- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.11.2023
- Impfdatum
- 12.01.2023
- Beginn
- 10.10.2023
- Tage bis Beginn
- 271,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Chest X-ray abnormal
Condition aggravated
Cough
Dyspnoea
Hypoxia
Lung infiltration
Lung opacity
Mobility decreased
Pulmonary congestion
SARS-CoV-2 test positive
Symptomtext
Patient is a 68 y.o. female patient of, MD with history of morbid obesity, chronic pain, IBS, ESBL UTI, OSA, abd pain presented to Doctors Hospital with SOB. Acute respiratory failure with hypoxia - resolved Chronic respiratory failure, reports 5 L home O2 requirement at nighttime and laying down COVID-19, POA Possible CAP Cough and SOB x 3 days. Called PCP prior to admission advised ED evaluation Currently requiring 5L all day; baseline 5L O2 only at night CXR (10/10) pulm vascular congestion, diffuse interstitial infiltrates and opacifications Afebrile, no leukocytosis Positive covid-19 test Started on remdesivir and steroids. Remdesivir course will not keep patient in hospital if she is medically improved for discharge otherwise. Pulm hygiene ID consulted for assistance with COVID-specific therapies Started on dexamethasone as well as remdesivir which was discontinued as patient was improved before course completion Morbid obesity BMI 65.37 Patient would benefit from bariatric surgery referral outpatient Reduced mobility, on admission Patient with wheelchair in her room which she utilizes much of the time at home Fibromyalgia Back pain Per history S/p L4 laminectomy by Dr. (NS) 10/2020 Resume home flexeril OSA Compliant with CPAP Ordered Chronic Abdominal pain Asymptomatic on arrival Recently admitted 10/5 for assistance with bowel prep for planned EGD/colonoscopy per Dr., GI Bowel prep was not ordered and procedure was not able to be completed Follow up with GI outpt Residence prior to admission: house or apartment Was patient transferred from outlying hospital or ED no
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.08.2023
- Impfdatum
- 25.04.2023
- Beginn
- 30.04.2023
- Tage bis Beginn
- 5,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood bicarbonate decreased
Blood chloride increased
Blood gases abnormal
Blood glucose increased
Blood lactic acid
Blood pH decreased
Blood potassium normal
Blood sodium decreased
Calcium ionised
Cardio-respiratory arrest
Chills
Death
Diarrhoea
Loss of consciousness
Malaise
PCO2 normal
PO2 increased
Pulseless electrical activity
Symptomtext
Had diarrhea, vomiting, chills and generalized malaise x2 days following Covid vaccine on 4/25/23, symptoms resolved by 4/28/2023. On 4/30/2023 husband paged on-call transplant coordinator to notify team that patient had passed out at home and EMS was called. Per EMS, the patient was observed to have syncope from the commode after which EMS was immediately called. EMS arrived within 4 minutes and initiated CPR. Prior to arrival in the emergency department EMS administered 11 rounds of epinephrine with continuous CPR, ROSC achieved and then rearrested. Code had been ongoing for 45 min on arrival. Pulse checks demonstrated PEA. CPR was resumed and epinephrine was readministered upon arrival to ED. 4/30/23 1813 Code started 4/30/23 1816 epi administered 4/30/23 1820 epi administered 4/30/23 1824 epi administered 4/30/23 1828 epi administered 4/30/23 1831 time of death
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- -
- Labordaten
- 4/30/2023 @ 1820 VBG pH 6.767/ pCO2 46.3/ pO2 80.7 /HCO3 6.5 4/30/2023 @ 1829 Whole Blood Glucose 532, Chloride 109, Sodium 133.6, Potassium 4.6, Lactic Acid 11.69, ionized Calcium 4.6
- Aktuelle Erkrankungen
- Abdominal hematoma following laparoscopic dor fundoplication on 3/8/2023 - size of grapefruit; Had diarrhea, vomiting, chills and generalized malaise x2 days following Covid vaccine on 4/25/23
- Vorgeschichte
- s/p lung transplant 10/1/2022 for hypersensitivity pneumonitis, GERD, gastroparesis, botox injection of pylorus 1/23/23, h/o gastric band, laparoscopic dor fundoplication 3/8/2023 complicated by hematoma
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG tablet budesonide (PULMICORT) 0.5 MG/2ML nebulizer suspension Cholecalciferol (VITAMIN D) 1000 UNIT TABS escitalopram (LEXAPRO) 10 MG tablet Estradiol 10 MCG TABS gabapentin (NEURONTIN) 100 MG capsu
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.07.2023
- Impfdatum
- 13.01.2023
- Beginn
- 10.04.2023
- Tage bis Beginn
- 87,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Alanine aminotransferase increased
Angiogram pulmonary abnormal
Aspartate aminotransferase increased
Blood bilirubin
Blood folate
Blood magnesium
Blood phosphorus
Blood potassium decreased
COVID-19
COVID-19 pneumonia
Calcium ionised
Chronic obstructive pulmonary disease
Condition aggravated
Cough
Dyspnoea
Electrolyte substitution therapy
Emphysema
Symptomtext
62 y.o. female patient of, DO with history of HTN, DM, tobacco use, CAD, PAD, COPD. Presents with dyspnea and cough. Found to be in acute hypoxic respiratory failure, requiring 2LNC 2/2 COVID and COPD exacerbation. Respiratory status initially improved with steroid therapy, but patient continues to require oxygen. Acute Hypoxic Respiratory Failure Suspected 2/2 covid PNA vs COPD exacerbation CTPA w/o PE, right upper lobe infilatrates, centrilobular emphysema Additional management as below Required continuous 2L NC oxygen on discharge Covid 19 Infection Acute COPD exacerbation Positive test on admission, symptom onset 4/4 Completed vaccinations Continued dexamethasone and remdesivir for COVID Continued azithro for COPD exacerbation Duoneb q 4 hr scheduled, IS, mucinex Hypokalemia - resolved K on admission 2.0 Monitored and repleted as needed T2DM 4/10 A1c 9.5% Likely worsened hyperglycemia in setting of seroids Home meds: glipizide and metformin, held On day of discharge patient received 74u lantus and 54u SSI Will need close outpatient follow up for titration of medications PCP notified Hypocalcemia Asymptomatic Ionized calcium 3.3 Phos 2.8, Mag 1.7 Repleted electrolytes PRN Transaminitis, resolved ALT/AST 51/133, T bili 2.1 on admission Denied daily use of alcohol, no reported hx of w/d seizures Hepatitis panel negative Monitored for signs of w/d Daily CMP Macrocytosis MCV 103 on admission Appeared chronically elevated B12 1784, folate 6.4 HTN Chronic, elevated on admission 2/2 to poor med adherence Asymptomatic Home medications: lisinopril, metoprolol, Continued metoprolol Held home lisinopril CAD PAD Hx of SVT Continued home meds with ASA, plavix, atorvastatin Continued home diltiazem for rate control Tobacco Use Disorder Smokes 0.5 ppd NRT prn Multinodular Goiter Incidentally noted on CT scan Recommend TSH and US in OP setting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 24.06.2023
- Impfdatum
- 20.06.2023
- Beginn
- 21.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- OT / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient was found expired in bed in the morning of next day ( after the vaccination); This is a spontaneous report received from a contactable reporter(s) (Physician). A 74-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Jun2023 at 11:00 as dose 5 (booster), single (Lot number: GJ6796) at the age of 74 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "A.fib," (unspecified if ongoing); "HTN" (unspecified if ongoing); "HLD" (unspecified if ongoing); "morbid obesity" (unspecified if ongoing); "OA" (unspecified if ongoing); "lymphedema" (unspecified if ongoing); "recurrent cellulitis of LEs" (unspecified if ongoing). Concomitant medication(s) included: ELIQUIS; FUROSEMIDE; LEVOTHYROXINE; METOPROLOL; ACETAMINOPHEN; VITAMIN D [ERGOCALCIFEROL]; TRAMADOL; NYSTATIN; MULTIVITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;FOLIC ACID;NICOTINAMIDE;PANTHENOL;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]. Vaccination history included: Covid-19 vaccine (DOSE 4 (BOOSTER); MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 3 (BOOSTER); MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 2; MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: DEATH (death, medically significant) with onset 21Jun2023 at 07:00, outcome "fatal", described as "Patient was found expired in bed in the morning of next day ( after the vaccination)". Therapeutic measures were not taken as a result of death. The patient date of death was 21Jun2023. The reported cause of death was unknown. It was not reported if an autopsy was performed. Clinical course: The patient did not take any other vaccines in four weeks and was not tested for COVID-19 prior to vaccination and post vaccination. Patient was found expired in bed in the morning of next day (after the vaccination).; Sender's Comments: Based on the information in the case report, a possible causal relationship between the event death and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate. ; Reported Cause(s) of Death: found expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Atrial fibrillation; Cellulitis; Hyperlipidemia; Hypertension; Lymphedema; Morbid obesity; Osteoarthritis
- Andere Medikamente
- ELIQUIS; FUROSEMIDE; LEVOTHYROXINE; METOPROLOL; ACETAMINOPHEN; VITAMIN D [ERGOCALCIFEROL]; TRAMADOL; NYSTATIN; MULTIVITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;FOLIC ACID;NICOTINAMIDE;PANTHENOL;RETINOL;RIBOFLAVIN;THI
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 06.04.2023
- Impfdatum
- 12.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Cough
Dyspnoea
Positive airway pressure therapy
SARS-CoV-2 test positive
Symptomtext
Patient with history of COPD, CHF, lung cancer. He was brought to the ED by EMS on 12/29/22. He tested positive for COVID-19 two days prior, and over the past few days has had increasing shortness of breath and coughing. That day he was found to be at 87% O2 and does not usually use oxygen so staff called for EMS. The patient was placed on a nonrebreathing mask by EMS, which increased his O2 sats to over 90%. Additional COVID-19 PCR test performed in the ED on 12/29/22 also resulted positive. He was admitted 12/29/22 - 1/4/23 with discharge diagnoses including acute hypoxemic respiratory failure and COVID-19 pneumonia, among other diagnoses. Initially on admission patient was requiring BiPAP and was able to go to 3L via nasal cannula, and eventually weaned to room air.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.03.2023
- Impfdatum
- 29.12.2022
- Beginn
- 12.01.2023
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anticoagulant therapy
Cerebrovascular accident
Facial paralysis
Monoplegia
Symptomtext
Stroke with right side hand and mouth paralysis. Patient was treated with plavix for 30 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- Patient was admitted to the hospital and determined she had a stroke.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 21.02.2023
- Impfdatum
- 02.02.2023
- Beginn
- 18.02.2023
- Tage bis Beginn
- 16,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac arrest
Dyspnoea
Pulseless electrical activity
Symptomtext
Pulseless electrical activity, Cardiac arrest, possible PE event, pt spouse reported shortness of breath 3-4 days prior to incident with no recent illness per hospital report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- PEA at rhythm checks 2/18/23
- Aktuelle Erkrankungen
- Hypothyroidism, Depression, Migraines, Dyslipidemia, RA, Hx colitis, Dog Bite in Jan 2023,
- Vorgeschichte
- Hyperlipidemia, Hypothyroidism
- Andere Medikamente
- citalopram 40mg take 1 tab daily. levothyroxine 50mcg take 1 tab daily. SUMAtriptam 25mg 1 tab as needed, may repeat 1 dose after 2 hours. zofran 4 mg take 1 tab as needed. Folic acid, Xeljanz, fexofenadine
- Allergien
- Latex, Sulfamethoxazole-trimethoprim, Banana, Iodine, Shellfish, Opium
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 16.02.2023
- Impfdatum
- 05.01.2023
- Beginn
- 08.01.2023
- Tage bis Beginn
- 3,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Blood test normal
Computerised tomogram abnormal
Dysarthria
Dysphemia
Hypoaesthesia
Intensive care
Magnetic resonance imaging abnormal
Myocardial infarction
Peripheral swelling
Postinfarction angina
Symptomtext
Days after receiving the vaccine, my arm was swelling and felt numb. I informed my wife who noticed my speech was slurred and stuttered. She took me to the emergency room; they diagnosed me with a heart attack. I was transported to the nearest medical center and put into ICU to be monitored overnight on 01/08/2023. The next morning, the neurosurgeon examined my test results including MRI scans, CT scans, bloodwork, and heart rate panel and confirmed I was suffering from a PIA (post-infarction angina) and put me on a temporary prescription of PLAVIX.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 1,0
- Labordaten
- 08JAN202 MRI scan abnormal; CT scan abnormal; Bloodwork normal; Heart rate test normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Back Pain
- Andere Medikamente
- Lisinopril; amlodipine; finasteride; atorvastatin; pregabalin; gabapentin; daily multivitamin; vitamin D3; vitamin C; calcium; zinc; coQ-10
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 20.12.2022
- Beginn
- 31.12.2022
- Tage bis Beginn
- 11,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cerebrovascular accident
Computerised tomogram
Hypoaesthesia
Laboratory test
Limb discomfort
Symptomtext
ON 12-31-22 CLIENT WOKE AT 5:15 AM, PLANNING TO TRAVEL. HE HAD GOTTEN DRESSED AND MADE BREAKFAST AND TOOK AM MEDS. STATED" ALL AT ONCE RIGHT ARM WENT NUMB, THEN RIGHT LEG FELT LIKE IT HAD A 10 POUND WEIGHT ON IT AND IT WENT NUMB. TOLD HIS WIFE, SHE THEN DROVE HIM TO HOSPITAL. WHEN ARRIVED AT ER, BLOOD PRESSURE WAS 200+/100+ (DID NOT KNOW VALUES) A CT-SCAN WAS COMPLETED AND LAB WORK. THEN WAS TRANSFERRED TO ALTERNATE HOSPITAL ER VIA GROUND AMBULANCE. HAD ANOTHER CT-SCAN WITH LABS. WAS ADMITTED AND RELEASED ON JANUARY 2, 2023. HE WAS TOLD THAT SOME PLAQUE HAD BROKEN LOOSE AND CAUSED A STROKE. STATED HAD A COUSIN THAT ALSO HAD A STROKE AFTER RECEIVING HER BIVALENT BOOSTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 2,0
- Labordaten
- CT SCAN - 12-31-22 IN HOSPITAL ER CT SCAN - 12-31-22 IN alternate HOSPITAL
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- WARFARIN 7.5 MG QD ; ATORVASTATIN @ HS; TAMSULOSIN .4 MG ; FINATERIDE 5 MG; GLYBURIDE 1 MG Q AM; AMLODIPINE 5 MG; CARVEDILO 3.125 MG; CARBAMAZEPINE 100MG BID; OMEPRAZOLE 20 MG Q AM; TRULICITY SHOT ONCE A WEEK; ASA 81 MG QD; MAZI VISION BID
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 18.01.2023
- Impfdatum
- 01.01.2023
- Beginn
- 01.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram pulmonary normal
Cardiac arrest
Chest pain
Computerised tomogram coronary artery normal
Death
Dyspnoea
Troponin increased
Symptomtext
On day of adverse event patient presented to ER with acute dyspnea and chest pain. Cardiac arrest in waiting room. Deceased. CT PE negative. Troponin elevated. Did not have cardiac cath as he died. Previously had normal coronary Calcium score 1/4/23, so shocked if this was acute coronary syndrome from Pre existing heart disease. While has risk factors, we had just done this reassuring calcium score of zero (low risk). No autopsy done. Ultimate cause of cardiac arrest not determined.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- Will need to request records from hospital
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, tobacco dependence
- Andere Medikamente
- Metformin, bupropion, atorvastatin
- Allergien
- Seafood
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 01.12.2022
- Beginn
- 11.01.2023
- Tage bis Beginn
- 41,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Facial paresis
Symptomtext
42 days after vaccination, patient was taken to the local ER with right side facial weakness, was dx with a stroke. Family friend called to report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- History of stroke, 3 years prior
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 05.01.2023
- Tage bis Beginn
- 8,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute kidney injury
Antineutrophil cytoplasmic antibody positive
Aspiration
Biopsy kidney abnormal
Cardiac arrest
Chronic kidney disease
Haematuria
Myocardial infarction
Pulmonary haemorrhage
Renal artery arteriosclerosis
Symptomtext
12/28/22: admit for myocardial infarction; started on piperacillin-tazobactam for possible aspiration pneumonia, AKI on CKD 01/05/23: pulmonary hemorrhage 01/05/23: ANCA (antineutrophil cytoplasmic antibiotics) vasculitis panel positive 01/08/23: new hematuria 01/09/23: renal biopsy performed, showed atherosclerotic changes but no evidence of ANCA vasculitis, due to limited sample from the renal biopsy ANCA vasculitis cannot be definitively ruled out 01/13/23: patient transitioned to comfort cares
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Recent hospitalization 12/20/22 - 12/28/22 for sepsis, received 7 day course of 3rd generation cephalosporin. Discharged 12/28/22. Re-admitted same day for cardiac arrest in setting of suspected food aspiration.
- Vorgeschichte
- PMH: hypertension, DM2, parkinson's, COPD, hypothyroidism, vascular dementia
- Andere Medikamente
- Aripiprazole, aspirin, atorvastatin, sinemet, citalopram, dulaglutide, empagliflozin, lantus, levothyroxine, lisinopril, lorazepam, metoprolol,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 30.12.2022
- Impfdatum
- 31.10.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiogram pulmonary normal
Anxiety
Bacterial test positive
Blood culture
COVID-19
COVID-19 pneumonia
Chest X-ray normal
Condition aggravated
Cough
Culture urine positive
Diarrhoea
Electrocardiogram normal
Escherichia test positive
Leukocytosis
Nausea
Pathogen resistance
Pyrexia
Symptomtext
78 y.o. male patient with history of UTIs, T2DM, paroxysmal atrial fibrillation, DVT, PAD, HTN, urinary incontinence, depression and anxiety who presented with anxiety and fever, found to have respiratory failure, COVID-19, severe sepsis and acute ESBL UTI. He was treated with steroids and was weaned off of O2 prior to discharge. He was treated with Ertapenem for 3 days until urine culture returned with typical E. Coli s/t Bactrim (same as before) and ID recommended that he finish 14 total days of Bactrim. Acute hypoxic respiratory failure -- resovled COVID-19 Virus Infection Date of onset of symptoms: 7 days prior to admission Symptoms present on admission: nausea, fever, diarrhea, cough Date of covid positive test: 11/29 Vaccination status: vaccinated CXR (reviewed personally): No acute pulmonary findings CTPA: No evidence of PE or acute pulmonary abnormality Oxygen requirements on admission: 3-4L NC in ED Current oxygen requirements: RA Medical therapy: steroids x10d, out of window for remdesivir (already took Paxlovid) Consultants following: Infectious Disease Anticipated special isolation end date: 12/8/22 Severe Sepsis, POA -- resolved Urinary Tract Infection Hx of ESBL E. Coli Hx of Pyelonephritis Patient febrile (101.8), tachypneic, with leukocytosis on admission Likely sources include UTI and COVID-19 pneumonia LA 4.4 on admission UA positive nitrite, large leukocyte esterase, 122 WBCs, >180 RBCs, many bacteria Blood cultures pending, urine cultures with ESBL E. Coli ID consulted -- PO Bactrim through 12/10 Type 2 Diabetes, Insulin Dependent A1c of 8.7 on 10/24/22 Home regimen 30u lantus nightly with SSI Continued on admission Urinary Incontinence Likely due to radiation after prostate cancer treatment Follows with doctor Home solifenacin 10mg daily Paroxysmal Atrial Fibrillation EKG with NSR Continue home BB and restart apixaban (especially in light of COVID infection) Pt will f/u with doctor to discuss further Peripheral Arterial Disease Hx of DVT Continue home lipitor, plavix Restarted apixaban as above HTN Continue home lisinopril, hydrochlorothiazide, toprol Anxiety/Depression Continue home buspar, cymbalta, ativan PRN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 04.11.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Blood creatinine increased
Blood iron decreased
Blood lactic acid increased
COVID-19
COVID-19 pneumonia
Cardiac failure congestive
Chest X-ray abnormal
Dyspnoea
Echocardiogram abnormal
Ejection fraction
Glycosylated haemoglobin normal
Haemoglobin decreased
Iron binding capacity total normal
Iron deficiency anaemia
Lactic acidosis
Normocytic anaemia
Symptomtext
Patient is a 72 y.o. male patient with history of type 2 diabetes hypertension BPH and a heart murmur presented to local Hospital with worsening shortness of breath Acute hypoxemic respiratory failure Sepsis POA due to COVID pneumonia COVID-19 pneumonia Covid-19 Virus Infection Date of onset of symptoms: 11/12/2022 Symptoms present on admission: Shortness of breath Date of covid positive test: 11/8/2022 Vaccination status: vaccinated Imaging: Bilateral multifocal airspace disease chest x-ray Oxygen requirements on admission: Nonrebreather mask Oxygen requirements: was on HF now on NC Medical therapy: steroids, remdesivir and received a dose of Tocilizumab Consultants following: Infectious disease Anticipated special isolation end date: 11/22/2022 Patient is doing well, on RA, hypoxia resolved, Discharge home stable on decadron. Loud heart murmur Location and provocation suggest MR Could be causing pulmonary congestion/CHF Echocardiogram, EF of 53% AS bicuspid. Lactic acidosis Presented with LA of 7.5 Resolved down to 1.9 Acute kidney injury on chronic kidney disease stage IIIb Baseline cr is 2.5-2.6, presented with cr of 3.13 Improved back to 2.6>2.78>2.5 Acute on chronic normocytic anemia Hemoglobin down to 7 baseline is close to 10 No evidence of bleeding at this point Iron studies completed on July 2022 showed iron 30 ferritin 16 iron saturation 7% and TIBC 446 suggest iron deficiency anemia Will guaiac stool and consider GI consultation if positive Hg at 8.1 Type 2 diabetes mellitus On Lantus daily A1c 5.9 on 11/4/2022 Will cover with sliding scale BPH Continue Flomax HTN On metoprolol succinate 25 mg daily
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 19.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac disorder
Death
Symptomtext
Patient received flu + COVID bivalent booster on 11/19/23, dies on 11/22/22 from an unknown heart issue. **I am a pharmacist, but not directly involved with this patient. She is a friend I knew from yoga class. I saw online she died suddenly from what her partner described as an unknown heart issue. I saw she recently had vaccines administered and wanted to make sure it was reported to VAERS**
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
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.05.2023
- Impfdatum
- 23.11.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 22,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Catatonia
Encephalitis
Fatigue
Infection
Intensive care
Lumbar puncture abnormal
Symptomtext
I was extremely fatigued, then catatonic. My husband brought me to the emergency room, where I was admitted to the ICU. I do not remember when the spinal tap I had done but it did reveal that I had encephalitis. I was in the hospital for eight weeks while the treated me to get rid of the infection. I was released for the hospital fifty-six days later. I am currently in speech therapy but am getting better every day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 56,0
- Labordaten
- 00NOV2022 - Spinal Tap - positive for encephalitis
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension: Hypothyroid; Aortic Valve Leak; Cancer Survivor; Osteoporosis
- Andere Medikamente
- Levothyroxine; Lisinopril; Atorvastatin; Anastrozole; Omeprazole; Calcitriol; Vitamin D; Calcium; Multivitamin; Preservision; Vitamin B Complex; CoQ10; Melatonin; Floragen
- Allergien
- Vancomycin; Hair Dye; Preservatives; Methylparaben
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 13.03.2023
- Beginn
- 14.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood thyroid stimulating hormone
Blood thyroid stimulating hormone decreased
Body height
Chills
Diarrhoea
COVID-19
Embolism
Haemoglobin
Vaccination failure
Vomiting
Eating disorder
Glycosylated haemoglobin
Glycosylated haemoglobin increased
Stress
Weight
Weight increased
Symptomtext
She had COVID after the vaccines.; She had COVID after the vaccines.; 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 76-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Mar2023 as dose 5 (booster), single (Lot number: GJ6796, Expiration Date: Jul2023) at the age of 76 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 31Mar2021 as dose 1, single (Lot number: EP7533, Expiration Date: Jul2021), on 21Apr2021 as dose 2, single (Lot number: EW017, Expiration Date: Aug2021), on 25Oct2021 as dose 3 (booster), single (Lot number: EW0183) and on 11Jul2022 as dose 4 (booster), single (Lot number: FP7135, Expiration Date: 17Aug2022) for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism", start date: 2007 (ongoing); "Hashimoto's disease" (ongoing); "Pre-diabetes" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID taken for hypothyroidism (ongoing). The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 14Mar2023, outcome "recovered" and all described as "She had COVID after the vaccines.". The patient underwent the following laboratory tests and procedures: Blood thyroid stimulating hormone: Low, notes: her TSH was too low; Embolism: Unknown results; Haemoglobin: 6.5. Clinical course: Synthroid: related to Hashimoto's, She did take Synthroid 112mcg , but now her doctor reduced her dose to 100mcg because her TSH was too low. She is pre diabetic and has lost 35 lbs between diet and exercise. She gained weight due to stress of being a care taker. Her A1C is now 6.5. She has hypothyroid from hashimoto's diagnosed in 2007. She did take Synthroid 112mcg , but now her doctor reduced her dose to 100mcg because her TSH was too low. She had COVID after the vaccines. Prior Vaccinations (within 4 weeks) were none.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300119765 same patient, different dose and event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolism
- Hospital-Tage
- -
- Labordaten
- Test Name: TSH; Result Unstructured Data: Test Result:Low; Comments: her TSH was too low.; Test Name: Thromboembolic; Result Unstructured Data: Test Result:Unknown results; Test Name: A1C; Result Unstructured Data: Test Result:6.5
- Aktuelle Erkrankungen
- Hashimoto's disease; Hypothyroidism
- Vorgeschichte
- Medical History/Concurrent Conditions: Pre-diabetes
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 13.03.2023
- Beginn
- 14.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood thyroid stimulating hormone
Blood thyroid stimulating hormone decreased
Body height
Chills
Diarrhoea
COVID-19
Embolism
Haemoglobin
Vaccination failure
Vomiting
Eating disorder
Glycosylated haemoglobin
Glycosylated haemoglobin increased
Stress
Weight
Weight increased
Symptomtext
She had COVID after the vaccines.; She had COVID after the vaccines.; 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 76-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Mar2023 as dose 5 (booster), single (Lot number: GJ6796, Expiration Date: Jul2023) at the age of 76 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 31Mar2021 as dose 1, single (Lot number: EP7533, Expiration Date: Jul2021), on 21Apr2021 as dose 2, single (Lot number: EW017, Expiration Date: Aug2021), on 25Oct2021 as dose 3 (booster), single (Lot number: EW0183) and on 11Jul2022 as dose 4 (booster), single (Lot number: FP7135, Expiration Date: 17Aug2022) for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism", start date: 2007 (ongoing); "Hashimoto's disease" (ongoing); "Pre-diabetes" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID taken for hypothyroidism (ongoing). The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 14Mar2023, outcome "recovered" and all described as "She had COVID after the vaccines.". The patient underwent the following laboratory tests and procedures: Blood thyroid stimulating hormone: Low, notes: her TSH was too low; Embolism: Unknown results; Haemoglobin: 6.5. Clinical course: Synthroid: related to Hashimoto's, She did take Synthroid 112mcg , but now her doctor reduced her dose to 100mcg because her TSH was too low. She is pre diabetic and has lost 35 lbs between diet and exercise. She gained weight due to stress of being a care taker. Her A1C is now 6.5. She has hypothyroid from hashimoto's diagnosed in 2007. She did take Synthroid 112mcg , but now her doctor reduced her dose to 100mcg because her TSH was too low. She had COVID after the vaccines. Prior Vaccinations (within 4 weeks) were none.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300119765 same patient, different dose and event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolism
- Hospital-Tage
- -
- Labordaten
- Test Name: TSH; Result Unstructured Data: Test Result:Low; Comments: her TSH was too low.; Test Name: Thromboembolic; Result Unstructured Data: Test Result:Unknown results; Test Name: A1C; Result Unstructured Data: Test Result:6.5
- Aktuelle Erkrankungen
- Hashimoto's disease; Hypothyroidism
- Vorgeschichte
- Medical History/Concurrent Conditions: Pre-diabetes
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 24.03.2023
- Impfdatum
- 13.03.2023
- Beginn
- 14.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood thyroid stimulating hormone
Blood thyroid stimulating hormone decreased
Body height
Chills
Diarrhoea
COVID-19
Embolism
Haemoglobin
Vaccination failure
Vomiting
Eating disorder
Glycosylated haemoglobin
Glycosylated haemoglobin increased
Stress
Weight
Weight increased
Symptomtext
She had COVID after the vaccines.; She had COVID after the vaccines.; 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 76-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Mar2023 as dose 5 (booster), single (Lot number: GJ6796, Expiration Date: Jul2023) at the age of 76 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 31Mar2021 as dose 1, single (Lot number: EP7533, Expiration Date: Jul2021), on 21Apr2021 as dose 2, single (Lot number: EW017, Expiration Date: Aug2021), on 25Oct2021 as dose 3 (booster), single (Lot number: EW0183) and on 11Jul2022 as dose 4 (booster), single (Lot number: FP7135, Expiration Date: 17Aug2022) for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism", start date: 2007 (ongoing); "Hashimoto's disease" (ongoing); "Pre-diabetes" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID taken for hypothyroidism (ongoing). The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 14Mar2023, outcome "recovered" and all described as "She had COVID after the vaccines.". The patient underwent the following laboratory tests and procedures: Blood thyroid stimulating hormone: Low, notes: her TSH was too low; Embolism: Unknown results; Haemoglobin: 6.5. Clinical course: Synthroid: related to Hashimoto's, She did take Synthroid 112mcg , but now her doctor reduced her dose to 100mcg because her TSH was too low. She is pre diabetic and has lost 35 lbs between diet and exercise. She gained weight due to stress of being a care taker. Her A1C is now 6.5. She has hypothyroid from hashimoto's diagnosed in 2007. She did take Synthroid 112mcg , but now her doctor reduced her dose to 100mcg because her TSH was too low. She had COVID after the vaccines. Prior Vaccinations (within 4 weeks) were none.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300119765 same patient, different dose and event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Embolism
- Hospital-Tage
- -
- Labordaten
- Test Name: TSH; Result Unstructured Data: Test Result:Low; Comments: her TSH was too low.; Test Name: Thromboembolic; Result Unstructured Data: Test Result:Unknown results; Test Name: A1C; Result Unstructured Data: Test Result:6.5
- Aktuelle Erkrankungen
- Hashimoto's disease; Hypothyroidism
- Vorgeschichte
- Medical History/Concurrent Conditions: Pre-diabetes
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.01.2023
- Impfdatum
- 09.01.2023
- Beginn
- 10.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Anticoagulant therapy
Computerised tomogram
Echocardiogram
Full blood count
Ischaemic stroke
Magnetic resonance imaging
Monoplegia
Symptomtext
Suffered ischemic stroke, hospitalized, treated with aspirin and atorvastatin Right hand paralysis persists now taking warfarin, aspirin, and lovanox
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ischaemic stroke
- Hospital-Tage
- 4,0
- Labordaten
- CT Scan, MRI, Heart ultrasound, CBC
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- history of dvt
- Andere Medikamente
- coumadin paroxetine
- Allergien
- sulfa drugs
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 13.01.2023
- Beginn
- 13.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Loss of consciousness
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Additional Details: Patient came in with parents to recieve pfizer boster shot and was anxious about recieving a shot. I asked patient to take time to calm down and after some time patient and parents confirmed they were comfortable recieving a shot. Patient passed out few minutes after recieving a shot. 911 was called and they stayed to confirm patient is stable and vitals are ok. Patient left after paramedics confirmed she was ok
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 06.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Computerised tomogram
Facial paralysis
Laboratory test
Loss of control of legs
Magnetic resonance imaging
Movement disorder
Posture abnormal
Symptomtext
7 am 12/28/22 felt leaning towards rt. side, couldn't control rt. arm, extended to rt. leg and facial droop. went to ER by 7:45 AM, started stroke protocol, CT scan done, given TNK. transferred to main hospital, admitted to hospital. continued improvement and went home 12/30/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- 3,0
- Labordaten
- CT scans, MRI scans, lots of labs
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- heart attack in 2005, stents
- Andere Medikamente
- Plavix 75 mg, Aspirin 325 mg, amalodipine 10 mg, citalopram 20 mg, ezetimide 10 mg, doxazosin 1 mg, avorstatin 80 mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 10.01.2023
- Beginn
- 10.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Syncope
Symptomtext
Client fainted and fell off the chair in waiting area after receiving vaccines. Client's legs raised while client was lying down. BP 130/80 HR 70. Ice compress placed on head. Provided juice and crackers, which client ate and drank. Client stated she bumped her head when she fell. Client walked to back area after stating she was feeling better. Vitals retaken. Supine: 134/79 HR 69 Sitting: 129/84 HR 62 Advised client and parents of signs of concussion and what to do if signs/symptoms appear . Client voided before being released at 30 minute mark per NP's advisement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 23.12.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Confusional state
Dizziness
Fatigue
Flushing
Hyperhidrosis
Lethargy
Nausea
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Chills-Severe, Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Severe, Systemic: Nausea-Severe, Systemic: Weakness-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Confusional state
Dizziness
Immediate post-injection reaction
Loss of consciousness
Seizure
Syncope
Tremor
Unresponsive to stimuli
Urinary incontinence
Symptomtext
Systemic: Confusion-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Seizure-Medium, Systemic: Shakiness-Medium, Additional Details: pt had a seizer less than 1 minute after receiving the flulaval in the right arm. before that she received, Pfizer bivalent covid 19 in the left arm. pt reported she was dizzy, then began to seize in the chair. she urinated on herself and lost consciousness for about 15 to 20 seconds. when i called EMS and was on the phone with them she seized again for 15-20 seconds. EMS took over and took patient to hospital and was given vaccine record to be presented to er doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 11.12.2022
- Beginn
- 11.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Flushing
Hyperhidrosis
Hypoglycaemia
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Mild, Additional Details: Although the patient didn't indicate history of fainting, he had fainted in the past to a flu shot, but thought it wouldn't happen again. He fainted next to wife while seated during 15 min wait. We had 911 on standby incase allergic reaction, but found out that he can be hypoglycemic and we got him some juice. He felt better after that with no injuries, but he was embarassed about fainting. We made sure he was able to walk and feeling OK before he left the store.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 11.12.2022
- Beginn
- 01.01.1900
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Computerised tomogram head
Computerised tomogram spine
Dizziness postural
Electrocardiogram
Eye contusion
Fall
Full blood count
Influenza virus test
Loss of consciousness
Metabolic function test
Myalgia
Myocardial necrosis marker
Pyrexia
Respiratory syncytial virus test
SARS-CoV-2 test
Skin laceration
Wound closure
Symptomtext
I received my booster on Sunday 12/11/22 at 4:30 PM. During the night of 12/11 I had muscle aches throughout my body. I got up at 7:30 AM on 12/12/22. Muscles no longer ached. Went to the bathroom. When I attempted to stand up I was momentarily very dizzy, apparently blacked out (syncope), fell, and was brought back to consciousness by my husband calling me. EMT arrived and while trying to get me onto a stretcher I had another syncope. I was taken to the emergency room at hospital, where I received the tests indicated below. When I fell I apparently whacked my head, resulting in 3 staples in my scalp and a black eye. I have had a fever varying from 99-101.4 since the shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EKG 12-lead, XR chest, comprehensive metabolic panel, cardiac injury panel, complete blood count, CT head-brain, CT cervical spine, SARS cov-2, flu, RSV, laceration repair
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high cholesterol, Gilbert's Sndrome
- Andere Medikamente
- baby aspirin, fish oil, magnesium glycinate, multivitamin
- Allergien
- sulfa, shellfish
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.12.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Seizure
Symptomtext
Systemic: seizure 12 hours after administration-Severe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 26.11.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: pt felt dizzt and fainted a few minutes after shot. watched the pt about 15 minutes and thet recovered fine and told me she was feeling better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 24.11.2022
- Impfdatum
- 20.11.2022
- Beginn
- 20.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Injection site pain
Nausea
Syncope
Unresponsive to stimuli
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Nausea-Mild, Additional Details: fainted 30 seconds after recieving both flu and pfizer shots. was unresponsive for about 1 min. was then nauseous and dizzy. was seen by emt and declined to go to hospital. left with a friend
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 22.11.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Laboratory test abnormal
Seizure
Symptomtext
Brief seizure occurred shortly after vaccines were administered as patient was leaving the office. He recovered quickly and had no lingering effects. His Depakote level was checked later in the day and found to be low.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- Depakote level: 41 (11/22/22 at 10:21), ref range 50-100
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bipolar Disorder, Seizure disorder, cerebral palsy, intellectual disability, constipation, tremor
- Andere Medikamente
- Depakote, Seroquel, benztropine, metoprolol, vitamin D, trazodone, Miralax
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 13.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Face injury
Syncope
Symptomtext
PT FAINTED THE NEXT MORNING AFTER VACCINATION. REQUIRED GLUE ON FACIAL LACERTAION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 21.09.2023
- Impfdatum
- 23.09.2022
- Beginn
- 29.07.2023
- Tage bis Beginn
- 309,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Hypotension
Symptomtext
I95.9 HYPOTENSION 7/29/2023 CELLULITIS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.07.2023
- Impfdatum
- 04.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injected limb mobility decreased
Injection site pain
Symptomtext
Began soreness in left shoulder down to elbow. Daily, got worse as the day went on. Weeks, months, went to my doctor on April 26th because pain would not go away. She gave me a steroid shot and it was better for 4 weeks, then started to get pain back. Lifting difficult with (L) arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Examination on 4-26-23 for SIRVA in left shoulder to elbow.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Xtra strength Tylenol Multi Vitamin
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.07.2023
- Impfdatum
- 02.12.2022
- Beginn
- 20.01.2023
- Tage bis Beginn
- 49,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 15.06.2023
- Impfdatum
- 17.11.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 43,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 11.06.2023
- Impfdatum
- 03.11.2022
- Beginn
- 16.03.2023
- Tage bis Beginn
- 133,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Blood culture negative
COVID-19
Chest X-ray normal
Computerised tomogram head normal
Dizziness
Ear pain
Echocardiogram abnormal
Fall
Muscular weakness
Nasal congestion
Pulmonary hypertension
SARS-CoV-2 test positive
Symptomtext
Patient is a 79 y.o. male patient of, MD with a history of fall Discharge Diagnoses: 1. Covid-19 Virus Infection 1. Date of onset of symptoms: 3/11/23 (nasal congestion) 2. Symptoms present on admission: nasal congestion and ear ache 3. Date of covid positive test: 3/17/2023 4. Vaccination status: vaccinated and boosters (x5) 5. Imaging: CXR no acute process 6. Anticipated special isolation end date 3/27/2023 Dizziness and fall H/O HTN, CAD, CAB Overweight with BMI 39 HOH Pulmonary hypertension appreciated on echo; follow up with pcp. Patient reports that on Friday his legs just felt like they were too weak he was able to get up and went to the bathroom but then fell. He reports that he did not lose consciousness. Head CT in the ER was negative. Patient reports that he just felt generally weak. ER noted he had a fever of 100. Blood cultures all negative. Was found to have COVID-19. States that he had symptoms starting on the 11th. He denied any shortness of breath. Chest x-ray was unremarkable. He is not requiring oxygen. Outside window for antivirals. Patient has been vaccinated. Was initiated on oral Decadron. Due to his hypertension also added hydralazine.. Due to dizziness he was having an echo was completed and was found to have pulmonary hypertension for which he states he will follow-up outpatient with Dr. as he no longer follows with his cardiologist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary hypertension
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 31.05.2023
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Bursal fluid accumulation
Bursitis
Injection site discomfort
Injection site pain
Injection site reaction
Joint range of motion decreased
Limb discomfort
Magnetic resonance imaging abnormal
Musculoskeletal discomfort
Musculoskeletal stiffness
Pain
Pain in extremity
Paraesthesia
Rotator cuff syndrome
Sleep disorder
Synovitis
Tendon disorder
Symptomtext
Received the Flu shot and Covid vaccine on left arm on the same day (12/08/2022). Had a constant pain, discomfort, stiffness and aching in the arm and shoulder since day one after the injection. Besides the pain, developed issues with limited range of motions in the arm and occasional pins and needles in the fingers after a few weeks. The pain got worse especially at nights, so I saw an orthopedic surgeon on 03/17/2023. Was diagnosed with post vaccine rotator cuff tendinopathy and subacromial bursitis. On the same day I did X-ray imaging of my shoulder and neck (finding: down sloping lateral acromion may contribute to rotator cuff impingement syndrome). My doctor ordered 8 weeks of physical therapy, for twice a week. Started my PT from 03/21/2023 for twice a week. I still had a lot of pain and limited range of motions. I couldn?t sleep at nights due to having lots of pain, so my doctor ordered an MRI. I did the MRI on 05/04/2023. The result came back with three findings: mild tendinopathy of the supraspinatus and subscapularis tendons, synovitis in the rotator interval which can be seen in frozen shoulder syndrome, a trace amount of fluid in the subacromial subdeltoid bursa. I had a follow up appointment with my doctor on 05/17/2023. Based on the current situation and persistent pain she suggested to do a Cortisone shot on the same day. She also suggested to continue with the physical therapy sessions. Since the injection, my constant pain got better specially at nights. But I still have a lot of pain when doing specific motions with my hand during physical therapy and also during normal routine, specifically raising my hand or reaching to some positions is with a lot of pain and in some cases impossible. I am still doing my physical therapy sessions. My follow up appointment with my doctor is on 07/19/2023 (I?m seeing her every other month).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- X-ray imaging on neck and shoulders on 03/17/2023: Findings: down sloping lateral acromion may contribute to rotator cuff impingement syndrome MRI imaging on 05/04/2023: Findings: mild tendinopathy of the supraspinatus and subscapularis tendons, synovitis in the rotator interval which can be seen in frozen shoulder syndrome, a trace amount of fluid in the subacromial subdeltoid bursa. Cortisone Injection on 05/17/2023
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Iron and Multivitamin pills
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 20.05.2023
- Impfdatum
- 18.05.2023
- Beginn
- 19.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Nausea
Tremor
Symptomtext
Woke up shaking with chills but no fever--had those for approx. 6 hours. Also woke up with nausea--had that for approx. 6 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Tachycardia
- Andere Medikamente
- Metoprolol Succinate (25mg), Sertraline HCL (100mg), Loratadine (10mg), vitamin D (25mcg), Esomeprazole Magnesium (20mg)
- Allergien
- -
- Vorherige Impfungen
- Nov 2021 had Moderna booster and woke up about 12 hours after injection with a fever and nausea
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 10.05.2023
- Beginn
- 10.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Decreased appetite
Diabetes mellitus
Dry mouth
Eye pain
Headache
Hypertension
Hypophagia
Magnetic resonance imaging normal
Mental impairment
Photophobia
Pyrexia
Visual impairment
Vomiting
Symptomtext
Nighttime came I started feeling fever and severe headache and I don't get headaches. it was on the left side and in my left eye in a stabbing pain. I could not think. I took 2 Advil to try and calm the headache but the headache did not cease. I threw up and the pain was getting more severe. I called an ambulance, I called 3 times before they got here. I went to the ER. The fever continued until after i left the ER. I had fever when I got home. The headache ceased and now I have spots and many colors that go across my eyes and I cant see off and on. I cant go outside because of the sunshine hurting my eyes. I have no appetite, I cant eat. I have dry mouth but I am drinking so much water and ginger ale for the nausea. I am weak as I cant eat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- MRI, normal. My pressure was high. I was told I am diabetic.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Sulfer
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 01.05.2023
- Impfdatum
- 27.10.2022
- Beginn
- 30.01.2023
- Tage bis Beginn
- 95,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dysgeusia
Ear pain
Malaise
Nausea
Oropharyngeal pain
Palpitations
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I began not feeling well on 01/29/2023 with a sore throat. I tested positive for COVID-19 on 01/30/2023. I had a sore throat, painful ears and a fever. I contacted my doctor and got a prescription for Paxlovid. I was nauseated and had the metallic taste in my mouth while taking Paxlovid. As of today, I am feeling better but it did bring back my heart palpitations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- 30JAN2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Levothyroxine
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 27.04.2023
- Impfdatum
- 06.04.2023
- Beginn
- 07.04.2023
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dyspnoea
Erythema
Impaired work ability
Influenza A virus test negative
Influenza B virus test
Influenza virus test negative
Pain in extremity
Productive cough
Pyrexia
SARS-CoV-2 test negative
Symptomtext
The day following my vaccine, my arm was sore and red. I also had a bit of a fever. On 04/08/2023, I had coughing, shortness of breath, and a slight fever. I continued having shortness of breath and coughing for the next 2 days. That Monday, I went to the doctor's office and got a shot of Rocephin. I was using an albuterol, steroid combined inhaler as well as Flovent inhaler. Tuesday, I still felt the same way with a fever of around 101 and still had a productive cough. Wednesday, I felt bad most of that morning. I thought I was feeling better that afternoon. However, Thursday morning, when I woke up, I felt really bad. I went to the doctor's office and received a shot of steroids. They also started me of Levaquin and oral steroids. They suggested admitting me into the hospital, but I declined. Friday, I felt a tiny bit better. Saturday and Sunday, things got better each day. I was able to return to work on Monday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 10APRL2023 - COVID-19 - Negative; Influenza A And B - Negative; 11APR2023 - COVID-19 Test - Negative; 12APR2023 - COVID-19 Test - Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD; Hyperlipidemia; Asthma; Anxiety
- Andere Medikamente
- Lipitor; Ambien; Paxil
- Allergien
- Feathers
- Vorherige Impfungen
- Dose One Moderna - 2020 - Headache Lasting Months
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 30.03.2023
- Impfdatum
- 28.12.2022
- Beginn
- 06.01.2023
- Tage bis Beginn
- 9,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Back pain
Brain fog
Condition aggravated
Eye pain
Fatigue
Hypoaesthesia
Memory impairment
Tinnitus
Vision blurred
Symptomtext
I experienced blurriness of my vision, I feel a stabbing pain in both my eyes. Joints that have never hurt before, hurts now and my back and hip seem amplified with pain, my neck will go numb from the middle of my left ear down to my shoulder and lots of ringing in my ears 5 days out of 7 days of the week, I'm always fatigued and having brain fog. I always lack energy when it comes to doing any errands or daily tasks, I am also always having trouble remembering stuff.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic back pain; Hip pain
- Andere Medikamente
- Hydrocodone; ADDERALL; atomoxetine; chlorpromazine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 07.03.2023
- Impfdatum
- 03.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia
Rash
Rash pruritic
Symptomtext
Patient got a prickly, itchy rash on her back that started within 24 hours of her injection and lasted about 4 or 5 days. She tried to treat with benadryl, but it didn't seem to help, but taking zyrtec did. She did not visit a doctor or go to an urgent care or ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Pregabalin 100mg, Losartan 50mg, Clopidogrel 75mg, Isosorbide mononitrate 30mg, Atorvastatin 40mg
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.02.2023
- Impfdatum
- 14.01.2023
- Beginn
- 01.01.2023
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Back pain
Blindness
Blood glucose decreased
Chest X-ray normal
Computerised tomogram normal
Condition aggravated
Dyskinesia
Electrocardiogram normal
Eye movement disorder
Hypertension
Muscular weakness
Fear
Vision blurred
Symptomtext
Couldn't see; Was able to see a little bit but everything was blurry; Eyes were kind of shaking; Wasn't able to smile all the way; Blood pressure was really high; Blood sugar was low; Lower back pain/pain in both lower and middle of back; Left hand still feels weaker; This spontaneous case was retrieved on 07-Feb-2023 from Vaccine Adverse Event Reporting System (VAERS) (reference number: 2565853-1), reported by other non-healthcare professional (consumer), and concerned a 40-year-old, female patient. The patient's concurrent conditions included high blood pressure, allergy to sulfa, garlic, pineapple, shellfish and seasonal allergies. The patient's concomitant medications were not reported. It was reported that on 14-Jan-2023, the patient was vaccinated with Fluad Quadrivalent (influenza vaccine inact sag 4v; dose: reported as '1'; route of administration: injection (reported as 'SYR'); anatomical location: right arm; indication: not reported). The batch number reported was P100465584. The reported batch number was identified by Seqirus to be linked to suspect product Afluria Quadrivalent (influenza vaccine inact split 4v) instead of reported suspect product Fluad Quadrivalent. Based on the reported batch number, the suspect product was changed to Afluria Quadrivalent. On the same date, the patient was vaccinated with non-company, co-suspect Pfizer-BioNTech COVID-19 Vaccine, Bivalent (tozinameran, riltozinameran; dose: reported as '3'; route of administration: injection (reported as 'SYR'); anatomical location: left arm; indication: not reported). The batch number reported was GJ6796. On the same date, that night, as reported, after receiving Afluria Quadrivalent and non-company, co-suspect Pfizer-BioNTech COVID-19 Vaccine, Bivalent, the patient felt lower back pain. On 15-Jan-2023, the next day, as reported, the patient started having pain in both lower and middle of back. On 16-Jan-2023, the next day, as reported, when the patient woke up the patient could not see. After five full minutes the patient was able to see a little bit, but everything was blurry. The patient went to an Urgent Care and was told that her blood pressure was really high and blood sugar was low. They called an Ambulance and took the patient to the emergency room (ER), where she underwent an electrocardiogram (EKG), computerised tomogram (CT) scan and chest X-ray, and all results were normal. The nurses noticed the patient's eyes were kind of shaking. The patient was not able to smile all the way and feared that could be a mini stroke, although it was never diagnosed. The patient was put on an unspecified intravenous (IV) therapy and blood pressure finally started coming down. On an unspecified date in Jan-2023, the patient's left hand started feeling weaker. On an unspecified date in Jan-2023, the patient was discharged with a prescription for lisinopril. The patient felt like she was just dismissed, and they did not listen to her. The patient was hoping to see a Primary Care Physician on 01-Feb-2023. At the time of initial reporting, the patient had not recovered from the event of 'hands weakness of', and was recovering from the event of 'blood pressure increased'. As reported, the patient's left hand still felt weaker. The outcome of all other events was unknown. The reporter did not provide a causality assessment. The events of 'vision loss' and stroke were considered to be medically significant by a Physician within Seqirus's Pharmacovigilance Department. Company comment: A 40-year-old patient experienced back pain on the same night after receiving the suspect product Afluria Quadrivalent and non-company, co-suspect Pfizer-BioNTech COVID-19 Vaccine. The patient also developed loss of vision for five minutes and blurry vision after that, as well as non-specified eye movement disorder, impaired mouth movement, increased blood pressure, and decreased blood sugar, two days after vaccination. Thereafter, the patient's left hand felt weaker. Underlying medical history of high blood pressure contributed to the development of the events. Reportedly, the patient underwent an electrocardiogram (EKG), computerised tomogram (CT) scan and chest X-ray, and all results were normal. Nevertheless, more information regarding patient's diagnostic findings is needed. Therefore, due to lack of information, causality is unassessable for all events.; Sender's Comments: A 40-year-old patient experienced back pain on the same night after receiving the suspect product Afluria Quadrivalent and non-company, co-suspect Pfizer-BioNTech COVID-19 Vaccine. The patient also developed loss of vision for five minutes and blurry vision after that, as well as non-specified eye movement disorder, impaired mouth movement, increased blood pressure, and decreased blood sugar, two days after vaccination. Thereafter, the patient's left hand felt weaker. Underlying medical history of high blood pressure contributed to the development of the events. Reportedly, the patient underwent an electrocardiogram (EKG), computerised tomogram (CT) scan and chest X-ray, and all results were normal. Nevertheless, more information regarding patient's diagnostic findings is needed. Therefore, due to lack of information, causality is unassessable for all events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230116; Test Name: Blood sugar; Result Unstructured Data: Low; Test Date: 20230116; Test Name: Blood pressure; Result Unstructured Data: Really high; Test Date: 20230116; Test Name: Chest X-ray; Result Unstructured Data: Normal; Test Date: 20230116; Test Name: CT scan; Result Unstructured Data: Normal; Test Date: 20230116; Test Name: EKG; Result Unstructured Data: Normal
- Aktuelle Erkrankungen
- Blood pressure high; Food allergy; Seasonal allergy; Sulfonamide allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 25.01.2023
- Beginn
- 26.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Incorrect route of product administration
Mobility decreased
Pain in extremity
Symptomtext
Vaccine appeared to be given slightly lower than deltoid muscle on arm. The injection itself did not cause pain but about 24 hours after receiving the vaccination patient reported that her hand became painful and numb. Patient reported she lost control of her hand for about a day or two. After a few days the pain subsided, and she regained control of her hand.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 22.01.2023
- Beginn
- 22.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Nausea
Pain
Peripheral swelling
Symptomtext
NAUSEATED, SEVERE BODY PAINS, WAS UNABLE TO LIFT ARMS, RIGHT ARM SWOLLEN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- no known health conditions
- Vorgeschichte
- no known health conditions
- Andere Medikamente
- bupropion xl 300mg, trazodone 200mg, venlafaxine er 75, ziprasidone 40mg, ziprasidone 80mg, pantoprazole 20mg, sertraline 100mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 21.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 11.01.2023
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac failure
Diuretic therapy
Dyspnoea
Heart rate irregular
Oxygen saturation decreased
Scan with contrast abnormal
X-ray abnormal
Symptomtext
Previous 3 shots of Covishield 1/6/2023 6:15 PM Covid shot Bivalent 1/11/2023 5:30 PM Unexplained sudden shortness of breath, drop in Sp02 to 84, heartbeat irregular XRAY and contrast showed a significant fluid buildup in the lungs Diagnosed as heart failure, pneumonia was ruled out on 1/12/2023 treated with IV Lasix to drain fluids out 1/14/2023 5:00 PM sudden increase in heart rate while in toilet >184 after medication heart rate came down to 100 bpm 1/14/2023 11:30 PM, Heart rate increased again to 137 IV treatment brought the heart rate down 1/19/2023 Discharged from Hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- digestion/gas-related problems.
- Andere Medikamente
- -
- Allergien
- Local Anesthetics such as novacane etc.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 15.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Dizziness
Headache
Migraine
Nausea
Tremor
Vomiting
Symptomtext
I received 5th Pfizer COVID vaccine on 12/30/2022. That night began violent vomiting. diarrhea and Global severe migraine on both sides of my head. On 12/31/2022 I sought Emergency care and was told I most likely had a reaction to the vaccine. I was treated with IV fluids, and medications for headache and nausea and vomiting. I am still nauseated and having loose stools and now I have developed additional symptoms of intermittent fine hand tremors, constant headache and lightheadedness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Local health care facility. Labs and treatment on 12/31/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Migraine, osteopenia, osteoarthritis, spinal degeneration, paroxysmal SVT, Hashimoto's thyroid, mild diverticulosis, hyperlipidemia, stage 2 kidney disease
- Andere Medikamente
- Levothyroxin, Multi vitamin, clonazepam, Tylenol
- Allergien
- Demerol
- Vorherige Impfungen
- Fever 102 for 3 days after Pfizer booster on 11/10/21 and 5/24/22
- Staat
- -
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 11.12.2022
- Beginn
- 11.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Eye movement disorder
Feeling cold
Pallor
Tremor
Unresponsive to stimuli
Symptomtext
At 1400 on 12/11/2022, Nurse, RN- Vaccinator notified Lead Nurse, RN, PHN about patient experienced loss of responsiveness for approximately 3 seconds with eyes rolling back after patient received the Pfizer Adult Bivalent booster dose (Lot: GJ6796, Exp:02/2023) in her left arm and Influenza dose (Lot: 9PG4D, Exp: 06/2023) on her right arm. Patient reaction was observed by nurse. At 1402 Nurse obtained vital signs; blood pressure: 98/64mmHg, heart rate: 87 bpm, oxygen saturation rate: 97%, respirations: 20 breaths per minute while sitting in chair. Patient reported to Nurse that she was experiencing a headache on her way to her today's COVID-19 vaccine appointment. Patient was offered water and cheese crackers by vaccination site staff. Per mother of patient, the patient had only a small bowl of cereal this morning. Patient's mother informed Lead Nurse that the patient had open-heart surgery in 2016, reported the patient does not take any medications, and has mild environmental allergies. Patient was transferred to an anti-gravity chair by Nurse. At 1415, nurse Nurse observed patient shaking and with pale skin. At 1417, 911 was activated by Lead Nurse, patient's vital signs were taken again by Nurse: heart rate: 100bpm, and oxygen saturation rate: 98%. Patient continued to experience shakiness and reported she was ?too cold." At 1433, Fire Department arrived and assumed care. At 1448 patient's mother declined transport to hospital. Patient's vital signs taken by Fire Dept: blood pressure: 100/62mmHg, respirations: 22, heart rate: 98bpm, and oxygen saturation rate: 98%. Lead Nurse educated patient's mother to follow-up with the patient's primary care provider. ER and urgent care precautions were provided. Patient's mother verbalized understanding. Patient and mother left vaccination site at 1450 with a steady gait and balance
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- -
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
Atrial fibrillation
Condition aggravated
Electrocardiogram abnormal
Heart rate irregular
Symptomtext
I received the Pfizer Bivalent booster on 12/1/22 at 11 am. I am a 72 year old female being treated for Afib. I had not had an incident of Afib since 9/12/22. At 10:06 pm the evening of 12/1 I started with an irregular heartbeat. I did an EKG on my watch and it indicate that I was in Afib. Fortunately it did not last too long that evening - just a few minutes. However, on the evening of 12/3/22 I hadan extensive Afib incident. I did 2 EKGs - one at 10:11 pm and one at 10:47 pm. They both showed Afib. The first showed an average of 116 beats per minute and the second showed an average of 105 beats per minute. I took my evening dose of Eliquis at the onset of the problem. I did not have any other symptoms with the irregular heartbeat. This incident continued much longer than a usual Afib event for me. It did not end until 11:30 PM. I did not see my cardiologist about the incident. I was considering going to the ER when it stopped. I am wondering if there could be a relationship between receiving the booster and the triggering of this Afib incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Never smoked
- Vorgeschichte
- Atrial fibrillation, high blood pressure, osteopenia
- Andere Medikamente
- CPAP for sleep apnea, Eliquis for Afib, Losartan for high blood pressure, Usana essentials vitamins and antioxidants, Vitamin D supplement, Red Rice Yeast with Co Q 10
- Allergien
- Adhesive, nickel
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 23.12.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
COVID-19
Dyspnoea
Exposure to SARS-CoV-2
Fatigue
Headache
Nasal congestion
Nausea
Neck pain
Neuropathy peripheral
Oropharyngeal pain
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Tachycardia
Vertigo
Vomiting
Symptomtext
I received the Pfizer Bivalent COVID-19 booster on 11/22/2022. Within an hour of getting the shot, I started to have pain in the right arm that extended to the neck and shoulders, fatigue, and headache. On 11/26/2022, I started to get severe vertigo with nausea and vomiting, which lasted for about 3 days. The pain in the neck, arm, and shoulders, the fatigue, and the headache also continued at this time, and it wasn't until about 11/29/2022 that I was back at my baseline. On 12/4/2022, I woke up with a very sore throat, increased nasal congestion, headache, and fatigue. I didn't yet have a fever, but my temperature was about a degree higher than normal. I wasn't really sure what was happening, so I just drank warm fluids to soothe my throat and rested. When I woke up on 12/5/2022, I still had the same symptoms, but they were intensified. I took my temperature, which was 101. I took a home antigen test and got a positive result. From that point, I began isolating. I had a telehealth appointment later that day and was prescribed Paxlovid, which I began taking the evening of 12/6/2022. I continued to have a fever on and off through about 12/15/2022. My sore throat waxed and waned, and at the time of this writing, I still sometimes have a sore throat. My congestion is now better, but not completely gone. I still have fatigue, plus I have increased neuropathy, especially in the fingertips of both hands. On 12/16/2022, I took a home antigen test, which yielded a negative result. I also got a negative result when I tested again on 12/18/2022. I also continue to have increased shortness of breath and tachycardia with any activity; these symptoms became more pronounced when I developed other COVID-19 symptoms on 12/4/2022. I would like to add that I believe I was exposed to COVID-19 on 11/25/2022 or earlier, because I had not left my home since 11/25/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 12/5/2022--Home Antigen Test--Positive Result; 12/16/2022 and 12/18/2022--Home Antigen Tests--Negative Results.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypothyroidism; Ehlers-Danlos Syndrome; Postural Orthostatic Tachycardia Syndrome; Small Fiber Neuropathy; Migraines; Visual Snow Syndrome; Mast Cell Activation Syndrome; Chronic Cerebrospinal Fluid Leak.
- Andere Medikamente
- Synthroid; Emgality; Vitamin D2; Pregabalin; Cromolyn Sodium; Estradiol Patch; Multivitamin; Tylenol; Acetaminophen Butalbital.
- Allergien
- NSAIDs; Sulfa Drugs; Ergotamine.
- Vorherige Impfungen
- I had an adverse event following the second dose of the Moderna COVID-19 vaccine. This is described in another report (e-report
- Staat
- MI
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 08.12.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Communication disorder
Computerised tomogram head abnormal
Computerised tomogram spine
Condition aggravated
Delirium
COVID-19
Cerebellar atrophy
Cerebral atrophy
Cerebral ischaemia
Cognitive disorder
Fall
Gait disturbance
Influenza A virus test positive
SARS-CoV-2 test positive
Spinal compression fracture
Spinal osteoarthritis
Toxic encephalopathy
Vertebral foraminal stenosis
Symptomtext
Discharge Provider: MD Primary Care Provider: MD Admission date: 12/19/2022 Discharge Date: 12/21/2022 Covid positive date: 12/19/2022 PRESENTING PROBLEM: COVID [U07.1] Toxic metabolic encephalopathy [G92.8] HOSPITAL COURSE: 92-year-old gentleman with medical history of chronic obstructive pulmonary disease/asthma, gout, hypertension, cognitive impairment and BPH presenting with encephalopathy 12/19. Patient was found to be positive for influenza A and COVID 19. Patient did not require any supplemental oxygen, No signs of respiratory distress thus He was not started on steroids/antivirals. His encephalopathy was considered metabolic in the setting of viral infections, delirium due to underlying history of cognitive impairment. 12/20 patient had a witnessed fall in his room when he wanted to go use the restroom and refused to get assistance from hospital staff. Patient did not hit his head or lost consciousness. Underwent noncontrast CT head that did not show any intracranial hemorrhage or acute intracranial abnormality, showed mild white matter hypoattenuation consistent with chronic microvascular ischemic disease and mild cerebral/cerebellar atrophy. CT spine showed mild T2 endplate compression fracture and moderate degenerative changes foraminal stenosis at multiple levels. Patient did not have any pain or tenderness in the spine. No focal deficits. Moving all extremities spontaneously. Discussed with Dr. from Ortho who did not recommend any brace since patient not having any symptoms. PT/OT evaluated, recommended discharge home with home health. SLP evaluated, patient found to have severe cognitive-communication impairment. Patient will require distant 24 hour supervision. He lives with his wife at home. Discussed with wife that given his severe cognitive impairment, any subtle changes including infections can cause significant decline in mental status. Informed that he will need to be formally assessed for dementia by Neurology/neuropsychology. Informed by his PCP will be able to send referrals for that. Discussed with wife how comfortable she be taking him. His wife stated that she would be okay taking him home. Her brother lives about 20 minutes away and can be at their house if she needs extra help. Mover our Case Management provided extensive list of resources in case if family wants to pursue long-term placement for patient given his dementia. Patient was discharged home in stable condition. All questions from the family answered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD with asthma (HCC) Influenza HTN (hypertension) CAD (coronary artery disease) Anemia Foot pain Left-sided low back pain with left-sided sciatica, unspecified chronicity Encephalopathy BPH (benign prostatic hyperplasia) Abnormal prostate biopsy Hyperuricemia PSA elevation Rash Decreased activities of daily living (ADL) Difficulty walking
- Andere Medikamente
- albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler allopurinol (ZYLOPRIM) 100 MG tablet aspirin 81 MG tablet benzonatate (TESSALON) 100 MG capsule cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) capsule col
- Allergien
- Demerol Meperidine
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 16.12.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dizziness
Headache
Hypertension
Symptomtext
headache, dizziness, high blood pressure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- respitory infectiom
- Vorgeschichte
- balance vertigo, dizziness
- Andere Medikamente
- belsomra
- Allergien
- -
- Vorherige Impfungen
- Pfizer ER8727Arm irritation 3/29/2021 62
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hypoaesthesia
Hypotension
Nausea
Pallor
Vomiting
Symptomtext
Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Severe, Systemic: Nausea-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Vomiting-Severe, Additional Details: She became lightheaded, dizzy and hypotensive as measured by BP cuff. She looked pale and also mentioned that her hands felt numb. I had her put her legs up, gave her water, offered Tylenol & Benadryl but patient was too nauseous. Patient then vomited, color came back to her face and she immediately felt much better. I kept her here to observe & suggested a salty snack to help with BP. When she felt better & after a snack, I retook her blood pressure and it had improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Visual impairment
Symptomtext
Client spouse called for booster dose appointment as client sight impaired, provided vaccine card showing primary series complete and monovalent dose, pre-visit screening did not note that client received the bivalent dose in 9/2022. Client was given a second bivalent dose on 12/20/2022 when a second vaccine card noted this as writer was documenting dose provided after administering the dose. Client received prior to the dose, screening completed prior to the dose and 15 minute wait completed after the injection. Client was stable throughout with no untoward effects noted. Client was notified that a second booster bivalent dose had been received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Vision deficit Others unknown
- Andere Medikamente
- Unknown
- Allergien
- None Known
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Palpitations
Throat irritation
Symptomtext
Pt had immediate feeling of racing heart, tickly throat, and lightheadedness. Felt fine after several minutes with no treatment. Did not lose consciousness at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- sinus cold
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Ear pain
Feeling abnormal
Headache
Injection site pain
Respiratory tract congestion
Tremor
Symptomtext
About 12:30 AM I decided to go to bed. I started shaking like I was convulsing. It could have been my anxiety. I settled down after I woke up in the chair about 4 AM. I went to bed and woke up that morning feeling awful. I had a major headache, my hips hurt and I felt clogged in my head. My ears were hurting like a earache. I just stayed in bed all day. That evening I decided to eat that evening at 6PM. I did not take any medicine. I contacted my PCP and was told to take ibuprofen. I feel much better today. My arm is still a little tender at the site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Levothyroxine; simvastatin; metoprolol; probiotic
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Muscle spasms
Neck pain
Pain in extremity
Symptomtext
severe left side neck spasms; severe left side neck spasms/Very very bad spasms. Came and went; little bit of a sore arm; Severe neck pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 71-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 30Nov2022 as dose 4 (booster), single (Lot number: GJ6796) at the age of 71 years intramuscular, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Blood Pressure" (unspecified if ongoing), notes: he takes a blood pressure pill and a tablet for urinating; "urinating" (unspecified if ongoing), notes: he takes a blood pressure pill and a tablet for urinating. Concomitant medication(s) included: SERTRALINE taken for urinary incontinence. Vaccination history included: BNT162b2 (Dose 1, Route of Administration: intramuscular, Lot number: EL9269), administration date: 13Feb2021, when the patient was 69-year-old, for COVID-19 Immunization, reaction(s): "little bit of a sore arm/like I've had on the other Pfizer shots"; BNT162b2 (Dose 2, Route of Administration: intramuscular, Lot number: EL9262), administration date: 07Mar2021, when the patient was 69-year-old, for COVID-19 Immunization, reaction(s): "little bit of a sore arm/like I've had on the other Pfizer shots"; BNT162b2 (Dose 3/first booster, Route of Administration: intramuscular, Batch/Lot number: FF8841), administration date: 28Oct2021, when the patient was 70-year-old, for COVID-19 Immunization, reaction(s): "little bit of a sore arm/like I've had on the other Pfizer shots". The following information was reported: NECK PAIN (non-serious) with onset 2022, outcome "unknown", described as "Severe neck pain"; PAIN IN EXTREMITY (non-serious) with onset 30Nov2022, outcome "unknown", described as "little bit of a sore arm"; CONDITION AGGRAVATED (non-serious) with onset 01Dec2022, outcome "not recovered", described as "severe left side neck spasms/Very very bad spasms. Came and went"; MUSCLE SPASMS (non-serious) with onset 01Dec2022 at 02:00, outcome "unknown", described as "severe left side neck spasms". The events "little bit of a sore arm", "severe left side neck spasms", "severe left side neck spasms/very very bad spasms. came and went" and "severe neck pain" required physician office visit. Therapeutic measures were taken as a result of pain in extremity, muscle spasms, condition aggravated, neck pain. Additional information:Patient had a very weird side effect. he figured should speak to someone. he trying to understand if what he experiencing may be a side effect. he had the Pfizer COVID bivalent vaccine (Lot: 6J6796) this Wednesday 30Nov2022 a little before noon. he had a little bit of a sore arm, like he had on the other Pfizer shots, but nothing major. he woke up 2 AM in the morning on Thursday 01Dec2022 with severe left side neck spasms. On a scale of 1-10, he would say 11. Very very bad spasms. Came and went. Went to the doctor and they prescribed Diazepam 5mg twice a day. Also, Diclofenac Sodium 75 mg for neck spasms. Patient assessed as non serious. Started taking those, and just struggled all day Thursday. Can only sleep for a couple hours at a time. these spasms were coming and going erratically. When they did come, they were 11 out of scale of 10. Managed to get a couple hours of sleep at a time. Last night, went to bed, then woke up about 3 AM Friday 02Dec2022. The entire spasm has moved from left side of his neck to his right side of his neck, but worse. Had the shot in the right arm. he feel like he never expected this. Severe neck pain out of the blue for no reason at all just threw him for a loop. his HCP didn't think it had anything to do with the shot, but he never experienced that in 7 years. he had a sore back/sore neck when you over exercise, but nothing like this out of nowhere. his spasm lasts 3-4 seconds to 10 seconds, very severe, and then they go away." Caller had four shots total. He had the bivalent COVID-19 vaccine on 30Nov2022. He had the neck spasms after the bivalent, and had pain to the left side of his neck starting at about 14 hours after getting it. Spasm Treatment: He didn't get the Diazepam or the Diclofenac until 05:00-06:00pm on 01Dec22, and he took them right away, at 6:30pm. Spasm outcome: Since he has been talking to call handler and agent he has had not one spasm. Prior to that he had spasms from about 02:00 to 03:00am this morning and he didn't count them, but there were at least 20 of them. While they were happening the spasms stayed about the same. He says he has a handwritten vaccine card, and it looks like the LOT is 6J6796, but if it is not supposed to be a six that could be a G. It looks like a six but then the other two sixes are different from it, so he thinks it is actually a G. NDC/EXP not provided on handwritten vaccine card. He clarifies that he got the bivalent COVID vaccine between 11:30AM and noon. He got dose one and two from Pfizer then had one booster which was shot number three, but he didn't have booster four, and then he had the bivalent. He asks, is that considered a booster or a shot? He had shot number five but didn't have number four, he skipped that one and didn't want to do it. Indication: The reason he got the bivalent vaccine was it was the latest shot and a booster that also covers COVID symptoms and latest Omicron. Historical AE: little bit of a sore arm: When he had sore arm he took some Tylenol and Ibuprofen, which was 500 mg for Tylenol, which he took a couple of times as needed. For the Ibuprofen dose would have been 200mg, which he took the same as the Tylenol, a couple of times as needed. Ibuprofen was taken at same time as Tylenol. His sore arm got better. Concomitant Medications: He takes his regular medications, like he takes a blood pressure pill and a tablet for urinating, and he takes Sertraline. Caller says he doesn't feel those are relevant, he has been taking all of them for 4-5 years and didn't have neck spasms. AE Outcome: They did tell him that if it doesn't clear up in a week to come back for some kind of CT Scan or x-ray, and maybe do physical therapy, but they were guessing and have no idea where this come from. They didn't believe it had nothing to do with the shot. He tended to agree with her at the time, but he totally does not agree now after Thursday night and then it went over to the right side. He thinks it is in direct relation to the shot; he is retired and has done nothing in the last couple days that would cause muscle spasms. He didn't have a sore neck or have one before. He thinks the chance that this is a side effect of the shot is very high in his opinion.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201350178 same patient, different vaccine dose number/event;US-PFIZER INC-202201350179 same patient, different vaccine dose number/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure abnormal (he takes a blood pressure pill and a tablet for urinating); Urinary incontinence (he takes a blood pressure pill and a tablet for urinating)
- Andere Medikamente
- SERTRALINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 23.11.2022
- Beginn
- 24.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray normal
Chills
Dyspnoea
Influenza virus test negative
Loss of personal independence in daily activities
Nausea
Pyrexia
SARS-CoV-2 test negative
Symptomtext
After the vaccine, I had short of breath, fever, chills, nausea; I went to the doctor on 11/28/2022 because the shortness of breath did not make me to function properly. I got medication and inhaler and steroid shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 28NOV COVID-19 test negative; 28NOV flu negative; 28NOV X-ray chest normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetic; Hyperlipidemia; Anemia; Asthma
- Andere Medikamente
- VICTOZA; biotin; ZYRTEC: atorvastatin; gabapentin; metformin; zinc; CENTRUM SILVER; ACTOS; aspirin, turmeric; B-12
- Allergien
- Iodine; penicillin; codeine; BACTRIM; morphine; latex
- Vorherige Impfungen
- 01/15/2021 Moderna 1st dose, could sore arm, where injection was placed. For over 1 week. Could not lift arm, lymph nodes for ov
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 10.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 12,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Headache
Mobility decreased
Myalgia
Neck pain
Pain in extremity
Pyrexia
Swelling face
Symptomtext
So I did have side effects from the injection on the 10th, I had a sore arm, muscle ache, fever, headache, severe pain from my neck to mid back on the right side, I could not turn my head. This lasted for about three days and gradually decreased. I took TYLENOL on the 11th at 6:00PM, then I started to take the ibuprofen, I do have an inhaler as needed as well. On the 22nd, I started noticing facial swelling, the 22nd and the 23rd I felt like I needed my inhaler, I took antihistamine, and ibuprofen, I stopped the antihistamine on the 26th I did not take it on the 27th, on the 28th I woke up with facial swelling and the same severe pain on my neck and mid back on the right side like I had when I first had the vaccine. This is why connected the two, on the 28th I went to the Dr. and he described prednisone, My O2 stats were normal, all usual stats normal. Did not go to the ER just my normal Dr.'s visit. the facial swelling is down from taking the medicine, and I am starting to feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- Mild Asthma; Hypothyroidism.
- Andere Medikamente
- Levothyroxine; omeprazole; ibuprofen; BENADRYL.
- Allergien
- Mineral oil; petroleum; nickle.
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 05.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenopia
Chills
Cough
Decreased appetite
Fatigue
Drug ineffective
Suspected COVID-19
Weight
Feeling cold
Gastric disorder
Malaise
Musculoskeletal chest pain
Pain
Sleep disorder
Visual impairment
Weight decreased
Symptomtext
aches; Fatigue; some kind of heaviness over the eyes; stomach issues; Chills; Cough; don't feel well; slept off and on; she still feels cold; it hurts around the ribs; she had to get magnifying glass to read vaccination; Lost weight; Appetite lost; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 85-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Nov2022 as dose 5 (booster), single (Lot number: GJ6796) at the age of 85 years, in arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EM980A), administration date: 04Feb2021, when the patient was 84-year-old, for Covid-19 immunization, reaction(s): "Diagnosed with Covid", "Diagnosed with Covid"; covid-19 vaccine (DOSE 2, SINGLE; Lot number: unknown), administration date: 03Mar2021, when the patient was 84-year-old, for Covid-19 immunization, reaction(s): "Diagnosed with Covid", "Diagnosed with Covid"; Covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE; Lot number: unknown), for Covid-19 immunization, reaction(s): "Diagnosed with Covid", "Diagnosed with Covid"; Covid-19 vaccine (DOSE 4 (BOOSTER), SINGLE; Lot number: unknown), for Covid-19 immunization, reaction(s): "Diagnosed with Covid", "Diagnosed with Covid". The following information was reported: CHILLS (non-serious) with onset 11Nov2022, outcome "not recovered"; COUGH (non-serious) with onset 11Nov2022, outcome "not recovered"; FATIGUE (non-serious) with onset 11Nov2022, outcome "recovering"; PAIN (non-serious) with onset 11Nov2022, outcome "not recovered", described as "aches"; ASTHENOPIA (non-serious) with onset 11Nov2022, outcome "recovering", described as "some kind of heaviness over the eyes"; GASTRIC DISORDER (non-serious) with onset 11Nov2022, outcome "not recovered", described as "stomach issues"; DECREASED APPETITE (non-serious) with onset Nov2022, outcome "unknown", described as "Appetite lost"; WEIGHT DECREASED (non-serious) with onset Nov2022, outcome "unknown", described as "Lost weight"; MALAISE (non-serious) with onset Nov2022, outcome "unknown", described as "don't feel well"; MUSCULOSKELETAL CHEST PAIN (non-serious) with onset Nov2022, outcome "unknown", described as "it hurts around the ribs"; VISUAL IMPAIRMENT (non-serious) with onset Nov2022, outcome "unknown", described as "she had to get magnifying glass to read vaccination"; FEELING COLD (non-serious) with onset Nov2022, outcome "unknown", described as "she still feels cold"; SLEEP DISORDER (non-serious) with onset Nov2022, outcome "recovering", described as "slept off and on". Additional information: Reporter called about her getting five injections of the different variants for the Covid-19 Vaccine. The last one she received was on 05Nov2022. She was diagnosed with covid this past Saturday, later confirmed as, 12Nov2022. However, the symptoms started on the 11Nov2022. About aches, she stated that it was hard to say when don't feel well. Later confirmed it was about the same. About the event fatigue, she commented she just got up this morning. On 12Nov2022 (Saturday) and 13Nov2022 (Sunday) pretty much slept off and on, or resting watching tv. She seemed to feel a little more alive today. She woke up couple hours ago. Then stated when little miserable don't know. Stomach issues, initially provided as a little better, but unsure. She would know a little later today. From coughing it hurted around the ribs. Still had a deep cough. However, her throat was not making her cough right now.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201303297 same patient/product, different dose/events;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 19.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest pain
Symptomtext
Some chest pain started about 24.5 h after injection. Has occurred a few more times today. Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- Resolved URI (sinus infection) about 3 weeks ago. Ended about 3 weeks ago w exception of mild residual cough.
- Vorgeschichte
- Overweight. Stroke presumed to be from PFO. PFO closed April 2022. No issues since 09/10/2021 stroke.
- Andere Medikamente
- Atorvastatin, aspirin, vitamin d
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Chills
Condition aggravated
Gastrooesophageal reflux disease
Symptomtext
I had the normal chills but this time starting Friday; I have chest pain I went to my primary doctor and she checked all my vitals she said everything was good she did mention that it has turned it into extreme chest pain and acid reflux.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- No tests
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- Anxiety; Acid reflux
- Andere Medikamente
- No medication was taken
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 06.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Immediate post-injection reaction
Tremor
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Shakiness-Mild, Systemic: Weakness-Mild, Additional Details: PATIENT FELT LIGHTHEADED AND DIZZY RIGHT AFTER RECEIVING THE VACCINES. MONITORED PT FREQUESTLY. PT OCMPANY GAVE WATER AND PT FELT BETTER AFTER FEW MINUTES. CALLED 911, WHILE WAITING FOR PARAMEDICS TO COME IN, PATIENT WAS BEING MONITORED. PER PT, SHE WAS FEELING BETTER BUT WE STILL WAITED FOR PARAMEDICS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 29.12.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ear pain
Fungal infection
Headache
Neuralgia
Salivary gland cancer
Skin burning sensation
Throat irritation
Symptomtext
Headache evening, 24 hrs later: facial, sinus & throat burning. Facial nerve path on Left burning. Day 2: Facial nerve path on Left & Right burning slightly. Day 3-10: Facial nerve path pain only on Right Side. Spastic headaches mostly in forehead. 15mg CBD oil started day 3. Used 2x/day 7 days got relief. Dentist ruled out dental problem. 12/15/2023 : Headaches returned, sinus & facial nerve Right side flared 7 days after wearing a mask for a week while at hospital with sick family member. CBD Oil 15 mg 1x/day for 5 days worked. Arnuity Elipta discontinued 12/23/2022 for recurrent oral yest infection. Fluconazole 100mg. Headaches returned 1/6-16/23 5/3/2023 Rt. below ear spastic pain, 9/8/2023 Parotid Cancer 1cm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Atypical asthma, bladder cancer survivor 5 yrs.,
- Andere Medikamente
- Arnuity Ellipta steroid inhaler, Allegra, Cal,Mag, Zinc, Vit D
- Allergien
- Iodine, sulfas, MSG, sulfites, NSAIDs
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 29.12.2023
- Impfdatum
- 08.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 12,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Antinuclear antibody
Eye pruritus
Giant papillary conjunctivitis
Immunology test
Lacrimation increased
Symptomtext
Developed itching in both eyes. Constant tearing. Treated with antibiotics for eyes:. Loteprednol, zylet, Pataday for 6 months. Seen by Optometrist and Specialist Optometrist. Also tested for Sjogrens syndrome which was negative. PFIZER COVID-19 BIVALENT (12+) mRNA, LNP-S, PF, 30 MCG/0.3 ML DOSE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- ANA IFA SCREEN WI REFLEX TO TITER Collected on August 1 4, 2023
- Aktuelle Erkrankungen
- Hypertension
- Vorgeschichte
- From December of 2022 to June of 2023 chronic giant papillary conjunctivitis post 5th vaccination. Last booster was Pfizer Bivalent GJ6796.
- Andere Medikamente
- LOSARTAN, MONTELUKAST, ASPIRIN, VIT D
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 30.08.2023
- Impfdatum
- 28.08.2023
- Beginn
- 30.08.2023
- Tage bis Beginn
- 2,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash pruritic
Urticaria
Symptomtext
client called 8/30/23 to report "I kind of broke out in a rash, I am taking Benadryl and applying itch cream". Client left this info on voicemail of this clinic nurse. Client called back 8/30/23 @ 12:00 pm to report welt-like rash started itching 8/28/23 after bedtime. Welts and itching (by next morning 8/29/23) then spread to both arms, front of chest and both armpits. Has not gotten worse since yesterday. Benadryl and itch cream are helping.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- not at this time
- Aktuelle Erkrankungen
- client denied at intake to clinic
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown, not reported
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- F
- Eingang
- 30.08.2023
- Impfdatum
- 25.08.2023
- Beginn
- 25.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site erythema
Injection site swelling
Injection site warmth
Lethargy
Symptomtext
Injection Site swollen, hot to touch and redness expanding from 1 inch circumference to 3-inch circumference in 72 hours. Patient also experience headache and was lethargic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 29.08.2023
- Impfdatum
- 27.06.2023
- Beginn
- 27.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Arm still sore 2 month later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 17.08.2023
- Impfdatum
- 13.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Loss of personal independence in daily activities
Magnetic resonance imaging abnormal
X-ray abnormal
Symptomtext
Sudden increase in L knee and ankle pain such that could no longer do daily hikes. Resulted in months of PT, multiple doctor visits, imaging. Dx peroneal tendinitis and unknown cause of knee pain, inflammation?
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- X-rays and MRI?s of L knee and ankle December 2022 and January 2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Gabapentin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.06.2023
- Impfdatum
- 13.06.2023
- Beginn
- 14.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 13.06.2023
- Impfdatum
- 08.06.2023
- Beginn
- 11.06.2023
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site swelling
Injection site warmth
Symptomtext
Resident rec'd Pfizer Biontech bivalent on 6/8/23 on 6/11/23 resident developed moderate amount swelling at inject site with some warmth, denies pain, resident had no c/o until 6/11 and reported to this nurse today that this happens with every vaccine I have rec'd all the way back to being a child. I reminded her that she told me prior to vaccination that she has "no problems" and she said she guess she forgot to mention that. She reports none of the previous episodes were treated with abx and they just resolve. Swelling is better today she reports and denies pain, slight warmth, resolving, seen by PCP and will continue to monitor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- resident in admitted with rt fibula fx., effusion rt knee, morbid obesity, GERD unsteady gait, muscle weakness type 2 morbid obesity, benign neoplasm of meninges, essential htn, hyperlipidemia, chronic kidney disease, artheroscclerotic heart disease,
- Andere Medikamente
- cholecalciferol, senna tabs, lisinopril, mom, verapamil, coumadin, duragesic patch, mirabegron, cyanocobalamin
- Allergien
- Morphine and related, NSAIDS, tape
- Vorherige Impfungen
- "every vaccine she has ever rec'd, same rxn"
- Staat
- PR
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 03.06.2023
- Impfdatum
- 19.05.2023
- Beginn
- 26.05.2023
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Pruritus
Swelling
Symptomtext
The patient reports that 1 week after the administration of the vaccine, she presented redness, itching and swelling in different areas of the body (face, legs, arms and neck).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Patient attended the ER, we are unaware of studies carried out in the hospital.
- Aktuelle Erkrankungen
- Patient with a history of thyroid extirpation
- Vorgeschichte
- Hypertension, Cholesterol.
- Andere Medikamente
- Losartan, Synthroid, Atorvastatin
- Allergien
- Patient refers to not being allergic to medications.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 24.05.2023
- Impfdatum
- 22.11.2022
- Beginn
- 20.03.2023
- Tage bis Beginn
- 118,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Cough
Fatigue
Headache
Lethargy
Malaise
SARS-CoV-2 test positive
Throat irritation
Symptomtext
3/20 I noticed a scratchy throat and malaise. 3/21 tested positive with at home COVID-19 test. I developed a severe headache with loss of taste and smell, and a terrible cough. 3/22 Televisit with doctor who prescribed PAXLOVID and recommended DELSYM cough syrup. 3/24 I felt better, with taste and smell returning. Felt much better by 3/27 with cough lingering for about a month longer. Fatigue and lethargy linger to time of reporting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 21Mar2023 at home COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Hydrochlorothiazide; metoprolol; atorvastatin; multivitamin; calcium; vitamin D3
- Allergien
- Peanuts
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 12.05.2023
- Impfdatum
- 23.02.2023
- Beginn
- 26.03.2023
- Tage bis Beginn
- 31,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza like illness
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I felt feverish and weak flu like symptoms, a home test was positive. I contacted healthcare provider via telehalth was prescribed Paxlovid took aregiment for five days, life returned
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 26MAR203 COVID-19 Test-Posirtive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 10.05.2023
- Impfdatum
- 09.05.2023
- Beginn
- 09.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Rash erythematous
Symptomtext
Patient was waiting for observation for 15 minutes, after that time she came to the pharmacy counter stating she was about to leave when she starting feeling hot and seeing a red rash appearing. Patient took 50mg diphenhydramine and was further observed for 30 minutes. After that point she was looking and feeling better and decided to go home. She declined to be seen by paramedics or emergency services.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- hypertension, hypothyroid
- Vorgeschichte
- hypertension, hypothyroid
- Andere Medikamente
- progesterone 100mg
- Allergien
- latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 01.11.2022
- Beginn
- 25.04.2023
- Tage bis Beginn
- 175,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
COVID-19
Chills
Fatigue
Feeling abnormal
Laryngitis
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 on 4/25/23. I started having laryngitis first and I thought it was because I went to a concert. The next night I started to feel bad, and I took a cough drop and couldn't taste it. I also had chills, body aches, fatigue, congestion, and fever of 101. I contacted my doctor and was prescribed PAXLOVID. I am still dealing with some of these symptoms at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 25APR2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol; Bronchiectasis; Depression
- Andere Medikamente
- Multivitamin; calcium; LIPITOR; gabapentin; hydroxyzine; EFFEXOR
- Allergien
- Ampicillin
- Vorherige Impfungen
- I broke out in welts after a Pneumonia shot years ago.
- Staat
- OH
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 28.04.2023
- Impfdatum
- 26.04.2023
- Beginn
- 26.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Chills
Headache
Injection site pain
Mental status changes
Pain
Symptomtext
Chills, loss of mental ability, overall pain, pain at injection site, headaches, loss of balance. Took Tylenol. Lingering - worse symptoms than when I actually had COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- high lipids high BP sleep issues allergies
- Andere Medikamente
- Vitamin D3 Amlodipine Klonipin Tylenol Metamucil polyethylene glycol
- Allergien
- Nsaids sulfa drugs steroids
- Vorherige Impfungen
- 1st one Pfizer
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 27.04.2023
- Impfdatum
- 19.11.2021
- Beginn
- 30.01.2023
- Tage bis Beginn
- 437,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Myalgia
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I was positive for COVID-19 on 30JAN2023, I was tired and fatigued, I had a headache, sore throat. I was also muscle aches and fever. I saw my doctor and got paxlovid, I starting feeling better about couple of days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 30JAN2023 COVID-19- Test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 12.04.2023
- Impfdatum
- 08.04.2023
- Beginn
- 08.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Needle issue
Symptomtext
Site: Pain at Injection Site-Mild, Additional Details: The patient's skin and muscle were a little tough and when my intern went to adminster the vaccine the needle bent a little and was not able to admnister the vaccine. I drew up a new dose with the vanish point needle and syringe and admnistered the vaccine to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 06.04.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy uterus normal
Biopsy vagina normal
Erythema
Pain in extremity
Pathology test
Pruritus
Urticaria
Vaginal haemorrhage
Symptomtext
Twelve hours after vaccine my arm got red welts, was painful and itchy. Went away after 3 days. Could only take Tylenol as treatment. Two months after vaccine started having vaginal heavy bleeding with blood clots. Changed Fem Ring and it stopped. Then after two weeks the bleeding started again. Went to doctor and did biopsies in vagina and uterus, all pathology was normal. Now applying topical estrogen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- 06MAR2023 Biopsies of Vagina and Uterus - normal pathology.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Previous Breast Cancer; Osteoarthritis; Diverticulosis; Anemia.
- Andere Medikamente
- Claritin; Armour Thyroid; Estradiol Fem Ring; Propranolol; Lorazepam; Multivitamin; Vitamin D3; Biotin; Cilium Fiber and Chi Seeds; Flax Seed; Probiotic.
- Allergien
- Codeine; penicillin; latex; bee's; mosquito's; orhis root; raw onions; nitrates; fast food; oils; soy; peanut's walnuts; mold; shell fish; fragrances.
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.04.2023
- Impfdatum
- 18.11.2022
- Beginn
- 17.02.2023
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dizziness
Ear discomfort
Fatigue
Headache
SARS-CoV-2 test positive
Secretion discharge
Sinus congestion
Sneezing
Symptomtext
I tested positive for Covid-19 on February 17, 2023 I experienced sneezing, sinus congestion, mucus, headaches, dizziness, fatigue, blockage in my ears. I was prescribed PAXLOVID for my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Anastrozole
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 03.04.2023
- Impfdatum
- 17.12.2022
- Beginn
- 04.02.2023
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Hip fracture
Pain in extremity
Pyrexia
Symptomtext
I had a sore arm and felt feverish for about a day. On 02/04/2023, I had a fall due to my dog getting under my feet. The fall was not due to a medical condition. I contacted my doctor who referred me to a specialist. I did fracture my hip born but I am recovering without surgery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteoporosis; Depression; ADHD
- Andere Medikamente
- Adderall; Vitamin D3; Turmeric; Fish Oil
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 06.02.2023
- Beginn
- 06.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dysphagia
Injection site swelling
Pain
Pyrexia
Throat tightness
Symptomtext
Site: Swelling at Injection Site-Medium, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Severe, Systemic: Fever-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 22.02.2023
- Impfdatum
- 28.01.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Illness
Lymphadenopathy
Pyrexia
COVID-19
Drug ineffective
Laboratory test
Symptomtext
swollen glands; She had fever and chills from fourth Pfizer COVID vaccine booster.; She had fever and chills from fourth Pfizer COVID vaccine booster.; Caller did get sick; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Jan2023 as dose 4 (booster), single (Lot number: GJ6796) at the age of 57 years for covid-19 immunisation. The patient's relevant medical history included: "Cold induced as asthma" (unspecified if ongoing). Concomitant medication(s) included: PRILOSEC [OMEPRAZOLE] (ongoing); DULERA taken for asthma (ongoing); LEVALBUTEROL [LEVOSALBUTAMOL], start date: Jun2019; PROBIOTICS NOS. Vaccination history included: BNT162b2 (First COVID Vaccine: it says 30mg/.3ml, LOT: ER8729), administration date: 12Apr2021, when the patient was 55-year-old, for COVID-19 immunization; BNT162b2 (Second COVID Vaccine: LOT: EW0172), administration date: 03May2021, when the patient was 55-year-old, for COVID-19 immunization; BNT162b2 (Third COVID Vaccine: LOT: FL3198), administration date: 13Jan2022, when the patient was 56-year-old, for COVID-19 immunization. The following information was reported: LYMPHADENOPATHY (non-serious), outcome "unknown", described as "swollen glands"; PYREXIA (non-serious), CHILLS (non-serious), outcome "unknown" and all described as "She had fever and chills from fourth Pfizer COVID vaccine booster."; ILLNESS (non-serious), outcome "unknown", described as "Caller did get sick". Additional Information: Other conditions, Investigations, no, other Products: Yes. Additional Information for Other medicines Prilosec: been on it years. She is down to one pill. Was taking it twice a day. When has cold and on steroid, it upsets her stomach and she goes to morning and night pill. Also received Multivitamin. Caller went over all medications on her list with doctor and caller doesn't think there is anything relevant. She takes a multivitamin, probiotic, and Prilosec. Caller clarified that she did use Albuterol and Dulera inhalers this morning.. She used Albuterol and Dulera this morning while waiting for the doctor's office to call. Has had problems in past with Dulera with taste kind of stuff. That was after a few days and long term use of Dulera, not on same day. This isn't the same taste or problem that she experienced with Dulera. Caller clarified that the Dulera killed her sense of taste before. What she is having now kind of reminds her of she doesn't want to say metallic taste, but kind of a chemical blah kind of taste. Therapy start date for Dulera: Used it on and off all season. She started with something in the beginning of fall or Sep. Caller has 13-year-old special needs son who brought something home from school and it moved to her chest. When it is in her lungs, nose, and upper respiratory it moves to her chest and she doesn't do well. That is why she started the Dulera. Then she stopped it because she didn't need it. Then she got RSV and started Dulera again and then stopped again. She flew and then things were tasting funny, so she stopped it again. Now yesterday when she talked to her provider the provider said if caller had respiratory symptoms to do it. Caller clarified Albuterol is actually Levalbuterol. Therapy start date for Levalbuterol in Jun2019 caller and her son went to. When she came home caller had upper respiratory thing that she developed. The funny taste she had reminded her of COVID but it was too early for COVID. There are people that said they had COVID before COVID was COVID. Caller was overseas since is considered. Caller clarified she was not having funny taste with Levalbuterol. The funny taste was before using Levalbuterol. Caller is not sure if that stuff deadens her taste buds. She hasn't used any of Levalbuterol or Dulera for over a month or quite some time. Caller clarified that the last time she used Levalbuterol and Dulera before today was Jan2023. She can't read because the put the writing so small on these things. Caller clarified that she is referring to the Levalbuterol and Dulera that has small writing. She was trying to read the information from the bottle. She was feeling pretty well. Caller and her daughter moved furniture and caller thought she had body aches form being out of shape and using muscles that she had not used in a while. Caller thought they had dusty and dirty boxes and that was giving her the sinus kind of infection, sneezy, and allergic kind of stuff. Caller had swollen glands and thought it was because she had her fourth Pfizer vaccine on the 28th. Everything caller was reading said it could still be side effects from that. Caller did get sick from fourth booster. She had fever and chills from fourth Pfizer COVID vaccine booster. The fourth dose doesn't say Bivalent, it doesn't say dose and that it was Bivalent. They only wrote the LOT. All of the others were a sticker. It kind of makes caller mad. On her son's they put a sticker for him, but wrote it on hers. It was supposed to be bivalent for her too. She has tried experimental drug in the past and had bad allergic reaction. Caller felt like her tongue was coated. As a single mom with a special needs child she wants to make sure she is not precuring herself for something. The fourth dose doesn't say Bivalent, it doesn't say dose and that it was Bivalent. They only wrote the LOT. She can't read because the put the writing so small on these things. Caller clarified that she is referring to the Levalbuterol and Dulera that has small writing. She was trying to read the information from the bottle.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300072243 same patient, different vaccine dose/AE;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- PRILOSEC [OMEPRAZOLE]; DULERA; LEVALBUTEROL [LEVOSALBUTAMOL]; PROBIOTICS NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 04.11.2022
- Beginn
- 18.12.2022
- Tage bis Beginn
- 44,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Impaired work ability
Influenza virus test negative
Nasal congestion
Oropharyngeal pain
Pain
Pyrexia
Respiratory syncytial virus test negative
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
I started to have aches, fever, sore throat, and nasal congestion. I went to my PCP, who tested me for various flu strains, RSV, and COVID-19, I tested positive for COVID-19 and negative for everything else. My PCP prescribed me Paxlovid. I took the medicine and had to wait for about five days before I could return to work. It was about day seven or day eight that I finally got a negative result on a home antigen test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 19DEC2022 - COVID-19 Test - Positive Result; 19DEC2022 - Various Flu Strain Tests - Negative Results; 19DEC2022 - RSV Test - Negative Result; 26DEC2022 - Home Antigen Test - Negative Result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Graves' Disease; History of Thyroid Removal; Thyroid Eye Disease; High Cholesterol
- Andere Medikamente
- Tirosint Levothyroxine; Cequa Eye Drops; Naltrexone; Multivitamin
- Allergien
- Lactose Intolerance
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 17.02.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bursitis
Injection site pain
Product administered at inappropriate site
Symptomtext
Administration was given proximal to intended location of deltoid muscle. Believed to have punctured bursa causing bursitis. Patient reported immediate pain upon injection reporting pain scale 10/10. Patient reported continual pain in upper arm and shoulder near acromion. Patient has been taking acetaminophen 500 mg twice daily to mitigate pain. At time of this report, patient still reports pain 5/10.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, hyperlipidemia, type 2 diabetes mellitus, lymphedema, history of DVT and PE, coronary artery disease with drug-eluting stent placement in 2016, obesity, factor V Leiden, obstructive sleep apnea, chronic low back pain, chronic kidney disease, recurrent UTI, urinary retention, dementia
- Andere Medikamente
- acetaminophen, atorvastatin, cholecalciferol, ezetimibe, losartan, metformin IR, omeprazole, warfarin
- Allergien
- donepezil
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 06.02.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
Dysphagia
Feeling abnormal
Illness
Oropharyngeal pain
Pain
Pain in extremity
Throat irritation
Symptomtext
sore throat; achiness/achy/achy feeling/always has a little bit of pain; sick; feeling bad; arm is extremely sore at the injection site; getting hard to swallow; scratchy throat; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. A 79-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Feb2023 as dose 4 (booster), single (Lot number: GJ6796, Expiration Date: 31Jan2024) at the age of 79 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (ongoing), notes: high blood pressure diagnosed long time ago; don't know when this was diagnosed.; "hyperthroid" (ongoing), notes: Thyroid was diagnosed a long time ago and she has been taking thyroid medicine for quite a while; "Fibromyalgia" (ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Lot EL9262), administration date: 27Jan2021, when the patient was 77-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, Lot EN6201), administration date: 24Feb2021, when the patient was 77-year-old, for COVID-19 immunization, reaction(s): "Dizziness/almost passed out"; BNT162b2 (Dose 3, Lot ALB4102 / 32030BD), administration date: 02Dec2021, when the patient was 78-year-old, for COVID-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 07Feb2023, outcome "not recovered", described as "arm is extremely sore at the injection site"; FEELING ABNORMAL (non-serious) with onset 07Feb2023, outcome "not recovered", described as "feeling bad"; DYSPHAGIA (non-serious) with onset Feb2023, outcome "not recovered", described as "getting hard to swallow"; THROAT IRRITATION (non-serious) with onset Feb2023, outcome "not recovered", described as "scratchy throat"; OROPHARYNGEAL PAIN (non-serious), outcome "not recovered", described as "sore throat"; PAIN (non-serious), outcome "unknown", described as "achiness/achy/achy feeling/always has a little bit of pain"; ILLNESS (non-serious), outcome "unknown", described as "sick". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of feeling abnormal, oropharyngeal pain, pain, illness, dysphagia, throat irritation, pain in extremity. Additional information: Female patient wanted to know if her 2nd booster dose of the Pfizer COVID-19 Vaccine Bivalent caused her to have symptoms of feeling bad, sore throat, and achiness. she stated it made her sick. Patient had high blood pressure diagnosed long time ago; don't know when this was diagnosed but she went to her doctor on Tuesday for a regular check up and it was low and was 112 over 60 something, thyroid condition hyperthyroid; was diagnosed a long time ago and she has been taking thyroid medicine for quite a while. Called about the Pfizer, her fourth injection which was a booster and clarified that this would be her 2nd booster which she got on Monday and started feeling bad Tuesday and now she has a sore throat, feels bad and is achy and she does not know if that is a side effect of the medication regarding the injection. She reported because she does not feel like doing anything else. This 2nd booster was Monday 06Feb2023. Feeling bad: ongoing and thinks it is a little worse today and states she is worse today and has not been out of the apartment today. Sore throat: she had a scratchy throat but today it is sore and is so scratchy and is now a sore throat; clarified the sore scratchy throat began since this 2nd booster injection and is getting worse and it is getting hard to swallow. Her arm is extremely sore at the injection site which was her right arm which began yesterday and is worse today than yesterday. Multiple attempts by this agent to clarify the full name of the Pfizer vaccines but caller unable to clarify further so details are captured as stated by the caller. Her vaccine patient card is handwritten and the 2nd shot she got, she had almost an immediate reaction to that but did not realize that is what it was until later and the reaction was that she got dizzy, had to be driven home and was in a chair at the store; she had gone to physical therapy and went to and almost passed out and someone had to come get her. The last booster which is her 2nd booster dose was on Monday 06Feb2023 and it was Pfizer Bivalent with lot GJ6796; states there is static on the phone line; for this 2nd booster dose bivalent, it has expiry date 31Jan2024 and no NDC is written on the card; she has two different cards and one is with three of her vaccines and one is with this last one. Almost did not get this most recent one wished had not gotten it and it says Bivalent. for this shot, they were there at her apartment complex and there was only three of us that got the shot; the facility was called outreach; unknown type of facility but it is not a military facility. She thought her third shot she got was for the third dose. For this current 2nd booster dose, the time she had it administered was unknown but was probably about 10:30am or 11:00am because she waited and drank coffee then went for it. AE did not required visit to Emergency Room; Physician Office; Intensive Care Unit; if admitted to ICU, duration of stay. she has not been outside. The event does not require the initiation of new medication/other treatment/ procedure. The achy feeling, she does not know when this began but probably always has a little bit of pain but nothing like this; she has fibromyalgia but does not know what pain this is; the fibromyalgia was diagnosed a long time ago but she has never been treated for it. Has been seeing physician's assistance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 202302; Test Name: blood pressure; Result Unstructured Data: Test Result:112/60
- Aktuelle Erkrankungen
- Blood pressure high (high blood pressure diagnosed long time ago; don't know when this was diagnosed.); Fibromyalgia; Hyperthyroidism (Thyroid was diagnosed a long time ago and she has been taking thyroid medicine for quite a while)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 09.02.2023
- Impfdatum
- 07.02.2023
- Beginn
- 08.02.2023
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Ear pain
Headache
Hyperhidrosis
Vomiting
Symptomtext
pt c/o sweats, chills, ha, vomiting, ears hurting, on 2/7/23 the night of vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- -
- Andere Medikamente
- Advised to take acetaminophen
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.02.2023
- Impfdatum
- 05.01.2023
- Beginn
- 08.01.2023
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase increased
Arthralgia
Blood alkaline phosphatase increased
Bone pain
Fatigue
Gamma-glutamyltransferase increased
Laboratory test abnormal
Myalgia
Symptomtext
noted persistent fatigue, new and more severe bone & joint pain esp. in feet and hands. Muscle soreness in thighs, groin pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- routine labs performed on 1/25/23 showed elevated ALT of 63 (12-59) and elevated Alkaline Phosphatase of 153 (45-117) and GGT on 1/27/23 was elevated at 295 (5-55) repeat labs on 2/8/23 were WNL for both ALT and Alk Phos - GGT not repeated.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- PCOS depression asthma breast cancer
- Andere Medikamente
- Lexapro, singular, metformin, pepcid, anastrozole allegra
- Allergien
- Cefzil seasonal allergies, pollen allergies, CAT, DOG
- Vorherige Impfungen
- normal sore arm, 1st COVID vaccine about 18 hour 'not feeling well" then back to normal.
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Lacrimation increased
Malaise
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
12/27/22 Started to feel sick. Tested positive for Covid (Binmax Now Covid kit) on 12/30/22. Symptoms: Coughing, watery eyes, runny nose, body ache, no energy. Called Primary care physician office but PCP doctor was on vacation and receptionist said there's nothing they can do. NOTE: I am two time cancer survivor, 65 yrs old and in high risk category. Since I was not feeling extremely sick I didn't go to the Emergency room (but my husband did go to the ER very sick). PCP came back from vacation on 1-9-23. We are passed 5 day period for Paxlovid so PCP advises NOT to take Paxlovid. To wait it out. Two days later on 1-11-23 I tested Negative for Covid (BinaxNow kit).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Two time cancer survivor (breast & melanoma)
- Vorgeschichte
- None.
- Andere Medikamente
- lisenpril 10mg,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.01.2023
- Impfdatum
- 12.01.2023
- Beginn
- 15.01.2023
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal dreams
Blood test normal
Fatigue
Feeling abnormal
Impaired work ability
Symptomtext
Brain fog, severe fatigue, very strange dreams. This lasted until 01/27/2023. I could not work for 6 days. I visited my doctor, they took blood tests which showed nothing wrong. They did not know what to tell me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Slight cold at the time. Had Covid 12/17/22
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Hydrochlorothiazide 25mg Lisinopril 10mg Multivitamin Calcium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 28.01.2023
- Impfdatum
- 16.01.2023
- Beginn
- 17.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Symptomtext
Systemic: Body Aches Generalized-Medium, Systemic: pain in both arms radiating from arm pit to elbow-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 02.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 26,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
We hosted a dinner for the family, and my granddaughter informed us she was around a friend who tested positive. I started experiencing mild body aches, fever, and runny nose through the weekend and decided to take an at-home COVID-19 test on 11/30/2022. The test came back positive and called my doctor since I originally had an in-visit office appointment that next day; I told my doctor about my symptoms, and he informed me since my symptoms were mild to just rest, stay hydrated and take ibuprofen if needed. After some days, my symptoms went away, and I recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test: 11/30/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Atrial Fibrillation; High Blood Pressure
- Andere Medikamente
- Coreg; Ramipril; Xarelto; Alopurinol; Crestor; Multivitamin; Vitamin C; Vitamin D; Ibuprofen
- Allergien
- Penicillin; Sypril
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 21.01.2023
- Beginn
- 21.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Flushing
Headache
Malaise
Nausea
Symptomtext
On 1/21/23 10:20 am, client received a Pfizer Bivalent in the right arm. At 11 am, a member came to the nurse table and stated the client is not feeling well. Client stated about 30 minutes after she received the vaccine while cleaning in kitchen felt the dizziness, nausea, headache, and flushed feeling all over the body. So, she sat and put her head down. Client does not know how long she was resting. Client stated she was starting to feel better when she was woken up and the dizziness, nausea, headache, and flushed feeling started all over again. Client also stated she did not have anything to eat for breakfast. Client was given snacks and drinks. Vitals recorded: 11:05 am BP= 154/84 HR 84, 11:10 am BP=148/93 HR 80, 11:20 am BP=145/76 HR 75. Client has a history of anxiety and obesity but denies taking any medications. Client denies any allergies or other medical history. At 11:30 am, client continued to eat and drink and reported feeling better. At 11:40 am last vitals BP=140/72 HR 70. At 11:45 am, client was walking around the hall with a mop. Client was advised to take it easy for the day and will be receiving a call from the nurse for a follow-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anxiety, Obesity
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 14.01.2023
- Beginn
- 15.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Administration site pain
Inflammation
Injection site pruritus
Symptomtext
pt called describing she recieved pfizer bivalant dose on 1/14/2023 and 1 day later had local itching, pain, and 'knot' on arm just at location of administration. I advised pt to ice the area to reduction pain/inflamation and adivised pt to seek medication attention if gets worse/ spreads to other areas or if remains 5-7 days after administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Administration site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- n/a
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 15.01.2023
- Beginn
- 15.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Sleep disorder
Symptomtext
chills got worse/rigors; headache; uncomfortable nights sleeps; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 56-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Jan2023 at 11:30 as dose 5 (booster), single (Lot number: GJ6796) at the age of 56 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Myopia" (unspecified if ongoing); "some hearing loss" (unspecified if ongoing); "I started to experience chills" (unspecified if ongoing). Concomitant medication(s) included: CENTRUM WOMEN 50+. Past drug history included: Contrast iodine, reaction(s): "known allergies: Contrast Iodine"; Morphine, reaction(s): "known allergies: Morphine", notes: known allergies: Morphine. Vaccination history included: BNT162b2 (prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand unknown: False, Is bivalent: False, Prev dose lot number: FJ4991, Prev dose lot unknown: False, Prev dose administration date: 14Jun2022, Prev dose dose number: 4, Prev dose vaccine location: Left arm), administration date: 14Jun2022, when the patient was 56-year-old, for COVID-19 Immunization; BNT162b2 (prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand unknown: False, Is bivalent: False, Prev dose lot number: FJ8762, Prev dose lot unknown: False, Prev dose administration date: 06Dec2021, Prev dose dose number: 3, Prev dose vaccine location: Left arm), administration date: 06Dec2021, when the patient was 55-year-old, for COVID-19 Immunization; BNT162b2 (prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand unknown: False, Is bivalent: False, Prev dose lot number: EW0176, Prev dose lot unknown: False, Prev dose administration date: 04May2021, Prev dose dose number: 2, Prev dose vaccine location: Left arm), administration date: 04May2021, when the patient was 55-year-old, for COVID-19 Immunization; BNT162b2 (prev dose product: COVID 19, Prev dose brand: Pfizer, Prev dose brand unknown: False, Is bivalent: False, Prev dose lot number: EW0162, Prev dose lot unknown: False, Prev dose administration date: 13Apr2021, Prev dose dose number: 1, Prev dose vaccine location: Left arm), administration date: 13Apr2021, when the patient was 55-year-old, for COVID-19 Immunization. The following information was reported: CHILLS (non-serious) with onset 15Jan2023 at 19:00, outcome "recovered" (Jan2023), described as "chills got worse/rigors"; HEADACHE (non-serious) with onset 15Jan2023 at 19:00, outcome "recovered" (Jan2023); SLEEP DISORDER (non-serious) with onset 15Jan2023 at 19:00, outcome "recovered" (Jan2023), described as "uncomfortable nights sleeps". Therapeutic measures were not taken as a result of chills, headache, sleep disorder. Additional information: At 7pm on Jan 15th after receiving the Covid 19 bivalent Vaccine I started to experience Chills. I went to bed and the chills got worse Than I started to have rigors and a Headache. I could not get warm waves of Chills kept coming over me. I had a very Uncomfortable nights sleeps with successive Waves of chills rigorsRapu2022.If covid prior vaccination: No. If covid tested post vaccination: No. The patient did not take any vaccine in four weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Chills; Hearing loss; Myopia
- Andere Medikamente
- CENTRUM WOMEN 50+
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 11.01.2023
- Beginn
- 11.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Ear discomfort
Feeling abnormal
Headache
Hypoaesthesia
Hypoaesthesia oral
Muscle spasms
Musculoskeletal pain
Nausea
Symptomtext
Muscle Knots and spasms on left side of upper body including scapula shoulder base of skull left arm; Muscle Knots and spasms on left side of upper body including scapula shoulder base of skull left arm; Numbness on left side of face and tongue; Numbness on left side of face and tongue; Headaches; Dizziness; Flushing with ears burning; Brain fog; Nausea; 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 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Jan2023 at 15:00 as dose 4 (booster), single (Lot number: GJ6796) at the age of 65 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Necrological Lyme Disease" (unspecified if ongoing), notes: Recovered from Neurological Lyme Disease. Concomitant medication(s) included: MAGNESIUM CITRATE; D3. Vaccination history included: Covid-19 vaccine (DOSE 1, Manufacturer unknown), for COVID-19 immunization; Covid-19 vaccine (DOSE 2, Manufacturer unknown), for COVID-19 immunization; Covid-19 vaccine (DOSE 3, Manufacturer unknown), for COVID-19 immunization. The following information was reported: FEELING ABNORMAL (non-serious) with onset 11Jan2023 at 15:00, outcome "not recovered", described as "Brain fog"; DIZZINESS (non-serious) with onset 11Jan2023 at 15:00, outcome "not recovered"; EAR DISCOMFORT (non-serious) with onset 11Jan2023 at 15:00, outcome "not recovered", described as "Flushing with ears burning"; HEADACHE (non-serious) with onset 11Jan2023 at 15:00, outcome "not recovered", described as "Headaches"; MUSCLE SPASMS (non-serious) with onset 11Jan2023 at 15:00, outcome "not recovered", MUSCULOSKELETAL PAIN (non-serious) with onset 11Jan2023 at 15:00, outcome "not recovered" and all described as "Muscle Knots and spasms on left side of upper body including scapula shoulder base of skull left arm"; NAUSEA (non-serious) with onset 11Jan2023 at 15:00, outcome "not recovered"; HYPOAESTHESIA (non-serious), HYPOAESTHESIA ORAL (non-serious) all with onset 11Jan2023 at 15:00, outcome "not recovered" and all described as "Numbness on left side of face and tongue". The events "muscle knots and spasms on left side of upper body including scapula shoulder base of skull left arm", "numbness on left side of face and tongue", "headaches", "dizziness", "flushing with ears burning", "brain fog" and "nausea" required physician office visit. Therapeutic measures were not taken as a result of muscle spasms, musculoskeletal pain, hypoaesthesia, hypoaesthesia oral, headache, dizziness, ear discomfort, feeling abnormal, nausea. Additional information: No other vaccine in four weeks. Other medication in two weeks included Magnesium citrate 200 mg BID (two times in a day). D3 2000 IU. Reported Muscle Knots and spasms on left side of upper body including scapula shoulder base of skull left arm. Numbness on left side of face and tongue. Headaches. Dizziness. Flushing with ears burning. Brain fog. Nausea. No COVID prior vaccination. Not tested for COVID post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Lyme disease (Recovered from Neurological Lyme Disease)
- Andere Medikamente
- MAGNESIUM CITRATE; D3
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 16.01.2023
- Impfdatum
- 15.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test abnormal
Body temperature increased
COVID-19
Chest X-ray
Cough
Dysphagia
Leukopenia
Malaise
Odynophagia
Oesophageal disorder
Oropharyngeal pain
SARS-CoV-2 test positive
Sensory disturbance
Sputum discoloured
Wheezing
White blood cell count decreased
Symptomtext
12/27/22 Started to feel sick. 12-29-22 Went Urgent Care for Infection medicine. Free covid tested kit arrived when I got home so I toke Covid test later in day. Tested positive for Covid (Binmax Now Covid kit) later in day on 12/29/22. 12/30/22 Temperature 100.4 at this time. Coughing, bad wheezing, bad sore throat, painful difficult swallowing, feels like esophagus is getting smaller, feel something in the chest not right, coughing up yellowish/green Phlegm constantly. Entered Hospital Emergency on 12/31/22. ER doctor did chest X-Ray and blood test. Prescribed Paxlovid (Covid treatment), cough medicine, and inhaler. 1/14/2023 I am 95% better but not 100%. I still have some wheeezing and cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- 12/31/22 X-ray (Dr. didn't discuss results on this). 12/31/22 Blood test Dr said I have Leukopenia (low white blood count). Prescribed Paxlovid and other med.
- Aktuelle Erkrankungen
- Smoldering Plasma Cell Myloma, Low white blood count.
- Vorgeschichte
- None.
- Andere Medikamente
- lisenpril 10mg,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 14.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Fatigue
Headache
Pain
Tinnitus
Symptomtext
Chills, headache, body aches, tiredness, weakness - lasted 2 days. Tinnitus - started a day after vaccine and it is still going on. This also happened after the 2 previous Covid vaccines that I received; however, I only now connected it to the vaccines. Symptoms had improved some from previous vaccine, but it is much worse since getting the 3rd vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- IBS
- Andere Medikamente
- NFH Menopause SAP Dietary Supplement
- Allergien
- Milk, Buckwheat, Sesame, Amoxicillin
- Vorherige Impfungen
- Pfizer - FP7139 on 7/8/22 and 7/29/22. Chills, body aches, headache, tiredness, weakness and tinnitus after both doses.
- Staat
- GA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Amnesia
Confusional state
Dizziness
Flushing
Headache
Hyperhidrosis
Symptomtext
Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Mild, Additional Details: Patient became very confused and lost her memory for about 15 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Inflammation
Pruritus
Rash
Skin fissures
Swelling
Symptomtext
Inflammation in my face followed by extreme rash and itching Emergency room visit on 12/26/22 resulting in subscription of Hydroxyzine HCL 25 MG which relieved itching, but resulted in extreme inflammation of my face. Extreme swelling and cracked skin. Visit to dermatologist on January 3, 2023 resulting in subscription for Medrol Dose Pack. Reduced inflammation to face, but rash and itching resumed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Blood work at the ER
- Aktuelle Erkrankungen
- Tested positive for Covid on December 17, 2022
- Vorgeschichte
- -
- Andere Medikamente
- Statin, Premerin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 07.01.2023
- Impfdatum
- 31.12.2022
- Beginn
- 31.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Myalgia
Symptomtext
Patient reports week-long muscle pain/aches and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 05.01.2023
- Impfdatum
- 21.12.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypoaesthesia
Injection site pain
Pain in extremity
Symptomtext
Site: Pain at Injection Site-Medium, Systemic: pt said his arm including wrist is numb after receiving vaccine-Medium, Systemic: Numbness (specify: facial area, extremities)-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 22.12.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Eye inflammation
Eye pain
Laboratory test normal
Pain
Pyrexia
Rash
Uveitis
Vasculitis
Symptomtext
Uveitis and vasculitis - abdominal cramping, fever, rash, body aches, eye pain and inflammation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Full lab tests done, all negative
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- -
- Andere Medikamente
- Fluoxetine HCl 20mg, Hailey 24 FE 1/20 (OCP)
- Allergien
- None
- Vorherige Impfungen
- Prior Covid vaccines - body ache and fever
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 23.12.2022
- Beginn
- 26.12.2022
- 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 bruising
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Itching at Injection Site-Medium, 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 bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 04.01.2023
- Impfdatum
- 02.01.2023
- Beginn
- 01.01.2023
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pyrexia
Symptomtext
Developed fever 12 hours after vaccination, then significant bodyaches all over 24 hours later. Fever resolved after 48 hours, but bodyaches still persisting after 48 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- seasonal allergies
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 12.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Pain in extremity
Symptomtext
Sore arm; This case has been considered invalid as other-Info not qualifying for AE reporting - Medical Information since patient experienced no adverse effect under suspect BNT162B2, BNT162B2 OMI BA.4-5. The initial case was missing the following minimum criteria: (other-Info not qualifying for AE reporting - Medical Information). Upon receipt of follow-up information on 28Dec2022 this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team, Program ID: The reporter is the patient. A 61-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Nov2022 as dose 5 (booster), single (Lot number: GJ6796) at the age of 61 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, lot number: EJ1685), administration date: 22Dec2020, when the patient was 59-year-old, for COVID-19 immunization, reaction(s): "Caller did not get swollen lymph nodes with 5th dose like caller did with the prior 4 doses"; BNT162b2 (DOSE 2, SINGLE, lot number: EK4176), administration date: 12Jan2021, when the patient was 59-year-old, for COVID-19 immunization, reaction(s): "Caller did not get swollen lymph nodes with 5th dose like caller did with the prior 4 doses"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot number: Assuming FH8020), administration date: 10Oct2021, when the patient was 59-year-old, for COVID-19 Immunization, reaction(s): "Caller did not get swollen lymph nodes with 5th dose like caller did with the prior 4 doses"; BNT162b2 (DOSE 4 (BOOSTER), SINGLE,, Lot number: FM9992), administration date: 12May2022, when the patient was 60-year-old, for COVID-19 Immunization, reaction(s): "Caller did not get swollen lymph nodes with 5th dose like caller did with the prior 4 doses". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Nov2022, outcome "not recovered", described as "Sore arm". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: It was inquired of wondering if patinet's last COVID vaccine was an older version. She was expecting one that it would provide protection against the most recent strains. She has had 5 vaccinations since 22Dec2020 and has just tested positive for COVID for the first time (24Dec2022 and still positive on 26Dec2022.) This was very disappointing, her last vaccine was 12Nov2022 from: GJ6796, Comirnaty, Pfizer-BioNTech COVID-19 Vaccine [Monovalent] and/or Bivalent, gray cap, original/omicron BA.4/BA.5 (Bivalent), above 12 years -15/15 mcg per dose. Caller performed a call back with regards to INT. Upon confirming details submitted in previous INT, caller stated that she has avoided covid all of this time with receiving 5 COVID vaccines. Caller stated that she reacted pretty severely, however this time she did not, but thought maybe her body was becoming used to the vaccines. Caller stated that she had been tested for COVID multiple times over the years and this was her first time that she had tested positive. Caller has had 5 vaccinations, confirmed all five vaccinations were the Pfizer COVID vaccine, since 22Dec2020 and caller just tested positive for COVID for the first time on 24Dec2022 and was still positive on 26Dec2022. Her last vaccine was on 12Nov2022, the lot number for the last dose was GJ6796. She usually reacts pretty severely however this time with the last vaccine caller did not. Upon transfer caller confirmed event details provided by transfer agent. Was just surprised that she came down with COVID, was careful, had a immunosuppressed daughter and grandkids. She has had many tests before which were negative. Originally called to make sure caller got the most recent vaccine that was available, which was verified with the agent that she got the most recent vaccine. She thought it would be interesting for Pfizer to know that she got COVID. Event details included that she did not get swollen lymph nodes with fifth dose like she did with the prior four doses. Just got the sore arm with the fifth dose. Sore arm started pretty much right away that evening, last dose was on 12Nov2022, so sore arm started maybe within 8 hours. Stop date: there was still some strange stuff going on with arm, does not know if related, something bugging arm going down into elbow, more like a nerve kind of thing. Event details included that she does not think there are any new events to report, thought caller reported all of this information on the Pfizer website. Just has a couple of questions and wanted to relay concerns to call handler first. She was surprised, caller had COVID after five vaccines and had not had COVID at all for two years, usually got pretty severe reactions to the prior four doses of the Pfizer COVID vaccine, this one, the fifth dose of the Pfizer COIVD vaccine, she did not get a severe reaction just pretty mild, just had a sore arm. So that was why she called in to see if caller had protection against the newest strain. Then clarified and confirmed that caller does not believe caller reported the sore arm on the Pfizer website. Reference number: took picture of form completed online but does not think there was any other reference number. Initially reported of having had 5 vaccinations of the Pfizer COVID vaccine and just tested positive for COVID. Fifth dose: Lot number: assuming first letter, handwritten on vaccination card so could not read, provided lot number as GJ6796. Product strength and count size dispensed were not provided. Additional lot numbers included: EJ1685; EK4176; FH8020; FM9992. Follow-up (28Dec2022): The initial case was missing the following minimum criteria: (other-Info not qualifying for AE reporting - Medical Information). Upon receipt of follow-up information on 28Dec2022 this case now contains all required information to be considered valid. This is a spontaneous follow-up report from a contactable Nurse. This 61-year-old female Nurse (Patient) reported for herself with updated information which included: Reporter title and occupation updated as Nurse. Reporter suffix added. Patient age and age at vaccination added. Age at vaccination, reaction and lot number added for dose 1 and Dose 2 in historical vaccine. Historical vaccine recoded to BNT162B2 for Dose 3 and Dose 4, vaccination date, reaction and lot number added as per SD. Lab test coded for COVID with Positive result as per VT: tested positive for COVID for the first time on 24Dec2022 and was still positive on 26Dec2022. Event onset date conservatively captured as Nov2022. As per VT: stop date of adverse event: There is still some strange stuff going on with arm, outcome of event conservatively captured as not recovered/not resolved. Additional information was updated. No new information provided.; Sender's Comments: Linked Report(s) :PFIZER INC-2021010707 same reporter/patient, different dose/events;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221224; Test Name: Tested positive for COVID; Test Result: Positive; Test Date: 20221226; Test Name: Tested positive for COVID; Test Result: Positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 12.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Pain in extremity
Symptomtext
Sore arm; This case has been considered invalid as other-Info not qualifying for AE reporting - Medical Information since patient experienced no adverse effect under suspect BNT162B2, BNT162B2 OMI BA.4-5. The initial case was missing the following minimum criteria: (other-Info not qualifying for AE reporting - Medical Information). Upon receipt of follow-up information on 28Dec2022 this case now contains all required information to be considered valid. This is a spontaneous report received from a contactable reporter(s) (Nurse) from medical information team, Program ID: The reporter is the patient. A 61-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Nov2022 as dose 5 (booster), single (Lot number: GJ6796) at the age of 61 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, lot number: EJ1685), administration date: 22Dec2020, when the patient was 59-year-old, for COVID-19 immunization, reaction(s): "Caller did not get swollen lymph nodes with 5th dose like caller did with the prior 4 doses"; BNT162b2 (DOSE 2, SINGLE, lot number: EK4176), administration date: 12Jan2021, when the patient was 59-year-old, for COVID-19 immunization, reaction(s): "Caller did not get swollen lymph nodes with 5th dose like caller did with the prior 4 doses"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot number: Assuming FH8020), administration date: 10Oct2021, when the patient was 59-year-old, for COVID-19 Immunization, reaction(s): "Caller did not get swollen lymph nodes with 5th dose like caller did with the prior 4 doses"; BNT162b2 (DOSE 4 (BOOSTER), SINGLE,, Lot number: FM9992), administration date: 12May2022, when the patient was 60-year-old, for COVID-19 Immunization, reaction(s): "Caller did not get swollen lymph nodes with 5th dose like caller did with the prior 4 doses". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Nov2022, outcome "not recovered", described as "Sore arm". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: It was inquired of wondering if patinet's last COVID vaccine was an older version. She was expecting one that it would provide protection against the most recent strains. She has had 5 vaccinations since 22Dec2020 and has just tested positive for COVID for the first time (24Dec2022 and still positive on 26Dec2022.) This was very disappointing, her last vaccine was 12Nov2022 from: GJ6796, Comirnaty, Pfizer-BioNTech COVID-19 Vaccine [Monovalent] and/or Bivalent, gray cap, original/omicron BA.4/BA.5 (Bivalent), above 12 years -15/15 mcg per dose. Caller performed a call back with regards to INT. Upon confirming details submitted in previous INT, caller stated that she has avoided covid all of this time with receiving 5 COVID vaccines. Caller stated that she reacted pretty severely, however this time she did not, but thought maybe her body was becoming used to the vaccines. Caller stated that she had been tested for COVID multiple times over the years and this was her first time that she had tested positive. Caller has had 5 vaccinations, confirmed all five vaccinations were the Pfizer COVID vaccine, since 22Dec2020 and caller just tested positive for COVID for the first time on 24Dec2022 and was still positive on 26Dec2022. Her last vaccine was on 12Nov2022, the lot number for the last dose was GJ6796. She usually reacts pretty severely however this time with the last vaccine caller did not. Upon transfer caller confirmed event details provided by transfer agent. Was just surprised that she came down with COVID, was careful, had a immunosuppressed daughter and grandkids. She has had many tests before which were negative. Originally called to make sure caller got the most recent vaccine that was available, which was verified with the agent that she got the most recent vaccine. She thought it would be interesting for Pfizer to know that she got COVID. Event details included that she did not get swollen lymph nodes with fifth dose like she did with the prior four doses. Just got the sore arm with the fifth dose. Sore arm started pretty much right away that evening, last dose was on 12Nov2022, so sore arm started maybe within 8 hours. Stop date: there was still some strange stuff going on with arm, does not know if related, something bugging arm going down into elbow, more like a nerve kind of thing. Event details included that she does not think there are any new events to report, thought caller reported all of this information on the Pfizer website. Just has a couple of questions and wanted to relay concerns to call handler first. She was surprised, caller had COVID after five vaccines and had not had COVID at all for two years, usually got pretty severe reactions to the prior four doses of the Pfizer COVID vaccine, this one, the fifth dose of the Pfizer COIVD vaccine, she did not get a severe reaction just pretty mild, just had a sore arm. So that was why she called in to see if caller had protection against the newest strain. Then clarified and confirmed that caller does not believe caller reported the sore arm on the Pfizer website. Reference number: took picture of form completed online but does not think there was any other reference number. Initially reported of having had 5 vaccinations of the Pfizer COVID vaccine and just tested positive for COVID. Fifth dose: Lot number: assuming first letter, handwritten on vaccination card so could not read, provided lot number as GJ6796. Product strength and count size dispensed were not provided. Additional lot numbers included: EJ1685; EK4176; FH8020; FM9992. Follow-up (28Dec2022): The initial case was missing the following minimum criteria: (other-Info not qualifying for AE reporting - Medical Information). Upon receipt of follow-up information on 28Dec2022 this case now contains all required information to be considered valid. This is a spontaneous follow-up report from a contactable Nurse. This 61-year-old female Nurse (Patient) reported for herself with updated information which included: Reporter title and occupation updated as Nurse. Reporter suffix added. Patient age and age at vaccination added. Age at vaccination, reaction and lot number added for dose 1 and Dose 2 in historical vaccine. Historical vaccine recoded to BNT162B2 for Dose 3 and Dose 4, vaccination date, reaction and lot number added as per SD. Lab test coded for COVID with Positive result as per VT: tested positive for COVID for the first time on 24Dec2022 and was still positive on 26Dec2022. Event onset date conservatively captured as Nov2022. As per VT: stop date of adverse event: There is still some strange stuff going on with arm, outcome of event conservatively captured as not recovered/not resolved. Additional information was updated. No new information provided.; Sender's Comments: Linked Report(s) :PFIZER INC-2021010707 same reporter/patient, different dose/events;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221224; Test Name: Tested positive for COVID; Test Result: Positive; Test Date: 20221226; Test Name: Tested positive for COVID; Test Result: Positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 31.12.2022
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- 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 inflammation
Symptomtext
10X10CM INFLAMMATION AROUND INJECTION SITE. PT TOOK A PREDNISONE TAPER (HAD SOME AT HOME) AND HAS BEEN FEELING BETTER. NO ANAPHYLACTIC EVENT REPORTED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site inflammation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pt mentioned compromised immune system
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- -
- Geschlecht
- M
- Eingang
- 31.12.2022
- Impfdatum
- 23.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body height
Pain in extremity
Poor quality product administered
Product administration error
Symptomtext
Bivalent, GRAY cap that was "open for 18 hours" and left at room temperature, in the vial.; Bivalent, GRAY cap that was "open for 18 hours" and left at room temperature, in the vial.; Sore arm; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Dec2022 as dose number unknown, 0.3 ml single (Lot number: GJ6796, Expiration Date: 31Jan2024), in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization complete; Manufacturer unknown), for Covid-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Dec2022, outcome "unknown", described as "Sore arm"; PRODUCT ADMINISTRATION ERROR (non-serious), POOR QUALITY PRODUCT ADMINISTERED (non-serious) all with onset 23Dec2022, outcome "unknown" and all described as "Bivalent, GRAY cap that was "open for 18 hours" and left at room temperature, in the vial.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of product administration error, poor quality product administered, pain in extremity. Additional information: The pharmacist reported that the patient received a dose of Pfizer Covid19 vaccine, Bivalent, Gray cap that was "open for 18 hours" and left at room temperature, in the vial. This happened on Friday, the patient was stable and ok. Created an AE Form because a vaccine was administered 6 hours past the 12 hour period time allowed. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received. Follow-up (27Dec2022): New information was reported from a contactable Pharmacist. This Pharmacist reported for a patient that: Updated information included: Reporter mailing address and institution, lab test, dosage regimen details and new event. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Name: Height; Result Unstructured Data: Test Result:Over 5'6" or 5'8"
- 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
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
patient only has rash on the abdomen and the back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- non
- Aktuelle Erkrankungen
- no thing
- Vorgeschichte
- no thing
- Andere Medikamente
- non
- Allergien
- no allergy
- Vorherige Impfungen
- redness on the injection site when she had moderna vaccine in the past
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 01.11.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 46,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cough
Fatigue
Gait disturbance
Rhinorrhoea
Thinking abnormal
Symptomtext
One day I had extreme join pain in the knees almost unable to walk followed in the evening by exhaustion and very strong fatigue. I had to lay down. It was a little bit better in the morning after sleeping. My nose started running with fatigue still. Unable to think straight. The doctor noticed I was coughing a lot and prescribed strong cough medicine for me. It has been ongoing for 10 days although I'm feeling a lot better. I had a telehealth interview with my doctor on Monday afternoon 12/19/2022. I started my first dose of PAXLOVID on the evening of 19th. I also only have one kidney so I got renal PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- -
- Andere Medikamente
- Alendronate; VAGIFEM
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- 24.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site pruritus
Injection site reaction
Rash
Rash macular
Rash papular
Rash vesicular
Urticaria
Symptomtext
Son had red splotchiness by the injection site on his arm, and it was itchy so he scratched in the evening the day after the injection. He woke parents up after midnight that night complaining of hives which were all over his body, especially located around mid section of torso. Hives were raised and bubble like and extremely uncomfortable. No fever accompanied hives. Father took him to the ER where he received steroids. Hives disappeared over the following week but reappeared sporatically on and off for 2 weeks. He has an appointment for skin testing on January 25th, 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicilian
- Vorherige Impfungen
- Hives at young age, 6 years old? due to Penicillin treatment
- Staat
- PA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 19.12.2022
- Impfdatum
- 19.12.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Muscular weakness
Symptomtext
About 15 minutes after vaccine patient felt dizzy and legs felt "rubbery". Patient was seated and drank water and felt find about 25 minutes after vaccination. Patient was called at home 5 hours later and she said she was find.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 18.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Headache
Incorrect product formulation administered
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Headache-Mild, Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 16.12.2022
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Urticaria
Symptomtext
Patient arrived to the vaccine clinic, received both the Pfizer Bivalent vaccine and the Flucelvax Quadrivalent Influenza Vaccine. Patient vaccinated at 0625 Patient complained of itchiness all over the arms, torso, legs, and back. Patient did not complain of swelling of the tongue, dysphagia, or trouble breathing. Medic, EMT, and RN verified symptoms and patient assessment. 0630 Assessed patient with vaccination team, no shortness of breath or swelling noted, lung sounds clear. Hive started to appear. 0635 Assessed vitals. Administer IM Benadryl, assessed patient and called medical team on site to assess patient. Hive started to dissipate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Patient was taken to Medical at 0640 12/16/22.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Insomnia
Malaise
Pain in extremity
Vaccination site pain
Symptomtext
I always get a sore arm where I get the shot; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. A female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), as dose 5 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "hip replacement" (unspecified if ongoing). Concomitant medication(s) included: AMOXICILLIN taken for hip arthroplasty. Vaccination history included: Bnt162b2 (Dose 1,Single), for Covid-19 immunization, reaction(s): "I always get a sore arm where I get the shot"; Bnt162b2 (Dose 2, Single), for Covid-19 immunization, reaction(s): "I always get a sore arm where I get the shot"; Bnt162b2 (Dose 3 (Booster), Single), for Covid-19 immunization, reaction(s): "I always get a sore arm where I get the shot"; Bnt162b2 (Dose 4 (Booster), Single), for Covid-19 immunization, reaction(s): "I always get a sore arm where I get the shot". The following information was reported: VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "I always get a sore arm where I get the shot". Additional information: She states she had to go to her dentist and had to take amoxicillin due to history of a hip replacement. She mentioned, at the time, she always get a sore arm where she got the shot. She did share information about friends that came down with Covid a few weeks (approximately 2 weeks) after receiving their Pfizer newest booster dose. The patient states she is being bombarded with multiple (8 packs) of mailed packages about the this information. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received.; Sender's Comments: Serious: No, Patient characteristics,,Patient: Privacy, Sex: Female,Reaction(s)/Event(s); MedDRA version for reaction/event term LLT: N/A; Reaction/event in MedDRA terminology (LLT): Medical Information Potential AE. Drug(s) Information; Characterization of drug role: Suspect Proprietary medicinal product name: Comirnaty, Pfizer-BioNTech COVID-19 Vaccine [Monovalent] and/or Biv. Identification of the country where the drug was obtained: private. Country of authorization/application: private. Active Substance Information: COVID-19 Vaccine, mRNA [Monovalent and/or Bivalent] Narrative case summary and further information: Originating AE Request: REQ-997387. Attachments:1 Reporter Subtype: Patient, PQC Present: No, AE Present: Yes. PQC Details: Request- Name: REQ-997387 Product: Comirnaty, Pfizer-BioNTech COVID-19 Vaccine [Monovalent] and/or Bivalent. Dose/Dosage Form: Gray cap,Original/Omicron BA.4/BA.5 (Bivalent), less than equal to 12 years-15/15 mcg per dos. Question: Caller states she called Pfizer a few weeks ago she informed the PMI agent that she had received the most newest booster. She states she had to go to her dentist and had to take amoxicillin due to history of a hip replacement. She mentioned, at the time, I always get a sore arm where I get the shot. I did share information about friends that came down with Covid a few weeks (approximately 2 weeks) after receiving their Pfizer newest booster dose. The patient states she is being bombarded with multiple (8 packs) of mailed packages about the this information. She stated Please do not send anymore questionaires to me. They are about 10 pages long and want more information about her experience. She would like this mail to STOP now. E-transmitting duplicate AE to agent: Please do not send anymore mailed packages to this caller. Its too much The information on the batch/lot number for [BNT162B2, BNT162B2 OMI BA.4-5] has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hip replacement
- Andere Medikamente
- AMOXICILLIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Immediate post-injection reaction
Pain in extremity
Symptomtext
Patient received Pfizer Bivalent vaccine on 11/30/22 and immediately started noticing shooting shoulder and arm pain. She came back on 12/12/22 to state that she is still experiencing the same pain symptoms. Advised patient to take OTC pain meds to treat symptoms and to make an appointment with PCP to discuss lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HAD PREVIOUS HISTORY OF FROZEN S HOULDER, PT MENTIONED SYMPTOMS FEEL LIKE FROZEN SHOULDER STARTING AGAIN AFTER RECEIVING VACCINE
- Andere Medikamente
- ANASTROZOLE 1 MG
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Symptomtext
About 12 hours after the vaccination, I developed terrible chills (no fever). I had to bundle up with lots of clothes and blankets and then continued to shiver while in bed that night. I also developed incredible fatigue which I am still having 3 days later. I did not have these symptoms with any of my previous COVID shots - 2 originals and 2 boosters before this. All of my shots give me soreness at the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid arthritis, Mast Cell Activation Syndrome
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 11.12.2022
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Lethargy
Nausea
Pain
Pyrexia
Vomiting
Symptomtext
Lethargy - started about 6 hours after dose Body aches/Chills/fever - started about 6-8 hours after dose Nausea/vomiting - about 12 hours after dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Glycopyrrolate
- Allergien
- N/A
- Vorherige Impfungen
- Similar adverse event for all prior Covid vaccines (all Pfizer). Previous vaccinations involved hives (possibly mitigated due to
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 13.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 6,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Feeling abnormal
Nasal congestion
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I started with a cough and a stuffy nose on 11/19/2022, in the evening I has a low-grade fever. I took two home COVID-19 test and they came back negative. I was still felling back so I called my doctor's office and made an appointment and was able to get in on 11/22/22. I did not have a fever when I went in for the appointment, I had a rapid COVID-19 in the doctor's office that came back positive. I was prescribed Paxlovid and cough medication. I decided not to take the Paxlovid. The cough is still lingering but I do feel better. I do consider my case very mild.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test - negative; Rapid COVID-19 test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Lipitor, Vitamin D; Multivitamin, Omega 3
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 09.12.2022
- Impfdatum
- 07.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blindness
Headache
Myalgia
Ophthalmological examination abnormal
Retinal infarction
Visual impairment
Symptomtext
When I woke up the following morning after dose five of my COVID-19 I had muscle aches and headaches. I work at a hospital and at about nine or ten AM that morning my vision diminished rapidly. At around ten AM as I was driving home, I called all my doctors. My eye doctor was the only doctor I heard back from on Wednesday November seventh 2022 and he scheduled an appointment for today Friday December ninth 2022. The vision loss has improved although still present as of today. I learned today I have an infarcted retinal artery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Eye exam discovered infarcted retinal artery.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines; Strokes; Tuberculosis; Stephen Johnson's Syndrome; IGG3 Deficiency; Anthrax; Myocarditis
- Andere Medikamente
- Losartan; hydrocortisone; amlodipine; metoprolol; SINGULAIR; FLONASE; aspirin; ALLEGRA
- Allergien
- Egg; LEVAQUIN; sulfa
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Feeling abnormal
Hyperhidrosis
Pain
Pyrexia
Symptomtext
fatigue and fever began initially, felt he was coming down with something by 6pm. He felt "bad by 7pm". He felt, "achy and painful to move". Was in bed by 10pm and had tried using heating pad as he felt, "severe chills, body aches, and sweating". He remained in bed until 10am the following morning. He still felt sore the following day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- no
- Andere Medikamente
- citerizine, multivitamin, vit C, vit D
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 01.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chapped lips
Diarrhoea
Feeling cold
Lip dry
Lip pain
Lip pruritus
Lip swelling
Oral pain
Pain
Toothache
Vomiting
Symptomtext
Fri Dec 2: Chills; body aches; oral pain in molars left side of mouth; dry, cracked, itchy, swollen lips Sun, Dec 4: vomiting, diarrhea Lip pain and swelling is persisting and medical treatment will be sought today
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pepcid Claritin Nasacort Florist or Vit D3 Iron Vit C Potassium Calcium Multivitamin Biotin Folate Vit E Vit Methyl B12
- Allergien
- Codeine Thimerasol
- Vorherige Impfungen
- Age 57 & 58: COVID does 3-4, all does Pfizer
- Staat
- OH
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Lymph node pain
Lymphadenopathy
Pain
Symptomtext
Experienced swelling in lymph node of acute left arm pit in pervious IM injections. Bivalent injection has created swelling and throbbing pain of left armpit but has also increased and spread to lymph nodes in left arm (upper and lower) and nearby left breast tissue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- All previous COVID IM injections have produced acute lymph node swelling in armpit. Each have been mild in discomfort and resolv
- Staat
- IN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19 immunisation
Chills
Peripheral swelling
Pyrexia
Vaccination site swelling
Symptomtext
CHILLS; FEVER; ARM SWELLED UP A LITTLE; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient concerned a 69 year old female of unspecified ethnicity. The patient's weight was 69.85 kilograms, and height was 163 centimeters. No past medical history or concurrent conditions were reported. The patient previously received dose 1 with covid-19 vaccine ad26.cov2.s (Dose number in series 1), (suspension for injection, route of admin, batch number and expiry date were not reported) dose was not reported, 1 total administered start therapy date were not reported for covid-19 prophylaxis. On an unspecified date, the patient got very sick and experienced chills and fever (Dose number in series 1). The patient received dose 2 with covid-19 vaccine ad26.cov2.s (Dose number in series 2), (suspension for injection, route of admin, batch number and expiry date were not reported) dose, start therapy date were not reported, 1 total administered for covid-19 prophylaxis. The batch number was not reported and has been requested. Age at time of vaccination 7 decade old. No concomitant medications were reported. On an unspecified date, the patient again got very sick and experienced recurrence of chills and fever (Dose number in series 2). The patient also received dose 3 with Non-company suspect vaccine Comirnaty (tozinameran), (Dose number in series 3), (intramuscular, batch number: GJ6796 expiry: 31-JUL-2023, form of admin was not reported) dose was not reported, administered on 18-NOV-2022 to left arm for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (Dose number in series 3). The patient also received Non-company suspect influenza vaccine (form of admin, route of admin, and batch number and expiry date were not reported) dose was not reported, administered on NOV-2022 for prophylactic vaccination. On 18-NOV-2022, the patient's arm swelled up a little (Dose number in series 3). The patient put ice on it. She had no fever, no headaches, nothing, she did not even get sick. The action taken with covid-19 vaccine ad26.cov2.s, tozinameran, and influenza vaccine was not applicable. The patient recovered from arm swelled up a little on night of 18-NOV-2022, and the outcome of fever, chills and revaccination with different covid-19 vaccine was not reported. This report was non-serious. This case, involving the same patient is linked to 20221201988 (Dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19 immunisation
Chills
Peripheral swelling
Pyrexia
Vaccination site swelling
Symptomtext
CHILLS; FEVER; ARM SWELLED UP A LITTLE; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient concerned a 69 year old female of unspecified ethnicity. The patient's weight was 69.85 kilograms, and height was 163 centimeters. No past medical history or concurrent conditions were reported. The patient previously received dose 1 with covid-19 vaccine ad26.cov2.s (Dose number in series 1), (suspension for injection, route of admin, batch number and expiry date were not reported) dose was not reported, 1 total administered start therapy date were not reported for covid-19 prophylaxis. On an unspecified date, the patient got very sick and experienced chills and fever (Dose number in series 1). The patient received dose 2 with covid-19 vaccine ad26.cov2.s (Dose number in series 2), (suspension for injection, route of admin, batch number and expiry date were not reported) dose, start therapy date were not reported, 1 total administered for covid-19 prophylaxis. The batch number was not reported and has been requested. Age at time of vaccination 7 decade old. No concomitant medications were reported. On an unspecified date, the patient again got very sick and experienced recurrence of chills and fever (Dose number in series 2). The patient also received dose 3 with Non-company suspect vaccine Comirnaty (tozinameran), (Dose number in series 3), (intramuscular, batch number: GJ6796 expiry: 31-JUL-2023, form of admin was not reported) dose was not reported, administered on 18-NOV-2022 to left arm for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (Dose number in series 3). The patient also received Non-company suspect influenza vaccine (form of admin, route of admin, and batch number and expiry date were not reported) dose was not reported, administered on NOV-2022 for prophylactic vaccination. On 18-NOV-2022, the patient's arm swelled up a little (Dose number in series 3). The patient put ice on it. She had no fever, no headaches, nothing, she did not even get sick. The action taken with covid-19 vaccine ad26.cov2.s, tozinameran, and influenza vaccine was not applicable. The patient recovered from arm swelled up a little on night of 18-NOV-2022, and the outcome of fever, chills and revaccination with different covid-19 vaccine was not reported. This report was non-serious. This case, involving the same patient is linked to 20221201988 (Dose number in series 1).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 02.12.2022
- Impfdatum
- 29.11.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Product administered to patient of inappropriate age
Symptomtext
Patient was given a 12+ Bivalent Booster of Pfizer when it should have been Peds Bivalent Pfizer (5-11yrs). Patients parents were called and notified of mistake and cleared that the only symptom he had was tiredness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 29.11.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site pain
Vaccination site swelling
Symptomtext
Approx 24 hours after 5th booster shot, (this is my 1st Pfizer Bivalent Booster), I have a raised, very red, and painful somewhat circular spot on my arm that received the vaccine. It measures approximately 2" x 2". I do have a photo available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Relapsing Polychondritis- Rare Autoimmune Disease that affects cartilage and, sometimes to a lesser extent, other proteoglycan-rich tissues in the body. It can be severe or fatal, though not for all patients.
- Andere Medikamente
- Prozac Lamictal Abilify
- Allergien
- Skin interaction with Nickel
- Vorherige Impfungen
- Missed menstrual cycles after every Pfizer Covid19 vaccine-I assume this is not serious, but I thought to mention this.
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 11.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash pruritic
Symptomtext
an hour or two after vaccine small rash lumps appeared on wrist and hand, as day went on they went all over my body, by 5pm they were becoming larger and red. They are a moderately painful and itchy. 24 hours laters I still have red rash all over my body, they mildly painful and itchy. Took two 1/2 Benadryls upon going to bed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- ritilan LA 20, fiber capsule,
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Headache
Myalgia
Nausea
Oropharyngeal pain
Pyrexia
Vaccination site pain
Symptomtext
Fever; headache; nausea; chills; muscle soreness; fatigue; soreness at injection site; sore throat; lightheadedness; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 12-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Nov2022 at 11:30 as dose 4 (booster), single (Lot number: GJ6796) at the age of 12 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Past drug history included: Augmentin, reaction(s): "known allergies: Augmentin", notes: known allergies Augmentin; Amoxicillin, reaction(s): "known allergies: amoxicillin", notes: known allergies amoxicillin. Vaccination history included: Covid-19 vaccine (Dose: 1, Manufacturer unknow, Lot batch number unknown), for COVID-19 immunization; Covid-19 vaccine (Dose: 2, Manufacturer unknow, Lot batch number unknown), for COVID-19 immunization; Covid-19 vaccine (Dose: 3, Manufacturer unknow, Lot batch number unknown), for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering", described as "Fever"; CHILLS (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering"; FATIGUE (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering"; HEADACHE (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering"; DIZZINESS (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering", described as "lightheadedness"; MYALGIA (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering", described as "muscle soreness"; NAUSEA (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering"; OROPHARYNGEAL PAIN (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering", described as "sore throat"; VACCINATION SITE PAIN (non-serious) with onset 19Nov2022 at 21:15, outcome "recovering", described as "soreness at injection site". Therapeutic measures were not taken as a result of pyrexia, headache, nausea, chills, myalgia, fatigue, vaccination site pain, oropharyngeal pain, dizziness. Additional information: If other vaccine in four weeks: no. Other medications in two weeks: no, If covid prior vaccination: no, If covid tested post vaccination: no. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Off label use
Pyrexia
Vertigo
Vomiting
Symptomtext
vomiting; fever and chills; fever and chills; significant and debilitating vertigo; Fluzone 08Nov2022; Fluzone 08Nov2022; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 36-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Nov2022 at 10:30 as dose 4 (booster), single (Lot number: GJ6796) at the age of 36 years intramuscular, in right arm for covid-19 immunisation; influenza vaccine (FLUZONE [INFLUENZA VACCINE]), on 08Nov2022 as dose 1, single (Lot number: UT7751MA), in left deltoid for immunisation. The patient's relevant medical history included: "ADHD" (unspecified if ongoing), notes: ADHD, Depression, Allergic Rhinitis; "Depression" (unspecified if ongoing), notes: ADHD, Depression, Allergic Rhinitis; "Allergic Rhinitis" (unspecified if ongoing), notes: ADHD, Depression, Allergic Rhinitis; "Latex Allergy" (unspecified if ongoing); "Sulfa Allergy" (unspecified if ongoing). Concomitant medication(s) included: CONCERTA; LEXAPRO; WELLBUTRIN; ALLEGRA [FEXOFENADINE HYDROCHLORIDE]; FAMOTIDINE. Past drug history included: Wasps, reaction(s): "Drug allergy: Wasps". Vaccination history included: BNT162b2 (Dose Number: 3, Batch/Lot No: FC3184, Route of Administration: Intramuscular), administration date: 21Oct2021, when the patient was 35-year-old, for covid-19 immunization; BNT162b2 (Dose Number: 2, Batch/Lot No: EL3247, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 25Jan2021, when the patient was 34-year-old, for covid-19 immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EK4176, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 04Jan2021, when the patient was 34-year-old, for covid-19 immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 08Nov2022, outcome "unknown" and all described as "Fluzone 08Nov2022"; PYREXIA (non-serious), CHILLS (non-serious) all with onset 09Nov2022, outcome "recovering" and all described as "fever and chills"; VERTIGO (non-serious) with onset 09Nov2022, outcome "recovering", described as "significant and debilitating vertigo"; VOMITING (non-serious) with onset 09Nov2022 at 17:00, outcome "recovering". The events "fever and chills", "significant and debilitating vertigo" and "vomiting" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia, chills, vertigo, vomiting. Additional information: Patient didn't receive other vaccine in four weeks. Started with fever and chills approximately 18 hours after the immunization. Early on morning of 09Nov2022 developed significant and debilitating vertigo with any type of position changes. Continued to fever for 48 hours despite Tylenol/Ibuprofen with a temperature around 101.1 F. Vertigo was significant enough to cause vomiting, limited ability to ambulate and also limited oral intake. Fever broke evening of 10Nov however Vertigo persisted requiring follow up with a medical provider and prescription medications. Facility type Vaccine: Doctor's office/urgent care. AE resulted in: Doctor or other healthcare professional office/clinic visit. Treatment drugs include Meclizine and Zofran. No Covid prior vaccination. No Covid tested post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 202211; Test Name: Body temperature; Result Unstructured Data: Test Result:101.1 Fahrenheit; Comments: with a temperature around 101.1 F
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: ADHD (ADHD, Depression, Allergic Rhinitis); Allergic rhinitis (ADHD, Depression, Allergic Rhinitis); Depression (ADHD, Depression, Allergic Rhinitis); Latex allergy; Sulfonamide allergy
- Andere Medikamente
- CONCERTA; LEXAPRO; WELLBUTRIN; ALLEGRA [FEXOFENADINE HYDROCHLORIDE]; FAMOTIDINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 05.11.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash pruritic
Urticaria
Vaccination site erythema
Vaccination site pruritus
Symptomtext
Started with a localized reaction right around where the vaccine site was located. Red and itchy for 3 days. Then progressed to a trunk rash that is very pruritic, small hives have been coming and going for the last 7 days. Rashi is mostly on buttocks, back and the R arm. Minimally on lower abdomen and groin area. Previous vaccines elicited a fever, but never a rash. No fevers, cough, sore throat or other changes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Eczema, asthma, Factor 5 Leiden (genetic clotting disorder)
- Andere Medikamente
- Multivitamin
- Allergien
- Bee stings
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 23.10.2022
- Beginn
- 23.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Insomnia
Myalgia
Nausea
Vomiting
Symptomtext
Chills Headache Insomnia Muscle Aches (Arm and Both Legs) Nausea Vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac Disease (Diagnosed June 2018, in Remission) Cholecystectomy (Performed February 2005)
- Andere Medikamente
- Amitriptyline Hydrochloride Dicyclomine Hydrochloride Gabapentine Ibuprofen Iron Mono-Linyah Multivitamin Omega-3 Pantoprazole Probiotic Supplement Tylenol Vitamin D3
- Allergien
- Dust mites Pet dander
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 12.12.2023
- Impfdatum
- 09.12.2022
- Beginn
- 01.11.2023
- Tage bis Beginn
- 327,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 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 53-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Dec2020 as dose 1, single (Batch/Lot number: unknown), in left arm, on 06Jan2021 as dose 2, single (Batch/Lot number: unknown), in left arm, on 20Dec2021 as dose 3 (booster), single (Lot number: FJ620), in left arm and on 09Dec2022 as dose 4 (booster), single (Lot number: GJ6796) at the age of 52 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "peanut allergy" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Nov2023, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive; Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received anti-viral Covid 19 treatment with Paxlovid from 28Nov2023 to 02Dec2023. The information on the batch/lot number for bnt162b2, bnt162b2 omi ba.4-5 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 Test; Test Result: Positive ; Test Name: Covid-19 Test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Peanut allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 08.12.2023
- Impfdatum
- -
- Beginn
- 01.11.2023
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
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(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 42-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), as dose 4 (booster), single (Lot number: GJ6796) 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: "High BP" (unspecified if ongoing); "overweight" (unspecified if ongoing); "Known allergies: Duck eggs" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE, start date: 01Sep2023. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Nov2023, outcome "unknown" and all described as "Treatment of COVID-19". The event "treatment of covid-19" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Nov2023) Positive, notes: Took course of Paxlovid within two days of symptom onset and positive test result. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received Paxlovid from 21Nov2023 to25Nov2023 for treatment of COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202311; Test Name: COVID test; Test Result: Positive ; Comments: Took course of Paxlovid within two days of symptom onset and positive test result.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high; Egg allergy; Overweight
- Andere Medikamente
- AMLODIPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 18.11.2023
- Impfdatum
- 10.01.2023
- 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
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 55-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Jan2023 as dose 4 (booster), single (Lot number: GJ6796) at the age of 54 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 29Mar2021 as dose 1, single (Lot number: EP7534), in left arm, on 21Apr2021 as dose 2, single (Lot number: FR8735), in left arm and on 08Nov2021 as dose 3 (booster), single (Lot number: FH8028), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Depression" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "anxiety induced High BP" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "allergies to food and medications" (unspecified if ongoing); "allergies to food and medications. Sulfer" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Codeine, reaction(s): "Allergies to codeine"; Erithmycin, reaction(s): "Allergies to erithmycin"; Epinephrine, reaction(s): "Allergies to epinephrine". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient took Paxlovid for treatment of Covid-19 from 03Nov2023 to 07Nov2023. Based on Investigational results for Batch/lot number FH8028 and EP7534: The complaint for lack of effect of the Pfizer biontech Covid-19 Vaccine lot FH8028 and EP7534 were investigated. The investigation included reviewing manufacturing and packaging batch records, retain samples, deviation investigations, analytical release test results, and an analysis of complaint history for the reported lot. The final scope of this investigation is limited to the reported finished goods lot FH8028, fill lot FH4341 and the bulk formulated drug product lot FH4347. The final scope included the reported finished goods lot EP7534, fill lot EP7532, and the formulated drug product lot EP7528. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300366134 Same patient, different drug/events;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety; Blood pressure high; Depression; Drug allergy; Food allergy; High cholesterol
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 15.11.2023
- Impfdatum
- 07.12.2022
- Beginn
- 16.10.2023
- Tage bis Beginn
- 313,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Cough
SARS-CoV-2 test positive
Sepsis
Urinary tract infection
Symptomtext
The patient was brought to the ED by EMS on 10/16/23 for weakness and a cough. In the ED, patient was found to be borderline febrile with a temperature of 100 F. A rapid COVID PCR test performed in the ED resulted positive. Ultimately, the patient was admitted 10/16/23 - 10/26/23. Discharge diagnoses included suspected sepsis secondary to UTI and COVID positive, among other diagnoses. Of note, the patient has received the Pfizer Monovalent COVID vaccine (given 3/7/2021; 4/4/2021; 12/6/2021; 8/16/202) and the Pfizer Bivalent COVID vaccine (given 12/7/2022).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- M
- Eingang
- 03.11.2023
- Impfdatum
- 28.04.2023
- Beginn
- 29.09.2023
- Tage bis Beginn
- 154,0
- Dosis
- 6
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
Symptomtext
Dose #6: Pfizer/ Dose #7: Moderna; 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. An 83-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Apr2023 at 13:15 as dose 6 (booster), single (Lot number: GJ6796), in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 29Sep2023 at 15:15 as dose 7 (booster), single (Lot number: AU3832B), in left arm for covid-19 immunisation; covid-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown), as dose 4 (booster), single (Batch/Lot number: unknown) and as dose 5 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Type II Diabetes" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Tetracycline, reaction(s): "Allergy: Tetracycline". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "COVID 19 Treatment"; INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 29Sep2023 at 15:15, outcome "unknown", described as "Dose #6: Pfizer/ Dose #7: Moderna". Therapeutic measures were taken as a result of drug ineffective, covid-19. Paxlovid used for COVID 19 treatment, from 17Oct2023 to 21Oct2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Type II diabetes mellitus
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 16.01.2023
- Beginn
- 11.03.2023
- Tage bis Beginn
- 54,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Disease recurrence
SARS-CoV-2 test
Vaccination failure
Deafness unilateral
Symptomtext
COVID test positive; COVID test positive; COVID test positive; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46-year-old female patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Jan2023 at 13:00 as dose 4 (booster), single (Lot number: GJ6796) at the age of 46 years intramuscular, in left deltoid for covid-19 immunisation; bnt162b2 (BNT162B2), on 15Jan2021 at 16:30 as dose 1, single (Lot number: EL3248) intramuscular, in left deltoid, on 05Feb2021 at 16:45 as dose 2, single (Lot number: EL9264) intramuscular, in left deltoid and on 22Dec2021 at 13:45 as dose 3 (booster), single (Lot number: FE3594), in left deltoid for covid-19 immunisation. A 3rd dose was administered due to high risk of frequent institutional or occupational exposure to coronavirus (and at risk of serious COVID-19 complications), patient indicated working at clinic and school. The patient's relevant medical history included: "COVID", start date: 10Nov2020 (unspecified if ongoing), notes: COVID test Positive. The patient's concomitant medications were not reported. Vaccination history included: Fluzone quadrivalent (yearly), for immunization. No other medical history or family medical history relevant to adverse events. The following information was reported: VACCINATION FAILURE (medically significant) with onset 11Mar2023, outcome "unknown", COVID-19 (medically significant) with onset 11Mar2023, outcome "unknown", DISEASE RECURRENCE (medically significant) with onset 15Sep2023, outcome "unknown" and all described as "COVID test positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (11Mar2023) Positive, notes: home test; (15Sep2023) Positive, notes: home test.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300294496 Same patient/ vaccine, different dose/ AE.;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deafness unilateral
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230311; Test Name: COVID test; Test Result: Positive ; Comments: home test; Test Date: 20230915; Test Name: COVID test; Test Result: Positive ; Comments: home test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (COVID test Positive)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 23.10.2023
- Impfdatum
- 09.01.2023
- Beginn
- 25.09.2023
- Tage bis Beginn
- 259,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Fall
SARS-CoV-2 test positive
Symptomtext
The patient has a history of diabetes type II. He was brought to the ED by EMS on 9/25/23 after sustaining multiple falls in the past 24 hours. His O2 sats were found by EMS to be in the mid 80's. In the ED, the patient also reported having a cough for the past few days. A COVID PCR test resulted positive in the ED. Ultimately, the patient was admitted to the hospital from 9/25/23 - 9/28/23, with discharge diagnoses including COVID infection, among other diagnoses. The patient did not require oxygen or steroids during his admission. Of note, he has received four doses of the Pfizer Monovalent COVID vaccine (given 2/2/2021; 2/23/2021; 10/14/2021; 4/5/2022) and one dose of the Pfizer Bivalent COVID vaccine (given 1/9/2023).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 09.10.2023
- Impfdatum
- 15.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Alopecia areata
Alopecia universalis
Biopsy skin abnormal
Exposure during pregnancy
Symptomtext
Discovered a bald spot (Alopecia Areata) in December 2022, 1 month after vaccine while 5 months pregnant which got larger over course of pregnancy. After giving birth, within 1 month, I had lost all of the hair and have been diagnosed with Alopecia Universalis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alopecia
- Hospital-Tage
- -
- Labordaten
- Derm did biopsy on scalp and confirmed alopeica.
- Aktuelle Erkrankungen
- A cold.
- Vorgeschichte
- N/A
- Andere Medikamente
- Pre natal supplement.
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.10.2023
- Impfdatum
- 31.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
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 60-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 31Oct2022 at 18:00 as dose 5 (booster), single (Lot number: GJ6796) at the age of 59 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), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "not recovered" and all described as "COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Other medication in 2 weeks was noted as no. Treatment of COVID-19 was Paxlovid (lot number 00069-0345-30) which started on 18Sep2023 and stopped on 22Sep2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 15.09.2023
- Impfdatum
- 08.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Oct2022 as dose 5 (booster), single (Lot number: GJ6796) at the age of 71 years for covid-19 immunisation; bnt162b2 (BNT162B2), on 18Feb2021 as dose 1, single (Lot number: EM9809), on 11Mar2021 as dose 2, single (Lot number: EP6955), on 07Oct2021 as dose 3 (booster), single (Lot number: 30155BA) and on 13Jul2022 as dose 4 (booster), single (Lot number: FK9895) for covid-19 immunisation. The patient's relevant medical history included: "CVID Common Variable Immune Deficiency" (unspecified if ongoing); "Known allergies: Codene Products" (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 "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid from 03Sep2023 to 07Sep2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Common variable immunodeficiency; Drug allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 15.09.2023
- Impfdatum
- 09.12.2022
- Beginn
- 06.09.2023
- Tage bis Beginn
- 271,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Atrial fibrillation
COVID-19
Liver function test increased
Physical deconditioning
Rhabdomyolysis
SARS-CoV-2 test positive
Symptomtext
Hospitalization for rhabdomyolysis, acute on chronic kidney failure, elevated liver enzymes, paroxysmal afib, physical deconditioning, COVID-positive on 9/7/23 on dates 9/6/23- 9/14/23. Treated with dexamethasone, baricitinib, Remdesivir, vitamin D 25 mcg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute kidney injury
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- statins (HMG-CoA Reductase Inhibitors), perfume
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 22.08.2023
- Impfdatum
- 15.08.2023
- Beginn
- 17.08.2023
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Glossodynia
Hypoaesthesia oral
Symptomtext
Extreme sensitivity of tongue. Mildly acidic foods cause pain. Spicy foods cause pain. Carbonated beverages cause pain. Mild numbness in lips. Has persisted for 5 days since symptoms started. Started two days after immunization. No history of mouth sensitivity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Glossodynia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 21.08.2023
- Impfdatum
- 19.01.2023
- Beginn
- 17.08.2023
- Tage bis Beginn
- 210,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Positive Covid test after feeling unwell; Positive Covid test after feeling unwell; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 49-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Jan2023 as dose 1, single (Lot number: GJ6796) at the age of 48 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 17Aug2023 at 13:00, outcome "recovering" and all described as "Positive Covid test after feeling unwell". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (17Aug2023) Positive. It was unknown if therapeutic measures were taken as a result of vaccination failure, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230817; Test Name: Nasal Swab; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 15.08.2023
- Impfdatum
- 09.08.2023
- Beginn
- 09.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HTN, Type 2 Diabetes
- Andere Medikamente
- Atorvastatin, Glipizide, Lisinopril, Metformin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 14.08.2023
- Impfdatum
- 03.06.2023
- Beginn
- 04.06.2023
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Memory impairment
Symptomtext
I forget things like that I had gallbladder surgery, I was experiencing many things. medical center.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Memory impairment
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.07.2023
- Impfdatum
- 16.11.2022
- Beginn
- 01.07.2023
- Tage bis Beginn
- 227,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Nov2022 as dose 4 (booster), single (Lot number: GJ6796) at the age of 66 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: "High blood pressure" (unspecified if ongoing); "glaucoma" (unspecified if ongoing); "Known allergies: Bacitracin" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jul2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Experienced a rebound of COVID symptoms approximately 3 days after finishing Paxlovid course. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300261669 same patient, different drug/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high; Drug allergy; Glaucoma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 19.07.2023
- Impfdatum
- 19.11.2022
- Beginn
- 04.12.2022
- Tage bis Beginn
- 15,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Foreign body in gastrointestinal tract
Hypersensitivity
Symptomtext
T78.40XA ALLERGIC REACTION, INIT 4/30/2023 FOREIGN BODY IN ESOPHAGUS, INIT T78.40XD ALLERGIC REACTION, SUBSEQ 5/3/2023 FOREIGN BODY IN ESOPHAGUS, INIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Foreign body in gastrointestinal tract
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 18.07.2023
- Impfdatum
- 30.05.2023
- Beginn
- 22.10.2022
- Tage bis Beginn
- -
- Dosis
- 6
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
Symptomtext
COVID-19; COVID-19; 1st dose-4th dose is Moderna vaccine, 5th dose, 6th dose is Pfizer vaccine; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 66-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Oct2022 as dose 5 (booster), single (Lot number: GH9702), in right arm and on 30May2023 as dose 6 (booster), single (Lot number: GJ6796) at the age of 66 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 18Jan2021 as dose 1, single (Lot number: 025J20-2A), in right arm, on 15Feb2021 as dose 2, single (Lot number: 032L20A), in right arm, on 05Nov2021 as dose 3 (booster), single (Lot number: 051C21A), in right arm and on 07Apr2022 as dose 4 (booster), single (Lot number: 007J21-2A), in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: ERYTHROMYCIN, start date: Jan2023; CLIMARA [ESTRADIOL], start date: Jan2023; VITAMIN D [VITAMIN D NOS], start date: Jan2023; CALCIUM, start date: Jan2023; FERROUS SULFATE, start date: Jan2023. Past drug history included: Dicloxacillin, reaction(s): "Known allergies: Dicloxacillin"; Betadine, reaction(s): "Known allergies: Betadine". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 22Oct2022, outcome "unknown", described as "1st dose-4th dose is Moderna vaccine, 5th dose, 6th dose is Pfizer vaccine"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient took the Paxlovid treatment from 02Jul2023 to 06Jul2023.; Sender's Comments: Considering interchange of vaccine, the contributory role of company suspect drug to all the reported events Drug ineffective, Covid 19 cannot be excluded completely.,Linked Report(s) : US-PFIZER INC-202300250572 same reporter/patient, different drug/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ERYTHROMYCIN; CLIMARA [ESTRADIOL]; VITAMIN D [VITAMIN D NOS]; CALCIUM; FERROUS SULFATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 28.06.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Circumstance or information capable of leading to medication error
Expired product administered
Symptomtext
Medical Assistant gave an expired covid Pfizer Bivalent that was drawn at 3:28 pm on 6/26/2023 and was at room temperature. The Medical Assistant asked another MA to get a Covid vaccine for a patient. The other MA did not check for expiration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 15,0
- Geschlecht
- U
- Eingang
- 16.06.2023
- Impfdatum
- 07.04.2023
- Beginn
- 07.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Pfizer bivalent gray booster given after discard date, expired 3/23/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 08.06.2023
- Beginn
- 08.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
Minor is not having any adverse reaction at this point. Minor received 2 doses of Covid bivalent in a period of 2 days difference.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None.
- Andere Medikamente
- None
- Allergien
- Allergy to milk
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 08.06.2023
- Impfdatum
- 08.06.2023
- Beginn
- 08.06.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
No adverse reaction, no treatment needed due to no adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKAD
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 08.06.2023
- Impfdatum
- 08.12.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Immunisation reaction
Symptomtext
Adverse effect of other vaccines and biological substances, initial encounter on 2022-12-14.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunisation reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergic rhinitis, unspecified; Acute cystitis with hematuria; Pain NOS; Special screening examination for infections with a predominantly sexual mode of transmission; Body mass index [BMI] 31.0-31.9, adult
- Vorgeschichte
- -
- Andere Medikamente
- OMEPRAZOLE 40 MG ORAL CPDR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 07.06.2023
- Impfdatum
- 05.04.2023
- Beginn
- 01.04.2023
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Was administered a vaccine past the BUD date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 21.03.2023
- Beginn
- 01.03.2023
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine was expired. The Pfizer vaccine was delivered on 12/8 and is viable in refrigeration for 10 weeks from that date is 2/16/23. The vaccine was administered on 3/21/23. So about 4 weeks expired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 01.06.2023
- Impfdatum
- 13.05.2023
- Beginn
- 01.05.2023
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient received dose too eary.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 01.06.2023
- Impfdatum
- 30.05.2023
- Beginn
- 31.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood culture
Blood lactic acid
Blood thyroid stimulating hormone
Computerised tomogram head
Confusional state
Culture urine
Electroencephalogram
Full blood count
Imaging procedure
Magnetic resonance imaging head
Mental status changes
Metabolic function test
Vitamin B1
Vitamin B12
Vitamin B6
Symptomtext
Altered mental status, confusion and weakness requiring hospital admission, metabolic evaluation, neuroimaging, EEG, neurologic consultation, empiric antibiotic administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 2,0
- Labordaten
- 5/31/2023 Head CT, brain MRI, blood and urine cultures, CMP, CBC, lactate, Vitamin B1, B6 and B12 measurement, TSH
- Aktuelle Erkrankungen
- CML with myelodysplasia essential thrombocytosis CKD 4 HFpEF hypertension hypothyroidism GERD
- Vorgeschichte
- CML with myelodysplasia essential thrombocytosis CKD 4 HFpEF hypertension hypothyroidism GERD
- Andere Medikamente
- Metoprolol XL, Jardiance, Hydralazine, Isordil, Levothyroxine, Aranesp, Amlodipine, Allopurinol, Tasigna, calcitriol, pantoprazole, torsemide.
- Allergien
- levaquin and doxycycline
- Vorherige Impfungen
- Arm pain after Shingrix vaccine 5/3/2023 with recurrence 5/24/2023.
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 27.05.2023
- Impfdatum
- -
- 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
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), as dose 4 (booster), single (Lot number: GJ6796), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) 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), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Information: Patient received Paxlovid treatment for COVID 19 from 15May2023 to 19May2023, patient received other medication in 2weeks product Nyquil, Tylenol, probiotics, ester C, vitamin D, Patient did not have Known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 18.05.2023
- Impfdatum
- 02.05.2023
- Beginn
- 02.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Health Department let us know that their was a excursion with our refrigerator and the vaccine was nonviable
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 18.05.2023
- Impfdatum
- 02.05.2023
- Beginn
- 02.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Poor quality product administered
Product storage error
Symptomtext
The Health Department reported our refrigerator had a excursion and the vaccine was nonviable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 12.05.2023
- Impfdatum
- 12.05.2023
- Beginn
- 12.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
Gave COVID-19 BIV 12+ to an 11 y.o female instead of the 5-11 BIV. No symptoms or adverse reaction during her 15 minutes here. The CRNP spoke with family and informed of reactions and if she has symptoms to have her seen in office and or ER depending on severity of reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 3,0
- Geschlecht
- M
- Eingang
- 05.05.2023
- Impfdatum
- 05.05.2023
- Beginn
- 05.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 10.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
COVID-19
Vaccination failure
Symptomtext
Got Covid; Got Covid; 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 79-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Nov2022 as dose 5 (booster), single (Lot number: GJ6796) at the age of 78 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 26Jan2021 as dose 1, single (Lot number: EL3302), in left arm, on 16Feb2021 as dose 2, single (Lot number: EN5318), in left arm, on 08Sep2021 as dose 3 (booster), single (Lot number: 30130BA), in left arm and on 21May2022 as dose 4 (booster), single (Lot number: FM9992), in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Got Covid". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: 128; 153; 149/56. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient got 5 of the Pfizer shots for Covid. She got Covid after being on a plane while out of town and was prescribed Paxlovid on Apr2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure measurement
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood pressure; Result Unstructured Data: Test Result:128; Test Name: Blood pressure; Result Unstructured Data: Test Result:153; Test Name: Blood pressure; Result Unstructured Data: Test Result:149/56
- 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
- -
- Staat
- TN
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 01.05.2023
- Impfdatum
- 01.05.2023
- Beginn
- 01.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
Patient given 0.2 mL dose of gray cap Pfizer Bivalent for 12years and older. Patients did not exhibit any adverse symptoms. Patient had no complaints prior to leaving post vaccinations area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 21.04.2023
- Impfdatum
- 11.01.2023
- Beginn
- 11.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Monovalent Pfizer was chart as a bivalent dose, which cause patient to get an additional bivalent dose two months later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 14.01.2023
- Beginn
- 14.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
CLIENT WAS ADMINISTERED INCORRECT VACCINE PRODUCT FOR AGE. NO REPORTED ABNORMAL EFFECTS FOLLOWING VACCINATION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 18.04.2023
- Impfdatum
- 09.12.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
Symptomtext
On approximately 12/19/2022, I went into AFIB, and stayed in AFIB for 4 or 5 days. I came out of it and have been fine since. I told my doctor, because I noticed it on my smart watch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Heart Disease
- Andere Medikamente
- Warfarin; metoprolol; aspirin; CRESTOR
- Allergien
- Sulfa; penicillin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 17.04.2023
- Impfdatum
- 12.04.2023
- Beginn
- 13.04.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphonia
Respiratory tract congestion
Secretion discharge
Symptomtext
Patient received two doses of J&J and got a dose of bivalent Pfizer as a booster dose. Within 24 hours of receiving this vaccine, patient reports onset of congestion in his head that is affecting his hearing as well as congestion in his throat and chest. He reports mucous/phlegm and loss of voice. No fever development. Symptoms present 5 days post-vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aphonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure, Diabetes
- Andere Medikamente
- Metformin, Amlodipine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 07.04.2023
- Impfdatum
- 06.04.2023
- Beginn
- 06.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
on 04/06/23 during patient appt visit, patient requested her 2nd dose of primary series pfizer covid vaccine, patient was given the consent forms and had signed them, and I went ahead and by mistake grabbed the pfizer bivalent booster vaccine when I should've grabbed the pfizer monovalent vaccine. I ordered and administered the vaccine to the patient. patient waited 15 minutes and had no adverse reaction. once I placed the vaccine in patients' chart, I then realized my mistake. my supervisor was notified, as well as provider was informed to see what was recommended. Dr. advised that patient should not have an adverse reaction and patient does not need a 2nd monovalent vaccine or booster vaccine. I went ahead and contacted patient to apologize for the inconvenience and for the error I have made, informed patient my supervisor and doctor was consulted of my error, and she should not be concerned, no further covid vaccines dosages are recommended. patient was very understanding and stated she feels well and has no concerns and thanked me for letting her know of my error. VAERS was also submitted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 31.03.2023
- Beginn
- 31.03.2023
- 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
No adverse event
Symptomtext
pt was confused. she presented with a copy of her vaccine card but forgot she received the booster 9-22-2022. No adverse effects noted at the time of this submission.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 20.02.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
PATIENT DID NOT REPORT ANY SYMPTOMS OR ADVERS EVENTS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
PATIENT REQUESTED A SECOND BOOSTER AND IT WAS ADMINISTERED, PATIENT DOES NOT HAVE ANY SIDE EFFECTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NOT KNOWN
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- NOT KNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 04.01.2023
- Beginn
- 04.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
No ADR Bivalent booster administered after improper storage
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 21.03.2023
- Impfdatum
- 21.03.2023
- Beginn
- 21.03.2023
- 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
Participant is vaccinated with Pfizer's Bivalent booster, when he was already vaccinated with it since 11/10/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hyperthyroidism, Rheumatoid Arthritis, Neuropathy, Fibromyalgia, Diabetes
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 20.03.2023
- Impfdatum
- 15.02.2023
- Beginn
- 15.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Product storage error
Symptomtext
Patient was given the correct vaccine requested, was clinically indicated, and the interval between the previous booster and the booster that was given was correct. However, the vaccine given to this patient was 5 days outside of its BUD (once removed from the freezer, they are good for 10 weeks in the refrigerator.....this was 5 days past that date). We contacted Pfizer for guidance and were provided with clinical and efficacy data that suggested that the potency/efficacy could not be verified for that time window outside the 10 week BUD. We provided this data from Pfizer to our clinical corporate pharmacist coordinator for guidance, and the recommendation was to re-vaccinate at no particular interval. No harm was implicated, and when we contacted the patient, she did not report any adverse effects. She was amenable to re-vaccination once she returned from travel.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No known health conditions.
- Vorgeschichte
- No known health conditions.
- Andere Medikamente
- We did not have any record of her taking any medications, prescription or OTC , at the time of vaccination.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 20.03.2023
- Impfdatum
- 26.02.2023
- Beginn
- 26.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Patient received the correct vaccine and was clinically appropriate (correct interval between dose 4 and 5). However, the vaccines, while they were in-date, were 16 days out of their beyond-use date (BUD) from their 10-week period of storage in the refrigerator after removal from the ultra-cold freezer. We contacted Pfizer, and the manufacturer provided us with stability and clinical efficacy data. The data suggested, after we consulted our corporate clinical pharmacist coordinator, that we need to re-vaccinate at no particular interval. No harm was implicated. We contacted the patient, and he had not had any adverse effects and was amenable to re-vaccination when he got the chance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Pre-diabetic, Hypertension
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Metformin
- Allergien
- NDKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 20.03.2023
- Impfdatum
- 03.02.2023
- Beginn
- 12.03.2023
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye haemorrhage
Nasopharyngeal swab
Ocular hyperaemia
Sinusitis
Symptomtext
On 02/03/2023 I received my Covid-19 vaccine. On 03/12/2023 I noticed my left lower eye was blood red. Throughout the next days the entire eye was red. After reaching out to my doctor I was diagnosed of a sinus infection and said I had a busted blood vessel in my left eye. I was prescribed AUGMENTIN and eyedrops. Symptoms ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye haemorrhage
- Hospital-Tage
- -
- Labordaten
- Sinus swab, positive for infection
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- NOW EVE; multivitamin; glucosamine chondroitin; vitamin D-3; biotin; vitamin B12; methocarbamol; naproxen
- Allergien
- Latex; codeine
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 17.03.2023
- Impfdatum
- 27.02.2023
- Beginn
- 27.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was administered the Pfizer Bivalent booster that was past its beyond use date. The vaccine he received was 7 days past its BUD of 2/10/23. Patient was contacted and made aware of this mistake on 3/17/23 and has rescheduled a time at the end of April to get re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 15.03.2023
- Impfdatum
- 05.12.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 58,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Increased viscosity of upper respiratory secretion
Influenza
SARS-CoV-2 test negative
Secretion discharge
Symptomtext
I was having a lot of thick mucus that collected at the back of my throat along coughing. The mucus was yellowish. I contacted my doctor, and she said if it was a flu, it would take 7-10 days to get over it. I got better after 7 days. I contacted her on Tuesday as my symptoms got worse over the weekend. The doctor prescribed an antibiotic for me. It helped but it took a while. I am down to my last 2. After a week it has begun to dry out my mucus. I do still have a little mucus, but I am more or less recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- N/A COVID-19 Home Test-02/2023-Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; High Cholesterol
- Andere Medikamente
- Female Fibrate; Losartan Potassium; Ibuprofen; Tylenol; Fish Oil; Multi Vitamin; Calcium; Magnesium; Flax Seed Oil; Vitamin B12; Lutein; Psyllium Husk Powder
- Allergien
- Cipro; Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 08.03.2023
- Impfdatum
- 06.12.2022
- Beginn
- 09.01.2023
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Tinnitus
Symptomtext
I experienced increased tinnitus and went to the doctor to discuss it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- 20FEB2023 Hearing test, High Frequency Hearing Loss
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Dissection of left internal Carotid Artery
- Andere Medikamente
- LIPITOR; aspirin; multivitamin; sumatriptan
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Provider ordered a Pfizer bivalent booster to be administered. Patient received vaccination then when he got home is mom told he had already received Moderna bivalent and did not need another booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ADD Bipolar affective Left wrist fracture lyme disease acute
- Vorgeschichte
- ADD Bipolar affective Left wrist fracture lyme disease acute
- Andere Medikamente
- lamotrigine 100 mg tablet
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 01.02.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
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
- -
- Staat
- -
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- 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
Nurse gave wrong dose of bivalent covid-19 vaccine booster. doctor immediately notified and spoke with family. Supervisor also notified immediately of event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known problems
- Vorgeschichte
- No known problems
- Andere Medikamente
- Benzoyl Peroxide 5% gel Clindamycin phosphate 1% gel
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- MS
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 20.02.2023
- Beginn
- 20.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Immunization given outside of approved temperature range during storage and handling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- PAD
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 01.02.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
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
- -
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 01.02.2023
- Beginn
- 01.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- 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
- -
- Staat
- PA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 01.02.2023
- Beginn
- 01.02.2023
- 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
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 22.02.2023
- Beginn
- 22.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 20.02.2023
- Beginn
- 20.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
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
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received a second Bivalent vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient received the 12+ year old dosing of Pfizer Bivalent COVID Vaccine instead of the pediatric dosing. No adverse effects noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient received the 12+ year old dosing of Pfizer Bivalent COVID Vaccine instead of the pediatric dosing. No adverse effects noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 05.02.2023
- Beginn
- 05.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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
- -
- Staat
- NE
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 04.12.2022
- Beginn
- 04.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 12.10.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 81,0
- Dosis
- 5
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased immune responsiveness
Hepatitis C antibody
Nucleic acid test
Symptomtext
weakened immune system; Hepatitis C antibody test reactive; Initial information received on 22-Feb-2023 regarding an unsolicited valid non-serious courtesy case received from Partner Pfizer. This case involves a 64 years old female patient (165 cm and 68 kg) who experienced hepatitis c antibody test reactive, nucleic acid test is nonreactive and weakened immune system while receiving vaccines influenza quadrival A-B high dose HV vaccine [fluzone high-dose quadrivalent] and pfizer biontech covid-19 vaccine. The patient's past medical history included Occupational exposure to toxic agent. The patient's past vaccination(s) included INFLUENZA VACCINE on 05-NOV-2021 and PFIZER BIONTECH COVID-19 VACCINE with Dose 1- 10-Mar-2021 with Lot number lot EM6204 Dose 2- 31-Mar-2021 with Lot number lot ER8737 Dose 3- 22-oct-2021 with Lot number lot FE3590 Dose 4- 10-Jun-2022 with Lot number lot FM7553 All in the left arm. The patient's past medical treatment(s) and family history were not provided. Concomitant medications included PNEUMOCOCCAL VACCINE CONJ 20V (CRM197) (PREVNAR 20) for Prophylactic vaccination. On 12-Oct-2022, the patient received a dose of suspect influenza quadrival A-B high dose HV vaccine (lot UJ919AB, expiry date, strength, form and dose was unknown) via unknown route in unknown administration site as prophylactic vaccination. On 22-Nov-2022, the patient received a dose 5 of suspect pfizer biontech covid-19 vaccine not produced by Sanofi Pasteur (lot GJ6796, with unknown expiry date, strength, form and dose) via unknown route in the left arm as prophylactic vaccination. On an unknown date in Jan-2023, the patient developed hepatitis c antibody test reactive, nucleic acid test is nonreactive (hepatitis c antibody positive) and on an unknown date developed weakened immune system (decreased immune responsiveness) (unknown latency) following the administration of influenza quadrival A-B high dose HV vaccine and pfizer biontech covid-19 vaccine. Relevant laboratory test results included: Hepatitis C antibody - On an unknown date: Positive Nucleic acid test - On an unknown date: Negative Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the outcome was Unknown for the events. Hepatitis c was assessed as medically significant. Sender's Comments: Sanofi Company Comment dated 27-Feb-2023: This case involves a 64 years old female patient (165 cm and 68 kg) who experienced hepatitis c antibody test reactive, nucleic acid test is nonreactive and weakened immune system while receiving vaccines influenza quadrival A-B high dose HV vaccine [fluzone high-dose quadrivalent] and pfizer biontech covid-19 vaccine. Based on the limited information provided, the causal role of the company suspect product cannot be excluded in occurrence of the events. However, lack of information regarding any concurrent conditions, any family history precludes the comprehensive case assessment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Decreased immune responsiveness
- Hospital-Tage
- -
- Labordaten
- Test Name: hepatitis c antibody test; Test Result: Positive ; Test Name: Hepatitis C nucleic acid test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Occupational exposure to toxic agent
- Andere Medikamente
- PREVNAR 20
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 25.02.2023
- Impfdatum
- 25.11.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 37,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hepatitis C antibody
Hepatitis C antibody positive
Immune system disorder
Nucleic acid test
Weight
Symptomtext
immunology system has been compromised; hepatitis C antibody test reactive, nucleic acid test is nonreactive; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 25Nov2022 as dose 5 (booster), single (Lot number: GJ6796) at the age of 65 years, in left arm for COVID-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (1st dose, NDC number, lot number, expiration date: thinks it is EM6204., Anatomical location: Given in top of left arm caller is pretty sure), administration date: 10Mar2021, when the patient was 63-year-old, for Covid-19 immunization; BNT162b2 (2nd dose:, NDC number, lot number, expiration date: Thinks ER8737., Dose amount, route, time received: Unknown, not on vaccination card., Anatomical location: Given in top of left arm caller is pretty sure.), administration date: 31Mar2021, when the patient was 63-year-old, for Covid-19 immunization; BNT162b2 (3rd dose:, NDC number, lot number, expiration date: FE3590, Dose amount, route, time received: Unknown, not on vaccination card., Anatomical location: Given in top of left arm caller is pretty sure.), administration date: 22Oct2021, when the patient was 64-year-old, for Covid-19 immunization, reactions: "Hepatitis C antibody test reactive", "immunology system has been compromised "; BNT162b2 (4th dose:, NDC number, lot number, expiration date: FM7553, Dose amount, route, time received: Unknown, not on vaccination card., Anatomical location: Given in top of left arm caller is pretty sure.), administration date: 10Jun2022, when the patient was 64-year-old, for Covid-19 immunization; fluzone high dose quad (Sanofi-Pasteur, Lot number: UJ919AB, Expiration date: 30Jun2023, NDC number: Unknown), administration date: 12Oct2022, when the patient was 65-year-old, for immunization; prevnar 20 (Manufacturer: Wyeth/Pfizer, Lot number: FJ2603, Expiration date: 30Jun2023, NDC number: Unknown, not on the CVS papers., Dose amount, route: 0.5ml), administration date: 21Oct2022, when the patient was 65-year-old, for immunization; flu (got the yearly flu vaccine, specific name, manufacturer, lot number, NDC number, expiration date: Unknown at time of call.), administration date: 05Nov2021, when the patient was 64-year-old, for immunization; Flu (specific name, manufacturer, lot number, NDC number, expiration date: Unknown at time of call. Confirmed prior to getting the Pfizer COVID vaccine.), administration date: 2020, for immunization. The following information was reported: HEPATITIS C ANTIBODY POSITIVE (non-serious) with onset Jan2023, outcome "unknown", described as "hepatitis C antibody test reactive, nucleic acid test is nonreactive"; IMMUNE SYSTEM DISORDER (non-serious), outcome "unknown", described as "immunology system has been compromised". The events "hepatitis c antibody test reactive, nucleic acid test is nonreactive" and "immunology system has been compromised" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient has given blood over the past 5 or 6 years about 12 times and just recently went to see physician because caller got rejected in Mar2022 and again in Jan2023 for the hepatitis C antibody test being reactive, but when the nucleic acid test was done, the nucleic acid test is nonreactive. The blood donors do the hep C virus antibody HCV which came back reactive so then did the more rigorous test, the nucleic acid testing HCV NAT, and that test came back nonreactive. Doctor thinks that caller's immunology system has been compromised due to the vaccine because doctor has been testing caller for the last 4 years and the hep C nucleic acid test has been nonreactive. Only thing different in caller's life is the fact that caller got the COVID vaccine and the 3 boosters. The patient can't give blood now for 6 months, then will have to get blood tested and pass certain tests.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300077790 Same patient/event/drug; different suspect dose;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hepatitis C antibody
- Hospital-Tage
- -
- Labordaten
- Test Date: 202203; Test Name: Hepatitis C antibody test reactive; Result Unstructured Data: Test Result:came back reactive; Test Date: 202301; Test Name: Hepatitis C antibody test reactive; Result Unstructured Data: Test Result:reactive; Test Date: 202203; Test Name: nucleic acid test; Result Unstructured Data: Test Result:nonreactive; Comments: nucleic acid testing HCV NAT; Test Date: 202301; Test Name: nucleic acid test; Result Unstructured Data: Test Result:nonreactive; Test Name: weight; Result Unstructured Data: Test Result:150 lbs; Comments: Patient weight: About 150 pounds
- 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
- -
- Staat
- IL
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- 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
We gave a 2nd bivalent shot when patient was not eligible for it. Patient did not have an adverse reaction to it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 02.02.2023
- Beginn
- 02.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Pt asked for booster covid vaccine. (Had reportedly received one dose of a vaccine in another country but was unable to provide information on what it was or when, exactly received.) Bivalent was given rather than original formulation to assure completion of primary series. Pt does not report any adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- aortic valve disorder, carotid stenosis, CAD, diastolic heart failure, hypertension, anemia, back pain, emphysema, leg edema, hypercholesterolemia,
- Andere Medikamente
- Albuterol, Alfuzosin, benzonatate, clopidogrel, norco, duoneb, nicotine, simvastatin, tadalafil, testosterone, anoro ellipta
- Allergien
- famotidine
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 21.02.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Administered a second Pfizer COVID Bivalent vaccine after patient received one on 9-3-22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Symptomtext
UNKNOWN spoke with mom she said no side effects have been reported yet
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 09.02.2023
- Beginn
- 09.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- 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
Extra dose administered
Symptomtext
This day the patient mentioned received an additional dose of Pfizer Bivalent. Prior to giving this vaccine he was looked up in database and database only showed his first 2 primary doses given 01/18/2021 and 02/08/2021. He received the first Pfizer Bivalent dose 10/21/2022 but it was not shown in database or our own patients records due to his last name being misspelled therefore we were not aware on 02/09/2023 he had previously received his bivalent dose. No ill or negative effects were noted on this day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- n/a
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 14.02.2023
- Impfdatum
- 21.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 59-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Nov2022 as dose 5 (booster), single (Lot number: GJ6796) at the age of 58 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient 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), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: COVID 19 Treatment; (30Jan2023) Negative, notes: Tested negative for Covid-19 on 30Jan2023; (04Feb2023) Positive, notes: Tested positive again for Covid-19 on 04Feb2023. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received treatment with paxlovid from 25Jan2023 to 29Jan2023. The patient had no known allergies, did not report administration of any concomitant medication within 2 weeks of Paxlovid therapy. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300058285 Same patient, different product and event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 20230130; Test Name: Covid-19 test; Test Result: Negative ; Comments: Tested negative for Covid-19 on 30Jan2023; Test Date: 20230204; Test Name: Covid-19 test; Test Result: Positive ; Comments: Tested positive again for Covid-19 on 04Feb2023
- 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
- -
- Staat
- MN
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 13.02.2023
- Impfdatum
- 03.11.2022
- Beginn
- 10.02.2023
- Tage bis Beginn
- 99,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 2/10/23 positive COVID PCR
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, CAD, COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- -
- Geschlecht
- M
- Eingang
- 09.02.2023
- Impfdatum
- 03.02.2023
- Beginn
- 03.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
patient came in for a shingles booster shot and was given a covid booster shot instead. Patient already had a bivalent covid booster in September of 2020.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 13.01.2023
- Beginn
- 20.01.2023
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Insomnia
Symptomtext
SEVERE INSOMNIA AFTER TAKING THE VACCINE. INABILITY TO FALL ASLEEP. INABILITY TO STAY ASLEEP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Insomnia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Diverticulitis
- Vorgeschichte
- Obesity issue, possible Cushing's Disease undiagnosed
- Andere Medikamente
- Amox-Clav 875 - 125 MG 1 tablet every 12 hrs
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 02.02.2023
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 26.12.2022
- Beginn
- 26.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 26.12.2022
- Beginn
- 26.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 24.12.2022
- Beginn
- 24.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 09.11.2022
- Beginn
- 09.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 29.10.2022
- Beginn
- 29.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 23.12.2022
- Beginn
- 23.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 04.12.2022
- Beginn
- 04.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 04.12.2022
- Beginn
- 04.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 09.11.2022
- Beginn
- 09.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 09.11.2022
- Beginn
- 09.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 22.12.2022
- Beginn
- 22.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 09.11.2022
- Beginn
- 09.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 22.12.2022
- Beginn
- 22.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 15.12.2022
- Beginn
- 15.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 04.12.2022
- Beginn
- 04.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 03.12.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 03.12.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 09.11.2022
- Beginn
- 09.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 27.11.2022
- Beginn
- 27.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 22.12.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 27.11.2022
- Beginn
- 27.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 26.11.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 26.11.2022
- Beginn
- 26.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 26.11.2022
- Beginn
- 26.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 19.12.2022
- Beginn
- 19.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 26.11.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 25.11.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 19.12.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 27,0
- Geschlecht
- U
- Eingang
- 01.02.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 03.12.2022
- Beginn
- 03.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 11.12.2022
- Beginn
- 11.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 03.12.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 11.12.2022
- Beginn
- 11.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 13.11.2022
- Beginn
- 13.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 23.11.2022
- Beginn
- 23.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 07.12.2022
- Beginn
- 07.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 10.12.2022
- Beginn
- 10.12.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 30.11.2022
- Beginn
- 30.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 27.01.2023
- Beginn
- 27.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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
- -
- Staat
- MI
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 26.01.2023
- Beginn
- 26.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pharyngeal swelling
Symptomtext
felt like her throat was swollen. Nurse checked stats to check on patient and confirmed with physician was doing good and able to leave the office
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal swelling
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 30.01.2023
- Beginn
- 30.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
The Covid vaccine was Pfizer-BioNTech (would not let me choose it from drop down) The patient did not have an allergic reaction. The patient was given a single dose from an expired Lot. The Lot expired 1/27/23 and was given today, 1/30/23. Our pharmacist at the hospital advised our office to file a report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- no adverse events
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 06.11.2022
- Beginn
- 06.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 06.11.2022
- Beginn
- 06.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 06.11.2022
- Beginn
- 06.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 06.11.2022
- Beginn
- 06.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 06.11.2022
- Beginn
- 06.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 05.11.2022
- Beginn
- 05.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 05.11.2022
- Beginn
- 05.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 05.11.2022
- Beginn
- 05.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 30.01.2023
- Impfdatum
- 05.11.2022
- Beginn
- 05.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- 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
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 29.01.2023
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 23.01.2023
- Beginn
- 23.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 16.11.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 34,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough Case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid + on 12/20/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 25.01.2023
- Beginn
- 25.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Product storage error
Symptomtext
patient received dose after beyond use date (exp 1/24/23). Supply had not been pulled from fridge and RA thought the date needed to be updated to today. No reactions that we can tell, provider and family notified of incident. No sign/symptoms noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Autism
- Andere Medikamente
- None
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Circumstance or information capable of leading to medication error
Symptomtext
Patient and ADON stated during the Prevaccination Checklist questioning that he had not had COVID-19 in the past 90 days. Vaccine was given and then the ADON found that he had actually had COVID-19 on 11/21/22. Treated with Paxlovid per standing orders at the nursing home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- COPD, Parkinnson's, Type 2 Diabetes Mellitus
- Vorgeschichte
- Encephalopathy, Postconcussional Syndrome, Major Depressive Disorder, Paranoid Schizophrenia, Mild Cognitive Impairment, Neuropathy, Anxiety Disorder, Hypo-Osmolality and Hyponatremia, Hyperlipidemia, Hypokalemia, SOB, Dysphagia, Muscle Weakness-generalized, Unspecified Lack of Coordination, Difficulty in Walking, History of Falling, Essential Primary Hypertension.
- Andere Medikamente
- Unknown
- Allergien
- Gabapentin, Metformin, Penicillin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- 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
Symptomtext
Patient received Pfizer Bivalent booster on 1/6/23, which was unnecessary due to having received the Moderna Bivalent booster on 9/18/22. Patient does not have additional risk factors that would warrant the additional bivalent booster at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 23.01.2023
- Beginn
- 23.01.2023
- 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 was given a Pfizer bivalent booster and did not need it. She had a J&J on 3/6/21, Moderna 1/7/22, and pfizer bivalent booster on 12/8/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 19.01.2023
- Beginn
- 19.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
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
- -
- Staat
- OH
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 30.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 22.01.2023
- Impfdatum
- 05.11.2022
- Beginn
- 05.11.2022
- 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
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 17.01.2023
- Beginn
- 17.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
COVID19 Pfizer Bivalent vaccine erroneously given as #1 dose of the primary series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Reports no Known allergies to food or other products.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 20.01.2023
- Impfdatum
- 17.01.2023
- Beginn
- 17.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
COVID19 Pfizer Bivalent vaccine given as dose #1 of the primary series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- unknown
- Allergien
- No Known food or drug allergies reported
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 16.01.2023
- Beginn
- 16.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
No Adverse event- patient received Covid 19 bivalent pfizer vaccine that had been at room temperature for 72 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Gave birth
- Vorgeschichte
- Anxiety
- Andere Medikamente
- Vitamin D, Prenatal vitamins, Fish oil
- Allergien
- Codeine, Crab, shrimp
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 19.01.2023
- Impfdatum
- 01.01.2023
- Beginn
- 19.01.2023
- Tage bis Beginn
- 18,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Pt. presented to the pharmacy requesting Bivalent vaccine, providing vaccine card. After administration of vaccination and documentation in the immunization registry it was discovered that a Bivalent vaccine was provided 10/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 17.01.2023
- Beginn
- 17.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Pt was administered the incorrect vaccine in series. No adverse effects with previous covid vaccinations or with vaccination just received
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Metastatic Breast cancer, COPD, Rheumatoid arthritis, Bipolar disease
- Vorgeschichte
- see above
- Andere Medikamente
- -
- Allergien
- effexor causes anxiety
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 18.01.2023
- Beginn
- 19.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
New employee went to obtain 2nd dose of primary series of COVID vaccine as requirement of employment. Patient stated she even told them beforehand that she had only had 1 dose of her primary series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A - instructed patient to follow-up with PCP to inform of report as well as ask for further recommendations
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- FOOD - cranberries; reaction- hives, throat swelling
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 18.01.2023
- Impfdatum
- 16.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- 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 a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Nov2022 as dose 5 (booster), single (Lot number: Gj6796) at the age of 62 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), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The patient had no known allergies. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovered with sequelae" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Treatment of COVID-19; (27Dec2022) Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Covid-19 treatment with Paxlovid from 21Dec2022 to 26Dec2022. It was reported that the patient recovered with lasting effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20221227; Test Name: COVID 19; 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
- -
- Staat
- NJ
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 17.01.2023
- Impfdatum
- 13.01.2023
- Beginn
- 13.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Pt received Pfizer Bivalent dose as his first covid vaccine. Pt was observed for 30 minutes no problems. Pt was called a few days later and had no symptoms or problems from vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- N/A
- Allergien
- Penicillin Aspirin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- 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
Administered the 12+ Pfizer COVID-19 Bivalent vaccine to 11 year old patient. No signs or symptoms present at the time of administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Benzoyl peroxide gel, clindamycin gel
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 12.01.2023
- Impfdatum
- 20.10.2022
- 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 (Consumer or other non-HCP). The reporter is the patient. A 46-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Oct2022 as DOSE 4 (BOOSTER), SINGLE (lot number: GJ6796) at the age of 46 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: "Known 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 which included Paxlovid treatment from 29Dec2022 to 02Jan2023. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 10.01.2023
- Beginn
- 10.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
A prepared vaccine syringe that was past the BUD was administered to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- WI
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Vaccination error
Symptomtext
7yo presented for COVID vaccine only. A vial was open on both prep trays in the med room. Staff member #1 drew up given 0.2ml dose from Pfizer-BioNTech COVID 19 in med room. Staff member #1 handed this syringe off to #2 to administer in room. Staff member #2 administered the vaccine and pt left. Staff member #2 was charting the NDC/lot/etc and noted the vaccine was not the correct dose. Staff member #2 noted that a 12 yr old and older bivalent COVID 19 vial was opened on both trays. That is when the med error was noted. Pharmacy was called: as pt should have received Pfizer-BioNTech 5-11 yr old Bivalent COVID 19 vial. Pharmacy reported that there should be only mild side effects if any with this error. Parents of the child were notified of the error and concern to monitor for. The NDC and lot info was not entered until after the child had received the vaccine. This is when the error was noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 18.12.2022
- Beginn
- 06.01.2023
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Tested positive for covid with symptoms; Tested positive for covid with symptoms; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 46-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Dec2022 as dose 3 (booster), single (Lot number: GJ6796) at the age of 46 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 08Apr2021 as dose 1, single (Lot number: EP6955) and on 06Dec2021 as dose 2, single (Lot number: FG3527) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Metachlopramide, reaction(s): "known allergies: Metachlopramide". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 06Jan2023, outcome "not recovered" and all described as "Tested positive for covid with symptoms". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were not taken as a result of drug ineffective, covid-19. The patient did not receive other vaccine in four weeks. The patient did not have covid prior vaccination. The patient tested for covid post vaccination.; Sender's Comments: Based on the available information in the case, an association between the reported events DRUG INEFFECTIVE & COVID-19 and The suspected drug cannot be ruled out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Nasal Swab; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 06.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- 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
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 08.01.2023
- Impfdatum
- 08.01.2023
- Beginn
- 08.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Bivalent booster given instead of primary series
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 08.01.2023
- Impfdatum
- 04.01.2023
- Beginn
- 04.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 08.01.2023
- Impfdatum
- 21.12.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 07.01.2023
- Impfdatum
- 03.01.2023
- Beginn
- 03.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- 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
- -
- Staat
- NC
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 05.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Patient received bivalent Pfizer( lot # GK1667)(age 6months-4 years) vaccine 0.2ml. inadvertently instead of the Pfizer (lot # GJ6796) adult vaccine dose(0.3ml). Clinical nurse consultant was contacted immediately and instructed to vaccinate patient immediately with correct vaccine for adult (12+).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 28.11.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient did not have any symptoms. This is just reporting inadvertently given the Bivalent when it should have been the Monovalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Aortic regurgitation, Low vitamin B12, anxiety, depression, autonomic dysfunction
- Andere Medikamente
- Mirtazapine, Vitamin C, Cyanocobalamin, Multi-Vitamin, Sodium chloride, Cryselle, Pristiq, Aldara cream, Duac, Ibuprofen
- Allergien
- Bee stings, Zithromax
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 15.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Patient received 2nd bivalent Pfizer covid vaccine; when should of only received one 1st bivalent 9/28/2022 2nd bivalent 12/14/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- liver transplant 11/6/2003 liver transplant 12/6/2004 Hep C
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 25.12.2022
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Shoulder injury related to vaccine administration
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Shoulder injury related to vaccine administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 23.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- 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
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 30Nov2022 as dose 5 (booster), single (Lot number: GJ6796) at the age of 68 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 01Mar2021 as dose 1, single (Lot number: EN6203), in left arm, on 22Mar2021 as dose 2, single (Lot number: ER2613), in left arm, on 05Oct2021 as dose 3 (booster), single (Lot number: FF2587), in left arm and on 18Jul2022 as dose 4 (booster), single (Lot number: FM7553), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Seizure" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "prostate cancer" (unspecified if ongoing); "Known allergies: Seasonal" (unspecified if ongoing). Concomitant medication(s) included: OXCARBAZEPINE; NEBIVOLOL; CETIRIZINE; ACETAMINOPHEN; DEXTROMETHORPHAN; GUAIFENESIN; PHENYLEPHRINE; TRIPROLIDINE. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Dec2022) Positive, notes: Result of antigen test was positive; (Dec2022) Negative, notes: Antigen test three days prior was negative. Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid (Treatment start date: 08Dec2022, Treatment stop date: 12Dec2022).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202212; Test Name: antigen test; Test Result: Positive ; Comments: Result of antigen test was positive.; Test Date: 202212; Test Name: antigen test; Test Result: Negative ; Comments: Antigen test three days prior was negative.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension; Prostate cancer; Seasonal allergy; Seizure
- Andere Medikamente
- OXCARBAZEPINE; NEBIVOLOL; CETIRIZINE; ACETAMINOPHEN; DEXTROMETHORPHAN; GUAIFENESIN; PHENYLEPHRINE; TRIPROLIDINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
CLIENT WAS GIVEN THE WRONG DOSE. INSTEAD OF A 2ND MONOVALENT VACCINE, THE CLIENT RECIEVED A BIVALENT DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 20.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Client called program requesting COVID vaccine dose. Review of Client record indicated one dose of Moderna previously given, client unable to identify which dose he was needing. Upon arrival and review of client vaccine card he had completed a primary series already so appeared eligible for a bivalent booster dose. Dose given after completion of screening. At that time a second vaccine card was produced showing that client had received bivalent booster on 9-22-2022. Situation was explained to client, 15 minute wait was completed, client has no change in condition noted, no untoward effects noted and had been provided an EUA prior to the dose with a verbal explanation of possible expected side effects from receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- None Known
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Adult formulation administered to 11 year old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 19.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaginal haemorrhage
Symptomtext
Non-menstrual vaginal bleeding, bright red (no clots). This has lasted for 6 days. No associated pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaginal haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Iodine IV Contrast
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 19.12.2022
- Beginn
- 19.12.2022
- 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
Symptomtext
Vaccine card improperly marked and did not indicate a bivalent covid vaccine was given. Patient received 2 doses of Pfizer bivalent covid vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.12.2022
- Impfdatum
- 16.12.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient notified staff that she had received Pfizer covid 19 booster on 10/11/22. Patient stating she is interested in receiving Pfizer Bivalent booster vaccine. Pfizer Bivalent booster administered o 12/16/22. Data states vaccine received on 10/11/22 was Pfizer bivalent booster. Phone call to patient to notify of vaccine administration error. Informed patient that data records show she received Pfizer Bivalent booster on 10/11/22. Per patient information must have been entered wrong due to her being told that she was receiving a covid vaccine booster and not bivalent booster. Patient states when she received her vaccine in October, she asked if the vaccine administered was the new covid vaccine. Patient states she was told it wasn't. Per patient, she was told that it was the covid vaccine booster and that they didn't have the bivalent booster. Patient went on to say that she was disappointed because she was hoping to receive bivalent booster that day. Patient disclosed, that is the reason why on 12/16/22 when she approached us at the event, she made sure to ask that the vaccine we were administering was in fact the bivalent vaccine, and not a booster vaccine. Patient denies any rash, sob, difficulty breathing. Patient denies any other symptoms such as: head ache, body aches, fever, pain, redness or swelling to injection site. ER precautions given. Patient verbalized understanding and denies any questions at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Client administered a bivalent dose as first dose of primary series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Mental illness
- Andere Medikamente
- Unknown
- Allergien
- Yes, not specified
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Client administered bivalent vaccine as second dose of primary series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Mental illness
- Andere Medikamente
- Unknown
- Allergien
- Yes, but not specified
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 16.12.2022
- Impfdatum
- 03.12.2022
- Beginn
- 04.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysmenorrhoea
Symptomtext
I had a severe menstrual cramps and had to go the emergency room on Tuesday from the booster I received.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Dec2022 at 15:00 as dose number unknown (booster), single (Lot number: GJ6796), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer), for COVID-19 Immunization; Covid-19 vaccine (Dose Number Unknown (Booster), Manufacturer Unknown), for COVID-19 Immunization.The following information was reported: DYSMENORRHOEA (non-serious) with onset 04Dec2022 at 09 :00, outcome "recovering", described as "I had a severe menstrual cramps and had to go the emergency room on Tuesday from the booster I received.". The events "i had a severe menstrual cramps and had to go the emergency room on tuesday from the booster i received." required emergency room visit. Therapeutic measures were taken as a result of dysmenorrhoea. Additional information: Patient had not been received any other vaccine within four weeks and other medication within two weeks. Medication to help with the excruciating pain. Patient not had Covid prior vaccination and not been tested post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysmenorrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 14.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient needed Pfizer BioTech 2nd dose and received Pfizer Bivalent Booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 13.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Wrong product administered
Symptomtext
client presented with Covid card and flu consent - Covid booster given before realized consent was for flu vaccine - once realized client only wanted flu vaccine was given that vaccine - client had already had bivalent booster in November
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 12.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type 2 diabetic without long term complication Benign hypertension Dyslipidemia Recurrent depression GERD
- Andere Medikamente
- Amlodipine 10 mg once daily Aspirin 81 mg PRN Buspar 5 mg tablet once daily Catapres 0.1 mg tablet once daily Lexapro 20 mg daily Prevacid 30 mg delayed release Metphormin 500 mg Metoprolol 100mg Ozempic 1 mg dose Valsartan Hydrochlorothia
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient was administered the Covid Bivalent Pfizer Vaccine instead of the Flu vaccine that patient had arrived at pharmacy to receive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 08.12.2022
- Impfdatum
- 08.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Swollen tongue
Symptomtext
Patient received Pfizer bivalent booster and after 15-minute wait time, patient complained of tongue swelling. Provider assessed and ordered Benadryl 50 mg po, patient sent to ER for higher level of care
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immediate post-injection reaction
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Cat hair Eggs, ok as ingredient in baked items Statins Topamax
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 07.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Bivalent booster shot given but patient had not yet received primary vaccine series
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- 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 already received a dose of Pfizer Bivalent in Sept 2022 but was unaware when she came in to get a dose today. She did not have her vaccine card with her. It was realized after she left through system that patient had already completed the Pfizer series. So today she received an extra dose of Pfizer Bivalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 03.12.2022
- Impfdatum
- 27.11.2022
- Beginn
- 27.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 03.12.2022
- Impfdatum
- 27.11.2022
- Beginn
- 27.11.2022
- 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
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 03.12.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 03.12.2022
- Impfdatum
- 15.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Electromyogram
Gait inability
Symptomtext
Patient received 4 vaccines on 11/15, Then received HepB on 11/16. Patient was from home self care, independent with all cares, but then on 11/17 patient was unable to walk on his own.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electromyogram
- Hospital-Tage
- -
- Labordaten
- Neurology was consulted and EMG was performed.
- Aktuelle Erkrankungen
- Acute pericarditis and recurrent large pericardial effusions after CABG (8/2022)
- Vorgeschichte
- perianal fistula, DM2, hypertension, hyperlipidemia, GERD
- Andere Medikamente
- -
- Allergien
- No known allergies.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 01.12.2022
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- 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
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 27.11.2022
- Beginn
- 27.11.2022
- 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
No adverse event
Symptomtext
Patient stated that she wanted to get the Pfizer booster vaccine that we are advertising at our pharmacy. I asked the questions on our form and it has been over 2 months since her last shot. I gave the vaccine and asked for her card and she said this was her first shot. Patient received the bivalent Covid vaccine as her first primary dose instead of the monovalent. No adverse effects have been reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Birth control
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 25.11.2022
- Impfdatum
- 25.11.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear swelling
Feeling hot
Skin warm
Swelling face
Symptomtext
Patient called after couple hours later since she left pharmacy, she feels swollen and warm cheek first then it goes to ear and neck area,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear swelling
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 24.11.2022
- Impfdatum
- 14.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oligomenorrhoea
Symptomtext
Menstrual cycle started 11/15 (normal date), but lasted 9 days. Normal cycle is 4-5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oligomenorrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Viral bronchitis - 1 month prior
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
COVID19 booster vaccine vial not discarded from previous day, incorrectly use to vaccinate patient d/t communication error between medical staff. Notified HCP Dr., as well as manager, CMA. No follow up treatment necessary d/t vaccine still being viable. CMA contacted Agency & spoke with staff for direction toward how to handle situation. CMA also contacted Pfizer manufacturer and was instructed that a punctured vial is good for 24 hours between degrees of 35 F and 86 F. Going forward officer closer will discard open vial, as well as a double check of morning opener will double check that old vial has been discarded & new vial has been opened. Dr. was advised regarding situation and per Dr. no further action is necessary.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- None Necessary
- Aktuelle Erkrankungen
- N / A
- Vorgeschichte
- Hyperlipidemia
- Andere Medikamente
- Simvastatin (Zocor) 40 mg - nightly Lisinopril (Prinivil; Zestril) 10 mg tablet - daily Cholecalciferol (Vitamin D3) 3000 units - daily Ranitidine (Zantac) 150 mg 2 times daily
- Allergien
- Medrol [Methylprednisolone] - causes rash
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
ADMINISTRATION ERROR, WRONG DOSE, PATIENT SHOULD HAVE GOTTEN PFIZER BIVALENT 5-11YEARS OLD, NOT PFIZER BIVALENT 12+
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 05.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Caller stated that she received 5 Pfizer immunization shots and the last one the omicron booster shot on 05Nov2022 (Lot number GJ6796), she was diagnosed covid positive; Caller stated that she received 5 Pfizer immunization shots and the last one the omicron booster shot on 05Nov2022 (Lot number GJ6796), she was diagnosed covid positive; 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. An 85-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Nov2022 as dose 5 (booster), single (Lot number: GJ6796) for covid-19 immunisation; BNT162b2 (BNT162B2), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Nov2022, and all described as "Caller stated that she received 5 Pfizer immunization shots and the last one the omicron booster shot on 05Nov2022 (Lot number GJ6796), she was diagnosed covid positive". The patient stated that she received five Pfizer immunization shots. On Saturday, Nov2022, the patient was diagnosed COVID positive shortly after receiving the last Pfizer COVID shot. The patient wanted to know if the COVID vaccine has an interaction with Paxlovid. The patient also asked if there are reports of contracting the COVID virus even though five COVID-19 shots were received, considering that the last shot was the omicron shot. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Nov2022) Positive, notes: she was diagnosed covid positive on Saturday. Outcome of the events was unknown. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202211; Test Name: SARS-CoV-2 test; Test Result: Positive ; Comments: she was diagnosed covid positive on Saturday
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 16.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Needle issue
No adverse event
Symptomtext
No adverse outcome. 5/8 needle used instead of 1-11/2' needle based on gender, age and weight.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Needle issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 16.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Needle issue
No adverse event
Symptomtext
No adverse event. a 5/8 needle was used instead of 1-11/2' needle based on gender, age and weight.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Needle issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 09.11.2022
- Beginn
- 09.11.2022
- 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
Pt got Bivalent dose instead of primary dose. Pt was informed and he was asked to call back if he had any side effects. He was instructed on most common side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- -
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Herpes zoster
Spinal disorder
Symptomtext
Mild case of shingles, left side T11 distribution
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN Hiatal hernia with GERD Environmental allergies
- Andere Medikamente
- Olmesartan/HCTZ 20/12.5 QD Allegra 180mg QD Fish oil 1200 has Magnesium 200 mg hs Famotidine
- Allergien
- Sulfa skin rash
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 06.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Pt entered dates on all four lines of Covid consent form. It was then thought that this was her booster does. Once the imm was given, it was noted this was pt's first dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 03.11.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient received 0.5ml imtramuscular of Flulaval to the Left Deltoid. Mom stated and patient's records documented that patient received flu vaccine in 8/2022. Mom and Dad informed. Post vac instructions provided and they were able to repeat them and stated they understood
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -