomach through posterior hemidiaphragm on the left. CT of the chest without contrast confirmed the findings. Patient was referred to General surgery. Surgery recommended diaphragmatic repair, patient had preop endoscopy on 11/16 which was otherwise normal. Patient had laparoscopic repair of congenital diaphragmatic hernia on 01/06/2022. --- Patient also tested positive for COVID-19 on 11/17, with symptoms of sweats, dyspnea, cough and fever. He did not need any therapeutics. He would be off isolation on 11/18. Consultations: Gastroenterology Procedures: CT thorax--showed large left diaphragmatic hernia with diaphragmatic defect BP 137/76 | Pulse 86 | Temp 36.9 ?C (Oral) | Resp 18 | Ht 1.829 m | Wt 114.3 kg | SpO2 98% | BMI 34.17 kg/m? Physical Exam Constitutional: General: He is not in acute distress. Appearance: He is well-developed. He is not ill-appearing or toxic-appearing. Eyes: Pupils: Pupils are equal, round, and reactive to light. Comments: Left eye strabismus Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: Normal heart sounds, S1 normal and S2 normal. Pulmonary: Effort: No respiratory distress. Breath sounds: Normal breath sounds. No wheezing or rales. Abdominal: General: There is no distension. Palpations: Abdomen is soft. There is no mass. Tenderness: There is no abdominal tenderness. Musculoskeletal: General: Normal range of motion. Cervical back: Normal range of motion and neck supple. Neurological: Mental Status: He is alert and oriented to person, place, and time. Psychiatric: Behavior: Behavior normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 2,0
Labordaten: Procedure Component Value Ref Range Date/Time CT THORAX WITH IV CONTRAST Collected: 11/18/22 2146 Order Status: Completed Updated: 11/18/22 2157 Narrative: EXAMINATION: CT Chest with IV Contrast EXAM DATE: 11/18/2022 7:57 PM TECHNIQUE: Standard protocol CT imaging of the chest with intravenous contrast was performed. Coronal and sagittal images were reconstructed. CONTRAST: The amount and type of contrast are recorded in the medical record. DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Lung/mediastinal abscess, covid . "gurgling in LLL" airfluid level noted on CXR, hx for pleurodesis, and subsequent eventration of diaphragm/Hiatal hernia, s/p repair COMPARISON: None ENCOUNTER: Initial ____________________ FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: There is no mediastinal or hilar lymph node enlargement. No significant esophageal dilation. Cardiovascular: Mild coronary artery calcification. No pericardial effusion. Mild aortic calcification. Lungs & Airways: Streaky left lower lobe and lingular consolidation. Right upper lobe 8 x 6 mm nodule (3/96). Focal right lower lobe bronchiectasis with abrupt termination of the bronchus and downstream decreased parenchymal density. Segmentally decreased density within the left upper lobe the region of lung containing upper lobe curvilinear 13 x 8 mm opacity (3/65). Pleural Space: Trace left pleural effusion. No pneumothorax. Upper Abdomen: Large left diaphragmatic hernia measuring approximately 69 mm in diameter containing approximately 50% of the stomach. Trace free fluid in the left upper quadrant of the abdomen. Right renal 16 mm cyst. Chest Wall & Musculoskeletal: Mild multilevel disc degeneration of the thoracic spine. ____________________ Impression: 1. Large left diaphragmatic hernia with diaphragmatic defect measuring approximately 69 mm in maximum diameter and contains approximately 50% of the stomach. 2. Trace free fluid in the left upper quadrant of the abdomen. 3. Trace left pleural effusion. 4. There is mosaic attenuation of the lung parenchyma with left upper lobe and right lower lobe segmental decreased attenuation lung parenchyma which could be seen with chronic mucus plugging as well as sequela of bronchial atresia or bronchial stenosis secondary to severe remote multifocal pneumonia. 5. Few scattered pulmonary nodules the largest measuring 13 x 8 mm in size. Follow-up guidelines are included below: Consensus guidelines for multiple solid lung nodules 6 mm or greater, not applicable if known malignancy or immunocompromise: Low risk: CT at 3-6 months, then consider CT at 18-24 months if stable. 2. Electronically signed by: MD on 11/18/2022 9:56 PM. DR CHEST 2 VIEWS FRONTAL AND LATERAL Collected: 11/17/22 2009 Order Status: Completed Updated: 11/17/22 2012 Narrative: EXAMINATION: Two View Chest Radiographs EXAM DATE: 11/17/2022 7:43 PM TECHNIQUE: Frontal and lateral views INDICATION: cp COMPARISON: 10/10/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: The heart, mediastinum, and pulmonary vasculature are stable. Rounded opacity at the left lung base with air-fluid level appears to measure 11.3 x 13.4 cm. Etiology is indeterminate by this examination. Differential considerations would include but are not limited to a hiatal hernia. Adjacent atelectasis. Need for further evaluation with CT thorax should be determined clinically. No pneumothorax Impression: As above. COVID-19, Influenza A/B, RSV PCR (Abnormal) Collected: 11/17/22 1925 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 11/17/22 2011 COVID-19 PCR Detected
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory Diaphragmatic hernia Pulmonary nodule---multiple, largest measuring 13 mm, will need repeat CT in 3-6 months Circulatory Essential hypertension Digestive Iron deficiency Infectious/Inflammatory COVID-19 Hematologic Symptomatic anemia
Andere Medikamente: aspirin 81 mg EC tablet Take 81 mg by mouth 1 (one) time each day. 0 04/26/2021 atorvastatin (LIPITOR) 40 mg tablet Take 40 mg by mouth at bedtime. 0 04/17/2021 lisinopriL (PRINIVIL,ZESTRIL) 20 mg tablet Take 20 mg by mouth 1
Allergien: No known allergies.
Vorherige Impfungen: -

VAERS 2493853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 11.07.2022
Beginn: 05.10.2022
Tage bis Beginn: 86,0
Dosis: 2
Route/Site: - / -

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

Adrenal mass Angiogram pulmonary normal Arteriosclerosis coronary artery Atelectasis Blood culture negative Blood glucose increased COVID-19 Condition aggravated Deep vein thrombosis Failure to thrive Fibrin D dimer increased Gastrostomy Glycosylated haemoglobin increased Heart valve calcification Hypernatraemia Infection Iron deficiency anaemia Leukocytosis

Symptomtext

"Patient with 2 COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: ""Reason for Admission: From, NP 84-year-old male patient with past medical history of Alzheimer's dementia, advanced, cerebral infarction, subdural hematoma, dysphagia, gastrostomy tube, chronic obstructive pulmonary disease, hypertension, NSTEMI, diabetes mellitus type 2, BPH with urinary retention, indwelling Foley catheter, resident of Timbers skilled nursing facility, presented with worsening altered mental status Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) found to be hypernatremic on admission, pressure ulcer infection Blood sugars on the high side , 250 PEG feeds changed to Glucerna gotCTA of the pulmonary artery rule out PE due to tachypnea, x2, negative Mild leukocytosis, improved at the time of discharge to 11 K Failure to thrive, due to advanced Alzheimer's dementia On PEG feeds, dietitian following Hypernatremia resolved Pressure ulcers Without evidence of osteomyelitis on MRI, repeated for inadequate imaging due to motion artifact, repeat MRI from 10/18 shows no evidence of osteomyelitis On Zosyn and doxycycline, from 10/11 and 10/14 respectively wound care, discontinued antibiotics 10/20 Being discharged on oral Augmentin for 1 week Leukocytosis- 13.4 COVID Off isolation, room air History of subdural hematoma Staph epidermidis 1/2 blood culture positive from 10/06 follow-up blood cultures negative, most likely contaminant DVT Evident on ultrasound imaging on admission, was discussed with family members, in the light of subdural hematoma it was decided not to anticoagulate the patient 10/19 has elevated D-dimer, had CTA 10/6 no evidence of pulmonary embolism 10/20 CTA pulmonary- No evidence of pulmonary embolism. 2. Patchy consolidation within the left lower lobe and a few scattered tree-in-bud nodular opacities within the right lower lobe, suspicious for multifocal pneumonia including atypical etiologies. 3. Extensive coronary artery and aortic valve leaflet calcifications. 4. Incidental note of a 4.3 x 6.7 cm intramuscular lipoma within the right shoulder musculature with areas of calcification and a 2.0 cm soft tissue component posteriorly, raising concern for possible liposarcoma. Further evaluation with MRI without and with contrast is recommended. 5. Indeterminate left adrenal nodule and partially visualized probable right adrenal nodule. These could be further evaluated with adrenal protocol CT or MRI on a nonemergent basis. Reviewed CTA pulmonary report with daughter, reassured that there is no PE however incidental finding of Right shoulder 4.3 3 x 6.7 intramuscular lipoma, with possible concerns of liposarcoma, she is okay and agreed to have it worked up outpatient Urinary retention, chronic Foley 10/20 Will get CT of the pulmonary artery rule out PE due to tachypnea Diabetes Last hemoglobin A1 c of 7.6, Lantus insulin, Glucerna tube feeds 10/18 increase Lantus insulin for high blood sugars of 250 Iron deficiency anem Was treated with IV Venofer in the beginning,repeat iron parameters, high ferritin of 800, cannot give IV iron No evidence of overt bleeding Kept daughter, guardian informed Got cognition to evaluation by speech, 10/20 however patient did not cooperate Condition at the time of discharge Vss Constitutional: No distress HENT: Normocephalic, Atraumatic, Normal oropharynx, Nose normal. Cardiovascular: Normal heart rate, Normal rhythm, No murmurs, No rubs, No gallops. Respiratory: Normal breath sounds, No respiratory distress, No wheezing, No chest tenderness. GI: Bowel sounds normal, PEG tube+ Soft, No tenderness, No masses, No pulsatile masses. , Foley catheter + Sacral wound noted , stage III bases appear clear, please see the picture from 10/nineteen wound care note Extremities: Intact distal pulses, No edema, No tenderness, No cyanosis, No clubbing. . Bilateral malleolar pressure ulcer, with clean base, Neurologic: Alert & oriented x1 , No focal deficits noted. Skin: Warm and dry Issues Requiring Follow Up: (Who, what, when, and how communicated?) Patient to follow-up with multiple specialist follow-up appointments fair med, For right shoulder lipoma/liposarcoma follow-up with general surgery, follow-up with Cardiology for calcification of coronaries, follow-up with Pulmonary Medicine for CT showing consolidation/atelectasis, follow-up with GI These appointments were made after discussing with the daughter, POA"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 16,0
Labordaten: COVID detected PCR on 10/6/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular HTN (hypertension) HLD (hyperlipidemia) Chronic deep vein thrombosis (DVT) of left femoral vein (HCC) Digestive Dysphagia Chronic constipation Endocrine Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) Integumentary Seborrheic dermatitis Skin ulcer of ankle with fat layer exposed (HCC) Psychological Alzheimer's dementia (HCC) Urinary Chronic indwelling Foley catheter Other Gastrostomy tube dependent (HCC) BPH (benign prostatic hyperplasia) Severe protein-calorie malnutrition (HCC) Failure to thrive in adult Vitamin D deficiency Pressure injury of sacral region, stage 3 (HCC) Chronic subdural hematoma (HCC) Multiple wounds Sepsis (HCC) Dehydration with hypernatremia Elevated troponin COVID-19 Iron deficiency anemia Elevated liver enzymes Alkaline phosphatase elevation
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2486923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 18.07.2022
Beginn: 15.10.2022
Tage bis Beginn: 89,0
Dosis: 3
Route/Site: - / -

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

Asthma Complication of pregnancy Delivery Exposure during pregnancy Foetal growth restriction Foetal heart rate deceleration abnormality Foetal heart rate indeterminate Haemorrhage Labour induction Perineal injury Postural orthostatic tachycardia syndrome Thrombocytopenia Thrombosis Uterine contractions during pregnancy Uterine dilation and evacuation Vacuum extractor delivery Vulvovaginal injury Wound closure

Symptomtext

Admission Date: 10/15/2022 Discharge Date: 10/18/2022 PROCEDURES PERFORMED: Vaginal delivery Tubal ligation: No HOSPITAL COURSE: Patient underwent an uncomplicated vaginal delivery and was discharged home in stable condition. DELIVERY TYPE: Vaginal, Vacuum (Extractor) ESTIMATED DUE DATE: Estimated Date of Delivery: 11/4/22 GESTATIONAL AGE AT DELIVERY: 37w2d G1P0000 FINDINGS: NEWBORN STATUS: Living NEWBORN SEX: girl Delivery Date/Time: 10/XX/22 9:53 AM WEIGHT: APGAR: 1 minutes 5 minutes 10 minutes 8 9 RESCUSITATION: Tactile stimulation PLACENTA REMOVAL: Spontaneous CORD VESSELS: 3 Vessels CORD COMPLICATIONS: Nuchal ANALGESIA METHOD: Epidural DELIVERY COURSE: Patiet is a 31 y.o. G1P0000 female who presented to L&D at 37 weeks gestation for induction of labor due to fetal growth restriction. Pregnancy was complicated by maternal POTS, asthma, thrombocytopenia. Labor course included vaginal cytotec. Labor course complicated by category II fetal heart tones after epidural which improved somewhat with intrauterine resuscitation and IV phenylephrine. She progressed to complete at 0900. She pushed well with contractions. Category II fetal heart tones noted with intermittent deep late and prolonged decelerations. With fetus at 3+ station, fetal heart rate dropped to the 70s. Patient was consented to operative vaginal delivery with vacuum. Kiwi omnicup was applied to flexion point on fetal head, ensuring that maternal tissue was excluded. Traction was applied along with maternal effort over one contraction to bring fetal head to a crown. There were no pop offs. The vacuum was removed and patient continued to push. She went on to deliver the fetal head in a controlled fashion. Head restituted to face maternal left. No nuchal palpated. Anterior shoulder delivered with gentle downward traction of the head, followed by the posterior shoulder. Rest of the body followed with ease. Time of delivery was 0953. NICU was present at the delivery due to operative delivery and fetal growth restriction. A female infant was placed on the maternal abdomen and dried by RN. Delayed cord clamping was performed for 60 seconds and then the cord was clamped x2 and cut by the patient. The infant was then placed skin to skin on maternal chest. APGARS 8 and 9 . Mixed cord blood was obtained. Arterial and venous blood gases were obtained. Placenta delivered with fundal massage and gentle downward traction on the cord. Placenta appears intact and a three vessel cord is present. Pitocin infusion started to actively manage the third stage. Active bleeding noted. Uterine massage performed, small amount of clots evacuated from uterine cavity. 1g IV TXA administered. Active bleeding noted from left sided vaginal wall laceration, this was repaired in running locked fashion with 3-0 Vicryl and good hemostasis achieved. A shallow second degree perineal laceration was repaired in usual fashion using 3-0 vicryl. QBL 500 ml. Mother and baby remain skin to skin and bonding in the immediate postpartum period. Sponge, instrument and sharp counts were correct. Mother plans to breastfeed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic pelvic pain in female History of abnormal cervical Pap smear -- LSIL 2015 PCOS (polycystic ovarian syndrome) Mild intermittent asthma without complication Celiac disease Family history of ASCVD Hyperlipidemia Gastric polyps POTS (postural orthostatic tachycardia syndrome) Numbness Generalized anxiety disorder Dysautonomia (HCC) MFM Plan of Care Autoimmune disorder (HCC) Abnormal prenatal test - high risk for triploidy on Panorama horizon carrier screen 14 dis panel negative Thrombocytopenia affecting pregnancy (HCC) Poor fetal growth affecting management of mother in third trimester IUGR (intrauterine growth restriction) affecting care of mother, third trimester, fetus 1
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin 81 MG enteric coated tablet busPIRone (BUSPAR) 5 MG tablet cromolyn (NASALCHROM) 5.2 MG/ACT nasal spray cromolyn (OPTICROM) 4 % ophthalmic solutio
Allergien: CephalexinRash GlutenGI Upset KeflexRash Turkey Allergy Diflucan [Fluconazole]Itching
Vorherige Impfungen: -

VAERS 2422606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: AL
Alter: 66,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 22.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Pain in extremity Thrombosis Ultrasound Doppler abnormal

Symptomtext

Woke up 7-29-22 with sore calf. Woke up Saturday 7-30-22 and went to urgent care. No ppler ultrasound was done and Xarelto was started due to dot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Doppler ultrasound of left calf.
Aktuelle Erkrankungen: No.
Vorgeschichte: HBP, High cholesterol - controlled with meds
Andere Medikamente: Lipitor, HCTZ, Lisinopril, B complex, Vit C, Rx vit - D.
Allergien: Bactrim, codeine.
Vorherige Impfungen: -

VAERS 2416819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: CT
Alter: 15,0
Geschlecht: F
Eingang: 20.08.2022
Impfdatum: 20.08.2022
Beginn: 20.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hyperhidrosis Syncope

Symptomtext

Patient was given vaccine. she stood up and was talking with her sister. I gave the father his vaccine after and instructed the family to wait for 15 minutes. I returned to the pharmacy and a minute or 2 later the older sister came back stating her sister had fainted. When I arrived, the younger sister was sitting in a chair, sweating profusely and conscious. I got her a bottle of water and contacted management. Management contacted EMS who took the patient to the hospital for observation. Before returning to the pharmacy, dad had asked the daughter if she had breakfast, she said no.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: At time of reporting, none that the pharmacy is aware of.
Aktuelle Erkrankungen: none reported
Vorgeschichte: none reported
Andere Medikamente: unknown. new patient to pharmacy at time of injection
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2405890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: SC
Alter: 17,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Skin discolouration Syncope

Symptomtext

patient had syncopal event approx5 minutes after vaccine injection. Did not lose consciousness - placed on floor on back with legs elevated - color returned within minutes and patient was smiling and laughing. Family declined '911' being contacted

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

VAERS 2397966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

schwer

Staat: VA
Alter: 17,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 20.06.2022
Beginn: 14.07.2022
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / -

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

Blood creatine phosphokinase increased Brain natriuretic peptide increased C-reactive protein increased Cardiac dysfunction Chest pain Electrocardiogram abnormal Fibrin D dimer Immunoglobulin therapy Inflammatory marker increased Intensive care Myocarditis Pericarditis Serum ferritin increased Troponin I increased Troponin increased

Symptomtext

myocarditis/pericarditis with chest pain, elevated inflammatory markers, EKG changes and elevated troponin, decreased heart function, requiring ICU admission, IVIG

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Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: CRP 27.4 (H) 08/01/2022 BNP 1,848 (H) 08/01/2022 FERRITIN 547.80 (H) 07/31/2022 CK 687 (H) 07/30/2022 TROPI 2.76 (HH) 08/01/2022 DDIMER 2.47 (H) 07/31/2022
Aktuelle Erkrankungen: covid ~1 month prior
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2397676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

schwer

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 31.07.2022
Impfdatum: 23.07.2022
Beginn: 24.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Anaphylactic reaction Pruritus Rash

Symptomtext

Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash Generalized-Medium

Weitere VAERSDATA-Felder

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

VAERS 2396718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: CA
Alter: 16,0
Geschlecht: M
Eingang: 29.07.2022
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: unbekannt Erholt: ja

Asthenia Cold sweat Dizziness Extra dose administered Gait disturbance Presyncope

Symptomtext

6 y.o., patient was vaccinated with Adult Pfizer Booster #1 on Friday, July 28 2022. At approx 1515 nurse administered the vaccine as an intramuscular injection into the L deltoid. In the vaccination was patients mother and sister. Previous to vaccination patient and mom had answered the pre-vaccination checklist with nurse, stating no previous adverse events to covid vaccines or other immunizations, nurse also asked about being properly hydrated and food intake to which the patient stated having done so. Immediately after vaccine was administered no reaction was noted. Nurse proceeded to escort the patient, patients mom and patients sister to the observations area. When the patient walked out of the vaccination room, approximately 10 feet from vaccination area and nurse behind him, nurse noted the client to have unstable gait. Nurse proceeded to place her arms under the patients axillary and call for help. Two other Nurses were prompt to respond and brought a wheelchair and folding cot. Another wo Nurses also responded to the area with vital signs kit and emergency kit. Nurse began to take the first set of vitals at 1520, BP: 100/60, HR: 67, SpO2: 98%, RR: 18, Temp: 97.6. Patient was A&O x4 with a clammy appearance. Patient stated that he began to feel dizzy and weak when he began to walk and that is why his gait became unsteady. Juice, water and crackers were provided to patients, as he began to disclose that he had not eaten since the morning. After 10 min the patient was transferred from the wheelchair to the cot where he was able to sit in a reclining position. Nurse proceeded to take vital signs for 30 minutes at 5 minute intervals, assessing the patients symptoms and alertness. Patients vital signs remained stable, last vital signs taken at 1350 were BP: 108/64, HR: 76, SpO2: 98%, RR; 18, Temp: 97.7, A&O x4. MD was made aware of the situation, stated the episode sounded like a vasovagal episode and recommended seeing his PCP. Patient and mom made aware of MD recommendation. Patient and mom stated understanding the situation and recommendations. During the event patient did not hit his head, did not loose consciousness, and no medications were administered. Mom and patient had no additional questions, were given the vaccine fact sheet and given information and instructions on what to do if patient were to develop additional vaccine reaction related symptoms.

Weitere VAERSDATA-Felder

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

VAERS 2379827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 23.07.2022
Impfdatum: 24.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia Dizziness Haematoma Malaise Nausea Syncope

Symptomtext

The day after receiving the second booster, I felt sick in the evening and 18 hours after the booster, I had nausea and fainted and sustained hematomas on my scalp and posterior right shoulder and had continued coccydynia for several weeks. I felt very weak and lightheaded most of the day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfas, amoxicylin, shellfish
Vorherige Impfungen: Covid 19 Moderna

VAERS 2363114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: MI
Alter: 13,0
Geschlecht: F
Eingang: 08.07.2022
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

Depressed level of consciousness Dizziness Dyskinesia Fall Immediate post-injection reaction Seizure Visual impairment Loss of consciousness Seizure like phenomena Tremor Vision blurred

Symptomtext

I (the pharmacist) gave the patient an HPV vaccine, then about 1 minute later gave a Pfizer vaccine. As I pulled out after administering the Pfizer vaccine, the patient began to lean back into the chair in a seemingly involuntary motion, and began shaking. I immediately thought this may have been a seizure, and grabbed behind her head to prevent it from banging on the table behind her. She seized for a few more seconds, then broke out of it, and fully regained consciousness. She described it as blacking out, and having lightheadedness and blurry vision afterwards. No Hx of seizures, but a few incidents of fainting spells have happened before when her blood sugar was low and she was anxious. She had skipped breakfast that morning, and was anxious about the shots (I couldn't tell just by look, but she said such afterwards), so perhaps a similar incident to the previous few, but with more visible shaking (vasovagal syncope perhaps?). Considering the timing and patient Hx, so quickly after 1 vaccine and during administration of another, and with possible precipitating factors, I doubt the vaccines were truly the cause, and the patient's stepmother agreed that they likely were not the cause. The patient was monitored for a half hour at the pharmacy, given some orange juice for possible low blood sugar, and then allowed to go home and rest, and call their PCP about the event. 911 was not called.

Weitere VAERSDATA-Felder

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

VAERS 2362604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: NY
Alter: 21,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope Vomiting

Symptomtext

After receiving shot, patient fainted for about one minute and then vomited. Paramedics came and cleared him, patient left on his own, walked out.

Weitere VAERSDATA-Felder

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

VAERS 2359844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: CA
Alter: 34,0
Geschlecht: F
Eingang: 06.07.2022
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: ja Erholt: nein

Asthenia Chills Dyspnoea Exposure during pregnancy Eye movement disorder Feeling abnormal Feeling cold Head titubation Interchange of vaccine products Loss of consciousness Malaise Nausea Pallor Syncope Unresponsive to stimuli Wheelchair user

Symptomtext

Patient previously had 3 Moderna (18+) COVID vaccines. This was their first Pfizer (12+). Patient received the Pfizer Adult (Age 12+) vaccine at 3:20pm. Patient started to not feel well 10 mins after the vaccine was given. Patient stated that they felt nauseous. Patient's eyes rolled back, head was leaning back in chair, and was unresponsive for 30 seconds to 1 minute. During that time patient made noises with throat and sounded like she was gasping for air. Patient regained consciousness, laid patient down, blood pressure was 77/51 on left arm, pulse was 55 and O2 was 97%. Patient stated that they do not know what happened. Patient stated that they are feeling weak, faint, cold, shivering, and "spacey". Patient was also pale. Patient stated that they have a history of fainting after blood draw, history of low blood pressure, history of brain lesion, and is currently pregnant. Patient stated she has never made the throat noises when she has fainted. Blood pressure at 3:35pm was 105/68, pulse 55. Nurses advised patient to call husband. Patient was advised to go to ED to get assessed. Patient was still feeling weak, cold, and shivering. Patient said they are feeling better but still feels weak. Patient blood pressure was at 110/66, pulse was 75 at 3:45pm. Patient's husband escorted patient out in wheelchair. clinical manager informed of the situation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: history of low blood pressure, history of fainting after blood draw, and history of brain lesion
Vorgeschichte: Cardiovascular Palpitations Mitral valve disorder Endocrine Hypothyroidism Gastrointestinal Celiac disease GU/Reproductive Ovarian cyst Cervical intraepithelial neoplasia grade 1 History of abnormal cervical Pap smear Encounter for supervision of normal first pregnancy in first trimester Heme/Onc Family history of melanoma Infectious COVID-19 Neurological Brain lesion Symptoms/Signs Syncope and collapse
Andere Medikamente: ondansetron 4 mg orally disintegrating tablet prenatal multivitamin 29 mg iron- 1 mg CHEW
Allergien: Gluten Morphine (itching, Pruritis, Hives/ urticaria)
Vorherige Impfungen: -

VAERS 2357827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

schwer

Staat: NY
Alter: 18,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 02.07.2022
Beginn: 02.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Flushing Hyperhidrosis Hypotension Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Weakness-Medium

Weitere VAERSDATA-Felder

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

VAERS 2341755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

schwer

Staat: AL
Alter: 62,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 16.06.2022
Beginn: 18.06.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Feeling hot Hyperhidrosis Loss of consciousness Nausea

Symptomtext

Patient became nauseous in the morning 2 days after getting both vaccines (had never had a problem with Pfizer vaccine). In the morning she even lost consciousness though she did not say or know for how long. Also became hot and started sweating a lot. Patient did not tell me treatments she used but she is fine now.

Weitere VAERSDATA-Felder

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

VAERS 2336476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

schwer

Staat: KY
Alter: 30,0
Geschlecht: M
Eingang: 27.06.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

pt passed out afterwards

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EMS workers took him to the hospital
Aktuelle Erkrankungen: stated he "could be dehydrated" and had been congested for 2 days
Vorgeschichte: none
Andere Medikamente: none, did have "lots of caffeine"
Allergien: nkda
Vorherige Impfungen: -

VAERS 2324197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: CA
Alter: 62,0
Geschlecht: M
Eingang: 20.06.2022
Impfdatum: 03.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: SYR / LA

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

Bell's palsy Ear pain Facial paralysis Glossitis Glossodynia Herpes zoster Herpes zoster oticus Neurological examination Pain in jaw

Symptomtext

Diagnosed with Ramsay Hunt Syndrome. 5 days after booster - noted inflammation and pain on tongue. 8 days after booster - experienced pain in ear/jaw. 9 days after booster - sought urgent medical care for facial paralysis on right side. Bell's palsy triggered by shingles suspected. 12 days after booster - Neurologist confirms Ramsay Hunt Syndrome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Initial Urgent Care Exam. Additional exam by Neurologist.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: daily multi-vitamin
Allergien: -
Vorherige Impfungen: -

VAERS 2323973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: CA
Alter: 58,0
Geschlecht: M
Eingang: 18.06.2022
Impfdatum: 14.06.2022
Beginn: 15.06.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Bell's palsy Eyelid function disorder Facial paralysis Hemiplegia Pain

Symptomtext

Soreness first and then diagnosed with Bells Palsy. Left side of the face paralyzed. Cannot keep left eye lid closed Being treated with Prednisone, Acyclovir and eye drops and eye ointment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Emergency care at Facility - Diagnosed adverse effect as bells palsy
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Low dose Aspirin, vitamin C, one a day multivitamin, fiber tab, vitamin D, calcium gummy
Allergien: None
Vorherige Impfungen: -

VAERS 2322123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: CA
Alter: 45,0
Geschlecht: M
Eingang: 16.06.2022
Impfdatum: 15.06.2022
Beginn: 15.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope

Symptomtext

I gave the 1st Pfizer in right arm, patient seemed fine at the time. He was to sit 15 minutes in our sight. A few minutes later after sitting, he fainted. He was conscious, we called 911. Emergency services came. After 30 minutes, patient said he felt fine and wanted to go, and he left

Weitere VAERSDATA-Felder

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

VAERS 2322064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: WI
Alter: 30,0
Geschlecht: M
Eingang: 16.06.2022
Impfdatum: 10.06.2022
Beginn: 12.06.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / -

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

Arteriogram coronary abnormal Cardiac imaging procedure abnormal Chest pain Ejection fraction decreased Hypokinesia Myocarditis Troponin

Symptomtext

Severe chest pain 2 post post vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: hsTroponin level markedly elevated: 325-- >454--- >394 Positive CMR for myocarditis EXAM: MR CARDIAC WITHOUT AND WITH IV CONTRAST COMPARISON: CT chest abdomen angiogram dated 6/15/2022 FINDINGS: LEFT VENTRICLE: Normal left ventricular chamber size. Normal wall thickness. Mildly decreased left ventricular ejection fraction. Left ventricular ejection fraction = 44%. Mild hypokinesis at the LV apex. Delayed enhancement in the epicardial surface greatest in the lateral wall at the mid and the apex (series 18, image 1; series 17 image 12; series 20, image 1). RIGHT VENTRICLE: Normal right ventricular chamber size. Normal systolic function. Right ventricular ejection fraction = 50%. ATRIA: Normal-sized left atrium. Normal-sized right atrium. PERICARDIUM: Normal pericardial thickness. No pericardial effusion. No abnormal pericardial enhancement. ADDITIONAL FINDINGS: No caliber thoracic aorta and pulmonary arteries. MEASUREMENTS: LEFT VENTRICLE: End-diastolic volume = 190 mL End-systolic volume = 107 mL Stroke volume = 84 mL Ejection fraction = 44% RIGHT VENTRICLE: End-diastolic volume = 150 mL End-systolic volume = 75 mL Stroke volume = 74 mL Ejection fraction = 50% MR Cardiac without and with IV Contrast Result Date: 6/16/2022 Impression: 1. Patchy delayed enhancement in a pattern that suggest myocarditis.
Aktuelle Erkrankungen: none
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: Pfizer dose 1 on 6/7/2021 Lot EW0180 Pfizer dose 2, EW0217 on 6/28/2021

VAERS 2316643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

schwer

Staat: MN
Alter: 55,0
Geschlecht: F
Eingang: 11.06.2022
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

Migraine Seizure

Symptomtext

HAD A SEIZURE THE NEXT DAY, NOT SURE IF RELATED...HAS HAD SEIZURES IN PAST AND HAD HAD A MIGRAINE AND LUNCH WAS VERY LATE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: HAS HAD SEIZURE HISTORY
Vorgeschichte: UNDOCUMENTED
Andere Medikamente: MANY
Allergien: MANY
Vorherige Impfungen: -

VAERS 2726882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 22.12.2023
Impfdatum: 29.07.2022
Beginn: 28.10.2023
Tage bis Beginn: 456,0
Dosis: 4
Route/Site: - / -

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

Acute kidney injury Asthenia Blood creatinine increased Blood gases normal Blood lactic acid Blood magnesium normal Blood phosphorus normal Blood thyroid stimulating hormone decreased COVID-19 Chest X-ray normal Cough Dehydration Diarrhoea Fatigue Hypokalaemia Hypophagia Hypopituitarism Hypothyroidism

Symptomtext

Patient is a 77 y.o. male patient CNP with history of Hypopituitarism, Essential HTN, Legal Blindness, Memory Impairment, HPL who presented to Medical Center with Dehydration, Diarrhea, Cough, Generalized Weakness and was found to have COVID infection and AKI . Covid-19 Virus Infection Date of onset of symptoms: 10/26 Symptoms present on admission: cough, diarrhea, N/V, fatigue, weakness, sore throat Date of covid positive test: 10/28 Vaccination status: vaccinated Imaging: CXR 10/28 negative Oxygen requirements on admission: none Current oxygen requirements: none Medical therapy: not indicated - is getting increased home steriod Consultants following: none Anticipated special isolation end date: 11/6 Does not meet sepsis criteria on admission WBC 14, VBG unremarkable, LA 2 Supportive care PT/OT Nausea, Vomiting - Resolved Loose Stool Secondary to covid Negative Lipase, LFTs No loose stool day of admission Poor po intake Zofran prn, imodium prn Hypopituitarism Hypothyroidism TSH low, free T4 normal on admission Continue synthroid Resume home prednisone Hypokalemia Replaced IV, recheck tomorrow Mag, phos normal Now resolved AKI - Resolved Secondary to GI lossess, poor po intake Cr 1.8 on admission, no prior hx of kidney disease Improving s/p hydration, Cr 1.49 > 0.94 Monitor closely Essential HTN Normotensive on admission with home med for 2 days Hypertensive this morning, resumed Norvasc

Weitere VAERSDATA-Felder

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

VAERS 2712024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: MI
Alter: 92,0
Geschlecht: F
Eingang: 09.11.2023
Impfdatum: 13.07.2022
Beginn: 09.08.2023
Tage bis Beginn: 392,0
Dosis: 4
Route/Site: - / -

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

Asthenia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram head normal Computerised tomogram spine Confusional state Fall Lung opacity Pancytopenia Platelet count decreased SARS-CoV-2 test positive

Symptomtext

BRIEF OVERVIEW: Admission Date: 8/9/2023 Discharge Date: Aug 19, 2023 Discharge Disposition: skilled nursing facility Active Issues Requiring Follow-up: PCP ? No future appointments. DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Weakness [R53.1] Fall, initial encounter [W19.XXXA] COVID [U07.1] COVID-19 virus infection [U07.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 93-year-old female with a past medical history of chronic thrombocytopenia, diabetes mellitus type 2, hypertension, hyperlipidemia and dementia who presents with a chief complaint of fall. Patient's daughter tested positive for COVID-19 a week prior to admission. She tested positive at home on 08/08/2023 for COVID. Family noted she had progressive weakness over the last week. She had an unwitnessed fall. Her daughter did not believe she hit her head. She also was noted to be increasingly confused for the last few days prior to admission. In the emergency department, she was hemodynamically stable. She was afebrile. She was not hypoxic. Her she was noted to have pancytopenia which was acute on chronic in terms of her platelet level. CT head and CT C-spine were unremarkable for acute injury, though there was questionable findings that could be consistent with compression fractures in her cervical spine. Chest x-ray showed bilateral opacities. She was admitted under observation to the hospitalist service for COVID-19 pneumonia. She was treated with IV remdesivir. PT/OT recommended SAR. The patient was discharged to subacute rehab 8/19. at the time of discharge patient was in good spirits and eager to leave. all questions and concerns addressed, all meds and follow-ups reviewed. advised to follow-up with PCP after rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Fracture of neck of left femur Type 2 diabetes mellitus, without long-term current use of insulin Essential hypertension, benign PMR (polymyalgia rheumatica) Anemia Chronic pain of right knee COVID Fall Generalized weakness Pneumonia due to COVID-19 virus
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet aspirin 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet carvedilol (COREG) 12.5 mg tablet cyclobenzaprine (FLEXERIL) 5 mg tablet folic acid (FOLVITE) 1 MG tablet glimepiride (AMARYL) 4 M
Allergien: Hydrocodone
Vorherige Impfungen: -

VAERS 2663684

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 31.07.2023
Impfdatum: 13.06.2022
Beginn: 09.03.2023
Tage bis Beginn: 269,0
Dosis: 3
Route/Site: IM / RA

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

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2661972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 70,0
Geschlecht: F
Eingang: 27.07.2023
Impfdatum: 18.08.2022
Beginn: 15.02.2023
Tage bis Beginn: 181,0
Dosis: 5
Route/Site: IM / LA

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

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2661282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FP7135

moderat

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 26.07.2023
Impfdatum: 07.09.2022
Beginn: 24.12.2022
Tage bis Beginn: 108,0
Dosis: 4
Route/Site: IM / RA

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

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2649101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

moderat

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 12.08.2022
Beginn: 12.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Cardiac function test Computerised tomogram Heart rate decreased Idiopathic intracranial hypertension Lumbar puncture Magnetic resonance imaging Paraesthesia

Symptomtext

Idiopathic intracranial hypertension (IIH) Tingling in arm, face, legs Low heart rate Pain in joints, hands toes, knees

Weitere VAERSDATA-Felder

Praegender Schweregrund: Idiopathic intracranial hypertension
Hospital-Tage: -
Labordaten: Emergency Room Cat Scan MRI Heart Test Lumbar Puncture
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: sulfa.penicillan
Vorherige Impfungen: -

VAERS 2646865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 19.06.2023
Impfdatum: 19.08.2022
Beginn: 05.09.2022
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: - / -

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

Hypotension Symptom recurrence Transient ischaemic attack

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE TRANSIENT CEREBRAL ISCHEMIA HYPOTENSION 9/6/2022, 12/19/2022, 1/20/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2636059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 24.05.2023
Impfdatum: 31.03.2022
Beginn: 15.05.2022
Tage bis Beginn: 45,0
Dosis: 5
Route/Site: UN / UN

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

Aortic arteriosclerosis Benign prostatic hyperplasia Cardiac failure Cardiac failure acute Cardiac failure congestive Chronic respiratory failure Condition aggravated Ejection fraction Ejection fraction normal Hypotension Left ventricular failure Respiratory failure

Symptomtext

HYPOTENSION 12/23/2022 BPH (BENIGN PROSTATIC HYPERPLASIA) CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 9/29/2022 BPH (BENIGN PROSTATIC HYPERPLASIA) HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 9/29/2022 BPH (BENIGN PROSTATIC HYPERPLASIA) HYPOTENSION 12/23/2022 BPH (BENIGN PROSTATIC HYPERPLASIA) CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 9/29/2022 BPH (BENIGN PROSTATIC HYPERPLASIA) HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 9/29/2022 BPH (BENIGN PROSTATIC HYPERPLASIA) HYPOTENSION 12/23/2022 DIASTOLIC HEART FAILURE, ACUTE ON CHRONIC CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 9/29/2022 DIASTOLIC HEART FAILURE, ACUTE ON CHRONIC HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 9/29/2022 DIASTOLIC HEART FAILURE, ACUTE ON CHRONIC HYPOTENSION 12/23/2022 CHF EXACERBATION, UNSPECIFIED CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 9/29/2022 CHF EXACERBATION, UNSPECIFIED HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 9/29/2022 CHF EXACERBATION, UNSPECIFIED HYPOTENSION 12/23/2022 ATHEROSCLEROSIS OF AORTA CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 9/29/2022 ATHEROSCLEROSIS OF AORTA HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 9/29/2022 ATHEROSCLEROSIS OF AORTA HYPOTENSION 12/23/2022 HEART FAILURE W NORMAL LVEF >=50%, UNSPECIFIED ACUITY CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 9/29/2022 HEART FAILURE W NORMAL LVEF >=50%, UNSPECIFIED ACUITY HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 9/29/2022 HEART FAILURE W NORMAL LVEF >=50%, UNSPECIFIED ACUITY HYPOTENSION 12/23/2022 ACUTE LEFT SIDED CHF CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 9/29/2022 ACUTE LEFT SIDED CHF HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 9/29/2022 ACUTE LEFT SIDED CHF HYPOTENSION 12/23/2022 ACUTE ON CHRONIC CHF, UNSPECIFIED CHRONIC HYPERCAPNIC RESPIRATORY FAILURE 9/29/2022 ACUTE ON CHRONIC CHF, UNSPECIFIED HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 9/29/2022 ACUTE ON CHRONIC CHF, UNSPECIFIED

Weitere VAERSDATA-Felder

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

VAERS 2634780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 07.06.2022
Beginn: 10.07.2022
Tage bis Beginn: 33,0
Dosis: 4
Route/Site: IM / RA

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

Hypotension

Symptomtext

CHRONIC HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2629011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 81,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 29.07.2022
Beginn: 23.10.2022
Tage bis Beginn: 86,0
Dosis: 3
Route/Site: IM / LA

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

Hypotension

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOTENSION

Weitere VAERSDATA-Felder

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

VAERS 2600070

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: TX
Alter: 47,0
Geschlecht: F
Eingang: 21.03.2023
Impfdatum: 30.07.2022
Beginn: 30.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Condition aggravated Magnetic resonance imaging normal Migraine

Symptomtext

I started experiencing severe Migraines a few years ago however the frequency and intensity has increased since receiving all of my vaccinations. In 09/2022 I was taken by ambulance to the ER with a severe migraine. The Physician on staff prescribed candesartan, and sumatriptan medication since then it has been replaced with NURTEC and was also put on UBRELVY. I had an MRI done in 10/2022 which showed no abnormalities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 10/2022 MRI no abnormalities
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes; Asthma
Andere Medikamente: ALLEGRA OTC; JANUMET XR; TRULICITY; fluoxetine
Allergien: Pineapple; cashews; VALTREX
Vorherige Impfungen: -

VAERS 2590303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: MN
Alter: 79,0
Geschlecht: F
Eingang: 02.03.2023
Impfdatum: 10.06.2022
Beginn: 11.06.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Injected limb mobility decreased Injection site pain Wrong technique in product usage process

Symptomtext

Patient complained of limited movement in left arm 24 hours after injection. She stated that she thinks the injector either "hit a tendon" or placed the injection off to the side of the deltoid. She also stated that that evening after injection she used both arms to carry buckets. This type of activity was not of the ordinary for her. As of 3/2023 she feels as if she can still locatethe site of injection due to tenderness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Patient stated that she did see a physical therapist for the limited movement in her left arm.
Aktuelle Erkrankungen: None
Vorgeschichte: Thyroid Disease
Andere Medikamente: none
Allergien: NKA
Vorherige Impfungen: -

VAERS 2563374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

moderat

Staat: GA
Alter: 49,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 20.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Chest pain Injection site pain Pain Pain in extremity

Symptomtext

Site: Pain at Injection Site-Severe.

Weitere VAERSDATA-Felder

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

VAERS 2563374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

moderat

Staat: GA
Alter: 49,0
Geschlecht: F
Eingang: 30.01.2023
Impfdatum: 20.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Back pain Chest pain Injection site pain Pain Pain in extremity

Symptomtext

Site: Pain at Injection Site-Severe.

Weitere VAERSDATA-Felder

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

VAERS 2560705

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: FL
Alter: 67,0
Geschlecht: F
Eingang: 16.01.2023
Impfdatum: 20.07.2022
Beginn: 24.12.2022
Tage bis Beginn: 157,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Chest discomfort Cough Dyspnoea Dyspnoea exertional Fatigue Headache Heart rate increased Malaise Oropharyngeal pain Paranasal sinus discomfort Respiration abnormal SARS-CoV-2 test positive

Symptomtext

I had never been that sick. I hadn't been sick at all for 3 years. I began feeling symptoms on 12/24/2022. I did test positive for COVID-19 on 12/25/2022. I had a sore throat, chest discomfort, fatigue, and shortness of breath when I would try to do things. I would start panting and my heartrate would go up. I also had a headache, a little dry cough like trying to clear your throat and sinus pressure. The tiredness lasted for two and a half weeks. I was prescribed PAXLOVID for the COVID-19 infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 25DEC2022 at home COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Eczema; Hypertension
Andere Medikamente: Valsartan; FLONASE nasal spray; calcium; women's ONE-A-DAY multivitamin; eye drops; moisturizing saline nasal spray; probiotic; collagen peptide
Allergien: DILANTIN
Vorherige Impfungen: -

VAERS 2559498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 13.01.2023
Impfdatum: 01.07.2022
Beginn: 01.08.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: IM / LA

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

Paraesthesia Temperature intolerance

Symptomtext

In August 2022 I started having a tingly and sensitivity to hot water. By September, I had an incident that I had to ice my hand down for over an hour, but it bothered me throughout the night. I called my primary care doctor to make an appointment, he referred me to a neurologist that I have yet to see as there is a long wait time. After using the glove on the one had for a month, I am now using cooler water as I do not want to experience that awful sensation again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Valacyclovir
Allergien: No
Vorherige Impfungen: -

VAERS 2548853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: IN
Alter: 59,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 10.06.2022
Beginn: 28.11.2022
Tage bis Beginn: 171,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal discomfort Asthma COVID-19 Condition aggravated Fatigue Influenza virus test negative Insomnia SARS-CoV-2 test positive

Symptomtext

I contracted covid which upset my asthma and caused G.I upset and fatigue. Insomnia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: positive covid test negative influenza test
Aktuelle Erkrankungen: NONE
Vorgeschichte: ASTHMA
Andere Medikamente: YES; DYDAMOTA; ADVAIR; GEBAPENTIN; VITAMIN E MULTIVITAMIN; FISH OIL SUPPLEMENT; VITAMIN D3
Allergien: YES, PERCOCET ;CELEXA; ADHESIVES
Vorherige Impfungen: -

VAERS 2547747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: SC
Alter: 53,0
Geschlecht: F
Eingang: 01.01.2023
Impfdatum: 29.06.2022
Beginn: 10.07.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: IM / LA

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

Angiogram Computerised tomogram Hypoaesthesia Laboratory test Lumbar puncture Paraesthesia Ultrasound scan

Symptomtext

numbness and tingling. Started in my legs and increasingly spread up to my chest, The numbness remains in my hands to this day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: spinal tap,, ultrasounds, lab work, angiogram. CT scan. Saw Infectious disease, neurology, primary care provider, endocrinology
Aktuelle Erkrankungen: none
Vorgeschichte: Mitral valve prolapse, arthritis, Vit D def
Andere Medikamente: VIt D,
Allergien: Red beans and rice, epinephrine
Vorherige Impfungen: -

VAERS 2528434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 10.12.2022
Impfdatum: 12.07.2022
Beginn: 08.12.2022
Tage bis Beginn: 149,0
Dosis: 4
Route/Site: - / -

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

Alanine aminotransferase normal Ammonia Ammonia normal Anaemia Anion gap Aspartate aminotransferase normal Bacterial test positive Base excess Basophil count decreased Basophil percentage decreased Bilirubin urine Blood albumin Blood alkaline phosphatase normal Blood bicarbonate normal Blood bilirubin normal Blood calcium normal Blood chloride decreased Blood creatinine normal

Symptomtext

Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on December 08, 2022 15:09 Verified By: MD on December 08, 2022 15:09 Encounter Info: Hospital, Inpatient, 12/08/22 - * Final Report * History of Present Illness/Subjective This is a 66-year-old female with past medical history of COPD, bipolar disorder, coronary artery disease presented to the ED with altered mental status. Patient's son visited her today in the morning and found her to be confused and hence brought her to the hospital. She was recently admitted on June 25 for sepsis due to uti and colitis. Previous admission was for for pneumonia in June as well This time she was not able to contribute much to the history due to being drowsy, On examination she was wheezing and had pinpoint pupils. Woke up during the middle of the examination and was able to answer 2 out of 3 orientation questions Lab values are significant for leukocytosis of 13.3 chronic stable anemia, mild hyponatremia of 129, hyperglycemia of 266, troponin elevation from 74-102, respiratory acidosis, UA shows protein ketones and glucose urea, negative for nitrate and leuk esterase. X-ray shows shows airspace opacities, and hilar lymphadenopathy Review of Systems 13 point review of system was not obtained due to patient's condition Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) None reported this timeframe Patient Weight Patient Height None Reported Constitutional: drowsy, Eyes: pin point pupils. ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: b/l expiratroy wheezing Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x2 Psychiatric: Cooperative but drowsy Assessment/Plan 1. Encephalopathy G93.40 The patient has been encephalopathy, metabolic versus toxic Likely due to hypertensive urgency, Follow drug screen Ammonia levels are 35 normal, CO2 level of 56, unlikely the cause No urinary tract infection Follow-up thyroid levels 2. Hypertensive urgency I16.0 Blood pressure 213/86 in the ED, last BP : 158/68. resolving 3. COPD exacerbation J44.1 methylprednisone q8 DUONEBS Q6, RT to assess and treat as per protocol 4. PNA (pneumonia) J18.9 - Ceftriaxone and doxy - pneumonia workup - Deescalate as necessary 5. Hyponatremia E87.1 new onset, serum osmolality, urine sodium , urine osmolality, unlikley the cause of AMS 6. Anemia D64.9 Chronic stable anemia monitor 7. Bipolar affective F31.9 - resume home medication 8. Hyperlipidemia E78.5 - resume home medication 10. Hypertension I10 resume home meds 11. Elevated troponin R77.8 trend, likley demand ischemia due to hypertensive urgency - monitor for chest pain 12. Diabetes E11.9 iss poct, insulin sliding scale Code Status None Recorded Chronic Problem List ADD (attention deficit disorder) Affective disorder Anemia Back pain with sciatica Bipolar affective CAD Chronic ankle pain Chronic pain Chronic pain of right hip Chronic ulcer of buttock CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min Closed fracture of right proximal humerus Diastolic dysfunction Encounter for medication management GERD Hyperlipidemia Hypertension Ileus Inflammatory arthritis Insulin long-term use Insulin long-term use Medication management Neurologic complication of diabetes mellitus Onychomycosis Pneumonia Preventive measure Tobacco use Type 2 diabetes mellitus with complications Urinary frequency Urinary incontinence in female Vertebral compression fracture Procedure/Surgical History ?Cholecystectomy ?Hysterectomy ?Left ankle ?left ankle surgery ?left shoulder surgery ?Lumpectomy ?pelvic ?right hip surgery Surgical History Internal 03/08/2017 Central Line Insertion. MD 06/16/2015 Lower Extremity Hardware Rem Deep (Left, Lower) MD 11/23/2012 Upper Extremity Open Reduction (Left) MD Medications Home Medications (28) Active acetaminophen 325 mg oral tablet 650 mg = 2 Tablet, PRN, Orally, Q6 aspirin 81 mg oral tablet 81 mg = 1 Tablet, Orally, QAM atorvastatin 20 mg oral tablet 20 mg = 1 Tablet, Orally, Daily busPIRone 10 mg oral tablet , TAKE 1 TABLET BY MOUTH 3 TIMES DAILY busPIRone 15 mg oral tablet , 21 Each, TAKE 1 TABLET BY MOUTH 3 TIMES DAILY calcium carbonate 750 mg chewable tablet 750 mg = 1 Tablet, PRN, Orally, TID carvedilol 12.5 mg oral tablet 12.5 mg = 1 Tablet, Orally, BID carvedilol 12.5 mg oral tablet 25 mg = 2 Tablet, Orally, BID carvedilol 25 mg oral tablet , 14 Each, TAKE 1 TABLET BY MOUTH TWICE DAILY dapagliflozin 5 mg oral tablet 5 mg = 1 Tablet, Orally, Daily DME (Vendor) Miscellaneous See DME Order Details or printed requisition for more information., This is a print requisition order, cannot be ePrescribed. docusate-senna tablet 50 mg-8.6 mg 1 Tablet, Orally, At Bedtime DULOXetine 20 mg oral delayed release capsule 20 mg = 1 Capsule, Orally, Daily DULOXetine 30 mg oral delayed release capsule 90 mg = 3 Capsule, Orally, Daily, do not crush or chew furosemide 40 mg oral tablet 40 mg = 1 Tablet, Orally, Daily gabapentin 600 mg oral tablet 900 mg = 1.5 Tablet, Orally, TID GaviLyte-G oral powder for reconstitution See Instructions, as directed HumaLOG (insulin lispro) KwikPen 100 units/mL subcutaneous injection 18 Units, Subcutaneous, With Meals insulin glargine 100 units/mL subcutaneous solution 30 Units, Subcutaneous, BID lactobacillus acidophilus and bulgaricus oral tablet, chewable , Orally, BID methocarbamol 500 mg oral tablet 1,500 mg = 3 Tablet, Orally, TID Nicorette 4 mg oral transmucosal gum 4 mg = 1 Each, PRN, Orally, Q2H ondansetron 4 mg oral tablet 4 mg = 1 Tablet, Orally, Q8H Protonix 40 mg oral delayed release tablet 40 mg = 1 Tablet, Orally, Daily simethicone 80 mg oral tablet, chewable 160 mg = 2 Tablet, PRN, Orally, 4 Times Daily sucralfate 1 g oral tablet 1,000 mg = 1 Tablet, Orally, BID Before Meals valsartan 80 mg oral tablet 80 mg = 1 Tablet, Orally, Daily Ventolin HFA 90 mCg/inh inhalation aerosol 2 Puff, PRN, Inhalation, 4 Times Daily Active Scheduled Inpatient Medications None Reported One-Time Medications Given 12/07/22 00:00:00 TO 12/08/22 15:08:52 None Reported PRN Medications (0600 - 0559) from 12/07 - 12/08 None Reported Allergies Spiriva Lyrica (swelling, Anxiety) Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School Applied for disability Home/Environment Lives with Children. Substance Abuse Denies Tobacco Tobacco Use: 10 or more cigarettes (1/2 pack or more)/day in last 30 days. Family History Diabetes mellitus type 2: Mother, Father and Sister. Disease: Mother and Father. Heart disease..: Sister and Brother. Hyperlipidemia..: Mother and Father. Hypertension..: Mother and Father. Lung cancer..: Sister. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 13.3 k/cumm High (12/08/22 08:38:00) RBC: 4.03 million/cumm (12/08/22 08:38:00) Hgb: 10.5 GM/dL Low (12/08/22 08:38:00) Hct: 34.8 % Low (12/08/22 08:38:00) MCV: 86 fL (12/08/22 08:38:00) MCH: 26 pg Low (12/08/22 08:38:00) MCHC: 30.1 GM/dL Low (12/08/22 08:38:00) RDW: 15.3 % High (12/08/22 08:38:00) Platelet: 403 k/cumm (12/08/22 08:38:00) MPV: 7.6 fL (12/08/22 08:38:00) Neutrophils %: 91 % (12/08/22 08:38:00) Lymphocytes %: 6 % (12/08/22 08:38:00) Monocytes %: 3 % (12/08/22 08:38:00) Eosinophils %: 0 % (12/08/22 08:38:00) Basophils %: 0 % (12/08/22 08:38:00) Absolute Neutrophil: 12 k/cumm High (12/08/22 08:38:00) Absolute Lymphocyte: 0.8 k/cumm Low (12/08/22 08:38:00) Absolute Monocyte: 0.4 k/cumm (12/08/22 08:38:00) Absolute Eosinophil: 0 k/cumm (12/08/22 08:38:00) Absolute Basophil: 0 k/cumm (12/08/22 08:38:00) Chemistry: Sodium SerPl QN: 129 mmol/L Low (12/08/22 08:38:00) Potassium SerPl QN: 4.3 mmol/L (12/08/22 08:38:00) Chloride SerPl QN: 94 mmol/L Low (12/08/22 08:38:00) Carbon Dioxide SerPl QN: 32 mmol/L High (12/08/22 08:38:00) Anion Gap: 3 mmol/L (12/08/22 08:38:00) BUN SerPl QN: 28 mg/dL High (12/08/22 08:38:00) Creatinine SerPl QN: 0.97 mg/dL (12/08/22 08:38:00) Estimated GFR (CKD-EPI, no race): 64 mL/min/1.73m2 (12/08/22 08:38:00) Estimated CRCL (CG): 67 mL/min (12/08/22 08:38:00) Glucose SerPl QN: 266 mg/dL High (12/08/22 08:38:00) Calcium Total SerPl QN: 9.1 mg/dL (12/08/22 08:38:00) Alkaline Phos SerPl QN: 109 Units/L (12/08/22 08:38:00) ALT SerPl QN: 10 Units/L (12/08/22 08:38:00) AST SerPl QN: 9 Units/L Low (12/08/22 08:38:00) Bilirubin Total SerPl QN: 0.3 mg/dL (12/08/22 08:38:00) Total Protein SerPl QN: 7.3 GM/dL (12/08/22 08:38:00) Albumin SerPl QN: 4 GM/dL (12/08/22 08:38:00) Troponin-I High Sensitivity: 102 ng/L High (12/08/22 09:59:00) BNP Pl QN: 558 pg/mL High (12/08/22 08:38:00) Ammonia Pl QN: 35 mCmol/L (12/08/22 08:38:00) Lactate Venous Pl QN: 1.2 mmol/L (12/08/22 08:38:00) Blood Gas Comment: O2 3L (12/08/22 07:58:00) pH Bld Arterial QN: 7.31 Low (12/08/22 07:58:00) PCO2 Bld Arterial QN: 56 mmHg High (12/08/22 07:58:00) PO2 Bld Arterial QN: 61 mmHg Low (12/08/22 07:58:00) Base Excess Bld Arterial: 1 mmol/L (12/08/22 07:58:00) Bicarb Bld Arterial Calc: 28 mmol/L (12/08/22 07:58:00) O2 Sat Bld Arterial Calc: 88 % Low (12/08/22 07:58:00) Patient Temperature: 37 DegC (12/08/22 07:58:00) Sample Type: Arterial (12/08/22 08:21:00) Urine Studies: Color: Yellow (12/08/22 09:26:00) Clarity: SL CLOUDY. (12/08/22 09:26:00) Specific Gravity: 1.020 (12/08/22 09:26:00) pH: 5.0 (12/08/22 09:26:00) Protein: 100 Abnormal (12/08/22 09:26:00) Glucose: >=1000 Abnormal (12/08/22 09:26:00) Ketones: TRACE. Abnormal (12/08/22 09:26:00) Bilirubin: NEGATIVE (12/08/22 09:26:00) Hgb Ur: TRACE. Abnormal (12/08/22 09:26:00) Nitrite: NEGATIVE (12/08/22 09:26:00) Urobilinogen: NormalUro (12/08/22 09:26:00) Leukocyte Esterase Ur: NEGATIVE (12/08/22 09:26:00) WBC: 0-5 (12/08/22 09:26:00) RBC: 0-2 (12/08/22 09:26:00) Bacteria: Moderate Abnormal (12/08/22 09:26:00) Squamous Epithelial: Few (12/08/22 09:26:00) Transitional Epithelial: Few (12/08/22 09:26:00) Mucous: PRESENT. (12/08/22 09:26:00) Amorphous Crys Ur: PRESENT. (12/08/22 09:26:00) All Other Labs: COVID 19 Specimen Source: Nasal (12/08/22 07:58:00) Coronavirus SARS-CoV2 Rapid: Not Detected (12/08/22 07:58:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (12/08/22 07:58:00) Rapid Influenza A PCR: Not Detected (12/08/22 07:58:00) Rapid Influenza B PCR: Not Detected (12/08/22 07:58:00) Diagnostics Radiology Results - Last 24 hours Across Visits 12/08/2022 09:05 - XR Chest PA or AP Portable IMPRESSION:1. Limited study due to hypoinflation with prominent interstitialand patchy airspace opacities, nonspecific and could be related toedema and/or infection.2. Prominent hila bilaterally, not appreciated previously. This isaccentuated by low lung volumes, and could be further evaluated withimproved inspiratory radiographs and/or CT of the chest if warranted.Lymphadenopathy or other etiologies not excluded.Thank you for consulting our team of subspecialty radiologists at Radiology. Healthcare providers wishing to discussthis case further can contact the Cardiothoracic Reading Room. For after-hours or emergency department cases, pleasecall. 12/08/2022 09:12 - CT Head W/o IV Contrast IMPRESSION: 1. No acute CT abnormality of the head. No acute intracranialhemorrhage, hydrocephalus, or large mass.Thank you for consulting our team of subspecialty radiologists at Radiology. Healthcare providers wishing to discussthis case further can contact the Neuroradiology Reading Room. For after-hours or emergency department cases, pleasecall.I, have personally reviewed the image(s) and theprepared and signed interpretation. Based on myreview, I agree with the findings. Signature Line Electronically Signed on 12/08/22 15:09 ________________________________________________________ MD

Weitere VAERSDATA-Felder

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

VAERS 2525573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 19.08.2022
Beginn: 20.08.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Abdominal discomfort Asthenia Fatigue Headache Hypophagia Loss of personal independence in daily activities Malaise Migraine Mobility decreased Neck pain Pain Pain in extremity

Symptomtext

Saturday at 3AM, I woke up with pain in my left arm. I sleep on the side, so I must have turned over on my left side and it hurt right away. It was my arm that was hurting and it felt like it was up my neck. I hurt down all my left side. Within minutes, it triggered a migraine. It makes sense if pain is coming from my neck, it can trigger a migraine. I got up and took my UBRELVY and that at least stopped the migraine. The pain in my body was still persistent from my head to my left side. By the time I got up, I was pretty exhausted. I couldn't go anywhere that day. I was supposed to go somewhere but I couldn't because I was sick all day. I couldn't get up and I barely ate. It was like a flu. I was sick to my stomach, very weak and I was in bed all day. I don't remember what happened over the night. By Sunday, I was feeling a little better. I didn't leave the house all day Saturday because I didn't feel well. I'm usually active doing things around the house or outside and doing normal daily activities, but I could not do any of that that day. By the beginning of the week on Monday, I was starting to feel back to normal. I talked to some neighbors and they also experienced some kind of flu like symptoms after their 2nd booster. These neighbors are all 70 years or older. I had three vaccines before this one, and I've never experienced the migraine and pain in the arm. It was unlike me to be in bed all day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: History of metastatic breast cancer - right side (1999); SVT; Migraines; History of colon cancer (2014); Actinomyces attacking lung system (lymph nodes); Autoimmune Disease attacking retina in right eye; Aneurysm behind right eye in brain; Car accident (2003) C7 damage
Andere Medikamente: NP Thyroid; metronidazole topical gel; cyclobenzaprine; penicillin; KLAIRELABS VITATAB CHEWABLES women's 50+ multivitamin; GI REVIVE supplement leaky gut REVIVE
Allergien: Sulfa drugs; TYLENOL; morphine; codeine; oxycodone; aspirin; ADVIL; ALEVE; NSAIDS; DILAUDID; narcotics; OTC cough medicine; long-term steroid tablets; metoprolol
Vorherige Impfungen: Flu vaccine 2009-2010, fainted and was sent to hospital, sick to stomach; 09/10/2021 1st Pfizer vaccine, flu symptoms, fever, si

VAERS 2515206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: FL
Alter: 37,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 18.11.2022
Beginn: 18.11.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain Headache Oropharyngeal pain Pain in extremity Throat irritation

Symptomtext

vaccine. later that day headache and sore arm. 2am next day throat itchy and painful, later extreme headache and chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Went to the ED x 2.
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma
Andere Medikamente: Albuterol MDI
Allergien: Spiders, bees, bed bugs == epi pen prn
Vorherige Impfungen: -

VAERS 2497743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 03.08.2022
Beginn: 31.10.2022
Tage bis Beginn: 89,0
Dosis: 4
Route/Site: IM / LA

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

Chest pain Headache Hypertension

Symptomtext

I was having chest pains and headaches, so I took my blood pressure at home. It was high enough that I needed to go into the local urgent care. I was given intravenous hydralazine to help get my blood pressure down. I will be having a follow up visit with my PCP today to hopefully learn more.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multivitamin
Allergien: AUGMENTIN
Vorherige Impfungen: -

VAERS 2464759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 29.06.2022
Beginn: 15.08.2022
Tage bis Beginn: 47,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Blood test normal Chills Hypoaesthesia Immediate post-injection reaction Laboratory test Neuropathy peripheral Pain Pain in extremity Paraesthesia Pyrexia Rash Rash erythematous Rash pruritic Swelling

Symptomtext

Right after I received dose 4, I felt soreness on my arm. That night I had chills and aching in my whole body. The next day I had the same symptoms and had a low-grade fever of about 99. In August 2022 I felt tingling and numbness in my right hand. I gradually started feeling pain in my elbows and then both hands. I now have joint pain in my knees. I noticed I had a rash in mid-September 2022. The rash is on my thigh, back of leg, lower abdomen, my neck, and my ear. The rash is bumpy, red and it itches. I met with a doctor, and she ran a couple of tests to eliminate arthritis. I was diagnosed neuropathy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Blood panel, normal;
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin; Amlodipine
Vorherige Impfungen: -

VAERS 2456320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FP7135

moderat

Staat: OH
Alter: 79,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 16.06.2022
Beginn: 24.08.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: UN / UN

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

Abdominal pain COVID-19 Coronavirus test positive Diarrhoea Dyspnoea

Symptomtext

Tested COVID positive, symptoms include shortness of breath, abdominal pain, and diarrhea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Nasopharyngeal test collected 08/24/2022 detected 2019 Coronavirus RNA on 08/24/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Autoimmune condition, anxiety, and depression.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2454769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: NY
Alter: 48,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 18.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: SYR / LA

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

Condition aggravated Extra dose administered Headache Hypertension

Symptomtext

I used to get headaches which would subside after some time. I started experiencing headaches 15 days post vaccine that were more severe and too a longer time to subside. I then noticed my bp was high and I was told to continue monitoring it. The bp remained high and the Dr. now has me on bp medication and has me making dietary changes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; Hypothyroidism
Andere Medikamente: Metformin; Glipizide; Baby aspirin; Synthroid; Centrum multivitamin; OTC pain killers
Allergien: No
Vorherige Impfungen: I had minor side effects with the 1st 3 COVID-19 vaccines that subsided.

VAERS 2452271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: TX
Alter: 72,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 12.08.2022
Beginn: 13.09.2022
Tage bis Beginn: 32,0
Dosis: 4
Route/Site: IM / RA

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

Chest X-ray abnormal Cough Decreased appetite Fatigue Headache Influenza virus test Myalgia Nausea Pneumonia SARS-CoV-2 test Streptococcus test

Symptomtext

On the morning of the 09/13 I woke up and felt extreme fatigue, nausea, headache and muscle soreness. I had no appetite. I went to the urgent care on 9/14 I was advised to take some vitamin C and vitamin D and a Zofran shot. I went to the urgent care again on 9/19 and was diagnosed with pneumonia after a chest x-ray. They gave me a c-pack, Augmentin, albuterol inhaler and flovent inhaler. It still currently hurts to cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: COVID-19 test and strep test and flu test
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Hypothyroidism; Depression; High cholesterol; restless leg syndrome;
Andere Medikamente: Levothyroxine; Bupropion; Letrozole; Calcium; Vitamin E; Vitamin B12; Folic Acid; Vitamin B6; Lysine; Vitamin D
Allergien: Dairy; Codeine; Morphine; Demurral; Hydrocodone
Vorherige Impfungen: Really swollen arm after 1st COVID vaccine

VAERS 2452069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 27.06.2022
Beginn: 10.09.2022
Tage bis Beginn: 75,0
Dosis: 4
Route/Site: UN / UN

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

Dizziness Tremor

Symptomtext

light-headedness, tremors

Weitere VAERSDATA-Felder

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

VAERS 2442919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 13.06.2022
Beginn: 06.09.2022
Tage bis Beginn: 85,0
Dosis: 4
Route/Site: SYR / AR

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

Chills Cough Headache Mobility decreased Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test negative Streptococcus test

Symptomtext

On 9.6.22, after returning on a flight, I became heavily congested. I awoke on 9.7.22 with a raging sore throat. Home COVID test was negative. Took an allergy pill (1x) at night thinking it was seasonal allergies. Awoke on 9.8.22 with sore throat, headache, and low grade temp. Another at-home COVID test returned a negative result. Had a antigen test at Pharmacy on 9.8.22 at around 4pm to make sure I was clear to attend a weekend wedding. When results weren't returned, I visited my local doctor on Friday, 9.9.22 in the morning for covid and strep test as sore throat and low grade fever were on and off present. Developed into bed for 2 days with on and off temp (highest was 100.6), sore throat (resolved on 9.11.22), chills, headaches, and cough which began on 9.9.22. Cough remains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Covid at home (9/7 and 9/8) Pharmacy 9/8/22 Doctor's office 9/9/22
Aktuelle Erkrankungen: none
Vorgeschichte: High BP
Andere Medikamente: candasartan; hydroclorotorozide, one-a-day women's vitamin
Allergien: voltarin flexerol benadryl
Vorherige Impfungen: On both 10/13/21 and 6/13/22, I had an immediate reaction to the boosters (Pfizer BioNTECH NDC 59267-1000-01 lot FF2593), I had

VAERS 2434041

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Dysgeusia Dysstasia Nausea Palpitations Paraesthesia Tunnel vision

Symptomtext

1047 Approx. 5 mins post vaccination Pt. states feeling lightheaded and dizzy. States sl. SOB and feels "like her heart is racing". c/o sl. nausea and metallic taste. States has tunnel vision. Unable to stand. Inst. to lower head between legs. 1049 Assisted to exam table to recumbent position. BP11/66 P64. Dizziness cont. Lungs clear to auscultation. 1056 BP 102/64 p64 r18. Dizziness and tunnel vision continues .1107 BP 102/74 P60. Denies difficulty breathing. PERL. Oriented and alert. Occas. stares into space but responds to questions. 1119 Assisted to sitting over edge of exam table. Immed. became dizzy and returned to recumbent position. . B/P 112/77 p60. 1124 EHS called. Pt. informed need to send to ER. Pt. in agreement. 1135 B/P 100/58 P60. 1142 C/o L arm tingling and mid sternal pressure. 1143 EMS arrived. 1148 Ems transported pt. to ER,

Weitere VAERSDATA-Felder

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

VAERS 2430014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 06.09.2022
Impfdatum: 14.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Chills Diarrhoea Dyspnoea Hypersensitivity Nausea Pruritus Swelling face Vaccination site pain Vomiting

Symptomtext

I felt like I couldn't breath; itchy everywhere; chills; nausea; vomiting; diarrhea; face swollen. I still have pain on my vaccination site. I went to the urgent care and they said it was an allergic reaction and put me on steroids for the itching and swollen face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: G6PD Deficiency; Diabetes; High blood pressure; Glaucoma; Breast Cancer survivor; Back issues
Andere Medikamente: Gabapentin; metformin; vitamin D3; ZOLOFT; ZYRTEC; probiotic; RITALIN; PROTONIX; LIPITOR; amlodipine; SYNTHROID; bimatoprost eye drops; COMBIGAN eye drops; melatonin; MOTRIN; soma; VALTREX; multivitamin
Allergien: Soy; KEFLEX; CT dye; NEULASTA; aspirin; sulfa
Vorherige Impfungen: -

VAERS 2427655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 02.09.2022
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: ja

Feeling hot Injection site erythema Injection site swelling Paraesthesia

Symptomtext

Patient complains of warm and tingly sensation entire left arm, redness and swelling at sight of injection. Patient using over the counter Ibuprofen to reduce swelling and redness. Patient states happens at least once a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Patient stated a couple of weeks before vaccine she had a cold.
Vorgeschichte: None known
Andere Medikamente: Over the counter IBUPROFEN
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2426449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: GA
Alter: 70,0
Geschlecht: F
Eingang: 01.09.2022
Impfdatum: 26.07.2022
Beginn: 06.08.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Mobility decreased Sleep disorder

Symptomtext

Patient has had pain in the shoulder and it has limited her movement. The pain is disturbing patient sleep. On Aug 30, patient had a visit with PCP where she received a steroid shot in hip and RX for naproxen 500mg 1bidprn.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Per patient no test were performed just a Dr. visit.
Aktuelle Erkrankungen: None documented
Vorgeschichte: Patient has chronic pain
Andere Medikamente: no OTC meds on file
Allergien: No Allergies reported
Vorherige Impfungen: -

VAERS 2418411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 23.08.2022
Impfdatum: 17.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Tremor

Symptomtext

patient described violent shaking

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: intermittent asthma, hyperlipidemia, acid reflux, osteoarthritis
Andere Medikamente: simvastatin, albuterol as needed, desonide ointment
Allergien: none
Vorherige Impfungen: -

VAERS 2416869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 21.08.2022
Impfdatum: 24.07.2022
Beginn: 25.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Asthenia Blood test Confusional state Fall Gait disturbance Head injury Mobility decreased Urinary incontinence X-ray

Symptomtext

The next morning, I tried to get up from bed, wet myself and fell on the floor and hit my head. I was not able to move. I was confused and needed help. My daughter tried getting me up for awhile and took me to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: They gave me fluids, ran xrays to make sure i did not injure my neck or back. I was so weak I was in the ER for several hours before I could walk. They ran bloodwork.
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Kidney Diease
Andere Medikamente: Trazodone 50mg; Hydrochlorothiazide 25mg; amolodipine Besylate; Trazodone 50mg; Hydrochlorothiazide 25mg; amolodipine Besylate 5mg; Atorvaslatin 10MG; Citalopram 10MG; Gabapentin 100mg; Omeprazole 40mg; Trospium 60mg; Vitamin D3 1000 IU; Vi
Allergien: None
Vorherige Impfungen: some nauseas

VAERS 2416784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 20.08.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Heart rate increased Tachycardia

Symptomtext

On 7/7/2022 patient received her first COVID-19 vaccine at 4:43 pm. One hour later mom said patient started having tachycardia. Her heart was beating faster than normal. This lasted until 10 pm. Patient did not receive treatment. Mom just gave her water.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Congenital cardiomyopathy
Andere Medikamente: -
Allergien: Eggs
Vorherige Impfungen: -

VAERS 2413503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: KS
Alter: 80,0
Geschlecht: F
Eingang: 17.08.2022
Impfdatum: 12.07.2022
Beginn: 10.08.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: SYR / LA

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

Cardiac monitoring Fatigue Heart rate increased Hypotension

Symptomtext

08/10/2022 I felt very tired my blood pressure was extremely low; I had high heart rate. I called my cardiologist and told him what was going on so he ordered a heart monitor. I am being monitored for 3 days. After 3 days my cardiologist will review the readings and will decide what I have to do next. He either will give me medications or something else. I will be going for a follow up with my PCP a week from tomorrow and cardiologist on the month of September.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: UTI; Neck pain caused by pinched nerve; High blood pressure; AFIF
Andere Medikamente: Amlodipine; Tamsulosin; Eliquis; Sotalol; Gabapentin; Atorvastatin; Tizanidine; Methenamine; Multivitamins; Calcium; COQ10; Cranberry tablets; Probiotics
Allergien: Levaquin; nitrofurantoin
Vorherige Impfungen: -

VAERS 2410989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 14.08.2022
Impfdatum: 21.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Injection site hypoaesthesia Injection site paraesthesia

Symptomtext

PATIENT REPORTS NUMBNESS AND TINGLING OF UPPER LEFT ARM APPROX 7 DAYS AFTER RECEIVING THEIR 1ST BOOSTER DOSE OF COVID 19 PFIZER. PATIENT RECEIVED PFIZER FOR ALL PREVIOUS DOSES AS WELL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: NONE.
Aktuelle Erkrankungen: NONE REPORTED. DID RECEIVE HEPATITIS A AND B VACCINE THAT DAY ON THE SAME ARM
Vorgeschichte: NONE REPORTED
Andere Medikamente: PFIZER COVID-19 VACCINE, (1ST BOOSTER)
Allergien: NONE
Vorherige Impfungen: -

VAERS 2408560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: OH
Alter: 23,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 25.07.2022
Beginn: 04.08.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Atelectasis Blood test abnormal Chest pain Computerised tomogram thorax abnormal Dizziness Dyspnoea Electrocardiogram normal Headache Mean platelet volume decreased Panic attack

Symptomtext

Onset over about 5 mins. Trouble breathing, dizziness, sudden headache with possible syncope event with sharp chest pain in left side of body. Went to bed assuming it was a random panic attack, but breathing did not get better and reported to local Urgent Care 8/08/2022. EKG came back normal and was recommended to go to local ER ASAP for further testing to ensure it wasn't a blood clot. At ER got another EKG, a chest CT, and basic blood work done. EKG came back normal, blood work came back with low MPV. CT came back with no signs of acute pulmonary illness and no embolism, but did come back with "dependent atelectasis in the lungs posteriorly bilaterally". Receiving follow-up with PCP next week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 2 EKGs - both came back normal blood work - low MPV CT - no signs of acute pulmonary illness and no embolism, "dependent atelectasis in the lungs posteriorly bilaterally".
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia, underactive thyroid (Hashimoto's)
Andere Medikamente: duloxotine 30mg/day, prasozin 1mg/day, testosterone cypionate 100mg/1ml/week, certrizine 10mg/day, ibuprofen 400mg/as needed
Allergien: Benadryl, nasal sprays, mushrooms, dust, seasonal (pollen)
Vorherige Impfungen: Gardasil Vaccine - 2014 - 15yo - HPV injection - fainting, weakness, migraines, full-body pain and inflammation, multiple ER vis

VAERS 2405577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: IN
Alter: 16,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 05.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysphagia Dyspnoea Hypersensitivity Hypoaesthesia Pruritus Throat tightness Visual impairment

Symptomtext

Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Medium, Systemic: Allergic: Itch Generalized-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Visual Changes/Disturbances-Mild, Additional Details: Pt said experiencing difficulty swallowing 10min post injection, consulted mom and decided to give benadryl, administered 37.5mg benadryl, mom also had pt use her inhaler, after about 10 more minutes pt said still having difficulty swallowing and now said also little trouble breathing, numbness in arm, and vision changes. Consulted mom and she said to go ahead and call 911. Monitored pt, did not appear in respiratory distress. EMS arrived minutes later, Pt walked out on own with mom and EMS.

Weitere VAERSDATA-Felder

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

VAERS 2404597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: NY
Alter: 45,0
Geschlecht: F
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: nein

Hypoaesthesia Paraesthesia oral

Symptomtext

patient describes a numb feeling on the left side of her face and a tingly sensation in the lips approx 5 minutes after vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: no OTC vaccinations
Allergien: no allergies stated- patient said she has no adverse events to prior vaccinations apart from chills and fever
Vorherige Impfungen: -

VAERS 2404455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: VA
Alter: 69,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 17.07.2022
Beginn: 18.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Condition aggravated Feeling abnormal Fibromyalgia Full blood count normal Hernia Laboratory test Loss of personal independence in daily activities Pain Somnolence Thyroid function test normal Vitamin D decreased

Symptomtext

Starting 07/18/2022, when I woke up, I had severe body aches like a very bad fibromyalgia flare up. Also, I felt very sleepy. This has been affecting my daily life and things I need to do. I have had to cancel appointments, dog sitting visits and more. Most of the time I feel bad, with a few days where I was able to do things. My fibromyalgia had been mostly under control for about 2 years before this happened. I have been seeing my regular internist and am trying to find a rheumatologist. Also, I have had a hernia for the last 2 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CBC count: normal, low vitamin D; Thyroid test: normal; Another test done unsure of name; Mammogram, Brain MRI, GI test, Breathing test to be scheduled.
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia; History of Ulcers; Hypothyroidism; Depression; Vertigo
Andere Medikamente: Gabapentin; omeprazole; losartan; trazadone; CYMBALTA; CELEBREX; naproxen; BUSPAR; WELLBUTRIN; fludrocortisone; levothyroxine; liothyronine; trospium; terbinafine; extra strength TYLENOL; ZYRTEC; polymyxin B eye drops; FLONASE; ipratropium
Allergien: Lactose intolerant; sulfa; oxycodone; PERCOCET; LYRICA
Vorherige Impfungen: -

VAERS 2404393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 08.08.2022
Impfdatum: 05.08.2022
Beginn: 07.08.2022
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 Gait disturbance Gout Pain in extremity

Symptomtext

Hi, I have a history of gout in my right foot, with my last flare hitting in May. On August 7, 2022, two days after my fourth Covid vaccine (ie, second booster) which was administered on August 5, I suffered a flare up of gout in my lower right foot. I am NOT asserting that the two are related. Just wanted to let you know. I've had a few of these gout "flares" before. I'd classify this one as "moderate". It hurts and I'm limping, but I don't need to use a hard show or crutches (yet -- this is now 3 days after the vaccine). To treat it, I'm resting and elevating and taking 500mg Naproxen twice per day. It's still there, but not debilitating.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Gout
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2400416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: NJ
Alter: 44,0
Geschlecht: M
Eingang: 03.08.2022
Impfdatum: 26.07.2022
Beginn: 26.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Decreased appetite Dyspnoea Feeling abnormal Headache Hypoaesthesia Malaise Nausea Pain in extremity Palpitations Vision blurred Vomiting

Symptomtext

My head started hurting really badly and I started getting pain in my left arm. I then became nauseated and vomited. I felt so ill that I went to sleep and when I woke up I did not feel like myself and started having heart palpitations and my headache was terrible. I still had pain in my arm and felt chest pains so bad I almost went to the emergency room. I had no choice but to go to work and I was sick all day long and I also started feeling numbness in my extremities. I have also had blurred vison, loss of appetite, and shortness of breath. The crazy thing was I had covid and did not feel half as bad as I do now. I was forced to get this vaccine because of a job and now everyday I feel myself getting worse and worse since taking it. I am really worried I am going to have a heart attack as my heart has not stopped doing strange things since I got the shot. I am not sure what to do, I guess there is nothing I can do now.

Weitere VAERSDATA-Felder

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

VAERS 2399287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 27.07.2022
Beginn: 28.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SC / LA

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

Asthenia Condition aggravated Gait disturbance Hypoaesthesia Impaired work ability Mobility decreased Motor dysfunction Multiple sclerosis

Symptomtext

This was my 2nd booster shot. Approximately 24 hours after, I started experiencing numbness in my hands and difficulty walking. It got to a point I could no longer work. I work on a computer. That night (~1 am) I couldn't get out of bed without help, my legs and arms unresponsive. To be fair, I do have difficulty with walking and numbness in my hands due to MS but this was completely debilitating. I normally walk without the need for any assistive aid. This extreme effect lasted approximately 12 hours but a more moderate form lingered long after. It is now 6 days later and I'm just starting to feel back to "normal."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Multiple sclerosis, high blood pressure
Andere Medikamente: Kesimpta, Atacand, Ampyra
Allergien: N/A
Vorherige Impfungen: I had an identical experience with the 1st booster shot, which was Moderna on 11/09/2021, batch/lot# 033F21A. I only had minor i

VAERS 2399141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: SC
Alter: 18,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 27.07.2022
Beginn: 28.07.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / -

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

Asthenia Bradykinesia Confusional state Dizziness Fatigue Feeling abnormal Headache Palpitations Speech disorder

Symptomtext

Heart palpitations, brain fog, confusion, difficulty with speech, headache, weakness, dizziness, extreme fatigue, moving slow, .palpitations are worse with activity.

Weitere VAERSDATA-Felder

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

VAERS 2397602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 30.07.2022
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: unbekannt

Chest pain Cold sweat Dizziness Dyspnoea Nasopharyngitis Oxygen saturation decreased

Symptomtext

After 15 minutes of receiving Pfizer booster shot, patient reports feeling dizzy, clammy, cold, chest pain, shortness of breath. Patient assisted to a chair initially and placed patient on her back with feet elevated. Provided water, snack and ice pack. Patient states she has not had anything to eat the whole day. Patient vital sign shows HR 130, Oxygen Saturation 99%, blood pressure 100/80. 911 called after patient oxygen level desaturated. Provided reports to Paramedics when they arrived and took over care of her.

Weitere VAERSDATA-Felder

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

VAERS 2391434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP 7135

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 18.07.2022
Beginn: 18.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Chest pain Heart rate increased

Symptomtext

Chest pain on left side of chest; rapid heartbeat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Rash under left arm, swelling of lymph nodes

VAERS 2387637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: CT
Alter: 65,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 02.07.2022
Beginn: 03.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / LA

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

Antibody test abnormal Arthralgia Blood immunoglobulin G Blood immunoglobulin M Hypoaesthesia Pain in extremity Paraesthesia Swelling Vitiligo

Symptomtext

extreme swelling and pain in hands and all joints; extreme swelling and pain in hands and all joints; hands, fingers and arms tingling; Legs feel numb and hurt at night; Legs feel numb and hurt at night; vitiligo spread exponentially and still spreading; low IgM and IgG class 4 antibodies; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 65 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hashimotos" (unspecified if ongoing); "vitiligo" (unspecified if ongoing); "sjogrens" (unspecified if ongoing); "possible RA" (unspecified if ongoing); "covid" (unspecified if ongoing), notes: If covid prior vaccination: Yes. Concomitant medication(s) included: CYMBALTA; AMBIEN; RAMIPRIL; LEVOXYL; LEVOTHYROXINE [LEVOTHYROXINE SODIUM]. Vaccination history included: BNT162b2 (Dose Number: 3, Lot No: FF2587, Location of injection: Arm Left), administration date: 26Sep2021, when the patient was 64-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 2, Lot No: ER2613, Location of injection: Arm Left), administration date: 19Mar2021, when the patient was 63-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 1, Lot No: EN6206, Location of injection: Arm Left), administration date: 02Mar2021, when the patient was 63-year-old, for Covid-19 immunization, reaction(s): "vitiligo spread exponentially". The following information was reported: HYPOAESTHESIA (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 03Jul2022, outcome "not recovered" and all described as "Legs feel numb and hurt at night"; PARAESTHESIA (non-serious) with onset 03Jul2022, outcome "not recovered", described as "hands, fingers and arms tingling"; ANTIBODY TEST ABNORMAL (non-serious) with onset 03Jul2022, outcome "not recovered", described as "low IgM and IgG class 4 antibodies"; VITILIGO (non-serious) with onset 03Jul2022, outcome "not recovered", described as "vitiligo spread exponentially and still spreading"; SWELLING (non-serious), ARTHRALGIA (non-serious) all with onset 04Jul2022, outcome "not recovered" and all described as "extreme swelling and pain in hands and all joints". The events "extreme swelling and pain in hands and all joints", "hands, fingers and arms tingling", "legs feel numb and hurt at night", "vitiligo spread exponentially and still spreading" and "low IGM and IGG class 4 antibodies" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of swelling. Additional information: There was no other vaccine in four weeks. Legs feel numb and hurt at night. After second booster shot two days later, extreme swelling and pain in hands and all joints. It has been two weeks and swelling still there and very painful, hands, fingers and arms tingling. After first shot, vitiligo spread exponentially and still spreading. Also now have low IgM and IgG class 4 antibodies. Treatment includes medrol pack for swelling which did not work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Name: IgG; Result Unstructured Data: Test Result:Low; Comments: Also now have low IgM and IgG class 4 antibodies; Test Name: IgM; Result Unstructured Data: Test Result:Low; Comments: Also now have low IgM and IgG class 4 antibodies
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes); Hashimoto's disease; RA; Sjogren's; Vitiligo
Andere Medikamente: CYMBALTA; AMBIEN; RAMIPRIL; LEVOXYL; LEVOTHYROXINE [LEVOTHYROXINE SODIUM]
Allergien: -
Vorherige Impfungen: -

VAERS 2379490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: WI
Alter: 56,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 19.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Dyspnoea Fatigue Feeling abnormal Flushing Headache Hot flush Hyperhidrosis Injection site pain Lymphadenopathy Malaise Myalgia Pain in extremity Peripheral swelling Tenderness

Symptomtext

sore arm started 6 hours after injection (same side and site and injection) day 1 (the next day, 24 hours later) hot flashes including sweating and flushing lasting 30 minutes, tiredness, headache (brief flashes of pain that did not last more than 1 minute) muscle aches and joint aches esp to large joints (hips, back to pelvis, shoulders) a general slight feeling if "i don't feel well or not quite right", and continued arm soreness day 2 (48 hours after injection) noted upoon awakening swollen tender axilla (ipsisteral to injection arm) fatigue and general feeling of not being well, including slight increased effort for breathing (deeper breaths more frequently than normal). no headache and joint pain less but not gone. day 3 (72 hours after injenction) back to my old crabby self :o) still have Left axilla adenopathy but less tender and swollen -this had happened previously with other vaccinations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none--did not seek medical treatment as these were not limiting my daily life activities including working
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: rabbits
Vorherige Impfungen: sore arm, adenopathy, one time cellulitis

VAERS 2376607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: CO
Alter: 58,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 30.06.2022
Beginn: 01.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / -

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

Asthenia Fall Gait disturbance Tremor

Symptomtext

Patient more unsteady gait, shakiness, and weakness on 7/01/2022 around 0300. No new orders from doctor. Patient was on Neuro checks due to a fall from symptoms. By 07/03/2022 symptoms improved.

Weitere VAERSDATA-Felder

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

VAERS 2372745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: WA
Alter: 42,0
Geschlecht: M
Eingang: 18.07.2022
Impfdatum: 10.07.2022
Beginn: 11.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Acoustic stimulation tests abnormal Acupuncture Condition aggravated Deafness neurosensory Tinnitus

Symptomtext

I noticed on Sunday afternoon a suspicion of tinnitus volume. It was a mild increase and I thought it was a normal daily variant. However, on Monday morning when waking up, the volume was higher than normal. I see an acupuncturist normally for assisting in control with this. It?s usually at 2/10 but on Monday it was 4/10. I received acupuncture treatment on Monday and Tuesday. I also exercised and gained additional rest. Still on Wednesday the volume was 4/10. Thursday, I received more acupuncture, and the volume was still relatively high. Friday, it was still high even with sleep, acupuncture, and exercise. On Friday, I contacted an auto neurologist, and he recommended a hearing test. I scheduled a hearing test for that Friday afternoon. I also scheduled an appointment with my local ENT Friday as well. It showed a hearing loss of 20db loss at 8khz, 15db loss at 6khz, 15db loss at 4khz. My threshold was reported at 55 Db. And the year before was at 35 Db, which is a 20Db difference. The last audiogram I had was in June 2021. I had very stable hearing in the Spring consistently. When I consulted my ENT, he said it was very unusual hearing loss for a drop of 20 Db in one year. We discussed exposure to loud events. I attended a baseball game recently and I didn?t experience anything after that event. I only experienced the increased hearing after the vaccine. My ENT said it?s best to treat it as sensory neuro hearing loss. He prescribed a 10-day prednisone course 60mg for 6 days then reducing to 40mg then 20mg. He also recommended hyperbaric oxygen treatment which I?ll get a consultation for soon after the ENT notes have been sent. I have started taking additional supplements that are helpful for anti-inflammatory reasons. I?m taking resveratrol, omega 3, ubiquinol, rosemary and oregano oil. I?m continuing with acupuncture, so I went today, and I went in case it?s helpful. I?m waiting for my hyperbaric referral to come through. I may be seeing some incremental benefit from the prednisone. It was 3/10 on the tinnitus, but it?s hard to tell with normal daily variants. My next audiogram is next Monday July 25, and following up with an additional hearing test and see if there was any benefit from the steroid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Hearing Test 07/15/2022 PTA Audio Test - showed a hearing loss of 20db loss at 8khz, 15db loss at 6khz, 15db loss at 4khz; Hearing Test 07/15/2022 OAE Audio Test - indicated sensory neuro hearing loss
Aktuelle Erkrankungen: None
Vorgeschichte: Mild Asthma; Tinnitus; Sensory Neuro Hearing Loss
Andere Medikamente: Tri-Magnesium; Vitamin B Complex; Vitamin D; Elderberry; Zinc
Allergien: None
Vorherige Impfungen: -

VAERS 2372149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 29.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Injection site pain Mobility decreased

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: Joint Pain-Severe, Additional Details: Patient complains of shoulder pain severe enough that she cannot lift her arm. She claims the vaccine was administered high on the arm and to the back of the arm. However upon review of the video of administration, it appears the immunizer administered the vaccine in the right place.

Weitere VAERSDATA-Felder

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

VAERS 2370720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: WA
Alter: 22,0
Geschlecht: U
Eingang: 15.07.2022
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Paraesthesia Pruritus

Symptomtext

15 minutes after injection c/o itching/tingling in entire left arm and body. Vital signs stable, no other symptoms. Given dexamethasone IM with near immediate resolution of symptoms, remained stable under additional observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: -
Andere Medikamente: testosterone, escitalopram, guanfacine, methylphenidate
Allergien: PCN, shellfish
Vorherige Impfungen: -

VAERS 2370186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fp7135

moderat

Staat: KS
Alter: 32,0
Geschlecht: M
Eingang: 15.07.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Aggression Anger Bruxism Burning sensation Chest pain Formication Insomnia Irritability Joint swelling Mood swings Restlessness

Symptomtext

Feeling like something is crawling on my skin all over my body, hands and joints swollen, restlessness/ insomnia Chest hurting Face burning Irritated Mood swings Clenched jaw/grinding teeth Short fuse temper Aggression Stupid shot I didn't want in the first place stupid labor laws...j have to get a shot to be considered for hire at some places.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2369395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: NV
Alter: 26,0
Geschlecht: M
Eingang: 14.07.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dyspnoea Heart rate increased Palpitations

Symptomtext

At 08:22, post vaccination, patient c/o heart palpitations, radial HR 103. 08:23 ice pack placed on neck, apple juice and water given to patient. 08:25: B/P 148/86. Patient c/o mild SOB but no obvious respiratory distress. 08:27 HR 92/irregular and offered EMS but he declined. 08:34 continued to be monitored. Reporter had patient perform slow, deep breaths to attempt to slow his heart rate; also offered EMS, but patient declined. 08:45 HR 80/regular. 08:47 B/P 126/78, asked patient to wait 10 more minutes to monitor patient. 09:00 patient states he felt better and left site. RN made aware.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Denied
Vorgeschichte: Denied
Andere Medikamente: None known
Allergien: Denied
Vorherige Impfungen: -

VAERS 2367768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: KS
Alter: 17,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Chest discomfort Chills Decreased appetite Diarrhoea Dizziness Dyspepsia Exercise tolerance decreased Fatigue Feeding disorder Feeling abnormal Gaze palsy Head discomfort Headache Hunger Hypersomnia Loss of personal independence in daily activities Malaise

Symptomtext

July 8th- Feeling weird, not hungry-nausea, tired, diarrhea, couldn't eat anything. July 9th-Intense Headache, severe nausea and diarrhea, couldn't eat , forced some fluids, drained, laying down the majority of the day, chills, pressure in chest, didn't eat at all. July 10th-Hungry but severe nausea, dizzy, felt like passing out, over all felt drained and weird, Intense headache, diarrhea, ate only once. July 11th-Headache, feeling weird, hungry but nauseated, forced down food twice (small amounts). Slept for long, couldn't do normal activities, drained, felt unwell. Upset stomach. July 12th-Constant headache-took Tylenol 1000 ml, didn't go away. Contacted local County Health Department, they told me to fill out this form and contact his primary Doctor. Contacted Primary Doctor, he advised to write everything down and that symptoms should be gone after one week. Upset stomach, indigestion and heartburn with food. Was able to eat twice, not normal yet. July 13th- Stomach still weird, tired, not exercising just yet, head still feels a little funny.

Weitere VAERSDATA-Felder

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

VAERS 2364153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 10.07.2022
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: unbekannt Erholt: unbekannt

Migraine Pain in extremity

Symptomtext

Patient says she experienced a really bad migraine starting the same day after she received the shots. The next day the migraine started getting better but it was still lingering. She also was experiencing the sore arms.

Weitere VAERSDATA-Felder

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

VAERS 2364118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: PA
Alter: 41,0
Geschlecht: F
Eingang: 10.07.2022
Impfdatum: 09.07.2022
Beginn: 09.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Chest discomfort Cough Dyspnoea Panic reaction Skin discolouration

Symptomtext

After patient was given her first Pfizer vaccination, she returned to the pharmacy within about 5-10 minutes with a violent and persistent cough. She was asked if she could make her way to the immunization booth for water and evaluation and she did so urgently. While staff retrieved water for the patient, she informed the pharmacist that her chest was tightening and that she was having trouble breathing. Patient had discoloration in face, panicked expression, and was grabbing at her throat and upper chest. At that point, the pharmacist administered an Epi-pen into her right thigh and sat beside the patient for observation. The patient's breathing began to improve and the pharmacist recommended that the patient allow for her to call for emergency services. The patient declined stating that she would have her companion take her if she felt the chest tightening return. Store management came to get a statement from the patient and within about 10 minutes from first Epi-pen administration the patient informed the pharmacist and managerial staff member that the Epi-pen was wearing off and that she wished for a second dose, which was then administered. Patient agreed that with the second dose given she should report to ER and continued to state that she would have her driver take her if she wished. She was adamant that she did not want 911 called. The following day, on 7/10/22 the pharmacist called to verify that the patient had recovered. The patient reported a night of coughing and some mild chest tightness but that she did not report to the ER or any other facility. She also reported feeling much improved on 7/10/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None to report
Aktuelle Erkrankungen: None known
Vorgeschichte: Asthma
Andere Medikamente: Trazodone 150 mg, amitriptyline 75 mg, quetiapine 200 mg, albuterol inhaler, albuterol nebulizer
Allergien: latex and aspirin
Vorherige Impfungen: -

VAERS 2359639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Chills Dehydration Diarrhoea Headache Nausea Pyrexia

Symptomtext

Fever, chills, headache, diarrhea, nausea, dehydration,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines, Osteoarthritis, Anxiety, IBS, Insomnia
Andere Medikamente: Buspirone, Celebrex, Celexa, Gabapentin, Melatonin, Topiramate, Trazodone, Zyrtec
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2357017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: AL
Alter: 58,0
Geschlecht: M
Eingang: 04.07.2022
Impfdatum: 30.06.2022
Beginn: 02.07.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / RA

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

COVID-19 Cough Dizziness Dyspnoea Headache Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

sob, ha, sore throat, dizziness, dry cough, body aches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: positive covid test on 07/04/2022
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, osa, htn,
Andere Medikamente: albuterol, Symbicort
Allergien: NKA
Vorherige Impfungen: -

VAERS 2356828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: FL
Alter: 71,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 28.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Injected limb mobility decreased

Symptomtext

difficulty moving left arm around to touch face (limited range of motion)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2355123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

moderat

Staat: OH
Alter: 27,0
Geschlecht: M
Eingang: 02.07.2022
Impfdatum: 02.07.2022
Beginn: 02.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Paraesthesia

Symptomtext

i administered pfizer 1st booster at 3:55pm and pt was sitting in the waiting area when his friend alerted me that he was feeling dizzy. i went out to him and laid him on the ground with his feet elevated. we put ice packs on his forehead and on his neck. he also had some tingling in his hands.he stated that he hadn't had anything to eat all day. we gave him orange juice and within 15 minutes he was feeling back to normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2348006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 29.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 1,0
Dosis: N/A
Route/Site: IM / LA

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

Blood test normal Chest X-ray normal Chest pain Computerised tomogram normal Fibrin D dimer increased Tachycardia

Symptomtext

severe chest pain and tachycardia following the shot. er visit resulted in iv fluid treatment, blood tests, chest x-ray and ct scan. hospital visit was over 6 hours and was released by the doctor stating that they have seen this recently after the second booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: chest x-ray, ct scan, blood panel, d-dimer tests. all scans and tests besides the d-dimer were clear. the d-dimer showed elevation but no clots were found.
Aktuelle Erkrankungen: sinus infection a few weeks ago
Vorgeschichte: asthma
Andere Medikamente: venlafaxine, apri
Allergien: naproxen, prednisone, paxil
Vorherige Impfungen: -

VAERS 2335844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: NY
Alter: 38,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 17.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / RA

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

Dyspnoea

Symptomtext

Shortness of breathe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes
Andere Medikamente: -
Allergien: Pcn Almonds milk Soy milk Pomegranate Apples
Vorherige Impfungen: -

VAERS 2329186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

moderat

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 12.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Headache Migraine Mobility decreased Muscle disorder Neck pain

Symptomtext

The next day after my vaccination, a little less than 12 hrs, I started having severe neck pain . I didn't wake up with the neck pain or do strenuous activity I was just at work typing at my desk. It got so bad I couldn't look up or down, it then turned into a headache. It got so bad the next day I went to urgent care. The Dr. said that the muscle was knotted at the base of my neck and gave me a muscle relaxer and 800mg ibuprofen. I the next day the headache had gone away and the pain was a little better. I couldn't take muscle relaxer 3 times a day because I'm a mom so I went to a massage spa and that helped a little. Today I just feel like I have a migraine and the pain is gone, It was just really odd the way it came on.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: obesity
Andere Medikamente: None
Allergien: no
Vorherige Impfungen: -

VAERS 2325528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: VA
Alter: 32,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 18.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain Pain in extremity Painful respiration

Symptomtext

Patient has been having pain in her arm and in her chest when she breaths in since she had the shot.

Weitere VAERSDATA-Felder

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

VAERS 2316992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

moderat

Staat: CT
Alter: 77,0
Geschlecht: M
Eingang: 13.06.2022
Impfdatum: 07.06.2022
Beginn: 09.06.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Injected limb mobility decreased Injection site pain

Symptomtext

Site: Pain at Injection Site-Severe, Additional Details: Patient wife came in to say patient having trouble moving right hand. Not able to open and close fist a couple of days since vaccine admin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2316681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

moderat

Staat: UT
Alter: 72,0
Geschlecht: F
Eingang: 11.06.2022
Impfdatum: 08.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / RA

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

Chest pain

Symptomtext

Patient called and complained of chest pain after the covid booster vaccine ( Pfizer) that she got few days ago. patient advised to see a Dr and seek medical attention as soon as possible.

Weitere VAERSDATA-Felder

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

VAERS 2313159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

moderat

Staat: FL
Alter: 41,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 07.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Auscultation Breath sounds abnormal Chest pain Cold sweat Drug hypersensitivity Dyspnoea Flushing Pain in extremity Pruritus Wheelchair user

Symptomtext

Vaccine received @ 0721, observation @ 0722. 0735 pt. states, "feeling itchy on body" appears flushed and clammy to touch. 02 :97%, BP 115/70,HR78,25mg chew. Benadryl admin. reassess 0740 pt states, "feeling better". Extended observation done and constant assessment. Pt states" very sensitive to Benadryl", her supervisor. is made aware of situation. 0810 patient appears flushed again assess and monitor 02:98%, BP 110/70. patient is talking with staff and is very anxious and states "her right arm and chest are sore" . lung sounds auscultated, slightly diminished in right lower lobe. Pt informed that a follow up is needed we recommend going with EMS. 0825 EMS called, pt placed in wheelchair. 0834 epi 0.3mg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: IM administered while in route to ems, after pt stated" I'm having trouble breathing"(02 :97%) . pt left with EMS @ 0846pm. BP 135/77, 02 99% HR 92. on ambulance. taken to hospital.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: nkda
Vorherige Impfungen: -

VAERS 2311743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

moderat

Staat: NY
Alter: 65,0
Geschlecht: M
Eingang: 07.06.2022
Impfdatum: 05.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Mobility decreased Somnolence

Symptomtext

patient woke up the day after immunization feeling dizzy and drowsy. patient stated they were unable to get out of bed and felt light headed.

Weitere VAERSDATA-Felder

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

VAERS 2716224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MN
Alter: 59,0
Geschlecht: M
Eingang: 21.11.2023
Impfdatum: 07.07.2022
Beginn: 25.10.2023
Tage bis Beginn: 475,0
Dosis: 4
Route/Site: IM / LA

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

Altered state of consciousness Asthenia COVID-19 Cough Influenza like illness Postoperative wound infection Pyrexia SARS-CoV-2 test positive

Symptomtext

The patient has a history of diabetes and PVD s/p bilateral BKA. He was seen in the ED on 10/25/23 for evaluation of weakness and altered level of consciousness. In the ED, his wife reported that the patient has had a cough, weakness, altered LOC, and flu-like symptoms for the past week. He was found to have a fever of 101.7 F. A COVID PCR test resulted positive in the ED. Ultimately, the patient was admitted 10/25/23 - 11/2/23. Discharge diagnoses include COVID-19 infection, among other diagnoses. He did not require oxygen during hospitalization. Of note, the patient is s/p bilateral BKA, and discharge diagnoses also included left stump wound infection. Of note, the patient has received the Pfizer Monovalent COVID vaccine (given 5/3/21; 5/22/21; 2/17/22; 7/7/22).

Weitere VAERSDATA-Felder

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

VAERS 2712497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FP7135

mild

Staat: CO
Alter: 65,0
Geschlecht: M
Eingang: 10.11.2023
Impfdatum: 10.03.2021
Beginn: 01.07.2021
Tage bis Beginn: 113,0
Dosis: 4
Route/Site: IM / LA

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

Biopsy site unspecified abnormal Injection site pain Laboratory test abnormal Lymphadenopathy Metastases to lymph nodes Nervous system disorder Oncologic complication Pain in extremity Peripheral nervous system neoplasm Positron emission tomogram abnormal Soft tissue neoplasm

Symptomtext

Left brachial Plexus tumor encompassing the left axillary artery; left axillary vein and the entire brachial plexus. The tumor is unable to be separated from these main structures in the left axillary area. Multiple lymph node involvement with metastasis to the node between the 1 and 2nd ribs of the chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: 10,0
Labordaten: Increasing neurological damage to the left arm with excruciating pain in the left should arm and hand to the finger tips. July 2023, PET scan revealed the tumor and the lymphadenopathy. Biopsy in August 2023 positive for grade 4 cancer with a grade 4 soft tissue tumor. DNA was so distorted, the source of the cancer could not be identified.
Aktuelle Erkrankungen: High cholesterol
Vorgeschichte: None
Andere Medikamente: Atorvastatin. 20 mg orally daily.
Allergien: None
Vorherige Impfungen: -

VAERS 2632963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MI
Alter: 76,0
Geschlecht: F
Eingang: 17.05.2023
Impfdatum: 21.07.2022
Beginn: 08.04.2023
Tage bis Beginn: 261,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

04/08/23 presents to ED for "fatigue". PMHx of "HTN, COPD, OSA, CAD, CHF, addison's disease"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 04/08/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2615036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: AL
Alter: 61,0
Geschlecht: M
Eingang: 14.04.2023
Impfdatum: 15.07.2022
Beginn: 17.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / -

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

Arthralgia Autoimmune disorder Joint range of motion decreased Neck pain Pain Pain in extremity Red blood cell sedimentation rate

Symptomtext

He is also having pain in his forearm and shoulder; He is also having pain in his forearm and shoulder; It is up like then worse, its migrated from my shoulder up into my neck; I been having some other pains in other parts of my body; having pain in my forearm on the other side of my body/ Little excruciating pain; He is having some kind of autoimmune reaction the vaccine; frozen shoulder; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. The reporter is the patient. A 61-year-old male patient received BNT162b2 (BNT162B2), on 15Jul2022 at 14:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 61 years for covid-19 immunisation. The patient's relevant medical history included: "Arthritis" (unspecified if ongoing); "Allergy" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing), notes: Indication for use in the case: Cholesterol. Concomitant medication(s) included: VALTRAX taken for hypersensitivity; ZOCOR taken for blood cholesterol; CELEBREX taken for arthritis. Vaccination history included: Covid-19 vaccine (DOSE 1, Single; Unknown Manufacturer), for COVID-19 IMMUNIZATION; Covid-19 vaccine (DOSE 2, Single; Unknown Manufacturer), for COVID-19 IMMUNIZATION; Covid-19 vaccine (DOSE 3 (BOOSTER), Single; Unknown Manufacturer), for COVID-19 IMMUNIZATION. The following information was reported: JOINT RANGE OF MOTION DECREASED (non-serious) with onset 17Jul2022, outcome "not recovered", described as "frozen shoulder"; AUTOIMMUNE DISORDER (medically significant), outcome "unknown", described as "He is having some kind of autoimmune reaction the vaccine"; PAIN IN EXTREMITY (non-serious), ARTHRALGIA (non-serious), outcome "not recovered" and all described as "He is also having pain in his forearm and shoulder"; NECK PAIN (non-serious), outcome "not recovered", described as "It is up like then worse, its migrated from my shoulder up into my neck"; PAIN (non-serious), outcome "unknown", described as "I been having some other pains in other parts of my body; having pain in my forearm on the other side of my body/ Little excruciating pain". The patient underwent the following laboratory tests and procedures: Red blood cell sedimentation rate: (28Mar2023) Normal, notes: I did you know I had a curiosity I had to check my SED rate and it come back you know, normal. Therapeutic measures were taken as a result of joint range of motion decreased, pain in extremity, arthralgia, neck pain. Therapeutic measures were not taken as a result of pain. Clinical course: It was reported that the patient had been told by his physician that he had autoimmune response to his last Covid booster shot. It has resulted in a frozen shoulder which has no persisted for nine. It was further stated that the patient was calling regarding the Pfizer COVID 19 booster dose and patient received Gray cap, Original (Monovalent), greater than equal to 12 years - 30 mcg/dose, Do not dilute. He received the booster shot around 15Jul2022 and he was having an issue with the shoulder since then. He went to his doctor and the doctor said that the shoulder was frozen. He was having some kind of autoimmune reaction the vaccine. The pain was still persisting. He was also having pain in his forearm and shoulder that is still persisting. He was taking physical therapy for the pain. He was wondering what he should do next for it. Caller added that he had his vaccination card with him, it mentions: 15Jul2022 and stated that it was different than the injection site, cause it was systemic and mentioned that when he went and saw doctor initially, he meant this was the last thing he expected to hear from him, was that he had an immune response to the vaccine. It was a surprise and given that it's persisted. The patient further stated that, he had been having some ongoing issues with his shoulder. It occurred immediately after giving last booster shot for the COVID-19 vaccine, and he went to his doctor after a couple of weeks, and he said that his shoulder was frozen and it because he have had an auto-immune reaction to the vaccine and his body was producing collagen which was freezing up his shoulder. When confirmed that patient was not sure that this pain in body is related to vaccine. He also stated that the shoulder happens to mediate it was like within a day but now he was having pain in his forearm on the other side of his body and that's only happened in last couple of weeks. The consumer stated that he thought it was about 2 weeks ago and they are just a little excruciating pain. When confirmed that consumer still experiencing the pain, consumer stated that it comes and goes a little bit not less than like it was about, so there was 3 or 4 episodes where it was so bad you had to stop whatever you were doing and now, he was feeling in the same location the pain but it's not as bad. When probed for treatment, consumer stated that he had not done anything for it now, he wanted to see his doctor and he was going to diagnose it, he was an orthopedic surgeon and he prescribed some physical therapy and so, he was been doing exercises which were just motion exercises, tried to keep that moves and he continued to do those, but they did not seem to have any effect on it. It was not constant but it's extremely regular, it's almost every day that he experienced it and if anything, it's probably little bit worst now. He thought they were like nine months now after the vaccination. When confirmed that pain is worsened, consumer stated, "It was up like then worse, its migrated from his shoulder up into his neck. It sometimes at night it wakes him up if he was sleeping on that side because its hurts. The patient also stated that he had been having some other pains in other parts of his body, having pain in his forearm on the other side of his body. The patient had not taken any vaccine 4 weeks prior to Pfizer COVID-19 vaccine. The patient did not take any Pfizer vaccine on same day. Other Products: Yes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Test Date: 20230328; Test Name: SED rate; Result Unstructured Data: Test Result:Normal; Comments: I did you know I had a curiosity I had to check my SED rate and it come back you know, normal.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Arthritis; Cholesterol (Indication for use in the case: Cholesterol)
Andere Medikamente: VALTRAX; ZOCOR; CELEBREX
Allergien: -
Vorherige Impfungen: -

VAERS 2603071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NC
Alter: 72,0
Geschlecht: M
Eingang: 24.03.2023
Impfdatum: 13.07.2022
Beginn: 19.10.2022
Tage bis Beginn: 98,0
Dosis: 4
Route/Site: - / RA

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

Papule Pruritus Rash

Symptomtext

Extreme rash and itch on arms and chest; Extreme rash and itch on arms and chest; Raised bumps that are symmetrical on body; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received BNT162b2 (BNT162B2), on 13Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 72 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Psoriasis" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing). Concomitant medication(s) included: FLU VACCINE VII taken for immunisation, on 27Sep2022 as unk unk, single; EZETIMIBE; ROSUVASTATIN; BABY ASPIRIN. Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Pfizer "Purple Cap"; lot number: FH8028; vaccine location: Right arm), administration date: 19Nov2021, when the patient was 71-year-old, for Covid-19 Immunisation; BNT162b2 (DOSE 2, SINGLE; Pfizer "Purple Cap"; lot number: EN6203; vaccine location: Left arm), administration date: 16Mar2021, when the patient was 70-year-old, for Covid-19 Immunisation; BNT162b2 (DOSE 1, SINGLE; Pfizer "Purple Cap"; lot number: EN0201; vaccine location: Left arm), administration date: 23Feb2021, when the patient was 70-year-old, for Covid-19 Immunisation. The following information was reported: RASH (non-serious), PRURITUS (non-serious) all with onset 19Oct2022, outcome "not recovered" and all described as "Extreme rash and itch on arms and chest"; PAPULE (non-serious) with onset 19Oct2022, outcome "not recovered", described as "Raised bumps that are symmetrical on body". The events "extreme rash and itch on arms and chest" and "raised bumps that are symmetrical on body" required physician office visit. Therapeutic measures were taken as a result of rash, pruritus, papule. Additional information: Patient received OTC Antihistamine, Prednasone 20 mg-ordered twice for events. Patient also received Pfizer Bivalent Sars-cov-2 Vaccine Booster 12+ Yrs (Lot number: GJ2524) on 25Oct2022 as dose 5 at right arm for covid-19 immunisation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Psoriasis; Sulfonamide allergy
Andere Medikamente: EZETIMIBE; ROSUVASTATIN; BABY ASPIRIN
Allergien: -
Vorherige Impfungen: -

VAERS 2581586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 14.02.2023
Impfdatum: 21.10.2022
Beginn: 05.01.2023
Tage bis Beginn: 76,0
Dosis: 2
Route/Site: - / -

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

Abdominal pain COVID-19 Imaging procedure abnormal Laboratory test abnormal Lipase increased SARS-CoV-2 test positive

Symptomtext

"Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: ""65 YO male w/ history of pancreatitis, tobacco, alcohol use, HIV presented with abdominal pain. Found to be COVID 19 positive.labs reveal mildly elevated lipase with imaging finding concerning for pancreatitis. During his stay, he was placed NPO for bowel rest. He tolerated slow diet advancement afterwards. His respiratory status was stable. Strict return precaution given. """

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 4,0
Labordaten: Covid PCR detected on 12/29/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular HTN (hypertension) HFrEF (heart failure with reduced ejection fraction) NSTEMI (non-ST elevated myocardial infarction) Hypertriglyceridemia Ischemic colitis, enteritis, or enterocolitis Digestive History of hepatitis C, now s/p curative treatment GERD (gastroesophageal reflux disease) Polyp of colon Proctitis Ileus Obstruction of cystic duct Acute cholecystitis Toxic megacolon C. difficile colitis Chronic pancreatitis Pancreatic duct stones Respiratory SOB (shortness of breath) CAP (community acquired pneumonia) Other Lumbago Status post laminectomy Seasonal allergies HIV (human immunodeficiency virus infection) Lumbar stenosis with neurogenic claudication Thoracic or lumbosacral neuritis or radiculitis, left lower extremity Synovial cyst of lumbar spine Numbness and tingling in right hand Neck pain Pain disorder Herpes Constipation Quit smoking Exposure to trichomonas Tobacco abuse Patient on methadone maintenance therapy Alcohol use disorder, severe, dependence (*) Abnormal stress test Toxic metabolic encephalopathy Polysubstance abuse Normocytic anemia Splenic infarct Clostridioides difficile infection S/P total colectomy Peritonitis Infected ascites Spondylolisthesis of lumbar region Ileostomy present
Andere Medikamente: acetaminophen (TYLENOL EXTRA STRENGTH) 500 mg tablet Take 1 tablet by mouth every 6 (six) hours as needed for up to 30 days for Pain. albuterol (PROVENTIL HFA,VENTOLIN HFA,PROAIR) 90 mcg/actuation inhaler Inhale 2 puffs into the lungs ever
Allergien: ApricotHives LisinoprilUnknown PeachesSwelling Peanut Butter FlavorHives Shellfish Containing ProductsSwelling
Vorherige Impfungen: -

VAERS 2566321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: OR
Alter: 41,0
Geschlecht: F
Eingang: 23.01.2023
Impfdatum: 06.07.2022
Beginn: 12.11.2022
Tage bis Beginn: 129,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Ear discomfort Headache Nasal congestion Nausea Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

I had a cough, sore throat, body aches, nausea, headache, fever, left ear was plugged up, and slight stuffy nose. I tested positive for COVID-19 at the place I worked at. I took TYLENOL, ibuprofen, and liquid cold medicine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test, positive, 11/14/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis; Hypothyroidism; Sirois
Andere Medikamente: Methotrexate; levothyroxine; tolterodine; multivitamin; iron; vitamin C; spironolactone; pantoprazole; TYLENOL
Allergien: Medroxyprogesterone; ampicillin
Vorherige Impfungen: -

VAERS 2561587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: KS
Alter: 50,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 06.06.2022
Beginn: 20.07.2022
Tage bis Beginn: 44,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Illness Malaise Oropharyngeal pain SARS-CoV-2 test positive Throat irritation

Symptomtext

I received a Pfizer COVID-19 booster on 6/6/2022. On 7/20/2022, I woke up feeling really tired. I also had a scratchy, sore throat. I decided to test myself, and the result was positive. I tested again 7/21/2022 and got another positive result. I didn't have too many symptoms during my illness. The main symptoms were fatigue and sore throat. I just took TYLENOL to treat my symptoms and waited out the virus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 7/20/2022, 7/21/2022 home antigen tests positive results.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Sulfa drugs.
Vorherige Impfungen: -

VAERS 2556294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 11.07.2022
Beginn: 28.11.2022
Tage bis Beginn: 140,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Cough Fatigue Malaise Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Sinus congestion Upper-airway cough syndrome

Symptomtext

I had my vaccination 07/11/2022. On 11/28/2022 I started to have extreme fatigue sinus congestion and low grade fever of 100 degrees. I tested COVID-19 negative on 11/29/2022. I went to urgent care on 11/30/2022 and I tested COVID-19 positive. I was prescribed a cough medicine and PAXLOVID. I stopped after the first 2 doses due to the horrible taste from the medication. I was very sick for 2 weeks. The 3rd and 4th week was full of congestion. I still have continuous post nasal drip on 01/10/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 11/30/2022 COVID-19 positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2553803

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: WA
Alter: 61,0
Geschlecht: F
Eingang: 08.01.2023
Impfdatum: 16.08.2022
Beginn: 18.08.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia C-reactive protein Musculoskeletal stiffness Polymyalgia rheumatica Red blood cell sedimentation rate

Symptomtext

Severe hips/shoulders pain, stiffness; in Dec 2022 diagnosed with polymyalgia arthritica. 4 month duration. Relieved with course of prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: ESR and C-reactive protein
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium, B12, D3
Allergien: Penicillin, steri strips
Vorherige Impfungen: -

VAERS 2553770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NM
Alter: 36,0
Geschlecht: F
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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 Rash

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent rash on arm and face that lasted for one day

Weitere VAERSDATA-Felder

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

VAERS 2551545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: PA
Alter: 65,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 22.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

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

Breast cancer female Feeling hot Lymphadenopathy Postmenopausal haemorrhage Rash erythematous Scab

Symptomtext

I had the routine side effects and wasn't expecting a rash but instead I experienced a rash. It felt scalding hot while at the beach when I noticed it from the shoulder down like little red dots they would open up then crust over. I am post menopausal and have spotting besides. It was so bad while on a trip I was asked if I had monkey pox, it went across my chest and down my back, now I have reaction to everything I take. I also had enlargement of the lymph nodes as well. I was diagnosed with breast cancer on August tenth 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: Breast cancer diagnosed 08/10/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin; vitamin D3
Allergien: Adhesive; silicon
Vorherige Impfungen: -

VAERS 2545769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: KS
Alter: 63,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 30.05.2022
Beginn: 02.10.2022
Tage bis Beginn: 125,0
Dosis: 4
Route/Site: - / LA

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

Cough Decreased appetite Feeling abnormal Headache Respiratory tract congestion

Symptomtext

Severe headache, much congestion, cough, loss of appetite. Was prescribed Paxlovid. Felt pretty bad for five days.

Weitere VAERSDATA-Felder

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

VAERS 2535245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CO
Alter: 52,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 11.06.2022
Beginn: 26.11.2022
Tage bis Beginn: 168,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Nasopharyngitis Oropharyngeal pain Paranasal sinus discomfort SARS-CoV-2 test positive

Symptomtext

I had COVID-19 and I had sinus pressure, head cold symptoms, sore throat, loss of taste and smell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 27NOV2022- COVID-19 - Positive 09DEC2022 - COVID-19- Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; PCOS; High Cholesterol; Chronic Insomnia
Andere Medikamente: Metformin;Amlodipine; Levothyroxine; Ibuprofen
Allergien: Penicillin; Sulfate Drugs
Vorherige Impfungen: Redness and swelling, Covid-19 vaccine, not serious

VAERS 2533286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: IA
Alter: 50,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 15.06.2022
Beginn: 10.12.2022
Tage bis Beginn: 178,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Chills Headache Nasopharyngitis Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had cold symptoms congestion and headache. I had chills but no fever. I was prescribed PAXLOVID which I am still taking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test two, both were positive.
Aktuelle Erkrankungen: None
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: OCREVUS; gabapentin; modafinil; baclofen; tizanidine; losartan; rosuvastatin; vitamin D3; alpha lipoic acid; fish oil
Allergien: None
Vorherige Impfungen: -

VAERS 2518017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: OH
Alter: 61,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 15.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 14,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Fatigue Pain Post-acute COVID-19 syndrome SARS-CoV-2 test positive

Symptomtext

I did not have a reaction to the vaccine. I started feeling symptoms on 06/28/2022 with feeling very tired and achy. I tested positive for COVID-19 the second time on 06/29/2022. I tested positive for COVID-19 the first time on 12/03/2021. I never had a fever nor lost my sense of taste or smell with either infection. I have long COVID-19 and a terrible cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 29JUN2022 COVID-19 Test - Positive; 02DEC2021 COVID-19 Test - Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Lung Disease; Diabetes; Depression
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2492179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 31.07.2022
Beginn: 18.10.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Cough Fatigue Respiratory tract congestion SARS-CoV-2 test positive Drug ineffective Sinus operation

Symptomtext

I tested positive for Covid 19 on October 18, 2022, I experienced a bad cough, no fever, lots of congestion, nasal drainage, tiredness. I was taking Tylenol, Sudafed, and Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid testing
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2492179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 31.07.2022
Beginn: 18.10.2022
Tage bis Beginn: 79,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Cough Fatigue Respiratory tract congestion SARS-CoV-2 test positive Drug ineffective Sinus operation

Symptomtext

I tested positive for Covid 19 on October 18, 2022, I experienced a bad cough, no fever, lots of congestion, nasal drainage, tiredness. I was taking Tylenol, Sudafed, and Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Covid testing
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2493747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: -
Beginn: 10.06.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Chest discomfort Dizziness Rash Rash pruritic

Symptomtext

Narrative: Shortly after vaccination reported substernal chest pressure and dizziness as well as a new mild itchy rash on the upper extremities and lower extremities. No dyspnea, swelling, or difficulty with swallowing. Reports he has needed to go the ED in the past after influenza vaccines when "he swelled up a lot". Did ok with the prior COVID vaccines but notes those were all Moderna rather than Pfizer. Triaged from clinic to the ED where he received IM epinephrine, IV diphenhydramine, and oral famotidine.

Weitere VAERSDATA-Felder

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

VAERS 2483901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NY
Alter: 79,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 19.07.2022
Beginn: 16.09.2022
Tage bis Beginn: 59,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Malaise Nasopharyngitis Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On 07/19/2022, I received the fourth dose of the COVID vaccine, Pfizer and on 09/16/2022, I started to experience symptoms of COVID-19. My husband had COVID the week prior, so I thought that I would be safe because I had the booster, and he did not. I was surprised that I tested positive on 09/17/2022. My symptoms were pretty mild, so I am thankful for that. I only had sniffles and what seemed like a cold.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Metoprolol; simvastatin
Allergien: Latex products
Vorherige Impfungen: COVID Vaccine Moderna - I was down for three days with headaches and pain after the first two doses.

VAERS 2480444

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge FP7135

mild

Staat: WI
Alter: 55,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 01.10.2022
Beginn: 01.07.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / -

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

Eczema Erythema Fungal skin infection Laboratory test normal Pruritus Psoriasis Skin disorder Skin exfoliation

Symptomtext

I began experiencing skin issues in the weeks/months after my booster. Extreme itching, red scaly patches on face, arms, legs. Also eczema type bumps on torso. Also psoriasis on scalp. Additionally yeast infection in arm pits that won't resolve with prescriptions ointments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: celiac tests were negative.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: amoxicillin, Zithromax, nuts, flaxseed, kiwi, cantaloupe
Vorherige Impfungen: -

VAERS 2470299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: IN
Alter: 57,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 20.07.2022
Beginn: 22.07.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Influenza like illness Lymphadenopathy Pyrexia

Symptomtext

Fever of 100.4, flu like symptoms, lymphadenopathy of right axillary.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin, stool softener, calcium +D, Effexor 75mg, Estradiol 1mg, and Allegra D.
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2469667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: PA
Alter: 75,0
Geschlecht: F
Eingang: 05.10.2022
Impfdatum: 12.07.2022
Beginn: 05.09.2022
Tage bis Beginn: 55,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia COVID-19 Contusion Fatigue Myalgia Oropharyngeal pain Pruritus SARS-CoV-2 test positive Sinus disorder Urticaria

Symptomtext

It started with sore throat and I took a COVID-19 test. I had just been at a wedding. I was positive that morning. For the first few days I had sinus and inflamed throat. At night I had joint and muscle pain. I trouble getting PAXLOVID so first few nights were really bad. Then after starting PAXLOVID it was more extreme fatigue. I felt better after a week and tested negative. Then 2 days later I tested positive. Later in the month I found strange bruises in odd places like my abdomen and had some itchy spots and what appeared as hives. I have had response like this to wheat gluten but I haven't consumed that in years, so I thought this flare up could be as a result to COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID-19 at home test - positive
Aktuelle Erkrankungen: No
Vorgeschichte: Celiac disease; Gastric reflux; Sinusitis; Cardiac abnormality
Andere Medikamente: REPATHA; levothyroxine; vitamin D; famotidine; fexofenadine; aspirin
Allergien: Celiac; Seasonal allergies
Vorherige Impfungen: In the 1977 I had a small pox vaccination and I became very ill and had diarrhea and vomiting.

VAERS 2465621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 30.09.2022
Impfdatum: 17.06.2022
Beginn: 14.08.2022
Tage bis Beginn: 58,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Decreased interest Discomfort Fatigue Hypersomnia Malaise Mental disorder Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

I traveled in August and when I returned home, I began to feel symptoms of COVID-19. I experienced a sore throat that rapidly worsened. The next morning, I did a self-test that was positive on August 14. I reported the test results to my doctor. They asked if I wanted to be treated and I said yes and was prescribed Paxlovid. I began the Paxlovid treatment right away on 8/15/22. The symptoms by then included aches and pains. No fever. I felt very tired and was sleeping a lot. Those symptoms continued and somewhat diminished with the Paxlovid over a period of three weeks. When I self-tested again, it was negative twice. I had self-isolated during that time and wore a mask around my family and separated from other members of my family who live with me which were my wife and mother-in-law. I maintained distance from them. They did not get COVID-19. Since the negative test, I had experienced some continued tiredness. More tiredness than I would experience previously. I also experience a heaviness in my body that is like an athlete after a strenuous workout. I am 69 years old, and I was a very active athlete. I would ride my road bike maybe more than 100 miles a week. In the weeks previously in July, I participated in a 100-mile bike ride. The contrast from being vibrant and energetic, then after COVID having to sleep all the time ? there is a stark contrast. Post-COVID-19, I?m still experiencing tiredness and a lack of interest in things. It is beginning to come back, but there is still a point of time in the day where when I wake up in the morning, I get the sense of depletion when I get tired. I get a sense of lack of mental acuity or clarity at times during the day particularly when I feel tired. These are not debilitating. The severity of it I would rate as not severe, mild post symptoms. Yes, I have recovered but still experience some mild symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Positive COVID-19 At-Home Test on 08/14/2022; Negative COVID-19 At-Home Test on 08/21/2022 Negative COVID-19 At-Home Test on 08/22/2022; Positive COVID-19 At-Home Test 08/26/2022; Positive COVID-19 At-Home Test 08/28/2022; Negative COVID-19 At-Home Test 09/01/2022; Negative COVID-19 At-Home Test on 09/07/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Partial lobectomy 10 years ago
Andere Medikamente: Multivitamin; Vitamin C; Vitamin D3; Methylphenidate
Allergien: None
Vorherige Impfungen: -

VAERS 2464407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: TX
Alter: 62,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 21.07.2022
Beginn: 24.09.2022
Tage bis Beginn: 65,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Pulmonary congestion Pyrexia SARS-CoV-2 test positive Stomatitis

Symptomtext

09/24 developed sores on the roof of my mouth. 09/26 I developed chest congestion and 100.6 fever. Took at home COVID-19 test and it was positive. I had no body aches, chills, or fatigue. I ran fever for 5 days and still have minimum chest congestion. Went in and saw PA on 09/26. Prescribed the antiviral molnupiravir began medication the evening of 09/26 and symptoms began resolving 09/27.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: COVID-19 - positive
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Vitamin D; trazadone; RITALIN
Allergien: No
Vorherige Impfungen: -

VAERS 2460757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MI
Alter: 91,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 17.06.2022
Beginn: 25.09.2022
Tage bis Beginn: 100,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Dizziness Fall SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID breakthrough. Patient presented to the emergency dept on 9/25 after feeling dizzy and falling. He has been feeling dizzy for a couple days. COVID+ on 9/25/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: 2,0
Labordaten: COVID+ PCR on 9/25/22
Aktuelle Erkrankungen: -
Vorgeschichte: CKD stage 2, Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2443221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: UT
Alter: 39,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 13.08.2022
Beginn: 20.08.2022
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: SYR / RA

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

Dizziness Headache Vomiting

Symptomtext

Dizziness, Vomiting and Headaches.

Weitere VAERSDATA-Felder

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

VAERS 2439747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 28.06.2022
Beginn: 01.06.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Abdominal distension Lymph node pain SARS-CoV-2 test Ultrasound scan

Symptomtext

lymph nodes under left arm was very painful. Although pain subsided, area still tender when touched.; fullness in my abdomen, from hip to hip.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jun2022 as dose 3 (booster), single (Lot number: FP7135) at the age of 54 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "HBP" (unspecified if ongoing); "known allergies: Latex" (unspecified if ongoing); "Known allergies: some preservatives" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Sulphur, reaction(s): "known allergies: Sulphur". Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: 33130BA; Anatomical location: Arm Left), administration date: 07Jan2022, when the patient was 54-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: FT1614; Anatomical location: Arm Left), administration date: 28Jan2022, when the patient was 54-year-old, for COVID-19 immunization, reaction(s): "What hasn't gone away since the 2nd shot leading to the 3rd one -is the fullness in my abdomen, from hip to hip". The following information was reported: ABDOMINAL DISTENSION (non-serious) with onset Jun2022, outcome "not recovered", described as "fullness in my abdomen, from hip to hip."; LYMPH NODE PAIN (non-serious) with onset Jun2022, outcome "not recovered", described as "lymph nodes under left arm was very painful. Although pain subsided, area still tender when touched.". The events "lymph nodes under left arm was very painful. although pain subsided, area still tender when touched." and "fullness in my abdomen, from hip to hip." required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of lymph node pain, abdominal distension. Additional information: The patient did not receive other vaccine in four weeks. The other medication in two weeks included over the counter (OTC) Supplements, DK which ones, not taken daily. It was unknown whether the patient had covid prior to vaccination. The patient had been tested for covid post vaccination. AE treatment was also reported as to receive diagnostic detailed ultrasound imaging.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: Test Date: 202208; Test Name: DK; Test Result: Negative ; Comments: Nasal Swab; Test Name: ultrasound imaging; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Latex allergy; Reaction to preservatives
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MI
Alter: 49,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 21.05.2021
Beginn: 14.08.2022
Tage bis Beginn: 450,0
Dosis: 4
Route/Site: - / -

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

Abdominal pain COVID-19 Computerised tomogram thorax abnormal Drug intolerance Intermenstrual bleeding Pulmonary mass SARS-CoV-2 test positive

Symptomtext

50 year old female with PMH of fibroids and ovarian cyst who presented to hospital with subacute abdominal pain. Patient still has menstrual periods every 28 days and has noted some mild inter-menstrual spotting over the past year- she has never been pregnant, has no known STI history, and is not currently sexually active. There is no known family history of breast or gynecologic malignancy. Patient will follow up with gynecologic oncology as an outpatient for further discussion of treatment. She did not tolerate Dilaudid or Tramadol due to nausea and dizziness and has an allergy to the Norco, so she was switched to Percocet. IR was consulted for biopsy of pleural nodules noted on chest CT, but determined they we not accessible due to size, and patient is encouraged to have the nodules surveyed with serial imaging at 3 month intervals. Patient had a mild fever to 100.2 without leukocytosis, we held Percocet and gave Tylenol, which resolved the episode. She is to follow up with gynecologic oncology within 1 week of discharge. Patient was medically stable for discharge with pain and anti-nausea medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 4,0
Labordaten: 8/14 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2429387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 03.09.2022
Impfdatum: -
Beginn: 08.08.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Rash Urticaria

Symptomtext

Narrative: Pt developed rash/hives on his forehead, upper back, arms, and legs 4 days after receiving 4th Pfizer COVID-19 vaccine on 8/4/22. Pt stated he took diphenhydramine and used calamine lotion which initially resolved the hived, however, they started to slowly come back on 8/9/22. Pt was prescribed methylprednisolone dosepak and famotidine to use in combination with diphenhydramine which resolved the reaction.

Weitere VAERSDATA-Felder

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

VAERS 2428439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: TX
Alter: 77,0
Geschlecht: M
Eingang: 03.09.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Pain in extremity

Symptomtext

Pain in his left arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. A 77-year-old male patient received BNT162b2 (BNT162B2), on 07Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 77 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "blood pressure problems" (unspecified if ongoing). Concomitant medication(s) included: VALSARTAN; AMLODIPINE BESILATE. Vaccination history included: BNT162b2 (First dose, Lot: EL9266), administration date: 21Feb2021, when the patient was 76-year-old, for COVID-19 Immunization; BNT162b2 (Second dose, Lot: EN6207), administration date: 14Mar2021, when the patient was 76-year-old, for COVID-19 Immunization; Bnt162b2 (1st Booster, 27Sep2021 or 29Sep2021, she has a hard time reading the date on the card., Lot: 30130BA), administration date: Sep2021, when the patient was 76 years old, for COVID-19 Immunization. The following information was reported: PAIN IN EXTREMITY (medically significant) with onset 07Jul2022, outcome "not recovered", described as "Pain in his left arm". The event "pain in his left arm" required physician office visit. Therapeutic measures were taken as a result of pain in extremity. Clinical course: Partner of a 77-year-old male patient called stating that they received the 2nd booster of the Pfizer COVID-19 Vaccine on 07Jul2022. Patient has been having pain in the arm ever since receiving it. The reporter wanted to know if this has been reported, what could be causing it, how to make it better, and when it should go away. As per caller: Caller stated that she also received the same vaccine on the same day around 15 to 20 minutes after the patient, but did not experience the side effect. Caller stated that that patient experienced it almost immediately. Caller stated that they have tried everything, heat, cold, and aspirin. Caller stated that they have gone to 2 PCPs and went to an orthopedic last week. Caller stated that the patient had a cortisone shot but the pain did not go away. Caller stated that she has called the CDC who referred her to VAERS. Caller stated that this was supposed to be something that will help someone but there is no information on how to remedy any adverse effect. Caller stated that this was supposed to be something that will help someone but there is no information on how to remedy any adverse effect. Specify Consumer or other non health professional: Wife. Other Conditions: Yes Investigations: No. NDC number, UPC number and Expiry Date of COVID-19 Vaccine were Unknown. Is Unspecified Medication a Pfizer product? Unspecified Unspecified Medication manufacturer: unspecified NDC number of Unspecified Medication: Unknown UPC number of Unspecified Medication: Unknown, Reason for no lot number: of Unspecified Medication: Other: Lot# could not be probed as the medication was unspecified, Expiry Date of Unspecified Medication: Unknown. Other Products: Yes Transferring agent stated, "I do have on the other line calling for her husband. The reason for the transfer is that after getting the second booster shot of the Pfizer COVID-19 Vaccine his husband got a bad reaction to the vaccine that is the reason for the transfer." Reporter stated, "Well he received, We received the dose same day I had no adverse effect he did and he still having it on 07Jul2022, he got his booster and since that time the pain in the arm on he has received the shot has given him so much pain that it has not stopped, have gone to two different doctors regular PCPs and then he has also gone to an Orthopedic because we thought that was it and they gave him a cortisone (Unspecified Medication) nothing has happen. They are trying to refer him to some other type of treatment but we are not getting any, It is not getting any better so I called the CDC and they said they can not help me they referred me to something. For my last thing let me go to Pfizer may be they have more information but we do not understand why the pain has not stopped? Why nobody can tell us? Well I need to find out is there anything that Pfizer can possibly tell us what we, who we need to go to find out what happened to him when he got the second shot?" Weight: Reporter stated, "About 170 (As reporter was unsure hence not captured in tab)." Treatment for side effect: Reporter stated, "They gave him a Cortisone, last week he got Cortisone." Anatomical site of injection: Reporter stated, "It is the left arm on the upper part." Date and time of vaccination: Reporter stated, "07Jul2022 and it does not have the time but that was before 12 O'clock in the morning that I can tell because we both went at that the same time." Vaccination Facility type: Reporter stated, "It was a Pharmacy which is # Pharmacy." Dosage and Relevant Information: Date and Time of Start of Drug: 21Feb2021 Batch/lot number: FP7135 Dosage text: Dose unknown, injection in the left arm Pharmaceutical form (Dosage form): Injection Indication for use in the case: Indication as Reported by the Primary Source: Covid-19 booster. Other Conditions: No, Investigations: No. Caller said that she was calling about the second booster dose for the Covid-19 Vaccine. She was calling for her partner. They received the booster dose on 07Jul2022 from a # pharmacy. Her partner has had pain in his left arm and has not stopped. They have seen 2 primary care doctors and a orthopedic doctor. Her partner received a Cortisone shot and it did not help. Caller would like to know what happened and how to make it better? The patient can hardly move the arm and it is getting bad. He is struggling with his arm. They don't know what to do. They were faithful about getting the boosters and the pain in his arm has not stopped. They thought he would get relief and the doctor said that they have seen people with the same issue. No further details provided. The evening of the 07Jul2022 he started complaining of the pain and said that the next day it got worse. He does not typically complain. When she would challenge him on it he would say that it hurt really bad. They were told to wait by the doctor to see if it would go away. The caller said that the doctors said that they have heard of it before and that people were reporting it after the booster. The doctor told the patient to take Advil and Tylenol and nothing would help. They went to a # hospital in #, # for the first 2 doses and a # pharmacy for the booster doses. Medical condition: She stated that he has blood pressure problems and he is pretty healthy. He is tall and skinny. He is not usually sick. This has worn him down though. Caller asked will it go away? Is it happening to other people? Time the Vaccination Was Given: In the morning before 12 noon. Anatomical Location of Administration of Pfizer vaccine considered as suspect: Arm Left. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available): First dose: 21Feb2021 Lot: EL9266 Expiry date: Unknown Site: Unknown; Second dose: 14Mar2021 Lot: EN6207 Expiry date: unknown Site: Unknown; First booster dose: 27Sep2021 or 29Sep2021, she has a hard time reading the date on the card. Lot: 30130BA Expiry date: Unknown Site: Unknown; Additional Vaccines Administered on Same Date of the Pfizer Suspect were None. Adverse Event: pain in his left arm, Time of Onset: (24-hour clock): between 2100-2200. Did any AE(s) require a visit to: Emergency Room? No; Physician Office? No; If Yes, which AE(s)? Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) were None. AE(s) following prior vaccinations were None. Patient's Medical History (including any illness at time of vaccination)? was None. Family Medical History Relevant to AE(s): None. Relevant Tests: None. Description of Product Complaint: Not suspect product, Description of complaint: Reported pain in the patient's left arm after Covid-19 second booster. Her partner received a Cortisone shot and it did not help. Last week received a cortisone shot and that did not help. No NDC, Lot, or expiry date. The patient received it at the orthopedist office. The doctor told the patient to take Advil and Tylenol and nothing would help. No NDC, Lot, or expiry provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal
Andere Medikamente: VALSARTAN; AMLODIPINE BESILATE
Allergien: -
Vorherige Impfungen: -

VAERS 2429332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 17.06.2022
Beginn: 17.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Headache Injection site pain Myalgia

Symptomtext

Headache, Myalgia, PAIN AT INJECTION SITE. Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2427939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 02.09.2022
Impfdatum: 28.12.2020
Beginn: 19.01.2021
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Inflammation Lip swelling Pain Pharyngeal swelling Skin lesion Swelling face Throat tightness

Symptomtext

Lips, face, tongue, throat swelling and inflammation. At day 2 my tongue, throat and mouth broke out in lesions. It took a steroid to lesson the swelling and pain after 4 days. I had to go to the ED as throat was closing. I had an event in Dec 2020, March 2021 and July of 2022 - following each dose: dec 2020, jan 2021, nov 2021, July 2022 Pfizer

Weitere VAERSDATA-Felder

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

VAERS 2425242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: IN
Alter: 71,0
Geschlecht: F
Eingang: 31.08.2022
Impfdatum: 26.06.2022
Beginn: 22.08.2022
Tage bis Beginn: 57,0
Dosis: 4
Route/Site: SYR / LA

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

Chills Cough Decreased appetite Headache Oropharyngeal pain Pain

Symptomtext

Sore throat, achy, cough, chills, slight headache, not much of an appetite

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure Cholesterol
Andere Medikamente: Lisinopril Pravastatin Zolpidem Hydrochlorothiazide Buspirone Centrum Probiotic Zinc Calcium plus D3 B complex Vitamin C
Allergien: None
Vorherige Impfungen: 4/30/2021 Moderna, age 70, lip swelling 03/01/2021, Moderna, age 70, flu like symptoms 10/22/2022, Moderna booster, age 70, flu

VAERS 2420053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: TN
Alter: 67,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 19.08.2022
Beginn: 19.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Diarrhoea Dizziness Erythema Fatigue Injection site pain

Symptomtext

Diarrhea, lightheadedness/dizzy, tired, erythema, injection-site pain. Symptoms resolved 3-4 days following vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Kidney transplant 6/2021, MI/CAD/, HTN, HLD, stroke, HFrEF
Andere Medikamente: Amlodipine, prograf/cellcept/prednisone, flomax, HCTZ, eliquis, crestor, mag-ox, protonix, imdur, coreg, aspirin 81mg, vitD3, vitB12, plavix, NTG
Allergien: none
Vorherige Impfungen: -

VAERS 2416842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: LA
Alter: 86,0
Geschlecht: F
Eingang: 21.08.2022
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: nein

Pruritus Rash

Symptomtext

Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild

Weitere VAERSDATA-Felder

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

VAERS 2414729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 27.07.2022
Beginn: 08.08.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: SYR / LA

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

Arthritis Computerised tomogram head abnormal Deafness bilateral Ear infection Ear pain Endodontic procedure Facial pain Fatigue Headache Laboratory test Middle ear effusion Neuralgia Pain in jaw Sinus disorder Temporomandibular joint syndrome Toothache X-ray normal

Symptomtext

I have had headaches, what felt like toothaches, one sided facial pain, ear aches, jaw pain, a lot of fatigue, sinus problems and I have had sever pain on the left side of my face, ear and pain. I went to the dentist and he could not find anything wrong with me, he sent me to an Endodontist, and he took and x-ray and test and could not find anything with the x-ray or scan, he did a heat and cold test and he did a root canal on my tooth, but that did not solve the pain at all. I went to urgent care with sever pain on the left side of my face and the Dr. stated I had TMJ and an ear infection and she prescribed a muscle relaxer and an antibiotic. The antibiotic cleared the ear infection, the muscle relaxer did not help at all but the pain. I was till feeling a lot of pain so a couple of days later I went to my primary care and the NP that saw me was concerned and she ordered a CT scan, and she disagreed with the diagnosis of TMJ but said that I l had a lot of fluid behind my ear, and the CT Scan did state that I had TMJ Arthritis but no infection, they set up an appoint for me to see someone for arthritis. I have also been referred to an oral surgeon for neuralgia, I was also advised to see an ENT which I saw on yesterday and she said I had hearing loss in both ears but no infection, she recommended hearing aides, and she also recommended that I go to an oral surgeon to look at the TMJ closer and come back to see her after that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: X-Ray July 20th; CT Scan August 3, 2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis; Sinus Tachycardia.
Andere Medikamente: CLARITIN; metoprolol tartrate; azelastine hydrochloride nasal spray; albuterol inhaler; nitroglycerin; TYLENOL.
Allergien: Prednisone; aerosolized garlic; CELEBREX; SEPTRA.
Vorherige Impfungen: COVID-19 2nd dose of the Vaccine, March 4, 2021.

VAERS 2414660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: MA
Alter: 26,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 21.07.2022
Beginn: 18.08.2022
Tage bis Beginn: 28,0
Dosis: 4
Route/Site: IM / -

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

COVID-19 Exposure to SARS-CoV-2 Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

reports sx of sore throat and feeling "stuffy" , reports known exposure in community from positive boyfriend- tested positive for covid 8/18/22- has had 4 doses of covid vaccine- initial series Moderna plus 2 doses of pfizer

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: 8/18/22 binax rapid antigen test positive for covid
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2414489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: DE
Alter: 66,0
Geschlecht: F
Eingang: 18.08.2022
Impfdatum: 25.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

Vaccination site pain

Symptomtext

If you were talking about adverse events of the Pfizer vaccine for go series. There were none other than pain at the injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Jun2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 66 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "hyper- cholesterolemia" (unspecified if ongoing). Concomitant medication(s) included: ATORVASTATIN, stop date: 05Aug2022; DILTIAZEM, start date: 03Aug2022. Vaccination history included: BNT162b2 (DOSE 3, SINGLE; Lot Number: 301458A, Anatomical location: Left arm), administration date: 29Sep2021, when the patient was 65-year-old, for Covid-19 Immunization; BNT162b2 (DOSE 2, SINGLE; Lot Number: EL9266, Anatomical location: Left arm), administration date: 25Feb2021, when the patient was 64-year-old, for Covid-19 Immunization; BNT162b2 (DOSE 1, SINGLE; Lot Number: EL9265, Anatomical location: Left arm), administration date: 28Jan2021, when the patient was 64-year-old, for Covid-19 Immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 2022, outcome "unknown", described as "If you were talking about adverse events of the Pfizer vaccine for go series. There were none other than pain at the injection site". Additional information: The patient had no known allergies. The patient received other medication in 2 weeks. It was reported that "If you were talking about adverse events of the Pfizer vaccine for go series", there were none other than pain at the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Hypercholesterolemia
Andere Medikamente: ATORVASTATIN; DILTIAZEM
Allergien: -
Vorherige Impfungen: -

VAERS 2408462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 10.08.2022
Beginn: 10.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Erythema Feeling hot Skin warm

Symptomtext

1521 Pt. states she started feeling slightly dizzy and lightheaded. Feeling "hot". Assist to lying down on exam table on R side. Alert and oriented x 3. Color pink. Skin warm and dry. 1523 BP 104/82 P84. 1526 BP 124/80. P93. States dizziness resolved. Assisted to sitting up on edge of exam table. 1534 BP110/82. P98. sitting up. Called family member for ride home. Sips of water given. 1543 BP 114/84. P86 1555 BP 124/80. amb. with assistance to waiting car. 1608. Brother in law arrived. and pt. home in car in stable condition.

Weitere VAERSDATA-Felder

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

VAERS 2408358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: AL
Alter: 67,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 13.07.2022
Beginn: 05.08.2022
Tage bis Beginn: 23,0
Dosis: 4
Route/Site: IM / RA

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

Back pain COVID-19 Cough Fatigue Neck pain Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

Developed COVID-19 about weeks after vaccination. Woke up with sore throat and persistent dry cough. I experienced sneezing, runny nose, fatigued and pain in back of neck and lower back. Went to walk in flu clinic and tested positive. Prescribed multi-symptom meds. Symptoms began resolving as soon as I began meds. Still experiencing extreme fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: COVID-19 x 2
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multivitamin; REPLENEX; probiotic; fish oil; coQ10; ACUITY
Allergien: Hay fever
Vorherige Impfungen: -

VAERS 2407318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CO
Alter: 49,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 19.07.2022
Beginn: 30.07.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: SYR / RA

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

Back pain COVID-19 Cough Dry throat Fatigue Feeling abnormal Headache Nasal congestion Pyrexia Respiratory tract congestion SARS-CoV-2 test positive Throat irritation Vaccine breakthrough infection

Symptomtext

Breakthrough case. My throat started feeling a scratchy and dry, then felt tired with a lower back ache and felt extremely tired. Started having a dry cough as well. Tested negative with a home COVID-19 test. My lower back pain worsened the next day and felt congested, took another at home test and tested negative again. Still feeling really bad, so went and got the PCR test and tested positive. Stayed home and rested, the next day I got a fever, headache and severe back pain went all the way up my back. I still hadn't had the results back from the PCR test, so I took another home test and it was positive. Just rested and started to slowly feel better a few days later except I got nasal congestion and still have it 3 weeks after testing positive for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: Home COVID-19 test - negative. Home COVID-19 test - negative. PCR test - was still waiting for the results. Took another home COVID-19 test and it was positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Fluoxetine; levothyroxine; vitamin D; magnesium glycinate; vitamin B complex
Allergien: Doxycycline
Vorherige Impfungen: -

VAERS 2405905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: AR
Alter: 51,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 25.06.2022
Beginn: 01.08.2022
Tage bis Beginn: 37,0
Dosis: 4
Route/Site: SYR / LA

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

Aphonia Influenza virus test negative Malaise Nasal congestion Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test negative Streptococcus test negative

Symptomtext

Starting 08/01/2022, I woke up with a very sore throat. The next day, I had a stuffy nose and thought it was the hotel air. On 08/02/2022, I got home and felt sickly, and took an at home test which was negative and then I went to urgent care and they did a COVID/strep test but they were both negative. On 08/05/2022, I went to another urgent care and got a COVID-19 test, Strep test and Flu test which all came back negative. The doctor put me on a Z-PAK because he didn't like the way my throat looked. I started feeling better by 08/06/2022. I feel fine today but still have some runny nose/nasal congestion and my voice hasn't returned to normal yet (I lost my voice on Saturday).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: COVID-19 test and Strep tests (08/02/2022): negative; COVID-19 test, Strep test and Flu test (08/05/2022): negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: GEMMILY
Allergien: Shellfish; latex; MACROBID; CHOLRAPREP
Vorherige Impfungen: -

VAERS 2405805

JANSSEN · COVID19 (COVID19 (JANSSEN)) · Charge FP7 135

mild

Staat: WA
Alter: 66,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 27.06.2022
Beginn: 07.08.2022
Tage bis Beginn: 41,0
Dosis: 4
Route/Site: IM / LA

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

Abdominal pain Diarrhoea Fatigue Myalgia Nausea SARS-CoV-2 test negative Somnolence Vomiting

Symptomtext

myalgias, fatigue, followed a couple of hours later by somnolence,, nausea, vomiting, abdominal pain, diarrhea all lasting about 36 hours then all resolved except abdominal pain and diarrhea, which are still going on.. Treated symptomatic a Lly. I have no reason to think this was related to the vaccine. Rapid COVID tests at onset and after 48 hours were negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, hypertension, depression
Andere Medikamente: Amlodipine, levothyroxine, NPThyroid, B12, folate, magnesium citrate
Allergien: Sulfa allergy, gluten sensitivity
Vorherige Impfungen: -

VAERS 2405669

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: AR
Alter: 72,0
Geschlecht: F
Eingang: 09.08.2022
Impfdatum: 16.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Fatigue Pain Respiratory tract congestion Rhinorrhoea Secretion discharge Sinus congestion

Symptomtext

I received my Covid 19 vaccine on 07/16/2022. On 07/29/2022 I started having a running noise. 07/30/2022 I woke up with lots of congestion and mucus. I felt achy and tired and lots of mucus with a stuffy head. On 07/31/2022 I went to the doctor and was diagnosed with Covid-19. I was prescribed PAXLOVID for 3x for 5 days. Symptoms gradually improved from next day and completely went away day 6.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetic; High Blood Pressure; High Cholesterol
Andere Medikamente: Losartan; metformin; pravastatin; multivitamin; calcium citrate; coQ10; krill oil; flax seed oil; vitamin D3; baby aspirin; OSTEO BI FLEX; NUSKIN eye formula
Allergien: Quinapril; AUGMENTIN
Vorherige Impfungen: -

VAERS 2404562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: OK
Alter: 60,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 02.08.2022
Beginn: 03.08.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Blood potassium decreased Chest X-ray normal Computerised tomogram thorax normal Dizziness Electrocardiogram Extra dose administered Fatigue Feeling abnormal Fibrin D dimer increased Full blood count Headache Hypersomnia Inflammation Laboratory test normal Muscle tightness Nausea Neck pain Pain

Symptomtext

Starting 08/03/2022, I ran a real high fever (102.6) even with tylenol or advil. I slept all day long. I was extremely fatigued, achy from head to toe even on the tops of my feet, headache and neck pain. Also, I was experiencing nausea. I was having the same reaction that I had to the 1st shot. On 08/04/2022, I was feeling basically the same but the temp only went to 101.6. On Friday and Saturday, I felt extremely exhausted and, on Sunday, 08/05/2022, I went out thinking I was okay and started feeling funny. So, I went back inside the house and grabbed my heart monitor (from when I had the bad reaction on 12/31/2020 from the first shot) and my HR was in the 150s. I was light headed, dizzy and my neck was feeling full. So, we went to the ER and they did a chest xray, labs and EKG. My D dimer was elevated and they were concerned I may have had a pulmonary embolism. So, they did the a CT scan of the chest which showed no embolism and the doctors concluded that it was likely inflammation as a result of receiving the vaccine that caused the elevated D dimer levels. They told me to follow up with the cardiologist and my regular doctor. I have an appointment coming up this Wednesday with them, and I am waiting to hear back from my cardiologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: CT scan of the chest: Normal; Chest X-ray: Normal; CBC/urine tests/Thyroid tests: Potassium low and D-Dimer was high. Other lab tests: Normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Ramipril; Hydrochlorothiazide; Metoprolol; Potassium; Baby Aspirin
Allergien: Cipro
Vorherige Impfungen: Same reaction after the 1st dose; High fever and aches/chills after 2nd and 3rd

VAERS 2403503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NM
Alter: 16,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 04.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Axillary pain Lymphadenopathy Muscle spasms

Symptomtext

Lymph node swelling, pain, and cramping under left armpit.

Weitere VAERSDATA-Felder

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

VAERS 2403084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: VA
Alter: 56,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 25.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / AR

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

Cough Dizziness Headache Influenza like illness Injection site erythema Injection site swelling Pyrexia

Symptomtext

About 10:00pm on the night of vaccination I started to feel like I had the flu. I was feverish, dizzy and coughing. It continued for over 24 hours. Two days after vaccination I woke up feeling better. I had a mild headache. Where I received the injection it was red and swollen. Everything got better but my arm. By five or six days after the shot the sore arm was gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Chron's disease
Andere Medikamente: Vitamins; Antidepressants
Allergien: Lysol; Penicillin
Vorherige Impfungen: Shingles

VAERS 2400552

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FP7135

mild

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 03.08.2022
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: ja

Dizziness Nausea

Symptomtext

minutes in observation I asked if she was feeling okay. She explained she "felt a little dizzy and nauseous" .She was guided to a cot to lie down. Water, crackers and ice pack were provided. Vital signs were taken an were as follows: BP 122/80 T 97.2 F P 86 R 16 02 98-99% RA. 50 minutes have passed and is feeling better. Patient slowly sat at the edge of the cot, dangled feet and stood up and is ambulating well. Vitals were taken a 2nd time after ambulating to the restroom and were as follows: BP 130/90 T: 97.3F P.87 02: 99% RA. Symptoms have resolved. Leena reports that she will start her period tomorrow and does usually have cramping the day before onset. She explains a history of pain and a heavy flow etc with each menstural cycle. She does mention a concern of endometriosis and will follow up with a GYN. She mentioned concern about GI issues and does see a specialist. Denies possibility of pregnancy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Vitals Signs - BP 122/80 T 97.2 F P 86 R 16 02 98-99%
Aktuelle Erkrankungen: GI issues
Vorgeschichte: NA
Andere Medikamente: Levothyroxine, omeprezole, zoloft, pamalor
Allergien: Zpack (SOB)
Vorherige Impfungen: -

VAERS 2399064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 02.08.2022
Impfdatum: 16.07.2022
Beginn: 16.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Chills Confusional state Delirium Extra dose administered SARS-CoV-2 test positive

Symptomtext

Systemic: Chills-Medium, Systemic: Confusion-Severe, Additional Details: The patient felt delirious after her 4th dose of the Pfizer COVID vaccine which lasted 3 days. The 4th day she tested positive for COVID. She wanted me to report her adverse effects because her previous doses she did not have any adverse effects.

Weitere VAERSDATA-Felder

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

VAERS 2398090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NC
Alter: 51,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 24.06.2022
Beginn: 19.07.2022
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia COVID-19 Influenza like illness Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

After the vaccine I felt flu like, achy and my joints ached for about 30 hours. The symptoms began about 12 hours after the booster. I started having a runny nose and congestion on July 18th. I took PCR that was positive. I continued to have nasal congestion and began to have a cough and runny. Paxlovid wasn't recommended because it had been several days and my symptoms were beginning to resolve. I felt good for a few days but then I still tested positive as of July 29th. As of today I do not have lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: PCR COVID-19 test, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Lymphedema;
Andere Medikamente: Vraylair; Multi Vitamin; Vitamin D
Allergien: Vodka; Metformin
Vorherige Impfungen: -

VAERS 2397638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: FL
Alter: 18,0
Geschlecht: M
Eingang: 30.07.2022
Impfdatum: 30.07.2022
Beginn: 30.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Cold sweat Dizziness Eye movement disorder Injection site pain Musculoskeletal stiffness Nausea Pain in extremity Pallor Somnolence

Symptomtext

Patient received a booster dose of the Pfizer COVID vaccine (Comirnaty) in his left deltoid muscle. Within 30 seconds, patient reported feeling extreme chills, nausea, dizziness, and a sore arm where the injection site was. Patient was within sight of the pharmacist for nearly 30 minutes. Patient felt cool, but not cold to the touch while patient experienced chills. He reported feeling the chills eased up within 15 minutes of receiving the vaccine. He stated that this episode was not as intense as the first dose, but still appeared in distress (patient clenching hands into fists, eyes rolling in the patient's head, general paleness). He was able to answer simple questions about his symptoms throughout the episode. Patient has a history of this reaction to previous doses of the COVID vaccine. Besides general verbal comforting from his father and sitting down in the waiting area, no intervention was taken. Patient was taken home by father and his brother after about 30 minutes. Called father for update a few hours later and patient is resting and doing better at home. Patient reports feeling groggy and dizzy, but chills resolved about 60-90 minutes after leaving pharmacy. Father did not know whether patient took any acetaminophen to relieve chills. Patient was reported to be well enough to eat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: -
Andere Medikamente: Divalproex DR 125mg, verapamil ER 180mg
Allergien: Penicillin/Cefdinir (rash), duloxetine (convulsions)
Vorherige Impfungen: Pfizer (primary series - during first dose, healthcare providers were considering taking him to ER, but symptoms resolved in abo

VAERS 2395917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MD
Alter: 75,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 21.06.2022
Beginn: 01.06.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / LA

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

Product administered at inappropriate site Urticaria Vaccination site pain Vaccination site pruritus Vaccination site swelling

Symptomtext

Itching around the site of injection; Hives; Received second dose of Pfizer COVID vaccine between shoulder and elbow instead of deltoid; Swelling around the site of injection; Pain around the site of injection; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A 75-year-old female patient received BNT162b2 (BNT162B2), on 21Jun2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 75 years intramuscular, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: FH8020), administration date: 01Nov2021, when the patient was 75-year-old, for COVID-19 immunisation; Covid-19 vaccine (DOSE 2, SINGLE), for COVID-19 immunisation; Covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE), for COVID-19 immunisation. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "Pain around the site of injection"; VACCINATION SITE SWELLING (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "Swelling around the site of injection"; PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 21Jun2022, outcome "unknown", described as "Received second dose of Pfizer COVID vaccine between shoulder and elbow instead of deltoid"; URTICARIA (non-serious) with onset 24Jun2022, outcome "not recovered", described as "Hives"; VACCINATION SITE PRURITUS (non-serious) with onset 24Jun2022, outcome "not recovered", described as "Itching around the site of injection". The events "swelling around the site of injection", "pain around the site of injection", "itching around the site of injection" and "hives" required physician office visit. Therapeutic measures were taken as a result of vaccination site pruritus, urticaria. Additional information: 2nd booster dose administered to left arm pharmacist assumes attempted intramuscular but it was not close. It was reported that a pharmacist that injected the patient between the shoulder and elbow instead of deltoid so wondering if she needs another dose of the vaccine. States for serious criteria of this event of injecting the patient between the shoulder and elbow, it is not life threatening but the patient did experience symptoms of swelling, pain and itching around the site of injection and the swelling and pain went away after 1.5 weeks and began about a day or two after getting the vaccine; states the patient still has the itching and the hives and she tried to reach out to the patient in the past week but has not heard back from the patient and the caller is not sure what is going on; the itching and hives began about 3 days after the vaccine and the last time she spoke with the caller maybe a week or two ago, the itching and hives were still ongoing and the patient stated nothing was helping the itching or hives so she has no idea if the itching and hives are ongoing now or not. The patient tried and did not help the hives and itching except the patient stated the Claritin did not help and caller has no product details for lot, expiry date or NDC to provide for the Claritin. No additional vaccines administered on same date of the pfizer suspect. The patient was not hospitalized. The patient did not receive other vaccines within four weeks prior to COVID vaccine. No Investigations was conducted. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received. Follow-up (21Jul2022): This is a spontaneous follow up report from a contactable pharmacist. This pharmacist reported for a female patient that: Updated information included: Primary reporter full address added, Corresponding reporter added. Patient information (patient initials added, other medical history added, historical vaccines added), Suspect product information (coding updated, vaccination date added, lot number added, dose description added, anatomical location added, vaccination facility details added), Event information (New events, onset dates, outcomes, treatments added and physician office visit ticked) and Concomitant therapy added.

Weitere VAERSDATA-Felder

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

VAERS 2388866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 22.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Pain Pain in extremity Throat irritation

Symptomtext

1. Arm is hurt 2. The whole body is pain 3. The throat is itchy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2388174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MD
Alter: 59,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 19.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Chills Eye pain Head discomfort Headache Injection site pain Nausea Pyrexia Sinus congestion Somnolence

Symptomtext

The following events occurred after receiving the second booster of Pfizer on 7/19/2022. I was very sleepy on the first day. On the morning of the second day, my head felt very heavy (congested); nagging headache; injection site pain for a couple of days (eventually went away); nausea 7/19 - 22/2022; fever beginning 7/24/2022 - 100.2, 99.9, 101.7; chills during the fever; my eyes also hurt to move during the fever period;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: Lyme Disease 2009 Vestibular issues since 2015
Andere Medikamente: Atorvastatin 40 mg Citalopram 10 mg Vitamin D3 2000 IU 50 mcg CoQ10 200 mg Centrum multivitamin
Allergien: Ampicillin Biaxin
Vorherige Impfungen: This was self-reported - vaccination date 4/27/2021 my second shot (not a booster) Pfizer EW0171 age 58 Nausea and vomiting; so

VAERS 2388073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MI
Alter: 77,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 12.06.2022
Beginn: 08.07.2022
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Dysphonia Headache Nasopharyngitis Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Sick relative Sneezing

Symptomtext

On the evening on 07/08/2022 I had a little bit of a sore throat and my voice dropped a bit. On the next day, I noticed some sneezing and a runny nose. Later in the day, I developed a significant headache which is unusual for me. I took 2 aspirin that night which got rid of the headache. I continued with common cold like symptoms and my husband seemed to be coming down with the same thing. At the suggestion of a friend, we tested for COVID-19 on 07/11/2022 with a PCR test and the results were positive the next day. I called my doctor after receiving the results and he prescribed PAXLOVID. After beginning the PAXLOVID, my symptoms continued to improve although I feel that they were progressing well on their own.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: PCR COVID-19 test 07/12/2022 positive.
Aktuelle Erkrankungen: None.
Vorgeschichte: Low Thyroid; Arthritis.
Andere Medikamente: Levothyroxine; latanoprost; acetaminophen; mature multivitamin; vitamin D3; magnesium citrate; TUMS; vitamin C; turmeric; AREDS2; probiotic.
Allergien: Penicillin.
Vorherige Impfungen: -

VAERS 2387970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: MD
Alter: 65,0
Geschlecht: F
Eingang: 25.07.2022
Impfdatum: 08.06.2022
Beginn: 08.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pain

Symptomtext

Site: Pain at Injection Site-Medium

Weitere VAERSDATA-Felder

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

VAERS 2387198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: GA
Alter: 35,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 01.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Headache SARS-CoV-2 test

Symptomtext

Severe headache; dull intractable headache; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Jul2022 at 17:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 35 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Multiple sclerosis" (unspecified if ongoing); "chronic migraine" (unspecified if ongoing). Concomitant medication(s) included: TECFIDERA; UBRELVY; ZOLOFT; BLISOVI FE 1/20; SEROQUEL. Vaccination history included: Covid-19 vaccine (Primary immunization series complete. , MANUFACTURER UNKNOWN), for Covid-19 immunization; Covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE , MANUFACTURER UNKNOWN), for Covid-19 immunization. The following information was reported: HEADACHE (non-serious) with onset 05Jul2022, outcome "not recovered", described as "Severe headache"; HEADACHE (non-serious) with onset 05Jul2022, outcome "not recovered", described as "dull intractable headache". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of headache, headache. Additional Information: No other vaccine in four weeks. No COVID prior to the vaccination. No known allergies. Severe headache starting on 05Jul (four days post-vaccination). Since then, dull intractable headache most days for the last two weeks. Migraine abortives don't seem to help. OTC painkillers help temporarily. Prednisone seems to help temporarily. COVID test post vaccination: COVID test type post vaccination: Nasal Swab on 07Jul2022, COVID test result : Negative. 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: Headache
Hospital-Tage: -
Labordaten: Test Name: Covid 19 test; Result Unstructured Data: Test Result:Unknown results; Comments: If covid tested post vaccination: Yes; Test Date: 20220707; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic migraine; Multiple sclerosis
Andere Medikamente: TECFIDERA; UBRELVY; ZOLOFT; BLISOVI FE 1/20; SEROQUEL
Allergien: -
Vorherige Impfungen: -

VAERS 2385357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: MI
Alter: 18,0
Geschlecht: F
Eingang: 23.07.2022
Impfdatum: 23.07.2022
Beginn: 23.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Blood glucose normal Dizziness

Symptomtext

Patient received her first dose of the pfizer vaccine and then went on to wait in the waiting area for 15 minutes. During that time, she began to feel light headed and dizzy. I went out to the waiting area to check on her and it appeared she was very lightheaded. She was responding to her father and I by nodding, I lifted her legs on the chair and gave her water. She began to feel better after drinking water. I called 611 to inform them while the patient's father called 911 from his cell phone. Patient started to verbally respond and said she was feeling better and was just dizzy and light headed. EMS did come and they checked her blood pressure which they confirmed to me was borderline low and they said her sugar levels were normal. By this time, patient was able to talk and stand and said she felt a lot better and EMS said that there is no need to transport her to the hospital.

Weitere VAERSDATA-Felder

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

VAERS 2382797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: IN
Alter: 72,0
Geschlecht: M
Eingang: 23.07.2022
Impfdatum: 21.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: SYR / LA

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

Asthenia Chills Pain Pyrexia

Symptomtext

Fever (around 101), chills and body aches, no energy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: From 2nd & 1st Pfizer Booster

VAERS 2379729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 90,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 20.07.2022
Beginn: 21.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Chills Dry mouth Headache Influenza like illness Myalgia

Symptomtext

I day after I received my vaccine I had extreme muscle aches and pains, an extremely dry mouth. The joints hurt all over my body, I felt as if I had a bad case of the flu. I had chills so bad that I could not get warm (it was 116F outside and I could not get warm). I experienced a headache that is very unusual for me. I did take a Tylenol on July 22, 2022 because I was still feeling achy. I do feel a bit better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: A-Fib; Peripheral Neuropathy; Relapsing Polychondritis Syndrome
Andere Medikamente: Lovastatin; Metoprolol Tartrate; Losartan; Xarelto; Tylenol;
Allergien: Sulfa
Vorherige Impfungen: First COVID-19 booster same symptoms but they lasted for 2 days. 08/20/2021 Pfizer

VAERS 2379462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CT
Alter: 64,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 16.06.2022
Beginn: 15.07.2022
Tage bis Beginn: 29,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Ear discomfort Fatigue Headache Impaired work ability Malaise Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Sneezing

Symptomtext

COVID-19 symptoms started 07/15/22; tested positive 07/17/22. By the 15th I had a sore throat that was significant and later that night I developed a headache and my ears were clogged up. By the 16th I continued to have he sore throat and headache but I did not develop a cough. By the 17th I was sneezing a lot and still had sore throat and headache and also developed a low grade fever that didn't go above 99.1. By the 19th my headache was gone and I experienced fatigue all weekend. so from the 15th-20th. I didn't lose taste or smell and on the evening of the 20th I started PAXLOVID. I am still currently taking medication and final dose is on the 25th. I still have ear stuffiness, fatigue, but no headache or throat pain. I am pretty good and have been cleared to go back to work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 Positive 07/15/22.
Aktuelle Erkrankungen: None
Vorgeschichte: Hemochromatosis; Hashimoto's thyroiditis; pacemaker because of heart disease.
Andere Medikamente: Standard SYNTHROID; levothyroxine
Allergien: All opioids (morphine; DILAUDID; DEMEROL; codeine); a bunch of antibiotics; sulfa drugs; doxycycline; cats.
Vorherige Impfungen: -

VAERS 2379273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: PA
Alter: 77,0
Geschlecht: M
Eingang: 22.07.2022
Impfdatum: 09.06.2022
Beginn: 15.07.2022
Tage bis Beginn: 36,0
Dosis: 4
Route/Site: SYR / RA

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

Body temperature decreased Chills Cough Fatigue Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test

Symptomtext

It started the evening of the 14th. I had a dry cough and a runny nose. That night I felt severe chills and took my temperature and it was below normal. It was 96.6. The chills lasted for days and I decided two days later and took a at home COVID-19 test. I started feeling very fatigue and congested. I never developed a fever. I contacted my PCP telehealth and he prescribed PAXLOVID. The symptoms never got worse and the symptoms have subsided and today 07/22/2022, I will finished my PAXLOVID. I feel much better than I have been.

Weitere VAERSDATA-Felder

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

VAERS 2375021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MA
Alter: 91,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 18.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / RA

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

Discomfort Injection site reaction Swelling

Symptomtext

Patient called the pharmacy to report swelling and injection site reaction on the arm with the vaccines. Had patient check for temperature, which was 98.1 degrees Farenheit. Advised patient to put ice on the area to minimize swelling and rotate arm to minimize discomfort. Called patient 2 other times during the day to make sure she was doing well. Patient reporting doing better and feeling better.

Weitere VAERSDATA-Felder

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

VAERS 2374885

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: VA
Alter: 56,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 03.07.2022
Beginn: 17.07.2022
Tage bis Beginn: 14,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Exposure to SARS-CoV-2 Headache Impaired work ability Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Contracted COVID 19 after exposure to known infected persons. Started experiencing symptoms on July 16 - sore throat, headache. Tested positive w rapid antigen home test on July 17 2022. Symptoms worsened to include fever, coughing, headache, congestion. Missed three days of work. Contacted primary care physician via phone to ask whether anti-retro viral therapy was appropriate. Dr did not recommend that option.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Home COVID 19 antigen test July 17, results positive.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Focalin XR 25mg, Centrum Silver for men multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2374879

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 19.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Injection site pain Pyrexia

Symptomtext

Fever; soreness in left arm where shot was given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None/Not applicable
Vorgeschichte: None/Not applicable
Andere Medikamente: None/Not applicable
Allergien: None/Not applicable
Vorherige Impfungen: -

VAERS 2374755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 28.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Blood pressure increased Extra dose administered Pain in extremity

Symptomtext

On 6/28/22 Patient received her 4th Pfizer vaccine at 12:24 pm. According to the daughter 4 hours later her arm was hurting. Patient took advil. Her blood pressure went up to 180 systolic. Pt. was taken to hospital and they recommended her to take tylenol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: N?A
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2373990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: WA
Alter: 33,0
Geschlecht: M
Eingang: 19.07.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
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 Lymph node pain Pain in extremity Pyrexia

Symptomtext

A second booster of Pfizer Covid 19 was given to a 33 year old healthy male. Upon realizing the mistake the client was called on 7/19/2022 to inform him that he received a dose that is currently not approved to be given to a person under 50 years of age. Client states he is not experiencing any complications that he did not experience with his other vaccines. The fever and arm soreness was gone with 24 hours, his lymph node is still sore but he states it is geting better.

Weitere VAERSDATA-Felder

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

VAERS 2372376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 18.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Cardiac flutter Extra dose administered Headache Heart rate irregular Injection site erythema Injection site induration Injection site warmth Nausea Pain in extremity

Symptomtext

RECEIVED VACCINE AT APPROXIMATELY 1PM. FINISHED WORK DAY AND WENT HOME. ARM WAS EXCESSIVELY SORE AT THIS TIME, MUCH WORSE THAN THE OTHER 3 DOSES. ARM ALSO NOTED TO HAVE A LARGE 10CM ROUND AREA OF INDURATION. PATIENT WENT TO BED THAT NIGHT AND WOKE UP WITH A TERRIBLE HEADACHE AND NAUSEA. THERE WAS REDNESS AND HEAT NOTED AT THE INJECTION SITE WHICH CONTINUED WITH REDNESS AND INDERATION. THE PATIENT NOTED SEVERAL IRREGULAR HEAT BEATS, SAYING SHE COULD FEEL HER HEART FLUTTERING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: HTN
Andere Medikamente: TYLENOL ARTHRITIS, CITALOPRAM, LISINOPRIL
Allergien: THYMERISOL
Vorherige Impfungen: -

VAERS 2371962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 16.07.2022
Impfdatum: 12.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Nausea Pain Pyrexia

Symptomtext

1:00 am, July 13 2022 to 6:00 pm July 14 2022: severe body aches, fever and nausea. 1:00 am, July 13 2022 thru today, July 16, 2022: severe nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: None. Urgent care doctor prescribed Zofran, which helps to a very limited degree.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Wellbutrin XL 300, Celexa 10mg, Nexium 20mg, Buspirone 15mg, Spironolactone 50mg, Cromolyn eye drops (occasionally), Flonase, Albuterol
Allergien: None
Vorherige Impfungen: 2/23/2021 Pfizer COVID-19 (age 58); 3/16/2021 Pfizer COVID-19 (age 58); 11/11/2021 Pfizer booster (age 59): With all the COVID-1

VAERS 2370580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MN
Alter: 65,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 02.06.2022
Beginn: 07.07.2022
Tage bis Beginn: 35,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sinus operation

Symptomtext

I started getting symptoms of sinus drainage. I then started getting fatigue, low grade fever, cough, runny nose, and more drainage. I took a COVID-19 test that was positive. I went to a clinic and had a PCR COVID-19 test that was positive. I was given antibody infusion. I feel like this help with my symptoms. I still have lingering symptoms of chest congestion, cough, and tiredness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 test - positive
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma (Controlled)
Andere Medikamente: Lisinopril ; Hydrochlorothiazide; Atorvastatin; Potassium
Allergien: Sulfa; Environment allergies
Vorherige Impfungen: Pfizer - lymph node swelling

VAERS 2369409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: LA
Alter: 40,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Expired product administered Injection site pruritus Product administration error Product storage error

Symptomtext

Pt was administered a first dose of Pfizer COVID Vaccine 0.3ml into her right deltoid muscle. This vaccine given after the BUD. Vaccine was originally punctured 07/13 at 10:10am with a BUD of 10:10pm on 07/13. The vaccine was maintained in the fridge at a temperature if 39 degrees celcius up until dose was drawn approximately at 03:20pm 07/14. Vaccine was given 07/14 at 3:25pm. After 15-20 minute monitoring, patient reported no serious side effects besides a slight itch at the injection site (and no where else). Pt was notified of the administration mistake and advised to monitor for any serious side effects and usual symptoms that last longer than 1-2 days and report to PCP or hospital. No additional dose was provided to patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: -
Vorgeschichte: diabetic
Andere Medikamente: Otezla, victoza, telmisartan, escitalopram, busprione
Allergien: none reported
Vorherige Impfungen: -

VAERS 2368888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: WI
Alter: 62,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 05.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Blood pressure increased Blood test abnormal Blood urine present Contusion Influenza virus test negative Nausea Pruritus Pyrexia Rash erythematous SARS-CoV-2 test negative Skin warm Urine analysis abnormal White blood cell count increased

Symptomtext

I started experiencing itching immediately after the vaccination while in the waiting room. It started with the palms of my hands and arms on both sides. The itchiness went away quickly but now I have itchy spots on my right leg. It is not constant but every other. There are red spots as well and they look like reddish pink bruises. On 7/12/2022 at night, my skin that felt unusually hot. The next morning I felt nauseous and hot. I took my temperature and it was elevated to around 99.3. I went to the ER due to the fever and had tests ran with COVID-19 negative, Flu was negative, blood test, and urinalyses. No major infection was indicated but blood test and urinalyses were higher than normal. My white blood cell count was higher at 11.5. My blood pressure was elevated and the reading was 140/86. My symptoms went away today about an hour ago and I now only have red itchy on my right leg. I have an appointment with my doctor on Monday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: COVID-19 test - negative; Flu - negative; Blood work - slightly elevated with white blood cell count 11.5, ASP higher than normal ; Urinalyses - blood indicated in urine; Blood pressure 140/86
Aktuelle Erkrankungen: None
Vorgeschichte: Pre Diabetes
Andere Medikamente: None
Allergien: Augmentin
Vorherige Impfungen: Flu vaccines - Headaches with all that I have had

VAERS 2366503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 05.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Inflammation

Symptomtext

Patient had shoulder pain and inflammation which was treated with steroids from an urgent care clinic

Weitere VAERSDATA-Felder

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

VAERS 2365866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NM
Alter: 2,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 06.07.2022
Beginn: 06.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Product use issue Rash

Symptomtext

rash around the shoulder area spread a little ways down towards belly and down the back; lot number FP7135; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). A 2-year-old female patient received BNT162b2 (BNT162B2), on 06Jul2022 at 14:30 as dose 1, single (Lot number: FP7135) at the age of 2 years, in left leg for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: PRODUCT USE ISSUE (non-serious) with onset 06Jul2022 at 13:30, outcome "unknown", described as "lot number FP7135"; RASH (non-serious) with onset 06Jul2022 at 13:45, outcome "recovering", described as "rash around the shoulder area spread a little ways down towards belly and down the back". The events "rash around the shoulder area spread a little ways down towards belly and down the back" required emergency room visit. Therapeutic measures were taken as a result of rash. Additional information: No other vaccine received in four weeks and no other medications in two weeks. Patient was not received covid prior vaccination and not tested covid post vaccination. It was reported that patient had a rash that wasn't a severe reaction couple of mins after the shot. Was around the shoulder area and under the neck both front and back and rash spread a little ways down towards belly and down the back. AE resulted in Emergency room/department or urgent care. Doctor checked and gave Benadryl. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2364697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fp7135

mild

Staat: CA
Alter: 60,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 08.07.2022
Beginn: 09.07.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

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

Headache Oropharyngeal pain Rhinorrhoea

Symptomtext

Headache, runny nose, sore throat

Weitere VAERSDATA-Felder

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

VAERS 2364365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 10.07.2022
Beginn: 10.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Axillary pain Nodule

Symptomtext

Patient states that the day after she received the vaccine, she developed a knot under her right arm close to her armpit, and the site of the knot is sore

Weitere VAERSDATA-Felder

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

VAERS 2364278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 06.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Fatigue Headache Lethargy Nausea

Symptomtext

Systemic: Exhaustion / Lethargy-Severe, Systemic: Headache-Severe, Systemic: Nausea-Severe

Weitere VAERSDATA-Felder

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

VAERS 2364277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: VA
Alter: 38,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 25.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Burning sensation Mass Pain in extremity

Symptomtext

Systemic: thigh pain and burning on night off vaccine, then 2 lumps appeared on upper thigh left side on 7/5-Severe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2364097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: KY
Alter: 71,0
Geschlecht: F
Eingang: 10.07.2022
Impfdatum: 09.07.2022
Beginn: 09.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Cough Nasal congestion Pain Pyrexia Rhinorrhoea Sneezing

Symptomtext

Achy Feverish Cough Sneezing Runny nose Stuffy nose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma MAC Pacemaker dependent
Andere Medikamente: -
Allergien: Pcn? Imetrex Vancomycin
Vorherige Impfungen: -

VAERS 2363949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 09.07.2022
Impfdatum: 05.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Additional Details: patient requested call 911, 911 came , check blood presuure , they said everything is fine and advised the patient to follow up with the provider

Weitere VAERSDATA-Felder

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

VAERS 2362700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: FL
Alter: 13,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 03.07.2022
Beginn: 04.07.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymphadenopathy Pain Swelling

Symptomtext

Systemic: Lymph Node Swelling-Severe, Additional Details: swelling under armpit that started Monday 7/4/22 afternoon. Swelling is currently the size larger than a golf ball and very painful. Advised mom to contact PCP and can use IBU for pain control

Weitere VAERSDATA-Felder

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

VAERS 2361189

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp 7135

mild

Staat: NM
Alter: 37,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 07.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Chills Dizziness Headache Nausea

Symptomtext

Patient became nauseous and dizzy 5 minutes post vaccine. Then developed a severe headache and chills 10 minutes later. Elevated legs, wrapped patient in fleece blanket. Pulse was normal rate- slightly weak. Patient had downed a half bottle of water directly after the vaccine administration. Sat with patient instructed on breathing and use of acupressure point for nausea. BEtter after 15 minutes but stayed 45 until I felt comfortable to escort her out.

Weitere VAERSDATA-Felder

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

VAERS 2361113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 23.06.2022
Beginn: 06.07.2022
Tage bis Beginn: 13,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia Diarrhoea Pyrexia

Symptomtext

weakenes, fever 101.5, diarrhea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: paxil, vitamins
Allergien: haldol, arithromyacin, percodan
Vorherige Impfungen: 62 yearsPfizer EL1283 1/15/2021

VAERS 2360969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: OH
Alter: 54,0
Geschlecht: M
Eingang: 07.07.2022
Impfdatum: 02.07.2022
Beginn: 02.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Burning sensation Rash

Symptomtext

started as burning sensation on right side of my head (forehead, scull, in front and around ear) developed rash, slightly panful on touch

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Visiting dermatologist on 7/7/2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None in the morning of vaccination day before vaccination: morning: bupropion, ezetimibe, digestive enzymes evening: baby aspirin, rosuvastatin, digestive enzymes
Allergien: None
Vorherige Impfungen: -

VAERS 2359817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 56,0
Geschlecht: M
Eingang: 06.07.2022
Impfdatum: 30.06.2022
Beginn: 01.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Gait inability Joint swelling Pain Pain in extremity Peripheral swelling Pyrexia

Symptomtext

The day after I received my fourth dose of Pfizer, I began to experience some aches and pain in my left foot and I also had a slight fever of 99 degrees. The next day my foot began to swell and the symptoms were similar to what I experience with Rheumatoid arthritis and I was unable to walk. Since then my left knee has also began to swell. The pain has subsided some, around 20-30% but the swelling has remained the same and my fever went away around 2-3 days after I first noticed it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Early May onset of Rheumatoid Arthritis lasting.
Vorgeschichte: None.
Andere Medikamente: Unwilling to provide.
Allergien: None.
Vorherige Impfungen: -

VAERS 2359662

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MN
Alter: 63,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 21.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 9,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Malaise Nasopharyngitis Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine but I tested positive for COVID-19 on 07/05/2022. I started feeling systems on 06/30/2022. I started with a sore throat and then a bad head cold. I had a telehealth visit with my doctor on 07/05/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Home test for COVID-19 which was positive on 07/05/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Bi-polar and irritable bowel syndrome
Andere Medikamente: Yes - declined to provide details
Allergien: Methylprednisolone
Vorherige Impfungen: -

VAERS 2359582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 02.07.2022
Beginn: 05.07.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Injection site rash

Symptomtext

Patient called via telephone to report a large red rash around the injection site. No other symptoms, no trouble breathings, no hives. No treatment required.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No previous illnesses.
Vorgeschichte: No known health conditions.
Andere Medikamente: MVI, and as needed OTC products.
Allergien: No known allergies.
Vorherige Impfungen: -

VAERS 2357241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: VA
Alter: 46,0
Geschlecht: F
Eingang: 04.07.2022
Impfdatum: 28.06.2022
Beginn: 29.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Headache Injection site pain Lymphadenopathy Pain Pyrexia

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Fever-Medium, Systemic: Headache-Medium, Systemic: Lymph Node Swelling-Medium, Additional Details: Patient told immunizer she has cancer

Weitere VAERSDATA-Felder

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

VAERS 2357060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 04.07.2022
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: nein

Injection site erythema Injection site pain Injection site swelling

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2356305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: FL
Alter: 1,9
Geschlecht: M
Eingang: 03.07.2022
Impfdatum: 24.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LL

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

Injection site injury Overdose Product administered to patient of inappropriate age Product use complaint

Symptomtext

a 23 month old child was inadvertently administered 0.2 mL of the Pfizer Covid vaccine gray cap adult vaccine; a 23 month old child was inadvertently administered 0.2 mL of the Pfizer Covid vaccine gray cap adult vaccine; it is very, very tiny on the bottle; injury; This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. A 23-month-old male patient received BNT162b2 (BNT162B2), on 24Jun2022 as dose number unknown, 0.2 ml single (Lot number: FP7135, Expiration Date: 30Nov2022) at the age of 23 months, in left thigh for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), OVERDOSE (non-serious) all with onset 24Jun2022, outcome "unknown" and all described as "a 23 month old child was inadvertently administered 0.2 mL of the Pfizer Covid vaccine gray cap adult vaccine"; INJECTION SITE INJURY (non-serious) with onset 24Jun2022, outcome "unknown", described as "injury"; PRODUCT USE COMPLAINT (non-serious) with onset 24Jun2022, outcome "unknown", described as "it is very, very tiny on the bottle". Additional information: It was reported that she called to advice that they have administered an adult dose grey cap Pfizer COVID-19 Vaccine to 23 months old baby. They have given 0.2 ml of the dose to the patient. She told that she handed the vaccine to the provider and it was checked by the provider but it was the provider who administered the COVID-19 Vaccine and also reported that he grabbed the needle as reporter stuck his leg, the dad didn't have his arms and when he grabbed it when the needle came out, it scratched his leg a little bit. So, but reporter didn't inject anything he grabbed it as soon as reporter stuck in reporter didn't get to put the plunger down. So, he got stuck again with the wrong and had the injury. Reporter grabbed the needle out of his hand and reporter just stuck him again, the provider was holding his legs down.

Weitere VAERSDATA-Felder

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

VAERS 2356208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: PA
Alter: 12,0
Geschlecht: M
Eingang: 03.07.2022
Impfdatum: 19.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Axillary pain Lymphadenopathy

Symptomtext

Pain in armpit; Swollen Lymph node; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 12-year-old male patient received BNT162b2 (BNT162B2), on 19Jun2022 at 19:00 as dose 3 (booster), single (Lot number: FP7135) at the age of 12 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: FL0007, Location of injection: Arm Left), administration date: 29Nov2021, when the patient was 11-year-old, for COVID-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: FK5127, Location of injection: Arm Left), administration date: 08Nov2021, when the patient was 11-year-old, for COVID-19 Immunization. The following information was reported: AXILLARY PAIN (non-serious) with onset 20Jun2022 at 01:00, outcome "not recovered", described as "Pain in armpit"; LYMPHADENOPATHY (non-serious) with onset 20Jun2022 at 01:00, outcome "not recovered", described as "Swollen Lymph node". Therapeutic measures were not taken as a result of axillary pain, lymphadenopathy. Additional information: The patient did not receive any other vaccine in four weeks. The patient did not receive other medications in two weeks. No COVID prior vaccination. COVID did not tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None Known allergies: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2355130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: WA
Alter: 63,0
Geschlecht: F
Eingang: 02.07.2022
Impfdatum: 22.06.2022
Beginn: 22.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Headache Malaise Pyrexia Thirst

Symptomtext

at 6 00 pm the same day I had a fever and headache felt week. was extremely thirstyI took tylennol and put eye pack on my forehead. I was ill until the next day around 9pm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: diabetic/high blood pressure
Andere Medikamente: none
Allergien: asprin
Vorherige Impfungen: -

VAERS 2351500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: -
Alter: 27,0
Geschlecht: F
Eingang: 02.07.2022
Impfdatum: 01.07.2022
Beginn: 01.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Disorientation Dizziness

Symptomtext

Patient received 1st dose of vaccine and within 5 minutes felt very light headed and became disoriented. Patient was laid on back with knees elevated and given an ice pack to rest on her head. After 5-10 minutes patient was sat up in a chair and given some cold water. Patient never lost consciousness and was able to communicate to a degree. Patient felt better after sitting in chair for another 10-15 minutes. Patient left on own accord.

Weitere VAERSDATA-Felder

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

VAERS 2347859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NC
Alter: 55,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 23.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Erythema Pruritus Rash Urticaria

Symptomtext

Broke out in hives on front of neck. Over several days hives spread to back of neck, upper arm, abdomen and butt. Severe redness and itching. Initial treatment prescribed 6/27/22 Triamcinolone 0.1% cream, apply 3x day for 1-2 weeks. Rash continued to spread so Dr called in Prednisone 10mg tablet tapering down for 12 days(?) beginning 6/29/22. Also taking zyrtec during the day and benadryl tablets at night.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: COVID positive May 10, 2022
Vorgeschichte: -
Andere Medikamente: benadryl, Multi Vitamin, Vitamin C, B12, D3, Tumeric, Advil.
Allergien: Penicillins, Tetracyclines, Quinolones
Vorherige Impfungen: -

VAERS 2341948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 13.06.2022
Beginn: 14.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Exposure to SARS-CoV-2 Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I did not have an adverse reaction to the vaccine. I was exposed to COVID-19 with my nephew while out with other family members. On June 14, I started having symptoms with a minor sore throat. I didn't feel bad at all because I thought it was allergies. I tested positive for COVID-19 on June 18 with a home test. I took Mucinex-D, Flonase, Tylenol and Advil for my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Home test for COVID-19 was positive on June18.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure and depression
Andere Medikamente: Zyrtec; Losartan; Amlodipine
Allergien: Penicillin and sulfa
Vorherige Impfungen: -

VAERS 2338902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MO
Alter: 26,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 28.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Flushing Heart rate increased Hyperhidrosis

Symptomtext

lightheadness, high heart rate, diaphoresis, flushing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: birth control
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2338841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NE
Alter: 76,0
Geschlecht: M
Eingang: 28.06.2022
Impfdatum: 26.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Full blood count Liver function test Metabolic function test Myocardial necrosis marker Nausea Pancreatic enzymes Vomiting

Symptomtext

Nausea & vomited 12 times in 8 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: CBC, Met profile, cardiac enzymes, pancreatic enzymes, liver studies all on 06/27/2022
Aktuelle Erkrankungen: Colitis
Vorgeschichte: -
Andere Medikamente: Amlodipine, Sildenafil, MVI, fish oil, Famotidine, Clopidogrel, Cholestyramine, Budesonide, Aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2338831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: VA
Alter: 24,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 27.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Headache Insomnia Nausea Vomiting projectile

Symptomtext

Pt. woke up night after booster with chills and severe headache. After about 30 minutes still had not been able to fall back asleep due to headache and chills. At this time experieced nausea followed by a large volume of projectile vomiting. Took ibuprofen for headache and presumed fever and was able to return to sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: levonorgestrel IUD
Allergien: n/a
Vorherige Impfungen: chills, headache, and nausea following second pfizer covid vaccine (2/18/21 age 22)

VAERS 2370334

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 13.06.2022
Beginn: 14.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Fatigue Headache Injection site pain Myalgia Pyrexia

Symptomtext

Headache, Myalgia, Fever, fatigue, pain at injection site Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2336509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: FL
Alter: 24,0
Geschlecht: M
Eingang: 27.06.2022
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

Anxiety Dizziness Nausea

Symptomtext

Patient had first dose for Pfizer, he was fine at the time of administration of vaccine. While he was waiting in the post vaccination area family member came to me to tell me he is dizzy and having anxiety attacks. She stated that he gets this kind of reactions when he sees needle. She also stated that he would be okay after 15-20 minutes. I gave him icepack to help for those reactions. He felt vomiting as well . He started feeling better after 15 minutes. He refused emergency call.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: Dizziness, vomiting, anxiety from any vaccines in the past. Unknown for name for vaccines. Patient has needle fear.

VAERS 2336501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: RI
Alter: 18,0
Geschlecht: M
Eingang: 27.06.2022
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

Cold sweat Vomiting

Symptomtext

Patient became clammy and vomited a few minutes after receiving vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vomiting
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: Dizziness (nervousness)

VAERS 2336498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 27.06.2022
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: unbekannt Erholt: ja

Chest discomfort Cough Diarrhoea Wheezing

Symptomtext

Patient started experiencing cough, chest tightness, wheezing 10 minutes after Pfizer vaccine administration. In 90 minutes after vaccine administration, patient started having loose stools. Given albuterol PRN. Patient refused to go to the ED. Patient stated symptoms relieved after taking the albuterol. During the course of observation, patient was able to verbalize needs and ambulate with assistance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: Albuterol PRN
Allergien: none
Vorherige Impfungen: -

VAERS 2335807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NE
Alter: 74,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 24.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia Chills Decreased appetite Fatigue Headache Pyrexia

Symptomtext

After the 4th injection...2nd booster...chills, fever, headache, loss of appetite, severe joint pain, extreme fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: oeseoarthritis
Andere Medikamente: Lisinipril, montelukast, pantoprazole, alprazalom, relief factor, calcium, cranberry, zinc, vitamin E, D3, multi vitamin, vitamin c, magnesium, iron, biotin
Allergien: none
Vorherige Impfungen: -

VAERS 2335312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: IN
Alter: 73,0
Geschlecht: M
Eingang: 25.06.2022
Impfdatum: 23.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Chills Pain Pyrexia

Symptomtext

Fever of 101, chills, aches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Lisinopril 30 mg, Atorvastin 20 mg, Tylenol
Allergien: none
Vorherige Impfungen: fever, chills, aches after 1st booster

VAERS 2329676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: AR
Alter: 56,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 15.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / LA

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

Injection site erythema Injection site swelling

Symptomtext

pt states she has redness and swelling at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2329023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 23.06.2022
Impfdatum: 22.06.2022
Beginn: 22.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Chills Injection site rash

Symptomtext

A half dollar coin sized rash under the injection site. Chills that lasted about 30 min during the night

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: Diabetes, HBP
Andere Medikamente: Levothyroxine, Losartan, Hydrochlorothiazide, Amlodipine, Metformin, Liquid Probiotic taken around 10:30pm
Allergien: No
Vorherige Impfungen: chills only

VAERS 2327624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 09.06.2022
Beginn: 10.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Body temperature increased Dysstasia Fall Fatigue Influenza like illness Malaise Vertigo

Symptomtext

Patient got her vaccine. The day after she got a temperature of 101 and flu like symptoms for 1.5 days (had with previous shots in this series). The second day she felt draggy, just not well. The 3rd day the patient got vertigo. She was out in her yard gardening, and it was so severe that when she bent over to turn on a faucet, she fell down in the yard. She got her vaccine on a Thursday and went to see her physician the following Tuesday due to continued vertigo. Her physician told her it would just have to run it's course. She is still having vertigo and when she closes her eyes feels like she can't stand.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: unknown
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2327265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: IN
Alter: 60,0
Geschlecht: M
Eingang: 22.06.2022
Impfdatum: 16.06.2022
Beginn: 17.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Computerised tomogram head normal Fall Lymphadenopathy Malaise Neurological symptom Nodule Pulmonary mass Skin test Ultrasound abdomen abnormal

Symptomtext

Patient experienced a fall approximatly 2 hours after the vaccine was administered. He appeared to have "stroke like" symptoms and complained of "not feeling well".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: It is noted that ultrasound at the hospital ( 6/18/22 ) shows "a prominent nodule measuring 4.1x2.4 cm adjacent to the pancreas." 6/17/2022 CT of head i snegative for acute findings. Calcified atherosclerosis throughout internal acrotid arteries. Scattered nodules throughout lungs . "New prominent lymph nodes throughout thre visualized upper mediastinum which could be reactive or could represent nodal metastatic disease as the patient has a history of malinancy." " Bulky right supraclavicular lymhadenopathy which is suspicious for nodal metatatic disease or less likely lymphoma.
Aktuelle Erkrankungen: GERD, Esophageal Ulcer w/o Bleeding, ASHD, Epilepsy, Weakness
Vorgeschichte: -
Andere Medikamente: Lamictal XR 200mg, Pantropazole 40mg, Sucralfate 1GM, TB Skin test administered 6/10/22. LFA Lot # 5077
Allergien: NKA
Vorherige Impfungen: -

VAERS 2326719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: AL
Alter: 75,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 16.06.2022
Beginn: 18.06.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / LA

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

Body temperature Chills Choking Dizziness Heart rate increased Heart rate irregular Nasal congestion Oxygen saturation Pyrexia Thermal burns of eye Vision blurred

Symptomtext

choking; Eye burn; Chills; low grade fever [99. - 101]; Fast pulse [114]; Oxygen 91; Eyes burn and are blurry; choking from nasal congestion; Slightly dizzy; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 75-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Jun2022 at 15:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 75 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Severe Scoliosis" (unspecified if ongoing); "Severe Spinal Stenosis" (unspecified if ongoing), notes: [Auto Acc. 7/1994]. The patient took concomitant medications. Vaccination history included: BNT162b2 ([{prev_dose_product=COVID 19,, prev_dose_brand=Pfizer FE 3590,, prev_dose_brand_unknown=False,, prev_dose_lot_number=FE3590,, prev_dose_lot_unknown=False,, prev_dose_administration_date=20Oct2021,, prev_dose_administration_time=02:45 PM,, prev_dose_dose_number=3,, prev_dose_vaccine_location=Left arm},), administration date: 20Oct2021, when the patient was 75-year-old, for COVID-19 immunization; BNT162b2 ({prev_dose_product=COVID 19,, prev_dose_brand=Pfizer ER6734,, prev_dose_brand_unknown=False,, prev_dose_lot_number=ER8734,, prev_dose_lot_unknown=False,, prev_dose_administration_date=08Apr2021,, prev_dose_administration_time=01:00 PM,, prev_dose_dose_number=2,, prev_dose_vaccine_location=Left arm},), administration date: 08Apr2021, when the patient was 74-year-old, for COVID-19 immunization; BNT162b2 ({prev_dose_product=COVID 19,, prev_dose_brand=Pfizer EN6206,, prev_dose_brand_unknown=False,, prev_dose_lot_number=EN6206,, prev_dose_lot_unknown=False,, prev_dose_administration_date=18Mar2021,, prev_dose_administration_time=02:30 PM,, prev_dose_dose_number=1,, prev_dose_vaccine_location=Left arm}]), administration date: 18Mar2021, when the patient was 74-year-old, for COVID-19 immunization. The following information was reported: CHILLS (non-serious) with onset 18Jun2022 at 02:30, outcome "not recovered"; THERMAL BURNS OF EYE (medically significant) with onset 18Jun2022 at 02:30, outcome "not recovered", described as "Eye burn"; VISION BLURRED (non-serious) with onset 18Jun2022 at 02:30, outcome "not recovered", described as "Eyes burn and are blurry"; HEART RATE INCREASED (non-serious) with onset 18Jun2022 at 02:30, outcome "not recovered", described as "Fast pulse [114]"; OXYGEN SATURATION (non-serious) with onset 18Jun2022 at 02:30, outcome "not recovered", described as "Oxygen 91"; DIZZINESS (non-serious) with onset 18Jun2022 at 02:30, outcome "not recovered", described as "Slightly dizzy"; CHOKING (medically significant) with onset 18Jun2022 at 02:30, outcome "recovered" (Jun2022); NASAL CONGESTION (non-serious) with onset 18Jun2022 at 02:30, outcome "recovered" (Jun2022), described as "choking from nasal congestion"; PYREXIA (non-serious) with onset 18Jun2022 at 02:30, outcome "not recovered", described as "low grade fever [99. - 101]". The patient underwent the following laboratory tests and procedures: Body temperature: (18Jun2022) 99. - 101; Heart rate irregular: (18Jun2022) Fast; Oxygen saturation: (18Jun2022) 91. Therapeutic measures Therapeutic measures Tylenol 500, Benadryl were taken as a result of choking, thermal burns of eye, chills, pyrexia, heart rate increased, oxygen saturation, vision blurred, nasal congestion, dizziness. Clinical course: It was reported that Facility type vaccine was pharmacy or drug store; patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient received other medication in two weeks. The patient did not have COVID prior vaccination and post vaccination, patient was not tested for COVID. Chills, low grade fever [99. - 101] two days.Fast pulse [114]. Oxygen 91. Tires. Eyes burn and are blurry. Slightly dizzy. Woke up on my back choking from nasal congestion. Improved with Benadryl & 500mg Tylenol, Treatment included Tylenol 500, Benadryl 4-6 hours, rest, fluids. [My husband is physician or I would go to ER]

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Date: 20220618; Test Name: low grade fever; Result Unstructured Data: Test Result:99. - 101; Test Date: 20220618; Test Name: Pulse [114]; Result Unstructured Data: Test Result:Fast; Test Date: 20220618; Test Name: Oxygen; Result Unstructured Data: Test Result:91
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Scoliosis; Spinal stenosis ([Auto Acc. 7/1994])
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2324168

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: FL
Alter: 36,0
Geschlecht: F
Eingang: 20.06.2022
Impfdatum: 10.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Eye swelling Pruritus

Symptomtext

Patient reports no immediate reaction after vaccination on friday the 10th. Said monday morning afterward her left eye was swollen, and throughout the day the rest of her face including her right eye got more swollen, and her arms/rest of body were red and itchy. Patient said she consulted a nursing friend, took benadryl, and the symptoms were relieved in the next 24-48 hours.

Weitere VAERSDATA-Felder

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

VAERS 2323928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fp7135

mild

Staat: WI
Alter: 23,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 16.06.2022
Beginn: 17.06.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site mass

Symptomtext

Quarter sized lump under skin at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site mass
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cold
Vorgeschichte: -
Andere Medikamente: -
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2323828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fp7135

mild

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 11.06.2022
Beginn: 11.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Fatigue Myalgia Pyrexia Vomiting

Symptomtext

low grade fever; muscle aches; vomiting all night; fatigue; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 11Jun2022 at 10:15 as dose 4 (booster), single (Lot number: Fp7135) at the age of 69 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Ms" (unspecified if ongoing); "chronic kidney disease" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "hasimotos thyroid" (unspecified if ongoing); "known allergies: Erythromycin" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN; LOSARTIN; LEVOTHYROXINE; B12 [CYANOCOBALAMIN]; D3; PRILOSEC [OMEPRAZOLE], 83 (as reported). Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: En6202, Location of administration: Right arm), administration date: 28Feb2021, when the patient was 67-year-old, for Covid-19 immunization; BNT162b2 (DOSE 2, SINGLE, Lot number: En6204, Location of administration: Right arm), administration date: 21Mar2021, when the patient was 67-year-old, for Covid-19 immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE , Lot number: 30130aa, Location of administration: Right arm), administration date: 04Oct2021, when the patient was 68-year-old, for Covid-19 immunization. The following information was reported: FATIGUE (non-serious) with onset 11Jun2022 at 12:00, outcome "recovered" (Jun2022); PYREXIA (non-serious) with onset 11Jun2022 at 12:00, outcome "recovered" (Jun2022), described as "low grade fever"; MYALGIA (non-serious) with onset 11Jun2022 at 12:00, outcome "recovered" (Jun2022), described as "muscle aches"; VOMITING (non-serious) with onset 11Jun2022 at 12:00, outcome "recovered" (Jun2022), described as "vomiting all night". Therapeutic measures were not taken as a result of pyrexia, myalgia, vomiting, fatigue. Additional information: The facility type vaccine was Pharmacy or Drug Store. The patient had not received any other vaccines within 4 weeks. Prior to vaccination, the patient was not diagnosed as COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to antibiotics; Blood pressure high; Chronic kidney disease; Hashimoto's thyroiditis; MS
Andere Medikamente: METFORMIN; LOSARTIN; LEVOTHYROXINE; B12 [CYANOCOBALAMIN]; D3; PRILOSEC [OMEPRAZOLE]
Allergien: -
Vorherige Impfungen: -

VAERS 2317475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 10.06.2022
Beginn: 10.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Body temperature Deafness Discomfort Headache Pain Deafness unilateral Ear disorder Hyperacusis Nausea Pain in extremity Immunisation Off label use Tinnitus Pyrexia

Symptomtext

I lost my hearing after having the vaccine on my left side; I now have a high pitch sound on my left ear; I have sensitivity to sound; 2nd booster dose.; 2nd booster dose.; 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 59-year-old female patient received BNT162b2 (COMIRNATY), on 10Jun2022 at 16:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 59 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: Covid-19 vaccine (Dose 3), for Covid-19 immunization; Covid-19 vaccine (Dose 2), for Covid-19 immunization; Covid-19 vaccine (Dose 1), for Covid-19 immunization. The following information was reported: OFF LABEL USE (medically significant), IMMUNISATION (medically significant) all with onset 10Jun2022 at 16:00, outcome "unknown" and all described as "2nd booster dose."; EAR DISORDER (non-serious) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I have sensitivity to sound"; DEAFNESS (medically significant) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I lost my hearing after having the vaccine on my left side"; TINNITUS (non-serious) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I now have a high pitch sound on my left ear". Therapeutic measures were taken as a result of deafness, tinnitus, ear disorder. Clinical Course: Caller called to report an adverse reaction she experienced with 2nd booster dose of the Pfizer Covid19 vaccine she received last Friday, 10June2022. I lost my hearing after having the vaccine on my left side, now have a high pitch sound on my left ear and have sensitivity to sound. Caller stated that she did not have any questions regarding the vaccine and that she wanted to report the adverse reaction she experienced with the booster dose. Transferring agent stated, "I do have a patient on the other line. This one is for the Pfizer COVID-19 vaccine second booster dose she said that she get this last Friday and has experienced adverse reaction for the vaccine, for the booster dose rather." Adverse reactions: Transferring agent stated, "She didn't say that to me and she just wanted to report it directly so, I transferred her immediately to you." On Paraphrasing: Consumer stated, "Yes, is this call being recorded? Good. I think it's horrible that Pfizer with all of the money they are making from this is using labor, from the third world country to get this information. Just once again more company greed. So, what would you like to know." Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2317475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 10.06.2022
Beginn: 10.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Body temperature Deafness Discomfort Headache Pain Deafness unilateral Ear disorder Hyperacusis Nausea Pain in extremity Immunisation Off label use Tinnitus Pyrexia

Symptomtext

I lost my hearing after having the vaccine on my left side; I now have a high pitch sound on my left ear; I have sensitivity to sound; 2nd booster dose.; 2nd booster dose.; 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 59-year-old female patient received BNT162b2 (COMIRNATY), on 10Jun2022 at 16:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 59 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: Covid-19 vaccine (Dose 3), for Covid-19 immunization; Covid-19 vaccine (Dose 2), for Covid-19 immunization; Covid-19 vaccine (Dose 1), for Covid-19 immunization. The following information was reported: OFF LABEL USE (medically significant), IMMUNISATION (medically significant) all with onset 10Jun2022 at 16:00, outcome "unknown" and all described as "2nd booster dose."; EAR DISORDER (non-serious) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I have sensitivity to sound"; DEAFNESS (medically significant) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I lost my hearing after having the vaccine on my left side"; TINNITUS (non-serious) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I now have a high pitch sound on my left ear". Therapeutic measures were taken as a result of deafness, tinnitus, ear disorder. Clinical Course: Caller called to report an adverse reaction she experienced with 2nd booster dose of the Pfizer Covid19 vaccine she received last Friday, 10June2022. I lost my hearing after having the vaccine on my left side, now have a high pitch sound on my left ear and have sensitivity to sound. Caller stated that she did not have any questions regarding the vaccine and that she wanted to report the adverse reaction she experienced with the booster dose. Transferring agent stated, "I do have a patient on the other line. This one is for the Pfizer COVID-19 vaccine second booster dose she said that she get this last Friday and has experienced adverse reaction for the vaccine, for the booster dose rather." Adverse reactions: Transferring agent stated, "She didn't say that to me and she just wanted to report it directly so, I transferred her immediately to you." On Paraphrasing: Consumer stated, "Yes, is this call being recorded? Good. I think it's horrible that Pfizer with all of the money they are making from this is using labor, from the third world country to get this information. Just once again more company greed. So, what would you like to know." Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2317475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 18.06.2022
Impfdatum: 10.06.2022
Beginn: 10.06.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

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

Body temperature Deafness Discomfort Headache Pain Deafness unilateral Ear disorder Hyperacusis Nausea Pain in extremity Immunisation Off label use Tinnitus Pyrexia

Symptomtext

I lost my hearing after having the vaccine on my left side; I now have a high pitch sound on my left ear; I have sensitivity to sound; 2nd booster dose.; 2nd booster dose.; 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 59-year-old female patient received BNT162b2 (COMIRNATY), on 10Jun2022 at 16:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 59 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: Covid-19 vaccine (Dose 3), for Covid-19 immunization; Covid-19 vaccine (Dose 2), for Covid-19 immunization; Covid-19 vaccine (Dose 1), for Covid-19 immunization. The following information was reported: OFF LABEL USE (medically significant), IMMUNISATION (medically significant) all with onset 10Jun2022 at 16:00, outcome "unknown" and all described as "2nd booster dose."; EAR DISORDER (non-serious) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I have sensitivity to sound"; DEAFNESS (medically significant) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I lost my hearing after having the vaccine on my left side"; TINNITUS (non-serious) with onset 11Jun2022 at 07:35, outcome "unknown", described as "I now have a high pitch sound on my left ear". Therapeutic measures were taken as a result of deafness, tinnitus, ear disorder. Clinical Course: Caller called to report an adverse reaction she experienced with 2nd booster dose of the Pfizer Covid19 vaccine she received last Friday, 10June2022. I lost my hearing after having the vaccine on my left side, now have a high pitch sound on my left ear and have sensitivity to sound. Caller stated that she did not have any questions regarding the vaccine and that she wanted to report the adverse reaction she experienced with the booster dose. Transferring agent stated, "I do have a patient on the other line. This one is for the Pfizer COVID-19 vaccine second booster dose she said that she get this last Friday and has experienced adverse reaction for the vaccine, for the booster dose rather." Adverse reactions: Transferring agent stated, "She didn't say that to me and she just wanted to report it directly so, I transferred her immediately to you." On Paraphrasing: Consumer stated, "Yes, is this call being recorded? Good. I think it's horrible that Pfizer with all of the money they are making from this is using labor, from the third world country to get this information. Just once again more company greed. So, what would you like to know." Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2323510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: WA
Alter: 27,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 15.06.2022
Beginn: 15.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site swelling

Symptomtext

redness and swelling at injection site for 2 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: depression
Andere Medikamente: oxycodone 5mg, acetaminophen 500mg, promethazine 25mg, cephalexin 500mg, ibuprofen 600mg,
Allergien: NKA
Vorherige Impfungen: -

VAERS 2323382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 15.06.2022
Beginn: 16.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Headache Limb discomfort Lymphadenopathy

Symptomtext

Patient presented to pharmacy this morning around 930am stating she woke up on day 2 with her lymph node under her left arm totally swollen and uncomfortable along with a headache in the back of her head on the right side. She said the swelling had continued into today along with the headache. The swelling is on the side where the covid shot was given...NOT the other two shots. I recommended she go to her dr or urgent care to follow up but she is visiting and has no insurance here and didn't want to go in. She wanted to know if lymphadenopathy was an adverse effect of the shot. It shows less than 2% however I still recommended she go be checked out due to her history and headache. She said she had taken Motrin and/or APAP for headache. Told her if she won't go in then if symptoms worsen or she gets fever she definitely needs to go in. She wished to just monitor at this time due to insurance being in another country and she is supposed to be heading back and she can see her Dr. at that time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: pt has a hx of lung cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: PA
Alter: 21,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 04.06.2022
Beginn: 05.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Headache

Symptomtext

No treatment. Significant headaches happening daily since last vaccine dose administered. Dizziness is accompanied with the severe headaches.

Weitere VAERSDATA-Felder

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

VAERS 2321928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

mild

Staat: MI
Alter: 74,0
Geschlecht: F
Eingang: 16.06.2022
Impfdatum: 11.06.2022
Beginn: 11.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Headache Peripheral swelling

Symptomtext

Patient called pharmacy on 6/16/22 to report that she developed a headache and swelling in her feet after receiving vaccine on 6/11/22. Swelling has gone down slightly. Patient was advised to inform her PCP right away for further evaluation.

Weitere VAERSDATA-Felder

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

VAERS 2320976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: AZ
Alter: 79,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 13.06.2022
Beginn: 13.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Cold sweat Nausea Vomiting

Symptomtext

Patient received Pfizer booster and Prevnar20 on 6/13 and began having severe nausea and vomiting, unable to keep even liquids down. No fever, just cold sweat. Advised patient to seek medical care due to concerns of dehydration. ER gave IV fluids, prescribed ondansetron. Patient felt better after receiving fluids but is nauseated again at home. ER physician suspects Prevnar.

Weitere VAERSDATA-Felder

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

VAERS 2320369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 14.06.2022
Beginn: 15.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Headache Pyrexia

Symptomtext

Headache, Fever

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Breast cancer
Vorgeschichte: -
Andere Medikamente: -
Allergien: Gluten
Vorherige Impfungen: -

VAERS 2320160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: GA
Alter: 58,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 11.06.2022
Beginn: 11.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Fatigue Lethargy

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Exhaustion / Lethargy-Mild

Weitere VAERSDATA-Felder

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

VAERS 2315608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 10.06.2022
Impfdatum: 08.06.2022
Beginn: 09.06.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SC / LA

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

Urticaria

Symptomtext

pt had whelps all over her body, under her arm pits, back, thighs, abdomen and arm. pt received whelps after 1 and 2nd booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: cancer survivor, remission
Vorgeschichte: pt had breast cancer, lumpectomy left, mastectomy right
Andere Medikamente: womens MVI, calcium with D
Allergien: codiene
Vorherige Impfungen: -

VAERS 2314563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: -
Alter: 17,0
Geschlecht: M
Eingang: 09.06.2022
Impfdatum: 06.06.2022
Beginn: 06.06.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

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

Dizziness Hyperhidrosis

Symptomtext

Patient felt dizziness once standing up to leave after waiting 10 min post vaccine. This resolved after lying on the ground and elevating his feet. He also experienced some sweating during the dizzy spell. After about 40 minutes, all his symptoms resolved.

Weitere VAERSDATA-Felder

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

VAERS 2313062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

mild

Staat: NY
Alter: 14,0
Geschlecht: F
Eingang: 08.06.2022
Impfdatum: 07.06.2022
Beginn: 07.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Cold sweat Feeling abnormal Nausea Vision blurred

Symptomtext

After about 10 minutes patient felt clammy, blurred vision and nauseous. She drank some water, sat on bench and tried to relax, was able to breathe but stated her vision was blurry and felt off. We called 911 and the paramedics took her vitals which were all normal and she felt better after some time. The paramedics did not take her to the hospital and believed she was very anxious after the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: Paramedics took patients vitals and were normal, the patient did not go to the hospital. She was able to walk and talk and her vision was back to normal.
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: none
Allergien: -
Vorherige Impfungen: -

VAERS 2728303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: IL
Alter: 55,0
Geschlecht: M
Eingang: 28.12.2023
Impfdatum: 29.07.2022
Beginn: 01.12.2023
Tage bis Beginn: 490,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a Consumer or other non HCP. A 57-year-old male patient received BNT162b2 (BNT162B2), on 29Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 55 years, in left arm for covid-19 immunisation; COVID-19 vaccine (COVID-19 VACCINE), as dose 1, single), as dose 2, single) and as dose 3 (booster), single) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2023, outcome "recovered" (Dec2023) and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Dec2023) Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19 with paxlovid from 10Dec2023 to 14Dec2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202312; Test Name: Covid-19 Virus test; 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 2718106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MN
Alter: 92,0
Geschlecht: F
Eingang: 27.11.2023
Impfdatum: 30.06.2022
Beginn: 21.11.2023
Tage bis Beginn: 509,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

hospitalization unrelated to COVID dx

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 6,0
Labordaten: 11/20/203 PCR positive
Aktuelle Erkrankungen: -
Vorgeschichte: HTN
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2675059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 0,3
Geschlecht: F
Eingang: 22.08.2023
Impfdatum: 29.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Expired product administered

Symptomtext

The patient was administered an expired dose of COVID-19 vaccine after the unfrozen date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2664139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 01.08.2023
Impfdatum: 06.06.2022
Beginn: 16.01.2023
Tage bis Beginn: 224,0
Dosis: 3
Route/Site: IM / LA

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

Dressler's syndrome

Symptomtext

PERICARDITIS POST ACUTE MI

Weitere VAERSDATA-Felder

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

VAERS 2663658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 31.07.2023
Impfdatum: 14.06.2022
Beginn: 14.01.2023
Tage bis Beginn: 214,0
Dosis: 3
Route/Site: IM / RA

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

Neuropathy peripheral

Symptomtext

NEUROPATHY

Weitere VAERSDATA-Felder

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

VAERS 2663598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 31.07.2023
Impfdatum: 02.07.2022
Beginn: 19.08.2022
Tage bis Beginn: 48,0
Dosis: 4
Route/Site: IM / RA

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

Hypoxia Symptom recurrence

Symptomtext

HYPOXIA 2/1/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2663588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 31.07.2023
Impfdatum: 02.07.2022
Beginn: 02.03.2023
Tage bis Beginn: 243,0
Dosis: 3
Route/Site: IM / LA

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

Angina unstable

Symptomtext

UNSTABLE ANGINA

Weitere VAERSDATA-Felder

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

VAERS 2663553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 31.07.2023
Impfdatum: 07.07.2022
Beginn: 29.10.2022
Tage bis Beginn: 114,0
Dosis: 5
Route/Site: IM / LA

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

Hypoxia Symptom recurrence

Symptomtext

HYPOXIA 11/8/2022, 1/15/2023, 1/7/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2663492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 42,0
Geschlecht: M
Eingang: 31.07.2023
Impfdatum: 14.07.2022
Beginn: 07.02.2023
Tage bis Beginn: 208,0
Dosis: 5
Route/Site: IM / LA

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

Hypoxia

Symptomtext

HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2662725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 28.07.2023
Impfdatum: 19.07.2022
Beginn: 13.02.2023
Tage bis Beginn: 209,0
Dosis: 2
Route/Site: IM / RA

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

Epilepsy

Symptomtext

EPILEPSY, INTRACTABLE

Weitere VAERSDATA-Felder

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

VAERS 2662706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 28.07.2023
Impfdatum: 22.07.2022
Beginn: 17.03.2023
Tage bis Beginn: 238,0
Dosis: 4
Route/Site: IM / LA

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

Obstructive sleep apnoea syndrome Symptom recurrence

Symptomtext

ADULT OBSTRUCTIVE SLEEP APNEA, MODERATE 2/28/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2662704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 28.07.2023
Impfdatum: 22.07.2022
Beginn: 27.02.2023
Tage bis Beginn: 220,0
Dosis: 4
Route/Site: IM / RA

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

Obstructive sleep apnoea syndrome

Symptomtext

ADULT OBSTRUCTIVE SLEEP APNEA, MODERATE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2661316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 26.07.2023
Impfdatum: 30.08.2022
Beginn: 13.02.2023
Tage bis Beginn: 167,0
Dosis: 4
Route/Site: IM / LA

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

Hypoxia Symptom recurrence

Symptomtext

HYPOXIA 1/6/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2660676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 25.07.2023
Impfdatum: 20.07.2022
Beginn: 03.12.2022
Tage bis Beginn: 136,0
Dosis: 3
Route/Site: - / -

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

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

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 3/4/21 lot# EN6206; Pfizer 3/22/21 lot# EN6206; Pfizer 7/20/22 lot# FP7135

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2648388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 22.06.2023
Impfdatum: 20.07.2022
Beginn: 06.02.2023
Tage bis Beginn: 201,0
Dosis: 4
Route/Site: IM / RA

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

Gastrooesophageal reflux disease Hypoxia Type 2 diabetes mellitus

Symptomtext

R09.02 HYPOXIA 4/19/2023 DM 2 WO COMPLICATIONS R09.02 HYPOXIA 4/19/2023 GERD COUNSELING

Weitere VAERSDATA-Felder

Praegender Schweregrund: Gastrooesophageal reflux disease
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2647579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 60,0
Geschlecht: M
Eingang: 21.06.2023
Impfdatum: 20.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old male patient received BNT162b2 (BNT162B2), on 20Jul2022 as dose 3 (booster), single (Lot number: FP7135) at the age of 60 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Chronic lymphocytic leukaemia" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative, notes: Paxlovid and testing negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient took paxlovid from 09Jun2023 to 15Jun2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300225165 Same patient, different drug/Event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 Test; Test Result: Negative ; Comments: Paxlovid and testing negative.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: CLL
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2645476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CO
Alter: -
Geschlecht: F
Eingang: 15.06.2023
Impfdatum: 21.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Anosmia Taste disorder

Symptomtext

lost her sense of smell; sense of taste is limited and makes eating quite unpleasant; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received BNT162b2 (BNT162B2), on 21Jul2022 as dose number unknown, single (Lot number: FP7135) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: ANOSMIA (non-serious) with onset 2022, outcome "unknown", described as "lost her sense of smell"; TASTE DISORDER (non-serious) with onset 2022, outcome "unknown", described as "sense of taste is limited and makes eating quite unpleasant". Additional information: Received the Pfizer vaccine on 21Jul2022. A few days after this vaccine patient lost her sense of smell. Her sense of taste is limited and makes eating quite unpleasant. It has been almost a year since this vaccine and her senses have not returned. She have never had COVID, only COVID vaccines. Her life is diminished due to this issue.

Weitere VAERSDATA-Felder

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

VAERS 2645214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 14.06.2023
Impfdatum: 04.08.2022
Beginn: 02.12.2022
Tage bis Beginn: 120,0
Dosis: 3
Route/Site: IM / RA

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

Hypersensitivity Prinzmetal angina

Symptomtext

PRINZMETAL ANGINA ALLERGIC REACTION, INIT

Weitere VAERSDATA-Felder

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

VAERS 2639663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 81,0
Geschlecht: F
Eingang: 01.06.2023
Impfdatum: 21.07.2022
Beginn: 29.08.2022
Tage bis Beginn: 39,0
Dosis: 4
Route/Site: IM / LA

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

Chronic respiratory failure Respiratory failure

Symptomtext

CHRONIC HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2635381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 51,0
Geschlecht: M
Eingang: 23.05.2023
Impfdatum: 08.08.2022
Beginn: 06.09.2022
Tage bis Beginn: 29,0
Dosis: 3
Route/Site: IM / RA

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

Chronic respiratory failure Respiratory failure

Symptomtext

CHRONIC HYPOXEMIC RESPIRATORY FAILURE

Weitere VAERSDATA-Felder

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

VAERS 2635380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 23.05.2023
Impfdatum: 25.07.2022
Beginn: 14.10.2022
Tage bis Beginn: 81,0
Dosis: 4
Route/Site: IM / LA

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

Angina unstable Symptom recurrence

Symptomtext

UNSTABLE ANGINA 11/16/2022 & 12/19/2022 -- RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

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

VAERS 2624172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 22.07.2022
Beginn: 27.04.2023
Tage bis Beginn: 279,0
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 1/26/21 Lot# EL3249; Pfizer 2/16/21 Lot# EN6200; Pfizer 10/6/21 Lot# Ew0183; Pfizer 7/22/22 Lot# FP7135

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2605007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 28.03.2023
Impfdatum: 01.08.2022
Beginn: 03.01.2023
Tage bis Beginn: 155,0
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 3/28/21 Lot# EN6207; Pfizer 4/23/21 Lot# EW0158 ;Pfizer 12/13/21 Lot# 33030BD; Pfizer 8/1/22 Lot# FP7135

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2588760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MO
Alter: 85,0
Geschlecht: M
Eingang: 28.02.2023
Impfdatum: 01.08.2022
Beginn: 15.02.2023
Tage bis Beginn: 198,0
Dosis: 4
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

unable to contact case following hospitalization

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 10,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2588111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: AZ
Alter: 70,0
Geschlecht: M
Eingang: 28.02.2023
Impfdatum: 29.06.2022
Beginn: 21.10.2022
Tage bis Beginn: 114,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Vaccine brand other=Moderna; This is a spontaneous report received from a contactable reporter(s) (Physician) from product quality group. The reporter is the patient. A 70-year-old male patient received BNT162b2 (BNT162B2), on 22Dec2020 as dose 1, single (Lot number: EH9899), on 12Jan2021 as dose 2, single (Lot number: EL1283), on 02Oct2021 as dose 3 (booster), single (Lot number: 30135BA) and on 29Jun2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 70 years for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 21Oct2022 as dose 5 (booster), single (Lot number: C52D22S) for covid-19 immunisation. The patient's relevant medical history included: "Benign Hypertension" (unspecified if ongoing), notes: Benign Hypertension. Concomitant medication(s) included: BYSTOLIC, start date: 01Dec2020; ROSUVASTIN, start date: 01Dec2020, stop date: 10Feb2023; LISINOPRIL, start date: 01Dec2020. The patient had no known allergies. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 21Oct2022, outcome "unknown", described as "Vaccine brand other=Moderna"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Feb2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 for which patient received PF-07321332, ritonavir (PAXLOVID) from to 10Feb2023 to 14Feb2023.; Sender's Comments: The efficacy of a vaccine varies from one patient to another and can be affected by different factors; however, a contributory role of the suspect vaccine product BNT162B2 to the reported events drug ineffective and COVID-19 cannot be ruled out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension (Benign Hypertension)
Andere Medikamente: BYSTOLIC; ROSUVASTIN; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 2582024

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MA
Alter: 61,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 15.06.2022
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; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Apr2021 at 14:00 as dose 1, single (Lot number: ER8729), in left arm, on 26Apr2021 at 14:00 as dose 2, single (Lot number: EW0175), in left arm, on 21Dec2021 at 14:00 as dose 3 (booster), single (Lot number: FH8030), in left arm and on 15Jun2022 at 14:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "osteoporosis"; "prediabetic". The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), outcome "unknown", COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of covid-19 and included treatment with PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Osteoporosis; Pre-diabetic
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2581547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 46,0
Geschlecht: F
Eingang: 14.02.2023
Impfdatum: 30.06.2022
Beginn: 04.01.2023
Tage bis Beginn: 188,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: "

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 3,0
Labordaten: Covid PCR detected on 01-04-2023
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular Hypotension Digestive Alcoholic hepatitis Erosive gastropathy Erosive esophagitis Pancreatic insufficiency Respiratory Influenza and pneumonia CAP (community acquired pneumonia) Urinary CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min Acute kidney injury superimposed on chronic kidney disease Renal mass, right Other Tobacco abuse Status post mitral valve annuloplasty H/O gastric ulcer Iron deficiency anemia due to chronic blood loss History of erosive esophagitis History of alcoholic gastritis with erosive gastropathy History of noncompliance with medical treatment, presenting hazards to health Acute on chronic anemia Hypomagnesemia Leukopenia Hyperglycemia Hypocalcemia Vitamin D deficiency Metabolic encephalopathy Malnutrition due to starvation Electrolyte abnormality Severe protein-calorie malnutrition Transaminitis Acute blood loss anemia Alcohol dependence Cachexia Alcohol abuse Abnormal CT scan Hyperkalemia Body mass index (BMI) less than 16.5 COVID-19 virus infection
Andere Medikamente: albuterol (PROVENTIL HFA,VENTOLIN HFA,PROAIR) 90 mcg/actuation inhaler 1-2 puffs every 4 (four) hours as needed. aspirin (LOW DOSE ASA) 81 mg EC tablet Take 1 tablet by mouth daily. cholecalciferol (VITAMIN D3) 125 mcg (5,000 unit) tab Ta
Allergien: DoxycyclineUnknown
Vorherige Impfungen: -

VAERS 2581112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 14.02.2023
Impfdatum: 06.07.2022
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

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter (Physician). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 06Jul2022 as DOSE 4 (BOOSTER), SINGLE (lot number: FP7135) at the age of 47 years old, administered in the left arm for COVID-19 immunization; Covid-19 vaccine (COVID-19 VACCINE), as DOSE 1, SINGLE (batch/lot number: unknown), as DOSE 2, SINGLE (batch/lot number: unknown) and as DOSE 3 (BOOSTER), SINGLE (batch/lot number: unknown) for COVID-19 immunization. The patient's relevant medical history included: "Depression" (unspecified if ongoing); "Knowm allergies: Penicillin" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19." The patient underwent the following laboratory tests and procedures: COVID-19 Test (SARS-CoV-2 test): Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of Drug ineffective, Covid-19.; Sender's Comments: 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 and COVID-19 cannot be ruled out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2573304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 01.02.2023
Impfdatum: 11.07.2022
Beginn: 29.12.2022
Tage bis Beginn: 171,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Confusional state Dementia Mental status changes SARS-CoV-2 test positive Vitamin B1 decreased

Symptomtext

Patient is a 74 y.o. female who presented from home on 12/12/2022 with altered mental status thought to be undiagnosed dementia. Expanded workup considered based on reported rapid progression but did not tolerate LP. Family elected to forego any further procedures. Found to have low B1 level. The patient was to be discharged on 12/30, though cancelled due to positive COVID test. During hospital course patient had remained pleasantly confused, out of COVID isolation 1/8. Patient discharged on 1/9/23.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 28,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560151

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: AR
Alter: 75,0
Geschlecht: M
Eingang: 14.01.2023
Impfdatum: 15.07.2022
Beginn: 21.09.2022
Tage bis Beginn: 68,0
Dosis: 1
Route/Site: IM / RA

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

Retinal vein occlusion Visual impairment

Symptomtext

The vaccine was administered 7/15/2022 and I had an eye stroke (ischemic retinal) on my right eye. I could only see through the bottom portion of my right eye. The top half was gray, completely non-transparent. After 15-20 minutes, the gray began to dissipate from right to left. Eye vision has been normal since the episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Retinal vein occlusion
Hospital-Tage: -
Labordaten: Optometrist examine my retina area and the photo showed the blood vessels on the bottom portion of my eye were not as robust as the top half. The Optometrist recommended I take an aspirin (81 mg) daily.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Simvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2554624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: TX
Alter: 50,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 08.07.2022
Beginn: 21.09.2022
Tage bis Beginn: 75,0
Dosis: 4
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

About two months after receiving the second booster of the Pfizer Covid vaccine, I started to have cold like symptoms. On 09/21/2022, I lost my sense of taste and smell. I performed an at home test and they were positive for COVID-19. I did not reach out to my GP because my symptoms were never severe enough to go to the doctor. My sense of taste and smell were only gone for about 24-48 hours. After that, I was able to taste and smell again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ageusia
Hospital-Tage: -
Labordaten: Covid-19
Aktuelle Erkrankungen: None
Vorgeschichte: Glaucoma; GERD; Sleep Apnea
Andere Medikamente: ALLEGRA; PRILOSEC; XALATAN eye drops; vitamin D3; vitamin E
Allergien: Sulfa; caffeine
Vorherige Impfungen: -

VAERS 2553943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 45,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 30,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 13,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 73,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553935

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 51,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 48,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 60,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 52,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553926

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 12,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553925

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 48,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 26,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 82,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 22,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 19,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 51,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 13,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 47,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 30,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 38,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 14,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 14,0
Geschlecht: M
Eingang: 09.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 67,0
Geschlecht: F
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 58,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 37,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 50,0
Geschlecht: F
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 69,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 36,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 50,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 13,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 15,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 15,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 31,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 72,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 70,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 69,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 53,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553773

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 16,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 63,0
Geschlecht: M
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 17,0
Geschlecht: F
Eingang: 08.01.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
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

Incorrect vaccine type, administered monovalent COVID19 dose instead of bivalent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2537811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: AR
Alter: 36,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 28.07.2022
Beginn: 18.12.2022
Tage bis Beginn: 143,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

hospitalized with covid; fully vaccinated

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 1,0
Labordaten: positive covid pcr 12/18/22
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2535197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 10.06.2022
Beginn: 18.08.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: SYR / LA

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

Atrial fibrillation Electrocardiogram normal

Symptomtext

In August I was diagnosed with Afib in which my doctor checked my heart with an EKG and my heart was fine. I was put on Metroprolol 50 mg. The medication appears to be working keeping my blood pressure down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial fibrillation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Coughing
Andere Medikamente: Synthroid 0.200mg, D3 3000iu, Multivitamin, Simvastatin 40mg, Fish Oil 1200mg, Plaquenil 400mg, Folic Acid 1mg, Arimidex 1mg, Vitamin B12, Bupropion HCL ER 300mg, Methotrexate 10mg weekly, Metoprolol 50mg, Lexapro 20Klonopin and Relpax
Allergien: NKA
Vorherige Impfungen: -

VAERS 2533714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 28.06.2022
Beginn: 22.10.2022
Tage bis Beginn: 116,0
Dosis: 3
Route/Site: - / LA

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

Herpes zoster SARS-CoV-2 test

Symptomtext

Shingles on left side of neck & left ear lobe; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jun2022 as dose 3 (booster), single (Lot number: FP7135) at the age of 54 years, in left arm for covid-19 immunisation. Patient was not pregnant at time of vaccination. The patient's relevant medical history included: "Sulfites Allergy" (unspecified if ongoing), notes: Known allergies: sulfites. Concomitant medication(s) included: FISH OIL [EICOSAPENTAENOIC ACID]; VITAMIN B12 [CYANOCOBALAMIN]. Other medication details reported as might have taken EPA/DHA fish oil, vitamin B12. DK. Vaccination history included: BNT162b2 (lot number: FT1614, dose number 2, vaccine location Left arm), administration date: 28Jan2022, when the patient was 54-year-old, for COVID-19 immunization; BNT162b2 (lot number 33130BA, dose number 1, vaccine location Left arm), administration date: 07Jan2022, when the patient was 54-year-old, for COVID-19 immunization. The following information was reported: HERPES ZOSTER (non-serious) with onset 22Oct2022, outcome "recovered" (2022), described as "Shingles on left side of neck & left ear lobe". The event "shingles on left side of neck & left ear lobe" required physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of herpes zoster. Additional information: Treatment included antibiotics & then antivirals with antibiotics. If other vaccine in four weeks reported as no.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: Test Date: 20221207; Test Name: Covid-19 test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy (Known allergies: sulfites)
Andere Medikamente: FISH OIL [EICOSAPENTAENOIC ACID]; VITAMIN B12 [CYANOCOBALAMIN]
Allergien: -
Vorherige Impfungen: -

VAERS 2533355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NC
Alter: 57,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 11.08.2022
Beginn: 01.09.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Computerised tomogram normal Electromyogram normal Immunisation reaction Magnetic resonance imaging normal Monoplegia Nervous system disorder Neuralgic amyotrophy

Symptomtext

A couple of weeks after the Pfizer covid injection in left arm I started to develop partial paralysis in my left arm as well as denervation and loss of strength, all originating in the scapula area. Three physicians, including a physiatrist, neurosurgeon and orthopedic surgeon all state that my malady was/is Parsonage Turner Syndrome and that it was caused by the vaccine. All other possible diagnoses were eliminated via many physical exams, MRIs, CTs, and EMGs. We are over three months out now and no change. Treatment is prednisone and lots of PT along with finger crossing and hope that the effects will one day pass.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: Several MRIs, CTs, EMGs, all in the last few months. I dont know the exact dates but can get them if needed.
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 2507260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: OH
Alter: 51,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 11.07.2022
Beginn: 03.09.2022
Tage bis Beginn: 54,0
Dosis: 3
Route/Site: SYR / LL

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

One week after COVID-19 vaccine, had to get a one week Rabies shot. Dr. decided to give an antibody treatment instead of PAXLOVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Home COVID-19 test positive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes; Hypertension.
Andere Medikamente: Metformin; lisinopril; vitamin B12; ONGLYZA; rosuvastatin; armor thyroid; metoprolol; ZYRTEC; MUCINEX; LANTUS; lispro.
Allergien: TYLENOL
Vorherige Impfungen: -

VAERS 2506538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: TX
Alter: 55,0
Geschlecht: F
Eingang: 12.11.2022
Impfdatum: 26.06.2022
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; 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 55-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 24Oct2021 as dose 3 (booster), single (Lot number: FF2593), in left arm and on 26Jun2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 55 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 11Jan2021 as dose 1, single (Lot number: 041L20A), in left arm and on 08Feb2021 as dose 2, single (Lot number: 0271n20A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: PCN" (unspecified if ongoing); "Von Willowbrande type 2A bleeding disorder" (unspecified if ongoing); "Celiac" (unspecified if ongoing); "feral cat bite" (unspecified if ongoing), notes: just took 5 rabies vaccines and immuglobin for a sick, feral cat bite. Concomitant medication(s) included: ESCITALOPRAM, start date: 01Feb2022; PROGESTERONE, start date: 01Feb2022; ESTRADIOL, start date: 01Oct2021. Past drug history included: Known allergies: cipro, reaction(s): "Known allergies: cipro"; Known allergies: keflex, reaction(s): "Known allergies: keflex"; Known allergies: amoxicillin, reaction(s): "Known allergies: amoxicillin". Vaccination history included: Rabies vaccines (just took 5 rabies vaccines and immuglobin for a sick, feral cat bite.), for IMMUNIZATION; Immuglobin (just took 5 rabies vaccines and immuglobin for a sick, feral cat bite.), for IMMUNIZATION; Just took 5 rabies vaccines (just took 5 rabies vaccines and immuglobin for a sick, feral cat bite.), for Immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Product: COVID19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient took other medication in two weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid test; Test Result: Positive ; Comments: Product: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cat bite (just took 5 rabies vaccines and immuglobin for a sick feral cat bite.); Celiac disease; Penicillin allergy; Von Willebrand's disease
Andere Medikamente: ESCITALOPRAM; PROGESTERONE; ESTRADIOL
Allergien: -
Vorherige Impfungen: -

VAERS 2502099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: IL
Alter: 44,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
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 No adverse event

Symptomtext

Patient was given an expired dose of Pfizer Covid vaccine. Patient has not reported any adverse reaction but lab staff realized it was expired after administering vaccine. Vaccine expired on 10/31/2022 and vaccine was administered on 11/1/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension sleep apnea asymptomatic microscopic hematuria hypertriglyceridemia
Andere Medikamente: Cetirizine Olmesartan-hydrochlorothiazide
Allergien: none
Vorherige Impfungen: -

VAERS 2495237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: IL
Alter: 48,0
Geschlecht: M
Eingang: 01.11.2022
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 No adverse event

Symptomtext

Patient received monovalent covid booster dose when monovalent booster is no longer recommended by the CDC as of this date. New bivalent booster is recommended instead. No adverse symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Major depressive disorder
Vorgeschichte: PMHx of alcohol and polysubstance use (heroin, cocaine, cannabis), MDD, panic attacks, anxiety unspecified
Andere Medikamente: -
Allergien: Chlorpromazine
Vorherige Impfungen: -

VAERS 2494002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 24,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / -

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

Expired product administered No adverse event

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2494001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 23,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / -

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

Expired product administered No adverse event

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2493997

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 38,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / -

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

Expired product administered

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2493995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 29,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / -

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

Expired product administered

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2493994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 34,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / -

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

No adverse event Product use issue

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

Weitere VAERSDATA-Felder

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

VAERS 2493981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 40,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / -

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

Expired product administered No adverse event

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2493978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 47,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / -

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

Expired product administered No adverse event

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2493976

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / -

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

Expired product administered No adverse event

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2493972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 27,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / -

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

Expired product administered No adverse event

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2493968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 38,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 27.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / -

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

Expired product administered No adverse event

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

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 2493945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 20,0
Geschlecht: M
Eingang: 31.10.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

No adverse event Product use issue

Symptomtext

Patient was administered the vaccine after the beyond use date, which was 8/15/2022. There was no symptoms or adverse reactions, however the vaccine was administered 12 days after its beyond use date.

Weitere VAERSDATA-Felder

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

VAERS 2491259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 84,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 29.01.2021
Beginn: 04.09.2022
Tage bis Beginn: 583,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Limb injury Motor dysfunction SARS-CoV-2 test positive

Symptomtext

09/04/22 presents to ED for "hand injury (motor skills issue)". PMHx of "DVT and PE"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 09/04/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2489522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: PA
Alter: 73,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 27.07.2022
Beginn: 30.08.2022
Tage bis Beginn: 34,0
Dosis: 4
Route/Site: - / -

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

Feeling abnormal Pollakiuria

Symptomtext

Urinary problems (urinary frequency); She is getting miserable here; 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 73-year-old female patient received BNT162b2 (BNT162B2), on 27Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 73 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "Pericarditis" (unspecified if ongoing), notes: When she was in her lower 20s she had pericarditis; "Knee arthritis problems" (unspecified if ongoing), notes: Knee arthritis problems. Concomitant medication(s) included: TYLENOL taken for arthritis. Vaccination history included: BNT162b2 (Dose: 1, LOT: FA6780 with no NDC/EXP provided), administration date: 14Jul2021, when the patient was 71-year-old, for COVID-19 immunization; BNT162b2 (Dose: 2, LOT: FA7680, no NDC/EXP provided), administration date: 04Aug2021, when the patient was 72-year-old, for COVID-19 immunization; BNT162b2 (Dose: 3, LOT: F36369 which she can't hardly read it how it was written), administration date: 27Jan2022, when the patient was 72-year-old, for COVID-19 immunization, reaction(s): "She is sickly, after she got the last, but not like when she got the first one", "After the first she was a little bit for a while"; flu shot (after the first booster which she got the Flu shot at the same time), administration date: 27Jan2022, when the patient was 72-year-old, for Immunization. The following information was reported: FEELING ABNORMAL (non-serious) with onset 2022, outcome "unknown", described as "She is getting miserable here"; POLLAKIURIA (non-serious) with onset 30Aug2022, outcome "not recovered", described as "Urinary problems (urinary frequency)". Additional information: She received the dose on 27Jul2022, 1 month after, on 30Aug2022, she started having urinary problems (urinary frequency). She wanted to know if this could be caused by the vaccine. She did not took other products. Consumer said she was concerned about a side effect she had since she took booster with Pfizer, she had the booster at the end of Jul. She wanted to know if urinary problems could be a side effect because she was concerned about something she heard on TV. She clarified it was the Pfizer COVID-19 vaccine booster. She said she first had two shots, and then the first booster, so the one she had problems after, that would have been the second booster. Her urinary problems trouble started about a month after the booster, she was not in pain or anything, she had urinary issues. She heard on TV last week for the booster there could be possible cancer or kidney stones and urinary tract infections, but she only heard part of the report. She was getting miserable here and was not sure if it could be the booster. She said she knows she was getting older, and this happened so quickly she does not know if there was some reason she was starting to have issues here. She was sickly, after she got the last, but not like when she got the first one. Caller does not clarify this statement. She said it took two weeks to get straightened out after the second booster, it was the worst, after the first she was a little bit for a while. She clarified after the first booster which she got the Flu shot at the same time, it did not affect her at all, she did not even have a sore arm. It happened after the second booster in late July, on 27Jul2022. Pfizer COVID-19 vaccine second booster adverse event It started 30Aug2022, it started while they were out and it has happened off and on ever since. She was not sickly, she doesn't have no temperature or nothing. She clarified her urinary problem was she has to urinate a lot, frequently, especially at night, so she was afraid to go anywhere. She doesn't have real pain. She was taking concomitant medications ever took was a little Tylenol for her knee arthritis problems, that has acted up for a few years, before getting the vaccines. Tylenol was the main thing she takes when she took it, she takes no prescriptions at all. No further details were provided about the Tylenol that she takes sometimes. When she was in her lower 20s she had pericarditis one time, she was a young girl and doesn't remember when, it was over forty years ago. She had never heard of it but they told her if she had it in her life time, she won't get it again. No follow-up attempts are possible. No further information is expected

Weitere VAERSDATA-Felder

Praegender Schweregrund: Feeling abnormal
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Knee arthritis (Knee arthritis problems); Pericarditis (When she was in her lower 20s, she had pericarditis.)
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 2482207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 19.10.2022
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: nein

No adverse event Product storage error

Symptomtext

Vaccine stored outside of recommended storage temperatures for greater than 2 weeks and administered to patient. Manufacturer contacted. Patient did not experience signs or symptoms of adverse outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: codeine, metoclopramide
Vorherige Impfungen: -

VAERS 2482203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 19.10.2022
Impfdatum: 22.09.2022
Beginn: 22.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product storage error

Symptomtext

Vaccine stored outside of recommended storage temperatures for greater than 2 weeks and administered to patient. Manufacturer contacted. Patient did not experience signs or symptoms of adverse outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 2482199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 19.10.2022
Impfdatum: 31.08.2022
Beginn: 31.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

No adverse event Product storage error

Symptomtext

Vaccine stored outside of recommended storage temperatures for greater than 2 weeks and administered to patient. Manufacturer contacted. Patient did not experience signs or symptoms of adverse outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2482196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 80,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 05.08.2022
Beginn: 05.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

No adverse event Product storage error

Symptomtext

Vaccine stored outside of recommended storage temperatures for greater than 2 weeks and administered to patient. Manufacturer contacted. Patient did not experience signs or symptoms of adverse outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Tizanidine
Vorherige Impfungen: -

VAERS 2482195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 90,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 22.07.2022
Beginn: 22.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

No adverse event Product storage error

Symptomtext

Vaccine stored outside of recommended storage temperatures for greater than 2 weeks and administered to patient. Manufacturer contacted. Patient did not experience signs or symptoms of adverse outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Ciprofloxacin, Diazepam, Erythromycin, Indocin [Indomethacin], Iodine And Iodide Containing Products, Penicillins
Vorherige Impfungen: -

VAERS 2482191

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 18.10.2022
Impfdatum: 19.07.2022
Beginn: 19.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

No adverse event Product storage error

Symptomtext

Vaccine stored outside of recommended storage temperatures for greater than 2 weeks and administered to patient. Manufacturer contacted. Patient did not experience signs or symptoms of adverse outcome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 07.07.2022
Beginn: 08.10.2022
Tage bis Beginn: 93,0
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 after three vaccines

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2473167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 05.07.2022
Beginn: 07.07.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2469445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 05.10.2022
Impfdatum: 10.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 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). The reporter is the patient. A 59-year-old male patient received BNT162b2 (BNT162B2), on 26Feb2021 as dose 1, single (Lot number: EN6021), on 25Mar2021 as dose 2, single (Lot number: FR2613), in left arm, on 27Sep2021 as dose 3 (booster), single (Lot number: 3C1308A), in left arm and on 10Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Sleep Apnea" (unspecified if ongoing); "Degenerative Disc Disease" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Known allergies : penicillin" (unspecified if ongoing), notes: Known allergies : penicillin; Sulfa; "Known allergies : Sulfa" (unspecified if ongoing), notes: Known allergies : penicillin; Sulfa. Concomitant medication(s) included: LIPITOR; NYQUIL; SUDAFED 12 HOUR. 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: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Course: Other medication in 2weeks reported as Lipitor, Nyquill and Sudafed. Patient received Paxlovid treatment from 23Sep2022 to 28Sep2022.

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: Degenerative disc disease; Hypertension; Penicillin allergy (Known allergies : penicillin; Sulfa); Sleep apnea; Sulfonamide allergy (Known allergies : penicillin; Sulfa)
Andere Medikamente: LIPITOR; NYQUIL; SUDAFED 12 HOUR
Allergien: -
Vorherige Impfungen: -

VAERS 2466916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 75,0
Geschlecht: M
Eingang: 02.10.2022
Impfdatum: 26.08.2022
Beginn: 26.08.2022
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

Patient was given vaccine that was beyond "use by" date of 8/16/22. Patient did not experience any adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2466913

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 28,0
Geschlecht: F
Eingang: 02.10.2022
Impfdatum: 30.08.2022
Beginn: 30.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Expired product administered No adverse event

Symptomtext

Patient was given vaccine past "use by" date of 8/16/22. patient did not experience any adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Acetaminophen
Vorherige Impfungen: -

VAERS 2466911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fp7135

gering

Staat: FL
Alter: 76,0
Geschlecht: F
Eingang: 02.10.2022
Impfdatum: 24.08.2022
Beginn: 24.08.2022
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

Symptomtext

Patient was given vaccine that was past its "use by" date of 8/16/22. patient did not report any adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2466910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 72,0
Geschlecht: F
Eingang: 02.10.2022
Impfdatum: 31.08.2022
Beginn: 31.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Expired product administered

Symptomtext

Patient was given vaccine that was beyond "use by" date of 8/16/22. Patient did not report any signs or symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: pneumovax23
Vorherige Impfungen: -

VAERS 2466907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 15,0
Geschlecht: F
Eingang: 02.10.2022
Impfdatum: 25.08.2022
Beginn: 25.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given vaccine that was beyond its "use by" date. Patient was contacted by pharmacy with no response.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2466904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 17,0
Geschlecht: F
Eingang: 02.10.2022
Impfdatum: 25.08.2022
Beginn: 25.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given a vaccine that was beyond "use by" date of 8/16/22. Patient was contacted by pharmacy supervisor and was not reached.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2466901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 23,0
Geschlecht: M
Eingang: 02.10.2022
Impfdatum: 22.08.2022
Beginn: 22.08.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given vaccine that was past "use by" date of 8/16/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2465267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WA
Alter: 44,0
Geschlecht: F
Eingang: 30.09.2022
Impfdatum: 27.06.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / RA

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

COVID-19 Incorrect dose administered Interchange of vaccine products SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Interchange of vaccine products; Inappropriate dose of Vaccine administered; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27Mar2021 as dose 1, single (Lot number: ER8730), in right arm, on 17Apr2021 as dose 2, single (Lot number: EW0161), in left arm, on 18Aug2021 as dose 3 (booster), single (Lot number: FD8448), in right arm and on 27Jun2022 at 13:00 as dose 5 (booster), single (Lot number: FP7135) at the age of 44 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 17Feb2022 as dose 4 (booster), single (Lot number: 031J21A), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Ankylosing Spondylitis" (unspecified if ongoing), notes: Other medical history: Ankylosing Spondylitis; "prolactinoma" (unspecified if ongoing), notes: Other medical history: Prolactinoma. Concomitant medication(s) included: COSENTYX, stop date: 09Sep2022; METHOTREXATE, stop date: 06Sep2022; MELOXICAM; LEXAPRO; CABERGOLINE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; FLONASE [FLUTICASONE PROPIONATE]; FOLIC ACID; VITAMIN D NOS. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown"; INCORRECT DOSE ADMINISTERED (non-serious), outcome "unknown", described as "Inappropriate dose of Vaccine administered". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19; Positive, notes: my rapid test went from the very faint line back up to strong positive result. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Course: The patient received COVID 19 Treatment Paxlovid on 16Sep2022 and stopped on 20Sep2022. Known allergies reported as No. Other medication in 2 weeks included Multivitamin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Name: rapid test; Test Result: Positive ; Comments: my rapid test went from the very faint line back up to strong positive result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Ankylosing spondylitis (Other medical history: Ankylosing Spondylitis); Prolactinoma (Other medical history: Prolactinoma)
Andere Medikamente: COSENTYX; METHOTREXATE; MELOXICAM; LEXAPRO; CABERGOLINE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; FLONASE [FLUTICASONE PROPIONATE]; FOLIC ACID; VITAMIN D NOS
Allergien: -
Vorherige Impfungen: -

VAERS 2464169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: OR
Alter: 50,0
Geschlecht: F
Eingang: 29.09.2022
Impfdatum: 02.06.2022
Beginn: 01.09.2022
Tage bis Beginn: 91,0
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

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 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Jun2022 at 16:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 50 years, in right 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) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hereditary elevated cholesterol" (unspecified if ongoing), notes: Hereditary elevated cholesterol; "Known allergies: Sulfa" (unspecified if ongoing), notes: Known allergies: Sulfa. Concomitant medication(s) included: SIMVASTATIN, start date: 01Jun2015, stop date: 14Sep2022. Past drug history included: Macrobid, reaction(s): "Known allergies: Macrobid". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Sep2022) Negative, notes: After Paxlovid treatment, felt fine and tested negative for two days; (Sep2022) Positive, notes: Then on the third day had mild sore throat and runny nose, tested and was positive again; (Sep2022) Negative, notes: After Paxlovid treatment, felt fine and tested negative for two days. Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202209; Test Name: Tested; Test Result: Negative ; Comments: After Paxlovid treatment, felt fine and tested negative for two days.; Test Date: 202209; Test Name: Tested; Test Result: Positive ; Comments: Then on the third day had mild sore throat and runny nose, tested and was positive again.; Test Date: 202209; Test Name: Tested; Test Result: Negative ; Comments: After Paxlovid treatment, felt fine and tested negative for two days.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol (Hereditary elevated cholesterol); Sulfonamide allergy (Known allergies: Sulfa)
Andere Medikamente: SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2462478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: AZ
Alter: 54,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 01.08.2022
Beginn: 01.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Vaccine was administered after 10 week received date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2461840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 49,0
Geschlecht: U
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered Incorrect product formulation administered

Symptomtext

Accidentally administered Pfizer monovalent when patient came to get booster dose. Error realized shortly post administration, patient counseled and given bivalent dose during same visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Moderate episode of recurrent major depressive disorder Chronic idiopathic constipation Dyslipidemia Essential hypertension PTSD (post-traumatic stress disorder) Insomnia HIV disease BMI 36.0-36.9,adult Gender dysphoria Lateral collateral ligament deficiency of left knee Tinea pedis of left foot Abnormal granulation tissue
Andere Medikamente: multivit with minerals/lutein (MULTIVITAMIN 50 PLUS ORAL) polyethylene glycol 3350 (DULCOLAX BALANCE ORAL) fenofibrate micronized (LOFIBRA) 134 mg capsule abacavir-dolutegravir-lamivud (TRIUMEQ) 600-50-300 mg tab aspirin 81 mg DR tablet est
Allergien: Spironolactone Sulfa (Sulfonamide Antibiotics)
Vorherige Impfungen: -

VAERS 2461787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: KS
Alter: 32,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
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 2461752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: KS
Alter: 37,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
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 2461751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: KS
Alter: 29,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: UNK
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 2461748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: KS
Alter: 41,0
Geschlecht: F
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
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 2461747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: KS
Alter: 37,0
Geschlecht: M
Eingang: 27.09.2022
Impfdatum: 23.09.2022
Beginn: 23.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / 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 2460420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 75,0
Geschlecht: M
Eingang: 26.09.2022
Impfdatum: 25.07.2022
Beginn: 24.09.2022
Tage bis Beginn: 61,0
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 9/25/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 40,0
Geschlecht: M
Eingang: 23.09.2022
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: ja Erholt: nein

Incorrect product formulation administered No adverse event

Symptomtext

Narrative: Wrong formulation of COVID-19 vaccine administered 09/01 FDA removes authorization to use monovalent COVID-19 (pfizer) vaccine as booster dose in individuals 12 and up, email communication sent to impacted staff 09/06 Pt administered COVID-19 (Pfizer) monovalent vaccine as booster dose instead of FDA approved bivalent booster No adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 23.09.2022
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: ja Erholt: nein

Incorrect product formulation administered No adverse event

Symptomtext

Narrative: Wrong formulation of COVID-19 vaccine administered 09/01 FDA removes authorization to use monovalent COVID-19 (pfizer) vaccine as booster dose in individuals 12 and up, email communication sent to impacted staff 09/06 Pt administered COVID-19 (Pfizer) monovalent vaccine as booster dose instead of FDA approved bivalent booster. No adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Narrative: Wrong formulation of COVID-19 vaccine administered 09/01 FDA removes authorization to use monovalent COVID-19 (pfizer) vaccine as booster dose in individuals 12 and up, email communication sent to impacted staff 09/06 Pt administered COVID-19 (Pfizer) monovalent vaccine as booster dose instead of FDA approved bivalent booster No adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2021
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Narrative: Wrong formulation of COVID-19 vaccine administered 09/01 FDA removes authorization to use monovalent COVID-19 (pfizer) vaccine as booster dose in individuals 12 and up, email communication sent to impacted staff 09/06 Pt administered COVID-19 (Pfizer) monovalent vaccine as booster dose instead of FDA approved bivalent booster No adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 23.09.2022
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: ja Erholt: nein

Incorrect product formulation administered No adverse event

Symptomtext

Narrative: Wrong formulation of COVID-19 vaccine administered 09/01 FDA removes authorization to use monovalent COVID-19 (pfizer) vaccine as booster dose in individuals 12 and up, email communication sent to impacted staff 09/06 Pt administered COVID-19 (Pfizer) monovalent vaccine as booster dose instead of FDA approved bivalent booster No adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 23.09.2022
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: ja Erholt: nein

Incorrect product formulation administered No adverse event

Symptomtext

Narrative: Wrong formulation of COVID-19 vaccine administered 09/01 FDA removes authorization to use monovalent COVID-19 (pfizer) vaccine as booster dose in individuals 12 and up, email communication sent to impacted staff 09/06 Pt administered COVID-19 (Pfizer) monovalent vaccine as booster dose instead of FDA approved bivalent booster No adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 50,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 06.09.2022
Beginn: 06.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Narrative: Wrong formulation of COVID-19 vaccine administered 09/01 FDA removes authorization to use monovalent COVID-19 (pfizer) vaccine as booster dose in individuals 12 and up, email communication sent to impacted staff 09/06 Pt administered COVID-19 (Pfizer) monovalent vaccine as booster dose instead of FDA approved bivalent booster No adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2658659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: -
Beginn: 06.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Narrative: Wrong formulation of COVID-19 vaccine administered 09/01 FDA removes authorization to use monovalent COVID-19 (pfizer) vaccine as booster dose in individuals 12 and up, email communication sent to impacted staff 09/06 Pt administered COVID-19 (Pfizer) monovalent vaccine as booster dose instead of FDA approved bivalent booster No adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2455938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 23.09.2022
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: ja

Incorrect product formulation administered

Symptomtext

The vaccine was given o 09/02/2022 @0900am. An email was sent on 09/02/2022 @ 1016am advising staff that the monovalent vaccine should not be given per CDC guidelines as of 09/01/2022. Patient made aware and will come back in 2 months for the bivalent vaccine. Provider is also aware and agreeable with the update

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Nervous Paresthesia of both feet Respiratory Allergic rhinitis due to pollen Vasomotor rhinitis Circulatory Varicose veins of lower extremity Digestive Vitamin D deficiency Gastro-esophageal reflux disease without esophagitis Musculoskeletal Disorder of bone and articular cartilage Endocrine/Metabolic Hypothyroidism Impaired fasting glucose Hyperlipidemia Other Hematochezia Dysthymia Dense breast tissue on mammogram
Vorgeschichte: Nervous Paresthesia of both feet Respiratory Allergic rhinitis due to pollen Vasomotor rhinitis Circulatory Varicose veins of lower extremity Digestive Vitamin D deficiency Gastro-esophageal reflux disease without esophagitis Musculoskeletal Disorder of bone and articular cartilage Endocrine/Metabolic Hypothyroidism Impaired fasting glucose Hyperlipidemia Other Hematochezia Dysthymia Dense breast tissue on mammogram
Andere Medikamente: albuterol HFA (ProAir HFA) 90 mcg/actuation inhaler Inhale 2 puffs. betamethasone valerate (VALISONE) 0.1 % cream APPLY A THIN LAYER TO THE AFFECTED AREA(S) BY TOPICAL ROUTE ONCE DAILY calcium carbonate/vitamin D3 (CALCIUM 500 + D ORAL) Cal
Allergien: NKDA NKFA
Vorherige Impfungen: -

VAERS 2455269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: FL
Alter: 1,9
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 25.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LL

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

Product administered to patient of inappropriate age

Symptomtext

Error: Wrong Age for Vaccine Given-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2454917

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 85,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 24.08.2022
Beginn: 24.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product use issue

Symptomtext

Patient was given vaccine that was pasted its "use by" date of 8/16/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product use issue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2454903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 38,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 22.08.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Patient was given vaccine that was beyond its "use by" date of 8/16/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2453150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NJ
Alter: 69,0
Geschlecht: F
Eingang: 21.09.2022
Impfdatum: 08.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

This is a spontaneous report received from a contactable reporter (physician). A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Mar2021 as dose 1, single (Lot number: EP6955), in left arm, on 06Apr2021 as dose 2, single (Lot number: EP7533), in left arm, on 12Sep2021 as dose 3 (booster), single (Lot number: FC3182), in left arm and on 08Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 69 years, in left arm for COVID-19 immunisation. The patient's relevant medical history included: "S/P Breast Cancer" (unspecified if ongoing); "Known allergies: Cephalosporin" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Ibuprofen, reaction: "Known allergies: Ibuprofen". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Paxlovid for treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, COVID-19 which included oral Paxlovid from 01Sep2022 to 05Sep2022. Sender's Comments: Based on available information and possible temporal relationship the causal role of suspect drug cannot be excluded for reported events. Case will be further reviewed on receipt of FU information. 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: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer female; Drug allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: TX
Alter: 28,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 02.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / AR

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

Incorrect product formulation administered

Symptomtext

ADMINISTERED PFIZER-BIONTECH NON BIVALENT BOOSTER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: TX
Alter: 20,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 02.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / AR

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

Incorrect product formulation administered

Symptomtext

ADMINISTERED PFIZER-BIONTECH NON BIVALENT BOOSTER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: TX
Alter: 21,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 02.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / AR

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

Incorrect product formulation administered

Symptomtext

ADMINISTERED MODERNA NON BIVALENT BOOSTER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: TX
Alter: 24,0
Geschlecht: M
Eingang: 20.09.2022
Impfdatum: 02.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / AR

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

Incorrect product formulation administered

Symptomtext

ADMINISTERED PRIZER-BIONTECH NON BIVALENT BOOSTER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2452030

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NC
Alter: 12,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 12.09.2022
Beginn: 12.09.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Product storage error

Symptomtext

BUD 9/2/2022 PATIENT RECEIVED VACCINE ON 9/12/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2452012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WI
Alter: 10,0
Geschlecht: M
Eingang: 20.09.2022
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: ja

Incorrect dose administered

Symptomtext

Patient is 10 years old and received 20 mcg/0.2 mL of the adult formulation (12 + age range). Patient received double of the intended dose due to use of the incorrect product.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Torticollis, plagiocephaly, hip dysplasia
Andere Medikamente: None
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2450327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MA
Alter: 66,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 18.07.2022
Beginn: 18.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; interchange of vaccine products; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 66-year-old male patient received BNT162b2 (BNT162B2), on 18Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 66 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 08Feb2021 as dose 1, single (Lot number: 030M20A), on 08Mar2021 as dose 2, single (Lot number: 026A21A) and on 12Nov2021 as dose 3 (booster), single (Lot number: 067F21A) for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: CITALOPRAM, start date: Jan2000, stop date: 13Sep2022; OMEPRAZOLE, start date: 01May2022, stop date: 13Sep2022; ATORVASTATIN, start date: Jan2007, stop date: 31Aug2022; VIT D [COLECALCIFEROL], start date: Jan2007, stop date: 13Sep2022. 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: Treatment of COVID-19. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Paxlovid was received from 01Sep2022 to 05Sep2022 (lot number:00069-0345-30) for the treatment of COVID-19. And experienced Headache, sore throat, body aches and fever resolved during treatment but recurred on 09Sep2022 (day 9).; Sender's Comments: The reported COVID-19 positive after BNT162b2 COVID-19 immunization is considered ineffective of BNT162B2, and the Company cannot completely exclude the possible causality between the reported events and BNT162B2 administration.Based on the information, the causal association between the event interchange of vaccine products and the use of suspect product BNT162b2 cannot be fully excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID 19 Test; Test Result: Positive ; Comments: Treatment of COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: None
Andere Medikamente: CITALOPRAM; OMEPRAZOLE; ATORVASTATIN; VIT D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 2447869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 01.09.2022
Beginn: 01.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Monovalent booster was given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2447866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 16.09.2022
Impfdatum: 01.09.2022
Beginn: 01.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Monovalent Booster was given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2447862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 16.09.2022
Impfdatum: 01.09.2022
Beginn: 01.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Monovalent Booster was given

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2443980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 55,0
Geschlecht: M
Eingang: 13.09.2022
Impfdatum: 31.08.2022
Beginn: 31.08.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient had no adverse event. We gave the patient primary pfizer vaccine for the patient's 4th dose and then after that we received an email that the primary pfizer vaccine should not be used for booster shot. We let the patient know that he could get another bivalent booster shot after 10/30/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2443245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 74,0
Geschlecht: M
Eingang: 13.09.2022
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

Expired product administered

Symptomtext

Expired vaccine administered to patient

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 diabetes, hyperlipidemia, hypertension, CKD stage 2
Andere Medikamente: Glipizide, metformin, aspirin, cholecalciferol, ipratropium, lisinopril-hydrochlorothiazide
Allergien: Allergies: Ciprofloxacin, Januvia
Vorherige Impfungen: -

VAERS 2442984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: ID
Alter: 62,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 13.09.2022
Beginn: 13.09.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

PATIENT INTENDED TO RECIEVE THE FIRST DOSE OF THE PFIZER BIVALENT COVID VACCINE, BUT RECEIVED ANOTHER BOOSTER OF THE ORIGINAL MONOVALENT PFIZER VACCINE, EFFECTIVELY HER 2ND BOOSTER OF THIS VACCINE OR 4TH TOTAL DOSE. THERE WAS NO ADVERSE REACTION, HOWEVER, WE ARE REPORTING TO VAERS BECAUSE THE PATIENT INTENDED TO RECEIVE THE BIVALENT VACCINE AND RECEIVED THE MONOVALENT INSTEAD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 90,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 23.06.2022
Beginn: 21.08.2022
Tage bis Beginn: 59,0
Dosis: 4
Route/Site: IM / RA

Tod: ja 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: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CO
Alter: 45,0
Geschlecht: F
Eingang: 12.09.2022
Impfdatum: 02.09.2022
Beginn: 01.09.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Monovalent booster was given in error after FDA's authorization of the omicron doses. No adverse reaction occurred as a result of this error. Pharmacist spoke to patient regarding error in not receiving the bivalent vaccine; she will be eligible for it in 2 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2439742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 37,0
Geschlecht: F
Eingang: 10.09.2022
Impfdatum: 16.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from product quality group. The reporter is the patient. A 37-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Dec2020 at 12:00 as dose 1, single (Lot number: EJ1685), in right arm, on 11Jan2021 at 13:00 as dose 2, single (Lot number: EL0140), in left arm, on 14Aug2021 at 15:00 as dose 3 (booster), single (Lot number: EW0198), in right arm and on 16Jul2022 at 12:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 37 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Multiple sclerosis" (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". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient did not received any other medication within 2 weeks. The patient received antiviral Covid-19 treatment with Paxlovid form 23Aug2022 to 27Aug2022. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on available information a contributory role of BNT162B2 to the reported events Covid-19 and vaccination failure cannot be totally excluded as efficacy of a drug varies from individual to individual depending upon the immune status. As with any vaccine, vaccination with BNT162B2 may not protect all vaccine recipients, so the expectedness of covid-19 and vaccination failure is : expected. The case will be reassessed further upon receipt of additional information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: SARS-CoV-2 test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Multiple sclerosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 66,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Incorrect product formulation administered

Symptomtext

The Monovalent COVID-19 vaccine was inadvertently given to the patient who was scheduled to receive the Bivalent COVID-19 vaccination as per the recent FDA approval of the Bivalent COVID-19 vaccines. The patient was notified of the error on the same day of the incident and written communication is being drafted and sent to all patients reiterating what was discussed over the phone with the patient. Further action is underway with the guidance of the Interim Clinical Considerations for using COVID-19 Vaccines. All patients were instructed to follow up with their primary care physician and were offered the opportunity to receive a booster dosage in line with the recommendations of the FDA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 08.09.2022
Beginn: 08.09.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Incorrect product formulation administered

Symptomtext

The Monovalent COVID-19 vaccine was inadvertently given to the patient who was scheduled to receive the Bivalent COVID-19 vaccination as per the recent FDA approval of the Bivalent COVID-19 vaccines. The patient was notified of the error on the same day of the incident and written communication is being drafted and sent to all patients reiterating what was discussed over the phone with the patient. Further action is underway with the guidance of the CDC Interim Clinical Considerations for using COVID-19 Vaccines. All patients were instructed to follow up with their primary care physician and were offered the opportunity to receive a booster dosage in line with the recommendations of the FDA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2426368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: FL
Alter: 65,0
Geschlecht: M
Eingang: 01.09.2022
Impfdatum: 21.07.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 Vaccination failure

Symptomtext

Paxlovid for COVID 19 Treatment; Paxlovid for COVID 19 Treatment; This is a spontaneous report received from a contactable consumer. The reporter is the patient. A 65-year-old male patient received BNT162b2 (BNT162B2), on 06Mar2021 at 12:30 as dose 1, single (Lot number: en6198), in left arm, on 27Mar2021 at 12:30 as dose 2, single (Lot number: er2613), in left arm, on 21Dec2021 at 12:30 as dose 3 (booster), single (Lot number: fh8028), in right arm and on 21Jul2022 at 13:15 as dose 4 (booster), single (Lot number: fp7135) at the age of 65 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Congenital syndrome" (unspecified if ongoing); "5 back surgeries" (unspecified if ongoing); "3 heart surgeries" (unspecified if ongoing); "Artificial heart valve" (unspecified if ongoing); "artificial aorta heart rhythm problems" (unspecified if ongoing), notes: artificial aorta heart rhythm problems associated with syndrome controlled by medicine.; "artificial aorta heart rhythm problems" (unspecified if ongoing), notes: artificial aorta heart rhythm problems associated with syndrome controlled by medicine. Patient has no known allergies. Concomitant medications included: DOFETILIDE (manufacturer: sun pharma), start date: Jan2019; METOPROLOL(manufacturer: rising), start date: Dec2013. Patient received Paxlovid from 18Aug2022 to 23Aug2022 for COVID-19 Treatment. Outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Aortic valve disease (artificial aorta heart rhythm problems associated with syndrome controlled by medicine.); Arrhythmia (artificial aorta heart rhythm problems associated with syndrome controlled by medicine.); Back surgery; Cardiac operation; Congenital anomaly; Heart valve replacement
Andere Medikamente: DOFETILIDE; METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2422703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MN
Alter: 100,0
Geschlecht: M
Eingang: 29.08.2022
Impfdatum: 15.07.2022
Beginn: 26.08.2022
Tage bis Beginn: 42,0
Dosis: 4
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Hospitalization.

Weitere VAERSDATA-Felder

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

VAERS 2420159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 25.08.2022
Impfdatum: 22.08.2022
Beginn: 22.08.2022
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 No adverse event

Symptomtext

Pt was given an expired vaccine. Vaccine expired on 8.19.2022 and was given on 8.22.2022. Pt did not have an adverse reactions at this time. Vaccine was pulled from deep freeze on 6.10.2022 which made the vaccine expire on 8.19.22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2420157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CO
Alter: 53,0
Geschlecht: F
Eingang: 25.08.2022
Impfdatum: 22.08.2022
Beginn: 22.08.2022
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 No adverse event

Symptomtext

Pt was given an expired vaccine. Vaccine expired on 8.19.2022 and was given on 8.22.2022. Pt did not have an adverse reactions at this time. Vaccine was pulled from deep freeze on 6.10.2022 which made the vaccine expire on 8.19.22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: None
Allergien: -
Vorherige Impfungen: -

VAERS 2420155

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CO
Alter: 54,0
Geschlecht: F
Eingang: 25.08.2022
Impfdatum: 22.08.2022
Beginn: 22.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

Pt was given an expired vaccine. Vaccine expired on 8.19.2022 and was given on 8.22.2022. Pt did not have an adverse reactions at this time. Vaccine was pulled from deep freeze on 6.10.2022 which made the vaccine expire on 8.19.22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: N/A
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2420069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 22.08.2022
Beginn: 22.08.2022
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 No adverse event

Symptomtext

Patient was given a dose 2 days after the BUD. No adverse effects reported. Valid dose and no need to revaccinate per clinical studies

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2420062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 17,0
Geschlecht: M
Eingang: 25.08.2022
Impfdatum: 21.08.2022
Beginn: 21.08.2022
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 No adverse event

Symptomtext

Patient was given a dose 1 day after the BUD. No adverse effects reported. Valid dose and no need to revaccinate per clinical studies

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2418439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 23.08.2022
Impfdatum: 12.08.2022
Beginn: 12.08.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Expired product administered

Symptomtext

This submission is to report accidental administration of Pfizer vaccine one day outside of beyond use date. Pfizer BUD was 8/11/22 and dose was given on 8/12/22. Pfizer was contacted and shared off-label stability studies that demonstrate a 1 to 2 day grace period to the usual 10 week BUD and indicated the dose was still stable. This pharmacist was still advised to submit VAERS report by supervisor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2417276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: IL
Alter: 82,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 19.08.2022
Beginn: 19.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / UN

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

No adverse event Product administration error Product storage error

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA administration error - vaccine dose given 26 hours after puncture of the vial. Pfizer offers excursion data for up 24 hours post-puncture. No symptoms as a result of the administration error.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: aspirin 81 mg qDay calcium-vitamin D 500 mg-200 intl units 1 Tablet(s) qDay cloNIDine 0.1 mg oral tablet 0.1 mg
Allergien: PCN, lisinopril, Latex, hydrochlorothiazide, amlodipine
Vorherige Impfungen: -

VAERS 2416855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 52,0
Geschlecht: M
Eingang: 21.08.2022
Impfdatum: 20.07.2022
Beginn: 30.07.2022
Tage bis Beginn: 10,0
Dosis: 4
Route/Site: SYR / LA

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

Herpes zoster Post herpetic neuralgia

Symptomtext

I got Shingles 10 Days after my 2nd Booster Shot. Now I'm diagnosed with PHN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: PHN due to Shingles
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Albuterol Astham Inhalers
Allergien: Prescription Asprine
Vorherige Impfungen: -

VAERS 2433488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 17.08.2022
Impfdatum: 14.06.2022
Beginn: 15.06.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

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

Fall

Symptomtext

Narrative: Pt received vaccine the previous day, fell in dining room following day. Also being assessed for concomitant UTI.

Weitere VAERSDATA-Felder

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

VAERS 2413247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: DE
Alter: 66,0
Geschlecht: F
Eingang: 17.08.2022
Impfdatum: 25.06.2022
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). The reporter is the patient. A 66-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jan2021 as dose 1, single (Lot number: EL9265), in left arm, on 25Feb2021 as dose 2, single (Lot number: EL9266), in left arm, on 29Sep2021 as dose 3 (booster), single (Lot number: 301458A), in left arm and on 25Jun2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 66 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "hypercholesterolemia" (unspecified if ongoing). Concomitant medication(s) included: ATORVASTATIN, stop date: 05Aug2022; DILTIAZEM HYDROCHLORIDE, start date: 03Aug2022. 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: (12Aug2022) Negative, notes: After having tested negative on 12Aug2022; (14Aug2022) Positive, notes: I tested positive today 14Aug2022. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: vaccine received reported as yes. Other medication in 2weeks reported as yes. COVID 19 Treatment includes Paxlovid with treatment start date 05Aug2022 and stop date 09Aug2022. Other medication in 2weeks product reported as Atorvastatin 40 mg with stop date 05Aug2022 and Diltiazem Er (cd) caps, 120 mg with start date 03Aug2022. Patient reported there were none other than pain add the injection site. If you are talking about adverse events regarding Paxlovid. Patient tested positive 14Aug2022, After having tested negative on 12Aug2022. Patient was asymptomatic. Known allergies reported as no.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220812; Test Name: COVID-19 Test; Test Result: Negative ; Comments: After having tested negative on 12Aug2022.; Test Date: 20220814; Test Name: COVID-19 Test; Test Result: Positive ; Comments: I tested positive today 14Aug2022
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Hypercholesterolemia
Andere Medikamente: ATORVASTATIN; DILTIAZEM HYDROCHLORIDE
Allergien: -
Vorherige Impfungen: -

VAERS 2413213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 53,0
Geschlecht: M
Eingang: 17.08.2022
Impfdatum: 17.06.2022
Beginn: 25.07.2022
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 53-year-old male patient received BNT162b2 (BNT162B2), on 26Dec2021 at 14:30 as dose 2 (booster), single (Lot number: 33130BA), in left arm and on 17Jun2022 at 14:00 as dose 3 (booster), single (Lot number: FP7135) at the age of 53 years, in right arm for covid-19 immunisation; janssen coviD-19 vaccine (JANSSEN COVID-19 VACCINE), on 20Mar2021 at 15:00 as dose 1, single (Lot number: 1805029), in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 25Jul2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (25Jul2022) positive, notes: Tested positive for COVID 19 on 25Jul; (31Jul2022) Negative, notes: tested negative on 31Jul and 04Aug; (04Aug2022) Negative, notes: tested negative on 31Jul and 04Aug; (07Aug2022) Positive, notes: Tested positive again on 07Aug. Paxlovid was taken on 25Jul2022 to 30Jul2022 as therapeutic measure as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220725; Test Name: COVID-19; Test Result: Positive ; Comments: Tested positive for COVID 19 on 25Jul; Test Date: 20220731; Test Name: COVID-19; Test Result: Negative ; Comments: tested negative on 31Jul and 04Aug.; Test Date: 20220804; Test Name: COVID-19; Test Result: Negative ; Comments: tested negative on 31Jul and 04Aug.; Test Date: 20220807; Test Name: COVID-19; Test Result: Positive ; Comments: Tested positive again on 07Aug
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Known allergies: None Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2409981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 13,0
Geschlecht: M
Eingang: 17.08.2022
Impfdatum: 12.08.2022
Beginn: 12.08.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered Underdose

Symptomtext

13-year-old patient received a pediatric Pfizer dose instead of an adult Pfizer dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2412886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: VA
Alter: 50,0
Geschlecht: F
Eingang: 16.08.2022
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: ja

Expired product administered

Symptomtext

Administered one day past BUD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2412884

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: VA
Alter: 83,0
Geschlecht: F
Eingang: 16.08.2022
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: ja

Expired product administered No adverse event

Symptomtext

A SHOT WAS ADMINISTERED A DAY PAST BUD. No adverse drug reactions were noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: not known
Vorgeschichte: not known
Andere Medikamente: not known
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2407398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: TX
Alter: 11,0
Geschlecht: F
Eingang: 10.08.2022
Impfdatum: 03.08.2022
Beginn: 01.08.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / UN

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

Inappropriate schedule of product administration

Symptomtext

No adverse event. First dose Pfizer vaccine administered 7/22/2022. Invalid follow up COVID-19 vaccine administered on 8/3/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2402989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NC
Alter: 92,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 20.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Blood pressure increased No reaction on previous exposure to drug Sleep disorder Blood pressure measurement Hypertensive crisis

Symptomtext

woke up to symptoms of high blood pressure /blood pressure and it was 222/111; This is a spontaneous report received from contactable reporter(s) (Pharmacist). A 92-year-old male patient received BNT162b2 (BNT162B2), on 20Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 92 years intramuscular, in left arm for covid-19 immunisation. The patient's family history included: "Phaeochromocytoma" (unspecified if ongoing), notes: Due to him having pheochromocytoma. Concomitant medication(s) in two weeks included: DOXAZOSIN; ELIQUIS; AMLODIPINE; METOPROLOL SUCCINATE; BUTALBITAL AND ACETAMINOPHEN; LEVOTHYROXINE. Vaccination history included: Bnt162b2 (Dose 1), for COVID-19 immunization, reaction(s): "no adverse effects"; Bnt162b2 (Dose 2), for COVID-19 immunization, reaction(s): "no adverse effects"; Bnt162b2 (Dose 3), for COVID-19 immunization, reaction(s): "no adverse effects". The following information was reported: HYPERTENSIVE CRISIS (medically significant, life threatening) with onset 20Jul2022 at 01:30, outcome "recovered", described as "woke up to symptoms of high blood pressure /blood pressure and it was 222/111". The events "woke up to symptoms of high blood pressure /blood pressure and it was 222/111" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood pressure measurement: (20Jul2022) 222/111. Therapeutic measures were taken as a result of hypertensive crisis. Clinical course: No covid prior vaccination. No covid tested post vaccination. Facility type vaccine was reported in Pharmacy or Drug Store. No other vaccine in four weeks. Patient reports that the night of his second booster of Pfizer he woke up to symptoms of high blood pressure. He checked his blood pressure and it was 222/111. Patient believes adverse effect is due to him having pheochromocytoma. He reports no adverse effects from his previous three doses of Pfizer. Adverse event resulted in Doctor or other healthcare professional office/clinic visit. The patient received Clonidine for events.; Sender's Comments: Based on the available information and known product profile, the causal relationship of the reported event and the use of BNT162B2 cannot be fully excluded. However, the underlying medical condition is confounding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood pressure increased
Hospital-Tage: -
Labordaten: Test Date: 20220720; Test Name: Blood pressure; Result Unstructured Data: Test Result:222/111
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pheochromocytoma (Due to him having pheochromocytoma.)
Andere Medikamente: DOXAZOSIN; ELIQUIS; AMLODIPINE; METOPROLOL SUCCINATE; BUTALBITAL AND ACETAMINOPHEN; LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2402989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NC
Alter: 92,0
Geschlecht: M
Eingang: 10.08.2022
Impfdatum: 20.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / LA

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

Blood pressure increased No reaction on previous exposure to drug Sleep disorder Blood pressure measurement Hypertensive crisis

Symptomtext

woke up to symptoms of high blood pressure /blood pressure and it was 222/111; This is a spontaneous report received from contactable reporter(s) (Pharmacist). A 92-year-old male patient received BNT162b2 (BNT162B2), on 20Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 92 years intramuscular, in left arm for covid-19 immunisation. The patient's family history included: "Phaeochromocytoma" (unspecified if ongoing), notes: Due to him having pheochromocytoma. Concomitant medication(s) in two weeks included: DOXAZOSIN; ELIQUIS; AMLODIPINE; METOPROLOL SUCCINATE; BUTALBITAL AND ACETAMINOPHEN; LEVOTHYROXINE. Vaccination history included: Bnt162b2 (Dose 1), for COVID-19 immunization, reaction(s): "no adverse effects"; Bnt162b2 (Dose 2), for COVID-19 immunization, reaction(s): "no adverse effects"; Bnt162b2 (Dose 3), for COVID-19 immunization, reaction(s): "no adverse effects". The following information was reported: HYPERTENSIVE CRISIS (medically significant, life threatening) with onset 20Jul2022 at 01:30, outcome "recovered", described as "woke up to symptoms of high blood pressure /blood pressure and it was 222/111". The events "woke up to symptoms of high blood pressure /blood pressure and it was 222/111" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood pressure measurement: (20Jul2022) 222/111. Therapeutic measures were taken as a result of hypertensive crisis. Clinical course: No covid prior vaccination. No covid tested post vaccination. Facility type vaccine was reported in Pharmacy or Drug Store. No other vaccine in four weeks. Patient reports that the night of his second booster of Pfizer he woke up to symptoms of high blood pressure. He checked his blood pressure and it was 222/111. Patient believes adverse effect is due to him having pheochromocytoma. He reports no adverse effects from his previous three doses of Pfizer. Adverse event resulted in Doctor or other healthcare professional office/clinic visit. The patient received Clonidine for events.; Sender's Comments: Based on the available information and known product profile, the causal relationship of the reported event and the use of BNT162B2 cannot be fully excluded. However, the underlying medical condition is confounding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood pressure increased
Hospital-Tage: -
Labordaten: Test Date: 20220720; Test Name: Blood pressure; Result Unstructured Data: Test Result:222/111
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pheochromocytoma (Due to him having pheochromocytoma.)
Andere Medikamente: DOXAZOSIN; ELIQUIS; AMLODIPINE; METOPROLOL SUCCINATE; BUTALBITAL AND ACETAMINOPHEN; LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2405937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 09.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
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 Product administration error

Symptomtext

Administration error. Pt over 50 years old, with no known immunocompromising conditions given a 5 dose (3rd booster) of pfizer; the patient had a 4th booster given May 26, 2022 . Pt made aware of un-indicated extra dose given in error. The patient's physician was called to inform. Patient left pharmacy in what appeared as same stay as when arrived; no signs of distress.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2405904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 15,0
Geschlecht: M
Eingang: 09.08.2022
Impfdatum: 09.08.2022
Beginn: 09.08.2022
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 No adverse event

Symptomtext

Pt arrived to receive covid vaccine booster, with grandmother's consent. Handed provider vaccination card, which showed 2 prior Pfizer doses. The above vaccine was administered, only for patient to then say "There was a sticker for my 3rd shot on my card, it fell off." Thus pt was inadvertently administered a 4th dose of the Pfizer Covid Vaccine. Pt is not immunocompromised, and thus did not qualify for a 4th dose. He was informed of what happened and left with no adverse reaction to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2405823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WI
Alter: 5,0
Geschlecht: M
Eingang: 09.08.2022
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: ja

Incorrect dose administered Incorrect product formulation administered

Symptomtext

Child is 5 years old but received the Pfizer vaccine for adults aged 12+. Received 0.3mL of the adult dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2404690

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 64,0
Geschlecht: F
Eingang: 08.08.2022
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

Aphonia Throat irritation

Symptomtext

Patient reported loss of voice and felt a scratchy sensation in her throat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Aphonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2404300

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FP7135

gering

Staat: FL
Alter: 79,0
Geschlecht: F
Eingang: 08.08.2022
Impfdatum: 08.08.2022
Beginn: 08.08.2022
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

Symptomtext

5TH DOSE GIVEN, NO ADVERSE REACTIONS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2402422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NV
Alter: 40,0
Geschlecht: F
Eingang: 05.08.2022
Impfdatum: 25.06.2022
Beginn: 01.07.2022
Tage bis Beginn: 6,0
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

COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Jun2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 40 years, in right 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) and as dose 3 (boster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Multiple sclerosis" (unspecified if ongoing). It was reported that the patient had no known allergies. Concomitant medication(s) included: DAYQUIL, start date: 25Jul2022, stop date: 27Jul2022; MUCINEX DM, start date: 27Jul2022, stop date: 29Jul2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jul2022, outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results. Therapeutic measures were taken as a result of covid-19. The COVID 19 Treatment received with Paxlovid with start date given as 28Jul2022 and stop date given as 30Jul2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Multiple sclerosis
Andere Medikamente: DAYQUIL; MUCINEX DM
Allergien: -
Vorherige Impfungen: -

VAERS 2402419

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: AL
Alter: -
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 01.07.2022
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 SARS-CoV-2 test

Symptomtext

COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-healthcare professional). The reporter is the patient. A 57-year-old male patient received BNT162b2 (BNT162B2), on 01Jul2022 as dose 4 (booster), single (Lot number: FP7135), in right 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) and as dose 3 (booster), single (Batch/Lot number: Unknown) for covid-19 immunisation. The patient relevant medical history included: "Known allergies: CT contrast dye" (unspecified if ongoing). Concomitant medication(s) included: VIT C, start date: Jul2022; VIT D [VITAMIN D NOS], start date: Jul2022, ZINC, start date: Jul2022. The following information was reported: DRUG INEFFECTIVE (medically significant), outcome "unknown", COVID-19 (medically significant), outcome "recovering'', 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, (25Jul2022) Negative, (31Jul2022) Positive. Therapeutic measures were taken because of drug ineffective, covid-19. The patient received treatment of Paxlovid for COVID-19 from 18Jul2022 to 23Jul2022. Clinical course: Patient Tested Covid negative 25Jul after treatment, and tested Covid positive 31Jul. Rebound Covid and patient experienced hardly any symptoms second time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19; Test Result: Positive ; Comments: COVID-19 Treatment; Test Date: 20220725; Test Name: COVID-19; Test Result: Negative ; Test Date: 20220731; Test Name: COVID-19; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Contrast media allergy
Andere Medikamente: VIT C; VIT D [VITAMIN D NOS]; ZINC
Allergien: -
Vorherige Impfungen: -

VAERS 2401658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 26.07.2022
Beginn: 30.07.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

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

Bloody discharge Dysmenorrhoea Postmenopausal haemorrhage Ultrasound scan normal

Symptomtext

I experienced menstrual cramps, brownish pink discharge that concerned me could be cancer symptoms. I was diagnosed with Post Menopausal spotting after a pelvic exam and Sonogram on 08/02/2022. I am still experiencing menstrual cramps and spotting daily. I was advised that it would resolve itself in time, and that my physician has seen this frequently after COVID-19 vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bloody discharge
Hospital-Tage: -
Labordaten: Sonogram showed no masses or abnormalities 08/02/2022.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Sertraline; estradiol patch; progesterone cream; women's multivitamin; vitamin D; magnesium; vitamin B complex
Allergien: N/A
Vorherige Impfungen: -

VAERS 2401426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CO
Alter: 11,0
Geschlecht: F
Eingang: 04.08.2022
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

Incorrect dose administered

Symptomtext

Patient was given the adult Pfizer dose for booster (3rd vaccine) instead of the pediatric Pfizer dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: None have been reported to us at this time.
Aktuelle Erkrankungen: -
Vorgeschichte: N/A
Andere Medikamente: -
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2400363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 16.07.2022
Beginn: 16.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Incorrect product formulation administered

Symptomtext

Patient was given a pediatric dose of Pfizer vaccine for her 4th shot. The error was immediately figured out and then patient was brought back and received the Adult Pfizer 4th dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2398143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: IL
Alter: 11,0
Geschlecht: M
Eingang: 01.08.2022
Impfdatum: 01.08.2022
Beginn: 01.08.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

Patient was given 12yrs> grey top instead of orange top 5yrs -11yrs. Patient did wait 15 min in office after vaccine and no reactions while in office. It is currently 3:42pm and parent has not called back to office reporting any adverse events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: allergy to food, allergic rhinitis
Andere Medikamente: Epi-pen 0.3mg/0.3ml injection as needed for peanut allergy, Nasal spray as needed, montelukast 5mg at bedtime, Zyrtec 10mg as needed, Multivitamins
Allergien: Peanut allergy, enviromental allergies
Vorherige Impfungen: -

VAERS 2397867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CT
Alter: 18,0
Geschlecht: F
Eingang: 01.08.2022
Impfdatum: 29.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Covid dose #2 given 6 days too early. It was given 15 days after the first dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2396719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: NH
Alter: 47,0
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: 15.07.2022
Beginn: 29.07.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / RA

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

no adverse reaction . patient was under 50 . had a Janssenn as primary , pfizer as ist booster . missed that he did not qualift for 2nd booster at this time

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2396152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: 06.07.2022
Beginn: 18.07.2022
Tage bis Beginn: 12,0
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

diagnosed with Covid; diagnosed with Covid; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), on 13Mar2021 as dose 1, single (Lot number: EN6198), on 03Apr2021 as dose 2, single (Lot number: EN6206), on 01Nov2021 as dose 3 (booster), single (Lot number: 30145BA) and on 06Jul2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 60 years for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (ongoing), notes: diagnosed for 5-10 years. The patient's family history included: "Covid" (unspecified if ongoing), notes: one of his brothers also had Covid and it took him months to get his taste and smell back. Concomitant medication(s) included: ADARBI taken for hypertension. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 18Jul2022, outcome "unknown" and all described as "diagnosed with Covid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18Jul2022) Positive, notes: Tested Positive for COVID after 4 Vaccines. Therapeutic measures were taken as a result of vaccination failure, covid-19. Caller states he was calling to report a benefit of Paxlovid. Stated he was diagnosed with Covid on Monday 18Jul2022, given Paxlovid medication, started the medication on Tuesday morning, 19Jul2022. The patient received Paxlovid (NDC number of Paxlovid: 0069-1085-30, Expiry Date: Mar2023, Batch/lot number: GC9447) three in the morning and three in the evening for COVID-19. Caller reported that by Monday 18Jul2022, he had already lost his sense of taste and smell due to the Covid. Stated that he was only on his fourth day of Paxlovid treatment and his taste and smell are back. States he noticed it a little bit yesterday but this morning when he ate breakfast his apple tasted like an apple and his milk tasted like milk, states he called his whole family to tell them. Caller stated he was worried because one of his brothers also had Covid and it took him months to get his taste and smell back. Caller did not know if it was because of the medication but he wanted to make sure Pfizer was aware of this potential benefit. The sample of the product was not available to be returned. The report was not related to a study or programme.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220718; Test Name: Covid-19 test; Test Result: Positive ; Comments: Tested Positive for COVID after 4 Vaccines
Aktuelle Erkrankungen: Blood pressure high (diagnosed for 5-10 years)
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (one of his brothers also had Covid and it took him months to get his taste and smell back)
Andere Medikamente: ADARBI
Allergien: -
Vorherige Impfungen: -

VAERS 2396080

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NJ
Alter: 64,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 16.06.2022
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). The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 22Mar2021 at 17:00 as dose 1, single (Lot number: EP7534), in left arm, on 21Apr2021 at 17:00 as dose 2, single (Lot number: ER8729), in left arm, on 02Dec2021 at 15:00 as dose 3 (booster), single (Lot number: FJ1611), in left arm and on 16Jun2022 at 15:00 as dose 4 (booster), single (Lot number: FP7135) at the age of 64 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hepatitis C" (unspecified if ongoing). Concomitant medication(s) included: CALCIUM MAGNESIUM ZINC [CALCIUM;MAGNESIUM;ZINC]; FISH OIL; GLUCOSAMINE CHONDROITIN [CHONDROITIN SULFATE SODIUM;GLUCOSAMINE HYDROCHLORIDE]; POTASSIUM [POTASSIUM CHLORIDE]; SIMVASTATIN; SERTRALINE; VITAMIN C [ASCORBIC ACID]. Past drug history included: Interferon, stop date: 1999, for hepatitis c, notes: I did have hepatitis c but was treated for it with interferon and riboviron for 11 months completing treatment in 1999.; Riboviron, stop date: 1999, for hepatitis c, notes: I did have hepatitis c but was treated for it with interferon and riboviron for 11 months completing treatment in 1999. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown Results, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient receive Paxlovid treatment (Lot- GA6765) from 20Jul2022 for COVID-19. The patient stated that, constant bad taste in mouth. Patient had only taken 3 doses. The patient had no known allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid Test; Result Unstructured Data: Test Result:Unknown Results; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hepatitis C
Andere Medikamente: CALCIUM MAGNESIUM ZINC [CALCIUM;MAGNESIUM;ZINC]; FISH OIL; GLUCOSAMINE CHONDROITIN [CHONDROITIN SULFATE SODIUM;GLUCOSAMINE HYDROCHLORIDE]; POTASSIUM [POTASSIUM CHLORIDE]; SIMVASTATIN; SERTRALINE; VITAMIN C [ASCORBIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2395017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 72,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 30.06.2022
Beginn: 25.07.2022
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: UN / UN

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

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

Symptomtext

Breakthrough COVID infection. Asymptomatic and tested for post discharge placement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asymptomatic COVID-19
Hospital-Tage: -
Labordaten: Positive SARS-COV-2 (COVID-19) by company collected 707/25/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2394943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 13.06.2022
Beginn: 25.07.2022
Tage bis Beginn: 42,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Inappropriate schedule of product administration SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 4 vaccines Pfizer 2/9/21 Lot# EL9267; 3/3/21 Pfizer Lot# EN6202; Pfizer 10/19/21 Lot# FF8841; Pfizer 6/13/22 Lot# FP7135

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2393674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MS
Alter: 71,0
Geschlecht: F
Eingang: 27.07.2022
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

Medication error Product storage error

Symptomtext

I have been keeping track of the covid vaccines in the clinic. LPN is a new hire to the clinic and was made aware of the covid vaccines and location for the covid book during her three-day clinic training. On 07/08/2022 I was out of the clinic due to a death in family and did not return until 07/15/2022. Upon my return I was notified that covid vaccines had been administered. There were two open vials (one Pfizer vaccine and one Moderna) in the refrigerator that I discarded on the morning of 07/15/2022 when performing vaccine daily inventory count. (There were no medication errors with Moderna vaccine, only Pfizer) The Pfizer count on the daily inventory log prior to me leaving on 07/07/2022 was 39 vials. The Pfizer count on the covid vaccine daily inventory log on 07/15/2022 was 39. There was one Pfizer vaccine given on 07/08/2022 administered to MRN# 13407855 by NP. There was one Pfizer vaccine administered on 07/12/2022 to MRN# 13150437 by RN. One Pfizer administered on 07/14/2022 to MRN # 13825361 by LPN. I checked the dates on the opened vials to make sure that what I was seeing on the daily log was the same as what was on the vial, and the date on the Pfizer vial was 07/08/2022. I spoke with LPN on 07/18/2022 who states she was not in clinic on 07/08/2022 and she administered one Pfizer vaccine on 07/14/2022. When asked if she opened a new vial of Pfizer vaccine on 07/14/2022 or if she gave from the previously open Pfizer vial, she stated that she did not open a new Pfizer vial, she used the Pfizer vial that was previously opened. I reported the incident to Dr. on 07/15/2022 and Clinic Manager on 07/27/2022. At this time, no one is administering covid vaccines other than myself and I continue to retrain others in the clinic on administration of covid vaccines and storage and safety of vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Medication error
Hospital-Tage: -
Labordaten: None reported.
Aktuelle Erkrankungen: None known
Vorgeschichte: Hypertension, Dementia, Hyperlipidemia, cardiac Pacemaker
Andere Medikamente: ASA 325mg daily Mucinex DM take q 12 hours as needed Tambocor 50mg take 1/2 tablet by mouth twice a day Zoloft 25mg take 1 daily cardizem CD 120mg daily
Allergien: No known Allergies
Vorherige Impfungen: -

VAERS 2393584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MS
Alter: 78,0
Geschlecht: M
Eingang: 27.07.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
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

No adverse events reports at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Patient was being seen by a pulmonologist for Chronic Bronchitis.
Vorgeschichte: Chronic Bronchitis.
Andere Medikamente: None listed
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2393303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WI
Alter: 84,0
Geschlecht: M
Eingang: 27.07.2022
Impfdatum: 28.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Extra dose administered No adverse event

Symptomtext

Pt. was in for an OV on 6/28/22, health maintenance flagged due for pfizer booster, MA discussed and verified he's truly due. Patient wasn't sure he had his card along, wasn't planned or known he was going to need it. After Pfizer booster was administered, before leaving the office the patient found his vaccine card, MA noticed he had one written on his card in bright blue ink dated 4/26/22, only then did pt. remember he had one recently with a BP check. The 4/26/22 one wasn't ordered or documented in system hence why it showed due. I looked back through our dose card for the covid vaccine and the story does match up. The doses given match what was on the schedule. We did go back into system on 4/26 and added the dose he received that day. As a result the patient was not due for another booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: no effect on patient
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: acetaminophen (TYLENOL) 325 mg oral tablet Take 650 mg by mouth every 4 hours as needed for fever or pain. amLODIPine (NORVASC) 10 mg oral tablet Take 1 tablet (10 mg total) by mouth every day. Indications: High Blood Pressure Disorder ator
Allergien: lisinopril
Vorherige Impfungen: -

VAERS 2393143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NE
Alter: 13,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 26.07.2022
Beginn: 27.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered No adverse event

Symptomtext

Patient brought to clinic by father for a well child visit. Father unaware of Covid booster being given to patient in January 2022. RN transcribes vaccines prior to patient visit in error, resulting in a booster data input error. Follow up with parent patient after visit- occurred with physician and nurse immediately after clinic visit. RN supervisor followed up with mother next day, at time of follow up patient was not experiencing side effects from vaccines received on 07/26/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: wears glasses keratosis pilaris
Andere Medikamente: none
Allergien: No medication or food allergies.
Vorherige Impfungen: -

VAERS 2391219

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MO
Alter: 11,0
Geschlecht: F
Eingang: 26.07.2022
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

Circumstance or information capable of leading to medication error Product administered to patient of inappropriate age

Symptomtext

Pt's DOB was typed in incorrectly. Pt given a 12+ Pfizer COVID vaccine instead of a 5-11 COVID vaccine. Father with pt and was notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Circumstance or information capable of leading to medication error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA, no food allergies or product allergies per pt's father
Vorherige Impfungen: -

VAERS 2388263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MO
Alter: 17,0
Geschlecht: U
Eingang: 25.07.2022
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: ja

Extra dose administered No adverse event

Symptomtext

PATIENT DID NOT QUALIFY FOR 4TH DOSE, BUT 4TH DOSE GIVEN. PATIENT HAS NOT EXPERIENCED ANY ADVERSE EFFECTS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2387542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fp7135

gering

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 14.06.2022
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; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Mar2021 at 15:00 as dose 1, single (Lot number: EN6202), in right arm, on 11Oct2021 at 12:00 as dose 2, single (Lot number: 330125BA), in left arm, on 05Mar2022 at 12:00 as dose 3 (booster), single (Lot number: EP7534), in right arm and on 14Jun2022 at 12:00 as dose 4 (booster), single (Lot number: Fp7135) at the age of 64 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: FLUOXETINE; JARDIANCE; METFORMIN HCL; METOPROLOL; MONTELUKAST SODIUM; OMEPRAZOLE; RAMIPRIL, stop date: 05Jul2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results, 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 test; Result Unstructured Data: Test Result:Unknown results; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Diabetes; Penicillin allergy
Andere Medikamente: FLUOXETINE; JARDIANCE; METFORMIN HCL; METOPROLOL; MONTELUKAST SODIUM; OMEPRAZOLE; RAMIPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 2377049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: FL
Alter: 36,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Extra dose administered Product administered to patient of inappropriate age

Symptomtext

Pt was not old enough to receive 4th pfizer shot ** 2nd booster**

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2375018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: AZ
Alter: 52,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 20.07.2022
Beginn: 20.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

patient waited 15 mins. no symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2374730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: PA
Alter: 10,0
Geschlecht: F
Eingang: 20.07.2022
Impfdatum: 11.07.2022
Beginn: 11.07.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

No adverse event patient received adult dose of Pfizer vaccine of 0.3ml instead of 5-11 dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2374323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 27,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
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

Error: Expired Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2374321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 20.07.2022
Impfdatum: 12.07.2022
Beginn: 12.07.2022
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

Error: Expired Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2374269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WA
Alter: 39,0
Geschlecht: F
Eingang: 19.07.2022
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: unbekannt Erholt: ja

Extra dose administered Interchange of vaccine products

Symptomtext

39yo female patient was here with her 3 kids for well child exam on 6/27/22. They were all there receiving COVID vaccines. Mom had asked provider if she could receive her booster as well since she is here and her kids are getting theirs. So I the patient received her Pfizer COVID vaccine booster on 6/27/22 (4th dose, 2nd booster of Pfizer COVID vaccine) that was signed off by provider. Patient previously received Pfizer COVID vaccine on 4/9/21, 5/8/21, and 12/18/21. This patient technically does not qualify for a 4th dose (or 2nd booster) because she is under 50 years of age and she's not immunocompromised. So this is an administration error without any adverse reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2373994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MD
Alter: 71,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

The patient was vaccinated with medication from a vial that had last been used 42 hours prior to the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No illnesses
Vorgeschichte: No known health conditions
Andere Medikamente: No none prescriptions or other medications
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2372774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: ME
Alter: 25,0
Geschlecht: M
Eingang: 18.07.2022
Impfdatum: 18.07.2022
Beginn: 18.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Inappropriate schedule of product administration No adverse event

Symptomtext

NOT REPORTING ADVERESE EVENT. ADMIISTRATION ERROR- PATIENT RECEIVED A 2ND BOOSTER DOSE (25 YO) 84 DAYS AFTER 1ST BOOSTER DOSE. PATIENT CAME IN TO GET BOOSTER DOSE PFIZER; PATIENT STATED DURING CONSULT HE RECIEVED HIS PRIMARY SERIES APRIL 2021; PATIENT CONFIRMED >5 MONTHS FROM LAST SHOT OF PRIMARY SERIES. IMMUNIZATION REGISTARY RECORD SHOWED PATIENT RECIEVED ONE PFIZER DOSE ON (1OF2) ON 4/4/22; AFTER ADMINISTRATION CALLED PATIENT TO DISCUSS WHEN BOOSTER DUE; PATIENT THEN DISCLOSED HE RECENTLY HAD A NAME CHANGE. PER IMMUNIZATION REGISTRY PRIMARY SERIES PFIZER WAS GIVEN ON 1/25/21 & 2/15/22. INFORMED PATIENT 2ND BOOSTER WAS GIVEN IN ERROR

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2372429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CO
Alter: 79,0
Geschlecht: M
Eingang: 18.07.2022
Impfdatum: 05.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 9,0
Dosis: 4
Route/Site: IM / UN

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

CSF test Lumbar puncture Magnetic resonance imaging head Magnetic resonance imaging neck Magnetic resonance imaging spinal Myelitis transverse Paraplegia

Symptomtext

Hospitalized with rapidly progressive transverse myelitis of thoracolumbar spine, onset of symptoms 9 days after second booster (fourth of series), currently paraplegic on high dose steroids. Multiple CSF and serologic studies sent and pending

Weitere VAERSDATA-Felder

Praegender Schweregrund: CSF test
Hospital-Tage: 2,0
Labordaten: Too many to document-has had MRI's brain, cervical/thoracic/lumbar spine, lumber puncture with multiple studies pending
Aktuelle Erkrankungen: none `
Vorgeschichte: None
Andere Medikamente: none
Allergien: HMG CoA reductase inhibitors (statins)
Vorherige Impfungen: -

VAERS 2372016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: MO
Alter: 93,0
Geschlecht: F
Eingang: 17.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series Given Too Early-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2371761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: OH
Alter: 66,0
Geschlecht: M
Eingang: 16.07.2022
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

COVID-19 Vaccination failure

Symptomtext

COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 66-year-old male patient received BNT162b2 (BNT162B2), on 29Dec2020 as dose 1, single (Lot number: EJ1685), in left arm, on 19Jan2021 as dose 2, single (Lot number: EL3249), in left arm, on 27Sep2021 as dose 3 (booster), single (Lot number: FE3592), in left arm and on 06Jun2022 as dose 4 (booster), single (Lot number: FP7135) at the age of 66 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "HTN" (unspecified if ongoing); "DM" (unspecified if ongoing); "Hypercholesterolemia" (unspecified if ongoing); "BPH" (unspecified if ongoing); "Known allergies: PCN" (unspecified if ongoing). Concomitant medication(s) included: TERAZOSIN; CLARITIN [LORATADINE]; PEPCID [FAMOTIDINE]; METFORMIN; HCTZ; MULTI VITAMINS. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. The patient took Anti-viral drug Paxlovid from 14Jun2022 to 19Jun2022 for treatment of COVID-19.; Sender's Comments: Based on the information in the case, an association between the reported events and the suspect product bnt162b2 cannot be ruled out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: BPH; Diabetes mellitus; Hypercholesterolemia; Hypertension; Penicillin allergy
Andere Medikamente: TERAZOSIN; CLARITIN [LORATADINE]; PEPCID [FAMOTIDINE]; METFORMIN; HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 2371613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: -
Geschlecht: M
Eingang: 16.07.2022
Impfdatum: 21.06.2022
Beginn: 10.07.2022
Tage bis Beginn: 19,0
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 rebound. Finished Paxlovid on July 2nd, tested positive July 10th; COVID rebound. Finished Paxlovid on July 2nd, tested positive July 10th; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33-year-old male patient received BNT162b2 (BNT162B2), on 30Mar2021 as dose 1, single (Lot number: ER8734), in left arm, on 20Apr2021 as dose 2, single (Lot number: ER8735), in left arm, on 09Nov2021 as dose 3 (booster), single (Lot number: 30145BA), in left arm and on 21Jun2022 as dose 4 (booster), single (Lot number: FP7135), in left arm for covid-19 immunisation. The patient's relevant medical history included: "One kidney" (unspecified if ongoing); "eczema" (unspecified if ongoing); "depression" (unspecified if ongoing). Concomitant medication(s) included: FLUOXETINE; BUPROPION; CETIRIZINE; ACETAMINOPHEN; IBUPROFEN; ATORVASTATIN. The following information was reported: COVID-19 (medically significant) with onset 10Jul2022, outcome "not recovered", VACCINATION FAILURE (medically significant), outcome "not recovered" and all described as "COVID rebound. Finished Paxlovid on July 2nd, tested positive July 10th". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown results; (10Jul2022) Positive, notes: Finished Paxlovid on 02Jul, tested positive 10Jul. Therapeutic measures were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220710; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Finished Paxlovid on 02Jul, tested positive 10Jul
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Eczema; Kidney absent
Andere Medikamente: FLUOXETINE; BUPROPION; CETIRIZINE; ACETAMINOPHEN; IBUPROFEN; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2370745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 15.07.2022
Beginn: 15.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Chest discomfort

Symptomtext

Pt states she started feeling chest pressure about 5 minutes after the vaccine was administered. Says she has had this feeling other times but never after a vaccines. BP checked WNL. States sometimes she has high BP. after talking with pt for about 5 mins she said it had decreased to a "little discomfort" and after another 5 mins she said she was feeling better. Advised check with PMD if pain or discomfort return.

Weitere VAERSDATA-Felder

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

VAERS 2370568

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WA
Alter: 15,0
Geschlecht: F
Eingang: 15.07.2022
Impfdatum: 14.07.2022
Beginn: 14.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

None observed

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: Not applicable
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Eggs - causes nausea
Vorherige Impfungen: -

VAERS 2369215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: ME
Alter: 21,0
Geschlecht: M
Eingang: 14.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Vaccination error

Symptomtext

Gave 4th dose outside of protocol. Mis-interpreted date range on protocol

Weitere VAERSDATA-Felder

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

VAERS 2369212

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: ME
Alter: 27,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Expired product administered Extra dose administered

Symptomtext

vaccine given outside of protocol. I mis-interpreted protocol and gave 4th dose outside of age range

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2369208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: ME
Alter: 19,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
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 Product administered to patient of inappropriate age

Symptomtext

Dose administered outside protocol. Not currently eligible for 4th shot based on age. I mis-understood the guidelines

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2369119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NM
Alter: 53,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 11.07.2022
Beginn: 11.07.2022
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 No adverse event

Symptomtext

Expired vaccine administered to the patient. No adverse effects reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: Mitral valve disorder, GERD, Diabetes, type 2; thrombocytosis, depression, phyllodes tumor of breast
Andere Medikamente: Aspirin EC 81mg, citalopram, metformin XR 500mg, MVI with minerals/ferrous fumarate
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2368121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 63,0
Geschlecht: F
Eingang: 13.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Patient received lower dose- 0.25mL administered instead of 0.3mL dose. No side effects reported after administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2368077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: ID
Alter: 4,0
Geschlecht: M
Eingang: 13.07.2022
Impfdatum: 13.07.2022
Beginn: 13.07.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient given adult Pfizer dose (grey cap) instead of pediatric Pfizer dose (maroon cap).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: N/A
Vorherige Impfungen: -

VAERS 2366531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 12.07.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

Non immunocompromise, 73 year old male patient arrived to vaccination site after a doctors appointment and reported he was here for his second booster dose per his doctors instructions. Patients chart and vaccine card were reviewed and it was determined he would be getting a second booster of Pfizer 0.3mL. Patient had Pfizer for all of his doses- first dose in primary series (per vaccine card and patients chart) was administered on 2/18/21, second dose of primary series administered on 3/11/21, and first booster administered on 10/4/21. Patient was given a 0.3mL Pfizer booster by LVN vaccinator. Upon going to place vaccine sticker with information about second booster on patients vaccine card, the vaccinator turned over the card (as there was no more room on the front) and noticed that patient had actually another documented vaccine on the back of the card. Patient reported he forgot aht he actually already had another booster in another state. This was a Pfizer 0.3mL IM dose given on 5/13/22. patients chart did not state this and patient reported he has been hospitalized 3 times recently and his mind has been "all over the place." Patient was given an extra dose (for a total of 5 doses of Pfizer now). No complaints of pain at this time. MD on call was contacted and patient was instructed to monitor self for any symptoms deviating from his normal baseline and to go to the nearest urgent care or ER if symptoms develop.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2366466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 9,0
Geschlecht: F
Eingang: 12.07.2022
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: unbekannt Erholt: unbekannt

Incorrect dose administered

Symptomtext

pfizer (grey cap) administered in error to 9 year-old

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2366402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: -
Alter: 68,0
Geschlecht: F
Eingang: 12.07.2022
Impfdatum: 11.07.2022
Beginn: 11.07.2022
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

Patient was given an expired dose of pfizer 30mcg/0.3ml vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2366052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 85,0
Geschlecht: M
Eingang: 12.07.2022
Impfdatum: 02.06.2022
Beginn: 02.07.2022
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: - / -

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

Anticoagulant therapy Ataxia Balance disorder COVID-19 Computerised tomogram normal Echocardiogram Ejection fraction Haemoglobin decreased Magnetic resonance imaging normal Muscular weakness Transferrin saturation decreased

Symptomtext

Discharge Provider: MD Primary Care Provider: None Physician, DO Admission Date: 7/2/2022 Discharge Date: Jul 5, 2022 PRESENTING PROBLEM: Ataxia Acute ataxia COVID-19 virus infection HOSPITAL COURSE: THIS IS AN 85-YEAR-OLD GENTLEMAN WITH A HISTORY OF PERMANENT ATRIAL FIBRILLATION WHO PRESENTED WITH ACUTE BILATERAL LOWER EXTREMITY WEAKNESS WITH CONCERN OF POSSIBLE STROKE. HAS BEEN ON ELIQUIS FOR PERMANENT ATRIAL FIBRILLATION AND HAS HAD A PREVIOUS SIMILAR NEUROLOGIC EVENT IN THE DISTANT PAST. HIS CT IMAGING IN THE EMERGENCY DEPARTMENT WAS NORMAL. HE WAS ADMITTED AND CONTINUED ON ELIQUIS, AND WAS TREATED WITH PT AND OT. HE HAD GRADUAL RESOLUTION OF HIS WEAKNESS AND WAS ESSENTIALLY BACK TO NORMAL BY DISCHARGE WITH ONLY MINOR DIFFICULTY WITH HIS BALANCE. MRI IMAGING WAS OBTAINED PRIOR TO DISCHARGE AND DID NOT SHOW ANY ACUTE ISCHEMIC EVENT. ECHOCARDIOGRAPHY WAS PERFORMED AND SHOWED EF OF 40% WITHOUT OTHER ABNORMALITIES. THE ONLY OTHER CONCERN DURING THE HOSPITAL STAY WAS THE FINDING MALE WITH A HEMOGLOBIN OF 11.5. IRON STUDIES WERE OBTAINED AND SHOWED A DECREASED IRON SATURATION OF 5%. HE WILL BE DISCHARGED WITH THE ADDITION OF FERROUS SULFATE TO HIS MEDICAL REGIMEN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anticoagulant therapy
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Acute stroke due to ischemia (HCC) Atrial fibrillation (HCC) Anemia Lab test positive for detection of COVID-19 virus Hematuria Essential hypertension Hyperlipidemia
Andere Medikamente: apixaban (ELIQUIS) 5 MG tablet atenolol (TENORMIN) 50 MG tablet atorvastatin (LIPITOR) 20 MG tablet ferrous sulfate 325 (65 Fe) MG tablet latanoprost (XALATAN) 0.005 % ophthalmic solution timolol (TIMOPTIC) 0.5 % ophthalmic solution
Allergien: None
Vorherige Impfungen: -

VAERS 2363992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WI
Alter: 74,0
Geschlecht: M
Eingang: 09.07.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

Pfizer Comirnaty vial was opened on Thursday 7/7/22 at 11:48 am. Vaccine was administered on Friday 7/8/22 at approx 3:15 pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: Not known
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2363989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WI
Alter: 74,0
Geschlecht: F
Eingang: 09.07.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
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

Pfizer Comirnaty vial opened on Thursday 7/7/22 at 11:48am. Vaccine administered on Friday 7/8/22 at approx 3:15pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: None reported
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2363977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: ME
Alter: 11,0
Geschlecht: F
Eingang: 09.07.2022
Impfdatum: 09.07.2022
Beginn: 09.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect dose administered No adverse event

Symptomtext

No adverse reaction during first 30 minutes. Adult Pfizer (12+yrs) dose given in error. Patient should have received the Pediatric (under 12yr) dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: Birth control
Allergien: pollen
Vorherige Impfungen: -

VAERS 2363149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 38,0
Geschlecht: F
Eingang: 08.07.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered Medication error

Symptomtext

Pt came in to receive, third shot of Pfizer, her booster. Pt was registered and brought back to vaccinators. According to pts vaccination card was she was good on time and date to receive third vaccine. Vaccination card only showed two prior shots. With lot numbers and dates. Pt mentioned prior to vaccine administration that she had trouble with getting her first shot, pt had gone to the convention center and was told she could not receive it as per the system she had already gotten it. According the pt this was false and in that instance was her first and onky shot. Per pt, ? had to spend 2 hours with onsite management ? of convention center vaccine clinc to resolve. In conclusion there was an identical persosn of the same name and similar DoB and SSN. For this reason she was ineligible at that time. Situation was resloved per the pt that day soemtime in April 2021. Pt came in today with a vaccine card showing two prior shots, no reason to suspect more, pt passed screening and willing wanted to receive the shot. Pfizer 0.3ml was given to the pt intramuscular in the Right Arm. Pt waited her 15 mins and left facility. Hours later during a quality check of vaccinated patients , this said pts information showed todays visit was her fifth, unknown how the system did not alert earlier or brought into question. Vaccinator thought it was resolved as per the pts story and vaccine card. Unable to prove whether the pts story is true or if the system is wrong, a medical error form is being filled up to address.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2362994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MO
Alter: 17,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 08.07.2022
Beginn: 01.07.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

Pfizer FP7135 dose #4 inadvertently given with no immunocompromised issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 2362630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: PA
Alter: 69,0
Geschlecht: M
Eingang: 08.07.2022
Impfdatum: 08.07.2022
Beginn: 08.07.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Product administered at inappropriate site

Symptomtext

Using 1 inch needle during injection per patient weight and arm appearance, felt like needle him bone from past experience, pulled back slightly and injected full dose to patient. By looking at patient arm thickness doesn't seem that the needle would have been long enough to hit bone. To best knowledge patient got injection in muscle. patient himself counseled and denies having any metal or anything in his arm. Patient reports "hard skin" due to diabetes and did not have any pain on injection or blood from injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered at inappropriate site
Hospital-Tage: -
Labordaten: None, patient reports no pain or adverse reaction.
Aktuelle Erkrankungen: None known
Vorgeschichte: Diabetic per patient
Andere Medikamente: Diabetic medication. glipizide, metformin, actos. unknown OTC medication
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2361109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: AZ
Alter: 39,0
Geschlecht: F
Eingang: 07.07.2022
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

Extra dose administered

Symptomtext

pt received a second booster when not recommended (pt is less than 50 years old and no immunosupression) no side effects or reaction

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2359809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: IL
Alter: 37,0
Geschlecht: F
Eingang: 06.07.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Inappropriate schedule of product administration No adverse event

Symptomtext

2nd Pfizer vaccine given 14 days after 1st Pfizer vaccine. Patient monitored 15 mins-No signs & symptoms present/noted

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Mild intermittent Asthma
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2357634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 29.06.2022
Beginn: 29.06.2022
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

Symptomtext

Patient received 5th dose of Pfizer COVID vaccine by error. Clinic was not notified until patient called clinic this morning stating he looked at his COVID vaccine card and noticed he received his 5th dose at our clinic yesterday (6/29/22).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2357522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: CA
Alter: 13,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 01.07.2022
Beginn: 01.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series Given Too Early-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2357521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 01.07.2022
Beginn: 01.07.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series Given Too Early-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2356794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: NY
Alter: 26,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 30.06.2022
Beginn: 03.07.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Vision blurred

Symptomtext

Blurry vision in one eye, feels like a film over the eye

Weitere VAERSDATA-Felder

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

VAERS 2356716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: OK
Alter: -
Geschlecht: U
Eingang: 03.07.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Adverse event

Symptomtext

Incorrect product storage (unknown if vaccine was administered); This case has been considered invalid-Unspecified AE. COVID-19 Vaccine temperature related enquiry by a costumer Product and costumer information: Product description: Pfizer BioNTech COVID-19 gray cap Batch/LOT number: FP7135 Expiry date: Nov2021 Date of shipment arrived at costumer and reference number for shipment (If applicable): 09May2022 Number of product unit impacted: 30 vials Costumer type: Pharmacy Temperature excursion information: Is the product diluted or undiluted: Undiluted Where the product stored when excursion occurred?: Freezer Maximum and minimum temperature reported/Measured during excursion: -5 to -6degree F Duration of excursion: 49 Provide the completed temperature data during storage at costumer location: Attached If Pfizer has not delivered product o the costumer location where excursion has occurred, provide the temperature data for the transport to this location to confirm this stock has not experienced any other /previous excursion: Pfizer delivered to this location Follow-Up (30Jun2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2356448

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fp7135

gering

Staat: -
Alter: 31,0
Geschlecht: F
Eingang: 03.07.2022
Impfdatum: 19.06.2022
Beginn: 20.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Lymphadenopathy Vaginal haemorrhage

Symptomtext

Swollen lymph node in left armpit; Vaginal bleeding/spotting; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received BNT162b2 (BNT162B2; Solution for injection), on 19Jun2022 at 09:15 as dose 3 (booster), single (Lot number: Fp7135) at the age of 31 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Anxiety" (unspecified if ongoing). Concomitant medication(s) included: FLUOXETINE; PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS FUMARATE;FOLIC ACID;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL ACETATE;RIBOFLAVIN;THIAMINE MONONITRATE;TOCOPHERYL ACETATE;ZINC OXIDE]. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: En6203, Location of injection: Arm Left), administration date: 25Feb2021, when the patient was 30-year-old, for Covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: El9269, Location of injection: Arm Left), administration date: 04Feb2021, when the patient was 30-year-old, for COVID-19 immunization. The following information was reported: LYMPHADENOPATHY (non-serious) with onset 20Jun2022, outcome "recovered", described as "Swollen lymph node in left armpit"; VAGINAL HAEMORRHAGE (non-serious) with onset 20Jun2022, outcome "recovered", described as "Vaginal bleeding/spotting". Therapeutic measures were not taken as a result of lymphadenopathy, vaginal haemorrhage. Additional information: Swollen lymph node in left armpit for 5 days, vaginal bleeding/spotting for 5 days. I have never had spotting before in my life. Even when pregnant. This is what concerns me the most. If covid prior vaccination: No. If covid tested post vaccination: No. No Known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymphadenopathy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety
Andere Medikamente: FLUOXETINE; PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS
Allergien: -
Vorherige Impfungen: -

VAERS 2354536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: IN
Alter: 38,0
Geschlecht: F
Eingang: 02.07.2022
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: nein

Expired product administered

Symptomtext

Vaccine was checked in by Pharmacist to be administered by Immunizing Tech. Tech did not realize the vial that was out was labeled and timed from the day prior and expired and new vial needed to be pulled out of fridge. Tech drew a dose out of expired vial and administered to patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2353786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fp7135

gering

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 02.07.2022
Impfdatum: 30.06.2022
Beginn: 01.07.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Lymphadenopathy

Symptomtext

Swollen lymph nodes under armpit

Weitere VAERSDATA-Felder

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

VAERS 2347174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 24.06.2022
Beginn: 25.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Contusion Lymphadenopathy

Symptomtext

Systemic: Lymph Node Swelling-Mild, Additional Details: Lymph node on the arm with injections swollen and BRUISES on that underarm.

Weitere VAERSDATA-Felder

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

VAERS 2344887

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 30.06.2022
Impfdatum: 29.06.2022
Beginn: 30.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

The patient was given the vaccine from a vial that should have been disposed of. The vial expired the night at midnight 6/29 and the patient received the vaccine 6/29 at 11:02 am. I spoke with the patient on 6/30/22 at 2;30pm and she denied any adverse affects. she stated she was doing fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, COPD.
Andere Medikamente: -
Allergien: Tenormin; Symbicort; Dulera.
Vorherige Impfungen: -

VAERS 2342239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: VA
Alter: 10,0
Geschlecht: M
Eingang: 29.06.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

Received 0.3 ml of Pfizer -grey top for 12 yr. and older.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: 6/14/2022-seen in clinic for a tick bite
Vorgeschichte: Ezcema Reactive Airway Disease
Andere Medikamente: Proventil MDI Pulmicort Epi-Pen
Allergien: Peanuts-anaphylaxis Shellfish derived products
Vorherige Impfungen: -

VAERS 2341979

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: VT
Alter: 77,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 07.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 17,0
Dosis: 4
Route/Site: SYR / RA

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

Discomfort Laboratory test abnormal

Symptomtext

I had been experiencing discomfort in my side and I thought it was muscle strain. I went into the hospital to have a CA2015 which is my cancer marker. The next day the doctors office called me and told me my CA2015 had gone to 10 from 2 months ago to 215. I couldn't imagine what would make it jump that high. I continue to have the discomfort in my side.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Discomfort
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Cancer
Andere Medikamente: FOSAMAX; calcium supplement; vitamin D3; vitamin C; milk thistle; omega 3 fish oil; magnesium; PERCUMIN; BENEFIBER.
Allergien: Sulfa.
Vorherige Impfungen: -

VAERS 2341834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WI
Alter: 11,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 23.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Incorrect dose administered

Symptomtext

An adult concentration of the Pfizer vaccine was given to an 11 year old patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: ketoconazole (NIZORAL) 2 % shampoo mometasone (ELOCON) 0.1 % solution
Allergien: none
Vorherige Impfungen: -

VAERS 2341821

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NH
Alter: 82,0
Geschlecht: F
Eingang: 29.06.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
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

vial was stored outside of parameters, spoke to manufacturer and determined that patient is safe and revaccination is not recommended. called pt and they are ok.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2341815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NH
Alter: 78,0
Geschlecht: M
Eingang: 29.06.2022
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: unbekannt Erholt: ja

Product storage error

Symptomtext

vial was stored outside of parameters, spoke to manufacturer and determined that patient is safe and revaccination is not recommended. called pt and they are ok.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2341809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NH
Alter: 72,0
Geschlecht: F
Eingang: 29.06.2022
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: unbekannt Erholt: ja

Expired product administered

Symptomtext

vial was stored outside of parameters, spoke to manufacturer and determined that patient is safe and revaccination is not recommended. called pt and they are ok.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2341798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NH
Alter: 68,0
Geschlecht: M
Eingang: 29.06.2022
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: unbekannt Erholt: ja

Product storage error

Symptomtext

vial was stored outside of parameters, spoke to manufacturer and determined that patient is safe and revaccination is not recommended. called pt and they are ok.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2341790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NH
Alter: 74,0
Geschlecht: M
Eingang: 29.06.2022
Impfdatum: 27.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Expired product administered

Symptomtext

vial used for injection was outside storage and handling limits. after speaking to manufacturer, recommend not revax and should not be safety issues. called patient and no side effects

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2339474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: -
Alter: 7,0
Geschlecht: M
Eingang: 28.06.2022
Impfdatum: 28.06.2022
Beginn: 28.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

PFIZER GREY CAP ADMINISTERED TO 7 YEAR OLD

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2338965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MI
Alter: 32,0
Geschlecht: M
Eingang: 28.06.2022
Impfdatum: 27.06.2022
Beginn: 27.06.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Expired product administered Product storage error

Symptomtext

Pfizer gray cap vaccine was punctured on 6/26/22 at 10:45 am and two doses were drawn and administered. The vaccine was not disposed of at the end of business day on 6/26/22. On 6/27/22 we gave an additional dose that came from the same vial. The vial had been expired (per storage conditions) since 10:45 pm on 6/26/22. The dose was drawn up and then administered at about 6:20 pm on 6/27/22. Upon calling Pfizer, they stated that they only have data to show stability for up to 24 hours after first puncture when the vial is held between 28 and 86 degrees Fahrenheit. Therefore, according to the CDC, the dose should be repeated immediately with no minimum interval. We have left a message on the patient's voicemail to have them call us back regarding their vaccination. Upon a call back, we will explain the discrepancy and recommend re-vaccination immediately. No adverse events have been reported yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2335569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: SC
Alter: 65,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 23.06.2022
Beginn: 23.06.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Eye swelling Mouth swelling Swelling face Swollen tongue Visual impairment

Symptomtext

Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Mild, Systemic: Visual Changes/Disturbances-Mild, Additional Details: Patient returned to pharmacy around 30 minutes after vaccination reporting narrowing of vision angle and possible swelling around the eyes. Administered 50mg Benaryl orally and monitored patient for around 30 minutes. Patient reported no further progression of symptoms while waiting and patient decided to return home. Instructed patient to continue to monitor and followed up by phone encounter around 3 hours later. Patient stated no further progression of syptoms at that time.

Weitere VAERSDATA-Felder

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

VAERS 2332401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: WA
Alter: 31,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 24.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Lymphadenopathy

Symptomtext

swollen lymph node

Weitere VAERSDATA-Felder

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

VAERS 2332171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: ID
Alter: 7,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 24.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Pt received child dose of adult Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: None at this time
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: None at this time
Allergien: NKDA/NKA
Vorherige Impfungen: -

VAERS 2332165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NE
Alter: 32,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 23.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Patient came in to clinic and received a COVID19 (Pfizer-BioNTech) vaccination on 06/23/22, she then came in for a second office visit on 06/24/22 and received another COVID19 (Pfizer-BioNTech) vaccination. Patient was not due for another Pfizer Covid 19 vaccine until 07/24/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None/NA
Aktuelle Erkrankungen: N/A
Vorgeschichte: OSA (Obstructive sleep apnea) Hiatal Hernia Abnormality of heart valve Class 3 severe obesity with serious comorbidity and body mass index (BMI) of 50.0 to 59.9 in adult (HCC) Iron deficiency Hypovitaminosis D Hypocalcemia Behavioral: H/O: substance abuse (HCC), PTSD (post-traumatic stress disorder), Depression Moderate episode of recurrent major depressive disorder (HCC) Neurology / Sleep: Intractable chronic migraine without aura and without status migrainosus Gastrointestinal: Gastroesophageal reflux disease Genetics: DiGeorge syndrome (HCC) Other: Family history of blood clots
Andere Medikamente: Famotidine 20mg (1 Tablet BID) Ferrous Sulfate 325 mg (1 Tablet daily) Fluoxetine (Prozac 20 mg capsule) 1 Capsule daily Fluticasone propionate (2 sprays by each nare route once daily) Pantoprazole 40 mg (1 tablet once a day) Topiramate 5
Allergien: Kiwi: Hives Phenylephrine HCL: Itching, red skin color Macrobid : Itching, red skin color, tremor Pseudoephedrine HCL: Throat irritation
Vorherige Impfungen: -

VAERS 2332165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: NE
Alter: 32,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 23.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / -

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

Inappropriate schedule of product administration

Symptomtext

Patient came in to clinic and received a COVID19 (Pfizer-BioNTech) vaccination on 06/23/22, she then came in for a second office visit on 06/24/22 and received another COVID19 (Pfizer-BioNTech) vaccination. Patient was not due for another Pfizer Covid 19 vaccine until 07/24/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None/NA
Aktuelle Erkrankungen: N/A
Vorgeschichte: OSA (Obstructive sleep apnea) Hiatal Hernia Abnormality of heart valve Class 3 severe obesity with serious comorbidity and body mass index (BMI) of 50.0 to 59.9 in adult (HCC) Iron deficiency Hypovitaminosis D Hypocalcemia Behavioral: H/O: substance abuse (HCC), PTSD (post-traumatic stress disorder), Depression Moderate episode of recurrent major depressive disorder (HCC) Neurology / Sleep: Intractable chronic migraine without aura and without status migrainosus Gastrointestinal: Gastroesophageal reflux disease Genetics: DiGeorge syndrome (HCC) Other: Family history of blood clots
Andere Medikamente: Famotidine 20mg (1 Tablet BID) Ferrous Sulfate 325 mg (1 Tablet daily) Fluoxetine (Prozac 20 mg capsule) 1 Capsule daily Fluticasone propionate (2 sprays by each nare route once daily) Pantoprazole 40 mg (1 tablet once a day) Topiramate 5
Allergien: Kiwi: Hives Phenylephrine HCL: Itching, red skin color Macrobid : Itching, red skin color, tremor Pseudoephedrine HCL: Throat irritation
Vorherige Impfungen: -

VAERS 2331901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

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Staat: OK
Alter: 28,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 23.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Reading disorder Vision blurred

Symptomtext

Pt had blurry vision on the second day after immunization was given. It was blurry enough that she cannot read.

Weitere VAERSDATA-Felder

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

VAERS 2331895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

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Staat: MI
Alter: 74,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 23.06.2022
Beginn: 24.06.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Incorrect dose administered Interchange of vaccine products No adverse event Wrong product administered

Symptomtext

NO Adverse Drug Event to report, however, the incorrect Covid-19 vaccine was drawn up and administerd. The wrong dose was administered. Patient had received the Moderna vaccine for dose #1 and was appropriate for second dose in primary series. Moderna vaccine (0.5ml) was ordered, but erroneously, 0.5ml of Pfizer vaccine was drawn up and administered. No adverse reaction or event reported. Nurse notified. Prescriber will be notified. Patient will be notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2329033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

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Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 23.06.2022
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: nein

Inappropriate schedule of product administration

Symptomtext

patient asymptomatic but was given Pfizer 2nd booster dose one month early.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: HTN, DM, COPD, Hypocholesteremia, vitamin b12 deficiency, osteoporosis
Vorgeschichte: HTN, DM, COPD, Hypocholesteremia, vitamin b12 deficiency, osteoporosis
Andere Medikamente: trazodone, metformin, diclofenac gel, miralax, magnesium citrate, buspar, chantix, vitamin b12, flexeril, albuterol, pravastatin, flovent, claritin, prolia, propranolol, duloxetine,
Allergien: erythromycin, adhesive tape
Vorherige Impfungen: -

VAERS 2326978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

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Staat: NE
Alter: 53,0
Geschlecht: F
Eingang: 22.06.2022
Impfdatum: 20.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Axillary mass

Symptomtext

I am self reporting this, as I have a very large mass under my right arm by my lymph nodes. Approximately, lemon size. I called the doctor's office and they said this wasa completely normal reaction.I disagree, and am submitting as an adverse reaction. I was told to ice, take Ibuprofen and range of motion exercises. I want to go on record to report this, however "normal" it is believed to be. As for Item 21, the outcome is unknown as of 6.22.22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary mass
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: I have high blood pressure and take the above medications for that.
Andere Medikamente: Hydroclorithyizde, Cartia XT, Vitamin E, Elderberry, Vitamin C & Zinc
Allergien: Eurthromycin
Vorherige Impfungen: -

VAERS 2325698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

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Staat: CA
Alter: 14,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 21.06.2022
Beginn: 21.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Device connection issue Product administered to patient of inappropriate age Syringe issue Underdose

Symptomtext

Pt was receving her 1st COVID-19 Pfizer booster vaccination. While nurse was administering the vaccine, the syringe hub separated from the syringe causing part of the vaccine to be administered while the rest spilt from the syringe. Given the loss of vaccine, this administration was followed with a pediatric dose of pfizer after consent from the patient and her mother.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Device connection issue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2324125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP 7135

gering

Staat: MA
Alter: 9,0
Geschlecht: M
Eingang: 20.06.2022
Impfdatum: 18.06.2022
Beginn: 18.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Incorrect dose administered No adverse event Incorrect product formulation administered

Symptomtext

NO ADVERSE EVENTS REPORTED FROM INCORRECT DOSE ADMINISTERED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2324125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FP7135

gering

Staat: MA
Alter: 9,0
Geschlecht: M
Eingang: 20.06.2022
Impfdatum: 18.06.2022
Beginn: 18.06.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered No adverse event Incorrect product formulation administered

Symptomtext

NO ADVERSE EVENTS REPORTED FROM INCORRECT DOSE ADMINISTERED

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -