- Staat
- NJ
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 13.05.2023
- Impfdatum
- 02.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebral haemorrhage
Death
Symptomtext
Brain Bleed on April 13 2022 and died April 17 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral haemorrhage
- Hospital-Tage
- -
- Labordaten
- At Hospital
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 08.05.2023
- Impfdatum
- 02.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Aortic arteriosclerosis
Hyperlipidaemia
Hypoxia
Symptomtext
J96.00 ACUTE RESPIRATORY FAILURE 6/24/2022 HYPERLIPIDEMIA J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/28/2022 HYPERLIPIDEMIA R09.02 HYPOXIA 6/24/2022 HYPERLIPIDEMIA J96.00 ACUTE RESPIRATORY FAILURE 6/24/2022 ATHEROSCLEROSIS OF AORTA J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/28/2022 ATHEROSCLEROSIS OF AORTA R09.02 HYPOXIA 6/24/2022 ATHEROSCLEROSIS OF AORTA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 18.04.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 248,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Anaemia
Anosognosia
Anticoagulant therapy
Anticoagulation drug level below therapeutic
Aspiration
Asthenia
Bacterial test positive
Blood creatinine increased
Blood potassium increased
Bronchoalveolar lavage abnormal
COVID-19
Chronic kidney disease
Citrobacter test positive
Cognitive disorder
Complication associated with device
Computerised tomogram head abnormal
Symptomtext
Patient is a 68 y.o. female, legally blind and chronically ill, originally presented 12/23/22 after being found confused and with hallucinations wandering around CVS, recently moved into new apartment (had been living with her mother). Initially treated for UTI and AKI; then became hypoxic and found to be COVID-positive prompting transfer to the ICU for intubation 12/26. She was extubated 12/29 and transferred out of ICU 12/31/22. Found to have Mycobacterium mucogenicum on BAL prompting ID consult with no further inpatient workup. Mental status was initially improved after ICU transfer to the floor, but then gradually worsened 1/5-1/7; with significant delirium, hypoxia and elevated WBC, suspicious for aspiration. Pt required re-intubation 1/7 per Pulm/CC team. Now extubated and back to the medical floor as of 1/11/23. Palliative consulted to assist with GOC, family currently wanting to continue current measures. Patient is currently stable for discharge to facility Assessment and Plan Acute Hypoxic Respiratory Failure Recent Covid 19 MRSA PNA - Developed sore throat 12/24 after admission, noted to be positive COVID 12/25 - Initially on RA but decompensated 12/26, requiring NRB and then intubation, then had septic like picture briefly requiring pressors; extubated 12/29. Also treated with antibiotics by ICU for possible concomitant pneumonia - Completed dexamethasone and remdesivir, removed from COVID isolation 1/5 - Bronch 12/26 with mycobacterium (see below) - Re-intubated on 1/7 upon transfer to ICU with concern for aspiration - Bronch Cultures w/ MRSA -Completed antibiotic therapy on January 14, currently afebrile hemodynamically stable with relatively stable white count - Urine cultures w/ Citrobacter - Extubated on 1/10; appears improved but remains very weak and would be high risk for repeat resp issues - Now weaned off O2 Acute toxic/metabolic encephalopathy Hospital associated delirium - Likely has chronic cognitive impairment or progressive dementia not formally diagnosed; presented with severe hallucinations, AKI, UTI, and wandering around pharmacy - Behavioral evaluated early in hospitalization, felt her encephalopathy was due to AKI and UTI; head CT was non-acute - Mental status improved with treatment of acute illness but remains with cognitive delay and poor insight; ultimately will need formal neuropsych testing at discharge AKI on CKD3 Hyperkalemia - In the setting of decreased PO intake and infection - Cr. 2.01 on admit, appears baseline is 1.4-1.7 -Kidney function improved. Cr was 1.10 on 1/15, now bounced back to 1.86 likely due to dehydration. -start gentle IVF and monitor. Encouraged oral fluid intake. -Intermittent hyperkalemia with unclear etiology -Received Lokelma, potassium improving We will continue to monitor Dysphagia - Multifactorial in setting of debility, acute illness and intubations - Came out of ICU with NG and tube feeds -Speech therapy on board -Discussed with nutrition and bedside nursing -Patient with a regular NG tube causing throat irritation. NG tube discontinued -Patient was reevaluated by speech therapy who recommended advancing diet. Patient is likely blind so needs help with meals Mycobacterium mucogenicum - Noted in BAL 12/26 - Pt with cough, emphysema, adenopathy on CT chest; also nodular and ground glass opacities; QuantiFERON negative - ID consulted and signed off; Recommended AFB sputum culture, CBC and CMP about a week prior to her follow-up appointment, which will be in about 6 weeks - She will need a CT chest without contrast prior to ID follow-up with Dr. Found on ground, possible fall in the hospital - Unwitnessed 1/1 PM, sounds like patient got frustrated and threw herself to the floor - CTH no significant change; fluid in R middle ear and mastoid air cells; CT C-spine without fractures - Continue supportive care with PT/OT Essential Thrombocytosis - Per history, previously supposed to be on Anagrelide 1 mg BID; appears not taking but still on COPC med rec; last visit noted 10/2021 - Plt elevated with this history and acute illness, peak 987 on 1/2, slight downtrend to 600-700s - Might need to have hematology see at some point in the OP setting once recovers from this acute illness Hypertension, essential - Had been holding antihypertensives when in ICU with pressors and soft bps - Added back on coreg 1/13/23 and monitor; will resume norvasc too - Monitor BP and adjust meds as needed Vitamin D deficiency - Vitamin D level low at 14, appears chronically low, started supplementation UTI, resolved - Noted early in admission - Initially urine culture with Providencia, Klebsiella, completed Rocephin, repeat UA 1/5 negative - UA and Cultures Positive for Citrobacter 1/7 - Treated with Cefepime Anemia, chronic - Unclear etiology, likely CKD contributing - Baseline appears to be around 9.5-11; currently ~9 - Monitor PVD - s/p aorto-fem bypass 1999, with thrombectomy 2004 - Continue medical management; resumed plavix and Zetia and transitioned to Eliquis per CCM History of CVA - Reports residual left sided weakness, not noted on exam - Occipital and parietal infarctions without significant carotid disease - Continue eliquis, resume statin at discharge History of DVT - s/p MVA in 1996 in RLE - Was on coumadin on admission although had been subtherapuetic - Transitioned to Eliquis COPD, without acute exacerbation - Per history, no exacerbation - Continue as needed Duonebs History of seizures - Per history - Previously on keppra but no longer taking AEDs Legally blind - Secondary to MVA in 1996 History of chronic hepatitis C - Recommend outpatient f/u with PCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 27,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 27.01.2021
- Beginn
- 09.08.2022
- Tage bis Beginn
- 559,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Brain cancer metastatic
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt was admitted for metastatic cancer to the brain and acute respiratory failure with hypoxia on 8/3. Pt was not tested for COVID on admission. She was tested on 8/9 due to placement and was found to be positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 03.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cerebral haemorrhage
Computerised tomogram head abnormal
Fall
Loss of consciousness
Symptomtext
Pt reports no issues with prior COVID vaccinations. Pt believes it was the combination of the first Shingrix and COVID second booster (dose 4) that caused this adverse event. No issues immediately following vaccination on 4/3/22. The morning of 4/4/22 the patient was found unconscious. CAT scan did not show any stroke or aneurysm, but pt reported having a brain bleed after the fall that left the patient unconscious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral haemorrhage
- Hospital-Tage
- -
- Labordaten
- CAT scan 4/4/22
- Aktuelle Erkrankungen
- no known illnesses
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 24.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Pulmonary embolism
Symptomtext
Patient states started experiencing shortness of breath ~5 days after vaccination leading to 3 day hospitalization for pulmonary embolism; no other risk factors for PE so best guess was combination of long-standing raloxifene therapy and recent vaccination combined (or coincidence)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 3,0
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Raloxifene 60 mg, atorvastatin 10 mg, others unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Angiogram pulmonary abnormal
Pulmonary embolism
Symptomtext
Pulmonary embolism with acute hypoxic respiratory failure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- CTPA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Cardiac And Vasculature Essential hypertension Mixed dyslipidemia Chromosomal And Congenital Misc MTHFR gene mutation Endocrine And Metabolic History of laparoscopic adjustable gastric banding Prediabetes Severe obesity Eye Combined form of senile cataract Presbyopia Diverticulosis Fatty liver Lipoma of left lower extremity Mental Health Mood disorder Musculoskeletal And Injuries Primary osteoarthritis of left knee S/P right knee arthroscopy Status post total shoulder arthroplasty, left Neuro Cognitive impairment DDD (degenerative disc disease), lumbar RLS (restless legs syndrome) Tension headache Interstitial lung disease: s/p R uniportal Wedge resection Upper, middle and lower lobes on 7/15/20 Lung interstitial disease Mild intermittent asthma without complication Sleep Obstructive sleep apnea Psychophysiologic insomnia
- Andere Medikamente
- acetylcysteine 600 mg capsule Sig: Take 600 mg by mouth every evening. Route: Oral ascorbic acid, vitamin C, (VITAMIN C) 500 mg tablet Sig: Take 500 mg by mouth daily. Route: Oral Class: Historical Med choleca
- Allergien
- Codeine Not Specified Allergy 1/6/2015 Other reaction(s): Nausea And Vomiting VOMITING Diphenhydramine Hcl Not Specified Unspecified 5/22/2019 Other reaction(s): Other (See Comments) Headache/dizziness Trimethoprim HEADACHE Not Specified Allergy 2/18/2022 Morphine Itching Low Allergy 1/6/2015 Adverse Reactions/Drug Intolerances Bactrim [Sulfamethoxazole-trimethoprim] UNKNOWN (SEE COMMENTS) Not Specified Contraindication 4/22/2016 Cefprozil UNKNOWN (SEE COMMENTS) Not Specified Contraindication 1/6/2015 Other reaction(s): Historical Data-Review with Patient Erythromycin GI REACTION Not Specified Contraindication 4/22/2016 Erythromycin Base Not Specified Contraindication 1/6/2015 Other reaction(s): Unknown GI SYMPTOMS Sulfa (sulfonamide Antibiotics) Not Specified Contraindication 4/22/2016 Other reaction(s): Other (See Comments) Headaches, dizziness
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 28.02.2022
- Beginn
- 05.03.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Endotracheal intubation
Inappropriate schedule of product administration
Intensive care
Positive airway pressure therapy
SARS-CoV-2 test positive
Symptomtext
Patient received Pfizer COVID vaccine on 2/5/22 and 2/28/22. On 3/5/22, patient admitted to our inpatient facility with acute respiratory failure with hypoxia due to COVID-19 pneumonia needing BiPAP (also positive COVID test during admission). Patient was intubated on 3/7/22 and as of today (3/8/22), patient is still intubated in.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- COVID status positive 3/5/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- dementia, depression and anxiety with agoraphobia, HTN, and CKD stage 3
- Andere Medikamente
- amlodipine, escitalopram, lisinopril, melatonin, memantine, mvi, trazodone
- Allergien
- morphine
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 02.02.2023
- Impfdatum
- 05.05.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 149,0
- Dosis
- 1
- Route/Site
- - / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Blood test
Colectomy
Colitis ulcerative
Colonoscopy abnormal
Computerised tomogram
Diarrhoea
Gastrointestinal disorder
Intensive care
Large intestinal ulcer
Migraine
Peripheral swelling
Symptomtext
Migraines and swollen hands were first experienced in October 2022. By November she was experiencing severe gut and diarrhea; she went to her PCP, who did bloodwork and sent her home. She went back again and then went for more bloodwork. They gave several diagnoses that proved incorrect after two different ER visits. On January 6, she was in the ER for the third time and they transferred her to the hospital and was admitted; they did a colonospy on January 9th and diagnosed 3/4 of her colon was ulcerated. On january 13 she was transferred to a local hospital and they removed her colon. Dr said that ' the colon disintegrated in his hands like a wet paper towel." She was in ICU for 5 days and did not get released until February 1, 2023. The diagnoses was ulcerative colitis, one of the adverse events listed by Pfizer as an 'adverse event'. The doctor said she would have died if they did n ot remove the colon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 22,0
- Labordaten
- Bloodwork, CAT scan, mulitple CAT scans and emergency surgery
- Aktuelle Erkrankungen
- sensitive stomach
- Vorgeschichte
- None
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 03.04.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Animal bite
C-reactive protein
COVID-19
Cardiac failure congestive
Chest X-ray abnormal
Condition aggravated
Decreased appetite
Diarrhoea
Dyspnoea
Fatigue
Nausea
Pulmonary oedema
SARS-CoV-2 test positive
Symptomtext
6/1/32022-Presents to ED, SOB, fatigue, decreased appetite, nausea and diarrhea. Pt on Augmentn for cat bite wound. Afebrile, On 2L NC 94% spo2.. Covid + test. CRP. Ordered Decadron, ceftriaxone and doxy. CXR-pulmonary edema. Admit CHF exacerbation Covid . 6/14/2022- Started on remdesivir and barictininb. 6/16/2022- Weaned down to RA, spo2 95%. 6/21/2022-Completed remdesivir , d/c steroids and baricitinib as no further resp symptoms at day 5. VSS afebrile. 6/24/2022- D/C to SNF .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, COPD, hyperlipidemia, hypothyroidism, A fib, CAD
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 21.04.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 77,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram pulmonary
Blood test
Chest X-ray
Dyspnoea
Pulmonary thrombosis
Ultrasound Doppler
Symptomtext
I experienced shortness of breath and blood clots in the bottom of my lungs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- -
- Labordaten
- Blood work Chest X-Ray CTA Ultra Sound of Lower Extremity
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Volost; Pepcid; Crestor
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 09.04.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 75,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Blood potassium decreased
Blood test
Chest X-ray normal
Nausea
SARS-CoV-2 test negative
Syncope
Symptomtext
I woke up to go to the bathroom and I was nauseous, very weak, and fainted. I had to go to the hospital by ambulance. This lasted for about 4 hours. When I was at the hospital the did several test, but they all came back normal. My potassium was a little low though and they had to gave me a little potassium. They also gave me a little fluid and then they sent me home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test- Negative; Blood Panel- Low Potassium; Chest X-Ray- Normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Irritable Bowel Syndrome
- Andere Medikamente
- Multivitamin; Calcium; Vitamin C; Vitamin B12; Aspirin; Citalopram; Simvastatin; Chlorthalidone
- Allergien
- Penicillin; Sulfa Drugs; Keflex
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 16.04.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 26,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Peripheral swelling
Pulmonary thrombosis
Thrombosis
Ultrasound Doppler abnormal
Symptomtext
Swelling in right calf. Blood clot in right leg that spread to lungs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- 2,0
- Labordaten
- Blood tests, CT scan, ultrasound to diagnose
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 19.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hyperhidrosis
Syncope
Symptomtext
Pt had shot and left pharmacy with not symptoms. He called the pharmacy from home stating he had light headedness, sweating, and fainted for 2-3 minutes. He had no other allergic symptoms signs or symptoms. He was told to call 911 but the refused.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- none per patient
- Allergien
- none per patient
- Vorherige Impfungen
- Stated he has felt similar after other shots in past.
- Staat
- CO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 08.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Head injury
Loss of consciousness
Myalgia
Syncope
Symptomtext
Patient fainted this morning after receiving pfizer booster yesterday. She said she fell and hit her head and doesn't know how long she was unconscious. I asked her how she is feeling now, if she is having any symptoms of concussion, syncope etc, she just reports muscle soreness. I encouraged her to seek medical attention and not drive herself to her provider. She had not had anything to eat this morning so I encouraged her to eat something and keep drinking fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Ear pain
Ear swelling
Facial pain
Full blood count
Headache
Immediate post-injection reaction
Metabolic function test
Pain
Swelling face
Symptomtext
Patient developed immediate body aches following second dose, followed by headache, swelling and pain left side of face and ear. Diagnosed with bell's palsy, unresolved 10 days post vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- CBC, CMP
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Diabetes, CAD, Hyperlipid, Thyroid goiter
- Andere Medikamente
- levemir, advair, singulair, humalog, amlodipine, losartan, potassium, vitamin d, meloxicam, gabapentin
- Allergien
- penicillin, ace inhibitors
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 24.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial paralysis
Injection site swelling
Paraesthesia
Swelling face
Symptomtext
PATIENT COMPLAINS OF SLIGHT SWELLING OF LEFT ARM (INJECTION SET) AND LEFT CHEEK IS ALSO SLIGHTLY SWELLING. FEELING A TINGLING SENSATION. LEFT EYE SLIGHTLY DROOPY. PT SAID 2ND DAY POST VACCINATION THE SWELLING HAS GONE DOWN BUT STILL TINGLING. OCCURED NEXT DAY AFTER SHOT. DOES NOT REPORT FEVER OR PAIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Laboratory test normal
Syncope
Symptomtext
vaccination received 4/20/22 syncopal event 4/23/22 followed by another on 4/25/22, which prompted his mother to bring him to the ED All labs were WNL, feeling better at clinic today
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- fluticasone propionate
- Allergien
- Shrimp
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Fear
Limb discomfort
Panic reaction
Thrombosis
Symptomtext
I left facility directly after vaccine. I was not instructed to stay. My husband and I nearly got down the road when I immediately started to feel as if my entire body were on fire from the inside. My limbs became heavy. It was the same feeling I get when stung by a wasp. I immediately took a few Benadryl. I also threw myself into a panic at that point and took an anti-anxiety pill that I carry on-hand incase of unanticipated events. It was very scary. I was alright in the end, however, I felt it necessary to bring attention to. And it seems as if I may have developed a blood clot in the palm of my hand. I am going to the doctors first thing next week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Celexa
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyskinesia
Fall
Loss of consciousness
Moaning
Restlessness
Seizure
Symptomtext
After vaccination, patient sat down in waiting area. After 5 minutes the patient starting groaning, and became restless in chair, moving legs. He started to have a seizure - specifically loss control of muscles, fell to the floor, unconscious for less than 1 minute. I, the pharmacist, came over and called his name and patted his chest to confirm alertness, and sat him on the chair from floor, as he started to produce saliva while eyes closed. Within 1 minute, he regained consciousness in the chair. He was able to confirm his name, where he was. The pharmacy called the ambulance. Paramedics took over, made sure he was ok to leave.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE ON RECORD
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- Dizziness from first dose of Pfizer reported by patient.
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 10.04.2022
- Impfdatum
- 10.04.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
Patient fainted 10 minutes after getting the vaccine in the store. she was feeling little dizzy after. Other than that She was doing fine and she was offered call emergency call but patents refused it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- n/a
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Memory impairment
Seizure
Symptomtext
Patient had a covid shot, passed out after 1 min. i lowered him to the floor. He was acting like he had convulsion, later he is breathing well. so, i gave him a 0.3 ml EpiPen. He woke up after a few mins later and wanted to know what happen. i called emergency, he asked me to call his roommate who brought him there. He later explains to me he has severe anxiety for needles, and he has passed out before at a blood bank after an injection. Emergency came and check his vitals and everything was ok. Re refuse to go to hospital and he sign a concern with emergency crew declining to go with them. His roommate drove him home after that
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- Peanut allergy
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fall
Myalgia
Pain in extremity
Pruritus
Injection site erythema
Injection site rash
Loss of consciousness
Pyrexia
Stomatitis
Symptomtext
Patient passed out about 10 hours after vaccination and was rushed to the hospital thru 911 the following day when she regained consciousness and was treated for fever, itching, rashes and redness in the injection site. Patient was hospitalized form 4/3/22 to 4/5/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- 3,0
- Labordaten
- Hospitalized from 4/3/22 to 4/5/22
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- unknown
- Allergien
- No known allergy
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site discolouration
Swelling
Thrombosis
Symptomtext
PATIENT EXPERIANCE SWELLING THE NEXT DAY WITH HEAD ACHE, FOLLOWED BY DISCOLORIZATION OF THE ENTORE UPER ARM FROM THE SITE IF INJECTION TO LOWER YELBOW WITH CLOTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- NONE , ADVISED PATEINT TO SEEK MEDICAL HELP
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HIGH BLOOD PRESSURE , HIGH CHOLESTROL, THYROID
- Andere Medikamente
- NO
- Allergien
- NKDA
- Vorherige Impfungen
- FLU
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Nausea
Pain
Symptomtext
Nausea and dizziness leading to momentary loss of consciousness for approx 5-10 seconds; Extreme generalized body pain everywhere
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetic
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Dizziness
Nausea
Syncope
Symptomtext
Aproximately 5 minutes after administration, patient let me know she was feeling dizzy, nauseous and fainted. Called 911 and the paramedics took care of patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- -
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Nausea
Vision blurred
Vomiting
Symptomtext
nausea/vomiting.. blurred vision.. Patient passed out.. ambulance called
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- no medication to my knowledge. pt had not eaten
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dehydration
Dizziness
Pyrexia
Syncope
Vomiting
Symptomtext
Pt stated she experienced dehydration, dizziness, fever, vomiting, and fainting spells.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Feeling hot
Interchange of vaccine products
Loss of consciousness
Symptomtext
Patient was administered booster dose of Pfizer Covid-19 vaccine after completing primary series of Moderna (3/11/21 & 4/8/21); he was aware he was receiving Pfizer vaccine. He claimed to have experienced dizziness after previous vaccinations. After administration, patient sat down in waiting area and was given a cold cloth after feeling hot and anxious; no observed hives or difficulty breathing. 911 was called after observing when going from hunched, seated position to sitting up straight, the patient lost consciousness for approximately ten seconds before becoming aware of his surroundings. Paramedics arrived to assess patient and he refused to be transported to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported at time of vaccination.
- Vorgeschichte
- None reported at time of vaccination.
- Andere Medikamente
- None reported at time of vaccination.
- Allergien
- None reported at time of vaccination.
- Vorherige Impfungen
- Dizziness to previous vaccinations (none specified, and dates not reported by patient).
- Staat
- NJ
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 20.06.2023
- Impfdatum
- 15.04.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 158,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Condition aggravated
Cough
Depression
Fatigue
Headache
Hypersomnia
Insomnia
Oropharyngeal pain
Parosmia
Peripheral swelling
Productive cough
Respiratory tract congestion
SARS-CoV-2 test positive
Serotonin syndrome
Taste disorder
Symptomtext
I had a massive headache for several days in September 2022. Then on 9/20/2022, I developed a very sore throat; it felt like I had rocks in my throat. By the end of that day, I developed a cough. It was a congested, productive cough. I finished my workday and then took a home antigen test and got a positive result. I called my physician on 9/21/2022 and arranged a telehealth appointment with her. She prescribed molnupiravir. I was to take four capsules twice a day for five days. I began taking the medication on 9/22/2022. During this time, I was extremely tired. I lost my senses of taste and smell at some point. I drank lots of tea with honey, because I know that honey has antibacterial properties. After three or four days of the antiviral, I began to feel better. It took several weeks before I began to regain my taste and smell, and even months later, things didn't smell or taste right. It's been several months since I had COVID-19, but I experience occasional swelling of the feet, though I don't know if it's related to that. I also had insomnia prior to having COVID-19, but since having it, my insomnia has been much worse. And then there are weekends in which I want to do nothing but sleep, but I don't know if it's because my body is worn down by that point. Before I had COVID-19, I had a history of depression. I had taken Zoloft until May 2021, when I was switched over to Cymbalta. After I began Cymbalta, I developed serotonin syndrome. I subsequently had to be taken off the Cymbalta, and I haven't taken any other antidepressants since then. Since having COVID-19, my depression has become even worse than before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 20SEPT2022 - Home Antigen Test - Positive Result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia; Hypertension; Acid Reflux; Osteoarthritis; Degenerative Joint Disease; Depression; Anxiety; High Cholesterol; Insomnia; Irritable Bowel Syndrome; Year-Round Post-Nasal Drip
- Andere Medikamente
- Colestipol; Gabapentin; Furosemide; Xyzal; Cozaar; Metformin; Prilosec; Pravastatin; Tramadol; Oxycodone with Acetaminophen; Cyclosporin Eye Drops; Ventolin Inhaler; Tizanidine; Flonase Nasal Spray; Tylenol; Zyrtec; Cinnamon; Ginger; Calciu
- Allergien
- Bactrim; Singulair; Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 16.06.2023
- Impfdatum
- 15.06.2022
- Beginn
- 20.05.2023
- Tage bis Beginn
- 339,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Atrial flutter
Malaise
Mobility decreased
Peripheral swelling
Symptomtext
I had a swollen arm and unable to lift my arm for about 24 hours. I was on a trip and on the third day, I started not feeling well. I was diagnosed with atrial flutter and AFIB. My first episode occurred on 03/23/2021. I went to the emergency room and got the help I needed. As of today, I feel better after starting new medication, and I have a follow-up appointment in two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diverticulitis; GERD
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 23.06.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 57,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Antineutrophil cytoplasmic antibody
Blood fibrinogen increased
C-reactive protein
Computerised tomogram thorax abnormal
Condition aggravated
Dyspnoea exertional
Fibrin D dimer increased
Interleukin level
Lung cancer metastatic
Pulmonary hypertension
Pulmonary mass
Respiratory symptom
Tricuspid valve incompetence
Troponin increased
Symptomtext
Pt with history of pulmonary fibrosis and a stable pulmonary nodule that had not changed much in years, but then took four RNA shots from January 2021-9/2021 and it is now clear that the lung mass is lung CA and now with mets., having worsening dyspnea with exertion of walking few feet. Last June/23/2022 had the second booster Pfitzer vaccine worsening the respiratory symptoms and 2 months later she was admitted at hospital for elevated D-Dimer and worsening dyspnea and was found to have elevated troponins , and severe tricuspid regurg and pulmonary hypertension.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- hs-CRP sky high at 48.9, MPO is high at 879, fibrinogen 698, IL-6 ls 13.7 and this is higher than 1/18/22. she has had mildly elevated baseline hs-CRP ranging from 2.8 to 4.1 prior to the Covid vaccinations x 2 in 1/2020, 3rd in 9/2021, and 4th in 6/22, hs-CRP was 4.8 after the 3rd shot. Elevated D-Dimer. Abnormal CT Thorax
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -Rheumatic aortic insufficiency, Cardiac arrhythmia, unspecified, Emphysema, unspecified, -Idiopathic pulmonary fib, Chronic obstructive pulmonary disease, unspecified, Nonrheumatic aortic (valve) Insufficiency, Nonrheumatic mitral (valve), Secondary pulmonary arterial hypertension Insufficiency, Nonrheumatic tricuspid (valve) Insufficiency, Chronic kidney disease, stage 3 (moderate), Presence of cardiac pacemaker.
- Andere Medikamente
- Levsin/SL; morphine; albuterol sulfate; lorazepam; dextromethorphan-guaifenesin; DHEA; Robitussin Cough-Chest Congestion DM; benzonatate; docusate sodium; Spectrazyme; aspirin; Omega 3 Fish Oil; Vitamin C; Prolia; Combivent Respimat; Traume
- Allergien
- Cipro
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 01.05.2023
- Impfdatum
- 26.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 36,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Catheterisation cardiac
Dyspnoea
Fatigue
Gait disturbance
Symptomtext
After the 4th dose, I discovered that it became very difficult for me to breathe, especially after going outside. I also experienced fatigue and difficulty walking because it became harder to breathe. My doctor gave me an albuterol inhaler around June 2022. After taking the 5th dose, the problems continued. I went to a cardiologist to check if I was having heart problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 7Mar2023 Heart catheterization
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Prior blood pressure issues; Heart murmurs
- Andere Medikamente
- Carvedilol; losartan potassium; atorvastatin; baby aspirin; AREDS 2 vitamins; PROLIA
- Allergien
- Erythromycin stearate; NOVOCAIN; mold; mildew; grass; pollen
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 14.04.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 181,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test abnormal
Giant cell arteritis
Headache
Hypertension
Infection
Nasopharyngitis
Neck pain
Symptomtext
On August I had a neck pain and headache. The headache continued till October. I took Advil . Around 10/20/2022 I went to the ER because I was experiencing headache and my blood pressure was high. They did some blood tests and said to go to a primary doctor. we did more blood where they diagnosed me as having Giant Cell Arteritis ( rare disease). My doctor prescribed Prednisone and Actemra weekly injections. I will be Seeing the Rheumatologist soon again June for a follow up. The disease that I have cannot be cured. It can be triggered by medication or infection but not sure where it exactly came from. . In October I had an infection (cold) may be It could be from there who knows. My doctor is not even sure where I developed this disease from.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- 20OCT2022 Blood Test- Abnormal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 07.04.2023
- Impfdatum
- 22.04.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 146,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Chest X-ray abnormal
Fatigue
Infantile spasms
Influenza
Malaise
Nasopharyngitis
Oropharyngeal pain
Pneumonia
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I started having a horrible sore throat, fatigue, fever, malaise. I took a home COVID-19 test that came back positive. I called my insurance COVID-19 hotline, to have a virtual health appointment. I elected to not take any medication for COVID-19. It did take three weeks for me to not test positive for the virus. This past week I had flu and cold symptoms, I started having rattling in my chest. I went to an Urgent Care where they did a chest X-ray, I was diagnosed with pneumonia. I was prescribed Doxycycline to help rid my body of the infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- 19MAR2023 Home COVID-19 test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Penicillin; Sulfa
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 10.06.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 168,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Fatigue
Headache
Nausea
Oropharyngeal pain
Pain
Pneumonia
Symptomtext
Fatigue, headache, body ache, nausea, sore throat, pneumonia and a bad cough, chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Simvastatin; gabapentin; omeprazole; amlodipine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 08.04.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 179,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Dyspnoea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 06.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 56,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody
Blood alkaline phosphatase
Blood creatine phosphokinase
Blood gastrin
Blood magnesium
Borrelia test
C-reactive protein
Chills
Colonoscopy
Culture
Dysphonia
Electromyogram
Full blood count
Heavy metal test
Laboratory test
Magnetic resonance imaging
Metabolic function test
Muscle twitching
Symptomtext
Twitching in arches of feet that progressed throughout my entire body and face. I also had an internal tremor all over my body that made my voice shaken and teeth chatter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- MRI, emg, colonoscopy, CBC, metabolic, Heavy Metals, Gastrin, Lyme, urinalysis, CK, Sedimentation, Ana screen/reflex titer, C reactive protein, ALK PHOS, TOTAL, CULTURE , urine T4, Magnesium
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- IBS, SVT, A-fib
- Andere Medikamente
- D3, B complex, magnesium, multi vitamin, pre/probiotic, butyrate, Metoprolol Tarterate(as needed for heart rate over 100)
- Allergien
- No NSAIDS
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 18.10.2022
- Impfdatum
- 15.04.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 139,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Atrial fibrillation
Dyspnoea
Electrocardiogram abnormal
Heart rate abnormal
Mobility decreased
Weight increased
Symptomtext
I went to my family doctor on 09/01/2022 and I noticed I was having trouble breathing, moving about. I had weight gain. During my physical he noticed my heart rate was out of sync. My heart valves were not following the sequence. Instead of all 4 chambers following in sequence, one chamber was not. My family doctor diagnosed me with A-Fib. The doctor sent me to a cardiologist. I met the cardiologist on 9/6/2022. The cardiologist put me on a regime of medications, and I have been on those medications since then. The medications the cardiologist put me on: XARELTO; valsartan; furosemide; carvedilol; amiodarone. To put my heart back into normal rhythm they need to shock my heart. At the end of October 2022, when I see my doctor, if I have lost sufficient weight, then they will do the shock to put my heart back into rhythm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- A series of EKGs, electrocardiogram. On 10/19/2022 I go in for a series of blood work up.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- None
- Andere Medikamente
- Krill oil
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 30.03.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 102,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood test
Computerised tomogram abdomen abnormal
Endoscopic ultrasound abnormal
Lymphadenopathy
Musculoskeletal chest pain
Pancreatitis
Pyrexia
White blood cell count increased
Symptomtext
After the vaccine my lymph nodes swelled under my arms. I was having sever joint pain. I also was having pain in my ribs on the right side. It became more significant and I started running a fever. My primary care doctor recommended I go to the doctor, so, I went to the emergency room. I was diagnosed with pancreatitis. After a lot of testing they were unable to determine how it happened. I think this was triggered by my vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- Blood Panel - 7/10/22 - Elevated White Blood Cells; CT scan - 7/24/22 - Pancreatitis; Endoscopic Ultrasound - 9/1/22 - Pancreatitis.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; GERD; Cardio Myopathy
- Andere Medikamente
- Verapamil; rosuvastatin; pantoprazole; famotidine; telmisartan; coQ10; multivitamin; vitamin D3; vitamin B12; probiotic
- Allergien
- Penicillin; sulfa; cefalexin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 22.07.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 48,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Anticoagulation drug level above therapeutic
Asthenia
Blood bicarbonate normal
Blood glucose increased
Blood ketone body
Blood pH increased
Blood sodium decreased
COVID-19
Chest X-ray normal
Condition aggravated
Diabetes mellitus management
Fatigue
Full blood count abnormal
Glycosylated haemoglobin increased
Gout
Hyperglycaemia
Insulin therapy
Symptomtext
Admission Date: 9/8/2022 Discharge Date: 09/16/2022 PRESENTING PROBLEM: Generalized weakness Chronic renal impairment, stage 4 (severe) Hyperglycemia due to diabetes mellitus Hyperosmolar hyperglycemic state (HHS) COVID-19 virus infection HOSPITAL COURSE: Patient is an 87 year old female with past medical history of NIDDM2, gout, PAF, mechanical aortic valve on coumadin, diastolic heart failure and CKD 4 who presented to ED to the ED with generalized fatigue. She had been on prednisone for 10 days leading up to admission for gout flare. In the ED, pt was found to have BS of 659, sodium of 129, normal AG, bicarb. pH was elevated and beta hydroxybutyrate of 1.08. Her CBC showed leukocytosis of 18. COVID positive and CXR showed no acute process. She was admitted for further treatment. She was started on endotool and director of medical services was consulted. She was transitioned to basal bolus on 9/9 but did continue to be hyperglycemic. Her a1c was found to be elevated to 12.1. The director of medical services assisted with management of basal bolus insulin. Recommendations to discharge on Novolog 70/30. The patient's husband is also on 70/30 at home and they feel comfortable with the management/administration of this. She should follow up with the director of medical services, or with her PCP for further management of DM. Regarding COVID diagnosis, she remained stable on room air. She did not require remdesivir or decadron. She was noted to have supratherapeutic INR but no active signs of bleeding. No reversal agent given but coumadin held. She subsequently became subtherapeutic, and was placed on heparin gtt while awaiting therapeutic INR. She was not a candidate for lovenox given CKD. Once INR therapeutic x 2 consecutive days, she was felt stable for discharge home. She was advised to have her INR checked on Monday 9/19 as her lab is not open over the weekend. PT/OT evaluated and recommended discharge home with assist and HHC. She was discharged home in stable condition with her husband on 9/16. All follow up recommendations discussed in detail with the patient and her husband prior to discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cardiac pacemaker in situ HTN (hypertension), benign Hyperlipidemia Anemia Depression with anxiety Osteoarthritis Hyperplastic polyps of stomach Type 2 diabetes mellitus with hyperglycemia GERD (gastroesophageal reflux disease) Glaucoma Hypothyroidism Thrombocytopenia Sarcoma History of artificial heart valve Paroxysmal atrial fibrillation Mobitz type II atrioventricular block H/O mechanical aortic valve replacement LBBB (left bundle branch block) CAD (coronary artery disease) Chronic diastolic congestive heart failure Tricuspid regurgitation CKD (chronic kidney disease) CHF (congestive heart failure) Allergic rhinitis Anxiety Aortic valve stenosis Atrioventricular block Bradycardia Endocarditis History of repair of rotator cuff History of spinal surgery Hypercalcemia Knee pain Restrictive lung disease Closed arm fracture, left, initial encounter Hypokalemia Hyperosmolar hyperglycemic state (HHS)
- Andere Medikamente
- Accu-Chek Aviva Plus Blood Glucose Monitor Accu-Chek Aviva Plus Test Strips Accu-Chek Softclix Lancets Acetaminophen (TYLENOL PO) atorvastatin (LIPITOR) 20 MG tablet busPIRone (BUSPAR) 15 MG tablet cholecalciferol (VITAMIN D3) 25 MCG (1000
- Allergien
- Adhesive Tape Sulfa Drugs Tape
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 16.03.2021
- Beginn
- 22.08.2022
- Tage bis Beginn
- 524,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute kidney injury
Alcohol use
COVID-19
Central venous catheterisation
Chest pain
Confusional state
Dizziness
Ex-alcohol user
Haemodialysis
Hepatorenal syndrome
Lethargy
SARS-CoV-2 test positive
Symptomtext
61y.o. male who presents on 8/22 with history of CABG, Hypertension, SBP, significant for alcoholic cirrhosis complicated by ascites and hydrothorax, and end-stage renal disease requiring dialysis M W F, presented to the ER from dialysis due to chest pain right-sided associated with dizziness. Found to be COVID positive, no indication for Remdesivir. Remained in isolation for 10 days, isolation precautions are removed. He reports that he began consuming alcohol in his 20s until April 9, 2022, when he stopped consumption due to symptoms. HRS with progressive AKI- initiated on hemodialysis July 8, 2022 -undergoing Intermittent HD 3 x week MWF via RIJ permacath- under care of Dr Upon exam, pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 8/22/22 SARS-COV-2 (COVID-19) by NAA, Micro -- detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 27.01.2021
- Beginn
- 03.08.2022
- Tage bis Beginn
- 553,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood culture negative
COVID-19
Chemotherapy
Chest pain
Echocardiogram abnormal
Ejection fraction
Febrile neutropenia
Haematocrit decreased
Haemoglobin decreased
Heart valve incompetence
Hyperdynamic left ventricle
Metabolic function test
Neutrophil count decreased
Oropharyngeal pain
Platelet count decreased
Platelet transfusion
Pyrexia
Red blood cell count decreased
Symptomtext
78 year old male with history significant for AAA (stable), HTN, HLD, DM type II, recent Covid-19 (7/21/22) presents to the hospital with chest pain. Cardiology consulted for further evaluation. Echocardiogram completed, revealing LVEF 70%. The left ventricular appears hyperdynamic. No segmental wall motion abnormalities are identified. There is moderately increased thickness of the interventricular septum without significant obstruction to outflow. There is trace valvular regurgitation. There is no pericardial effusion. Pt discharged to home. well. She received half dose of Neulasta after chemotherapy. Physical examination was only remarkable for in injected pharynx. Labs on presentation showed WBC of 0.2, RBC 2.69, Hct 25.2, RDW 16, Platelets 45, neutrophil 0.1, Hb 8.8 and CMP was within normal limits. Afterwards, blood culture were sent from oncology, normal saline fluid bolus initiated in clinic, and patient received first dose of cefepime at 14: 30 in clinic. And patient was started on Paxlovid (nirmatrelevir & ritonavir)1 dose orally twice per day. Patient was diagnosed with febrile neutropenia and was admitted to the inpatient ward to continue IV antibiotics, fluids and for monitoring. On 08/04 at midnight, patient developed a fever of 100.7 and was started on Tylenol. Aftwerwards, her congestion and sore throat improved and patient has been afebrile since. On 08/05, patient was doing well with no fevers, chills or night sweats. However, patient's platelet count decreased to 27 and was given 1 dose of platelet transfusion and no transfusions reactions occured. Furthermore, blood cultures showed no growth at 1 day. Patient was deemed stable for discharge on 08/05 to home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 4,0
- Labordaten
- 8/3 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 28.04.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Chest X-ray normal
Chest pain
Cough
Dyspnoea
Electrocardiogram normal
Eye discharge
Nasal congestion
Paranasal sinus hypersecretion
Pulmonary congestion
Throat irritation
Symptomtext
I had a stuffy nose and scratchy throat on the 28th. I did a test on the 29th it was negative. I arrived home on the 30th I had chest congestion and trouble with congestion. On July 3, 2022, I went to the ER, I was having chest pain and trouble inhaling. I was given a EKG, x-ray. I developed a cough that MUCINEX helped with the cough. The cough lasted about three days total. The chest pain stopped after the visit to the ER was over. My nose did drain uncontrollably throughout the COVID-19. On the forth of July I had green discharge coming out of my tear ducts. I had a video visit with a doctor and she prescribed eye drops for me. I never had fever or fatigue. Just eye discharge, congestion and cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 07/03/2022 EKG normal, 07-03/2021 chest X-ray- normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; Allergies; Cardiac Microvalve Disorder
- Andere Medikamente
- Probiotics; magnesium lactate; calcium, glucosamine; fish oil; omeprazole; baby aspirin; levothyroxine
- Allergien
- Pineapple; mushrooms; soy; penicillin; sulfa drugs; peanuts; iodine; mustard; statin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 59,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Feeling abnormal
Headache
Influenza like illness
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I woke up early feeling achy and had a headache. I took a home test which came back positive. I isolated and stayed home until the 20th. 06/20, I went back to work and I didn't feel bad at the beginning of the day as the day went on I started feeling run down and just wanted to crawl into bed. Body aches, headaches, fatigue, shortness of breath. Called the doctor and they sent me to the hospital for the antibody infusion for the next day. 06/21, Went and did the infusion, shortness of breath, chest congestion, flu like symptoms. This day was by far the worst day while having COVID-19. 06/22, I started to feel much better and was on isolated for the rest of the week. 06/27, I went back to work with no issues and I had fully recovered from the illness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Ehlers-Danlos Syndrome; Mast Cell Activation Syndrome; Raynaud's Syndrome
- Andere Medikamente
- Omega 3; TYLENOL 3; ZYRTEC; atorvastatin; DEXILANT; metoprolol; lorazepam; metaxalone; vitamin D3; B12; multivitamin; potassium; magnesium
- Allergien
- NSAIDS; penicillin; sulfa; iodine; PERCOCET; VICODIN
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 70,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Fatigue
Feeling abnormal
Headache
Mobility decreased
Pain
SARS-CoV-2 test positive
Sensory disturbance
Throat clearing
Upper-airway cough syndrome
Symptomtext
04/11/2022 Vaccination 06/20/2022 That evening I was coming down with something. I had that feeling behind my eyes that something was like a post nasal drip, clearing my throat, and unusually tired. 06/21/2022 I went to the Doctor. I was tired all day. Did not test for COVID-19. He prescribed Z-pack. 06/22/2022 I had headache, chills, body aches, and fatigue. I did not take my fever during this time. I couldn't get off the couch I was so tired. I contacted the Doctor again and he stated to keep on the Zpack. I had done the home test; COVID-19 POSITIVE. My wife was POSITIVE a couple days after.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- COVID-19 POSITIVE
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- History of Headaches
- Andere Medikamente
- Amitriptyline; Latanoprost Eye Drop; Vitamin D; Multivitamin
- Allergien
- Keflex
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 62,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest pain
Cough
Diarrhoea
Exposure to SARS-CoV-2
Fatigue
Headache
Malaise
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I attended a wedding on 06/11/22 out of state. On 06/12/22 I noticed some chest pain while I was walking. The next day I was notified that multiple people at the wedding had tested positive for COVID-19. I had done some at home testing for COVID-19 and those were negative but I was feeling sick with coughing and a runny nose. So I went to a local hospital for a PCR test on 06/15/2022 and I received my positive results the next day. I had a telehealth appointment on 06/17/22 and was prescribed PAXLOVID. After I began the medication, my cough and congestion became much better but I developed headaches and diarrhea that persisted for a week after completing the medication. All of my symptoms improved with the exception of fatigue that lasted until this week. The week of 07/11/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR test 06/15/2022 positive; COVID-19 at home tests negative.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure; Third stage kidney disease.
- Andere Medikamente
- Atenolol; losartan; meloxicam; multivitamin; vitamin D; fiber.
- Allergien
- Tetracycline; tetanus shot.
- Vorherige Impfungen
- Tetanus shot age 53, swollen glands in arms, allergic reaction.
- Staat
- AZ
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Ear discomfort
Musculoskeletal chest pain
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sneezing
Symptomtext
6/27/2022 I had a hacking cough that hurt my ribs, sore throat on one side with pressure in the ear on that same side. I sneezed a lot too. Developed a fever that peaked at 103 on 6/29. At home test positive on 6/27. I spoke to the doctor on 6/27 who prescribed Paxlovid. Tested positive again on 6/28 with an At Home COVID 19 test. A Cough medication was also prescribed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- At home COVID tests 6/27 and 6/28, both positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High blood pressure; Hypothyroid; Gout
- Andere Medikamente
- Olmesartan; Furosemide; Spironolactone; Levothyroxine; Allopurinol; Bethanechol Chloride; Hydralazine; Fenofibrate; Nifedipine; Lorazepam; Co Q 10; Flax Seed Oil; Turmeric; Vitamin C and D3
- Allergien
- Sulfa; Levaquin; Dust; Dander; Oxycodone; Tramodol
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 05.04.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 53,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Chest discomfort
Cough
Decreased appetite
Dyspnoea
Fatigue
General physical condition abnormal
Head discomfort
Headache
Influenza A virus test negative
Influenza B virus test
Malaise
Myalgia
Oropharyngeal pain
Pain
Paranasal sinus discomfort
Pulmonary congestion
Respiratory syncytial virus test negative
Symptomtext
Contraction of Covid-19 Patient presents today for urgent care due to covid symptoms and positive home test. He has been fully immunized. He has fatigue, head and chest congestion, sore throat, some shortness of breath and body aches. Review of Systems Constitutional: Positive for activity change, appetite change and fatigue. Negative for chills and fever. HENT: Positive for congestion, sinus pressure, sinus pain and sore throat. Respiratory: Positive for cough, chest tightness and shortness of breath. Negative for wheezing. Cardiovascular: Negative for chest pain. Gastrointestinal: Negative. Musculoskeletal: Positive for myalgias. Neurological: Positive for headaches. Pulse 84 | Temp 99.3 ?F (37.4 ?C) (Oral) | SpO2 91% Constitutional: General: He is not in acute distress. Appearance: He is obese. He is ill-appearing. HENT: Head: Normocephalic and atraumatic. Eyes: General: No scleral icterus. Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, and reactive to light. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: Normal breath sounds. No wheezing. Musculoskeletal: Cervical back: Neck supple. Skin: General: Skin is warm and dry. Neurological: General: No focal deficit present. Mental Status: He is alert and oriented to person, place, and time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19/FLU/RSV PCR PANEL, Collection Time: 05/29/22 2:35 PM / Specimen: Nasopharynx; Swab COVID-19/FLU/RSV PCR PANEL, Collection Time: 05/29/22 2:35 PM Specimen: Nasopharynx; Swab Respiratory syncytial virus, Negative Influenza A by PCR, Negative Influenza B by PCR, Negative SARS-Coronavirus-2 PCR, Positive (A)
- Aktuelle Erkrankungen
- None indicated
- Vorgeschichte
- Obesity, Hypertension (HTN), Coronary artery disease (CAD)
- Andere Medikamente
- nebivoloL 5 mg Tab amLODIPine 10 mg Tab chlorthalidone 25 mg Tab losartan 50 mg Tab cholecalciferol 25 mcg (1,000 unit) Tab sildenafiL (pulm.hypertension) 20 mg Tab Opurity Multivitamin 30 mg iron- 800 mcg Chew cyanocobalamin 1,000 mcg Tab
- Allergien
- None indicated
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 43,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Decreased appetite
Dysphonia
Fatigue
Feeling abnormal
Headache
Illness
Mobility decreased
Oropharyngeal pain
SARS-CoV-2 test positive
Sick relative
Speech disorder
Vomiting
Symptomtext
I was having a sore throat which lasted for a few days. By Monday it was worse and I took a home COVID-19 test and that was negative. I ended up going to the Doctor and they tested me and it was positive. The next day I was violently ill and was trying to throw up but I was so weak I was just on the floor and could not even lift my head to throw up in the toilet. I could not move or get up. My husband who was also positive called EMS who was able to get me up but I was able to sit and talk with them and we did not end up taking me to the ER. I was having a horrible cough and headache at this point and was so tired. I had no appetite and ended up calling my doctor back because I was still so sick. As of now I do not have the cough but my voice is gruff and I am still fatigued all the time. I have brain fog and it is hard to hold a conversation. I know that most things I do will make me exhausted so I have to pick and choose what I do because I still have this lingering fatigue. While I have tested negative I am still impacted with lingering issues and would say I have not recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- At Home COVID-19 Test, COVID-19 PCR Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Loratadine; Tylenol;
- Allergien
- Celebrex; Fluconazole
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Pain in extremity
Symptomtext
Patient initially described typical arm soreness that is known to occur with Covid 19 vaccinations. By the weekend he was having difficulty raising arm and that has continued to date. Patient can raise raise left arm all directions except for forwards in front of his body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Dizziness
Hypertension
Hypoaesthesia
Vertigo
Symptomtext
10 MINS AFTER VACCINE PT FELT DIZZY, LIGHT HEADED, VERTIGO, ABDOMINAL PAIN, LEG NUMBNESS, HTN, CALLED 911, EMS ADVISED HOSPITAL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- POSSIBLY A NAUSEA MEDICCATION
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Back injury
Computerised tomogram thorax
Condition aggravated
Dehydration
Dyspnoea
Emphysema
Extra dose administered
Fall
Feeling abnormal
Headache
Impaired self-care
Influenza like illness
Laboratory test normal
Magnetic resonance imaging
Malaise
Nasal congestion
Nausea
Symptomtext
Within a week after getting the vaccine I felt like I was having the flu. I didn't feel good. I haven't been running a fever. I was very weak. I felt like I was sick with covid again. During that time I did fall and hurt my back again. This time it was really bad. My breathing got worse. I wake up in the morning with headaches. My underlying health conditions has gotten worse. I'm continuously losing weight. I used to weigh around 115 lbs, but now I am down to 93 lbs. If I eat I feel nauseas and sick. I went to the hospital on June 13th and they told me I was dehydrated. I was throwing up and having headaches. They hydrated me and gave me some medicine for my nausea. I haven't been able to take care of myself. The doctor is slowly trying to rule things out to figure out what is going on. I did finally get a Prolia shot. My lung doctor changed my medication. I have been having bad headaches and brain fog. I'm being referred to a gastrologist. My nose is very congested and stuffy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Lab work- all normal X-rays MRI with contrast (6/8/2022) CT scan of chest (6/16/2022) CT Scan with dye of GI Tract- scheduled
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Sever Osteoporosis, Emphysema
- Andere Medikamente
- Buprenorphine-naloxone, Clonazepam, Fosteum Plus, Singulair, Spiriva, Albuterol, Aspirin, CoQ-10 Plus Red Yeast rice, Over 50 Women's Multivitamin, Omega Fish Pill, Turmeric with Curcumin, Vitamin D3, Magnesium, B-Complex, Melatonin, Tylen
- Allergien
- Azithromycin
- Vorherige Impfungen
- 3rd dose Pfizer covid vaccine (Lot #330308D)- I started getting sick. I felt like I had the flu. It lasted for a month or 2. The
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 06.05.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Computerised tomogram normal
Dysstasia
Fatigue
Laboratory test normal
Mobility decreased
Muscle fatigue
Symptomtext
Starting 2 days after the vaccine dose, I had severe fatigue that went on to last at least 7 days. Then, it slowly faded. About the same onset of time, I had sort of weakness. I couldn't even stand up for very long periods of time. Holding my arms up to wash my hair, my arms would get really fatigued. I would describe it as a muscle fatigue. I had zero strength. Going up my floor of stairs in my house, I would get really tired. It was kind of all over in all muscle groups but more noticeable in my shoulders and thighs, large muscle groups that I wouldn't expect a lot of fatigue from. It's a remarkable change for me because I run and hike around 40 miles per week. So, not even being able to hold my arms up to wash my hair is extremely unusual.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- CT Scan normal. General lab work normal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Losartan 25mg 1xday; nifedipine 5mg 1xday
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 08.06.2022
- Impfdatum
- 25.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac stress test
Electrocardiogram
Palpitations
Respiratory disorder
Sleep disorder
Symptomtext
After the 3rd vaccination. It happened end of last fall. It woke me up out of my sleep around 1AM. I woke my wife up and told her something was wrong with my heart. We went to the ER by the time I got there it calmed down and they ran a bunch of test. They referred me to see a cardiologist and she put me through a a lot of test, physical stress test, EKG. They came back okay. I see her now every six months to a year. I also noticed that every once in a while I get a singular heart palpitation and reoccurred after the 4th vaccination. After the 4th vaccination I developed a very aggressive respiratory condition that is the worse at night. It lasts all day. My wife has the same thing as well. Overall the heart palpitations come here and there and I am still dealing with the respiratory condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Physical Stress test, EKG.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes Type II- Controlled by Diet and Exercise
- Andere Medikamente
- LUMIGAN .01%; dorzolamide HCL; omega 3 krill oil 500mg; D3/K2 supplement 10,000 iu; zinc 20mg; magnesium 100mg; pancreatin 200 mg
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 30.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 30.04.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arrhythmia
Symptomtext
Onset of arrhythmia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- heart 6th nerve bundle branch
- Andere Medikamente
- Eliquis Atrovstatin Metaprolol
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 06.04.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 38,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Cough
Dizziness
Fatigue
Feeling abnormal
Lethargy
Malaise
Nasal congestion
Nasopharyngitis
Nausea
Paraesthesia
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sleep disorder
Symptomtext
It started on Saturday evening. I was tired, really tired and had a very terrible cough. Kept waking me up all night. The next day, Sunday morning I was really fatigued and felt like I had a fever. Had a low-grade fever and that passed pretty quickly then felt decent for a bit. Up and down. I was still coughing a lot. I also had a cold, runny nose, stuffy nose. It has been so much better today. I had an interesting event a couple nights ago. I had been feeling lethargic all day and I was by myself at home. I was reading a book on my phone and suddenly, I started to get so dizzy and so spaced out. I got pins and needles up and down my arms and legs. I got nauseated but didn?t throw up. These are all the symptoms for a heart attack so my husband came home, and I went to bed and we were worried so he called 911. They came quickly and I told them I was pretty fatigued, and I did a COVID test Sunday morning, and it was negative. Everything vitals wise was normal. They noted to come with them as a precaution or follow up with a cardiologist. I just got sicker with the horrible runny nose. The next day I did make an appointment and got on a virtual call. I told him what happened, and he said it was just more COVID. He noted it wasn?t a heart attack and I noted this went on from 6-9pm. started to feel gradually better around 8:30PM and then by 9pm I felt fine and just needed to eat. Asked about the anti-viral and I got the prescription for the Paxlovid. But I didn?t take it because I started to feel better already. I haven?t taken it and he just recommended Vitamin C 3000mg and lots of water. He also suggested 40-50mg of zinc per day, but I am doing better. I decided just not to take the Paxlovid because I?m feeling so much better. I have been more energic than I had been the last 3 days, not completely normal, but getting there. No more fever except for a low grade one on Sunday. Everything was perfectly normal yesterday for the temperature. So I believe I?m on the mend.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- 05/15/2022 - At-Home COVID Test - Negative 05/18/2022 - At-Home COVID Test - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma Multiple Sclerosis (Benign) Standing Tremors (Orthostatic Tremors)
- Andere Medikamente
- Vitamin D3
- Allergien
- Penicillin Sulfa Dust Mites Shellfish Lone Star Tick bite in 2014, 2017 (Delayed Anaphylaxis) ? Alpha Gal Sugar Levels Elevated ? Caused an allergy to Mammalian Meat Wasp stings Bee stings Molds and mildews
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast pain
Chest pain
Hypoaesthesia
Injected limb mobility decreased
Lymph node pain
Lymphadenopathy
Mammogram normal
Neuralgia
Pain
Pain in extremity
Paraesthesia
Rash
Tenderness
Tinel's sign
X-ray limb abnormal
Symptomtext
Patient is a 31-year-old female here today for concerns regarding left arm pain and numbness after receiving COVID-19 third booster vaccination on 3-29-2022. She reports after she received COVID-19 booster in left arm, she has been experiencing numbness from her left shoulder radiating to left hand. She also reports limited range of motion in left shoulder. She also reports sharp pain of the left side of chest radiating to the left breast. She reports that pain and numbness and tingling seem to be constant. She reports that sometimes her pain is a excruciating, 8 out of 10 pain. She will take ibuprofen 800 mg every 6 hours as needed for pain. She reports that ibuprofen helps some with pain. She reports that the lymph nodes under her left axilla appear to be swollen and are painful. She denies fever or chills. She denies injury to her left arm. She reports all of her symptoms occurred right after her vaccination and did not resolve. She reports that numbness and tingling goes from her left shoulder and radiates down to her left, third through fifth digits. Rash on Left Hand. Swollen Lymph Node present under left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 1. Vaccines and biological substances causing adverse effect in therapeutic use, initial encounter (Primary) 2. Numbness and tingling in left arm - Ambulatory referral to Neurology 3. Left arm pain - meloxicam (MOBIC) 15 mg tablet; Take one tablet (15 mg dose) by mouth daily., Starting Mon 5/16/2022, Normal Dispense: 30 tablet; Refill: 2 - Xr Shoulder Min 2 Views Left; Future 4. Axillary lymphadenopathy - Mammo Diagnostic Bilateral; Future 5. Breast pain, left - Mammo Diagnostic Bilateral; Future - meloxicam (MOBIC) 15 mg tablet; Take one tablet (15 mg dose) by mouth daily., Starting Mon 5/16/2022, Normal Dispense: 30 tablet; Refill: 2 Based on physical exam, pain appears to be nerve related. Positive Tinel's sign of ulnar nerve of the left side. Will refer patient to neurology for nerve conduction study of the left arm. Will also obtain left shoulder x-ray due to limited range of motion of left shoulder as well as tenderness to palpation. Will obtain diagnostic mammogram and ultrasound of the left breast due to left axillary lymphadenopathy after COVID-19 vaccination. COVID-19 third booster occurred almost 2 months ago. Advised patient to report to CDC adverse effects. Patient verbalized understanding. Follow up if symptoms worsen or fail to improve.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- ibprofen
- Allergien
- Rye
- Vorherige Impfungen
- Fainting, Vomiting, Fatigue, Low grade fever.
- Staat
- NY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Cardiac monitoring
Condition aggravated
Electrocardiogram normal
Heart rate increased
Palpitations
Symptomtext
About 3 weeks after receiving my fourth dose of the vaccine, I woke up with a racing heart rate. It was so fast, I was not able to count the beats. My son tried also, but he was not able to either. I called for an ambulance, but by the time they got there, my heart rate had slowed a little. It was still high, as well as my blood pressure when they checked it. I made an appointment with my Cardiologist and he has me wearing a heart monitor which I will take back tomorrow. I had an EKG done and everything was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I had an EKG, but it was normal.
- Aktuelle Erkrankungen
- I was not experiencing any illness.
- Vorgeschichte
- I have high blood pressure (controlled); I have 2 hernia's; I am pre-diabetic.
- Andere Medikamente
- I was taking Valsartan; metoprolol; fish oil; vitamin D.
- Allergien
- I am allergic to NSAID's; Ceclor (antibiotic); Reclast; I cannot take any statin.
- Vorherige Impfungen
- After receiving my second dose of Pfizer, I had arm/shoulder pain and I was given a steroid shot which helped with being able to
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 11.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest X-ray normal
Chest pain
Chills
Cough
Injection site pain
Musculoskeletal stiffness
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test negative
Sinusitis
Sneezing
Symptomtext
It began as a sore throat. By the evening of 4/21, there was a burning in the chest, congestion, coughing, sneezing. By the morning of 4/22, fever up to 101.6, and chills ensued through the day and into the next day. Throughout, and still today, there is stiffness and pain in the shoulder of the injection site. I had no such reactions to the previous three Pfizer vaccinations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Two home Covid test showed negative. Visited Urgent Care center. Exam and xrays showed no pneumonia or Covid. Diagnosed sinusitis and prescribed 10-day Doxycycline regimen.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- PE X 3, Past history of bladder and prostate cancer
- Andere Medikamente
- 20mg Xarelto, 20 mg Pravastatin, Multivitamin, CoQ10, D3, Niac
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 23.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Chills
Confusional state
Electrocardiogram normal
Fatigue
Injected limb mobility decreased
Injection site pain
Injection site swelling
Lymphadenopathy
Mobility decreased
Symptomtext
The next day after vaccine, I had swelling and pain in my arm at the injection site. I felt very tired and fatigued with chills. I laid in bed for 2 days. I had pain in my arm with limited range of motion. I have lymphatic swelling under both arms. I went to my doctor on 4/28/2022, when I started having chest pressure, chest pain, and confusion. I have had an EKG which was normal and blood work which is scheduled. I have started taking OTC Guaifenesin which does help.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Fatigue Fibromyalgia Slow Lymphatic System Phase 1 Fast and Phase 2 Slow
- Andere Medikamente
- Amlodipine Niacin DMAE Fish Oil Glutathione
- Allergien
- N/A
- Vorherige Impfungen
- Pfizer dose 1
- Staat
- KY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Condition aggravated
Symptomtext
I developed severe joint pain in my hips and knees. I had knee arthritis previously but it seemed to be exacerbated afterwards. I am unsure if its related but wanted to note it. Ankle pain was minimal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis in the knees Type II diabetes
- Andere Medikamente
- Claritin Aspirin 81mg
- Allergien
- Tetracycline
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Limb immobilisation
Mobility decreased
Monoplegia
Pain in extremity
X-ray normal
Symptomtext
It started as a sore arm that has continued for about 3 weeks. Last weekend the pain spread to my shoulder and down to my fingertips. I was in excruciating pain and had to go to the emergency room. My arm is now in a sling and I am not able to lift my arm over my head. They indicated that the x-ray was normal and that I needed to see an orthopedist. My arm is more or less paralyzed. I was given a short term amount of oxycodone which has not help. I have also taken Tylenol and Ibuprofen which has only helped minimally. My primary care doctor had to submit the prescription on my behalf.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- X-ray-normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sleep apnea Asthma Borderline personality disorder Depression
- Andere Medikamente
- Bupropion Atorvastatin Duloxetine Topamax
- Allergien
- None
- Vorherige Impfungen
- Pfizer 3-experienced sore arm.
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure fluctuation
Ear infection
Ear pain
Fatigue
Headache
Mobility decreased
Pain
Pain in extremity
Symptomtext
I was extremely fatigued. I could barely move throughout the house for about a week. It got better as the week progressed. I also had a headache and very little arm pain. I only felt the arm pain when I took a shower. I was so tired as well. When I went to the doctor they said I have an ear infection. My blood pressure has also been sporadic up and down. I have headaches all the time. I was prescribed Neomycin-Polymyxin-Hydrocortisone Otic 3.5 10,000-1 Sol Sand 2 drops into left ear 2xdaily. I still have shooting pain in my left ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid Reflux; Anticardiolipin Syndrome Antibodies; Atrial Tachycardia; Carotid Artery Stent Implant in March 2020; Chronic Insomnia; Degenerative Disc Disease; Diastolic Dysfunction; Dry eyes; Essential Tumors; Hypertension (diagnosed November 2019); Lupus SLE (mild); Lymphedema; Mitral Valve Prolapse (mild); MGUS; Osteopenia; Sarcopenia
- Andere Medikamente
- Ambien 5mg 1xday, Aspirin 81mg 1xday, Bystolic 20mg 1xday, Estradiol Transdermal Patch 3.75mh 2xweek, Hydralazine 25mg (if blood pressure exceeds 160), Torsemide 10mg 2xday as needed, Lipitor 20mg 1xday, Magnesium Oxide 400mg 1xday, Nitrogl
- Allergien
- Penicillin; Shrimp; Morphine; Vicodin
- Vorherige Impfungen
- (2/9/2021) COVID-19 Vaccine 1st dose- I was very sick. I had chills. I felt like I was going to die. I felt very weak, and then
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Hypersensitivity
Pruritus
Rash
Urticaria
Symptomtext
an allergic reaction; really bad hives; itchiness; it got worse and worse and worse; rash and irritation; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 27-year-old female patient received BNT162b2 (BNT162B2), on 29Mar2022 as dose 3 (booster), single (Lot number: FJ9943) at the age of 27 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1, Manufacturer unknown), for Covid-19 immunization; Covid-19 vaccine (Dose 2, Manufacturer unknown, Expiry date: EW0170), for Covid-19 immunization. The following information was reported: HYPERSENSITIVITY (non-serious) with onset 01Apr2022, outcome "unknown", described as "an allergic reaction"; CONDITION AGGRAVATED (non-serious) with onset 01Apr2022, outcome "unknown", described as "it got worse and worse and worse"; PRURITUS (non-serious) with onset 01Apr2022, outcome "unknown", described as "itchiness"; URTICARIA (non-serious) with onset 01Apr2022, outcome "unknown", described as "really bad hives"; RASH (non-serious) with onset 2022, outcome "unknown", described as "rash and irritation". The events "rash and irritation", "really bad hives" and "itchiness" required emergency room visit. Therapeutic measures were taken as a result of rash, urticaria. Additional information: It was reported that the patient had an allergic reaction, and she was taking high dosage of medication for the rash and irritation. It was reported that she was required by her employer to take the booster dose and she has an appointment with her PCP on 02May2022. she wanted to know if she can get a medical certificate to show her employer. The patient mention that she had reported her side effects. Advised caller that her doctor was the best person who can provide her with the medical certificate and informed caller that we have a document discussing how long side effects last which caller accepted. It was reported that she got her third dose of COVID (clarified as Pfizer COVID vaccine), the booster on 29Mar2022. So, three days later she started experiencing really bad hives and itchiness and she thought it was 'scheduled with the allergy or something else' but it got worse and worse and worse. But today, she went in and out urgent care nonstop from the rashes and the hives and itchiness. So, she just wanted to see reporting it, having it. She does not know what else to do? otherwise with her job that she got hired for we 'fired' the vaccine so she have seen doctor's doing there but she haven't been able to actually work due to the factor she really have a very bad rashes and stuff." Consumer stated, "Its EW0170 and she have another one it says FJ9943, the third one this was for the third vaccine. she believes its (EW0170) for the second dose she just has it." It was reported that It doesn't gave her me an expiration, it just says 02712, it doesn't have any expiration date. Reportedly for the hives she had this medication that they gave her. There are 4 different one. First one was called Hydroxyzine pamoate, this was one tablet and it was going to be 25mg." It was reported that she work in the medical field, she is a biller (hence captured as consumer or other non-health professional. Prior Vaccinations: Consumer stated, "No." It was queried by the patient that what she was supposed to do right now. She can't work right now. They won't see her till 02May2022, and she just started her job at the clinic she honestly does not know what else she needs to give them. They are okay with her missing, but she has to have like a paper work to see that she was going through this whole because of the vaccine. Reportedly the patient was provided with the number of Pfizer Medical Information and was requested to select option 3, timings as 8 am to 9 pm Monday to Friday. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Peripheral swelling
SARS-CoV-2 test negative
Wheezing
Symptomtext
First, I had immediate excessive swelling of arm, then led to breathing difficulty, wheezed when I exhaled and inhaled, tried albuterol inhaler, gave me temporary relief, did the best I could do to function the last couple of weeks. Saturday, I went to Urgent Care they gave me a breathing treatment, shot of steroids' and prescribed for prednisone. Proud to say I am 90% better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 test was negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal Allergies; Eczema; High Blood Pressure
- Andere Medikamente
- Amlodipine, Lisinopril, Doxazocin, Chlorthalidone, Dorsal, Ketorolac, Dorzolamide
- Allergien
- Penicillin; Mold
- Vorherige Impfungen
- COVID-19 dose 1-headache.
- Staat
- ID
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 24.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Migraine
Symptomtext
On 04/24/2022 at 06:30PM I had back to back migraines for two hours. I had the same occurrence at the exact same time the next day 04/25/2022. I do have a history of Migraines but it is unusual to have them back-to-back and at the same time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Hypertension
- Andere Medikamente
- Losartan 100mg once daily, Amlodipine 2.5mg daily, Simvastatin 20mg daily, Progesterone 100mg, Prilosec 20mg, Cetirizine 2 dose of 20 mg AM/PM total 40mg, Asthma inhalers Symbicort 160mcg, Fluticasone inhaler, ProAir rescue inhaler. Suppl
- Allergien
- Penicillin; Sulfa
- Vorherige Impfungen
- On 10/19/2021 I had my Booster (Pfizer) and Flu Shot on the same day and I did experience body aches, pains, soreness, fatigue,
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 25.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Tinnitus
Symptomtext
Dramatic increase in tinnitus, bordering on unbearable within 2 hours. This occurred with the previous 3 doses as well. It subsided over many months after each previous dose, but it never decreased close to the level of tinnitus that I had before the 1st dose. Previous doses were as follows: Dose #1 - 3/17/2021 Dose #2 - 4/7/2021 Dose #3 - 8/27/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Allergies, amyloids in esophagus, aneurysm, asthma, demyelination of the pons, dysautonomia, eczema, fasciculations, immunodeficiency, GI dysmotility, ischemia, hypoperfusion, & moderate to severe vascular reserve compromise, MGUS, mitochondrial disease, MTHFR, mitral valve prolapse, neuropathy (peripheral and small fiber), Raynaud's syndrome, scoliosis (fusion and instrumentation), small vessel disease (brain), soft aortic murmur, tinnitus
- Andere Medikamente
- Pentasa, Phazyme, VSL#3DS (probiotic), Allegra, Astelin nasal spray, Advair (generic), Nimodipine, Lorazepam, Baclofen, carnitine, COQ10, creatine, methyl folate, alpha lipoic acie, N-Acetyl Cysteine, L-Glutamine, Systane Balance Lubricant
- Allergien
- Latex, Prozac, Valtrex, Acyclovir, Cartia XT, Zofran Prolia, Leviquin, Cipro, Avelox, Prepartion-H, Hydrocort-Pramoxine cream, cats, dogs, mold, ragweed, grass, pollen, trees, dust, fragrances, nickel, latex, mercapto mix, thorium mix, Euxyl K 400, flaxseed, egg, pineapple, plum, strawberry
- Vorherige Impfungen
- As in #18 above. Also, pneumovax (hives, adult, date unknown) and flu ((raised & red around injection sit (raised & red around i
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
Patient reports numbness and tingling in legs and feet
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Flushing
Tremor
Symptomtext
pt presented with shakiness, flushed face and shortness of breath at 7 pm, after receiving her vaccination the previous day at 2 pm. Pt attested that symptoms developed at 5-6 pm, and immediately took 50 mg of liquid diphenhydramine and came to the store. Pt began to look remarkably better after resting in the patient area for 30 minutes. Pt declined transportation to the hospital/urgent care/home, and told me she'd call in the morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- unknown
- Andere Medikamente
- vitamin b12 100 mcg, atorvastatin 10 mg
- Allergien
- penicillin, naproxen, erythromycin
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 10.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Diarrhoea
Injection site erythema
Injection site mass
Injection site pain
Injection site rash
Injection site swelling
Injection site vesicles
Injection site warmth
Pain
Paraesthesia oral
Pruritus
Rash
Sleep disorder
Urticaria
Symptomtext
Tingling sensation of mouth, tongue, and lips. Hives appeared across upper chest, arms, and cheeks. After taking 50mg Benadryl (diphenhydramine), the mouth sensation subsided quickly. Approximately 24-36 hours later, I experienced mild localized pain and lump in left arm at injection site. Large rash with fluid filled blisters on left upper arm. Redness, warmth, swelling of upper arm. Burning/itching sensation (bad enough to wake me up at night). I experienced this reaction with all three COVID vaccines (3/26/21, 4/16/21, 4/10/22). with the first two doses, the mouth/tongue reaction occurred within 30 minutes and subsided with Benadryl. With the third dose, I took Benadryl proactively and did not experience the mouth sensation, just the painful rash. The rash lasts approximately 7-10 days and does not improve much with Benadryl every 6 hours and application of hydrocortisone cream. I also experience sever diarrhea approx 3-4 days after each shot when the rash is at its worst.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Losartan-HCTZ 100-25mg 1x day
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 16.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Constipation
Migraine
Nausea
Pyrexia
Symptomtext
Migraine; Severe constipation; nausea; Fever of about 101 degrees; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 04Apr2022 16:15 (Lot number: FJ9943) at the age of 68 years as dose 4 (booster), single for covid-19 immunisation. Relevant medical history included: "Known allergies:Shellfish" (unspecified if ongoing), notes: Known allergies:Shellfish. Concomitant medication(s) included: ATORVASTATIN; FOLIC ACID; BIOTIN; VIT C. Past drug history included: Neomycin, reaction(s): "Allergies: topical neomycin", notes: Known allergies: topical neomycin; Formaldehyde, reaction(s): "Allergies: formaldehyde producers", notes: Known allergies: formaldehyde producers. Vaccination history included: Bnt162b2 (Dose Number: 3, Batch/Lot No: FF2588, Location of injection: Arm Left, Fever of about 101 degrees), administration date: 20Sep2021, when the patient was 67 years old, for Covid-19 Immunization, reaction(s): "Fever", "Migraine"; Bnt162b2 (Dose Number: 2, Batch/Lot No: ER8727, Location of injection: Arm Left, Vaccine Administration Time: 04:00 PM), administration date: 24Mar2021, when the patient was 67 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6205, Location of injection: Arm Left, Vaccine Administration Time: 04:00 PM), administration date: 03Mar2021, when the patient was 67 years old, for Covid-19 Immunization. The following information was reported: MIGRAINE (non-serious) with onset 05Apr2022 06:00, outcome "recovering", described as "Migraine"; CONSTIPATION (non-serious) with onset 05Apr2022 06:00, outcome "recovering", described as "Severe constipation"; NAUSEA (non-serious) with onset 05Apr2022 06:00, outcome "recovering", described as "nausea"; PYREXIA (non-serious) with onset 05Apr2022 06:00, outcome "recovering", described as "Fever of about 101 degrees". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of migraine, constipation, nausea, pyrexia. Additional information: Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Also she received medication Centrum within 2 weeks of vaccination. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220405; Test Name: Fever; Result Unstructured Data: Test Result:about 101; Comments: degrees
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Shellfish allergy (Known allergies:Shellfish)
- Andere Medikamente
- ATORVASTATIN; FOLIC ACID; BIOTIN; VIT C
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Discomfort
Hypoaesthesia
Immediate post-injection reaction
Lymphadenopathy
Pyrexia
Sensitive skin
Skin burning sensation
Tremor
Symptomtext
Numbness in face immediately after receiving shot, which lasted several hours. Later that evening, hypersensitive skin on upper arms, back, thighs (felt like a bad sunburn). I also had severe chills that seemed more like a seizure to my husband because the shaking was quite violent. This lasted for several hours, until about 5 am the next day (22nd of March). Other more common symptoms were fever for a few hours , and swollen lymph nodes which lasted about 2 weeks. Today (April 12, 2022), I am experiencing hypersensitive skin sensation again. I don?t know if it?s related, but I think so, since this was what I experienced the day of the vaccine. It is very uncomfortable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None, just a telehealth visit with my provider
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, osteoarthritis
- Andere Medikamente
- None
- Allergien
- Raw mango, raw pineapple, lychee fruit, scallop
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Pneumonia
Sputum culture
Upper respiratory tract infection
X-ray
Symptomtext
Woke up next day with sore arm and beginning of upper respiratory infection which turned into pneumonia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- X-ray, sputum culture
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, chronic rhino sinusitis, gerd
- Andere Medikamente
- Seroquel X-ray, brio ellipta, xyzal, montelukast, nuvigil, rexulti, cymbalta, vitamin a, b, c, calcium, fish oil, humira
- Allergien
- Lithium
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Diarrhoea
Dizziness
Fatigue
Pain
Pyrexia
Symptomtext
Severe diarrhea Fever Severe body pain Severe tiredness Chest pains Dizziness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Metformin/ Atenolol
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Dyspnoea
Erythema
Onycholysis
Pain in extremity
Hypoaesthesia
Injection site discharge
Joint swelling
Nail bed infection
Onychomadesis
Pain
Peripheral swelling
Paronychia
Product complaint
Skin odour abnormal
Vaccination site pustule
Symptomtext
She would like to know if this could have been from the vaccine being expired or the needle being bad; thumb was hurting so bad; had a red line going down her arm from the injection site to her thumbnail; She touched her thumbnail and the nail came off and her thumb was filled with puss; She touched her thumbnail and the nail came off and her thumb was filled with puss; it smelt like she was dying and she had never smelt something so bad; the injection site began to ooze pus; chest pain lasted 5 hours from the injection; short of breath; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 71 year-old female patient received bnt162b2 (BNT162B2), administration date 31Mar2022 (Batch/Lot number: unknown) at the age of 71 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetes" (not ongoing); "Angina pectoris" (unspecified if ongoing); "tooth removed" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose 1), for Covid-19 immunization, reaction(s): "with no issues"; Bnt162b2 (Dose 2), for COVID-19 immunization, reaction(s): "with no issues"; Polio vaccine, for Immunization. The following information was reported: CHEST PAIN (medically significant) with onset 31Mar2022, outcome "recovered", described as "chest pain lasted 5 hours from the injection"; DYSPNOEA (medically significant) with onset 31Mar2022, outcome "unknown", described as "short of breath"; PRODUCT COMPLAINT (non-serious), outcome "unknown", described as "She would like to know if this could have been from the vaccine being expired or the needle being bad"; VACCINATION SITE PUSTULE (non-serious) with onset 01Apr2022, outcome "unknown", described as "the injection site began to ooze pus"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "thumb was hurting so bad"; ERYTHEMA (non-serious), outcome "unknown", described as "had a red line going down her arm from the injection site to her thumbnail"; ONYCHOLYSIS (non-serious), PARONYCHIA (non-serious), outcome "unknown" and all described as "She touched her thumbnail and the nail came off and her thumb was filled with puss"; SKIN ODOUR ABNORMAL (non-serious), outcome "unknown", described as "it smelt like she was dying and she had never smelt something so bad". Therapeutic measures were taken as a result of vaccination site pustule, onycholysis, paronychia. At the time of booster dose administration the patient reported she became short of breath and blew it off as angina. She stated she had dealt with angina for 15 years on and off and knows when to go to the hospital. The pharmacist wanted to call an ambulance but she declined. She went home and her neighbor was home in case she needed someone. She stated that the chest pain lasted 5 hours from the injection. The next day (01Apr2022) the injection site began to ooze pus. She stated that she had had many shots and vaccines (give examples of polio vaccine and DMAR) and never had a injection site ooze pus before. She relays that she used to be diabetic but was no longer a diabetic. Stated that because of her years as a diabetic she knows how to clean wounds and mentioned packing wounds and knows that they have to heal from the inside out. She stated that she cleaned the injection site with rubbing alcohol and saline before taking some antibiotics, amoxicillin, that she had on hand because she was having a tooth removed. Took Tylenol for pain. She goes on to explain that she was wearing a sweatshirt later on and when she took off the sweatshirt because her thumb was hurting so bad, she had a red line going down her arm from the injection site to her thumbnail. She touched her thumbnail and the nail came off and her thumb was filled with puss. She stated that it smelt like she was dying and she had never smelt something so bad. She also relays that the injection site was right on top of her shoulder. She cleaned her thumb wound in the same manner as the injection site, with alcohol, saline and antibiotics. The patient did not seem interested in seeking healthcare when referring her multiple times. She would like to know if this could have been from the vaccine being expired or the needle being bad. The lot number for bnt162b2 was not provided and will be requested during follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Angina pectoris; Diabetes; Tooth extraction
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Condition aggravated
Decreased appetite
Extra dose administered
Hot flush
Immediate post-injection reaction
Injection site pain
Mobility decreased
Night sweats
Sleep disorder
Symptomtext
No reaction immediately following injection. Arm became sore at the injection site as the day progressed, but not red and not worse than any other vaccine (flu, etc.). Went to bed earlier than usual but did not sleep through the night. Got up for breakfast on Tuesday 5 April, then went back to bed for about 3 hours sleep. Got up again about noon, took two aspirin and lazed around all afternoon, finally showering at about 4pm (NOT my usual routine). Not hungry, but ate a little dinner. Took one tylenol. Now I felt as if I were having a constant "hot flash" of the very worst kind I had experienced 20+ years ago: as if a wire brush were inside me pushing out of my skin. Also chills/shivering inside my torso. At about 2:30am on Wednesday 6 April, I awoke and my nightgown arms, chest and torso were soaked with sweat, but I felt better at that point and have had no other problems since then. This is the first time (of the four shots) that I have had immediate side effects. I will be on the lookout in about two weeks for dizzy spells, which have accompanied the previous shots about 14 days after the injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- seasonal allergies - mild at this time of year
- Vorgeschichte
- seasonal allergies
- Andere Medikamente
- Allegra; Singulair generic; fish oil; fluticasone; Preservision/AREDS2 multi; D-3; milk thistle
- Allergien
- perhaps not an allergy, but certainaly an adverse reaction to Clindamycin HCL and to Doxycycline Hyclate
- Vorherige Impfungen
- Dizziness 2 weeks after the first 3 shots
- Staat
- WA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mobility decreased
Pain in extremity
Peripheral swelling
Shoulder injury related to vaccine administration
Symptomtext
Patient (my wife) received 3rd covid shot ( booster shot) in right arm. The pharmacy tech who administered the vaccine was not under any supervision by the pharmacist on duty, nor did the pharmacist have direct line of sign during the vaccine. The patient was also not counseled by the pharmacist on duty about adverse effects or what to expect after. The tech injected the vaccine too high and administered into the shoulder, she didn't find the top of the shoulder joint the acromion and go two fingers widths down and inject into the deltoid. patient started experiencing symptoms within 2-3 hours after the vaccine that where consistent with SIRVA, loss of mobility, extreme pain, swelling redness in the right arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Patient went to see PCP next day 3-16-2022 and was diagnosed with SIRVA.
- Aktuelle Erkrankungen
- none.
- Vorgeschichte
- none.
- Andere Medikamente
- none.
- Allergien
- none.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthritis
Headache
Mobility decreased
Myalgia
Neuralgia
Pain
Symptomtext
Patient experienced severe headache, muscle and nerve shooting pain throughout her entire body, inflamed joints and was not able to get out of bed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None at this time. Patient will contact primary care doctor to schedule appointment soon.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Asthma and Diabetic
- Andere Medikamente
- Cymbalta Votaren gel Trazodone Meloxicam Methocarbamol Propranolol Crestor Tylenol #3 Advair Diskus ProAir HFA Omeprazole Zofran Trulicity Hydroxyzine Micardis Benadryl Pepto Bismo
- Allergien
- Stadol
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Hypertension
Scleroderma renal crisis
Systemic scleroderma
Symptomtext
I have been diagnosed with a very rare autoimmune disease, systemic sclerosis with the variant SRC, which causes periodic high blood pressure events, usually 1 to 4 events per month. I keep a record of all events. The best literature I have seen suggests an 85-90% fatality within 1 year of diagnosis. I was diagnosed 4 years ago and am doing excellent. However, after having an SRC event the day after receiving the 2nd booster, I looked back through my notes and realized that I have had high BP events following all 4 vaccine doses. Most recently, I had an event the day after the 2nd booster vaccine. I also had a high BP event the day after the 3rd Covid-19 vaccine. I also had high BP hours after both the 1st and 2nd vaccine doses, followed by high BP on 3, 4 and 5 days following the 1st dose (noting that it is unprecedented to have a multi-day event). It was only after this 4th dose that I have taken notice of the apparently strong association of all 4 doses with high BP. While I did not definitely associate some of these instances with my disease because of the lack of early symptoms (for some reason, I am able to accurately detect that I will have an onset of an event many hours before I manifest symptoms. I describe this as sensing something is wrong in every cell of my body. I cannot better articulate this), in this particular instance the presence of early morning symptoms on April 1 cause me to identify this day as a Scleroderma Renal Crisis (SRC) event arising from systemic sclerosis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Systemic sclerosis with SRC Crohn's disease/ulcerative colitis Sjogren's probable psoriatic or rheumatoid arthritis
- Andere Medikamente
- -
- Allergien
- sulfamethoxazole and sulfa drugs dairy, soy and many other foods
- Vorherige Impfungen
- see prior note
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Headache
Muscular weakness
Tremor
Visual impairment
Symptomtext
adverse effects happened about 20 minutes after the vaccine. patient experienced severe dizziness (described having squared visions), tremor on all extremities, muscle weakness (caused him to collapse), headache (back of the head)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 13.03.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Dyspnoea
Heart rate
Heart rate increased
Hyperhidrosis
Hypoaesthesia
Symptomtext
Sweating; Numbing of arms and legs; Rapid heart beat; Trouble breathing.; This is a spontaneous report from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 35-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 13Mar2022 at 17:00 (Lot number: FJ9943) at the age of 35 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19?:Yes. Concomitant medication included: FISH OIL. The following information was reported: HYPERHIDROSIS (non-serious) with onset 13Mar2022 at 17:00, outcome "recovered with sequelae" (an unknown date in Mar2022), described as "Sweating"; HYPOAESTHESIA (non-serious) with onset 13Mar2022 at 17:00, outcome "recovered with sequelae" (an unknown date in Mar2022), described as "Numbing of arms and legs"; HEART RATE INCREASED (non-serious) with onset 13Mar2022 at 17:00, outcome "recovered with sequelae" (an unknown date in Mar2022), described as "Rapid heart beat"; DYSPNOEA (non-serious) with onset 13Mar2022 at 17:00, outcome "recovered with sequelae" (an unknown date in Mar2022), described as "Trouble breathing". The events "Sweating", "Numbing of arms and legs", "Rapid heart beat" and "Trouble breathing" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of hyperhidrosis, hypoaesthesia, heart rate increased and dyspnoea. Additional Information: It was reported that the patient didn't take any medications to know about allergies. The patient did not receive any other vaccines within four weeks prior to COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Treatment taken as a result of the reported events included 50mg Benadryl. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220313; Test Name: Heart rate; Result Unstructured Data: Test Result:rapid heart beat; Comments: at 17:00
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes)
- Andere Medikamente
- FISH OIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 13.03.2022
- Beginn
- 13.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Dyspnoea
Heart rate
Heart rate increased
Hyperhidrosis
Hypoaesthesia
Symptomtext
Sweating; Numbing of arms and legs; Rapid heart beat; Trouble breathing.; This is a spontaneous report from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 35-year-old male patient received bnt162b2 (BNT162B2), administered in left arm, administration date 13Mar2022 at 17:00 (Lot number: FJ9943) at the age of 35 years as dose 1, single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19?:Yes. Concomitant medication included: FISH OIL. The following information was reported: HYPERHIDROSIS (non-serious) with onset 13Mar2022 at 17:00, outcome "recovered with sequelae" (an unknown date in Mar2022), described as "Sweating"; HYPOAESTHESIA (non-serious) with onset 13Mar2022 at 17:00, outcome "recovered with sequelae" (an unknown date in Mar2022), described as "Numbing of arms and legs"; HEART RATE INCREASED (non-serious) with onset 13Mar2022 at 17:00, outcome "recovered with sequelae" (an unknown date in Mar2022), described as "Rapid heart beat"; DYSPNOEA (non-serious) with onset 13Mar2022 at 17:00, outcome "recovered with sequelae" (an unknown date in Mar2022), described as "Trouble breathing". The events "Sweating", "Numbing of arms and legs", "Rapid heart beat" and "Trouble breathing" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of hyperhidrosis, hypoaesthesia, heart rate increased and dyspnoea. Additional Information: It was reported that the patient didn't take any medications to know about allergies. The patient did not receive any other vaccines within four weeks prior to COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Treatment taken as a result of the reported events included 50mg Benadryl. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220313; Test Name: Heart rate; Result Unstructured Data: Test Result:rapid heart beat; Comments: at 17:00
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes)
- Andere Medikamente
- FISH OIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 28.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Cold sweat
Dehydration
Diarrhoea
Pyrexia
Symptomtext
COLD SWEATS, FEVER, DEHYDRATION, WEAK, NO ENERGY, DIARRHEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 27.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood urine present
Chest pain
Symptomtext
Bloody urine, sudden onset. Chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None yet.
- Aktuelle Erkrankungen
- POTS
- Vorgeschichte
- POTS
- Andere Medikamente
- Macrobid, Vyvanse, Wellbutrin
- Allergien
- Nougat, Zoloft
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.10.2023
- Impfdatum
- 16.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
None from vaccines except sore arm; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 76-year-old patient received bnt162b2 (BNT162B2), on 16Apr2022 as dose 3 (booster), single (Lot number: FJ9943) for covid-19 immunisation. The patient's relevant medical history included: "Crohn's disease" (unspecified if ongoing); "known allergies: Sulpha" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Pfizer / Biontech COVID-19 vaccine (DOSE 1, SINGLE, Lot number: EL9262), administration date: 22Jan2021, for COVID-19 immunization, reaction: "None from vaccines except sore arm"; Pfizer / Biontech COVID-19 vaccine (DOSE 2, SINGLE, Lot number: EL9266), administration date: 02Feb2021, for COVID-19 immunization, reaction: "None from vaccines except sore arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "recovered" (2022), described as "None from vaccines except sore arm". Therapeutic measures were not taken as a result of pain in extremity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Crohn's disease; Sulfonamide allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.06.2023
- Impfdatum
- 14.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Echocardiogram
Electrocardiogram
Urticaria
Vaccination site reaction
Vaccination site swelling
X-ray
Symptomtext
very severe site reaction; it swelled up very significant swelling; incredible welt; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient received BNT162b2 (BNT162B2), on 14Mar2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 69 years for covid-19 immunisation. The patient's relevant medical history included: "MS", start date: Aug1998 (ongoing); "Immunosupressed" (unspecified if ongoing), notes: has an underlying condition and is immune suppressed. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1; Lot#: EL9263), administration date: 25Jan2021, when the patient was 68-year-old, for COVID-19 immunization, reaction(s): "sore arm", "did not feel 100 percent but felt ok"; BNT162b2 (DOSE 2; Lot#: EN6201), administration date: 15Feb2021, when the patient was 68-year-old, for COVID-19 immunization, reaction(s): "typical sore arm", "did not feel 100 percent"; BNT162b2 (DOSE 3; Lot#: FC3184), administration date: 06Sep2021, when the patient was 68-year-old, for COVID-19 immunization, reaction(s): "typical sore arm", "did not feel 100 percent". The following information was reported: VACCINATION SITE REACTION (non-serious), outcome "unknown", described as "very severe site reaction"; VACCINATION SITE SWELLING (non-serious), outcome "unknown", described as "it swelled up very significant swelling"; URTICARIA (non-serious), outcome "unknown", described as "incredible welt". The events "very severe site reaction", "it swelled up very significant swelling" and "incredible welt" required emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of vaccination site reaction, vaccination site swelling, urticaria.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300214232 Same product, patient, different event, different dose;US-PFIZER INC-202300215225 Same product, patient, different event, different dose;US-PFIZER INC-202300215226 Same product, patient, different event, different dose;US-PFIZER INC-202300215227 Same product, patient, different event, different dose;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood Test; Result Unstructured Data: Test Result:Negative; Test Name: Dima test; Result Unstructured Data: Test Result:Negative; Test Date: 20230523; Test Name: Echo; Result Unstructured Data: Test Result:acute pericarditis; Comments: the echocardiogram confirmed it as acute pericarditis with fluid around her heart. 23May2023 was the echo.; Test Name: EKG; Result Unstructured Data: Test Result:Negative; Test Name: X-Ray; Result Unstructured Data: Test Result:Negative
- Aktuelle Erkrankungen
- MS
- Vorgeschichte
- Medical History/Concurrent Conditions: Immunosuppression (has an underlying condition and is immune suppressed)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 25.05.2023
- Impfdatum
- 18.04.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 166,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bronchitis
Chest X-ray abnormal
Malaise
Oropharyngeal pain
Productive cough
SARS-CoV-2 test negative
Sputum discoloured
Streptococcus test negative
Symptomtext
10/1/2022 I had a sore throat, coughing, spitting clear mucous and was diagnosed with acute Bronchitis. I started an antibiotic and prednisone. I was sick for the entire month of October. Since then, I have been sick two more times with the same symptoms. I was prescribed antibiotics and prednisone for both times. The first night after starting these medications, I wake up soaking wet. Since the 4th vaccination, I have been sick with these symptoms every other month. On 5/22/23 I had a sore throat, nonstop coughing, spitting clear mucous at first then turned yellow. I went to the doctor yesterday. I was tested for Strep. The rapid test was negative, but am still waiting for the results of the one sent off. I was prescribed antibiotics and prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- (?)OCT22 at home COVID test negative; (?)OCT Chest X-Ray, Bronchitis; (?)DEC22 at home COVID test negative (?)FEB23 at home COVID test negative; (?)MAR23 Chest X-Ray, Acute Bronchitis; 24MAY23 at home COVID test negative; 24MAY23 Strep test rapid was negative, waiting results for send off test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; Acid Reflux
- Andere Medikamente
- Omeprazole; amlodipine; pravastatin; low dose aspirin; vitamin D3; cod liver oil; ALPHAGAN eye drops
- Allergien
- Oxycodone; doxycycline; latex; cats
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 22.05.2023
- Impfdatum
- 20.04.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 111,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Arthralgia
Brain fog
COVID-19
Chills
Cough
Decreased appetite
Ear discomfort
Headache
Malaise
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Taste disorder
Symptomtext
On the morning of 8/9/2022, I woke up with sore throat, headache, general body aches and joint aches, a cough, and general malaise. The headache and the joint aches lasted for a couple of days. I coughed for probably two or two and a half weeks. I experienced loss of appetite. I had chills and a low-grade fever of 99 degrees. I took Tylenol, but it didn't help much with the headache, though it did help with the fever and chills. I experienced a slight pressure in the ears and brain fog, which both last concurrently with the cough. On 8/10/2022, I took a home antigen test and got a positive result. I called the doctor's office that day and got a prescription for Paxlovid, which I took for five days. The Paxlovid caused me to have intermittent diarrhea and nausea. On the rare occasions in which I had any appetite, I would eat something as simple as a piece of toast and immediately feel sick afterwards. The doctor also recommended that I take an OTC expectorant for the cough. I took Robitussin DM, which helped. The lack of appetite and upset stomach lasted for about six weeks. Also, some things tasted different than they did before I had COVID-19. Some of the taste changes have persisted to this day. Sweets especially don't taste the same. Sometimes they taste good, but not always. I have more of a normal appetite now, but it took maybe four or five months for it to return.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 10AUG2022 - Home Antigen Test - Positive Result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hashimoto's Disease; Restless Legs Syndrome; Osteoarthritis; Sjogren's Disease; Partial Block in Left Ascending Cardiac Artery (40%); Gastroesophageal Reflux Disease; Depression; Anxiety; Age-Related Macular Degeneration; Low Ferritin; Osteopenia of the Forearm
- Andere Medikamente
- Levothyroxine; Pantoprazole; Atorvastatin; Pramipexole (As Needed); Vitamin C; Ferrous Sulfate; Flonase (As Needed); Meloxicam; TUMS with Calcium; Puritan's Pride Healthy Eyes Lutigold Extra; Vitamin D3; Sertraline; Clonazepam; Tylenol (As
- Allergien
- Wellbutrin; Keflex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 19.03.2022
- Beginn
- 20.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Amino acid level
Anti-cyclic citrullinated peptide antibody
Antibody test
Antinuclear antibody
Arthralgia
Blood creatinine
Blood homocysteine
Blood magnesium
Blood thyroid stimulating hormone
C-reactive protein
Complement analysis
Complement factor C3
Complement factor C4
Differential white blood cell count
Full blood count
HLA marker study
Liver function test
Metabolic function test
Symptomtext
Beginning the day after the booster dose, diffuse widespread joint pain began. Continued to progress with no relief, so made appointment to see my PCP. Ongoing medical appointments since last year and therapies to try and help, with no relief. Now seeing a specialist since the progression has gotten worse. Awaiting PT, PM&R, and currently seeing a rheumatologist. Medical documentation can be provided for all visits.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 10/22/22 CBC w/diff, ANA, TSH, Metabolic Panel, C-reactive protein, RBC, Vitamin D, ESR, Magnesium Serum, Homocysteine, Methylmalonic Acid, Ferritin, Xrays 5/15/23 C-reactive protein, C3 compliment, C4 compliment, CH50 total, CBC, Creatinine, Cyclic Citrullinate peptide antibody, HLA, Liver panel, Rheumatoid factor, Sedimentation rate, SJOGRENS antibody screen. xrays cortisone injections x3
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Rizatriptan
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 30.04.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 220,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Alopecia
Blood test
COVID-19
Computerised tomogram neck
Computerised tomogram thorax
Diagnostic aspiration
Oropharyngeal pain
SARS-CoV-2 test positive
Swelling
Ultrasound scan
Symptomtext
I tested positive for Covid-19 on 11DEC2022. Around 25FEB2023 I started to get a really bad sore throat and loosing a lot of hair. On 08MAR2023 I noticed my neck swelling on 10MAR2023 the left side of my neck blew up the swelling went from left side of the Thyroid and the swelling continued below the sternal notch past the midline and a little bit tot the right with no fever and no problems breathing. 11MAR2023 I went to a local urgent care and CT Scan of the chest and neck with blood work was performed. An Ultrasound was performed on 28MAR2023 and on 03APR2023 fine needle aspirate was performed and the biopsy was benign.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 11DEC2022 COVID-19 test positive. Biopsy benign.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Levothyroxine; NEXIUM; hydrochlorothiazide; phenetamine; dicyclomine; CENTRUM SILVER; CALTRATE; vitamin D; coQ10; ARED 2; biotin; ALEVE
- Allergien
- Penicillin; AUGMENTIN; DEXILANT; PHENERGAN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 30,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood cholesterol increased
Blood glucose increased
Glucose tolerance impaired
Malaise
Myalgia
Symptomtext
On May 22nd of 2022 I felt under the weather and tested positive for COVID-19. My symptoms lasted until May 30th. Since August 2022 I have become pre-diabetic. I have experienced random muscle aches and pains.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Blood tests, cholesterol levels high and blood sugar high, Fall2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multi Vitamin; St. John's Wart; Melatonin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 21.04.2023
- Impfdatum
- 18.04.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 196,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Asthma
Back pain
COVID-19
Chills
Cough
Decreased appetite
Fatigue
Headache
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19. I had severe chills and a fever of 103. Soon after, I developed a cough, severe headache, back pain, fatigue, general weakness all over my body, and a lack of appetite. I spoke to my doctor and she prescribed me PAXLOVID and a back up of antibiotics called ZITHROMAX. COVID-19 also reactivated my asthma as well, so I had to take a nebulizer treatment every 6 hours for a week that was given to me when I went to urgent care. I had a cough, fatigue, and asthma issues for about 6 weeks later but it has now cleared up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- 31Oct2022 home COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure; High cholesterol; Diabetes; Asthma; Chronic Kidney Disease; Gastric reflux; Fibromyalgia; Osteoarthritis; Mild heart attack
- Andere Medikamente
- Baby aspirin; SINGULAIR; losartan; HCTZ; PROTONIX; atorvastatin; iron supplement; B12 supplement; vitamin D; clopidogrel; gabapentin; CLARITIN; tramadol; multivitamin; TYLENOL; ADVAIR inhaler; DILANTIN
- Allergien
- Opiates; beta blockers; figs
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 13.04.2023
- Impfdatum
- 31.03.2022
- Beginn
- 21.02.2023
- Tage bis Beginn
- 327,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Headache
Pain
Symptomtext
My COVID experience started out as a normal headache which lasted the entire time that than became a very bad headache. I also had some body aches and chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Pernicious Anemia
- Andere Medikamente
- Synthroid; Vitamin B-12 Injection; Folate; Iron Tablets; Acyclovir; Fluticasone; Albuterol; Estrate Cream; Celebrex; Gabapentin; Vitamin D; Calcium; MiraLAX
- Allergien
- Nitrofurantoin; Lidocaine; Aspirin; Advil
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 10.04.2023
- Impfdatum
- 07.04.2022
- Beginn
- 28.03.2023
- Tage bis Beginn
- 355,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Nasopharyngitis
Pain
Pyrexia
Respiration abnormal
SARS-CoV-2 test positive
Symptomtext
It started out with head stuffiness, cold symptoms, body aches, and a fever. I didn't get the temperature, but I knew I had a fever and chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 29MAR2023 COVID-19 test positive; 02APR2023 COVID-19 test positive; 04APR2023 COVID-19 test positive; 07APR2023 COVID-19 test positive; 10APR2023 COVID-19 test positive; COVID-19 test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood pressure; PMR
- Andere Medikamente
- ELIQUIS; metformin HCL; amlodipine; CARDURA; HCL; ZETIA; prednisone; amitriptyline HCL; alendronate sodium; fexofenadine
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 07.04.2023
- Impfdatum
- 06.04.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 270,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Nasopharyngitis
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
My COVID-19 infection symptoms started on 01/2023 in the morning. I had fever, chills, body aches, and head cold. It felt like I had a stuffy head. I did 2 COVID-19 home tests on 01/30/2023 which were positive. I called my doctor on the same day and did a telehealth. I was prescribed Paxlovid for 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 30JAN2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Low Thyroid
- Andere Medikamente
- Citalopram; Atorvastatin; Levothyroxine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 01.04.2022
- Beginn
- 18.01.2023
- Tage bis Beginn
- 292,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
Brain fog
COVID-19
Decreased appetite
Fatigue
Headache
Pyrexia
SARS-CoV-2 test positive
Sick relative
Symptomtext
My husband had been sick for three days and I started getting sick so we took COVID-19 Home Tests and we were both positive. I had a fever, I was exhausted, I had a horrible headache for a few days. I had no appetitive and I could not taste or smell anything. I called my health care provider, and they did not give me anything for my positive case. I also had this brain fog that lingered for awhile.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; High Cholesterol
- Andere Medikamente
- Lovastatin; Calcium; Simvastatin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 03.04.2023
- Impfdatum
- 03.03.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood test normal
Brain fog
Cardiac function test normal
Fatigue
Inflammatory marker test
Myalgia
Symptomtext
From the first shot, fatigue, sore muscles and joints, brain fog. starts to get better then I have the next Covid shot and it starts all over again
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Tested for heart problems, inflammatory problems, lots of blood work, everything is always ok
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism Restless legs Hbp
- Andere Medikamente
- Synthroid Levothyroxine Pramipexole
- Allergien
- Penicillin Hydroxychoriquin ( sp ?)
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 07.04.2022
- Beginn
- 03.03.2023
- Tage bis Beginn
- 330,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Nasal congestion
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
On 03/03/2023, in the night, I woke with nasal congestion, sore throat, headache, body aches, very tired. I tested negative on 03/03/2023, I tested positive on 03/06/2023. I had a telehealth appointment that day. She prescribed Paxlovid. I have had lingering fatigue and nasal congestion, but now I am good.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 03MAR2023 - COVID-19 Test- Negative; 06MAR2023 - COVID-19 Test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism; Anxiety
- Andere Medikamente
- L-Thyroxine; Citalopram; Calcium with Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 13.03.2023
- Impfdatum
- 09.03.2021
- Beginn
- 10.03.2023
- Tage bis Beginn
- 731,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Symptomtext
Constant, pervasive fatigue since booster May 5, 2022 and from the 2 injection COVID shots on March 9, 2021 & March 30, 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Celerac Horse dander Seasonal hay feaver
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.02.2023
- Impfdatum
- 12.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
Arm soreness after received the Pfizer COVID 19 Vaccines; 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 received BNT162b2 (BNT162B2), on 12Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 64 years for covid-19 immunisation. The patient had no relevant medical history. The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Lot: ER8733, Expiry/NDC: Unknown), administration date: 02Apr2021, when the patient was 63-year-old, for COVID-19 Immunization, reaction(s): "Arm was sore with all of her Pfizer COVID 19 doses"; BNT162b2 (Dose 2, Lot: EW0173, Expiry/NDC: Unknown), administration date: 30Apr2021, when the patient was 63-year-old, for COVID-19 Immunization, reaction(s): "Arm was sore with all of her Pfizer COVID 19 doses"; BNT162b2 (Dose 3, Lot: FJ8757, Expiry/NDC: Unknown), administration date: 24Nov2021, when the patient was 64-year-old, for COVID-19 Immunization, reaction(s): "Arm was sore with all of her Pfizer COVID 19 doses". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset Apr2022, outcome "recovered" (Apr2022), described as "Arm soreness after received the Pfizer COVID 19 Vaccines". Additional information: No Investigations, Other Products reported. States that she takes vitamins. Normally her arm is sore for a little while, which even happened with the COVID vaccines. Has had multiple family members that have died from Pneumonia. Verifies that her arm was sore with all of her Pfizer COVID-19 doses. States that if you give her any kind of shot, her arm will hurt. Her mother had cancer, and when they did radiation on her, her skin turned green. The doctors took a bunch of pictures and put her in a medical journal. Arm soreness after received the Pfizer COVID-19 Vaccines began the night she received the vaccine and lasted about 2-3 days. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available): None. Additional Vaccines Administered on Same Date of the Pfizer Suspect: If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect: None. Prior Vaccinations (within 4 weeks): If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): None. States that if you give her any kind of shot, her arm will hurt. Each dose was received at a different facility and she doesn't remember where she got which dose. One of the doses was received in a building, and one was in the car at the hospital. If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): None. Family Medical History Relevant to Adverse Events (AEs): None.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cancer (Her mother had cancer, and when they did radiation on her, her skin turned green); Pneumonia (multiple family members that have died from Pneumonia); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.02.2023
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: unbekannt
Immediate post-injection reaction
Injection site mass
Injection site pain
X-ray limb
Pain
Pain of skin
X-ray
Symptomtext
Immediate pain that has never subsided. I have had shoulder muscle pain since the injection and exists today. I can go to the point of injection on my are because pain and a lump navigates me there. I have spent many hours at physical therapy now and visited an orthopediac sports doctor. The sports doctor's solution to my injury was chortizone steroids. Once the chortizone wore off the pain is still there. My primary doctor tried to convince me that I must of injured my shoulder to cause the severity and length of the pain. I thought through my doctor's declaration once I left his office. I thought maybe the pain was not the shot but was prolonged in the spot due to another injury
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Physical therapy from 08012022 till 01012023. Orthopedic doctor two visits 12142022 Exray and chortisone. Follow up visit 01182023.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, Emphysema
- Andere Medikamente
- Metformin, Ventolin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.02.2023
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: unbekannt
Immediate post-injection reaction
Injection site mass
Injection site pain
X-ray limb
Pain
Pain of skin
X-ray
Symptomtext
Immediate pain that has never subsided. I have had shoulder muscle pain since the injection and exists today. I can go to the point of injection on my are because pain and a lump navigates me there. I have spent many hours at physical therapy now and visited an orthopediac sports doctor. The sports doctor's solution to my injury was chortizone steroids. Once the chortizone wore off the pain is still there. My primary doctor tried to convince me that I must of injured my shoulder to cause the severity and length of the pain. I thought through my doctor's declaration once I left his office. I thought maybe the pain was not the shot but was prolonged in the spot due to another injury
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Physical therapy from 08012022 till 01012023. Orthopedic doctor two visits 12142022 Exray and chortisone. Follow up visit 01182023.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, Emphysema
- Andere Medikamente
- Metformin, Ventolin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.02.2023
- Impfdatum
- 24.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: unbekannt
Immediate post-injection reaction
Injection site mass
Injection site pain
X-ray limb
Pain
Pain of skin
X-ray
Symptomtext
Immediate pain that has never subsided. I have had shoulder muscle pain since the injection and exists today. I can go to the point of injection on my are because pain and a lump navigates me there. I have spent many hours at physical therapy now and visited an orthopediac sports doctor. The sports doctor's solution to my injury was chortizone steroids. Once the chortizone wore off the pain is still there. My primary doctor tried to convince me that I must of injured my shoulder to cause the severity and length of the pain. I thought through my doctor's declaration once I left his office. I thought maybe the pain was not the shot but was prolonged in the spot due to another injury
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Physical therapy from 08012022 till 01012023. Orthopedic doctor two visits 12142022 Exray and chortisone. Follow up visit 01182023.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, Emphysema
- Andere Medikamente
- Metformin, Ventolin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 04.01.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 325,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pyrexia
Renal transplant
Symptomtext
11/25/22 presents to ED for "fever". PMHx of "ESRD secondary to FSGS s/p kidney transplant 6 months ago"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 30.04.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 52,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Malaise
Oropharyngeal pain
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
I received my second Pfizer COVID-19 booster on 4/30/2022. At 7 AM on 6/21/2022, I woke up and took a home antigen test, because I had developed symptoms during the night, and the test response was positive. I had a sore throat, sinus congestion, and fatigue. We were on vacation at the time, so we notified the hotel where we were staying, and we agreed that I would self-isolate from my family during my stay there. The first day was the worst, because the sore throat, sinus congestion, and fatigue were especially intense. After the first day, the symptoms gradually improved, though I did develop a mild cough a few days later. The cough lasted for only a couple of days. After the fifth day, I left my isolation. During this time, I didn't really self-medicate much. I just used an OTC nasal spray. I took multiple tests during this time, and the first time I got a negative result was about 7/1/2022. Overall, I made a quick recovery and had no residual symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 6/21/2022 home antigen test positive result; 7/1/2022 home antigen test negative result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Simvastatin; vitamin D; CENTRUM multivitamin; saw palmetto; coQ10.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 06.10.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 48,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asymptomatic COVID-19
Exposure to SARS-CoV-2
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Patient up to date on COVID vaccines who tested detected for COVID during her stay. Patients spouse had been visiting and called to report positive test. Patient with sore throat at time. Received Remdesivir. No hypoxia noted. Asymptomatic at time of d/c.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- 9,0
- Labordaten
- COVID Detected PCR on 11/25/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Hypertension Pure hypercholesterolemia Varicose veins of bilateral lower extremities with other complications Digestive GERD (gastroesophageal reflux disease) Endocrine Other specified hypothyroidism Integumentary Rosacea Staph skin infection Psychological Depression Other Macrocytosis without anemia Other insomnia Arthritis Leg swelling that resolves with lasix Closed nondisplaced fracture of right pubis with routine healing Closed stable burst fracture of fifth lumbar vertebra with routine healing Fall from ground level
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 29.11.2022
- Impfdatum
- 01.05.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Malaise
Oropharyngeal pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptom recurrence
Symptomtext
About two months after getting vaccine I tested positive for COVID. Began feeling ill on 07/27 and tested positive on morning of 07/28 on at home test. I had fatigue, aches, pains. Called PCP and was prescribed PAXLOVID which I began taking that evening. 07/29 added fever, cough, congestion, and sore throat to symptoms. 07/30 symptoms continued except for fever. By 08/03 still experiencing fatigue and lingering cough. 08/05 had negative COVID-19 test. On 06/11 symptoms returned and I retested, testing positive. My final negative was 08/20.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home test x 4, 2 positive and two negative.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Enlarged prostate; glaucoma
- Andere Medikamente
- PROSPAR; LUMIGAN eye drops for glaucoma; multivitamin; FLOWMAX
- Allergien
- No
- Vorherige Impfungen
- 05/2021 Shingrix vaccine, spent two days in bed.
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 16.06.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 89,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Feeling hot
Gait inability
Magnetic resonance imaging abnormal
Meniscus injury
Oedema
Pain
Scan with contrast abnormal
Wheelchair user
Symptomtext
I noticed while on vacation I started hurting and it got to the point that I could not walk. I ended up in a wheelchair and ended my vacation early. It felt like I had hot marbles going up and down left leg. I went to the emergency room where they did an MRI with and without contrast. I have had a gel shot in my left knee. I am scheduled to go in for my right knee so I can get the MRI with and without contrast and get the gel shot in it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- MRI with and without contrast, complex tear of the meniscus, mild subcutaneous edema.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Dry AMB; Obesity; RND Positive; Oral Lesion; Sleep Apnea; Anemic; Arthritis
- Andere Medikamente
- Vitamin D; iron; multivitamin; iron infusions; B-12 injections
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 07.11.2022
- Impfdatum
- 29.04.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 126,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
No adverse event
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
No adverse effects from the vaccination. Tested positive to COVID 09/02/2022. Very minor symptoms. Runny nose, slight sore throat. Prescribed Paxlovid. Symptoms gone in less than a day. Tested positive again 3 days after final Paxlovid dose. Again, very minor symptoms gone the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Home COVID tests between 9/2/2022 and 9/18/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Atorvastatin (20mg), Exforge (5/320),
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 29.10.2022
- Impfdatum
- 22.09.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
COVID-19
Cough
Fatigue
Headache
Influenza like illness
Liver function test
Nasal congestion
Nasopharyngitis
Oropharyngeal pain
Pain
Renal function test
SARS-CoV-2 test positive
Sneezing
Symptomtext
Tested positive for COVID 19 on 10/22/2022. Started Paxlovid afternoon of 10/22/2022. Experience cold and flu like symptoms: sore throat, fatigue, cough, achiness, headache, sneezing, nasal congestion. Symptoms generally resolved after 5 days with only mild headache and cough remaining. Negative tests on 10/27/2022, 10/28/2022 and 10/29/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Blood tests to check kidney and liver functions.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amlodopine, calcium, multivitamin, vitamin D, Tumeric, Flax seed oil
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 23.04.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 152,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Feeling abnormal
Headache
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
I had sore throat and headache for the first two days. Then I had congestion and fatigue for the next 5 days. Then the congestion started to break after a week, and all the symptoms started to gradually reduce after week. I took over the counter cold medication, acetaminophen, and ibuprofen. I also had head fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 09/23/2022 COVID-19 test negative; 09/24/2022 COVID-19 test negative; 09/26/2022 COVID-19 test positive; 09/27/2022 PCR COVID-19 test positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Cholesterol
- Andere Medikamente
- Atorvastatin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 10.04.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 159,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchitis
COVID-19
Chills
Cough
Feeling abnormal
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Vomiting
Symptomtext
On 9/16/2022 I had a sore throat and a cough. I felt a little achy like a cold or flu was coming on. I threw up a little bit, fever 102 +, and chills. I just did not feel good at all. It lasted for a good day and a half. On Sunday, 9/18/22, I started feeling a little bit better. I called my doctor on Monday he prescribed antibiotics, BIAXIN, and steroids, prednisone. Typically, I develop bronchitis and I was trying to get ahead of it. I was prescribed antibiotics, Z-PAK and another course of steroids, prednisone by another allergist, 10/18/2022. The steroids I am still taking the prednisone until I am done. I have 2 days' worth. The only symptom remaining is the cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test over a period of 10 days, I remained positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- None
- Andere Medikamente
- ALLEGRA; losartan; tamsulosin; tadalafil; ARNUITY inhaler; TYLENOL; AIRBORNE gummies; FIBER WELL gummies; vitamin D3
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 67,0
- Geschlecht
- U
- Eingang
- 21.10.2022
- Impfdatum
- 19.04.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 130,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal discomfort
COVID-19
Diarrhoea
Ear infection
Fatigue
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Sinusitis
Symptomtext
I started with a sore throat, fatigue, headache. I also had upset stomach and diarrhea. I tested myself 3 times before finally testing positive on September 02, 2022. 5 or 6 days into it, I went to an urgent care clinic on September 07, 2022. I had developed and ear and sinus infection and was given Doxycycline. I took acetaminophen for my headache. It took me up until September 10 to start to feel better, but I was still having some ear and sinus issues. By September 14 I had completely recovered from all symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID 19 Home Test-August 31, 2022-Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Sinusitis; Hypertension
- Andere Medikamente
- Losartan; Multi-Vitamin; Alendronate; Fluticasone; Mucinex; Calcium with Vitamin D; Zinc
- Allergien
- Penicillin; Environmental Allergies
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 14.04.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 162,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cough
Fatigue
Oropharyngeal pain
Symptomtext
Symptoms: sore throat, fatigue, cough, chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cancer - tumor on right kidney - in remission. Diagnosed June 2015.
- Andere Medikamente
- Atorvastatin Tabs 20 mg, L-Thyroxine 112 mg, NIFEdipine CC 30mg, Famotidine Tabs 20 mg I received the 3rd Covid booster on 10/19/2022.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 14.04.2022
- Beginn
- 17.09.2022
- Tage bis Beginn
- 156,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Coughing, sore throat, fatigue, fever 99 degrees, lasted about 5 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Still coughing but less and less as time goes by.
- Andere Medikamente
- Finestride 5mg 1 tab per day Metoprolol 25 mg 1 tab twice a day Tansulosin 0.4 mg 1 cap per day L-Thyroxine 75 mcg. 1 tab per day Eliquis 5 mg 1 tab twice a day Vitamin D 3 1 tab per day Tears received 3rd booster 10/19/22
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 14.10.2022
- Impfdatum
- 14.04.2022
- Beginn
- 02.10.2022
- Tage bis Beginn
- 171,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
COVID-19
Cough
Drainage
Fatigue
Pain
Pulmonary congestion
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
On 10/2/2022 my symptoms were draining into my throat, a bit of a cough, and later in the day congestion and body aches. I took a COVID-19 home test on 10/2/2022 and it was negative. The next day, 10/3/2022, I felt worse, and I tested again, and it was positive. I had a fever, chest congestion, stomach upset, and fatigue. I sent my doctor a message on 10/3/2022 that I had tested positive, and she said she wanted to do a video call with me on 10/4/2022. The doctor felt that I had a lot of symptoms, and she was going to put me on PAXLOVID. But because of my liver problems she decided that was not a good medication to take. So, she prescribed molnupiravir. I started taking the medication on 10/4 in the evening and I took the last dose on the morning of 10/9. When I stopped taking the medication my symptoms had decreased. I tested on 10/10/22 and the results were negative. Then I had a rebound, I tested positive on 10/11/2022 and the results were positive. Today, 10/14/2022 I have a congestion and a little bit of a cough and fatigue, and I tend to have an upset stomach.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Fatty liver disease
- Andere Medikamente
- ALIGN probiotic; omega 3; HELIOCARE advance
- Allergien
- Penicillin; fenofibrate
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 02.04.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 104,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Irritability
SARS-CoV-2 test positive
Symptomtext
On 7/15/2022- I had awful cough, fatigue, and very grumpy. On 7/15/2022, I took a home test COVID-19 and it was positive. I called health line, they called in a prescription. They prescribed a medication that started with an "M". It was not Paxlovid. I started feeling better after a couple of days after taking the prescription. I did not feel horrible. I just had a bad cough and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 7/15/2022- COVID-19 home test- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- asthma; Type 2 Diabetes; overweight; high blood pressure
- Andere Medikamente
- Metformin; Montelukast; Crestor; Levocetirizine; Losartan; Dulera; glucosamine; A Red; turmeric; vitamin D; Ginger; Magnesium; Probiotic; Mometasone Furoate
- Allergien
- mint; Penicillin
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 09.04.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Feeling abnormal
Headache
Malaise
SARS-CoV-2 test positive
Symptomtext
For three days I felt ill, I tested using the home COVID-19 test but it came back negative every time. On day four it came back positive, I called my PCP and asked if I should start on any of the antiviral medications. They did not suggest them since I was not that sick. I am feeling better with the exception that I do still get a headache most every day and have lingering brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Home COVID-19
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Atorvastatin; Tamsulosin; Synthroid; Pepcid; Propranolol ER;
- Allergien
- Percocet; Oxycontin; Betadine
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 06.04.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 87,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Body temperature increased
COVID-19
Feeling abnormal
Lacrimation increased
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Sinusitis
Symptomtext
The first day I had runny nose and runny eyes. The next day I was achy and had a temperature. I just felt really crappy. The hospital said I had a bit of a sinus infection. I ended up going to the ER twice.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test- Positive; PCR COVID-19 test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Thyroid issue; Atrial Fibrillation; Low red blood count
- Andere Medikamente
- Magnesium; Riboflavin; Iron; B-12 shot; Levothyroxine; Sotalol; Eliquis; Valtrex; Vitamin D3; Lynparza
- Allergien
- Sulfites; Walnuts; Aged Cheese
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 07.04.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 169,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Decreased appetite
Feeling abnormal
Feeling of body temperature change
Headache
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sinus congestion
Sinus operation
Symptomtext
I received my second Pfizer booster for COVID-19 on 4/7/2022. On the night of 9/23/2022, I began having a lot of head congestion, a severe headache, and a runny nose. I had been outside working in the yard earlier that day, so I figured that maybe I just had an allergy. On 9/24/2022, I felt worse. I had no appetite, and I still had a lot of head congestion, a headache, and sinus drainage. I also felt a strange sensation of being hot and cold at the same time. I took a home test and got a positive result. I had a fever that may have been about 101. I just drank cold water from the refrigerator. When I woke up on the morning of 9/25/2022, the fever was gone. However, the fever returned later that day. During this entire time, my severe headache persisted; I took Tylenol, but it didn't get rid of the pain. I also still had the head congestion and drainage. On 9/26/2022, I called my doctor's office and had a telehealth visit with his PA, who prescribed me Paxlovid, which I started taking that evening. I still had some fever on the night of 9/26/2022, but the fever went away that night and never returned. On 9/27/2022, I felt much better. The fever was gone, the congestion and drainage had improved greatly, and the headache was gone. While I was on the Paxlovid, the drainage seemed to almost be completely gone. At the time of this writing, though, I still have a little bit of residual congestion and drainage, but it's not major. For all I know, they could be due to hay fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test--9/24/2022--Positive Result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension.
- Andere Medikamente
- Losartan; Tylenol (As Needed).
- Allergien
- Sulfa Drugs; Skin Sensitivity to Some Chemicals in Cosmetics, Skin Creams, and Hair Products.
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 27.04.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 134,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I received my second Pfizer booster for COVID-19 on 4/27/2022. I traveled to an international airport on 9/6/2022 on a domestic flight. Of course, there is no way to be certain that this is when and where I came into contact with COVID-19, but I strongly suspect it. On the morning of 9/8/2022, I was experiencing symptoms that included runny nose, a mild fever, and dry cough. I went to an urgent care to get a rapid test, and the result was negative. The symptoms continued to develop and would not go away. On 9/10/2022, I took a home test, which yielded a positive result. I then did a telehealth visit with the urgent care and informed them of my test result, and they immediately prescribed me PAXLOVID. I began taking PAXLOVID on 9/10/2022. Within 24 hours of starting it, the symptoms subsided substantially. I finished the 5-day course and was completely symptom-free by the end of the course. About 2-3 days later, I took another home test and got a negative result. Since then, I have not had any residual issues, and I believe starting the PAXLOVID early helped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 9/8/2022 urgent care rapid test, negative result; 9/10/2022 home test, positive result; later home test (date uncertain), negative result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension; Type II Diabetes; Borderline Hypercholesterolemia.
- Andere Medikamente
- Amlodipine; telmisartan hydrochlorothiazide; baby aspirin; CENTRUM for men 55+; vitamin D; metformin; fenofibrate; FARXIGA.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 05.04.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 139,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
COVID-19
Dizziness
Fatigue
Feeling abnormal
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
08/22/2022 around noon I didn't feel good and by evening I felt congestions. On 08/23/2022 I felt fever, body aches, congestions in my throat and chest, fatigue. I felt like I had the worst flu ever. I test positive on the 08/23/2022. I went to the urgent care on 08/24/2022 I asked about the medication side affects I got the prescription but I never got it filled out because I was worried about the rebound. I drank a lot of fluids and I took rest for my symptoms. I am still experiencing tiredness, balance issue, fatigued and dizziness so I went to a neurologist on Friday 09/30/2022 just to make sure if something else wasn't affecting me or my health.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test- Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid; Hypertension; Fibular neuritis; GERD
- Andere Medikamente
- Does not want to disclose
- Allergien
- Sulfa; Morphin; Codeine; Zosyn
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 04.04.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
COVID-19
Chills
Cough
Fatigue
Injection site pain
Malaise
Pain
SARS-CoV-2 test positive
Throat irritation
Symptomtext
On 4/4/22 that evening and the next day I had a mild elevation in my temperature, I felt fatigue, chills and a little achy. I had a little soreness at the site of the injection, but no swelling or redness. It lasted about 36 hours. On 6/22/2022, it started with a little dry cough. That night I had a scratchy throat. The next morning the cough was worse, the throat was worse, and I started feeling achy and generally sick. On 6/23/2022 I took a at home antigen test, and it was positive. I called my doctor, and he prescribed me Paxlovid. It took me around 4 or 5 days to completely recover.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 6/23/2022 - at home test antigen test- positive
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- hypertension; paroxysmal atrial fibrillation; elevated cholesterol
- Andere Medikamente
- Lisinopril; Rosuvastatin; Aspirin; CoEnzymeQ10; Nature made stress vitamins B12; multivitamins; vitamin C 500mg; Vitamin D
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 04.04.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 173,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Blood test normal
COVID-19
Cough
Diarrhoea
SARS-CoV-2 test positive
Vomiting
X-ray normal
Symptomtext
First I was constantly coughing all night long. had a dry hack for the whole night. I thought it was a cold because that night I tested negative. The following day my son said I need to get Paxlovid so I had to go to the emergency room. They did blood, work, x-ray, oxygen test, blood pressure. All the tests came back fine. They tested for COVID-19 and that came back positive. I took the medicine but I ended up vomiting them back up. It was perfuse, it lasted the rest of the afternoon. I was given a nausea medicine, Ondansetron, to keep the medication down. I also had diarehea. I didn't have a fever. I was told to check after 5 days to see if I was still positive. My whole abdomen was aching from coughing so much.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Blood work; X-ray; Oxygen; COVID-19 test- Negative; COVID-19 test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 31.03.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 101,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
SARS-CoV-2 test positive
Symptomtext
About 4 months after the third dose of my COVID-19 vaccine my wife had tested Positive for Covid-19 and then I came down with it. I had a cough and some fatigue. I was prescribed Paxlovid immediately after testing positive at a clinic. I started to feel better pretty quickly. I tested negative after five days. About five days after testing negative my symptoms rebounded and they were little more severe, but they were still relatively moderate. I took some decongestant and a cough suppressant and I recovered after about a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Simvastatin
- Allergien
- Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 15.04.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 161,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest discomfort
Cough
Fatigue
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
Sneezing, running nose, tight chest, no fever, painful coughing, and tiredness. Symptoms were mild. I contacted the doctor and she wrote me a script for PAXLOVID for 5 days. I've completed the meds and feel normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Insulin; PRILOSEC; aspirin; supplements
- Allergien
- Statins
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 26.09.2022
- Impfdatum
- 01.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy
Burning sensation
Rash
Rash pruritic
Symptomtext
A couple days after my vaccine I broke out . It went into my back, legs, scalp and it burns and itches. I went to my primary care doctor and they put me on prednisone for five days and the seemed to ease the itching, but when I went off the medication it came right back. Then, I went to a dermatologist and she prescribed three different ointments and they didn't do any good. Then, she gave me a steroid shot and put me on a new medication, acitretin, which is very pricy. She said that it would take a little while for the medication to start working because it has to build up in my system before it will start working.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Biopsy- 3/07/22- Came back as having Grover's Disease.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Grover's Disease; High Blood Pressure; Hypothyroidism
- Andere Medikamente
- Benazepril; Amlodipine; Doxazosin; Chlorthalidone; Omeprazole; Levothyroxine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 31.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Pyrexia
Symptomtext
fever; chills; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 80-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31Mar2022 at 10:00 as dose 4 (booster), single (Lot number: FJ9943), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Thyroid issues" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Vascular issues with stents" (unspecified if ongoing); "Seafood" (unspecified if ongoing), notes: Known allergies : Seafood. Concomitant medication(s) included: TOPROL XL; LISINOPRIL; BABY ASPIRIN; SYNTHROID; Z-PAK. Past drug history included: Mycins, reaction(s): "Drug allergy", notes: Known allergies : Yes many meds (most mycins). Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EL9263, Anatomical location: Arm Left), administration date: 27Jan2021, when the patient was 78-year-old, for COVID-19 immunisation, reaction(s): "sore arm"; BNT162b2 (DOSE 2, SINGLE; Lot number: EL9267, Anatomical location: Arm Left), administration date: 17Feb2021, when the patient was 78-year-old, for COVID-19 immunisation, reaction(s): "sore arm"; BNT162b2 (DOSE 3 (BOOSTER) SINGLE; Lot number: FC3184, Anatomical location: Arm Left), administration date: 25Aug2021, when the patient was 79-year-old, for COVID-19 immunisation, reaction(s): "Chills", "Fever". The following information was reported: CHILLS (non-serious) with onset 2022, outcome "recovered" (2022); PYREXIA (non-serious) with onset 2022, outcome "recovered" (2022), described as "fever". Therapeutic measures were taken as a result of pyrexia, chills that included Tylenol. Additional information: The patient did not receive any other vaccine within the four weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID -19. Around 10 hours after vaccination dose 5, the patient awoke with fever and chills which lasted around 10 to 12 hours and which responded to Tylenol. Exact same response for vaccination dose 4. With dose 3, was more intense and same symptoms lasted for 3 days. Oddly no after effect other than sore arm for dose 1 or dose 2. Since the vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension; Seafood allergy (Known allergies : Seafood); Thyroid disorder; Vascular disorder
- Andere Medikamente
- TOPROL XL; LISINOPRIL; BABY ASPIRIN; SYNTHROID; Z-PAK
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 06.02.2021
- Beginn
- 29.08.2022
- Tage bis Beginn
- 569,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Fatigue
Laboratory test abnormal
SARS-CoV-2 test positive
Symptomtext
08/29/2022 presented to ED for abnormal lab values and fatigue. PMHx of breast cancer and multiple myeloma.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 08/29/2022 SARS-CoV-2 (COVID-19) by NAA detected.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 06.03.2021
- Beginn
- 02.08.2022
- Tage bis Beginn
- 514,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal distension
Abdominal pain
COVID-19
Chills
Computerised tomogram abdomen
Constipation
Gastrointestinal tube insertion
Nausea
SARS-CoV-2 test positive
Small intestinal obstruction
Vomiting
Symptomtext
Patient is a 66-year-old male with PMH significant for IBS, open b/l inguinal hernia repair, and prostate cancer s/p robotic prostatectomy who presented to ER for abdominal pain with associated constipation, bloating, nausea, chills and vomiting on 8/2/2022. In the ED, the patient was afebrile and hemodynamically stable. CT A/P demonstrated small bowel obstruction with transition in the TI and an additional 1 or 2 foci of caliber transition of small bowel. NGT was placed and pain medications given. Patient was admitted to general surgery service for medical management of SBO with isolation precautions due to having tested positive for COVID-19 on 7/29/2022. NGT output monitored. On 8/3/2022, NGT was removed. Diet advanced to which patient tolerated well. Discharge instructions reviewed. Was given instructions to follow up as indicated. Reference chart for further information. To be sent home with instructions to drink lots of water and continue daily Miralax.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 2,0
- Labordaten
- 8/2 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 28.03.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 132,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had a very mild fever for 12 hours. I continued testing positive for the week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 - positive on 08/07/2022
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Aspirin exasperated respiratory disease; TRIAD asthma
- Andere Medikamente
- Dupilumab injection; allergy shots; cetirizine; montelukast; birth control; ADDERALL
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 29.04.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 117,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
COVID-19
Nausea
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
reports sx of sore throat, nausea, and stomach ache started 8/22/2022- tested positive for covid 8/24/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- rapid antigen test positive for covid 8/24/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 01.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Headache
Pain in extremity
Symptomtext
COVID positive after vaccination; COVID positive after vaccination; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient received BNT162b2 (BNT162B2), on 21Feb2021 as dose 1, single (Lot number: EN5318), on 16Mar2021 as dose 2, single (Lot number: EN6205), on 18Aug2021 as dose 3 (booster), single (Lot number: FA7484) and on 01Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 70 years, in left arm for covid-19 immunisation. No additional vaccines administered on same date of the Pfizer suspect. No other vaccinations within four weeks prior to the first administration date of the suspect vaccine. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID positive after vaccination". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: unknown, notes: Tested herself for COVID using Binax antigen home tests; positive, notes: received Paxlovid treatment; It was all fine It was all fine, notes: She did travel over seas this past spring and had to have an antigen test. Therapeutic measures were taken as a result of vaccination failure, covid-19 (Paxlovid, 24Jul2022 to 28Jul2022).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Name: Binex antigen home tests; Result Unstructured Data: Test Result:unknown; Comments: Tested herself for COVID using Binax antigen home tests; Test Name: covid-19; Test Result: Positive ; Comments: received Paxlovid treatment; Test Name: COVID-19 antigen test; Result Unstructured Data: Test Result:It was all fine; Comments: She did travel over seas this past spring and had to have an antigen test.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 29.05.2022
- Beginn
- 06.08.2022
- Tage bis Beginn
- 69,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Throat irritation
Vaccine breakthrough infection
Symptomtext
Breakthrough case of COVID-19; on August 6, 2022 I woke up fine and then after moving around a bit my throat got scratchy and sore, and I took a COVID-19 home test and it was positive and I called my Dr. and they prescribed the PAXLOVID. I had a slight headache, a dry cough and very tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test -positive August 6, 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Asthma; Overweight; Cancer Survivor.
- Andere Medikamente
- Alendronate; amitriptyline; cetirizine; vitamin B12; vitamin D3; fluticasone propionate diskus; levothyroxine; losartan; magnesium; montelukast; fish oil; potassium; pregabalin; topiramate; triamterene hydrochlorothiazide; warfarin.
- Allergien
- Walnuts; ZOFRAN; codeine; sulfa drugs; penicillin; cephalosporins; NEOSPORIN; adhesives.
- Vorherige Impfungen
- Swine Flu in 1977 I was extremely ill, I lost motor function and ran an extremely high fever.
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 21.04.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal distension
Arthralgia
Asthenia
COVID-19
Decreased appetite
Diarrhoea
Fatigue
Headache
Illness
Nausea
SARS-CoV-2 test positive
Weight decreased
Symptomtext
I received my second Pfizer booster for COVID-19 on 4/21/2022. On 7/8/2022, I began feeling bloated, nauseous, and tired. These symptoms continued for about a week and they worsened during this period. On 7/9/2022, I developed a headache and joint pains. The bloating was pretty significant; I looked about 5 months pregnant, and I'm normally pretty slim. I also experienced a loss of appetite, which I didn't regain until about 7/16/2022. On 7/10/2022, I had loose stools, though I wouldn't classify them as diarrhea. On 7/11/2022, though, I experienced diarrhea multiple times. The diarrhea continued off and on until about 7/15/2022. The headaches, bloating, joint pain, and fatigue continued. On 7/11/2022, I took a home test for COVID-19, and I got a positive result. I called my doctor's office that day and had a telemedicine visit with a nurse practitioner, who prescribed me molnupiravir. I started the molnupiravir that evening, and I also took OTC Tylenol to help with the headache and joint pain. The Tylenol provided some relief for the headache and joint pain, but it didn't eliminate them completely. As I was taking the molnupiravir for the prescribed 5 days, my symptoms gradually improved. The bloating became less pronounced and painful. The headache gradually diminished over a couple of days until it was finally gone. The joint pain went away within the day I started taking the antiviral. The diarrhea also resolved within a couple of days after I started taking the molnupiravir. I just gradually got better and was eventually able to return to my normal activities. I took another home test for COVID-19 on 7/16/2022, and the result was negative. During my illness, I lost 4 lbs. I had to gradually rebuild my strength after my recovery, and at the time of this writing, I feel that I have completely recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 7/11/2022--Home COVID-19 Test--Positive Result; 7/16/2022--Home COVID-19 Test--Negative Result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Oral Esophageal Cancer (In Remission); Acid Reflux Disease; Atopic Dermatitis.
- Andere Medikamente
- Pantoprazole; Montelukast; Clobetasol Propionate Ointment; Tylenol; Vitamin B; Vitamin C; Vitamin D3; Vitamin A; Omega 3 Fish Oil; Red Yeast Rice with CoQ10; Pepcid AC.
- Allergien
- Penicillin; Fluticasone; Carmine; Cocamidopropyl Betaine; Ethyl Acrylate; Formaldehyde; Nickel Sulfate; Potassium Dichromate.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 29.04.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 84,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Fatigue
Nasal congestion
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sneezing
Symptomtext
Starting 07/22/2022, in the morning, I had a sore throat, nasal congestion, low grade fever and chills. I tested myself with an at-home COVID-19 test on 07/23/2022 which was negative. I went the same day to the pharmacy to get tested and the PCR test came back positive on 07/24/2022. I called my doctor and they prescribed me a 5 day course of prednisone. They didn't think I was sick enough for PAXLOVID. The fever lasted for a few more days then stopped. The sneezing basically stopped within a day of taking the prednisone. The past couple of days I have felt pretty much normal except some slight fatigue. I have had no real respiratory symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- At-home COVID (07/23/2022): negative; COVID-19 PCR test (07/23/2022): positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Atenolol; WELLBUTRIN; vitamin D; vitamin C; magnesium; calcium
- Allergien
- None
- Vorherige Impfungen
- I felt sick for about 24 hours after each COVID-19 vaccine
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 27.04.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 69,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
COVID-19
Cough
Diarrhoea
Feeling abnormal
Pain
SARS-CoV-2 test positive
Sinusitis
Symptomtext
On July 5th I woke up feeling not good and having diarrhea with stomach cramps with aches and pains. I tested negative this day. Two days later I still had those symptoms but now had sore throat and dry cough. Tested positive July 7th. I had a PCR test on same day and it was positive. That same day I called my doctor to see about PAXLOVID. We decided that I wouldn't take it because of drug interactions with current medications. (Amoxicillin and prednisone for continued sinus infections). I isolated at home. After another couple of days I was feeling better but still had cough and sore throat. This continued until the 6th day after the first symptom. As of July 14 I was symptom free.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- Home COVID-19, positive; PCR, positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Mild Asthma; Post Heart Attack
- Andere Medikamente
- FLONASE; ALVESCO; spironolactone; metoprolol; atorvastatin; aspirin; ALLEGRA; multivitamin; biotin
- Allergien
- Seasonal to trees; grasses; sulfa
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 26.04.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
COVID-19
Headache
Paranasal sinus discomfort
SARS-CoV-2 test positive
Symptomtext
I woke up on the morning of the 06/15/2022 with a really bad headache and sinus pressure. So I had a over the counter test that I administered and it tested positive. I quarantined on a ship for 5 days that I was on. When I got off the ship I stayed in a hotel and then went to a urgent care who recommended I go to the hospital to get PAXLOVID. I got it filled at the hospital and took the PAXLOVID for 5 days. After 11 days I finally tested negative. After the first 3 days my symptoms went away. I haven't had any problems since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Blood test - 06/28/2022.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- PAXLOVID; vitamin B; vitamin D3; berberine; ALLEGRA.
- Allergien
- Sulfa.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Sore throat, cough, fatigue. Cough and Lasted 3 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test strip positive. Tested 3 times.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Atrial Fibrillation
- Andere Medikamente
- Xarelto, Plavix, Metformin. B12, Tylenol as needed
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Bone densitometry
Gait disturbance
Joint swelling
Musculoskeletal stiffness
Pain
Posture abnormal
Walking aid user
Symptomtext
About a week after my shot I was feeling really sore and stiff. I could hardly walk and was bent over and in pain and was taking OTC medications to help with the pain. I was having to hold onto things as I was walking because I was having such a hard time. I had a trip planned and I took my cane because I could not walk and move as normal. My family was concerned because I was so unstable. I saw my PCP and he is having me get a bone and density test. My knee has also been swelling and that is not normal at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- DXA Bone Density Test on 07/27/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Valsartan HCTZ; Amlodipine; Lorazepam; Tylenol
- Allergien
- Cymbalta; Lyrica; NSAIDS
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 67,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cough
Headache
Oropharyngeal pain
Pyrexia
Secretion discharge
Symptomtext
I had a fever at first. It was low grade. I had a sore throat for two days and a vague headache. I had no respiratory problems except a cough. I had low energy for a week. By July 2nd, I felt good. We contacted our doctor. Our doctor prescribed PAXLOVID. The only side effect I had was a very funny taste in the mouth for the five days. I had mucus in the throat for a couple of weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ezetimibe; RESTASIS; calcium; vitamin B12; vitamin D3
- Allergien
- Aspirin; ibuprofen
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 20.04.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Extra dose administered
Fatigue
Headache
Malaise
Pain
SARS-CoV-2 test positive
Sleep disorder
Symptomtext
Tested positive for COVID-19 on 06/09/2022. I received my 4th dose on 04/20/2022 and my COVID-19 symptoms stated on the morning around 06:00AM. I woke up with a severe headaches; body aches; tiredness. I called nurse practitioner on the same day 06/09/2022 and she prescribed PAXLOVID for 5 days. I went to the ER for COVID test which was positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID19 test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Antiestrogen; letrozole; vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 60,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Head discomfort
Headache
Paranasal sinus discomfort
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On 6-18, 2022 I started having sinus pressure and headache. The following day, 6-19-2022, I woke up with head congestion, a dry cough and fatigue. I used a Covid19 home test with positive results. My doctors office was closed 6-20 so I called them on 6-21 and they ordered a prescription for PAXLOVID. I started taking the medication on the same day. I was also taking OTC DAYQUIL severe. I am recovered. I am reporting a breakthrough case of Covid19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 6-19-2022 Covid19 home test with positive results. 6-24-2022 Covid19 home test with positive results. 6-26-2022 Covid19 home test with negative results.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cold Urticaria; Osteoarthritis
- Andere Medikamente
- Omeprazole; alendronate; vit D supplement, METAMUCIL
- Allergien
- Cold water; possibly allergy to sulfa drugs; iodine
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 67,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Fatigue
Headache
Odynophagia
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
On June 25, 2022, it started with sore throat, headache and minor body aches. I was very tired. I tested at home for COVID-19 and it was positive. I never got fever. We waited until Monday June 27, 2022, to call the doctor and got PAXLOVID. Then my symptoms were feeling better actually before PAXLOVID. My worst day was Saturday through Sunday. My worse symptom was the sore throat, just painful to swallow like razor blades. I also had a dry cough at night. The fatigue and lack of stamina lasted the longest. I believe I didn't regain my strength July 13, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lisinopril; tramadol; mirtazapine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 75,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Fatigue
Headache
Pain
Pyrexia
Symptomtext
I had fever, body aches, fatigue, cough, and infrequent headaches which only lasted for about 5 days i was prescribed the antiviral medications Paxlovid for my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Losartin; atorvastin; hydrochlorothiazide; aspirin; prilosec; vitamin b 12
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 79,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Head discomfort
Headache
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Symptoms: scracthy throat, headache, fever, stuffy head, lack of energy Time course: 2 days from symptoms until fever broke and symptoms began to go away Treatment: Dr. prescribed 5 days of Paxlovid and treatment completed Note: Symptoms were already diminishing greatly by time I was able to meet with Dr. and began Paxlovid treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- At home Covid test, 6/18/2022 - positive At home Covid test, 6/24/2022 - negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Atorvastatin, Benazepril, Vitamin D3, CoQ10
- Allergien
- Penicillin family
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 10.04.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 90,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
COVID-19
Cough
Exposure to SARS-CoV-2
Fatigue
Headache
SARS-CoV-2 test positive
Sinus congestion
Vaccine breakthrough infection
Vertigo
Symptomtext
On 7-9-2022, several family members tested positive for Covid19 so I tested using a home kit for Covid 19 with a positive result. I had no symptoms at this time. I went to the urgent care to get medication. They tested me at the urgent care with a positive result. The Physicians Assistant prescribed Paxlovid. I started taking it that day. I did start having a cough, head congestion, fatigue, vertigo, backache and a headache on 7-10. I am feeling better but still have fatigue and head congestion. I am reporting a breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- 7-9-2022 home Covid19 test with positive result 7-9-2022 Urgent Care with positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure, Hyperlipidemia; GERD; "slight kidney problem"(name unknown); "heart condition with too much calcium in my veins"; Irritable Bowel Syndrome
- Andere Medikamente
- Lisinopril/HCTZ; Ezetimibe; Tricor; Lansoprazole; Potassium chloride, Procardia XL; Topamax; Amitriptyline; Lunesta; Fioricet; Acetaminophen; Aspirin; Vit B6; Vit C; Vit D3
- Allergien
- Sulfa drugs; Clarithromycin
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 75,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Decreased appetite
Fatigue
Feeling cold
Headache
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Taste disorder
Vaccine breakthrough infection
Vertigo
Symptomtext
On 6-28, 2022, I had a headache, vertigo, fatigue, weakness and felt very cold (did not check temp). I took tylenol ES and went to bed. On 6-29, I continued to have the headache and weakness, a cough, runny/stuffy nose, poor appetite and sense of taste was altered. I did an at home Covid 19 test and it was immediately positive. I called the doctors office and scheduled an appointment for the next day. On 6-30, I was feeling a little better but I still went to the doctors office and tested positive for Covid19 and they gave me a prescription for Paxlovid. I am feeling alot better now. I am reporting a breakthru case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 6-29-2022 at home Covid 19 test - positive result 6-30-2022 Covid19 test at doctor's office - positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia
- Andere Medikamente
- Rosuvastatin; Allegra; Zinc; Calcium; Multivitamin; Fish Oil; Probiotic; Emergencee; Collagen peptide; Trim Sunmed;
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 43,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Dizziness
Fatigue
Symptomtext
I had a cough and fatigue and i experienced a little dizziness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Diarrhoea
Fatigue
Feeling abnormal
Gastrointestinal disorder
Respiratory tract congestion
SARS-CoV-2 test positive
Sick relative
Symptomtext
I was feeling bad June 30 AM. I took a home test that was negative. Lots of fatigue and diarrhea cough and congestion later that day, I was positive. 07/1, Followed up with a PCR test that confirmed my findings from the day before. Called my doctor and prescribed medication and said give it a week and call me back if it doesn't get better. I was in isolation for five days. July 3, my wife tested positive. Friday I was in recovery even walked a little over five miles and was feeling fine. 07/9, Weird that I was recovering and out of nowhere as soon as I completed the prescription, I started having congestion and a weak stomach with diarrhea and fatigue. I called my doctor and county hospital. I was unsure why the symptoms came back. The county health department told me to act as if I was re-infected. PCP told me it's the same illness it was roller-coaster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- PCR
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Heart Issues; A fib; Pace Maker
- Andere Medikamente
- Lisinopril; amlodipine; atorvastatin; ELIQUIS
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 84,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Extra dose administered
Fatigue
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test
Symptomtext
I contracted COVID-19 approximately 3 months after my 4th dose vaccination and had the following symptoms: Fatigue, Sore Throat, Drippy nose. I called my Doctor and was prescribed with Paxlovid for 5 days. So far, it did help with my symptoms and as of 07/15/2022 I feel so much better but still feeling a little bit tired,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; High Cholesterol
- Andere Medikamente
- Rovastatin; Lisinopril; Fish Oil; Calcium; Glucosamine; Multivitamins; Low dose aspirin; Magnesium; B Complex; Loratadine; Tylenol; Levothyroxine
- Allergien
- Septin; Chlorhexidine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 60,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Fatigue
Headache
SARS-CoV-2 test positive
Symptomtext
My husband was positive so I was exposed to COVID-19, I started having a headache and was tired so I tested with home COVID-19 test that came back positive. I called my doctor who said I did qualify for the Paxlovid and called it in to my pharmacy and I started taking it immediately. For about eight days after the medication I was tired but I am feeling better now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Lisinopril; Liothyronine: Progesterone: Slow Release SQ Progesterone/Testosterone; Hemp Oil; Zinc
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 73,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Body temperature increased
COVID-19
Cough
Decreased appetite
Diarrhoea
Fatigue
Feeling abnormal
Myalgia
Oropharyngeal pain
Pain
Pharyngitis
Respiratory tract congestion
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough Case: 06/23/2022 I was on a cruise and I started to get a cough and continued into 06/25/2022. Flew through multiple terminals and got home on 06/25/2022. On the plane I was feeling terrible and getting back was very hard. I had aches and pains and I had home COVID-19 Test and it came out a faint red but no where near what it was suppose to look like. I took another test and it came out negative as well. I called urgent care and was able to get in around noon and after getting swabbed it was positive. Paxlovid was prescribed to me and I had to stop taking my statin medication and felt terrible for a few more days and then started to feel much better. I went back to urgent care on July 13th and had a sore throat but no fever or other symptoms. Some of the symptoms I was experiencing were coughing and fatigue right away and muscle aches as well. I also had congestion, and my temperature on the 25th it was 100.5 and then on the morning of the 26th it was 101.3. Appetite was not great, taste and smell were fine, did have some diarrhea as well. After taking the Paxlovid I was starting to feel better after a few days of taking it. Now I am only dealing with a throat infection and I am taking an antibiotic and steroid for the congestion as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Tests: Negative; COVID-19 Test at Urgent Care: Positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Acid Reflux; Barrett's Disease; Rosacea; Enlarged Prostate; High Cholesterol
- Andere Medikamente
- Atorvastatin; Doxazosin; Finasteride; Pantoprazole;
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dizziness
Dysphonia
Fatigue
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Vertigo
Symptomtext
First experienced dizziness/vertigo when I first woke up. Had that for 2 days. Then the cough & sniffles started with body aches about the 3rd day. Did a home COVID test and it was positive. Cough and fever got worse so I went to an care clinic and I tested positive on their antigen covid test. They prescribed me a cough medicine during the day versus a liquid cough medicine at bedtime and a medicine for my dizziness. Had slight fever, no sore throat, and fatigue that lasted 3-1/2 weeks. Finally tested negative 12 days later from when I first contracted it. Post Covid, I'm still experiencing some coughing and a hoarse voice 4 weeks after contracting Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma and allergies
- Andere Medikamente
- Metformin 1000mg, Pravastatin, Losartan 100mg, Calcium & Vitamin D, Iron, both Lantus (long acting) and Humalog (fast acting) insulins.
- Allergien
- Vicodin, sulfa, niacin, lactose intolerant
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Compression garment application
Hypoaesthesia
Oedema peripheral
Pain
Swelling
Symptomtext
Started 05/18/2022, I started getting pain. I called the doctor the next day and they prescribed a MEDROL dose pack. It did not help me and I called them again and they put me on a high dose of prednisone and instructed me to also take ibuprofen or ALEVE. It helped with the pain but didn't resolve the numbness I was feeling in my right foot up through my knee. I went in and was advised to get an MRI scan to see how to treat it. Unfortunately, due to my insurance they will not approve an MRI until I have had at least 6 weeks of conservative treatment. After the 6 weeks passed (06/30/2022), I went back into the office and they requested the MRI again. Last Friday, 07/07/2022, I was approved for the MRI and I am scheduled to have one done tomorrow (07/15/2022). I have a follow up with a Dr. on 07/28/2022 to interpret the MRI. When the prednisone ran out, I was prescribed gabapentin and I have been taking that twice daily along with ALEVE. When I wake up in the morning, the numbness and pain are worse. The medicine helps the pain but not the numbness. Also, I am experiencing edema in the ankle that is worse at night. Within the last week, I have been wearing compression socks and that is helping slightly for swelling during the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- MRI of the low back and right leg (07/15/2022).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Amlodipine; allopurinol; hydrochlorothiazide; PRAVACHOL; vitamin D3; multivitamin; baby aspirin; fish oil; tamsulosin; ALEVE; ibuprofen; PEPCID; METAMUCIL
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 04.05.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Influenza A virus test
Influenza B virus test
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID infection. Tested positive 07/13/2022. Fever and worsening fatigue starting 07/13/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Positive SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification test 07/13/2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Essential Hypertension, stage 4 chronic kidney disease
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Exposure to SARS-CoV-2
Headache
Malaise
Paranasal sinus discomfort
SARS-CoV-2 test positive
Sinus disorder
Symptomtext
Found out we had been exposed to a friend, felt sinus pressure. Took home COVID-19 test and it was negative. Took another home test the next day and it was positive. Wend to Urgent Care, was extremely sick with headache and sinus problems. Told to take Mucinex, Vitamin C and vitamin D,. Said she was too far into the process and decided not to prescribe Paxlovid, instead they recommended Zinc. Starting to slowly feel better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 test.
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Prempro; synthroid; Vitamin D; flaxseed oil; chromium; vitamin B
- Allergien
- Phenergan, muscles
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 10.04.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 7/8/22. I had fatigue, sore throat, runny nose, and cough. I had a slight fever for a day and a half and it is gone now. I was prescribed PAXLOVID and I take my last dose tonight.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test- 7/8/22- positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Methotrexate; folic acid; vitamin D; multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Fatigue
Malaise
Nasal congestion
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
COVID-19 symptoms started on evening of 07/04/22; tested positive on 07/05/22. I had a fever that spiked and so I had mobile medical service come out and test me. I also had runny nose, cough, chills when fever got high, and sore throat. I still have ongoing symptoms but fever has subsided and occasionally I have slight fever of 99.1 but my normal temperature is 98 something. I took a test yesterday and it was still positive. I still have a mucousy cough and I wouldn't say nose is running but it's stuffy. Sore throat is gone and fever for the most part if gone. I had extreme fatigue the first 4 days and I would say I still have a bit of it but not as bad. I'm still not feeling super energetic but fatigue is 90% improved. They discouraged me from taking the antiviral. It's just taking a while and I am better but not done yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive 07/05/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperthyroidism
- Andere Medikamente
- Levothyroxine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Headache, Fever, runny nose, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home Covid-19 antigen test - Positive idicator
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cerebral Palsy High Blood Pressure
- Andere Medikamente
- Cardura Amlodapine Multi Vitamin Valsartin HCL low dose aspirin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 09.04.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Decreased appetite
Fatigue
Influenza like illness
Malaise
SARS-CoV-2 test positive
Symptomtext
I started getting symptoms of flu like symptoms except no fever. I took an at home COVID-19 test that was positive. I contacted my doctor and was prescribed molnupiravir. My symptoms were weakness, loss of appetite, and fatigued. My symptoms lasted for 4-5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes since after partial Pancreas surgery in 2012
- Andere Medikamente
- None
- Allergien
- Sulfa; atenolol
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 09.04.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 60,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Influenza like illness
Malaise
Night sweats
SARS-CoV-2 test positive
Symptomtext
COVID-19 symptoms started on 06/08/22 at night time; tested positive on 06/11/22. I had night sweats on the 8th, 9th, and 10th, and on the 11th I felt flu-like symptoms. On the 13th I went to the Doctor and then I recovered on either the 19th or 20th when I had a negative COVID-19 test. I had two nights of bad coughing and that's about it. It wasn't until I had the night sweats that I realized I had COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 Positive 06/11/22
- Aktuelle Erkrankungen
- Mastoiditis
- Vorgeschichte
- High blood pressure; high cholesterol; psoriasis; acid reflux; PTSD; herpes simplex; mastoiditis; 2 replacement composite discs in neck.
- Andere Medikamente
- Diltiazem; Zaltidine; levothyroxine; atorvastatin; pantoprazole; estradiol; fluocinolone acetonide topical oil; derma-smooth; Clobetasol propionate topical solution; cyclobenzaprine; aspirin; melatonin; folic acid; multivitamin; Cyclobenzap
- Allergien
- Dogs; Cats
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 07.04.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 76,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Chest discomfort
Cough
Dysphonia
Exposure to SARS-CoV-2
Fatigue
Productive cough
Pyrexia
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
I received my second Pfizer booster for COVID-19 on 4/7/2022. On the night of 6/22/2022, I felt a tightness in my chest and used my inhaler. I knew that I had previously been exposed to COVID-19, so on 6/23/2022 I took both a rapid test and a PCR test. The rapid test yielded a negative result, but the PCR test yielded a positive result. On the afternoon of 6/23/2022, I began having a productive cough. On 6/24/2022, I called my doctor's office, and I was prescribed a 5-day course of Paxlovid, which I started that day. The coughing became very persistent, and I developed a very deep, raspy voice. On 6/25/2022, I still had a cough and was very fatigued. That evening, I had a low-grade fever for about an hour. On 6/26/2022, the symptoms were about the same. I had coughing, hoarseness, and fatigue, but no fever. On 6/27/2022, I felt better. I had more energy, and the coughing had diminished some. I was able to walk my dogs for the first time in several days. The symptoms continued to improve gradually. I would say that my symptoms were completely gone by 7/1/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 6/23/2022-PCR test-positive result; 6/23/2022-rapid test-negative.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Herniated Disk; Hypertension; Osteoporosis; Reactive Airway Disease.
- Andere Medikamente
- Vitamin D3; Amlodipine; Nortriptyline; Allegra; Omeprazole; Meloxicam.
- Allergien
- Meloxicam; Diclofenac.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Malaise
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Upper respiratory tract congestion
Symptomtext
When I caught COVID-19 I had mild symptoms. I had a mild headache, some upper respiratory congestion, a runny nose, and sneezing. I took acetaminophen to treat my symptoms. I was also mildly fatigued. My doctor prescribed paxlovid. After I had recovered from the acute, beginning phases of COVID-19 I was still experiencing some fatigue, mild congestion, and occasional coughing that has lingered. I did have a low grade fever of about 97 to 98.8 degrees.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 6/24/2022- COVID-19 Antigen Test- Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lovastatin; Hydrochlorothiazide; Myrbetriq
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 80,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Nasal congestion
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Vaccine breakthrough infection
Symptomtext
I had a breakthrough case. I was vaccinated on 03/31/2022 then on 06/18/2022 I started having symptoms of a scratchy throat, stuffy nose and a fever. On 06/19/2022 I got a really high fever. I did a home COVID-19 test and it came back positive so I called my Dr.'s office and they prescribed me PAXLOVID. I felt fever, stuffy nose symptoms for a few days. I never recovered from the scratchy throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Heart Disease
- Andere Medikamente
- Aspirin; atorvastatin; multivitamin; vitamin B12
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
Cough
Dysphonia
Headache
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test
Symptomtext
I woke up on June 27, 2022 and felt like I had a fever, I had a raspy voice, sore throat, headache, cough. My wife took my temperature for me and we used a home COVID-19 test that came back immediately. I could not get in to see him but was able to have a phone visit on June 28, 2022. He prescribed PAXLOVID that I was able to start that day along with TESSALON PERLES for the cough. He advised me to rest. I am now feeling better. My sense of taste and smell are coming back, still have slight congestion and cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Blood Pressure; High Triglycerides; High Cholesterol
- Andere Medikamente
- Amlodipine; TOPROL XL; triamterene; HCTZ; CRESTOR; losartan; timolol; vitamin D3; TYLENOL
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 63,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Malaise
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 06/08/2022 with symptoms of congestion, and dry cough. I was prescribed PAXLOVID on 06/11/2022 at the urgent care. I was ill for 18 days before my symptoms fully resolved. I had also continued to test positive until 06/22/2022. I am fully recovered now with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 06/11/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Estradiol
- Allergien
- Augmentin; TYLENOL; clindamycin
- Vorherige Impfungen
- Shingrix vaccine left me extremely fatigued for 24 hours on 06/2022.
- Staat
- WA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 03.07.2022
- Tage bis Beginn
- 88,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Diarrhoea
Dysgeusia
Fatigue
Oropharyngeal pain
Oxygen saturation decreased
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 07/03/2022 with symptoms of cough, fever, congestion, body aches, slight decline in oxygen level, fatigue, and sore throat. I was prescribed Paxlovid on 07/05/2022. I am still experiencing symptoms of sore throat and cough. I have a metallic taste in my mouth and diarrhea from the Paxlovid. I am not recovered yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab was positive on 07/03/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin; Calcium; Aspirin; Vitamin B12; CoQ10; Vitamin C; Pravastatin; Amlodipine; Hydrochlorothiazide
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 05.04.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 68,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Fatigue
Headache
Pyrexia
SARS-CoV-2 test
Sinus operation
Symptomtext
I have a lot of allergies so when I awoke on June 12, 2022with a headache and sinus drainage I thought it was just my allergies. Later that day I called my doctor and had a telehealth visit after having taken a home COVID-19 test once my symptoms had progressed to fatigue, cough with a fever. He prescribed Paxlovid that I started taking the next day for five days. I have been feeling much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diapetes; high Blood Pressure; Anxiety; Allergies
- Andere Medikamente
- Losartan; Glimpiride; Metformin; Fluticiosone; Sertraline; Baby Aspirin, Quutiapine
- Allergien
- Sulfaites, Grasses
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
COVID-19
Cough
Headache
Malaise
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I started with achiness, headache, runny nose, and coughing. I did a home test that was positive on July 03rd. I went to urgent care at 11:30am and retested with a COVID-19 PCR Test and was positive. I was prescribed Paxlovid. I started the medication on the same day and started to have improvement in symptoms at about a rate of 10% per day. I am still experiencing low energy with a mild cough. I also have mild to moderate achiness. I have not recovered as I still have symptoms but I am improving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19-Home Test-Positive-July 3rd, 2022 COVID-19 PCR-Positive-July 3rd, 2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Simvastatin; Ipratropium Nasal Spray; Alendronate; Daily Vitamin; Low Dose Aspirin; Guaifenesin; Vitamin D3; MSM
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 05.04.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Memory impairment
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Sputum discoloured
Throat irritation
Symptomtext
I contracted COVID-19 on 05/19/2022 with sore throat, itchy throat, sneezing, congestion, and headache. I was prescribed PAXLOVID on 05/20/2022 via a telemedicine visit. I was ill for 8 days before my symptoms resolved. I flew to another area 05/29/2022 and my COVID-19 symptoms returned that evening and worsened. My sputum was no longer clear and eventually was a magenta color, which made me concerned it was blood. The congestion was far worse, and I had to have another medical visit where I was given a Z-PAK on 06/05/2022. On 06/06/2022 I was not feeling improved at all so I had a HCF do a home call where they gave me a steroid shot and an albuterol inhaler prescription. I felt much better after that and my symptoms fully resolved after 8 days. I do feel my memory has been affected by my illness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal home test was positive on 05/20/2022; COVID-19 rapid nasal home test was negative on 05/28/2022; COVID-19 rapid nasal test was positive 05/29/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Coronary Heart Disease; Arterial Sclerosis; Hypertension
- Andere Medikamente
- Vitamin C; vitamin D3; atorvastatin; metoprolol; tartrate; losartan; ezetimibe; aspirin
- Allergien
- Penicillin; latex
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Fatigue
Headache
Influenza like illness
Nasopharyngitis
Oropharyngeal pain
Pain
Parosmia
Pyrexia
SARS-CoV-2 test positive
Symptomtext
When I caught COVID-19 I had a cold, sore throat, coughing, headache, and a little bit of body aches. I felt like I had the flu. I had a slight fever of 100 degrees at the highest, but it didn't last very long. I went to an urgent care clinic. I was put on prednisone and PAXLOVID. I have had a terrible smell of smokiness in my nose, but my sense of taste is fine. I am a little tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 6/27/2022- Covid test- positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Amlodipine; hydrochlorothiazide; meloxicam; VASCEPA; fluticasone; DETROL; omeprazole; VENTOLIN; SYMBICORT; vitamin D3; calcium
- Allergien
- Betadine; erythromycin; BIAXIN; ZITHROMAX; levofloxacin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
COVID-19
Oropharyngeal pain
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I tested positive on 6/24/22. I developed a throat tickle that evolved to a sore throat. Spoke to the Dr. on the 24. Wasn't able to take PAXLOVID because I was taking ELIQUIS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- AFIB; Heart problems
- Andere Medikamente
- ELIQUIS; gabapentin; rosuvastatin
- Allergien
- Azithromycin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 01.07.2022
- Impfdatum
- 01.05.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 45,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest X-ray normal
Cough
Fatigue
Injection site pain
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
After receiving the vaccine I had pain at the site of injection. When I caught COVID-19 I had congestion, cough, a low grade fever between 99 to 101 degrees, body aches, and fatigue. I called an urgent care and they gave me a prescription for Paxlovid. I took the 5 day course of it, and then 3 days after not taking the Paxlovid anymore the cough and congestion came back. I called urgent care again. I have been taking Sudafed, Afrin nasal spray, Tylenol, Robitussin DM during the day, and Robitussin with codeine at night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 6/14/2022- COVID-19 Test- Negative; 6/15/2022- COVID-19 Test- Positive; 6/30/2022- COVID-19 Test- Positive; 6/28/2022- Chest X-Ray- Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; GERD; High Cholesterol
- Andere Medikamente
- Losartan; Nebivolol; Hydrochlorothiazide; Amlodipine; Protonics; Lipitor; Uroxatral; Tadalafil
- Allergien
- Bactrim; Sulfa
- Vorherige Impfungen
- Shingrix-I had a low grade fever and body aches for 24 hours. That was 2 or 3 years ago.
- Staat
- DE
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 30.06.2022
- Impfdatum
- 30.03.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I tested positive for COVID-19 on 5/16/22. I had fatigue, runny nose, and sneezing. I was prescribed Paxlovid the next day and the symptoms cleared up within 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test- 5/16/22- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type 2 Diabetic; High Cholesterol; High Blood Pressure
- Andere Medikamente
- Farxiga; Tamsulosin; Metformin; Amlodipine Besylate; Bisoprolol - HCTZ; Atorvastatin
- Allergien
- Amoxicillin; Penicillin; Prednisone
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 25.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal distension
Blood pressure increased
Cardiac monitoring normal
Chest X-ray normal
Computerised tomogram normal
Dizziness
Extra dose administered
Fatigue
Immunisation reaction
Magnetic resonance imaging normal
Nausea
Vertigo
Symptomtext
I received my second booster on May 25th at 03:00 in the afternoon. On May 26th around noon, I started getting nauseas, bloated, and lightheaded. On May 30th, around 04:00PM, I went to urgent care as my blood pressure went up to 183/81. I do not have blood pressure problems. I was diagnosed with fatigue. On June 15th, I went to the doctor as an annual visit, but I still had all the symptoms. Right before I went to that appointment, after 8 days of being nauseous 24 hours a day, I called my primary doctor. He prescribed Ondansetron HCL 4mg to be taken every 6 hours. Nausea went away. My doctor examined me and said there was nothing he could do for me because of it being vaccine related. He called it vaccine syndrome. He did prescribe Vitamin B12. Saturday, June 25th, I had a very dizzy spell. I had to call an ambulance. I spent the night admitted to the hospital where many tests were done. I was discharged with vertigo likely secondary to COVID-19 Booster. I went home with a prescription Meclizine 12.5mg. On June 29th, I went to see primary doctor. He examined me. He is sending me to therapy for crystal adjustments and referral to an ENT doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- 1,0
- Labordaten
- 06/25/2022: Chest x-ray - Normal; CAT Scan-Normal; Blood Pressure Test-Normal; Heart Monitor-Normal; 06/26/2022: MRI-Normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Temazepam
- Allergien
- Sulfa; Penicillin; Levofloxacin; Hydrocodeine; Codeine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 29.03.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
SARS-CoV-2 test positive
Taste disorder
Symptomtext
On 6/20/2022, I did a PCR test for COVID-19 in preparation for a trip. On 6/22/2022, I got the results, and they were positive. I got a sore throat later that same day. I spoke to my doctor that day, and he prescribed me PAXLOVID. I was hesitant to take it at first, because I had heard of the side effects. The sore throat continued into 6/23/2022. On 6/24/2022, I started coughing. Despite my prior misgivings about the PAXLOVID, I began taking it to treat my symptoms. Within 24 hours, I felt a complete difference, though I got a horrible taste in my mouth, which continues at the time of this writing. Peppermint candy helps that, though. Today is the last day I have to take the PAXLOVID, and I no longer have symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- PCR test--result positive.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Mild Emphysema; Pre-Diabetes; Hyperthyroidism; High Cholesterol.
- Andere Medikamente
- LEVOXYL; simvastatin; metformin; vitamin B2; turmeric; probiotic; baby aspirin; omega fish oil; vitamin D3; mag ox; vitamin B12; glucosamine chondroitin; alpha lipoic acid; bilberry extract; cinnamon; BOSWELLIA; calcium; MIRALAX.
- Allergien
- Penicillin; codeine; tomatoes.
- Vorherige Impfungen
- I had a red, swollen arm for a week after taking both doses of Shingrix.
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 15.05.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Chills
Cough
Fatigue
Headache
Night sweats
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
Symptomtext
I got COVID-19 and I have severe headache, sore throat, fatigue, congestion, fever, chills, night sweats, coughing and tightness in chest. Is been a week and it fluctuates. I had a video visit. Recommended me to not take PAXLOVID and prescribed albuterol and benzonatate. They did help with some symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Lisinopril
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Crying
Decreased appetite
Discomfort
Dizziness
Fear
Insomnia
Pain
Screaming
Visual impairment
Vomiting projectile
Weight decreased
Symptomtext
I've lost 13 pounds in the last 23 days. I lost 6 of those pounds within the first 5 days. It is hard to keep food down because I projectile vomit 20 minutes after eating and I am never hungry anymore. I only know I need to eat if I feel like I am going to faint. A couple days after the first dose and the night of the second dose I had severe pain, the worst I've experienced in my life, and it lasted for about 8 hours each time. I felt like all my nerves and all my bones were on fire. It was terrifying. My vision gets grey and splotchy and there is a swollen lump in my armpit that is half the size of a baseball. I have not been able to sleep a full 8 hours a night since I received this vaccine due to pain and discomfort. I take vitamin C & D, got a vitamin C IV, aspirin, my mom had to massage me for hours so I could stop screaming and crying. I am still not ok and I am scared.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypothyroidism
- Vorgeschichte
- -
- Andere Medikamente
- Thyroid NP, Progesterone, Adderall, Amantadine
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- -
- Geschlecht
- M
- Eingang
- 18.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pain
Symptomtext
He too started a couple days later experiencing these type of situation, these type of pains; he too has suffered from that and to this day;; still have that in our muscles; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). An 85-year-old male patient received BNT162b2 (BNT162B2), as dose 1, single (Lot number: FJ9943) and as dose 2, single (Lot number: FJ9943) for covid-19 immunisation. The patient's relevant medical history included: "High Blood Pressure" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: PAIN (non-serious), outcome "unknown", described as "He too started a couple days later experiencing these type of situation, these type of pains; he too has suffered from that and to this day;"; MYALGIA (non-serious), outcome "unknown", described as "still have that in our muscles". Therapeutic measures were not taken as a result of pain, myalgia. Additional Information: Reporter stated, "Sometimes I don't hear really well. Well, you know, I had the second booster I believe it was like 05Apr and so that mean my fourth shot okay, my fourth Pfizer shot. I had the two regular you know, in the beginning, I had everything recorded in my little card and everything and now I had the first booster and then I had the second booster I think it was like maybe 8 months later. So, I did not had any reactions to the first three but on this particular second booster, I have had a terrible reaction to my muscles and my joints and I have been fighting this since, well I got the shot on 05Apr, it seems like the 6th was fine I had no, by the way I had no, I don't remember you know, anything major with the other ones like red arms or anything like that but this one the first day nothing, second day same nothing but the third day I could not move, I could not get out of bed. My muscles and joints were like frozen, and I just could not move out of bed and it took me quite a while to find and I am an active person by the way it's not like I am not an active person and so, I don't remember exactly how it finally happened. I think, I kept rubbing my leg or trying to make it move or helping it to move with both of my hands, but it was hard to do that too because the main muscles in my upper arms were so sore and my legs. So, when I would stand up it seems like it was just intense pain that went from my I guess just under my shoulders. I guess it was around through the bicep starts you know, the bicep and all the way down my body and I could hardly walk." Treatment for Adverse Event: Reporter stated, "No, he did not. He did not take it; he did not go to the doctor. I went to the doctor and, but he did not, but he experiences the same muscle but not as intense as mine but in the same area the biceps and the hips and the lower back." No follow-up attempts are needed. No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 31.03.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Polymyalgia rheumatica
SARS-CoV-2 test
Symptomtext
Polymyalgia rheumatica; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received BNT162b2 (BNT162B2), on 31Mar2022 at 12:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 69 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Gout" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, other vaccine same date product= Pfizer,, other vaccine same date lot number= 5318,, other vaccine same date vaccine location= Right arm), for COVID-19 immunization; Bnt162b2 (DOSE 2, other vaccine same date product=Pfizer,, other vaccine same date lot number= 6199,, other vaccine same date vaccine location= Right arm), for COVID-19 immunization; Bnt162b2 (DOSE 3, other vaccine same date product= Pfizer,, other vaccine same date lot number= 3182,, other vaccine same date vaccine location=Right arm), for COVID-19 immunization. The following information was reported: POLYMYALGIA RHEUMATICA (medically significant) with onset 20Apr2022, outcome "recovering". The event "polymyalgia rheumatica" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (07Jun2022) Negative, notes: Nasal swab. Therapeutic measures were taken as a result of polymyalgia rheumatica. Clinical Course: The patient did not receive any other vaccine in four weeks. No other medications received in two weeks. Prior vaccination, the patient not had covid vaccination. Post vaccination, the patient had tested for covid. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Polymyalgia rheumatica
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220607; Test Name: Rapid Test; Test Result: Negative ; Comments: Nasal swab.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Gout
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 02.05.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 40,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
COVID-19
Fatigue
Headache
Productive cough
Pyrexia
Symptomtext
5/31 to 6/9 or 10th on cruise ship. 6/11/2022 Developed a cough and fatigue struck late in the evening accompanied by a headache that got progressively worse. Fever in the night of 101. At home test for Covid tested positive. 6/12 Cough became wetter and phlegmier. Fever shifted between 99 and 101 for about 15 hours. On call doctor advised to go to ER. ER doctors provided Monoclonal antibodies and saline. Symptoms improved after time in ER and I was released. Symptoms have been steadily improving, but not fully recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home covid test positive on 6/11. ER on 6/12 blood work to assess.
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- metastatic cancer, High blood pressure
- Andere Medikamente
- Centhroid, losartan, gabapentin, d3, milkthissle, magnesium, preservision
- Allergien
- Sulfa, Morphine, Oxycodone, Macrobid, carboplatin
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 30.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
C-reactive protein
Disability
Full blood count
Joint range of motion decreased
Loss of personal independence in daily activities
Pain in extremity
Red blood cell sedimentation rate
Symptomtext
Right arm soreness, reduced ROM despite daily exercises, hydration, tylenol, and benadryl. Symptoms have been ongoing daily and have been constant, worsened with ROM. No loss of sensation or motor function. Partial disability resulted in that pt is now using the alternate upper extremity to complete tasks that require UE gross motor funciton.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- ESR, CRP, CBC
- Aktuelle Erkrankungen
- see item 12.
- Vorgeschichte
- Hypermobility Spectrum Disorder Hypogammaglobulinemia/CVID Osteoporosis MVA age 18-severe trauma loss of control of my bowels diarrhea COVID-19 Vaccine oa Seasonal allergies/allergic rhinitis Obesity Joint replacements Insomnia Hospitalized (past six months) History of falls High blood pressure Diabetes Depression COPD Chronic pain Asthma Arthritis Anxiety
- Andere Medikamente
- Metformin, levothyroxine, glipizide, morphine, clopidogrel, bisoprolol
- Allergien
- Ciprofloxacin (rash, pruritus) Gadolinium Containing Compounds (nausea) Sulfa Drugs (Childhood reaction) Aspirin (Childhood reaction) Penicillins (Syncope)
- Vorherige Impfungen
- November 2019, Influenza Vaccine, right arm with edema/erythema. Symptoms had resolved within 1.5 months
- Staat
- OR
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 04.04.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 55,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
Cough
Fatigue
Pyrexia
SARS-CoV-2 test
Sneezing
Symptomtext
coughing, sneezing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home Covid Test Blood Test at Facility
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Paxlovid was prescribed by doctor for 5 days Previous Vacinnations: 03/03/2021 (1st Vaccination) 03/24/2021 (2nd Vaccination) 09/30/2021 (1st Booster)
- Allergien
- None
- Vorherige Impfungen
- Slight Fever and fatigue after all 4 vacinnations
- Staat
- ID
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 20.04.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
COVID-19
Decreased appetite
Diarrhoea
Fatigue
Gastric disorder
Headache
Lymphadenopathy
Malaise
Odynophagia
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
5/27 I experienced headache, sore throat, and fatigue. Symptoms got worse on 5/28, I had painful swallowing, stomach cramping and diarrhea started late in the day, into 5/29. 5/29 loss of appetite along with increased fatigue. Tested positive with At home test on 5/29. Telemedicine with doctor on 5/29, who prescribed Paxlovid. 5/30 Swollen glands in neck. 6/4 symptoms noticeably improved, stomach pain continued. Fatigue, Stomach issues, sore throat persist to present. No fever at any point.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- At home covid test positive on 5/29
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetic; High Blood Pressure; hypothyroidism
- Andere Medikamente
- Hydrochlorothiazide, Synthroid, co q 10, metformin, Zyrtec, pravastatin, Diltiazem, Bupropion, Glipizide, telmisartan, multi vitamin, Vitamin D3, insulin
- Allergien
- LOTANITIN; codeine; black and white pepper
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 05.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Gait disturbance
Symptomtext
While walking to the restroom got out of bed and felt extremely dizzy. Almost fell to the ground but held on to the walls for support. I was able to make it back to the bed and lay down. I still feel scared to walk, so I'm staying in bed, for now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 16.04.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 36,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 approximately one month after the 2nd booster. My symptoms (acute sore throat and wracking cough) lasted 2 days. Exhaustion is ongoing nearly 2 weeks after onset of symptoms and positive text result.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Daily antigen testing.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure, Type 2 diabetes, minor heart blockage, depression, anxiety
- Andere Medikamente
- Levothyroxine, Fluoxetine, Lisinopril, Naproxen, Metformin, Rosuvastin Calcium, Famotidine, Alprazolam, Baby Aspirin, Calcium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 20.04.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 40,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
COVID-19
Headache
Malaise
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID breakthrough case. I received my 2nd booster shot on 04/20/2022 and my COVID symptoms started on 05/30/2022 I felt a little achy at first in the morning but as the day began I was feeling more achy in my whole body. I had runny nose and I thought it was from allergies or from a cold. I started feeling worse as the day went by and I said to myself something was not right so I decided to do a COVID home test at about 6pm which was positive. I have slight fever. I also had very mild headache. I did a telehealth with my doctor and she prescribed me with medication I haven't received it yet but will be taking med soon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID home test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Last month I was diagnosed with AFIB
- Andere Medikamente
- Ampicillin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Fatigue
Feeling abnormal
SARS-CoV-2 test
Symptomtext
she started to feel really bad; weakness; fatigue; light headed; 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 93-year-old female patient received BNT162b2 (BNT162B2), on 10May2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 93 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing), notes: controlled by diet and exercise no medicine. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1; Lot Number: EN6199; Anatomical location: left arm, She has never had a bad reactions.), administration date: 06Mar2021, when the patient was 92-year-old, for Covid-19 immunization, reaction(s): "sore arm"; BNT162b2 (DOSE 2; Lot Number: ER8730; Anatomical location: left arm), administration date: 27Mar2021, when the patient was 92-year-old, for COVID-19 immunization; BNT162b2 (DOSE 3 (BOOSTER); Lot Number: 33025BD; Anatomical location: left arm), administration date: 05Jan2022, when the patient was 93-year-old, for COVID-19 immunization. The following information was reported: FEELING ABNORMAL (non-serious) with onset 13May2022, outcome "not recovered", described as "she started to feel really bad"; FATIGUE (non-serious) with onset May2022, outcome "unknown"; DIZZINESS (non-serious) with onset May2022, outcome "unknown", described as "light headed"; ASTHENIA (non-serious) with onset May2022, outcome "unknown", described as "weakness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of feeling abnormal, asthenia, fatigue, dizziness. Additional information: The patient experienced some side effects as a delayed reaction, stating that she felt well the first few days after getting the vaccine and the on 13May2022 she started to feel really bad. On 10May2022 in late afternoon (when vaccine was administered) She was fine the next day and in fact she felt good. The 3rd day and 4th day were really bad days including today. She feels about the same. She feels pretty bad. At her age she does have a bad day every once and a while. Now she has been going on sick for almost 4 days. No additional vaccines administered on same date of the Pfizer suspect. No events require a visit to emergency room or physician office. No other product administered prior vaccinations (within 4 weeks). No relevant tests.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Negative ; Comments: test came out negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes (controlled by diet and exercise no medicine)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
Severe itching on feet, ankles, lower legs, hands, wrists, forearms developed in the evening and has continued intermittently (daily, but generally in the evening and night). It is only relieved with ice packs. I had similar itching episodes following the first two vaccines and the first booster, but I did not report them because I did not realize they might be related to the shots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression, migraines
- Andere Medikamente
- Nortriptyline, levothyroxine, lamotrigine, trintellix, Centrum daily vitamin
- Allergien
- Several antibiotics, sulfa drugs. No food allergies
- Vorherige Impfungen
- Same itching following first two Covid vaccines and first booster. Also itching following Shingrex shots and flu shot. All shots
- Staat
- AZ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 13.04.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sick leave
Sneezing
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID case: The symptoms started around 06:00PM on Wednesday, May 18th. They started with congestion and sneezing. I went to bed after taking an Alka-Seltzer night time, one tablet. When I woke up in the morning of the 19th, I was achy and congested. I was scheduled to work that day, but my husband suggested I take a COVID test before leaving for work. Taking the COVID test, my result showed positive within 5 minutes at the most. I called in sick and looked for a place that carried antivirals. I made an appointment at the clinic for 05:00PM. I took the antivirals around 06:00PM. I'm still feeling pretty congested. It's been over a week now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- 05/19/2022 home test positive. 05/19/2022 clinic Covid test positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of Hemiplegic Migraines
- Andere Medikamente
- Fluoxetine 20mg 1xday; gabapentin 100mg 1xday; simvastatin 20mg 1xday; coq10 200mg 1xday; folate 1000mg 1xday; b12 1000mg 1xday; vitamin d3 5000mg 1xweek; baby aspirin 83mg 1xday
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 13.04.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Dizziness
Ear infection
Ear pain
Ear swelling
Erythema
Symptomtext
My right ear felt like I had an infection. Very painful with swelling and redness. I had trouble with being dizzy and very unsteady a good two weeks. I communicated with my doctor about my symptoms. It was not determined to not me an infection. The symptoms could be related to the vaccine or the allergies. My doctor put me on prednisone, Claritin and nasal spray all for treating as anti inflammatory.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Thyroid; pancreas cyst (IPMN)
- Andere Medikamente
- Synthroid; Cytomel; vitamin D3; calcium; vitamin B12; daily vitamin 50+ chewable; Prolia
- Allergien
- Penicillin; codeine (pain medication); Ilosone (off the market)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
On May 17, 2022 I had a headache and I thought that it was allergies as it I do take Zyrtec. On May 19, 2022 I took a home COVID-19 test that came back positive and called my doctor he prescribed my Paxlovid. On May 22, 2022 I went to the pharmacy and took another test. For me it felt more like a sinus cold and I was really, really tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19; COVID-19 test at pharmacy
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Allergies
- Andere Medikamente
- Zyrtec
- Allergien
- Soy; flax; coffee sensitivity; milk sensitivity
- Vorherige Impfungen
- Pneumococcal Vaccine, Enlarged Lymph Nodes.
- Staat
- NC
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Feeling abnormal
Impaired work ability
Malaise
Nasal congestion
SARS-CoV-2 test positive
Throat irritation
Vaccine breakthrough infection
Symptomtext
Breakthrough case of COVID - 05/11/2022 My sx started on the evening of 05/10/1022, I started with nasal congestion and scratchy throat. I went to bed, woke up the next morning with the same sx, did a rapid test and it was positive. I called my doctor's office and the doctor called back that afternoon, that he prescribed Paxlovid which I started that evening, I took for 5 days, I started feeling better almost instantly, I was pleased with how it worked. I went back to work and worked Tue - Friday, Saturday was fine. Sunday I felt terrible, I felt like a brand new case of Covid, bad as ever. I spoke via telehealth to my doctor yesterday, she stated that it could be Post Covid Syndrome and a rebound effect from the Paxlovid. I am now on a Z-Pack, albuterol inhaler and Tessalon pearls for cough. I was instructed not to go back to work until June 1st, but I am able to work from home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home Rapid Covid Test - positive
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- psoriasis, arthritis, hypertension, Type II diabetes
- Andere Medikamente
- simvastatin, HCTZ, Otezla, alive, multi-vitamin, Occu-Vit, Ramipril, famotidine,
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Throat irritation
Symptomtext
I started thinking that I was having bad seasonal allergies. I was sneezing, had a runny nose with congestion. Thursday it was worse and by Friday I was having a cough that was coming from like a tickle in my throat but it was intermittent. I did a home test and it was positive. By Saturday the fatigue had set in and I ended up going in for a PCR test and to get the Paxlovid. I am doing a little better but have been very tired and just felt like its a bad allergy season aside from the cough which is not constant or productive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid 19 home test, Covid 19 PCR Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cardiac Patient
- Andere Medikamente
- Aspirin, Omeprazole, Atorvastatin, Xyzal, Vitamin B D and Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 40,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Exposure to SARS-CoV-2
Fatigue
Feeling abnormal
Influenza virus test negative
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Somnolence
Throat irritation
Symptomtext
I started with a scratchy throat and by the afternoon I got chills and a fever. Took Tylenol it didn't help the fever any. On the 12th I made and appointment to see my doctor, I took at home test it was negative before I saw my doctor I did another test it was negative. I saw a doctor that afternoon and she did a flu test and a Covid test and it was negative she gave me antibiotic. I still had chills, coughing, body aches and congestion. I stuck it out but my fever went up to 103 on Friday. Saturday morning I called my doctor and they thought it was a virus. I got a call that I was exposed on Monday and I did another test it was positive. I still had all my symptoms until the 14th. On the 15th my fever broke. And through all this I also was sleepy. I also had brain frog that that stayed until the 19/20. Today was the first day that I felt pretty good. I am tired now but I am feel a lot better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Covid positive, flu negative.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Allergies; Gerd; High Blood Pressure
- Andere Medikamente
- Vitamin D
- Allergien
- Sulfur
- Vorherige Impfungen
- Covid, sore arm, sick for 4 days with fever and aches and congestion.
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
COVID-19
Dizziness
Feeling abnormal
Malaise
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
On 05/13 I started sneezing and I felt like I was having an Allergic. On 05/14 I took Flonase for allergies in the morning. After which I went outside and started feeling sick. I had severe pain in my back and I started feeling congested, dizzy and "brain fog." Tested positive for COVID on 05/15. Dr. prescribed Paxlovid for symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Home Covid Test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lung Disease (in remission)
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
COVID-19
Cough
Nausea
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
Retching
Rhinorrhoea
SARS-CoV-2 test positive
Sleep disorder
Symptomtext
I had two days of a sore throat and on Tuesday I ran fever, sever congestion, nausea, dry heaving, couldn't sleep and I guess that was about it. It lasted till I contacted the Dr. on Wednesday morning. The doctor asked me questions about how I was feeling and he prescribed the Paxlovid and told me to stop taking my Lipitor while taking that medication. I still don't have no sense of smell or taste, runny nose, and a cough but not too bad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test 5/9/22 negative. COVID-19 home test 5/10/22 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraines
- Andere Medikamente
- Topamax 150 mg; Lipitor 10mg; vitamin D3; calcium
- Allergien
- Penicillin; sulfa; aspirin
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 12.04.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram
Confusional state
Dysphagia
Electrocardiogram
Electroencephalogram
Full blood count
Headache
Magnetic resonance imaging
Symptomtext
I had severe headache and aphagia that started at 5AM May 8, 2022. I went to the emergency where they ran a CT scan, MRI, ECG, EEG, complete blood panel. I am still having intermittent much milder headaches and much confusion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Bad Back
- Andere Medikamente
- Vitamin D Vitamin C Vitamin B12 Zinc Ocuvite Losartan Hctz Duloxetine Testosterone Cream Metoprolol Omeprazole Adderall only once or twice Tylenol Ibuprofen Metamucil Capsule
- Allergien
- Penicillin Neomycin Nickel
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 30.04.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Feeling abnormal
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
05/11/2022 - runny nose cough 05/12/2022 - runny nose and cough, cough got worse, in the late afternoon I had chills and late afternoon I had a slight fever 99.7 ( I do not ever get a high fever - my normal is 97) I went right to bed. I did a home test which came back positive in 2 minutes, My doctor called in Paxlovid and I took my first dose that evening, 05/13/2022 - I woke up feeling what seemed to be better, but later I started feeling worse again, but I never go super sick. I was able to function. I am feeling better than before, but I am doing better, I cough less and doing better. Plus I am a real active person, I am not a normal 79 year old.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Home test - positive
- Aktuelle Erkrankungen
- nope
- Vorgeschichte
- no
- Andere Medikamente
- levothyroxine, amlodipine, metoprolol, simvastatin, multi-vitamin, fish oil
- Allergien
- Demerol
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 10.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Decreased appetite
Dyskinesia
Illness
Nasal congestion
Nasopharyngitis
Pain in jaw
SARS-CoV-2 test positive
Symptomtext
I started getting symptoms of general illness. I took an at home COVID test that was negative so the next day, I had a positive COVID test. I had head cold symptoms like a stuffy nose, loss of appetite, and cough. I was prescribed Paxlovid. I took that for 5 days. I also take Nyquil at nights. I tested positive for 10 days then got a negative COVID test. Then I started getting nasal congestion again. I tested positive again. On 5/15/2022, I started feeling an ache in my right jaw and I couldn't close my mouth properly. I did research and it looks like I have COVID jaw. I have a night guard that I wear at night and this morning it felt some better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in jaw
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Probiotic, Vitamin C, Vitamin D, Cranberry
- Allergien
- None
- Vorherige Impfungen
- 12/2021 - Shingles vaccine Shingrix 1st dose - flu like symptoms for 1-2 days
- Staat
- NV
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 17.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 35,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
COVID-19
Cough
Decreased appetite
Headache
Night sweats
Ocular hyperaemia
SARS-CoV-2 test positive
Sinusitis
Sputum discoloured
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID Case: I had a lot of weakness and was coughing. I also had headaches a day or so later. I felt like I had a sinus infection. I was bringing up sputum that was thick and yellow. My eyes were red and I had night sweats. I sort of lost my appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 05/06/2022 - Home Covid Test - Positive; 05/07/2022 - PCR Test - Positive -Hospital
- Aktuelle Erkrankungen
- Sinus infection
- Vorgeschichte
- Lymphoma Non-Hodgkin's; High Blood Pressure; Diabetes-Type 2
- Andere Medikamente
- Imbruvica 420mg 1xday, Dexilant 60mg 1xday, Gabapentin 600mg 3xday, Lisinopril 2.5mg 2xday, Valacyclovir 500mg 1xday, Flomax 0.4mg 2xday, Singulair 10mg 1xday Metformin 500mg 2xday, Zetia 10mg 1xday, Allegra 180mg 1xday, Lipitor 40mg 3xweek
- Allergien
- FELDENE
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 17.05.2022
- Impfdatum
- 30.03.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Hives started on arms within a week of vaccination; hives itch; hives rash/spread to my leg/knee area; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46-year-old male patient received BNT162b2 (BNT162B2), on 30Mar2022 at 18:45 as dose 3 (booster), single (Lot number: FJ9943) at the age of 46 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Not that I'm aware of besides weeds" (unspecified if ongoing). Concomitant medication(s) included: ALLERGY MEDICINE. Past drug history included: Poison ivy, reaction(s): "known allergies". Vaccination history included: BNT162b2 (Dose 2, Product: COVID 19, Brand: COVID 12 yrs (Purple CAP Pfizer), Lot number: FF2588, Dose administration time: 07:45 PM, Vaccine location: Left arm), administration date: 20Sep2021, when the patient was 46-year-old, for COVID-19 immunization; BNT162b2 (Dose 1, Product: COVID 19, Brand: COVID 12 yrs (Purple CAP Pfizer), Lot number: FC3182, Dose administration time: 07:45 PM, Vaccine location: Left arm), administration date: 30Aug2021, when the patient was 46-year-old, for COVID-19 immunization. The following information was reported: URTICARIA (non-serious) with onset 06Apr2022, outcome "not recovered", described as "Hives started on arms within a week of vaccination"; PRURITUS (non-serious) with onset 06Apr2022, outcome "not recovered", described as "hives itch"; RASH (non-serious) with onset 06Apr2022, outcome "not recovered", described as "hives rash/spread to my leg/knee area". The events "hives started on arms within a week of vaccination", "hives itch" and "hives rash/spread to my leg/knee area" required physician office visit. Therapeutic measures were taken as a result of urticaria, pruritus, rash. Additional information: The patient had not other vaccine in four weeks. Patient had received other medications in two weeks with allergy medicine. Reporter stated, hives started on arms within a week of vaccination. The hives itch as well. Still have hives rash almost 6 weeks after vaccine shot, had for about 5 of those 6 weeks. It has now spread to my leg/knee area. Sought medical attention on 25Apr2022 for relief, was prescribed prednisone tablets and relieved itching, but still have hives. Sought additional medical attention from allergist on 05May2022 for further relief and prescribed Fluocinonide Ointment to put on rash. It relieves itching, but still have hives and appearing in other areas on body. Does not seem to be going away anytime soon. The patient was visited to doctor or other healthcare professional office/clinic visit for adverse event. Prednisone tablets and fluocinonide ointment as treatment was received for the events. The patient had not covid prior vaccination and had not covid tested post vaccination. Other medical history was none. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Ragweed allergy
- Andere Medikamente
- ALLERGY MEDICINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 30.03.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash macular
Symptomtext
Hives rash beginning on arms; have more spots mostly on arms and wrist and other random areas; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Mar2022 at 19:15 as dose 3 (booster), single (Lot number: FJ9943) at the age of 41 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: KIRKLAND SIGNATURE ALLERGY MEDICINE taken for hypersensitivity. Past drug history included: Known allergies : cephalexin, reaction(s): "Known allergies : Cephalexin". Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Batch/Lot No: FC3182, Location of injection: Arm Left, Vaccine Administration Time: 08:00 PM), administration date: 30Aug2021, when the patient was 40-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Batch/Lot No: FF2588, Location of injection: Arm Left, Vaccine Administration Time: 08:00 PM), administration date: 20Sep2021, when the patient was 40-year-old, for COVID-19 immunization. The following information was reported: RASH (non-serious) with onset 18Apr2022, outcome "not recovered", described as "Hives rash beginning on arms"; RASH MACULAR (non-serious) with onset 18Apr2022, outcome "not recovered", described as "have more spots mostly on arms and wrist and other random areas". The events "hives rash beginning on arms" and "have more spots mostly on arms and wrist and other random areas" required physician office visit. Therapeutic measures were taken as a result of rash, rash macular. Additional information: Hives rash beginning on arms started two to three weeks after injection on 30Mar2022. Been almost six weeks since vaccine and have more spots mostly on arms and wrist and other random areas. Rash does not itch but gets spots get bigger if scratched. No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ALLERGY MEDICINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 01.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Oral pain
Pyrexia
SARS-CoV-2 test positive
Toothache
Symptomtext
Covid 19, mouth, tooth, head pain, mild fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- POC Rapid Covid-19, Positive
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Aspirin Exacerbated Respiratory Disease (AERD), also called Samter's Triad
- Andere Medikamente
- Triamcinolone AC, Montelukadt Sod Tabs 20mg, Flowvent HFA 12gm, Azelastine
- Allergien
- Asprin, NSAIDs
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 30.04.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Malaise
Myalgia
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I contracted Covid19 on 04/30/2022 with symptoms of sore throat, runny nose, and congestion until I began Paxlovid. When I began taking Paxlovid on 05/02/2022 and I developed additional symptoms of low grade fever, chills, myalgia, and a cough. I was ill for 7 days, but then my symptoms returned on 05/13/2022. I am still experiencing mild symptoms, and I have a lingering cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Covid19 rapid nasal swab home test was positive 04/30/2022.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Vienna graves
- Andere Medikamente
- Azathioprine; montelupo sodium; finasteride; atorvastatin
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Body temperature increased
COVID-19
Fatigue
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I had a little bit of a scratchy throat and a slight sniffle. Then, my temperature was 100.4 and 100.3 then would go down to normal. I was tired also but wasn't sure if it was related to travel or not. Symptoms continued for about 4-5 days and I ended up testing positive (at home) and then went to the HCF and got a PCR test which was positive. I called my doc the next day to see if I was a candidate for Paxlovid. He called it in the next day and I ended up taking the 5 day course of Paxlovid. I felt okay and stayed home. Today was the first real day I have been out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID test at home and PCR test: positive. COVID test (05/11/2022 and 05/16/2022): negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Atorvastatin; Prozac; Konsyl
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site reaction
Pruritus
Rash erythematous
Rash pustular
Skin exfoliation
Symptomtext
A couple of days after my vaccine, I noticed a severe itch on my right arm that I received the vaccine. I noticed a red bumps that looked like they were filled with pus in it coming from my shoulder down to my elbow. It became not to bother me as much to do anything about and I let it go away on its own as it got scaly and dried up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Duloxetine; meloxicam; omeprazole; cyclobenzaprine; lisinopril; Singulair
- Allergien
- Hydrochlorothiazide
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 11.05.2022
- Impfdatum
- 16.04.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 17,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Malaise
No adverse event
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
No adverse effect from vaccine. Breakthrough COVID infection; started feeling ill 5/3/2022. Antigen test positive result 5/6/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Antigen test negative result 5/3/22 Antigen test negative result 5/4/22 POCT MOLECULAR COVID-19 test negative 5/4/22 Antigen test negative result 5/5/22 Antigen test positive result 5/6/22 Antigen test positive result 5/7/22 Antigen test positive result 5/9/22 Antigen test positive result 5/10/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes Type II
- Andere Medikamente
- Metformin 100mg 2x per day. Januvia 50mg 1x per day. Atorvastatin 10mg 1x per day Vitamin D3 50mcg per day
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 16.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Dizziness
Gait disturbance
Head discomfort
Thyroid function test
Symptomtext
Dizziness: head feels full and when I stand up to move, I feel like I want to go left or right like after a few drinks although not having had any.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood draw: Thyroid and Anemia check
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Sulfa
- Vorherige Impfungen
- Moderate dizziness after dose 3.
- Staat
- IL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pyrexia
Vaginal haemorrhage
Symptomtext
PATIENT IS 3 YEARS POST MENOPAUSAL AND WAS VACCINATED 5-5-22. PATIENT HAD 102 FEVER DAY AFTER VACCINATION 5-6-22 AND THE 2ND AFTER VACCINATION 5-7-22. SHE BEGAN BLEEDING/SPOTTING VAGINALLY. WHEN PATIENT HAD 1ST 2 COVID VACCINATIONS SHE HAD NO SUCH SYMPTOMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothroidism
- Andere Medikamente
- Synthroid
- Allergien
- No know allergy
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 10.05.2022
- Impfdatum
- 04.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bone pain
COVID-19
Cough
Fatigue
Feeling abnormal
Headache
Nasopharyngitis
Oropharyngeal pain
Respiratory tract congestion
Restlessness
SARS-CoV-2 test positive
Symptomtext
I took a PCR test on April 29th with a negative result. I became symptomatic over the weekend and tested positive on May 2nd, 2022. My symptoms are similar to a bad cold. I developed bad cough, sore throat, some congestion, headache, fatigue, restlessness, and some fogginess. I do resistance training and have a usual pain in my clavicle bone area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Lichen Planus externally a year and a half ago Immune Deficiency
- Andere Medikamente
- Daily Men's Vitamin Daily Probiotic Statin 10 mg daily Sleep Apnea Nasal Spray Nasal Court nightly Melatonin 2-3 mg
- Allergien
- Morphine Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 10.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Fatigue
Pain in extremity
SARS-CoV-2 test
COVID-19
Vaccination failure
Symptomtext
caller mentioned that she had her 4th Pfizer covid vaccine booster and recently was diagnosed with covid./ She stated they all have had the Pfizer Covid vaccine for their vaccinations.; caller mentioned that she had her 4th Pfizer covid vaccine booster and recently was diagnosed with covid./ She stated they all have had the Pfizer Covid vaccine for their vaccinations.; Caller states just sore arm and tiredness maybe after all of her COVID-19 vaccines; Caller states just sore arm and tiredness maybe after all of her COVID-19 vaccines; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team and product quality group. The reporter is the patient. A 66-year-old female patient received BNT162b2 (BNT162B2), on 25Jan2021 as dose 1, single (Batch/Lot number: unknown), on 15Feb2021 as dose 2, single (Batch/Lot number: unknown), on 10Oct2021 as dose 3 (booster), single (Batch/Lot number: unknown) and on 20Apr2022 at 10:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 66 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Migraine" (unspecified if ongoing), notes: Comments: Migraine Caller states she has been getting migraines for a long time.; "Arthritis" (unspecified if ongoing), notes: Comments: Arthritis Caller states she was diagnosed with arthritis 2 years ago.; "Prediabetes" (unspecified if ongoing); "palpitations" (unspecified if ongoing). Concomitant medication(s) included: NIRMATRELVIR; RITONAVIR; METFORMIN taken for glucose tolerance impaired (ongoing); BYSTOLIC taken for palpitations (ongoing); LIVALO (ongoing). The following information was reported: PAIN IN EXTREMITY (non-serious), FATIGUE (non-serious) all with onset 2021, outcome "unknown" and all described as "Caller states just sore arm and tiredness maybe after all of her COVID-19 vaccines"; VACCINATION FAILURE (medically significant) with onset 29Apr2022, outcome "unknown", COVID-19 (medically significant) with onset 29Apr2022, outcome "recovering" and all described as "caller mentioned that she had her 4th Pfizer covid vaccine booster and recently was diagnosed with covid./ She stated they all have had the Pfizer Covid vaccine for their vaccinations.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (29Apr2022) Positive. Therapeutic measures were taken as a result of covid-19. Clinical course: Question: Does Nurtec (Rimegepant) interact with Paxlovid? Caller states that she takes the Nurtec for migraine and has recently felt the beginning of one coming. She was also put on dexamethasone (unknown manufacturer) for her cough while she is being treated with the Paxlovid for her Covid infection. She also stated that it is cloudy outside and that will also cause her to get migraines. In addition, caller mentioned that she had her 4th Pfizer Covid vaccine booster and recently was diagnosed with Covid. Her brother was also boosted with his 4th booster and recently was diagnosed with Covid. And her son also has Covid but has not yet had a booster. She stated they all have had the Pfizer Covid vaccine for their vaccinations. Medicinal Product Name as Reported by the Primary Source: Metformin. Additional Information for Other medicines Metformin: Caller states she has taken Metformin for several years. Her dose is 500 but she is not sure. She takes Metformin 3 times a day and she takes 3 pills. Additional Context: Warm transfer from (withheld) with Medical Information. Agent reports she has a consumer on line reporting she has been taking Paxlovid and has had the beginning of a migraine. Caller also reported she has been prescribed Dexamethasone. She reports she has had her 4th booster of Pfizer COVID-19 vaccine and recently got COVID. Caller also reported her brother also had the Pfizer COVID-19 vaccine and has gotten COVID and her son also has COVID. Agent reports the caller had a drug interaction question which was addressed. Caller clarifies the details provided by transfer agent. Caller states she got COVID a week after her 4th booster dose of the COVID-19 vaccine and clarifies a week or week and a half. She states she received the COVID-19 vaccine on Wednesday and had symptoms the following Thursday. Caller states her brother had his 4th booster dose of the COVID-19 Vaccine but she doesn't know the exact dates he got the booster. She states her brother got the booster dose of COVID-19 a week or so before her and tested positive yesterday for COVID and he just started Paxlovid today. Caller states her son also has COVID and has had his 3rd booster dose of the COVID-19 vaccine but hasn't gotten his 4th booster dose. She states her son received COVID from 2 kids that are unvaccinated. She states her other grandson after one shot of the COVID-19 vaccine got COVID and then got his second shot of the COVID-19 vaccine. Caller states she does not have the details on shots. Reporter details: Caller states she probably has the longest name in the system. She states she is not a doctor, nurse, or pharmacist but her husband is a doctor. Caller clarifies that her area code for her phone number is # not #. Prescribing HCP details: Caller states she does not have mailing address, email address, or phone number available. Positive for COVID after 4th COVID-19 vaccine booster dose: Caller states her symptoms started on Thursday and she tested positive on Friday, 29Apr2022. She didn't know when to test again but will test again tomorrow after she finishes her Paxlovid. She states that was a question she had as well. Caller states she is still having symptoms but her symptoms have definitely improved. Caller states she asked the pharmacist and was told she received the full dosage. She states the COVID-19 Vaccine was an injection in her left arm. Indication: Caller states she received the COVID-19 vaccine for protection for her age and for her grandkids as she thinks she gave COVID to her grandkids. Concomitant Medications: Caller states she does get a lot of medications but she doesn't have her medication list with her. Additional Vaccines Administered on Same Date of the Pfizer Suspect. Vaccines were not administered on same date with the Pfizer vaccine considered as suspect. No other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) were administered. For Lack of Efficacy, request the following information if not included in the initial report is not available. Caller declined to complete report on her brother, her son, and her grandson. Full details unable to be obtained. Caller states she is glad Pfizer has these vaccines and her symptoms could have been a lot worse if she didn't have the vaccines. Caller declined to complete reports for her brother, her son, and her grandson. Full details unable to be obtained. Caller phone went in and out during report. Attempts made to clarify details. There was product complaint to report. Product strength and count size dispensed not provided on call. Sample of the product available to be returned, if requested (Y/N) was not provided on call. Packaging sealed and intact was not provided on call. 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
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220429; Test Name: COVID; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis (Comments: Arthritis Caller states she was diagnosed with arthritis 2 years ago.); Migraine (Comments: Migraine Caller states she has been getting migraines for a long time.); Palpitations; Prediabetes
- Andere Medikamente
- NIRMATRELVIR; RITONAVIR; METFORMIN; BYSTOLIC; LIVALO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 17,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I felt really tired and fatigued on Monday night, 05/02/2022. So I took a COVID-19 test and it came back negative. The next morning on Tuesday, I had a bad headache and sore throat so I decided to take another test. This time, it came back positive. I contacted my physician and scheduled a telehealth virtual appointment, told her my symptoms, and she prescribed me Paxlovid. I went to the pharmacy the next day to pick it up and have been taking it ever since. This morning (05/09/2022) I took my last dose and feel way better than I was last week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 tests: 05/02/2022 and 05/03/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteoporosis Glaucoma
- Andere Medikamente
- Eye Drop Lumigan Timolol Lisinopril Zyrtec Calcium Supplement Vitamin D Supplement Vitamin C Supplement Multivitamin Supplement
- Allergien
- Penicillin Sulfur Drugs Viramidine Benadryl
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chromaturia
Dizziness
Fatigue
Feeling abnormal
Headache
Pyrexia
Symptomtext
They started on the 4th and have continued since. I have had fever (99-100.1), headache, dizziness, fatigue, brain fog, intensely dark urine. Even while being hydrated the urine color remains the same.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- Cpap machine
- Andere Medikamente
- Amlodipine Olmesartan Simfibrate Atorvastatin Aspirin Claritin Flonase
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 24.04.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Oropharyngeal pain
Respiratory tract congestion
Symptomtext
Sore throat and chest congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Monoclonal treatment on 04/24/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- -
- Andere Medikamente
- Multivitamin and psyllium husk
- Allergien
- Plavix
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Biliary colic
Hot flush
Injection site pain
Malaise
Pain assessment
Symptomtext
yesterday she was not feeling well; severe gall bladder pain; feeling kind of having hot flashes' during that night; abdominal distress; had some pain at the sight; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old female patient received BNT162b2 (BNT162B2), on 27Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Irritable bowel syndrome" (ongoing), notes: Irritable bowel syndrome manages with diet and supplements, currently her bowel is irritated, diagnosed 7-8 years or so.; "gallbladder issues diagnosed" (unspecified if ongoing), notes: gallbladder issues diagnosed about a year and a half ago. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose 1, Lot: EP6955), administration date: 17Mar2021, when the patient was 57-year-old, for Covid-19 immunization; BNT162b2 (Dose 2, Lot: EW0153), administration date: 08Apr2021, when the patient was 58-year-old, for COVID-19 immunization; BNT162b2 (Dose 3 (1st Booster), Lot: FH8020), administration date: 22Oct2021, when the patient was 58-year-old, for Covid-19 immunization. The following information was reported: ABDOMINAL DISCOMFORT (non-serious) with onset 27Apr2022, outcome "unknown", described as "abdominal distress"; HOT FLUSH (non-serious) with onset 27Apr2022, outcome "unknown", described as "feeling kind of having hot flashes' during that night"; INJECTION SITE PAIN (non-serious) with onset 27Apr2022, outcome "unknown", described as "had some pain at the sight"; BILIARY COLIC (non-serious) with onset 27Apr2022, outcome "not recovered", described as "severe gall bladder pain"; MALAISE (non-serious) with onset 28Apr2022, outcome "unknown", described as "yesterday she was not feeling well". The events "severe gall bladder pain", "feeling kind of having hot flashes' during that night", "abdominal distress", "had some pain at the sight" and "yesterday she was not feeling well" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: caller states Patient has already been had this gallbladder ejection frequency issue prior to the vaccines, states has been working with acupuncturist to help in an attempt to avoid having surgery. Patient had gall bladder pain and sometimes it was not there and sometimes its maybe 0-3 pain and then sometimes, like this morning, Patient has surging acute pain. Patient received Covid-19 vaccine within Pharmacy In A Grocery Store facility type. Patient did not received vaccine In military facility. Patient does not require to visit emergency room. Patient had not prior vaccination within 4 weeks of first administration date of the suspect vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220427; Test Name: sometimes its maybe 0-3 pain; Result Unstructured Data: Test Result:0 - 3
- Aktuelle Erkrankungen
- Irritable bowel syndrome (manages with diet and supplements, currently bowel irritated, diagnosed 7-8 years.)
- Vorgeschichte
- Medical History/Concurrent Conditions: Gallbladder disorder (Diagnosed about a year and a half ago.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 09.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allodynia
Facial pain
Magnetic resonance imaging head
Trigeminal nerve disorder
Symptomtext
Allodynia of right side of face and neck Trigemminal distribution in addition to neck and back of head and ear lobe
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- MRI brain neurology visit Dental/facial pain evaluation Gabapentin
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypothyrioid Vitamin d def Menopause GER Constipation High cholesterol Burning mouth syndrome
- Andere Medikamente
- Synthroid, Linzess, HRT,Dexilant,Mobic Vitamin D, MgOxide,Atorvostatin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 18.04.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 378,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 5/1/2022 with symptoms of cough, congestion, headache, body aches, and fatigue. I began taking Paxlovid 5/2/2022 after a telemedicine visit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swap was positive 5/2/2022.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
I had a delayed reaction of a rash no pimples or anything splotchy and raised. Doctor said to use cold compresses and took Benadryl.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- No,
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- No.
- Andere Medikamente
- Simistatin Vitamin D Baby Aspirin Fish oil Premarin
- Allergien
- No.
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 26.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Symptomtext
BRUISING AT INJECTION SITE BRUISE ON CALF
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site erythema
Injection site infection
Injection site scab
Injection site swelling
Symptomtext
Patient received second booster dose on 4/20/2022 and had reported a few days later that she had swelling and redness around the injection site. Almost a week later, patient reported that the injection site had scabbed over and went to doctors office to be examined. Doctor reported that the site was infected and prescribed an antibiotic ointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 30.04.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Feeling cold
Headache
Myalgia
Similar reaction on previous exposure to drug
Symptomtext
After first day: Muscle aches, headache, feeling cold, temperature at 99.5 degrees, tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Arthritis, Two treated brain anuerysms July 2021, kidney stones, gall stone
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Atorvastatin 5mg.
- Allergien
- No, I have not experienced any allergies to food, but was told I was allergic to shellfish, tumbleweeds and cockaroaches
- Vorherige Impfungen
- Similar to current
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 27.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Nausea
Skin discolouration
Symptomtext
Patient was vaccinated on 04/27/2022 at 4:30pm and began to experience symptoms (primarily joint pain) at 9AM on 04/28/2022. Symptoms included joint pain throughout entire body (mostly upper body), nausea, whiteness at fingertips, and overall progressive worsening up to time of reporting symptoms via phone call on 04/29/2022 around 10AM. There was no redness, no fevers, no chills, and no shortness of breath (patient denied all).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 24.04.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Pain in extremity
Peripheral swelling
Skin discolouration
Skin exfoliation
Symptomtext
About 2-3 weeks post immunization, toes of both feet became swollen, purple, burning and painful to touch...within one week all symptoms abated...skin on toes is peeling off slowly and painlessly...after about two weeks, toes will be completely healed. Identical symptoms after first dose...2.4.2021...Telemed visit with physician...suspected post-immunization immune response...little was known about patient immune-response to vaccine...since problem was already abating, and Covid numbers were high, I did not request an office visit for an official diagnosis. There was no reaction after doses 2 & 3. Thank you.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension
- Andere Medikamente
- losartan, atorvastatin
- Allergien
- penicillin
- Vorherige Impfungen
- Same as described above.
- Staat
- NY
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 16.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Joint stiffness
Movement disorder
Pain
Symptomtext
.Extreme pain in the left shoulder, with stiffness in the joint, unable to move anywhere. The pain began at the time of vaccination and the pain increased each day, with the maximum bearable pain being on day 7 after vaccination. I went to the hospital on April 26th where I received care and then went to the orthopedist April 27th
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- No
- Allergien
- Opioid
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Myalgia
Symptomtext
I had muscle soreness and the next day I had fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes Type II; High blood pressure; High cholesterol; Obesity
- Andere Medikamente
- Metoprolol; Benicar; Eliquis; Lyrica; Crestor; Tamsulosin; ACTZ; Hydralazine; Humalog; Vitamin D3; Vitamin C; Centrum senior multivitamin; Tylenol
- Allergien
- None
- Vorherige Impfungen
- Shingles vaccine, 65 years old, soreness.
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Culture urine
Diarrhoea
Headache
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Head Ache starting on 4/6/2022 through 4/8/2022 Fever 100.5 starting on 4/7/2022 through 4/8/2022 Diarrhia starting on 4/7/2022 through 4/10/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Covid Rapid Antigen Test self administered on 4/7/2022 - negative Covid PCR test 04/08/2022 administered by the Urgent Care - negative Urine culture 04/08/2022 Urine culture 04/08/2022 - negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Glaucoma, high blood pressure, high cholesterol
- Andere Medikamente
- Losartin, Simvastatin, Latanoprost, CoQ10, Vitamin D,
- Allergien
- Scallops
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID-19 breakthrough infection on April 18, 2022. Mild symptoms: low grade fever, sore throat, headache, cough and runny nose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Administered self-test, COVID-19 Antigen Rapid Test. Test was positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seizure disorder following measles at age 8 (there was no vaccine at the time). Last seizure was April 3, 1977. Taken some combination of phenytoin and phenobarbital since age 8. Went off phenytoin in 1982 and switched to phenobarbital and have been on vardoses
- Andere Medikamente
- Phenobarbital, Atorvastatin, CQ10, B12, D3, Baby Aspirin, Magnesium, Iron
- Allergien
- Mesuximide, erythromycin (delivered in eye), corn, flonase
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Musculoskeletal stiffness
Myalgia
Nausea
Neck pain
Pain in extremity
Symptomtext
The next morning, I woke up with stiff and sore neck and that lasted for a couple of days. I took arthritis strength Tylenol every 8 hours for a day and a half and the pain went away. But then for the next two weeks I was having muscle aches in my legs. Like a general achiness in my lower legs. That persisted for another week and a half in different intensities. I also felt queasy off and on for two weeks, maybe every other day, and gradually diminished. There were a couple of days immediately after the neck pain went away that I felt quite fatigued.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Stage 2 Prostate Cancer; Celiac Disease; Pace maker
- Andere Medikamente
- Metoprolol Succinate Doxazosin Losartan Atorvastatin Aspirin Magnesium Gluconate Multivitamin Pataday Xiidra
- Allergien
- Celiac Disease Cipro Sulfa Based Antibiotics
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 11.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Rash
Skin exfoliation
Urticaria
Symptomtext
Rash, hives, swelling of arms legs, peeling skin arms neck.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- I have pictures of reactions.
- Aktuelle Erkrankungen
- Breast cancer; Sjogren syndrome; Hypertension; Essential tremors
- Vorgeschichte
- Hypertension; Breast cancer; Sjogren syndrome; Essential tremors
- Andere Medikamente
- Lisinopril; Triamterene; Hydroxychloroquine; Pravastatin
- Allergien
- Environmental allergy
- Vorherige Impfungen
- Flu vaccine in 2012
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bronchial disorder
Bronchitis
COVID-19
Cough
Delirium
Dysstasia
Pyrexia
Respiratory symptom
SARS-CoV-2 test positive
Symptomtext
So the immediate thing that happened was getting a fever within a hour or two after the vaccine and then became delirious and I was unable to stand and had respiratory symptoms that were prevalent which is why I had to go to the doctor. This lasted for 2 or 3 days. As time progressed and it was a common thing for me that I had bronchitis and the doctor gave me more medication due to the coughing and bronchial issues. I was diagnosed with acute bronchitis, I still have a shade of it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 Test negative on 4/9/22. Home COVID-19 Test positive on 4/19/22.
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- Diabetes; Hypertension; Asthma; Allergies; Coronary Artery Disease
- Andere Medikamente
- Montelukast; Benazepril/HCTZ; Metformin; Glimepiride; Aspirin; Loratadine; Fluticasone; Multivitamin; D3 Vitamin; AREDS Preservision
- Allergien
- None
- Vorherige Impfungen
- Shingles with fever and delirium in 2020 62 age unknown brand.
- Staat
- NJ
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 24.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye haemorrhage
Eye pain
Ocular hyperaemia
Symptomtext
Hemorrhage in right eye with pain behind the eye and in the eye itself. Looks very bloody, red and hurts. I had problems with my right shoulder after my 1st booster/3rd shot of Pfizer COVID-19 vaccine. Self-treating with eye drops and saline solution. Taking Tylenol for pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Slight cold
- Vorgeschichte
- Non-contractile bladder, heart disease, high blood pressure
- Andere Medikamente
- Blood pressure meds; Repatha for cholesterol; Hiprex for urinary condition; Toprol for heart.
- Allergien
- Injected iodine for contrast
- Vorherige Impfungen
- Pfizer, 3rd shot. Acute tendonitis in right shoulder.
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 24.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Urticaria
Wheezing
Symptomtext
Anticipating a reaction I took Zyrtec and received the Pfizer booster. Was "fine" that day. The following morning I stopped taking Zyrtec. By midday I was covered with red, itchy welts all over my body and I dealt with wheezing. Went back on Zyrtec. It's day five and I'm still itchy but the red welts are starting to dissipate. On April 2 2021 I received the J & J vaccine and was covered with red welts all over, for five days. I was hot to the touch but it was not itchy, nor did I experience respiratory issues. Stayed in bed taking Benadryl every few hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Erythromycin Penicillin Vancomycin Compazine Valium Morphine
- Vorherige Impfungen
- Johnston & Johnston
- Staat
- DC
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 23.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Urticaria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- AFIB, HYPERTENSION
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 17.04.2022
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Decreased appetite
Diarrhoea
Flatulence
Gastric dilatation
Vomiting
Symptomtext
On 4/6/22, I received my first dose of the Covid vaccine. From Saturday 4/09/22-Saturday 4/16/22, I was on vacation. I ate almost every meal out. Throughout the day on 4/17/22, I did not have an appetite. I ate a small meal at 2pm (salad, sweet potatoes, brussel sprouts/pecans/some bacon bits/apples and bread). By 4pm I was having diarrhea and gas. At about 9pm, I vomited and continued having diarrhea. I went to bed shortly after and slept through the night. The next morning I vomited again, but it was just bile as my stomach was empty. I ate a piece of toast and a banana. No more diarrhea or vomiting for the rest of the day. Yesterday, 4/21/22, I went out to eat. I got a warm bowl with rice, tomatoes, avocado. Last night, 4/21/22, I woke in the night with extreme bloating. My belly looked like it had a balloon in it. I went to the bathroom and had very watery diarrhea. I vomited a lot at one time. I had excessive gas. I was in the bathroom for about an hour. I stayed home from school the next day and did not vomit again. I had some diarrhea earlier around 5pm but nowhere near as bad as before. I still feel a little gassy but other than that, symptoms have resolved for now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- I am trying a gluten free diet for the next few weeks to see if that helps. After 3 weeks I will slowly reintroduce gluten and see if it makes me sick or not.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Anxiety/depression
- Andere Medikamente
- Sertraline Risperidone Zyrtec (generic) Vitamin D Zinc
- Allergien
- Environmental
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 17.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram pulmonary
Dizziness
Lymphadenopathy
Oxygen saturation decreased
Pain in extremity
Peripheral swelling
Symptomtext
Two days later participant woke up with a lot of pain and swelling in left arm. Also had Lymph node swelling. Next became very lightheaded and dizzy. Oxygen level dropped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- CTPA
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Autoimmune Disease
- Andere Medikamente
- Allegra; Zyrtec; Pepcid; Singulair; Nasal spray; Xolair; Nexium; Larin; Inhaler; Aspirin; Multivitamins
- Allergien
- Antipox; Prednisone
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
pain on left arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- advil
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash pruritic
Symptomtext
On April 15th 2022, I broke out in a rash that started in the middle of my neck like a bite. It was a red raised itchy small round lump. In the next few days it spread down my neck onto my upper and lower chest, but now it was much more pronounced and in clusters, red and many more bumps. Very itchy! It is now April 21st and It is spreading to mu right shoulder with smaller bumps that are less itchy. The Dr. put me on Claritin, 10mg which I started April 20th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eczema
Rash
Symptomtext
Extreme eczematous rash on neck, chest, breasts, back of shoulders, back of arms, inner forearms, abdomen, waist, thighs front and back, behind knees, sides of knees, inner and outer elbows, buttocks, and tops of hands. Treatment has included a six-day course of Methylprednisolone (21 pills at 4mg each), twice daily application of triamcinolone acetonide ointment 0.1%, Claritin once daily, 50 mg Benadryl daily, three times daily application of itch relief spraydiphenhydramine hydrochloride 2% with zinc acetate0.1%, colloidal oatmeal baths daily. OTC Topical treatments have been ongoing since April 3. Prednisone and Triamcinolone treatment started on April 11. As of today, April 21, symptoms have not changed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Physical examination only
- Aktuelle Erkrankungen
- Arthritis
- Vorgeschichte
- Asthma, arthritis, seasonal allergies
- Andere Medikamente
- Hydroxychloroquine, Acetaminophen, Claritin, Multi-vitamin
- Allergien
- None. Seasonal allergies/pollen.
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Diarrhoea
Feeling abnormal
Headache
Lymph node pain
Nausea
Pain
Vomiting
Symptomtext
NAUSEA, VOMITING, DIARRHEA, SORE LYMPH NODE UNDER LEFT ARM. SHOOTING PAIN IN LEFT ELBOW AND SHOOTING PAIN IN HEAD AND RIGHT KNEE. LASTED ABOUT 24 HOURS, GOT SHOT ON FRIDAY , STARTED FELLING BAD FRIDAY NIGHT, FEELING BETTER ON SUNDAY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- morphine
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 17.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site cellulitis
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Mild to moderate cellulitis at and distal to the injection site, covering an area approximately 4" X 2". Swelling, erythema and heat present, but no visible pustules or other signs of infection. Mildly pruritic. Signs began approximately 24hr after the injection, and progressed for the next 48hrs. Patient is currently 5 days post injection with no signs of improvement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- reflex sympathetic dystrophy, osteoarthritis, myofascial pain syndrome
- Andere Medikamente
- oxycodone tizanidine venlafaxine vitamin D3
- Allergien
- penicillins sulfa antibiotics
- Vorherige Impfungen
- Moderate to severe cellulitis after tetanus toxoid injection. Date of injection unknown, but patient was in her 50s at the time
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Myalgia
Pyrexia
Symptomtext
Chills, high fever, muscle aches and pains. Resolved in 12 hours ( much shorter than the 3 days in vaccine 3)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure Cardiac artery issues
- Andere Medikamente
- Synthroid, Toprol XL, Lisinipril, baby aspirin, vitamins d, c, b and calcium with magnesium.
- Allergien
- Shellfish, penicillin, mycin drugs, latex
- Vorherige Impfungen
- Pfizer 3 08/21/2022, chills and fever for 3 days, hep a , b 11/2019. Fever and nausea
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness unilateral
Fatigue
Headache
Hyperacusis
Pyrexia
Sudden hearing loss
Tinnitus
Symptomtext
mild fever , head ache ,fatigue ringing in right ear - sudden hearing loss in right ear treated at Urgent care on 4/16/22 with 60 mg of prednisone daily. followed up on 4/18/22 with a audiology test and ENT doctor and noted event was triggered by Pfizer booster and to stay the coarse with prednisone therapy and to schedule another hearing test in one month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Urgent Care visit on 4/16/22 Hearing test dated 4/18/22 and ENT Doctor visit 4/18/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure ( controlled) Diabetes type 2 ( controlled) Sleep apnea ( controlled)
- Andere Medikamente
- Allopurinol 100mg ,lisinopril 5mg ,Lipitor 40mg none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
itching intensely all over his body; just a lot of intense itching; he feels like even his eye balls are itching; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received BNT162b2 (BNT162B2), on 08Apr2022 at 18:00 as dose number unknown, single (Lot number: FJ9943) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PRURITUS (non-serious) with onset 08Apr2022, outcome "unknown", described as "itching intensely all over his body; just a lot of intense itching; he feels like even his eye balls are itching". Additional information: Reporter stated, "My husband and myself (Further clarifications unknown) received the Pfizer COVID Vaccine at about 6 'O' clock this evening. My husband is now having, he doesn't have a rash but he is itching intensely all over his body but there is no rash. It's just a lot of intense itching. He said even, he feels like even his eyeballs are itching, is that any, I can't find anything about that being reported." No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Fatigue
Pulmonary pain
Symptomtext
Extreme pain in left lung and fatigue. Temperature of 102f for three days Visited Urgent care and later prescribed inhaler Next day prescribed steroids for a week
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- No labs Two visits to doctors and the phone calls with nurse Counseling at pharmacy on how to use inhaler and steroid treatment
- Aktuelle Erkrankungen
- Achy hip and back muscles Artheritis
- Vorgeschichte
- Spinal care through chiropractor Counseling through therapist Family counseling through marriage counselor
- Andere Medikamente
- Zoloft Multi vitamin Calcium/magnesium
- Allergien
- Penicillins Progesterone Sulfites Aspartame Jello
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Breast pain
Dysgeusia
Ear infection
Ear pain
Eye pain
Facial pain
Flatulence
Myalgia
Pain
Pyrexia
SARS-CoV-2 test negative
Toothache
Symptomtext
After my second booster vaccine, muscle from armpit to my left breast has been extremely sore since the vaccine was administered however, the pain has slowly dissipated after. My fever went up to 103.2F and slept it off took Tylenol and slept. I had some strange chemical taste coming from my mouth and gas from my chest. I also had an ear infection that started with sharp pains on the sides of my face. The pain shot up from my teeth to my eyes as well. The next day it moved to just one side, and it goes from my ear to my eye. I do notice that my fever has gone down to 99.7F and Ear infections seem to be the major lingering issues. In the past vaccinations I have had somewhere between a few weeks post vaccines a herpes simplex virus outbreak as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- COVID Test: Negative
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- History of Pneumonia Bilateral since birth; Head injury from birth that causes Seizures; Leg injury; Obesity
- Andere Medikamente
- Nicomiid, Tylenol 800 mg
- Allergien
- Many Allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
rash on right arm, itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Cymbalta 30mg
- Allergien
- seasonal pollen
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Gait disturbance
Pain in extremity
Vaccine positive rechallenge
Symptomtext
Leg pain and lower back all on the right-side. Causes me to limp. Starts 2-3 days after every vaccine. This time worse than all previous vaccines. It takes about almost 2 weeks before it goes away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Penicillin
- Vorherige Impfungen
- Previous 3 COVID-19 Pfizer vaccines, same reaction.
- Staat
- -
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pruritus
Urticaria
Symptomtext
hives and itching. taking Benadryl. getting better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Nausea
Thinking abnormal
Symptomtext
Initial Nausea - lasted for about 2-3 hours Brain Fog (fuzziness, not thinking clearly) - lasted 1.5 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Injection site extravasation
Symptomtext
Vaccination for COVID19 Pfizer 4th dose/booster was administered to patient by a certified technician with a 1inch, 1ml vanishpoint safety syringe/needle. After administration, the technician activated the safety feature by retracting needle into syringe, a small amount of liquid came out of the patient's arm. The patient stated that there was a "bubbling." Patient does not feel that she received the entire dose. I assured patient during a phone call after the vaccination date, that I believe she received the entire dose, as the syringe requires the entire dose to be administered. There may have been some that came out from the retraction, but the entire dose was administered. No adverse event has occured but that patient believes she may not receive full protection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site extravasation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 07.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Neck pain
Swelling
Symptomtext
Swelling in his neck area and soreness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- atorvastatin, lumigan eye drops, omega 3
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Chills
Injection site erythema
Injection site pain
Pain
Symptomtext
injection site pain, redness at site, 2 days later abdominal pain, chills, aches, still ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- vit. C,E, D3, Calcium, Alpha lipoic Acid, potassium, magnesium, Co-enzyme Q10, B-50 complex, Glucosamine-Chondroitin MSM.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Investigation
Limb discomfort
Malaise
Symptomtext
Dizzy; not so steady on her feet; Chills; wasn't feeling well; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 03Apr2022 (Lot number: FJ9943) at the age of 76 years as dose 4 (booster), single for covid-19 immunisation. Relevant medical history included: "Blood pressure" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN taken for blood pressure measurement; NORVASC taken for blood pressure measurement. Vaccination history included: Bnt162b2 (Dose 1, Lot number: EN6208), administration date: 10Mar2021, when the patient was 75 years old, for Covid-19 Immunization, reaction(s): "Sore arm"; Bnt162b2 (Dose 2, Lot number: EW0150), administration date: 31Mar2021, when the patient was 75 years old, for Covid-19 Immunization, reaction(s): "Sore arm"; Bnt162b2 (Dose 3, Lot number: FD0809), administration date: 29Oct2021, when the patient was 76 years old, for Covid-19 Immunization, reaction(s): "Sore arm". The following information was reported: CHILLS (non-serious) with onset 04Apr2022, outcome "recovered" (04Apr2022), described as "Chills"; DIZZINESS (non-serious) with onset 04Apr2022 07:30, outcome "recovered" (04Apr2022 07:30), described as "Dizzy"; MALAISE (non-serious) with onset 04Apr2022, outcome "unknown", described as "wasn't feeling well"; LIMB DISCOMFORT (non-serious) with onset 04Apr2022 07:30, outcome "recovered" (04Apr2022), described as "not so steady on her feet". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of chills, dizziness, malaise, limb discomfort. Additional information: Caller states she went yesterday to get her 4th booster for the BA5 and clarifies BA2 Variant. Caller states last night she had chills. She reports this morning she wasn't feeling well and thought she was coming down with COVID-19. Caller states she never had these side effects before except a sore arm that she has had before. She was concerned because she didn't want her husband to catch anything. Email Address: unknown; Caller states she will leave the report at her house address. She states she is sure Pfizer receives a few phone calls regarding this. Patient details: Caller states she thinks that she has shrunk. Caller states weight is unknown, but she is not big and fat. She states she tells the doctor she does not want to be weighed as she is not fooling with that. She states maybe 170 pounds. Caller states the phone broke up. Caller confirms the call is regarding the COVID-19 vaccine. Caller states a 4th dose is recommended for the new variant and clarifies the sub variant she thinks. Caller states her symptoms are not a big deal. HCP Details: Caller states she has Medicare. Caller declines consent for follow up with primary care physician since she states she will be okay. Caller states she was afraid she had caught COVID-19 but states she was told she didn't. Chills: Caller states the chills began around 1:00 am today, 04Apr2022 and stopped after about 3 hrs. She states she put blankets on the bed and the chills stopped. Caller states after talking to the pharmacist she feels better now. The pharmacist told her 24-48 hours for her symptoms to resolve. Dizzy: Caller states when she got out of bed her head was spinning and she had to hold on to something because she didn't want to fall. Caller reports she woke up and got out of bed at 7:30am, 04Apr2022. Not steady on feet: Caller states she was not feeling good. She reports the not steady on her feet began at the same time as the dizziness at 7:30am, 04Apr2022. She states she took Tylenol and feels better now. She states her vaccination card is in her purse. Caller reports the pharmacy gave her some paperwork yesterday maybe her vaccination information will be there. She states the pharmacy gave her a lot of papers. Dose: Caller states the vaccination took like 3 seconds in her left arm. Indication: She states she does not know if she is immune compromised, but she is old. She reports her granddaughter comes to her house and her granddaughter is not vaccinated. Caller states all her test results came back fine but she needs her physical this month. She reports that she hasn't had her physical since last year, but all her tests were fine last year. Caller declined to complete supplemental form as she states she has someone calling on the other line. No further details to provide. Description of Product Complaint: Description of complaint: She reports this morning she wasn't feeling well and thought she was coming down with COVID-19. She thought she may have got COVID-19 from the vaccine but the pharmacy told her she didn't catch COVID-19. Patient underwent lab test procedures which included: Investigation came back fine. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: Lab test; Result Unstructured Data: Test Result:came back fine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure.
- Andere Medikamente
- LOSARTAN; NORVASC.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Gastrointestinal disorder
Hyperhidrosis
Nausea
Symptomtext
Sweating real bad like he had a fever. Nausea, stomach and extreme fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- stepped on nails 2 days prior so he took a tetanus shot
- Vorgeschichte
- COPD, arthritis
- Andere Medikamente
- gabapentin, omeprazole, hydrochlorothiazide, Motrin
- Allergien
- latex
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Product storage error
Symptomtext
Vaccine was administered with a vial that was punctured or more than 12 hrs. Patient reported sore arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Immediate post-injection reaction
Malaise
Nausea
Symptomtext
Patient appeared faint and nauseous immediately following injection. Pt. started to slump in chair and complained that she felt hot and sick. Patient was told to lay on ground and was given water and ice. Pt. did not go into syncope or have any further reaction, and recovered after about 20 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 05.03.2022
- Beginn
- 06.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Lymphadenopathy
Pain
Symptomtext
Throbbing headache and golf ball size swollen lymph node after each vaccine. Swelling had almost disappeared after first vaccine under left arm. Swelling appeared under right arm the next day after second vaccine. All day after the second vaccine I was achy and very tired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- Protronix, Gabapentin, Lorsartan
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 19.03.2022
- Beginn
- 20.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Symptomtext
Red area around injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Arthralgia
Asthenia
Fatigue
Headache
Injection site pain
Insomnia
Muscle spasms
Myalgia
Pain
Pain in extremity
Symptomtext
insomnia, bloating, headaches, fatigue, body aches, muscle aches, muscle cramping, pain at injection site, arm pain, low energy, constantly tired, joint pain, this has been going on for two weeks now
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- stomach issues
- Andere Medikamente
- Fenefibrate, Celexa, Tramadol, Omeprozole, Abilify, Promethazine, multi vitamin
- Allergien
- PCN, Motrin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 11.10.2023
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Symptomtext
she developed the fluttering heart 2 weeks later; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 72-year-old female patient received bnt162b2 (BNT162B2), on 01Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 72 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: bnt162b2 (DOSE 1, SINGLE, Batch/lot number: EK4176), administration date: 15Jan2021, for COVID-19 immunisation, reaction(s): "allergic reaction of numbness and swelling of her lips", "allergic reaction of numbness and swelling of her lips", "allergic reaction of numbness and swelling of her lips"; bnt162b2 (DOSE 2, SINGLE), administration date: 10Feb2021, for COVID-19 immunisation, reaction(s): "no reaction"; bnt162b2 (DOSE 3 (BOOSTER), SINGLE, Batch/lot number: 301US8A), administration date: 29Sep2021, for COVID-19 immunisation, reaction(s): "she developed the fluttering heart". The following information was reported: CARDIAC FLUTTER (medically significant) with onset Apr2022, outcome "unknown", described as "she developed the fluttering heart 2 weeks later". Therapeutic measures were not taken as a result of cardiac flutter. Clinical course: She said on her last three doses, she took an anti-histamine prior to getting those doses. Before her last three dose of this Pfizer COVID-19 vaccine, she took an anti-histamine prior to getting those doses and she did not have an allergic reaction. However, she develops fluttering of the heart two weeks later. She developed a fluttering heart two weeks later, on all of three of her last doses. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300320687 same patient/vaccine, different dose number/event;US-PFIZER INC-202300321099 same patient/vaccine, different dose number/event;US-PFIZER INC-202300321098 same patient/vaccine, different dose number/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac flutter
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.08.2023
- Impfdatum
- 12.04.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 129,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Pfizer 3/11/21 lot# EN6207; Pfizer 4/1/21 lot# ER8730; Pfizer 4/12/22 Lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 15.06.2023
- Impfdatum
- 16.04.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 153,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 1/25/21 lot# EL9261; Pfizer 2/5/21 lot# EL9267; Pfizer 8/27/21 lot# EW0173; Pfizer 4/16/22 lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.02.2023
- Tage bis Beginn
- 306,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 2/24/21 Lot# EN6200; Pfizer 3/27/21 Lot# En6208; Pfizer 9/21/21 lot# FF8825; Pfizer 4/21/22 lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 24.04.2023
- Impfdatum
- 30.04.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 246,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood thyroid stimulating hormone decreased
Graves' disease
Hyperthyroidism
Metabolic function test
Thyroid function test abnormal
Symptomtext
On 28DEC2020 my doctor had a TSH test done and my value was 1.23 ml UL within standard range. Upon changing doctors in 01JAN2023 a new TSH test was done and the value was les than 0.008mU/L. I was sent to an Endocrinologist who did a full thyroid workup and stated I have an overactive thyroid and graves disease. I have been prescribed methimazole to control my thyroid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood thyroid stimulating hormone decreased
- Hospital-Tage
- -
- Labordaten
- Full metabolic work up. Diagnosis overactive thyroid and grave disease.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lyme's Disease
- Andere Medikamente
- Atorvastatin; multivitamin; fish oil; probiotic
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 21.04.2023
- Impfdatum
- 05.05.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 180,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 1/8/21 Lot# EL3249; Pfizer 2/8/21 Lot# EM9810; Pfizer 10/16/21 Lot# 301558A; Pfizer 5/5/22 Lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 13.04.2023
- Impfdatum
- 11.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 1/20/21 Lot# El3249; Pfizer 2/7/21 Lot# EL9265; Pfizer 9/26/21 Lot# FF8841 ; Pfizer 4/11/22 Lot# FJ9943;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 03.04.2022
- Beginn
- 20.02.2023
- Tage bis Beginn
- 323,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Nasopharyngitis
Sinusitis
Symptomtext
I had a sinus infection following having COVID-19. I received ten days of antibiotics. The COVID-19 itself came and gone in a couple days. It wasn't that bad. The cold I experienced afterwards was worse. I never saw a doctor for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Lymphocytic Leukemia
- Andere Medikamente
- Propranolol; levothyroxine; loratadine; vitamin D
- Allergien
- Cold air
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 26.03.2023
- Impfdatum
- 04.10.2022
- Beginn
- 09.03.2023
- Tage bis Beginn
- 156,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 14.03.2023
- Impfdatum
- 01.04.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 116,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy skin abnormal
Limb mass
Malignant melanoma
Mass excision
Symptomtext
At my yearly Dermatologist appointment, doctor found a mass near my thigh. Doctor performed a Punch Biopsy and found that is was Melanoma. Had the mass removed. I go to a Dermatologist every 3 months for a check-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy skin abnormal
- Hospital-Tage
- -
- Labordaten
- 2022JUL26 Punch Biopsy on leg - Melanoma.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hashimoto's Disease; Acid Reflux; Bile Reflux; Fibromyalgia; Asthma; High Blood Pressure; High Cholesterol.
- Andere Medikamente
- L-thyroxine; Losartan; Famotidine; Citracal; Vitamin D3; Vitamin B12; Methyl folate; D Mannose; Cranberry Supplements; Montelukast; Rosuvastatin; Naltrexone; Flonase; Xopenex Inhaler.
- Allergien
- Nitrofurantoin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 13.03.2023
- Impfdatum
- 09.09.2022
- Beginn
- 15.02.2023
- Tage bis Beginn
- 159,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
Symptomtext
A-fib, referred to cardiologist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- Nonees
- Vorgeschichte
- HBP, high cholesterol
- Andere Medikamente
- Atorvastatin Baby aspirin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.03.2023
- Impfdatum
- 08.09.2022
- Beginn
- 24.01.2023
- Tage bis Beginn
- 138,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
This wasn?t really an adverse event from the vaccine. It was just that I did have Covid even though I had five vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None I had a very mild case of Covid four months after the fifth vaccine. I also had influenza a in November 2022. I am not able to take the flu shot because of the risk of Guillain-Barr?.
- Vorgeschichte
- Rheumatoid arthritis, osteoporosis.
- Andere Medikamente
- Plaquinel and pantoprazole
- Allergien
- Gluten, beans, legumes, criciferous vegetables, animals, plants.
- Vorherige Impfungen
- Fever, arm soreness, tiredness.
- Staat
- CT
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 08.03.2023
- Impfdatum
- 14.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- 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 77-year-old male patient received BNT162b2 (BNT162B2), on 14Apr2022 at 14:00 as dose 5 (booster), single (Lot number: FJ9943) at the age of 77 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure" (unspecified if ongoing); "cholesterol" (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 2023, outcome "unknown" and all described as "COVID-19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19: Treatment with Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure abnormal; Cholesterol
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 22.02.2023
- Impfdatum
- 06.04.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 86,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gout
Pericardial effusion
Pleural effusion
Spinal osteoarthritis
Thoracic operation
Weight
Symptomtext
gout; Pericardial effusion; turned into pleural effusion cardiologist almost killed her; Had thoracic surgery; Cervical spondylosis; This is a spontaneous report received from contactable reporter (Consumer). The reporter is the patient. A 67-year-old female patient received BNT162b2 (BNT162B2), on 06Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 67 years for covid-19 immunisation. The patient's relevant medical history included: "Coronary artery disease with 7 stents" (unspecified if ongoing); "Coronary atherosclerosis" (unspecified if ongoing); "Angina" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "diabetes type 2" (unspecified if ongoing); "Acquired hypothyroidism" (unspecified if ongoing); "Osteopetrosis" (unspecified if ongoing), notes: from taking Synthroid Started Probably like 3 years ago; "Seronegative arthritis" (unspecified if ongoing); "Adhesive capsulitis" (unspecified if ongoing), notes: Adhesive capsulitis Known as frozen shoulder; "Skin allergies" (unspecified if ongoing); "Osteoarthritis" (unspecified if ongoing); "autoimmune inflammation" (unspecified if ongoing); "non rheumatic mitral regurgitation" (unspecified if ongoing), notes: Still trying to get answer about that one; "thyroid cancer" (ongoing); "Diabetes" (ongoing); "chronic responsive pain syndrome from ankle injury" (ongoing); "heart" (ongoing); "Cholesterol" (ongoing); "stroke" (ongoing); "guess it is mood stabilizer" (ongoing); "Constipation" (ongoing); "nausea from swallowing all these pills" (ongoing), notes: nausea from swallowing all these pills; "Cervical spondylosis", start date: Jul2022 (unspecified if ongoing); "Blood pressure" (ongoing); "immunocompromised" (unspecified if ongoing); "multiple vitamin" (ongoing). Concomitant medications included: SYNTHROID [reported has been taking about 10 years ] taken for thyroid cancer (ongoing); METFORMIN [reported probably about 10 years] taken for diabetes mellitus (ongoing); HUMALOG [reported been taking probably 9 years] taken for diabetes mellitus (ongoing); LEVEMIR [reported has been taking for 10 years]taken for diabetes mellitus (ongoing); PREGABALIN [reported been taking a couple years] taken for complex regional pain syndrome (ongoing); ASPIRIN [ACETYLSALICYLIC ACID] [reported been forever, 20 years] taken for cardiac disorder (ongoing); CARVEDILOL [been taking, probably about a year] taken for cardiac disorder, blood pressure abnormal (ongoing); ENALAPRIL [reported been taking probably different dose for 20 years] taken for blood pressure measurement (ongoing); ATORVASTATIN [reported probably been taking for 5 or 7 years] taken for blood cholesterol abnormal (ongoing); VASCEPA [reported been taking probably 2 years] taken for blood cholesterol abnormal (ongoing); XANAX [has been on it about 23 years] taken for cerebrovascular accident (ongoing); FLUOXETINE taken for affective disorder, start date: 2017 (ongoing); COLACE [reported taking maybe like 3 years] taken for constipation (ongoing); VITAMIN D3 [reported to be on it a few years ago] (ongoing); CENTRUM SILVER WOMEN 50+ [reported as always taken vitamins] taken for vitamin supplementation (ongoing); TYLENOL (ongoing); ZOFRAN [ONDANSETRON] [reported at least 3 or 4 years] taken for nausea (ongoing); COLCHICINE taken for inflammation, start date: Aug2022 (ongoing); BRILINTA taken for anticoagulant therapy, start date: Aug2022 (ongoing). Past drug history included: Metformin, reaction(s): "has significant B12 deficiency", notes: he never tested her for B12. As result of B12, she is now anemic. Vaccination history included: BNT162b2 (Dose 3; Lot number: EW0185), administration date: 03Sep2021, when the patient was 66-year-old, for COVID-19 immunization; BNT162b2 (Dose 2; lot number: EP7533), administration date: 26Mar2021, when the patient was 66-year-old, for COVID-19 immunization; BNT162b2 (Dose 1; lot number: EN6206), administration date: 05Mar2021, when the patient was 66-year-old, for COVID-19 immunization. The following information was reported: SPINAL OSTEOARTHRITIS (non-serious) with onset Jul2022, outcome "unknown", described as "Cervical spondylosis"; THORACIC OPERATION (medically significant) with onset Aug2022, outcome "unknown", described as "Had thoracic surgery"; PERICARDIAL EFFUSION (medically significant, life threatening) with onset Sep2022, outcome "unknown"; PLEURAL EFFUSION (life threatening) with onset Sep2022, outcome "unknown", described as "turned into pleural effusion cardiologist almost killed her"; GOUT (non-serious), outcome "unknown". The patient underwent the following laboratory tests and procedures: Weight: 150, notes: Probably about 150 today. Therapeutic measures were taken as a result of thoracic operation, gout. Additional information: The patient reported that she had to receive a 3rd and subsequent dose administered since CDC said so. She received her 3rd dose in her house. The adverse events did not require any visit (facility). The patient inquired if an additional dose is required as they are recommending another booster for compromised patients
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gout
- Hospital-Tage
- -
- Labordaten
- Test Name: weight; Result Unstructured Data: Test Result:150; Comments: Probably about 150 today
- Aktuelle Erkrankungen
- Blood pressure abnormal; Cholesterol; Complex regional pain syndrome; Constipation; Diabetes; Heart disorder; Mood disorder; Nausea (nausea from swallowing all these pills); Stroke; Thyroid cancer; Vitamin supplementation.
- Vorgeschichte
- Medical History/Concurrent Conditions: Acquired hypothyroidism; Adhesive capsulitis (Adhesive capsulitis Known as frozen shoulder); Allergic skin reaction; Anginal syndrome; Blood pressure high; Cervical spondylosis; Coronary artery disease; Coronary atherosclerosis; Immunocompromised; Inflammation; Mitral regurgitation (Still trying to get answer about that one); Osteoarthritis; Osteopetrosis (from taking Synthroid Started Probably like 3 years ago); Seronegative arthritis; Type II diabetes mellitus.
- Andere Medikamente
- SYNTHROID; METFORMIN; HUMALOG; LEVEMIR; PREGABALIN; ASPIRIN [ACETYLSALICYLIC ACID]; CARVEDILOL; ENALAPRIL; ATORVASTATIN; VASCEPA; XANAX; FLUOXETINE; COLACE; VITAMIN D3; CENTRUM SILVER WOMEN 50+; TYLENOL; ZOFRAN [ONDANSETRON]; COLCHICINE; BR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.01.2023
- Impfdatum
- 03.05.2022
- Beginn
- 02.01.2023
- Tage bis Beginn
- 244,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after two vaccines ; Pfizer x2; Pfizer 10/5/21 Lot# FF2589; Pfizer 5/3/22 Lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 22.12.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
Vaccine brand: Pfizer/BioNTech/Vaccine dose number: 4; 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 68-year-old male patient received BNT162b2 (BNT162B2), on 04Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 68 years for covid-19 immunisation; coviD-19 vaccine nrvv MVa (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)), on 11Sep2022 at 11:30 as dose 5 (booster), single (Lot number: AS7148B), in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 05Mar2021 as dose 1, single (Lot number: 002A21A), on 02Apr2021 as dose 2, single (Lot number: 046A21A) and on 12Nov2021 as dose 3 (booster), single (Lot number: 032F21A) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 04Apr2022, outcome "unknown", described as "Vaccine brand: Pfizer/BioNTech/Vaccine dose number: 4"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (10Dec2022) Negative, notes: COVID rebound after testing negative on 10Dec2022 and 11Dec2022; (11Dec2022) Negative, notes: COVID rebound after testing negative on 10Dec2022 and 11Dec2022; (18Dec2022) Unknown results, notes: I retested on 18Dec2022 due to runny nose, sneezing, and cough symptoms. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: COVID rebound after testing negative on 10Dec2022 and 11Dec2022. I retested on 18Dec2022 due to runny nose, sneezing, and cough symptoms. The patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221210; Test Name: COVID-19 test; Test Result: Negative ; Comments: COVID rebound after testing negative on 10Dec2022 and 11Dec2022.; Test Date: 20221211; Test Name: COVID-19 test; Test Result: Negative ; Comments: COVID rebound after testing negative on 10Dec2022 and 11Dec2022.; Test Date: 20221218; Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown results; Comments: I retested on 18Dec2022 due to runny nose, sneezing, and cough symptoms.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 28.04.2022
- Beginn
- 18.12.2022
- Tage bis Beginn
- 234,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 3/4/2 Lot# EN6205; Pfizer 3/25/21 Lot# Er8733; Pfizer 10/4/21 Lot# FF2588; Pfizer 4/28/22 Lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- external COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 10.03.2022
- Beginn
- 16.12.2022
- Tage bis Beginn
- 281,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after three vaccines Pfizer 2/15/21 Lot# El9267; Pfizer 3/8/21 Lot# EN6199; Pfizer 3/10/22 Lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 17.12.2022
- Impfdatum
- 10.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure measurement
COVID-19
Electrocardiogram
SARS-CoV-2 test
Vaccination failure
Weight
Symptomtext
got confirmed Covid; got confirmed 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 63-year-old female patient received BNT162b2 (BNT162B2), on 23Mar2021 as dose 1, single (Lot number: EN6207), in left arm, on 13Apr2021 as dose 2, single (Lot number: EP7533), in left arm, on 22Oct2021 as dose 3 (booster), single (Lot number: FF8841), in left arm and on 10Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 63 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Breast cancer" (unspecified if ongoing), notes: She had breast cancer like 7 years ago; "irregular heart beat", start date: 16Mar1982 (unspecified if ongoing), notes: irregular heart beat don't know the cause tied tubes in 15Mar1982 when woke up did EKG and showed it; "high blood pressure" (unspecified if ongoing), notes: high blood pressure diagnosed 10-15 years ago; "lung cancer surgery", start date: Jul2022 (unspecified if ongoing), notes: lung cancer surgery Jul2022; "slow down the little acid producers in her stomach" (unspecified if ongoing), notes: slow down the little acid producers in her stomach. Concomitant medication(s) included: LOSARTAN oral taken for hypertension (ongoing); PANTOPRAZOLE oral taken for achlorhydria, start date: Mar2022 (ongoing); VITAMIN C [ASCORBIC ACID]; ZINC; D3; TYLENOL EXTRA STRENGTH. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "got confirmed Covid". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: (unspecified date) High; Electrocardiogram: (15Mar1982) irregular heart beat, notes: irregular heart beat don't know the cause tied tubes in 15Mar1982 when woke up did EKG and showed it. didn't know she had; SARS-CoV-2 test: (unspecified date) Positive, notes: positive for Covid after Pfizer Covid 19 vaccine; Weight: (unspecified date) 128-130 lbs, notes: Weight - at this point about 128-130 pounds. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The report was not related to a study or program. Vaccine Administered was not at specific Facility. The patient had not received Prior Vaccinations (within 4 weeks). The patient has had 2 doses shot and the 1st 2 boosters and queried if it normal to get sick for more than more a couple days. She was on day 4-5 now and does not know what to think. The patient got confirmed Covid on Thursday at home test and went to pharmacy and had more extensive quick one done. The patient received Paxlovid on 09Dec2022 at 11 AM pink and white pills. took twice a day, ongoing. NDC number of Paxlovid: 0069-0345-30. Product investigation summary conclusion included Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER-BIONTECH COVID-19 VACCINE lot FJ9943 was 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 was limited to the reported finished goods lot FJ9943, fill lot FJ9942 and the bulk formulated drug product FJ9940. The final scope included the reported finished goods lot FF8841, fill lot FF8835, and the formulated drug product lot FA9156. The final scope was determined to be the reported finished goods lot EP7533, fill lot EP7531, and the bulk formulated drug product lot EP7527. The final scope included the reported finished goods lot EN6207, fill lot EN5340, and the formulated drug product lot EN5328. A complaint sample was not returned. No related quality issues were identified during the investigation. There was no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure measurement
- Hospital-Tage
- -
- Labordaten
- Test Name: high blood pressure; Result Unstructured Data: Test Result:High; Test Date: 19820315; Test Name: EKG; Result Unstructured Data: Test Result:irregular heart beat; Comments: irregular heart beat don't know the cause tied tubes in 15Mar1982 when woke up did EKG and showed it. didn't know she had; Test Name: Covid home test; Test Result: Positive ; Comments: positive for Covid after Pfizer Covid 19 vaccine; Test Name: Weight; Result Unstructured Data: Test Result:128-130 lbs; Comments: Weight - at this point about 128-130 pounds.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (high blood pressure diagnosed 10-15 years ago); Breast cancer (She had breast cancer like 7 years ago); Heart beat abnormal neonatal (irregular heart beat don't know the cause tied tubes in 15Mar1982 when woke up did EKG and showed it); Hypochlorhydria (slow down the little acid producers in her stomach); Lung cancer (lung cancer surgery Jul2022)
- Andere Medikamente
- LOSARTAN; PANTOPRAZOLE; VITAMIN C [ASCORBIC ACID]; ZINC; D3; TYLENOL EXTRA STRENGTH
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 09.12.2022
- Impfdatum
- 09.05.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 210,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 2/12/21 Lot# ELk9267; Pfizer 3/5/2 Lot# EN6202;' Pfizer 11/3/21 Lot# FH8020; Pfizer 5/9/22 Lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 30.03.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 187,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive covid test in fully vaccinated and boostered x2 pt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 06.05.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 154,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
caller already had two boosters and he was diagnosed with COVID-19 early this month; caller already had two boosters and he was diagnosed with COVID-19 early this month; 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 80-year-old male patient received BNT162b2 (BNT162B2), on 26Jan2021 as dose 1, single (Batch/Lot number: unknown, FL9265 or maybe EL9265), on 16Feb2021 as dose 2, single (Batch/Lot number: unknown, EL9267 or might be EI9267), on 27Sep2021 as dose 3 (booster), single (Batch/Lot number: unknown, FE2588 or FI2588) and on 06May2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 80 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 07Oct2022, outcome "recovered" and all described as "caller already had two boosters and he was diagnosed with COVID-19 early this month". Patient already had two boosters and he was diagnosed with COVID-19 early this month 07Oct2022. Patient also stated that he took a complete course of Paxlovid, though he was symptom free from the second day on. Patient had an appointment for the gray cap bivalent Pfizer BioNTech COVID 19 vaccine and asked if he should get it. 07Oct2022, was diagnosed with Covid-19. Symptoms were very mild and only lasted for 1 day. Doctor put him on Paxlovid, the 5 day regimen, that it helped immensely. By the second day, the symptoms were gone. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (07Oct2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. 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: 20221007; Test Name: COVID-19; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 23.04.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 145,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza like illness
Nasopharyngitis
Peripheral swelling
SARS-CoV-2 test positive
Varicose vein
Symptomtext
I got a cold after we docked from a cruise, and I tested on the 9th and the 13th, and they were both negative. I thought I just had a common cold, but my left leg started swelling on the 15th. I had something like varicose veins up my shin. When I got off the ship, I tested positive one the 22nd and was give PAXLOVID. The treatment did help the flu like symptoms, but I still have swelling in my lower leg. I went to my doctor, and they didn't think so but to be safe they are going to order some tests.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Cholesterol; thyroid activities
- Andere Medikamente
- Fenofibrate; finasteride; atorvastatin; SYNTHROID
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 25.04.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 92,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
On 7/27 began sneezing and horrible runny nose this happened for two days and I decided to test and tested positive for COVID-19. On day 3 I began heavy coughing and decided to go to walk in clinic. The dr prescribed Paxolovid. After 36 hours I saw an improvement in symptoms, and they completely resolved in 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Positive at home COVID-19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- NP thyroid;
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 22.10.2022
- Impfdatum
- 31.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Immunisation reaction
Muscular weakness
Weight
Symptomtext
After developing great weakness after both Pfizer booster shots; severe reactions to his 1st and 2nd booster; would fall over like he had no muscle control; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. An 83-year-old male patient received BNT162b2 (BNT162B2), on 31Mar2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 83 years for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing); "heart trouble" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (First Dose: 14Jan2021 NDC, LOT, EXP: Unknown), administration date: 14Jan2021, when the patient was 82-year-old, for COVID-19 immunization, reaction(s): "sore arm"; BNT162b2 (Second Dose: 04Feb2021 NDC, LOT, EXP: Unknown), administration date: 04Feb2021, when the patient was 82-year-old, for COVID-19 immunization, reaction(s): "sore arm"; BNT162b2 (First Booster: 16Oct2021 LOT: FF2589 NDC, EXP: Unknown., Patient became very weak on 17Oct2021 after his 1st booster), administration date: 16Oct2021, when the patient was 83-year-old, for COVID-19 immunization, reaction(s): "weakness"; Bnt162b2 (fell), for COVID-19 immunization, reaction(s): "Fall"; Bnt162b2 (couldn't walk a straight line), for COVID-19 immunization, reaction(s): "Gait disturbance"; Bnt162b2 (BP dropped), for COVID-19 immunization, reaction(s): "Blood pressure decreased"; Bnt162b2 (Patient was found to have UTI and was treated for it), for COVID-19 immunization, reaction(s): "Urinary infection"; Bnt162b2 (Patient could barely get up from the chair.), for COVID-19 immunization, reaction(s): "Activities of daily living impaired"; Bnt162b2 (hit his head), for COVID-19 immunization, reaction(s): "Headache"; Bnt162b2 (Patient's head was checked and had a superficial cut), for COVID-19 immunization, reaction(s): "Skin laceration". The following information was reported: ASTHENIA (non-serious), outcome "unknown", described as "After developing great weakness after both Pfizer booster shots"; MUSCULAR WEAKNESS (non-serious), outcome "unknown", described as "would fall over like he had no muscle control"; IMMUNISATION REACTION (non-serious), outcome "unknown", described as "severe reactions to his 1st and 2nd booster". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Patient reported developing great weakness after the both Pfizer booster shots and was enquired if it would be same with the current booster or the ingredients are different. Caller stated that the patient had the Pfizer COVID-19 Vaccine for his primary series and 1st and 2nd booster doses. Patient was fine with the primary series. Patient wanted to get his 3rd booster but had severe reactions to his 1st and 2nd booster. Patient became very weak after his 1st booster. During the patient's 2nd booster, when he sat on the side of the bed, he would fall over like he had no muscle control. Patient was very weak for about two days. Caller mentioned that they had spoken to the primary care doctor who told them to wait if anyone has any type of reaction with the Pfizer COVID-19 Vaccine Bivalent Booster. Caller stated that they were wondering if there were any changes other than the variants with the new bivalent booster to encourage them to take the booster. No other conditions and investigations reported. Patient wrote a letter to Pfizer and received number they gave him. He has had a rather severe reaction to the last 2 boosters of the Covid-19 vaccine. With the original 2 vaccines, the injections, really had nothing more than usual. They were all Pfizer. Had the usual sore arm and nothing else. With the last 2, he had a really severe reaction and became extremely weak. Would like to take the latest, third booster with the new variant and asked if it is made up of the same ingredients as the other vaccines. He was trying to make up his mid, whether to take vaccine or not. Caller passed phone to her husband, the patient. Clarified with the patient, his full name as (withheld) who's details were entered in formal field as reporter and provided remaining details for report. Clarified with patient that he was asking about the ingredients of the latest Covid booster for the new variant. Knows he has to make his own mind up but wanted to find out what information there was. Clarified that patient got number from Pfizer, previously provided online on Pfizer website. Clarified that he did not report anything but had asked question about the ingredients and was told to call. The patient does not remember the treatment details. After the second booster, it was about the same. Didn't fall down but if he was sitting up, he would just fall over, he was so weak. Clarified that he did not go to hospital the second time and this reaction occurred after first and second booster of Covid vaccine. Did not have any real problems with first 2, original doses Covid vaccine. Clarified that patient had 4 total doses Pfizer Covid-19 vaccine, including 2 original doses and 2 booster doses. Concomitant Products/Medical Conditions: Has got several medical conditions and is on gobs of medicine. No additional vaccines administered on same date of the Pfizer suspect. No prior vaccinations, No family medical history relevant to AE and no relevant tests reported.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201240238 Same patient, drug, and event separated in time;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- Test Name: Weight; Result Unstructured Data: Test Result:167; Comments: Weight: About 167.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes; Heart disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 01.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Apr2022 as dose number unknown, single (Lot number: FJ9943) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL, start date: Mar2021, stop date: Oct2022. Past drug history included: Gabapentin, reaction(s): "taking gabapentin for damaged femoral nerve", notes: taking gabapentin for damaged femoral nerve 600mg 3x daily(program would not allow more than one med) doubled vaxxed and double boosted; Tetanus toxoid, reaction(s): "Known allergies: Tetanus toxoid"; Gadolinium, reaction(s): "Known allergies: gadolinium". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 Test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension
- Andere Medikamente
- LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 07.04.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 127,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Nasopharyngitis
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 via a home test on 08/12/2022. I felt like I had a bad cold with congestion, runny nose and coughing. I called my doctor and she put me on PAXLOVID. I took the medication for 4 out of the 5 days but I had a reaction to it with throwing up, diarrhea, loss of muscle control and super tired. I stopped taking it and did not take anything else for my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home test for COVID-19 was positive on 08/12/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Diabetes; High Cholesterol
- Andere Medikamente
- N/A
- Allergien
- Metformin; adhesive tape; seasonal allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 11.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 22Feb2021 as dose 1, single (Lot number: EN6200), in left arm, on 15Mar2021 as dose 2, single (Lot number: EN6208), in left arm, on 27Sep2021 as dose 3 (booster), single (Lot number: 301458A), in left arm and on 11Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). Concomitant medication(s) included: TRAZODONE; ESTRADIOL; MELOXICAN; MONTELUKAST; ACYCLOVIR [ACICLOVIR]; DEXAMETHASON [DEXAMETHASONE], start date: 08Sep2022, stop date: 17Sep2022; WELLBUTRIN; OMEPRAZOLE; XANAX. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Treatment of COVID-19; (12Sep2022) Negative, notes: 1st covid tested negative on day 5; (25Sep2022) Positive, notes: tested positive 13 days after testing negative from 1st covid. Therapeutic measures were taken as a result of vaccination failure, covid-19. Additional information: The patient was given Paxlovid as treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20220912; Test Name: COVID; Test Result: Negative ; Comments: 1st covid tested negative on day 5; Test Date: 20220925; Test Name: COVID; Test Result: Positive ; Comments: tested positive 13 days after testing negative from 1st covid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- TRAZODONE; ESTRADIOL; MELOXICAN; MONTELUKAST; ACYCLOVIR [ACICLOVIR]; DEXAMETHASON [DEXAMETHASONE]; WELLBUTRIN; OMEPRAZOLE; XANAX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 15.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Mar2021 as dose 1, single (Lot number: EP7534), in right arm, on 08Apr2021 as dose 2, single (Lot number: EW0153), in right arm, on 14Oct2021 as dose 3 (booster), single (Lot number: FF8839), in right arm and on 15Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 52 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). Concomitant medication(s) included: BUDESONIDE, stop date: 21Sep2022; OMEPRAZOLE. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: positive, notes: Treatment of COVID-19; positive, notes: Recurrence if Covid symptoms, positive test results. Therapeutic measures were taken as a result of vaccination failure, covid-19. Additional information: Anti viral medication received by patient due to the event was Paxlovid, from 21Sep2022 to 26Sep2022. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE lot EP7534 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EP7534, fill lot EP7532, and the formulated drug product lot EP7528; lot EW0153, fill lot EP8692 and the bulk formulated drug product EW8071; lot FF8839, fill lot FF8833, and the bulk formulated drug product FA9148; and lot FJ9943, fill lot FJ9942 and the bulk formulated drug product FJ9940. A complaint sample was not returned, and photographs were not received. There were no deviations that may have caused a complaint of this nature. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Name: COVID-19 test; Test Result: Positive ; Comments: Recurrence if Covid symptoms, positive test results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- BUDESONIDE; OMEPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 06.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Disease recurrence
Drug ineffective
SARS-CoV-2 test
Symptomtext
had 4 shots and I have had COVID; had 4 shots and I have had COVID; have had 4 shots and I have had COVID, got it again; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team and product quality group. The reporter is the patient. A 67-year-old male patient received BNT162b2 (BNT162B2), on 27Jan2021 as dose 1, single (Lot number: EL3247), in left arm, on 17Feb2021 as dose 2, single (Lot number: FL9267), in left arm, on 22Sep2021 as dose 3 (booster), single (Lot number: FD8448), in left arm and on 06Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure" (unspecified if ongoing). Concomitant medication(s) included: IRBESARTAN taken for blood pressure measurement (ongoing); AMLODIPINE taken for blood pressure measurement (ongoing). Vaccination history included: Shingrix (Prior Vaccinations (within 4 weeks): , Stated may have had the Shingrix Vaccine in February. Manufacturer: Unknown , Lot Number: Unknown , Route, Anatomical Location: Unknown), administration date: Feb2022, for Immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "had 4 shots and I have had COVID"; DISEASE RECURRENCE (medically significant) with onset 2022, outcome "unknown", described as "have had 4 shots and I have had COVID, got it again". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (2022) had covid in Jun 2022 or Jul 2022. Therapeutic measures were taken as a result of drug ineffective, covid-19, disease recurrence. Clinical course: It was reported that, Patient have had 4 covid 19 injections with Pfizer with no problem and he was not 6 months out since the last one and he have an appointment in 3 hours for the other one. His wife was all of a sudden concerned and he told her he would call Pfizer and ask. Is there anything different, really different with this Pfizer shot than the other 4 that he previously got. any side effects from any of it Are the side effects worse, Caller stated, he had no side effects from any of it. During conversation with the caller, he does also mention having had COVID. Further clarification provided and he did contract COVID after already having received his Pfizer COVID 19 Vaccination. Caller said "It didn't happen right away, it happened in June or July, not right away. Had the shot in April. There are break through cases." He have had 4 shots and he have had COVID, got it again, such a slight case, didn't know he had it, pretty much he was thinking 6 months down the line the proper precautions would be to take the new product at this time. He was calling about the Pfizer Covid 19 vaccine. He has had a total of four. He will get the Bivalent Booster today. However, he mentioned he had Covid in June or July. His last dose of the Covid-19 vaccine was in April; about six months ago. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: covid; Result Unstructured Data: Test Result:had covid in Jun 2022 or Jul 2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure
- Andere Medikamente
- IRBESARTAN; AMLODIPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 153,0
- 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 contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 77-year-old male patient received BNT162b2 (BNT162B2), on 01Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 76 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: LIPITOR. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Sep2022) Positive, notes: Treatment of COVID-19; (Sep2022) Negative, notes: after testing negative; (Sep2022) Positive, notes: Rebound about 2 days after testing negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient was treated with Paxlovid HR9 from 19Sep2022 to 23Sep2022 for COVID-19. Patient had no known allergy. Patient has received Other medication in 2weeks was yes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202209; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 202209; Test Name: COVID-19 Test; Test Result: Negative ; Comments: after testing negative; Test Date: 202209; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Rebound about 2 days after testing negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: Known allergies no Other medical history none
- Andere Medikamente
- LIPITOR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 04.10.2022
- Impfdatum
- 04.04.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 119,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Macular hole
Ophthalmological examination abnormal
Retinal detachment
Surgery
Symptomtext
I had a macular hole and a detached retina after receiving the 4th dose. I had surgery on 09/22/2022. I am still in recovery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Macular hole
- Hospital-Tage
- -
- Labordaten
- Eye exams in July 2022
- Aktuelle Erkrankungen
- Cold
- Vorgeschichte
- Skin cancer
- Andere Medikamente
- Lisinopril; simvastatin
- Allergien
- Bacitracin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 20.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Ataxia
Dysstasia
Gait inability
Symptomtext
Severe ataxia to the extent patient was unable to walk or stand up without assistance. Evaluated at a local Medical Center where code stroke was called, cardiac and infectious evaluation were done. No cause of his ataxia was found. Patient returned to baseline function after another 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ataxia
- Hospital-Tage
- -
- Labordaten
- As above, all done 9-21-2022
- Aktuelle Erkrankungen
- No acute illnesses.
- Vorgeschichte
- Cerebellar hemorrhagic CVA, 5-24-2019 Idiopathic pulmonary fibrosis HTN
- Andere Medikamente
- 1. Lisinopril 2. Carvedilol 3. Pantoprazole 4. Aspirin 5. Multivitamin 6. Perfenidone 7. Doxazosin 8. Simvastatin 9. Acetaminophen 10. Amlodipine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 13.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 84-year-old male patient received BNT162b2 (BNT162B2), on 23Jan2021 as dose 1, single (Lot number: FL3246), in left arm, on 12Feb2021 as dose 2, single (Lot number: EN9581), in left arm and on 13Apr2022 as dose 3 (booster), single (Lot number: FJ9943) at the age of 83 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Patient had no known allergies. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19 including PAXLOVID (lot number: 2796 as reported) given from 25Sep2022 to 27Sep2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19; Test Result: Positive ; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: Other medical history: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- -
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 153,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 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. An adult female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Mar2021 at 11:00 as dose 1, single (Lot number: EN6206), in left arm, on 26Mar2021 at 10:30 as dose 2, single (Lot number: EP8730), in left arm, on 17Aug2021 at 11:00 as dose 3 (booster), single (Lot number: EC3132), in left arm and on 01Apr2022 at 14:00 as dose 4 (booster), single (Lot number: FJ9943), in left arm for covid-19 immunisation. The patient's relevant medical history included: "RA" (unspecified if ongoing); "over weight" (unspecified if ongoing). Concomitant medication(s) included: L-THYROXINE [LEVOTHYROXINE SODIUM], start date: 30Jun2020. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Treatment of COVID-19; (25Sep2022) Positive, notes: Rebound Covid positive on 25Sep2022. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient received Xeljanz Xr (From 14Aug2022 to 11Sep2022), Simvastatin (From 30Jun2022 to 11Sep2022).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20220925; Test Name: Covid; Test Result: Positive ; Comments: Rebound Covid positive on 25Sep2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Overweight; RA
- Andere Medikamente
- L-THYROXINE [LEVOTHYROXINE SODIUM]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 24.09.2022
- Impfdatum
- 02.04.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 152,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old male patient received BNT162b2 (BNT162B2), on 22Jan2021 as dose 1, single (Lot number: 210122-137), in left arm, on 15Feb2021 as dose 2, single (Lot number: EL9266), in left arm, on 06Oct2021 as dose 3 (booster), single (Lot number: 30130BA), in left arm and on 02Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "type 1 diabetes" (unspecified if ongoing); "hypothyroid" (unspecified if ongoing), notes: Other medical history: hypothyroid. There was no known allergies. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Sep2022) Positive, notes: Treatment of COVID-19; (21Sep2022) Positive, notes: Return of positive home test. Therapeutic measures were taken as a result of vaccination failure, covid-19 for which included Paxlovid from 13Sep2022 to 17Sep2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202209; Test Name: COVID-19 test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20220921; Test Name: COVID-19 test; Test Result: Positive ; Comments: Return of positive home test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypothyroidism (Other medical history: hypothyroid); Type 1 diabetes mellitus
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 24.09.2022
- Impfdatum
- 10.05.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 114,0
- 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; COVID-19; This is a spontaneous report received from contactable reporter(s) (Physician) from product quality group. The reporter is the patient. A 63-year-old male patient received BNT162b2 (BNT162B2), on 10May2022 at 13:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 63 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Sleep Apnea" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing). Concomitant medication(s) included: CRESTOR, start date: 01Jan2021, stop date: 10Sep2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Negative, notes: previous no symptoms and negative test; (Sep2022) Positive; (20Sep2022) Positive, notes: 20Sep with retested positive. Therapeutic measures were taken as a result of drug ineffective, covid-19.; Sender's Comments: As there is limited information in the case provided, the causal association between the events and the suspect drug cannot be excluded. The case will be reassessed once new information is available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: covid-19 test; Test Result: Negative ; Comments: previous no symptoms and negative test.; Test Date: 202209; Test Name: covid-19 test; Test Result: Positive ; Test Date: 20220920; Test Name: covid-19 test; Test Result: Positive ; Comments: 20Sep with retested positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: High cholesterol; Sleep apnea
- Andere Medikamente
- CRESTOR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 03.04.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 116,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
SARS-CoV-2 test positive
Symptomtext
07/28/2022 in the morning I had cough and I was feeling weak so, I decided to test for COVID-19. I was positive. I did a tele health with my doctor the same day who prescribed me with Paxlovid for 5 days. It took me 3 days to get better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test- Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amlodipine; Doxycycline; Fish oil; Black seed oil; Multivitamin; Zyrtec
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 17.05.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 76,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
3 doses of the Moderna Covid-19 vaccine and one dose of Pfizer.; his wife and himself had Covid mid Aug2022 after getting 3 doses of the Moderna Covid-19 vaccine and one dose of Pfizer; his wife and himself had Covid mid Aug2022 after getting 3 doses of the Moderna Covid-19 vaccine and one dose of Pfizer; This is a spontaneous report received from contactable reporter(s) (Physician). Other Case identifier(s): MOD22-022731 (MODERNA), 147942 (MODERNA). A female patient received BNT162b2 (BNT162B2), on 17May2022 as dose 4 (booster), single (Lot number: FJ9943) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 05Feb2021 as dose 1, single (Lot number: 011M20A), on 05Mar2021 as dose 2, single (Lot number: 002A21A) and on 08Nov2021 as dose 3(booster), single (Lot number: 065F21A) 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 Aug2022, outcome "unknown" and all described as "his wife and himself had Covid mid Aug2022 after getting 3 doses of the Moderna Covid-19 vaccine and one dose of Pfizer"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown", described as "3 doses of the Moderna Covid-19 vaccine and one dose of Pfizer.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Aug2022) positive.; Sender's Comments: Based on the information provide and plausible temporal association, the causality between BNT162B2 and events cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202208; Test Name: Covid; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- -
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Body temperature increased
COVID-19
Confusional state
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
his wife and himself had Covid mid Aug2022 after getting 3 dosesof the Moderna Covid-19 vaccine and one dose of Pfizer; his wife and himself had Covid mid Aug2022 after getting 3 dosesof the Moderna Covid-19 vaccine and one dose of Pfizer; Interchange of vaccine products; he ran a temperature of 102.5; confused; This is a spontaneous report received from non-contactable reporter(s) (Physician) from product quality group. The reporter is the patient. Other Case identifier(s): MOD22-022731 (MODERNA), 147943 (MODERNA), 147942 (MODERNA). A male patient received BNT162b2 (BNT162B2), on 17May2022 as dose 4 (booster), single (Lot number: FJ9943) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 05Feb2021 as dose 1, single (Lot number: 011M20A), on 05Mar2021 as dose 2, single (Lot number: 002A21A) and on 08Nov2021 as dose 3 (booster), single (Lot number: 065F21A) for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 17May2022, outcome "unknown"; CONFUSIONAL STATE (non-serious) with onset 2022, outcome "unknown", described as "confused"; BODY TEMPERATURE INCREASED (non-serious) with onset 2022, outcome "unknown", described as "he ran a temperature of 102.5"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "his wife and himself had Covid mid Aug2022 after getting 3 dosesof the Moderna Covid-19 vaccine and one dose of Pfizer". The events "his wife and himself had covid mid aug2022 after getting 3 dosesof the moderna covid-19 vaccine and one dose of pfizer", "he ran a temperature of 102.5" and "confused" required physician office visit. The patient underwent the following laboratory tests and procedures: Body temperature: (2022) 102.5; SARS-CoV-2 test: (Aug2022) Positive. Clinical course: A retired Physician reports that his wife and himself had Covid mid Aug2022 after getting 3 doses of the Moderna Covid-19 Vaccine and one dose of Pfizer. He had to seek an out patient consult when he had the covid as he ran a temperature of 102.5 and he was confused. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the pfizer-biontech covid-19 vaccine lot FJ9943 was 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 FJ9943, fill lot FJ9942 and the bulk formulated drug product FJ9940. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications.; Sender's Comments: Based on the available reported information, the causal association between the events and the suspect drug BNT162B2 cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: Body temperature; Result Unstructured Data: Test Result:102.5; Test Date: 202208; Test Name: Covid test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 10.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), on 19Jan2021 as dose 1, single (Lot number: EL3246), in left arm, on 09Feb2021 as dose 2, single (Lot number: EM9809), in left arm, on 10Oct2021 as dose 3 (booster), single (Lot number: FH8020), in left arm and on 10Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 68 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing), notes: other medical history : Diabetes; "Hypertension" (unspecified if ongoing), notes: other medical history : Hypertension. Concomitant medication(s) included: IBUPROFEN. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Paxlovid for COVID 19 Treatment was received from 30Aug2022 to 03Sep2022.No known allergies.; Sender's Comments: As there is limited information in the case provided, the causal association between the Reported events Vaccination failure and Covid-19 cannot be excluded for the suspect drug. The case will be reassessed once new information is available.
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: Diabetes (other medical history : Diabetes); Hypertension (other medical history : Hypertension)
- Andere Medikamente
- IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 05.02.2021
- Beginn
- 17.05.2022
- Tage bis Beginn
- 466,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
COVID-19
COVID-19 immunisation
Confusional state
Interchange of vaccine products
Symptomtext
confused; Patient had COVID-19; Interchange of vaccine products; Revaccination with different covid-19 vaccine; This spontaneous case was reported by a physician and describes the occurrence of COVID-19 (Patient had COVID-19), CONFUSIONAL STATE (confused), INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different covid-19 vaccine) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 065F21A, 002A21A and 011M20A) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. No Medical History information was reported. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-May-2022, the patient received fourth dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 17-May-2022, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different covid-19 vaccine). In August 2022, the patient experienced COVID-19 (Patient had COVID-19). On an unknown date, the patient experienced CONFUSIONAL STATE (confused). At the time of the report, COVID-19 (Patient had COVID-19) and CONFUSIONAL STATE (confused) outcome was unknown and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different covid-19 vaccine) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 102.5. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The onset date of COVID-19 was reported as mid of Aug-2022. No treatment medications were reported. Company comment: This spontaneous case concerns a 76-year-old male patient, with no medical history reported, who experienced the non-serious unexpected AESI of COVID-19 approximately 9 months after receiving a booster dose of mRNA-1273. Patient had initially received mRNA-1273 in an appropriate schedule as primary vaccination series, and had also received a second booster dose with Pfizer COVID-19 vaccine approximately 3 months prior to event onset (interchange of vaccine products and well as revaccination with different COVID-19 vaccine were noted). Patient states that he had to seek an outpatient consult since he had a temperature of 102.5 and was confused. No information on diagnostic test, treatment received, course and outcome of the events was provided. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to US-MODERNATX, INC.-MOD-2022-642018 (E2B Linked Report).; Sender's Comments: This spontaneous case concerns a 76-year-old male patient, with no medical history reported, who experienced the non-serious unexpected AESI of COVID-19 approximately 9 months after receiving a booster dose of mRNA-1273. Patient had initially received mRNA-1273 in an appropriate schedule as primary vaccination series, and had also received a second booster dose with Pfizer COVID-19 vaccine approximately 3 months prior to event onset (interchange of vaccine products and well as revaccination with different COVID-19 vaccine were noted). Patient states that he had to seek an outpatient consult since he had a temperature of 102.5 and was confused. No information on diagnostic test, treatment received, course and outcome of the events was provided. The benefit-risk relationship of mRNA-1273 is not affected by this report. US-MODERNATX, INC.-MOD-2022-642018:Crosslinked with AE (Wife's Case)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: 102.5
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 05.02.2021
- Beginn
- 01.08.2022
- Tage bis Beginn
- 542,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 immunisation
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
Revaccination with different COVID-19 vaccine; Interchange of vaccine products; It was reported that patient experienced COVID-19 on mid of Aug-2022 after getting 3 doses of the Moderna COVID-19 vaccine and one dose of Pfizer; This spontaneous case was reported by a physician and describes the occurrence of COVID-19 (It was reported that patient experienced COVID-19 on mid of Aug-2022 after getting 3 doses of the Moderna COVID-19 vaccine and one dose of Pfizer), COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in a 76-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 065F21A, 002A21A and 011M20A) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. No Medical History information was reported. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Nov-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-May-2022, the patient received fourth dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. In August 2022, the patient experienced COVID-19 (It was reported that patient experienced COVID-19 on mid of Aug-2022 after getting 3 doses of the Moderna COVID-19 vaccine and one dose of Pfizer). On an unknown date, the patient experienced COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). At the time of the report, COVID-19 (It was reported that patient experienced COVID-19 on mid of Aug-2022 after getting 3 doses of the Moderna COVID-19 vaccine and one dose of Pfizer), COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In August 2022, SARS-CoV-2 test: (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. No treatment medication were provided. Company comment: This spontaneous case reported by a physician concerns a 76-year-old female patient with no reported medical history who experienced the unexpected non-serious AESI of COVID 19. The event occurred approximately 9 months after the third dose of mRNA-1273 Vaccine and approximately 3 months after tozinameran given as fourth dose. Other details are not available. Revaccination with different COVID-19 vaccine and Interchange of vaccine products were considered as additional events as fourth dose was given with Tozinameran vaccine. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to US-MODERNATX, INC.-MOD-2022-642055 (E2B Linked Report).; Sender's Comments: This spontaneous case reported by a physician concerns a 76-year-old female patient with no reported medical history who experienced the unexpected non-serious AESI of COVID 19. The event occurred approximately 9 months after the third dose of mRNA-1273 Vaccine and approximately 3 months after tozinameran given as fourth dose. Other details are not available. Revaccination with different COVID-19 vaccine and Interchange of vaccine products were considered as additional events as fourth dose was given with Tozinameran vaccine. The benefit-risk relationship of mRNA-1273 is not affected by this report. US-MODERNATX, INC.-MOD-2022-642055:Crosslinked with AE (Husband's Case)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202208; Test Name: COVID-19 Virus test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 10.09.2022
- Impfdatum
- 06.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Chronic inflammatory demyelinating polyradiculoneuropathy
Infusion
Symptomtext
CIDP IV infusions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic inflammatory demyelinating polyradiculoneuropathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 25.03.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 159,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Disease recurrence
Drug ineffective
SARS-CoV-2 test
Symptomtext
This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Mar2022 as dose 4 (booster), single (Lot number: fj9943) at the age of 35 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) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "crohn's" (unspecified if ongoing). Concomitant medication(s) included: REMICADE. The following information was reported: DISEASE RECURRENCE (medically significant) with onset 31Aug2022, outcome "not recovered", described as "Rebound of symptoms and positive test"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Covid-19 treatment: Paxlovid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: COVID 19 treatment: Paxlovid; (31Aug2022) positive, notes: Rebound of symptoms and positive test. Therapeutic measures were taken as a result of drug ineffective, covid-19. Therapeutic measures were not taken as a result of disease recurrence. Clinical information: Antiviral details: COVID 19 treatment was Paxlovid, treatment started on 22Aug2022, and treatment stopped on 27Aug2022. Other medication in 2 weeks was Remicade. Adverse event was rebound of symptoms and positive test. Adverse event started on 31Aug2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Positive; Comments: COVID 19 treatment: Paxlovid; Test Date: 20220831; Test Name: COVID-19 Test; Test Result: Positive; Comments: Rebound of symptoms and positive test.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Crohn's disease
- Andere Medikamente
- Remicade
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 05.04.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 147,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Appetite disorder
Dyskinesia
Weight abnormal
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
activity change, appetite change, unexpected weight change
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 05.04.2022
- Beginn
- 30.08.2022
- Tage bis Beginn
- 147,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Appetite disorder
Dyskinesia
Weight abnormal
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
activity change, appetite change, unexpected weight change
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.09.2022
- Impfdatum
- 08.04.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 115,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 56-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31Mar2021 as dose 1, single (Lot number: EW0151), on 22Apr2021 as dose 2, single (Lot number: EW0175), on 21Nov2021 as dose 3 (booster), single (Lot number: 33030BD) and on 08Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 56 years for covid-19 immunisation. The patient's relevant medical history included: "diabetes" (unspecified if ongoing); "asthma" (unspecified if ongoing); "paroxysmal a-fib" (unspecified if ongoing), notes: paroxysmal a-fib; "hypertension" (unspecified if ongoing); "left atrial fascicular block" (unspecified if ongoing), notes: left atrial fascicular block; "Right bundle branch block" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "COVID-19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient had no known allergies. The patient received Paxlovid from 22Aug2022 to 26Aug2022 for the treatment of COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Diabetes; Hypertension; Left anterior fascicular block (left atrial fascicular block); Paroxysmal atrial fibrillation (paroxysmal a-fib); Right bundle branch block
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 30.08.2022
- Impfdatum
- 29.01.2021
- Beginn
- 18.08.2022
- Tage bis Beginn
- 566,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
Admitted to Allegan Hospital for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 02.04.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 121,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 52-year-old male patient received BNT162b2 (BNT162B2), on 11Mar2021 as dose 1, single (Lot number: EN6207), in left arm, on 01Apr2021 as dose 2, single (Lot number: EW0150), in left arm, on 23Oct2021 as dose 3 (booster), single (Lot number: RA1570), in left arm and on 02Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 51 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient was taking other medications/products within 2 weeks of starting COVID-19 treatment. Covid-19 treatment Paxlovid was given form 13Aug2022 to 18Aug2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Known allergies: No Other medical history: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- 02.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 11Jan2021 as dose 1, single (Lot number: EK9231), on 01Feb2021 as dose 2, single (Lot number: EL3249), on 25Sep2021 as dose 3 (booster), single (Lot number: FC3184) and on 02Apr2022 as dose 4 (booster), single (Lot number: FJ9943) for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing); "hypothyroidism" (unspecified if ongoing); "hypercholesterolemia" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL; LEVOTHYROXINE; ROSUVASTATIN, start date: Mar2022, stop date: 04Aug2022. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient had no known allergies. Paxlovid was received as a therapeutic measures for the adverse events. Covid rebound symptoms began 15Aug2022 which was five days after completion of paxlovid. mild symptom course. Rebound symptoms still resolving 9 days later. also had significant metallic taste in mouth throughout treatment course. worsened 1-2 hours after each dose. Resolved with end of paxlovid course. present 05Aug-10Aug2022. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on available information in the case the reported events Vaccination failure and Covid 19 are assessed as related to suspect drug .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19 Treatment; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypercholesterolemia; Hypertension; Hypothyroidism
- Andere Medikamente
- LISINOPRIL; LEVOTHYROXINE; ROSUVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- 31.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Jan2021 at 10:00 as dose 1, single (Lot number: EL9264), in left arm, on 19Feb2021 at 11:30 as dose 2, single (Lot number: EL9264), in left arm, on 24Sep2021 at 16:00 as dose 3 (booster), single (Lot number: FF8839), in left arm and on 31Mar2022 at 16:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "heart failure" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: positive. Therapeutic measures were taken as a result of vaccination failure, covid-19.Treatment of Anti-viral details for COVID 19 Treatment: Treatment start date10Aug2022 and Treatment stop date15Aug2022. Patient had no known allergy. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 Test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Heart failure
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 13.04.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case. Started feeling mild flu symptoms, took home COVID-19 test negative, next day is was positive. Dr. prescribed PAXLOVID. Had tested positive for two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test negative, COVID-19 home test positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Crohn's
- Andere Medikamente
- Infliximab; vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 20.08.2022
- Impfdatum
- 12.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
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 68-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Feb2021 as dose 1, single (Lot number: el9264), on 23Feb2021 as dose 2, single (Lot number: en6202), on 25Sep2021 as dose 3 (booster), single (Lot number: ff2589) and on 12Apr2022 as dose 4 (booster), single (Lot number: fj9943) at the age of 67 years for covid-19 immunisation. The patient's relevant medical history included: "coronary artery disease" (unspecified if ongoing); "CKD" (unspecified if ongoing); "hypertension" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (11Aug2022) Negative; (13Aug2022) Negative. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient was treated with Paxlovid from 04Aug2022 to 08Aug2022. Received 2 negative covid tests 48 hours apart (11Aug2022 and 13Aug2022) after Paxlovid treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20220811; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20220813; Test Name: COVID-19 test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Chronic kidney disease; Coronary artery disease; Hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 15.05.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 89,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccine breakthrough infection
Symptomtext
Breakthrough infection August 12, 2022; last vaccine date before infection May 15, 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccine breakthrough infection
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- IBS
- Andere Medikamente
- Multivitamin, IBGard
- Allergien
- Morphine sensitivity
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 09.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Dec2020 as dose 1, single (Lot number: EL0140), in left arm, on 20Jan2021 as dose 2, single (Lot number: EL3302), in left arm, on 04Oct2021 as dose 3 (booster), single (Lot number: 30145BA), in left arm and on 09Jun2022 as dose 4 (booster), single (Lot number: FJ9943) 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. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jul2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient received Paxlovid from 14Jul2022 to 19Jul2022 as treatment of COVID-19.
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
- MI
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 153,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 8/10/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 80-year-old male patient received BNT162b2 (BNT162B2), on 07Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 80 years, in left arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 29Jan2021 as dose 1, single (Batch/Lot number: unknown), in left arm, on 26Feb2021 as dose 2, single (Batch/Lot number: unknown), in left arm and on 02Sep2021 as dose 3 (booster), single (Batch/Lot number: unknown), in left arm for covid-19 immunisation. The patient's relevant medical history included: "COPD" (unspecified if ongoing); "Diabetes" (unspecified if ongoing). Concomitant medication(s) included: ATORVASTATIN; METFORMIN; TRAZODONE. 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: Negative, notes: Tested negative; Positive, notes: then tested positive again after a couple of days. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient was treated with Paxlovid for COVID-19 from May2022 to May2022. The patient was on other medications in 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Negative ; Comments: Tested negative; Test Name: COVID-19 test; Test Result: Positive ; Comments: then tested positive again after a couple of days.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COPD; Diabetes
- Andere Medikamente
- ATORVASTATIN; METFORMIN; TRAZODONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 01.04.2022
- 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 contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Apr2022 at 14:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 63 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Bilateral Duane Syndrome" (unspecified if ongoing); "Penicillan" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 Included Paxlovid from 21Jul2022 to 26Jul2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Duane's syndrome; Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 06.08.2022
- Impfdatum
- 27.04.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 65,0
- 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 contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received BNT162b2 (BNT162B2), on 27Apr2022 at 11:30 as dose 4 (booster), single (Lot number: FJ9943) at the age of 69 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (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 patient was not taken any other medications/products within 2 weeks of starting COVID-19 treatment. patient had previously received a COVID-19 Vaccine. There was no known allergies. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jul2022, outcome "not recovered" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (01Aug2022) Positive, notes: continued to test positive for COVID-19 on 9th day after starting Paxlovid; (03Aug2022) Positive, notes: Also tested positive on 11th day after starting. Therapeutic measures were taken as a result of covid-19. COVID-19 Treatment of Paxlovid started from 23Jul2022 to 28Jul2022 No follow-up attempts are possible. No further information is expected
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220801; Test Name: COVID test; Test Result: Positive ; Comments: continued to test positive for COVID-19 on 9th day after starting Paxlovid; Test Date: 20220803; Test Name: COVID test; Test Result: Positive ; Comments: Also tested positive on 11th day after starting.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 21.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Physician) from product quality group. The reporter is the patient. A 66-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Dec2020 as dose 1, single (Lot number: EL0140), in right arm, on 18Jan2021 as dose 2, single (Lot number: EK9231), in right arm, on 30Sep2021 as dose 3 (booster), single (Lot number: FE3592), in right arm and on 21Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 66 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: SYNTHROID oral. Past drug history included: Trimethoprim, reaction(s): "Known allergies: trimethoprim"; Sulfamethoxazole, reaction(s): "Known allergies: sulfamethoxazole". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown Results, notes: indication was Treatment of COVID-19. Therapeutic measures were taken as a result of vaccination failure, covid-19. Anti viral treatment was started from 20Jul2022 to 25Jul2022 by oral route.; Sender's Comments: Based on the available information, the reported events cannot be excluded for the suspect drug.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown Results; Comments: indication=Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypothyroidism
- Andere Medikamente
- SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 02.03.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 121,0
- 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
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 68-year-old male patient received BNT162b2 (BNT162B2), on 15Mar2021 as dose 1, single (Lot number: EN6198), in left arm, on 22Sep2021 as dose 2, single (Lot number: EN6204), in left arm, on 13Nov2021 as dose 3 (booster), single (Lot number: FF8841), in left arm and on 02Mar2022 at 02:30 as dose 4 (booster), single (Lot number: FJ9943) at the age of 68 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jul2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Jul2022) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical information: No known allergies. Patient received no other medication in 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202207; Test Name: Covid-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 31.07.2022
- Impfdatum
- 29.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eyelid disorder
Eyelid oedema
Swelling of eyelid
Symptomtext
Adverse Event: Eyelid edema in right eye Signs: Eyelid appeared droopy Symptoms: Eyelid felt heavy and fuller to the touch Time Course: First noticed after waking up at 8 am. Did not worsen but remained swollen throughout the day, slowly improving. By the next morning, eyelid was back to normal. Treatment: Damp, warm cloth press for 10 minutes Outcome: Problem resolved within 24 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eyelid disorder
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- -Asthma -Seasonal Allergies -Raynaud's Disease
- Andere Medikamente
- -Tri Lo Milli (birth control) -Breo -Zyrtec
- Allergien
- -Sudafed -Tobramycin
- Vorherige Impfungen
- Adverse Event: Injection Site swelling and irritation following improper administration low on the left arm. For weeks the skin
- Staat
- MD
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 22.04.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 54,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy bone marrow
Blood test abnormal
Plasma cell myeloma
Protein total abnormal
X-ray
Symptomtext
I had a routine blood screening for a physical in June and that came back with an abnormal protein that was indicative of myeloma. I was referred to an Oncologist/Hematologist and am still having testing done without any course of treatment decided yet but will probably begin next month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy bone marrow
- Hospital-Tage
- -
- Labordaten
- Blood Test-06/16/2022-abnormal protein found. Bone Marrow Testing; X-ray Survey.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin; Vitamin D Supplement.
- Allergien
- Tetracycline; Amoxicillin.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 24.07.2022
- Impfdatum
- 15.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
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 71-year-old male patient received BNT162b2 (BNT162B2), on 09Jan2021 as dose 1, single (Lot number: EL3246), in left arm, on 31Jan2021 as dose 2, single (Lot number: E5318), in left arm, on 31Aug2021 as dose 3 (booster), single (Lot number: FC3183), in left arm and on 15Mar2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 71 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (15Jul2022) Positive, notes: Recurrence of positive Covid antigen test 4 days after completing Paxlovid. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Recurrence of positive Covid antigen test 4 days after completing Paxlovid and new symptoms (bad nasal congestion, fluctuating fever up and down: normal, fever, normal, fever, sleepiness, headache, tinnitus). No other medication was received within 2 weeks of vaccination. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220715; Test Name: Covid-19 Test; Test Result: Positive ; Comments: Recurrence of positive Covid antigen test 4 days after completing Paxlovid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 24.07.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
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 76-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Feb2021 at 10:00 as dose 1, single (Lot number: EL9267), in left arm, on 03Mar2021 at 12:00 as dose 2, single (Lot number: EN0205), in left arm, on 28Sep2021 at 12:00 as dose 3 (booster), single (Lot number: 30135BA), in left arm and on 05Apr2022 at 14:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 75 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: Anti viral details product COVID 19 Treatment, brand Pfizer, treatment start date 06Jul2022,treatment stop date 10Jul2022,indication. Treatment of COVID-19,COVID vaccine details vaccine brand=Pfizer / BioNTech, Adverse event: Fever, sore throat, congestion , cough, Adverse event start date: 14Jul2022,Adverse event start time: 04:00 PM. NO other medication in 2weeks.Seriousness criteria-Results in death: No, Seriousness criteria-Life threatening: No, Seriousness criteria-Caused/prolonged hospitalization: No, Seriousness criteria-Disabling/Incapacitating: No, Seriousness criteria-Congenital anomaly/birth defect: No. AE resulted in: None of the above, If patient recovered: Recovering,If treatment Ae: No
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: Penicillin); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 24.07.2022
- Impfdatum
- 30.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old male patient received BNT162b2 (BNT162B2), on 05Feb2021 as dose 1, single (Lot number: EM9810), in left arm, on 23Feb2021 as dose 2, single (Lot number: EN6202), in left arm, on 25Sep2021 as dose 3 (booster), single (Lot number: FC3184), in left arm and on 30Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "CARDIAC PATIENT" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL, start date: 01Jul2022; ZETIA, start date: 01Jul2022; METFORMIN, start date: 01Jul2022; ASPIRIN (E.C.), start date: 01Jul2022; ROSUVASTATIN, start date: 01Jul2022, stop date: 04Jul2022. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "recovering" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Covid test positive; (Jul2022) Negative, notes: Paxlovid 5 days, then Covid negative; (Jul2022) Positive, notes: Symptoms returned 3 days later Covid tested positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient received Paxlovid treatment from 05Jul2022 to 09Jul2022 for covid-19. Covid symptoms sore throat, cough, mucous in throat build up, covid test positive. Paxlovid 5 days, then covid negative, symptoms returned 3 days later covid tested positive. Patient had no known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Comments: Covid test positive.; Test Date: 202207; Test Name: COVID-19 test; Test Result: Negative ; Comments: Paxlovid 5 days, then Covid negative; Test Date: 202207; Test Name: COVID-19 test; Test Result: Positive ; Comments: Symptoms returned 3 days later Covid tested positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Cardiac disorder
- Andere Medikamente
- METOPROLOL; ZETIA; METFORMIN; ASPIRIN (E.C.); ROSUVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 24.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 03Feb2021 as dose 1, single (Lot number: EL9265), in left arm, on 24Feb2021 as dose 2, single (Lot number: EN6198), in left arm, on 02Nov2021 as dose 3 (booster), single (Lot number: FF259), in left arm and on 12Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Irritable bladder" (unspecified if ongoing). Concomitant medication(s) included: MYRBETRIQ, start date: 01Sep2021; PRAVASTATIN, start date: 01Jun2019. Past drug history included: Tetracycline, reaction(s): "known allergies:Tetracycline", notes: known allergies:Tetracycline; Erythromycin, reaction(s): "known allergies:erythromycin", notes: known allergies:erythromycin. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jun2022, outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course included: Patient received COVID 19 treatment with Paxlovid on 21Jun2022 and stopped on 25Jun2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Irritable bladder
- Andere Medikamente
- MYRBETRIQ; PRAVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 24.07.2022
- Impfdatum
- 09.04.2022
- 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 contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 65 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) 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: COVID-19 (medically significant), DRUG INEFFECTIVE (medically significant) all with onset 2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (13Jul2022) positive, notes: tested positive. Therapeutic measures were taken as a result of covid-19, drug ineffective. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220713; Test Name: COVID-19 test; Test Result: Positive ; Comments: tested positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 18.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bile duct stenosis
Blood ketone body decreased
Bone marrow disorder
Liver disorder
Platelet count decreased
Red blood cell count decreased
Symptomtext
I started to have problems after my first dose. But since the fourth dose I had a second bone marrow because my blood tones keep dropping. My liver blocked off my bile duct and currently in the hospital now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bile duct stenosis
- Hospital-Tage
- 3,0
- Labordaten
- Platelet went down to 31. Red cells went down.
- Aktuelle Erkrankungen
- Blood thinning problems; Cancer; Blood pressure going down
- Vorgeschichte
- Hx of Pulmonary Embolism x2 on Coumadin 2015. Breast carcinoma status post mastectomy and chemotherapy in 2017. History of breast carcinoma status post mastectomy and chemotherapy in 2017
- Andere Medikamente
- Gabapentin; ARIMIDEX; coumadin; allopurinol; SINGULAIR; LASIX; potassium cl; magnesium; calcium; fish oil; B complex; acetaminophen; acetaminophen PM; D3; multivitamin
- Allergien
- MAXZIDE; travoprost; penicillin; aspirin
- Vorherige Impfungen
- 1st dose COVID-19
- Staat
- MI
- Alter
- 99,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 03.04.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 110,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 2/9/21 Lot# EL9267; Pfizer 3/2/21 Lot# EN6202'; 10/4/21 PFizer Lot# FE3592; Pfizer 4/3/22 Lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 92,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 2/22/21 Lot# EN6200; Pfizer 3/16/21 Lot# EN6207; Pfizer 10/25/21 Lot# FE3590; Pfizer 4/6/22 Lot# FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID + external test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 10.04.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 233,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gastritis
Impaired gastric emptying
Overgrowth fungal
Symptomtext
Gastro paresis is the term given me, however that is being researched. I do have gastritis, pretty chronic and severe, yeast in my throat and stomach, being treated. I don't think this is an adverse reaction but I was told to report anyway
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gastritis
- Hospital-Tage
- -
- Labordaten
- see above
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- emphysema
- Andere Medikamente
- uro-mp, Allegra d, metaxalone, linzess, Relpax, Fmotidine, thryoid np, metoprolol er, Simvastatin, Symbicort, methenamine hippurate., Dandelion Root, Magnesium, b6, b12, 81 mg aspirin,
- Allergien
- narcotic, citalopram, newly blueberries
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 77,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Feeling abnormal
SARS-CoV-2 test positive
Symptomtext
07/05/2022, I started feeling bad. I went downstairs and took a test and it went to positive immediately. I called my doctor and started PAXLOVID that afternoon. I went to bed for 4 or 5 days. I was feeling better when I ran out of PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 07/05/2022 COVID-19 test- positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Diphenhydramine; multivitamin; terazosin; amlodipine; EXCEDRIN migraine
- Allergien
- N/A
- Vorherige Impfungen
- 50 years ago, the plague shot, passed out.
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Insomnia
SARS-CoV-2 test positive
Symptomtext
I was having trouble sleeping. I woke up the next morning and took a COVID-19 test at home and it was positive. I called my doctor and since I had mild symptoms she did not recommend me taking PAXLOVID. I felt very tired for about 4-5 days. I did not have any other symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 test- positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteoarthritis
- Andere Medikamente
- Ibandronate sodium; probiotics; multivitamin; vitamin D; C; E; zinc; slippery elm; vitamin D3
- Allergien
- Sulfa; penicillin
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 16.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), on 04Apr2022 at 14:30 as dose 4 (booster), single (Lot number: FJ9943) at the age of 68 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (09Jul2022) Negative, notes: tested negative on 09Jul and was without symptoms for 3 days; (13Jul2022) Positive, notes: on 13Jul runny nose, headache and I tested positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Paxlovid (Lot number: GA9630) was started in 04Jul2022 till 08Jul2022 for the COVID-19 Treatment. After completing a round of Paxlovid on 08July2022, the patient tested negative on 09Jul2022 and was without symptoms for 3 days. On 12Jul2022 02:30PM runny nose started, again and on Jul 13 runny nose, headache and the patient tested positive. The patient was not recovered. The patient did not have any allergies and did not have a treatment adverse event. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220709; Test Name: COVID-19 test; Test Result: Negative ; Comments: tested negative on 09Jul and was without symptoms for 3 days; Test Date: 20220713; Test Name: COVID-19 test; Test Result: Positive ; Comments: on 13Jul runny nose, headache and I tested positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 19.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID positive; COVID positive; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 72-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 05Feb2021 at 18:00 as dose 1, single (Lot number: EL9269), in left arm, on 02Mar2021 as dose 2, single (Lot number: EN6206), in left arm, on 06Oct2021 at 13:30 as dose 3 (booster) single (Lot number: FF2590), in left arm and on 19Apr2022 at 13:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 72 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "known allergies: Sulfa drugs" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing); "seasonal allergy" (unspecified if ongoing); "auto immune angio edema" (unspecified if ongoing); "glaucoma" (unspecified if ongoing). Concomitant medication(s) included: ZYRTEC ALLERGY; METOPROLOL; CALTRATE [CALCIUM CARBONATE]; D3; VITAMIN C [ASCORBIC ACID]. Past drug history included: Metoprolol, reaction(s): "Minor cardiac pvc's", notes: Minor cardiac pvc's (metoprolol). The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Jun2022) Positive; (29Jun2022) Negative; (30Jun2022) Negative; (01Jul2022) Negative; (02Jul2022) Negative; (08Jul2022) Positive, notes: Tested twice on 08Jul2022. Both immediately Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Addition information: Start date of treatment for COVID-19 was 24Jun2022. Stop date of treatment for COVID-19 was 29Jun2022. Paxlovid rebound- return of COVID symptoms 5-8 days after first negative test. (First negative test and last day of paxlovid 5 day caourse are same). 3 consecutive days of negative tests to follow. Initial COVID positive on 22Jun2022. 1st dose paxlovid 24Jun2022 in pm. Last dose paxlovid 29Jun2022 in am. Negative tests 29Jun2022; 30Jun2022; 01Jul2022; 02Jul2022; new mild symptoms may have started as early as 01Jul2022. Or as late as 06Jul2022. Cold symptoms with mild congestion and intermittent cough due to raw throat more apparent on 07Jul2022. Tested twice on 08Jul2022. Both immediately Positive. Slight fever and headache with some congestion on 08Jul2022. I am in the throes of it now.; Sender's Comments: The contribution of the suspect drug to the onset of "COVID positive" cannot be ruled out since drug efficacy varies from one patient to another and affected by different factors.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220622; Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20220629; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20220630; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20220701; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20220702; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20220708; Test Name: COVID-19 test; Test Result: Positive ; Comments: Tested twice on 08Jul2022. Both immediately Positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Angioedema; Glaucoma; Penicillin allergy; Seasonal allergy; Sulfonamide allergy
- Andere Medikamente
- ZYRTEC ALLERGY; METOPROLOL; CALTRATE [CALCIUM CARBONATE]; D3; VITAMIN C [ASCORBIC ACID]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 11.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19; 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 74-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Feb2021 at 12:00 as dose 1, single (Lot number: EN6202), in right arm, on 26Mar2021 at 12:00 as dose 2, single (Lot number: ER8730), in right arm, on 01Oct2021 at 12:00 as dose 3 (booster), single (Lot number: FF2589), in right arm and on 11Apr2022 at 12:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 74 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: statin drugs" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Percocet, reaction(s): "Known allergies: Percocet"; Naproxen, reaction(s): "Known allergies: Naproxen". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: No chronic conditions or illnesses at this time other than Covid. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid 19; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Drug allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 16.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 58,0
- 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
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 72-year-old male patient received BNT162b2 (BNT162B2), on 22Jan2021 as dose 1, single (Lot number: EL9262), in left arm, on 24Sep2021 as dose 3 (booster), single (Lot number: FF2588), in left arm and on 04Apr2022 at 12:15 as dose 4 (booster), single (Lot number: FJ9943) at the age of 71 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), on 11Feb2021 as dose 2, single (Lot number: EL9267), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "kidney stones" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: COVID-19 (medically significant), DRUG INEFFECTIVE (medically significant) all with onset Jun2022, outcome "recovering" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Jun2022) Positive. Therapeutic measures were taken as a result of covid-19, drug ineffective. Clinical course: Anti viral details included COVID 19 Treatment, (brand was Paxlovid), started on 28Jun2022 to 03Jul2022. Other medication in 2 weeks product was Amlodipine, valsartan, atorvastatin. The patient previously received a COVID-19 Vaccine. It was reported as Covid recurred, positive test. No known allergies were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202206; Test Name: Covid; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension; Kidney stones
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 16.07.2022
- Impfdatum
- 20.05.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment/Covid Test: positive; COVID 19 Treatment/Covid Test: positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34-year-old male patient received BNT162b2 (BNT162B2), on 09Mar2021 as dose 1, single (Lot number: EN6204), in left arm, on 30Mar2021 as dose 2, single (Lot number: EP6955), in left arm, on 10Nov2021 as dose 3 (booster), single (Lot number: FH8028), in left arm and on 20May2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 34 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 08Jul2022 at 08:30, outcome "unknown" and all described as "COVID 19 Treatment/Covid Test: positive". Other medication in 2 weeks. AE resulted in: [None of the above]. Known allergies: No Known Allergies. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (08Jul2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220708; Test Name: Covid Test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
After being vaccinated, & receiving 2 boosters, I contracted Covid Variant 2
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- May 22, 2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- osteoporosis arthritis
- Andere Medikamente
- doxycycline
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 08.07.2022
- Impfdatum
- 29.03.2022
- 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/ Re-occurance of Covid- Rebound Covid; Treatment of COVID-19/ Re-occurance of Covid- Rebound Covid; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 77-year-old male patient received BNT162b2 (BNT162B2), on 29Mar2022 at 17:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 76 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "lung cancer" (not ongoing), notes: Recovered lung cancer; "emphysema" (unspecified if ongoing). Concomitant medication(s) included: PANTOPRAZOLE, start date: Jan2020, stop date: 05Jul2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19/ Re-occurance of Covid- Rebound Covid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown Results. Therapeutic measures were taken as a result of drug ineffective, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: covid-19 test; Result Unstructured Data: Test Result:Unknown Results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Emphysema; Lung cancer (Recovered lung cancer)
- Andere Medikamente
- PANTOPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 67,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 19Jan2021 as dose 1, single (Lot number: EL8982) at the age of 66 years, in right arm, on 09Feb2021 as dose 2, single (Lot number: EN9581) at the age of 66 years, in right arm, on 26Sep2021 as dose 3 (booster), single (Lot number: FE3592) at the age of 67 years, in right arm and on 01Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 67 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Thyroid" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing); "mild asthma" (unspecified if ongoing), notes: Mild asthma. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 07Jun2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (07Jun2022) Positive; (16Jun2022) Negative; (17Jun2022) Negative; (04Jul2022) Positive, notes: Home test. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient did not have known allergies. Tested positive for COVID on 07Jun2022. Started Paxloid on 09Jun2022. Finished her last dose on 13Jun2022. Tested negative for COVID on 16Jun2022 and negative again on 17Jun2022. She was experiencing COVID mild symptoms on 03Jul2022 and she tested positive for COVID on 04Jul2022 using a home test. She have an appointment for a PCR test on 05Jul2022 at 7:15 am. Patient had received Anti-viral medication Paxloid as COVID 19 treatment and the treatment was started on Jun2022 and stopped on 13Jun2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220607; Test Name: tested for covid; Test Result: Positive ; Test Date: 20220616; Test Name: tested for covid; Test Result: Negative ; Test Date: 20220617; Test Name: tested for covid; Test Result: Negative ; Test Date: 20220704; Test Name: tested for covid; Test Result: Positive ; Comments: Home test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (Mild asthma); Blood pressure high; Thyroid disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature fluctuation
COVID-19
Cough
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I had a stuffy nose, cough, and temperature regulation problems one night. I decided to take an at-home COVID-19 test on 06/24/2022, and it came back positive. I called my doctor, and they informed me to go to a telehealth visit online to consult a physician. I was prescribed PAXLOVID to help remediate my symptoms faster. I began taking my prescription that evening and completed my dosage. I tested negative on 06/30/2022; but a few days later on 07/03/2022, I tested positive again. I recovered after the initial infection, but since finishing the prescription, I've still had a cough, runny nose, and sneezing so often.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature fluctuation
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- Root canal
- Vorgeschichte
- Asthma
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 01.01.2021
- Beginn
- 25.06.2022
- Tage bis Beginn
- 540,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Covid 19 positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid home test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Amlodipine losartan atorvastatin Hydrochlorothiazide Aspirin Fish Oil Pramipexole
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
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 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 50 years, in right arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (COVID-19 VACCINE MODERNA), on 18Jan2021 as dose 1, single (Lot number: 071856), on 10Feb2021 as dose 2, single (Lot number: 004M20A) and on 20Sep2021 as dose 3 (booster), single (Lot number: 048F2A) for covid-19 immunisation. The patient's relevant medical history included: "Mitral valve prolapse" (unspecified if ongoing); "Known allergies: Penicillin" (unspecified if ongoing). Concomitant medication(s) included: PREMARIN, start date: 31Dec2019, stop date: 19Jun2022; PREMPRO, start date: 01Aug2021, stop date: 19Jun2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Positive home test day 10; Negative, notes: Negative home test on day 7.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Home test; Result Unstructured Data: Test Result:Positive; Comments: Positive home test day 10; Test Name: Home test; Result Unstructured Data: Test Result:Negative; Comments: Negative home test on day 7
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Mitral valve prolapse; Penicillin allergy
- Andere Medikamente
- PREMARIN; PREMPRO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 27.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 73 years, in right arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 25Jan2021 as dose 1, single (Lot number: 029L20A), in right arm, on 28Feb2021 as dose 2, single (Lot number: 010A21A), in right arm and on 29Oct2021 as dose 3 (booster), single (Lot number: 939905), in right arm for covid-19 immunisation. The patient's relevant medical history included: "breast cancer", start date: 2010 (unspecified if ongoing); "osteoporosis" (unspecified if ongoing); "Interchange of vaccine products" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Amoxicillin, reaction(s): "known allergies: amoxicillin", notes: known allergies: amoxicillin; Gentamycin, reaction(s): "known allergies: gentamycin", notes: known allergies: gentamycin. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: positive, notes: positive test after taking Paxlovid; Negative, notes: testing negative; unknown results, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of covid-19. Patient had Known allergies of amoxicillin, gentamycin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid; Test Result: Positive ; Comments: positive test after taking Paxlovid; Test Name: Covid; Test Result: Negative ; Comments: testing negative; Test Name: Covid; Result Unstructured Data: Test Result:unknown results; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Breast cancer; Interchange of vaccine products; Osteoporosis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 16.03.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 110,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after three vaccines Pfizer 3/26/21 Lot# ER8727; Pfizer 4/16/21 Lot# Ew0158; Pfizer 3/16/22 Lot # FJ9943
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 04.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- 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 68-year-old male patient received BNT162b2 (BNT162B2), on 13Apr2022 at 09:00 as dose number unknown, single (Lot number: FJ9943) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient had no known allergies. There were no concomitant medications. The patient did not receive other medication in 2weeks. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown results, notes: COVID 19 Treatment; (28Jun2022) positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Patient received covid-19 treatment from 16Jun2022 to 20Jun2022. On 28Jun2022, a rebound infection occurred including sore throat, dry cough and fatigue. Positive Covid test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: covid test; Result Unstructured Data: Test Result:Unknown results; Comments: COVID 19 Treatment; Test Date: 20220628; Test Name: covid test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 05.04.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
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), on 09Mar2021 as dose 1, single (Lot number: PAA156051), in right arm, on 30Mar2021 as dose 2, single (Lot number: ER8272), in right arm, on 30Sep2021 as dose 3 (booster), single (Lot number: 30130BA), in right arm and on 05Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 62 years, in right arm 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 14Jun2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Jun2022) Positive; (23Jun2022) Negative; (25Jun2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220614; Test Name: COVID test; Test Result: Positive ; Test Date: 20220623; Test Name: COVID test; Test Result: Negative ; Test Date: 20220625; Test Name: COVID test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
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 55-year-old male patient received BNT162b2 (BNT162B2), on 01Apr2022 at 15:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 55 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: "Hypertension" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE, start date: 24Jan2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown Results. Therapeutic measures were taken as a result of drug ineffective, covid-19. Additional Information: The patient received other medication in 2weeks. The patient took Paxlovid for COVID 19 treatment. The treatment start date was reported as 20Jun2022 (lot number: GC0490). The patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Result Unstructured Data: Test Result:Unknown Results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Borderline hypertension
- Andere Medikamente
- AMLODIPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 26.04.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 42,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Positive COVID 19; Positive COVID 19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 84-year-old male patient received BNT162b2 (BNT162B2), on 28Jan2021 as dose 1, single (Lot number: EL3247), on 19Feb2021 as dose 2, single (Lot number: EL9263), in right arm, on 04Oct2021 as dose 3 (booster), single (Lot number: FF2590), in right arm and on 26Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 82 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: LOVASTATIN, stop date: 06Jun2022. The following information was reported: VACCINATION FAILURE (medically significant) with onset 07Jun2022, outcome "unknown", COVID-19 (medically significant) with onset 07Jun2022, outcome "not recovered" and all described as "Positive COVID 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (07Jun2022) Positive; (16Jun2022) Negative; (21Jun2022) Positive. Therapeutic measures were taken as a result of covid-19. Clinical Course: Tested Positive COVID19 07Jun2022, took Paxlovid 5 days 08Jun2022 to 12Jun2022. Tested negative 16Jun2022. On 21Jun2022 not feeling well tested Positive COVID 19 again. Milder symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220607; Test Name: Tested Positive COVID19; Test Result: Positive ; Test Date: 20220616; Test Name: Tested Positive COVID19; Test Result: Negative ; Test Date: 20220621; Test Name: Tested Positive COVID19; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LOVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 01.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 88,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Extra dose administered
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Three months after 4th dose, tested positive with a home COVID-19 test. His Dr. prescribed Paxlovid. Breakthrough case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- High Blood Pressure; High Cholesterol; had Prostate Cancer, and received Radiation treatments from 1/2021 through 3/2021. Is now Cancer free.
- Andere Medikamente
- Diovan; Lipitor; Priolosec; Celebrex; Flomax; multivitamin
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Extra dose administered
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
Three months after getting 4th dose of Pfizer, developed COVID-19. Took home test. Breakthrough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Synthroid; Valtrex; Vitamin D
- Allergien
- NANA
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 28.06.2022
- Impfdatum
- 04.04.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 72,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspepsia
Symptomtext
I didn't have any issues until 2 months after my vaccine and didn't associate it as an issue with the vaccine. But I began to have persistent heart burn and around 06/15/2022 my doctor prescribed a prescription strength PRILOSEC which has completely resolved the issue so far.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspepsia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Sinus cold.
- Vorgeschichte
- Thyroid and Kidney Cancer (in remission since 2011.)
- Andere Medikamente
- Synthroid; alopurinol.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 11.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Patient reported to me that the developed tinitis in both ears 2-3 days following vaccination. The ringing is constant with the patient's left ear being much more severe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- The patient reported they had not had an appointment with a provider regarding this issue as of June 18th 2022
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- None reported
- Allergien
- Corticosteroids
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 14.04.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 66,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Mar2021 as dose 1, single (Lot number: en6205), in left arm, on 30Mar2021 as dose 2, single (Lot number: ew0150), in left arm, on 06Oct2021 as dose 3 (booster), single (Lot number: 3015584), in left arm and on 14Apr2022 as dose 4 (booster), single (Lot number: fj9943), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Rheumatoid arthritis" (unspecified if ongoing); "salicylates" (unspecified if ongoing), notes: known allergies: salicylates and small pox vaccination. Concomitant medication(s) included: FOLIC ACID, start date: 03Nov2018, stop date: 19Jun2022; CIMZIA, start date: 02Jun2022, stop date: 02Jun2022; METHOTREXATE, start date: 03Jun2022, stop date: 03Jun2022. Past drug history included: Small pox vaccination, reaction(s): "known allergies: small pox vaccination", notes: known allergies: salicylates and small pox vaccination. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 19Jun2022, outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Jun2022) Positive, notes: reinfection on day 10- was symptom free after initial covid but still testing positive until 19Jun2022. overnight 19Jun into 20Jun sinus pressure built and cold like symptoms developed. No fever, no appetite, no energy and positive covid test; (20Jun2022) Positive, notes: reinfection on day 10- was symptom free after initial covid but still testing positive until 19Jun2022. overnight 19Jun into 20Jun sinus pressure built and cold like symptoms developed. No fever, no appetite, no energy and positive covid test. Therapeutic measures were taken as a result of vaccination failure, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220619; Test Name: Covid-19 test; Test Result: Positive ; Comments: reinfection on day 10- was symptom free after initial covid but still testing positive until 19Jun2022. overnight 19Jun into 20Jun sinus pressure built and cold like symptoms developed. No fever, no appetite, no energy and positive covid test; Test Date: 20220620; Test Name: Covid-19 test; Test Result: Positive ; Comments: reinfection on day 10- was symptom free after initial covid but still testing positive until 19Jun2022. overnight 19Jun into 20Jun sinus pressure built and cold like symptoms developed. No fever, no appetite, no energy and positive covid test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Rheumatoid arthritis; Salicylate (known allergies: salicylates and small pox vaccination)
- Andere Medikamente
- FOLIC ACID; CIMZIA; METHOTREXATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 67,0
- Geschlecht
- U
- Eingang
- 22.06.2022
- Impfdatum
- 11.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 51,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old patient received BNT162b2 (BNT162B2), on 18Jan2021 at 08:30 as dose 1, single (Lot number: EL1283), in left arm, on 08Feb2021 at 08:30 as dose 2, single (Lot number: EM9809), in left arm, on 04Oct2021 at 10:00 as dose 3 (booster), single (Lot number: FE3592), in left arm and on 11Apr2022 at 11:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure (controlled)" (unspecified if ongoing), notes: High blood pressure (controlled). The patient's concomitant medications were not reported. Past drug history included: O, reaction(s): "O drug allergy". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jun2022, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. This report was about COVID-19 treatment. Patient did receive the vaccine. Patient received treatment for COVID-19 as Paxlovid from 07Jun2022 to 11Jun2022. Seriousness criteria was reported as no for Results in death, Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating, Congenital anomaly/birth defect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (High blood pressure (controlled))
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- 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
Extra dose administered
Symptomtext
MOM STATED DOB 5/1/2010 ON CONSENT FORM AND VERIFIED SO PATIENT RECEIVED PFIZER GRAY CAP VIAL DOSE 0.3 ON 5/24/22. INSURANCE REJECTED 2ND DOSE 6/21/22 DUE TO INVALID DOB. ACTUAL DOB 5/1/2011 (11YRS) . MOM VERFIED SHE PROVIDED INCURRENT DOB ON CONSENT FORM ON 1ST DOSE AND ALSO ON 2ND DOSE CONSENT FORM.
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
- NJ
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 06.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old male patient received BNT162b2 (BNT162B2), on 25Feb2021 at 09:00 as dose 1, single (Lot number: EN6203), in left arm, on 18Mar2021 at 14:00 as dose 2, single (Lot number: EN6207), in left arm, on 02Oct2021 at 14:00 as dose 3 (booster), single (Lot number: 301458A), in left arm and on 06Apr2022 at 14:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 56 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing); "hyperlipidemia" (unspecified if ongoing); "benign prostatic hyperplasia" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown results, notes: COVID 19 Treatment; (14Jun2022) Negative, notes: initially tested negative one day after completion of treatment; (17Jun2022) Positive, notes: I initially tested negative one day after completion of treatment and then tested positive four days later. Therapeutic measures were taken as a result of covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid; Result Unstructured Data: Test Result:Unknown results; Comments: COVID 19 Treatment; Test Date: 20220614; Test Name: Covid; Test Result: Negative ; Comments: initially tested negative one day after completion of treatment; Test Date: 20220617; Test Name: Covid; Test Result: Positive ; Comments: I initially tested negative one day after completion of treatment and then tested positive four days later.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Benign prostatic hyperplasia; Hyperlipidemia; Hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
DOSE DELIVERED HAD A BEYOND USE DATE OF 05/26/2022 AND WAS GIVEN 06/01/2022. DISCUSSED WITH PATIENT'S PARENT. PARENT DID NOT WISH TO REPEAT THE DOSE. PATIENT DOING WELL TODAY. NO COMPLAINTS RELATING TO THE DOSE BEING GIVEN PAST THE BEYOND USE DATE. DISCUSSED WITH PHARMACY MANAGER, AND REPORTING TO VAERS PER PROTOCOL. NO COMPLAINTS FROM PATIENT PER MOTHER. SHE WAS MADE AWARE THAT THIS ERROR REPORT WOULD BE SENT ON 6/15/2022 PER PHONE CALL AT 5 PM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 15.06.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
PATIENT IS UNDER AGE 50 AND IS NOT IMMUNOCOMPROMISED OR TAKING ANY OTHER MEDICATIONS THAT WOULD WEAKEN HIS IMMUNE SYSTEM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 09.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- - / RA
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 65-year-old male patient received BNT162b2 (BNT162B2), on 11Mar2021 as dose 1, single (Lot number: EN6208), in left arm, on 01Apr2021 as dose 2, single (Lot number: ER8737), in left arm, on 31Aug2021 as dose 3 (booster), single (Lot number: FE3184), in right arm and on 09Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 64 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing); "Ulcerative Colitis" (unspecified if ongoing). Concomitant medication(s) included: XELJANZ, start date: 01Dec2017. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset May2022, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Paxlovid Rebound. Two days after completing Paxlovid I developed a runny nose, congestion & cough with fatigue. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy; Ulcerative colitis
- Andere Medikamente
- XELJANZ
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 11.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body mass index
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Nurse) from product quality group. A 67-year-old male patient received BNT162b2 (BNT162B2), on 03Mar2021 as dose 1, single (Lot number: EN6205), on 23Mar2021 as dose 2, single (Lot number: EP7534), on 26Sep2021 as dose 3 (booster), single (Lot number: FF2587) and on 11Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 67 years for covid-19 immunisation. The patient's relevant medical history included: "CAD" (unspecified if ongoing), notes: CAD; "dyslipidemia" (unspecified if ongoing); "prediabetes" (unspecified if ongoing); "CABG x 5" (unspecified if ongoing), notes: CABG x 5; "Carotid atherosclerosis" (unspecified if ongoing), notes: carotid atherosclerosis; "Sulfa antibiotics" (unspecified if ongoing), notes: known allergies Sulfa antibiotics. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: Body mass index: 33; SARS-CoV-2 test: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19 included Anti viral details product of oral Paxlovid from 21May2022 to 26May2022. product quality group providing investigation results: As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in PQS Q# and/or Q#. PR ID (CR): 7266074 Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1 Lot-# (CR): EN6205. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EN6205 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EN6205, fill lot EN5337, and the formulated drug product lot EN5326. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 5801756 PR Link (Previously Investigated CR): 5797466 PR ID (CR): 7266076. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1Lot-# (CR): EP7534. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EP7534 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EP7534, fill lot EP7532, and the formulated drug product lot EP7528. A complaint sample was not returned, and photographs were not received. There were no deviations that may have caused a complaint of this nature. No root cause or corrective/preventati ve actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 5862218. PR Link (Previously Investigated CR): 5851167. PR ID (CR): 7266080. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): FF2587. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FF2587 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot FF2587, fill lot FF2556, and the formulated drug product lot FE5315. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventati ve actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 6446122. PR Link (Previously Investigated CR): 6443978. PR ID (CR): 7266082. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): FJ9943. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FJ9943 was 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 FJ9943, fill lot FJ9942 and the bulk formulated drug product FJ9940. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 7121106. PR Link (Previously Investigated CR):7120223. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in PQS Q# and/or Q#. PR ID (CR): 7266074. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): EN6205. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EN6205 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EN6205, fill lot EN5337, and the formulated drug product lot EN5326. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 5801756. PR Link (Previously Investigated CR): 5797466. PR ID (CR): 7266076. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): EP7534. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EP7534 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EP7534, fill lot EP7532, and the formulated drug product lot EP7528. A complaint sample was not returned, and photographs were not received. There were no deviations that may have caused a complaint of this nature. No root cause or corrective/preventati ve actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 5862218 PR Link (Previously Investigated CR): 5851167. PR ID (CR): 7266080. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1 Lot-# (CR): FF2587. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FF2587 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot FF2587, fill lot FF2556, and the formulated drug product lot FE5315. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventati ve actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 6446122. PR Link (Previously Investigated CR): 6443978. PR ID (CR): 7266082. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): FJ9943. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FJ9943 was 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 FJ9943, fill lot FJ9942 and the bulk formulated drug product FJ9940. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 7121106 PR Link (Previously Investigated CR):7120223. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in PQS Q# and/or Q#. PR ID (CR): 7266074. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): EN6205. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EN6205 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EN6205, fill lot EN5337, and the formulated drug product lot EN5326. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 5801756. PR Link (Previously Investigated CR): 5797466. PR ID (CR): 7266076. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1 Lot-# (CR): EP7534. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EP7534 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EP7534, fill lot EP7532, and the formulated drug product lot EP7528. A complaint sample was not returned, and photographs were not received. There were no deviations that may have caused a complaint of this nature. No root cause or corrective/preventati ve actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 5862218. PR Link (Previously Investigated CR): 5851167. PR ID (CR): 7266080. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for. intramuscular 2ml multiple dose vial X 1. Lot-# (CR): FF2587. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FF2587 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot FF2587, fill lot FF2556, and the formulated drug product lot FE5315. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventati ve actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 6446122. PR Link (Previously Investigated CR): 6443978. PR ID (CR): 7266082. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): FJ9943. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FJ9943 was 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 FJ9943, fill lot FJ9942 and the bulk formulated drug product FJ9940. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 7121106. PR Link (Previously Investigated CR):7120223. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in PQS Q# and/or Q#. PR ID (CR): 7266074. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): EN6205. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EN6205 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EN6205, fill lot EN5337, and the formulated drug product lot EN5326. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 5801756. PR Link (Previously Investigated CR): 5797466. PR ID (CR): 7266076. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): EP7534. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EP7534 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EP7534, fill lot EP7532, and the formulated drug product lot EP7528. A complaint sample was not returned, and photographs were not received. There were no deviations that may have caused a complaint of this nature. No root cause or corrective/preventati ve actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 5862218 PR Link (Previously Investigated CR): 5851167. PR ID (CR): 7266080. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1 Lot-# (CR): FF2587. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FF2587 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot FF2587, fill lot FF2556, and the formulated drug product lot FE5315. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact to product quality. No root cause or corrective/preventati ve actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 6446122. PR Link (Previously Investigated CR): 6443978. PR ID (CR): 7266082. Product Description (CR): Compound BNT 162 covid-19 vaccine suspension for intramuscular 2ml multiple dose vial X 1. Lot-# (CR): FJ9943. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FJ9943 was 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 FJ9943, fill lot FJ9942 and the bulk formulated drug product FJ9940. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality. No root cause or CAPA were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. PR ID of Previously Completed Inv: 7121106. PR Link (Previously Investigated CR):7120223; Sender's Comments: Based on the available information and possible temporal association the causal relationship between the reported event and suspect cannot be excluded.The case will be reviewed further with FU information. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body mass index
- Hospital-Tage
- -
- Labordaten
- Test Name: BMI; Result Unstructured Data: Test Result:33; Test Name: Covid test; Result Unstructured Data: Test Result:COVID 19 Treatment
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Atherosclerosis (carotid atherosclerosis); Coronary artery bypass graft (CABG x 5); Coronary artery disease (CAD); Dyslipidemia; Prediabetes; Sulfonamide allergy (known allergies Sulfa antibiotics)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 18.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 antibody test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 43-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Feb2021 as dose 1, single (Lot number: EM9810), in left arm, on 15Mar2021 as dose 2, single (Lot number: EN6208), in left arm, on 24Oct2021 as dose 3 (booster), single (Lot number: FH8028), in left arm and on 18Apr2022 as dose 4 (booster), single (Lot number: fj9943) at the age of 43 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Ankylosing spondylitis" (unspecified if ongoing); "Known allergies: Peanuts" (unspecified if ongoing), notes: Known allergies: Peanuts. Concomitant medication(s) included: PREDNISONE, start date: Mar2020, stop date: 31May2022; METOPROLOL, start date: Mar2018, stop date: Jun2022; VERAPAMIL, start date: 01Sep2019, stop date: 31May2022; HYDROCODONE, start date: Sep2014, stop date: 09Jun2022; REMICADE, start date: Mar2022, stop date: 09Jun2022. Past drug history included: Cipro, reaction(s): "Known allergies: Cipro", notes: Known allergies: Cipro. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 antibody test: (unspecified date) Negative, notes: After testing negative for 3 Days; (unspecified date) Positive, notes: COVID 19 Treatment; (unspecified date) Negative, notes: After testing negative for 3 Days; (unspecified date) Negative, notes: After testing negative for 3 Days; (09Jun2022) Positive, notes: Rebound infection after testing negative for 3 Days. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Rebound infection after testing negative for 3 Days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19; Test Result: Negative ; Comments: After testing negative for 3 Days.; Test Name: Covid-19; Test Result: Positive ; Comments: COVID 19 Treatment; Test Name: Covid-19; Test Result: Negative ; Comments: After testing negative for 3 Days.; Test Name: Covid-19; Test Result: Negative ; Comments: After testing negative for 3 Days.; Test Date: 20220609; Test Name: Covid-19; Test Result: Positive ; Comments: Rebound infection after testing negative for 3 Days.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy to nuts (Known allergies: Peanuts); Ankylosing spondylitis
- Andere Medikamente
- PREDNISONE; METOPROLOL; VERAPAMIL; HYDROCODONE; REMICADE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 61,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Pulmonary congestion
SARS-CoV-2 test positive
Symptomtext
positive COVID, cough and chest congestion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive COVID 19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- xyzal
- Allergien
- seasonal allergy, beets and artichokes
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 04.04.2022
- 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 antibody test
Symptomtext
covid-19; covid-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 04Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 67 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing); "Thyroid" (unspecified if ongoing); "Psoriasis Arthritis" (unspecified if ongoing). The patient took concomitant medications. Past drug history included: Known allergies: acyclovir, reaction(s): "Allergy"; Known allergies: dicyclomine, reaction(s): "Allergy"; Known allergies: flagyl, reaction(s): "Allergy"; Known allergies: liothyronine, reaction(s): "Allergy"; Known allergies: nabumetone, reaction(s): "Allergy"; Known allergies: sulfasalazine, reaction(s): "Allergy". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "covid-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 antibody test: (unspecified date) Unknown results, notes: Indication: Covid-19 treatment; (May2022) Positive, notes: Tested COVID positive 8, 9, and 11 days after Paxlovid; (May2022) Positive, notes: Tested COVID positive 8, 9, and 11 days after Paxlovid; (May2022) Positive, notes: Tested COVID positive 8, 9, and 11 days after Paxlovid. Therapeutic measures were taken as a result of drug ineffective, covid-19. Additional information: If vaccine received: Yes, Other medication in 2weeks: Yes. Adverse event: COVID rebound after Paxlovid series. Tested COVID positive 8, 9, and 11 days after Paxlovid and still feeling ill (13 days after end of series). Known allergies: Acyclovir, Dicyclomine, Flagyl, Liothyronine, Nabumetone, Sulfasalazine. Other medical history: Diabetes, Thyroid, Psoriasis Arthritis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Result Unstructured Data: Test Result:Unknown results; Comments: Indication: Covid-19 treatment; Test Date: 202205; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Tested COVID positive 8, 9, and 11 days after Paxlovid; Test Date: 202205; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Tested COVID positive 8, 9, and 11 days after Paxlovid; Test Date: 202205; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Tested COVID positive 8, 9, and 11 days after Paxlovid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes; Psoriatic arthritis; Thyroiditis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- 01.04.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 51,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Covid rebound. Covid symptoms 5/21/22, positive PCR test taken afternoon of 5/22. First Paxlovid dose evening of 5/23, complete course morning of 5/28. Two negative antigen tests on 5/29/22.; Covid rebound. Covid symptoms 5/21/22, positive PCR test taken afternoon of 5/22. First Paxlovid dose evening of 5/23, complete course morning of 5/28. Two negative antigen tests on 5/29/22.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 10Mar2021 as dose 1, single (Lot number: EN6206), in left arm, on 31Mar2021 as dose 2, single (Lot number: ER8730), in left arm, on 05Oct2021 as dose 3 (booster), single (Lot number: 30155BA), in left arm and on 01Apr2022 at 16:30 as dose 4 (booster), single (Lot number: FJ9943) at the age of 51 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "PCOS" (unspecified if ongoing); "blood clot in leg", start date: 2017 (unspecified if ongoing), notes: blood clot in leg in 2017. The patient's concomitant medications were not reported. Past drug history included: Biaxin, reaction(s): "Allergy". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 22May2022, outcome "not recovered" and all described as "Covid rebound. Covid symptoms 5/21/22, positive PCR test taken afternoon of 5/22. First Paxlovid dose evening of 5/23, complete course morning of 5/28. Two negative antigen tests on 5/29/22.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (29May2022) Negative; (29May2022) Negative; (02Jun2022) Positive, notes: in the afternoon; (22May2022) Positive, notes: positive PCR test taken afternoon of 22May. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Course: No Other medication in 2 weeks.Covid rebound. Covid symptoms 21May2022, positive PCR test taken afternoon of 22May. First Paxlovid dose evening of 23May2022, complete course morning of 28May2022. Two negative antigen tests on 29May2022. Headache, sore throat, upset stomach morning of 02Jun2022 and Positive antigen test in the afternoon of 02Jun2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220529; Test Name: Antigen test; Test Result: Negative ; Test Date: 20220529; Test Name: Antigen test; Test Result: Negative ; Test Date: 20220602; Test Name: Antigen test; Test Result: Positive ; Comments: in the afternoon; Test Date: 20220522; Test Name: PCR test; Test Result: Positive ; Comments: positive PCR test taken afternoon of 22May
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Clot blood (blood clot in leg in 2017); Polycystic ovary
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jan2021 as dose 1, single (Lot number: EL9265), in left arm, on 18Feb2021 as dose 2, single (Lot number: EL9267), in left arm, on 09Oct2021 as dose 3 (booster), single (Lot number: FE3590), in left arm and on 07Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "HTN" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "hypothyroid" (unspecified if ongoing); "depression" (unspecified if ongoing); "allergies" (unspecified if ongoing), notes: known allergies Yes. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset May2022, outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Patient received treatment with Paxlovid, treatment start date=31May2022, lot number=GA1189, indication=Treatment of COVID-19.; Sender's Comments: The reported Covid 19 positive after both the doses of COVID-19 immunization is considered ineffective of BNT162B2, and the Company cannot completely exclude the possible causality between the reported events and BNT162B2 administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy (known allergies Yes); Asthma; Depression; Hypertension; Hypothyroidism
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 04.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 14,0
- 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
tested positive for covid; tested positive for covid; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Feb2021 as dose 1, single (Lot number: EN5318), in right arm, on 18Feb2021 as dose 2, single (Lot number: EN6201), in left arm, on 03Dec2021 as dose 3 (booster), single (Lot number: FH8030), in left arm and on 04Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 63 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: OMEPRAZOLE. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 18Apr2022, outcome "not recovered" and all described as "tested positive for covid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: I did a home test and it was a strong positive; (unspecified date) Positive, notes: I had a PCR on 31Apr2022 that confirmed positive; (18Apr2022) Positive, notes: tested positive for Covid on 18Apr which was confirmed with a PCR test; (24Apr2022) Negative, notes: I did a rapid test and was negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Patient tested positive for Covid on 18Apr which was confirmed with a PCR test. She started Paxlovid the evening of 19Apr2022 till 24May2022 for the treatment of COVID-19. Started feeling better within a day. Cough was gone, still very fatigued. Followed CDC guidelines. On 24Apr she did a rapid test and was negative. Still fatigued but no other symptoms. On 28Apr2022, she woke up with extreme nasal congestion, watering eyes, sneezing, and slight headache. She did a home test and it was a strong positive. She had a PCR on 31Apr2022 that confirmed positive. Patient did not have other medical history. She did not know that she had known allergy. Patient received Zyertec medication in 2weeks and Prednisone from 12May2022 to 16May2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: PCR test; Test Result: Positive ; Comments: I did a home test and it was a strong positive; Test Name: PCR test; Test Result: Positive ; Comments: I had a PCR on 31Apr2022 that confirmed positive.; Test Date: 20220418; Test Name: PCR test; Test Result: Positive ; Comments: tested positive for Covid on 18Apr which was confirmed with a PCR test; Test Date: 20220424; Test Name: Rapid Test; Test Result: Negative ; Comments: I did a rapid test and was 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
- OMEPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 27.04.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 30,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
C-reactive protein
COVID-19
Chest X-ray normal
Cough
Fall
Hypoxia
Leukocytosis
SARS-CoV-2 test positive
Symptomtext
79 year old male with known atrial fibrillation (on AC and amiodarone), HTN came here with three weeks history of cough and two days of weakness with recent fall due to this weakness, no head trauma. In the ED he was found to be profoundly weak and became hypoxemic with minimal exertion. Work-ups were significant for mild leukocytosis, chest x-ray unremarkable and patient tested positive for COVID-19. Patient was admitted under hospitalist service. Patient stayed in hospital for approximately 3 days. Patient started on Decadron 6 mg daily. Patient has been weaned off oxygen and 1st 24 hours of stay. He was monitored and continued to be stable. His CRP were monitored as well and down trended. PTOT evaluation initially recommended subacute rehab but with the reassessment and patient much improved recommendations had changed to home health and patient discharged home stable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 3,0
- Labordaten
- DR CHEST 2 VIEWS FRONTAL AND LATERA Resulted: 05/27/22 2034 Order Status: Completed Updated: 05/27/22 2036 Narrative: EXAMINATION: Frontal and Lateral View Chest EXAM DATE: 5/27/2022 7:58 PM TECHNIQUE: Frontal and lateral views INDICATION: Cough, weakness. COMPARISON: January 31, 2022 ENCOUNTER: Initial _________________________ FINDINGS: Cardiac silhouette is prominent although I believe large part of this is due to prominent epicardial (pericardial fat pads. Pulmonary vascularity is normal. There are no infiltrates or pleural effusions. _________________________ Impression: No acute cardiopulmonary disease is present. COVID-19 PCR - Rapid (Abnormal) Collected: 05/27/22 1900 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 05/27/22 1925 COVID-19 PCR Detected
- Aktuelle Erkrankungen
- Persistent atrial fibrillation 4/5/2022
- Vorgeschichte
- Respiratory OSA (obstructive sleep apnea) Circulatory Atrial flutter Essential hypertension Palpitations Persistent atrial fibrillation Digestive (BMI) of 31.0 to 31.9 Nervous Chest pain Endocrine/Metabolic Dyslipidemia Other History of cardiomyopathy Fatigue
- Andere Medikamente
- amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 5 MG tablet benzonatate (TESSALON) 200 MG capsule beta carotene 10000 UNITS capsule BREWERS YEAST PO Calcium Carbonate-Vit D-Min (CALCIUM 1200 PO) Coenzyme Q10 200 MG CAPS dexamethasone
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 04.04.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 51,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Covid 19 - verified by home testing - patient is fully recovered. Paxvolid was prescribed (5 days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- A-Fib
- Andere Medikamente
- Paxvolid was prescribed for 5 days Previous Vaccinations: 03/03/2021 (Vaccination #1) 03/24/2021 (Vacinntaion #2) 09/30/2021 (1st Booster)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 31.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26Mar2021 at 12:00 as dose 1, single (Lot number: EN6207), in left arm, on 16Apr2021 at 12:00 as dose 2, single (Lot number: EW0169), in left arm, on 20Oct2021 at 12:00 as dose 3 (booster), single (Lot number: FE3590), in left arm and on 31Mar2022 at 12:00 as dose 4 (booster), single (Lot number: FJ9943) at the age of 53 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Breast cancer" (unspecified if ongoing); "melanoma" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Erythromycin, reaction(s): "Known allergies: Erythromycin". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (May2022) Negative, notes: 1 week after testing negative on PCR; (May2022) Positive, notes: Tested positive again (rapid) on 5th day; (unspecified date) Unknown results; (May2022) Positive, notes: tested positive again. Therapeutic measures were taken as a result of vaccination failure, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202205; Test Name: PCR; Test Result: Negative ; Comments: 1 week after testing negative on PCR; Test Date: 202205; Test Name: rapid; Test Result: Positive ; Comments: Tested positive again (rapid) on 5th day.; Test Name: tested; Result Unstructured Data: Test Result:Unknown results; Test Date: 202205; Test Name: tested; Test Result: Positive ; Comments: tested positive again
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Breast cancer; Melanoma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 29.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Physician). The reporter is the patient. A 52-year-old male patient received BNT162b2 (BNT162B2), on 15Dec2020 as dose 1, single (Lot number: EK5730), in left arm, on 05Jan2021 as dose 2, single (Lot number: EL3246), in left arm, on 24Sep2021 as dose 3 (booster), single (Lot number: EW0185), in left arm and on 29Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 50 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing). Concomitant medication(s) included: ATORVASTATIN. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), all with latency 11 days after the suspect product(s) administration, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: No known allergies. Patient received other medication in 2 weeks was Atorvastatin. Coivd-19 treatment with Paxlovid day 1-5 completed from 12May2022 to 15May2022. Rebound Covid-19 symptoms at day 12 on 23May2022 and was not recovered. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the information available and close temporal association, a possible contributory role of the suspect Product cannot be excluded for the reported events . The case will be reassessed once new information is available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: covid test; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: High cholesterol; Hypertension
- Andere Medikamente
- ATORVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
One month after my 4th dosage I tested positive for COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home Covid test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Degenerative Disc Disease
- Andere Medikamente
- Restasis 1 drop twice daily; vitamin B complex; calcium supplement
- Allergien
- Seasonal
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 29.05.2022
- Impfdatum
- 28.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
I CALLED PT'S MOM 4 TIMES BUT I DID NOT GET ANY RESPONSE. SO, I AM NOT SURE IF THE PATIENT EXPERIENCE ANY SIDE EFFECT OF THE INJECTION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- NO INFORMATION AVAILABLE AT THIS TIME. I WAS NOT ABLE TO CONTACT MOM TO FIND OUT IF THE PATIENT EXPERIENCE ANY SIDE EFFECT.
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
EXPIRED VACCINE WAS ADMINISTERED TO PATIENT - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOW N
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE WAS EXPIRED WHEN ADMINISTERED TO PATIENT - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- ACCUTANE
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 11.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE ADMINSTERED TO PATIENT WAS EXPIRED - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
EXPIRED VACCINE WAS ADMINISTERED TO PATIENT - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
EXPIRED VACCINE WAS ADMINISTERED TO PATIENT - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 17.05.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 15.05.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
EXPIRED VACCINE WAS ADMINISTERED TO PATIENT - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 15.05.2022
- Beginn
- 15.05.2022
- 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
EXPIRED VACCINE WAS ADMINISTERED TO PATIENT - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- SULFA MEDICATIONS
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 15.05.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
EXPIRED VACCINE WAS ADMINISTERED TO PATIENT - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- NONE KNOWN
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE ADMINISTERED TO PATIENT, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 14.05.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE WAS EXPIRED AT TIME OF ADMINISTRATION - EXPIRED ON 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE KNOWN
- Andere Medikamente
- NONE KNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
ADMINISTERED EXPIRED VACCINE, VACCINE EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine given to patient - expired on 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- unknown
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 28.05.2022
- Impfdatum
- 02.05.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
EXPIRED VACCINE GIVEN TO PATIENT, EXPIRED 5/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 26.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Drug ineffective
Suspected COVID-19
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 77-year-old male patient received BNT162b2 (BNT162B2), on 15Apr2022 at 12:30 as dose 4 (booster), single (Lot number: FJ9943) at the age of 76 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 had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant), all with latency 10 days 18 hrs. after the suspect product(s) administration, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, suspected Covid-19. Clinical course: Vaccine received and no other medications with in 2 weeks. Adverse event: Symptoms were completely gone on 13May, but came back worse than they originally were on 15May. No known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Drug ineffective
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 04.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old male patient received BNT162b2 (BNT162B2), on 03Apr2021 as dose 1, single (Lot number: EW0150), in left arm, on 01May2021 as dose 2, single (Lot number: EW0173), in left arm, on 16Oct2021 as dose 3 (booster), single (Lot number: FF2590), in left arm and on 04Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 54 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "HIV" (unspecified if ongoing). Concomitant medication(s) included: TIVICAY, start date: Jan2017; DESCOVY, start date: Jan2017; MONTELUKAST, start date: Jan2016. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: Treatment of COVID-19; (14May2022) Negative, notes: 2 negative at-home tests (Days 7 & 8); (15May2022) Negative, notes: 2 negative at-home tests (Days 7 & 8); (16May2022) Positive, notes: viral rebound occurred on Day 9 (after initiating treatment). Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: No vaccine received and no other medication with in in 2weeks. Adverse event: After completing 5-day treatment course and symptoms (soar throat, fatigue, congestion, cough, headache and brain fog) surged back later the same day of viral rebound and were greater in severity than during initial infection. No known allergies, Other medical history: HIV No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20220514; Test Name: Covid-19; Test Result: Negative ; Comments: 2 negative at-home tests (Days 7 & 8); Test Date: 20220515; Test Name: Covid-19; Test Result: Negative ; Comments: 2 negative at-home tests (Days 7 & 8); Test Date: 20220516; Test Name: Covid-19; Test Result: Positive ; Comments: viral rebound occurred on Day 9 (after initiating treatment)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: HIV disease
- Andere Medikamente
- TIVICAY; DESCOVY; MONTELUKAST
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Drug ineffective
SARS-CoV-2 test
Suspected COVID-19
Symptomtext
Pfizer / BioNTech: Dose Number: 4; Paxlovid: Treatment of COVID-19; Pfizer / BioNTech: Dose Number: 4; Paxlovid: 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 71-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 71 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. No known allergies. The patient's relevant medical history included: "atrial fibrillation" (unspecified if ongoing), notes: Very rare instances (less than 1 per year) of atrial fibrillation. Concomitant medication(s) included: VALACYCLOVIR [VALACICLOVIR], start date: 20Jan2022, stop date: 12May2022. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant), outcome "unknown" and all described as "Pfizer / BioNTech: Dose Number: 4; Paxlovid: Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results. Therapeutic measures were taken as a result of suspected covid-19 included Paxlovid. Clinical course: Treatment: Paxlovid, on 13May2022 to 14May2022. Follow-up attempts completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Drug ineffective
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Atrial fibrillation (Very rare instances (less than 1 per year) of atrial fibrillation)
- Andere Medikamente
- VALACYCLOVIR [VALACICLOVIR]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 36,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
One month after my 4th dose of Pfizer, I tested positive for COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; High Blood Pressure
- Andere Medikamente
- Triamterene 37.5mg, Citalopram 20mg, Pantoprazole 40mg, Singular 10mg, Zyrtec, Nasal Spray as needed, Ludden Zeaxanthin 25mg, Multivitamin, Calcium and Vitamin D3 twice daily, Vitamin C, Digestive Aid, Inhaler as needed.
- Allergien
- Seasonal allergies; grass; amoxicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 44,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID a month after getting my 4th dose of Pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Heart Disease
- Andere Medikamente
- Wellbutrin 200mg; Abilify 1mg; isosorbide mononitrate 90mg; Zetia 10mg; Cozaar 100mg; Prilosec 20mg; metoprolol succer 25mg; 81mg aspirin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 16.04.2022
- Beginn
- 30.04.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Hypersensitivity
Lacrimation increased
Mononucleosis heterophile test negative
Pharyngeal erythema
Pharyngeal swelling
Rhinorrhoea
Streptococcus test negative
Tonsillar inflammation
Symptomtext
I started having this feeling like my throat was swollen, almost like someone had their hand on my throat, and around about the same time I was having watery eyes, runny nose, and drainage at night. I looked at my tonsils, where I've never been able to see before, they were inflamed and my throat was red. I didn't have any pain, just the feeling of pressure on neck. I didn't think anything of it until it started occurring more frequently. I made appt with doctor who performed mono test and strep test, both negative. She believed it was allergy related because we've had a lot of wind here recently. Although i've experienced allergies every year, i've never had issues with my throat. She prescribed zyrtec d, flonase, and benadryl and told me to take those daily until they went away. That was last week (5/18/22). The symptoms are fine in the morning time, I'm in an enclosed room with a purifier. Its throughout the day when I'm out and about that my throat feels like its starting to swell, which has continued with the medication. She said it might continue for a while and advised that once symptoms have receded to continue to take zyrtec D at night before bed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discomfort
- Hospital-Tage
- -
- Labordaten
- Mono test, strep test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- systemic lupus, ulcerative colitis (remission), fibromyalgia
- Andere Medikamente
- Hydroxychloroquine, pantaprozal, Probiotic/prebiotic, fish oil, D3, Bariatric Multivitamin, calcium, cyclobenzaprine
- Allergien
- seasonal allergies, pet dander
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 17,0
- Geschlecht
- U
- Eingang
- 20.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Product administered to patient of inappropriate age
Symptomtext
Looked in registry for previous Covid19 shots. Listed as getting 2 shots. 1st shot on 4/2/21 and 2nd shot on 5/30/21. Patient and father confirmed patient only got 2 shots in the past and no boosters yet. They left their vaccine card at home. I told them they can always bring back in the future and we can fill it out for them. Billed as a 3rd (booster) shot. Patient came in with vaccine record card. Has gotten a booster shot on 1/14/22 that they do not recall receiving. Reporting that this 17yo patient has now gotten a 4th shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product use issue
Symptomtext
Administered pfizer covid vaccine gray cap for patient on 5/20/2022 with the beyond use date of 5/19/2022. Called pfizer and confirmed the total time pfizer covid vaccine gray cap can be stored in the fridge is 72 days which is good until 5/21/2022. patient does not have to revaccinate. Called patient and explained about the incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product use issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE.
- Vorgeschichte
- NONE.
- Andere Medikamente
- FOSAMAX, PRAVASTATIN.
- Allergien
- NONE.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 18.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from Regulatory Authority. The reporter is the patient. A 60-year-old male patient received BNT162b2 (BNT162B2), on 05Mar2021 as dose 1, single (Lot number: En205), in right arm, on 26Mar2021 as dose 2, single (Lot number: Er8727), in right arm, on 26Oct2021 as dose 3 (booster), single (Lot number: 3203080), in right arm and on 01Apr2022 as dose 4 (booster), single (Lot number: Fj9943) at the age of 60 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing). Concomitant medication(s) included: STATIN [ATORVASTATIN CALCIUM]. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (12May2022) negative. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course-After the 5 day treatment the patient felt fine.Tested negative on day 6. 5 days after the 5 day treatment have a head full, sinus, cough. Sore throat. It was reported that, the patient taking other medications within 2 weeks of starting COVID-19 treatment. The patient previously also received a COVID-19 Vaccine. Device Date: 12May2022 No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220512; Test Name: COVID test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high; High cholesterol
- Andere Medikamente
- STATIN [ATORVASTATIN CALCIUM]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 21.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Drug ineffective
Suspected COVID-19
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 04Apr2021 as dose 1, single (Lot number: EP7533), in left arm, on 25Apr2021 as dose 2, single (Lot number: EU 0170), in left arm, on 27Nov2021 as dose 3 (booster), single (Lot number: FH8030), in left arm and on 21Apr2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 64 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant) all with onset May2022, latency 2 days 30 min after the suspect product(s) administration, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, suspected covid-19. Clinical course included: Treatment of COVID-19 included Paxlovid from 7May2022. On 9May2022 the patient experienced muscle cramps. No known drug allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Drug ineffective
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 17.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Nasopharyngitis
Rhinorrhoea
Secretion discharge
Sneezing
Symptomtext
Runny nose, sneezing and. Deep cough with mucus present. It felt like a cold. I got over it within 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- coronary artery disease (stint in place 30 years ago)
- Andere Medikamente
- I do not have the dosage for these. fosinopril, atenolol, loratadine, 81 mg of aspirin, triamterene, alopurinol, amlodipine, centrum silver vitamin.
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 31.03.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 42,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 22.04.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose decreased
Symptomtext
I have had, up until getting the vaccine, my diabetic numbers were under control regularly. But once getting the vaccine, my diabetic numbers increased tremendously for about a week regardless what medications to took.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood glucose decreased
- Hospital-Tage
- -
- Labordaten
- Glucose test
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- diabetes
- Andere Medikamente
- Crestor, Metformin 2000mg, probiotic, vitamin D, cinnamon supplement, apple cider supplement
- Allergien
- tetanus vaccine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 04.04.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 32,0
- Dosis
- 4
- Route/Site
- - / LA
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 a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76-year-old female patient received BNT162b2 (BNT162B2), on 04Apr2022 at 13:00 as dose 4 (booster), single (Lot number: Fj9943) at the age of 76 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) 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. Past drug history included: Known allergies mo, reaction(s): "Known allergies Mo", notes: Known allergies Mo. The following information was reported: COVID-19 (medically significant) with onset 06May2022, outcome "recovering", DRUG INEFFECTIVE (medically significant) with onset 2022, outcome "unknown" and all described as "COVID 19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Treatment received included Amici Clav857.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 19.03.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. An 85-year-old male patient received BNT162b2 (BNT162B2), on 04Jan2021 as dose 1, single (Lot number: EK5730), in left arm, on 15Jan2021 as dose 2, single (Lot number: EL3248), in left arm, on 08Sep2021 as dose 3 (booster), single (Lot number: FC3182), in left arm and on 19Mar2022 as dose 4 (booster), single (Lot number: FJ9943) at the age of 85 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "mild hypertension" (unspecified if ongoing); "CA of prostate" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: COVID-19 (medically significant) with onset 05May2022, outcome "not recovered", VACCINATION FAILURE (medically significant), outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. Follow-up attempts are completed. No further information is expected.; Sender's Comments: The reported Covid 19 positive after both the doses of COVID-19 immunization is considered ineffective of BNT162B2, and the Company cannot completely exclude the possible causality between the reported events and BNT162B2 administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension; Prostate cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 11.05.2022
- Impfdatum
- 12.04.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Nasopharyngitis
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Break through Covid case. I started feeling symptoms May 5th and tested positive on Monday May 9th. I developed a head cold and I treated with ibuprofen and later on with Mucinex cough syrup. As of today the only symptoms I have are residuals from head cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Nasal swap Covid test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Simvastatin Prilosec Lotrel
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 05.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
patient had pfizer as first dose and moderna as second dose. no symptoms, signs, or reactions noted as per staff giving vaccine as well as monitoring after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- asthma, low back pain, nicotine dependence
- Andere Medikamente
- albuterol cyclobenzaprine meloxicam
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- U
- Eingang
- 30.04.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Blood pressure measurement
Symptomtext
This is a spontaneous report received from a contactable consumer or other non-HCP (the patient); program ID: (005570). A patient (no qualifiers provided) received the 1st, 2nd, 3rd and 4th dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, batch/lot# unknown); all single dose, for COVID-19 immunization. Medical history and concomitant medications not reported. The patient experienced increased blood pressure, with outcome of unknown. Patient described, "I am experiencing an unusually high blood pressure since receiving my 2nd booster shot. I noticed increased blood pressure after the first dose and the 2nd dose and my 1 booster." Relevant laboratory tests and procedures available in the appropriate section. The information on the batch/lot number for BNT162B2 requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure increased
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood pressure; Result Unstructured Data: Test Result: High blood pressure.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Normal shot reaction This is being reported as a breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Binax home test POSITIVE Urgent Care confirmation antibody infusion
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- ramapril synthroid lipitor
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Lymphoedema
Symptomtext
armpit lymph node swollen the night of vaccination then drainage to left side formed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mammogram abnormal
Ultrasound scan abnormal
Symptomtext
I had a routine mammogram and ultrasound and the results were abnormal, I am scheduled for a follow-up biopsy of my left axillary lymph node.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mammogram abnormal
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Coronary Artery Disease; Hyperlipoidemia; Obesity; Hypothyroid; Hypertension; Pinched Nerves.
- Andere Medikamente
- Lotrel; Cinnamon; Caltrate; Centurium Silver; Toprol XL; Vitamin D3; Vitamin B-12; Metformin; Loratadine; Onglyza; Lipitor; Levothyroxine; Low Dose Aspirin; Aleve.
- Allergien
- Ambien
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Amnesia
Blood test
Magnetic resonance imaging
Transient global amnesia
Urine analysis
Symptomtext
One hour after receiving vaccine, I had lost my memory until the next afternoon. I woke up in the hospital and was diagnosed With TGA (Transient global amnesia). Took a few days to get back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amnesia
- Hospital-Tage
- 1,0
- Labordaten
- blood, urine, mri
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril, Baby Aspirin, Vitamin B, Vitamin D, Efudex
- Allergien
- Penicillin, Cipro
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 09.04.2022
- Beginn
- 10.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Constant ringing in ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, migraines, rosacea, hypercalcemia
- Andere Medikamente
- Synthroid, Simvastatin, Hydochlorothiazide, Nurtec, fish oil, flax oil, calcium, vitamin D, high potency vitamins, metrogel
- Allergien
- Dilaudid
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lymphadenopathy
Symptomtext
Ipsilateral lymphadenopathy affecting L axillary, L humeral, & L pectoral lymph nodes. Onset approx. 24 h after vaccine administered. Duration 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Limb discomfort
Swelling
Symptomtext
I woke up late the following night after receiving the vaccine I felt something in my left arm that was different. I looked in the mirror and saw swelling above my clavicle at the base of my next going over to my shoulder. I went to see the doctor on Monday morning around 11AM to have his check this out. He advised me to wait a week or two see if the swelling would go down. Most of the swelling has come down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Limb discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Irbesartan 75mg QD; HCTZ 6mg QD; Crestor 3 days a week; Vitamin D3
- Allergien
- Sulfite Sensitivity
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Lip swelling
Symptomtext
After 1 hour patient called and said lip is swollen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- patient was observed at emergency room Doctor was concern maybe his blood pressure medication ,losartan can cause the same side effect
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- DIABETIC HYPERTENSION
- Andere Medikamente
- LOSARTAN POTASSIUM METFORMIN AMIODARONE
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye irritation
Vitreous floaters
Symptomtext
a floater in his left eye; has a floater in his left eye that is very irritating; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 73-year-old male patient received BNT162b2 (BNT162B2), on 11Apr2022 at 15:30 as dose 4 (booster), 0.3 ml single (Lot number: FJ9943, Expiration Date: 22May2022) at the age of 73 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Blood Pressure" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (Pfizer Covid vaccine Dose #1 on 20Feb2021. Caller does not have NDC, expiry or dose to provide. lot EL9267. Given in his left arm around 6am., Caller is asking if others have reported or is this a common experience after the vaccine. States he had nothing like this with his previous 3 shots.), administration date: 20Feb2021, when the patient was 72-year-old, for COVID-19 immunization; BNT162b2 (Pfizer Covid vaccine Dose #2 on 13Mar2021. Caller does not have NDC, expiry or dose to provide. lot EN6205. Given in his left arm around 6am., Caller is asking if others have reported or is this a common experience after the vaccine. States he had nothing like this with his previous 3 shots.), administration date: 13Mar2021, when the patient was 72-year-old, for COVID-19 immunization; BNT162b2 (Pfizer Covid vaccine booster #1 on 30Nov2021. Caller does not have NDC, expiry or dose to provide. lot FE3692. Given in his left arm about 10am., Caller is asking if others have reported or is this a common experience after the vaccine. States he had nothing like this with his previous 3 shots.), administration date: 30Nov2021, when the patient was 73-year-old, for COVID-19 immunization; Flu shots (States just a sore arm from the shot location with flu shots. Caller does not have name, NDC, lot, or expiry to provide.), reaction(s): "just a sore arm from the shot location". The following information was reported: VITREOUS FLOATERS (non-serious) with onset 11Apr2022, outcome "not recovered", described as "a floater in his left eye"; EYE IRRITATION (non-serious) with onset 11Apr2022, outcome "not recovered", described as "has a floater in his left eye that is very irritating". Therapeutic measures were taken as a result of vitreous floaters, eye irritation. Additional information: Caller stated he got the 4th dose, his booster of Pfizer yesterday and within 1 hour he experienced a vision side effect. Stated he has a floater in his left eye that was very irritating, very distracting and sort of like looking through a bug on the windshield and it moves around. Caller was asking if others have reported or was this a common experience after the vaccine. Stated he had nothing like this with his previous 3 shots. Vaccination Facility Type was Pharmacy/Drug Store. Vaccine was not Administered at Facility. Vaccination Facility Address: Facility Name was pharmacy. Caller stated he thought that might be it might go away after sleeping but it's still there. Stated he has tried general eye drops. Additional Vaccines Administered on Same Date of the Pfizer Suspect was none. Patient had no Vaccinations (within 4 weeks). There were no Relevant Tests.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye irritation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood cholesterol abnormal; Blood pressure abnormal
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Patient should have received the pediatric dose for 5-11 years old but patient was given the dose for 12+ years old.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 09.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Sensory loss
Symptomtext
Patient is feeling loss of sensation in bicep muscle. no tingling or pins and needles feeling. Not necessarily complete numbness but does not have the feeling in her arm like she thinks that she should. No treatment has been initiated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sensory loss
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism, GERD, IBS, epsiten barr virus reactivated after J&J (4/9/2021)
- Andere Medikamente
- trazodone, allegra, dexliant, klonopin amitiza, levothyroxine
- Allergien
- scallops levaquin
- Vorherige Impfungen
- After J&J vaccine patient fainted in the middle of a conversation. Epstein Barr reactivated
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Upper respiratory tract infection
Symptomtext
upper resitory infectionm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Upper respiratory tract infection
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 13.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Swelling
Symptomtext
Patient developed swelling without pain in left axilla after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swelling
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Hypertension hyperlipidemia erectile dysfunction
- Andere Medikamente
- amlodipine 5mg rosuvastatin 10mg clopidogrel 75mg tadalafil 10mg
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was given the Pfizer Covid-19 ADULT dose instead of the Pfizer Covid 19 PEDIATRIC (PEDS) dose. After 24 hours, no adverse reaction or side effects reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysgeusia
Glossodynia
Hypoaesthesia oral
Symptomtext
Patient stated she had numbness in the lips and a metallic taste in her mouth. She then stated that her tongue was stinging about 15 minutes later. She experienced NO swelling, hives, or shortness of breath. Patient was monitored for 45 minutes. Patient was encouraged to take some liquid benadryl which alleviated her symptoms. Patient stated that these symptoms resolved around 15 minutes after taking the liquid benadryl. Patient was encouraged to follow-up with PCP and to go to the ER if any new or worsening symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- COVID rash from initial Moderna vaccine. Received Pfizer booster with no issues besides metallic taste in mouth.
- Staat
- IN
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Patient received .2ML of the adult COVID-19 vaccine (grey cap)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Patient received .2ML of the adult COVID-19 vaccine (grey cap)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Symptomtext
Patient states that her hands began to turn beet red about 2 hours after the vaccination. She did not report any itching or pain, just a bright red color on both hands. The redness persisted for about 6 hours before it went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 02.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Dose is a second booster that was administered 8 days too soon 112 days after the third shot instead of 120 days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Flushing
Hot flush
Hyperhidrosis
Immediate post-injection reaction
Symptomtext
PATIENT REPORTS "HOT FLASH" SYMPTOMS (SWEATING, FLUSHING) BEGINNING IMMEDIATELY AFTER INJECTIONS THAT LASTS APPROXIMATELY 2 HOURS. PATIENT HAS EXPERIENCED THIS REACTION AFTER EACH OF HER 4 COVID VACCINATIONS (ALL PFIZER)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- -
- Andere Medikamente
- DICYCLOMINE, FAMOTIDINE
- Allergien
- NKDA
- Vorherige Impfungen
- HOT FLASH SYMPTOMS ; PFIZER COVID 19 ON 10/28/2021
- Staat
- OR
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Immunisation
Off label use
Poor quality product administered
Symptomtext
received a shot of the Pfizer-BioNTech Covid 19 Vaccine (gray cap) more than 12 hours after the first puncture of the vial; Off label use; Initially stated that the date was Aug2023. Later clarified that the date is fuzzy and looks like Aug2021.; Dose 4 Booster; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team for a Pfizer sponsored program (159558). A 55 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 29Mar2022 10:41 (Lot number: FJ9943, Expiration Date: Aug2021) at the age of 55 years as dose 4 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer, DOSE 1), for COVID-19 immunization; Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer, DOSE 2), for COVID-19 immunization; Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer, DOSE 3), for COVID-19 immunization. The following information was reported: POOR QUALITY PRODUCT ADMINISTERED (medically significant) with onset 29Mar2022, described as "received a shot of the Pfizer-BioNTech Covid 19 Vaccine (gray cap) more than 12 hours after the first puncture of the vial"; OFF LABEL USE (medically significant) with onset 29Mar2022, described as "Off label use"; EXPIRED PRODUCT ADMINISTERED (medically significant) with onset 29Mar2022, described as "Initially stated that the date was Aug2023. Later clarified that the date is fuzzy and looks like Aug2021."; IMMUNISATION (medically significant) with onset 29Mar2022, described as "Dose 4 Booster". Therapeutic measures were not taken as a result of poor quality product administered, off label use, expired product administered, immunisation. Clinical Course: Caller stated that a patient received a shot of the Pfizer-BioNTech Covid 19 Vaccine (gray cap) more than 12 hours after the first puncture of the vial. First puncture was yesterday March 28th 2022 at 12:58 pm and the patient received the shot today 29Mar2022 at 10:41 am. Regulatory authority Support CEP 159558 has a pharmacist has a Covid 19 vaccine (gray cap) that expired that they already administered to one of their patients. Stated that they will do a report with VAERS. Is her fourth dose since she is immunocompromised. Stated that she was immunocompromised prior to getting the vaccine. Patient details: Height, weight and ethnicity unknown. Stated that the vaccine was pharmacy prescribed. Product details: Stated that she cannot read the expiration date. Stated that she has the bottle. Initially stated that the date was Aug2023. Later clarified that the date is fuzzy and looks like Aug2021 No follow-up attempts are possible. No further information is expected; Sender's Comments: Based on the information provide and plausible temporal association, the causality between BNT162B2 and events cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
PATIENT RECEIVED A 2ND BOOSTER DOSE OF PFIZER COVID VACCINE WHEN SHE WANTED A 2ND DOSE OF SHINGRIX VACCINE. THERE WAS VERBAL MISCOMMUNICATION WITH THIS INCIDENT WHEN PERFORMING OUR 2ND CHECK TO VERIFY CORRECT VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetes
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Patient's mother stated her son was 12 years old and wanted to get the COVID-19 vaccine. Filled out the form; verified age with patient; administered the vaccine. When processing the form, rejected thru insurance because patient was under the age of 12. Pharmacy did not have vaccine for <12 years old. Administered wrong Pfizer vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Activated partial thromboplastin time
Blood urine present
Complement factor C3
Complement factor C4
Culture urine negative
Full blood count
Haematuria
International normalised ratio normal
Proteinuria
Prothrombin time abnormal
Renal function test
Ultrasound kidney
Urine analysis abnormal
Urine calcium
Urine protein/creatinine ratio
Symptomtext
Gross hematuria for 3 days after the 2nd and 3rd doses (1st and 2nd boosters). Hematuria was not observed after initial dose. Subject was worked for hematuria, complete blood works including Complement (C3 and C4), total protein/creatinine ratio, APTT, PROTIME-INR, renal function panel, urinanalysis, calcium/random urine, urine culture, and kidney ultrasound. No treatment given. Gross hematuria resolved within 3 days and proteinuria persisted for about 3 months before resolving. Same follow done after 2nd booster and proteinuria follow up is still pending.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Activated partial thromboplastin time
- Hospital-Tage
- -
- Labordaten
- The following tests were done 3/25/22: Urine culture: negative Calcium/random urine: normal Urinalysis: abnormal (positive for blood) Renal function panel: normal PROTIME-INR: slightly abnormal (12.2s) INR: normal (1.1) APTT: abnormal (29.2s) C4 complement: normal (28) C3 complement: normal (94) Total protein/creatinine ratio: abnormal (2.97g) Note: Same labs were done after the 1st booster w very similar results.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None, however, the same reaction reported here after the 3 dose (2nd booster) also occurred after the 2nd dose (1st booster) as well. 3 doses received were of Pfizer mRNA.
- Andere Medikamente
- Multi-vitamins daily and vitamin D3 (2000IU) twice weekly
- Allergien
- No known allergies to medications or foods. Known allergy to baby wipes around mouth
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Vaccine positive rechallenge
Symptomtext
Lower lip swelling. Vaers also filled out by Mom with first dose lip swelling. Refilled prednisone as had with previous reaction. Continue cetirizine and consider adding famotidine. Has EpiPen on hand for other allergies. Pt with hx of urticaria and family history of mast cell activation. Mom to let allergist know as well
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- urticaria
- Andere Medikamente
- -
- Allergien
- almonds, corn, peanuts, tree nuts
- Vorherige Impfungen
- previous covid shot. Mom reported
- Staat
- CT
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Symptomtext
Two inch long by one inch wide echymotic bruise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Contusion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ehlers Danlos syndrome hyper joint mobility
- Andere Medikamente
- Multiple vitamins, biotin, iron , vitamin d,
- Allergien
- Shrimp
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
pt received the third dose of Pfizer COVID that had expired. This vial was prepared more than 12 hrs prior to injection, and its window of stability haf already passed when pt received this vaccine. When contacted pt once this error was identified, she did not experience any side effect from the dose. Pt will come back to pharmacy to get re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
pt received her second dose of Pfizer COVID that was expired. This vial was prepared more than 12 hrs and its window of stability was already passed when pt received this vaccine. When contacted pt once this error was identified, she did not experience any side effect from the dose. Pt will come back to pharmacy to get re-vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia oral
Throat tightness
Symptomtext
pt had janseen for her first dose, and this is the first pfeizer shot she's gotten, she started getting numbness in her lips and throat started closing in a little.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia oral
- Hospital-Tage
- -
- Labordaten
- 911 was called they came and assessed her and we gave her bendaryl 50 mg
- Aktuelle Erkrankungen
- not sick
- Vorgeschichte
- no known health condition
- Andere Medikamente
- benadryl 50 mg
- Allergien
- nkda
- Vorherige Impfungen
- -
