- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 01.08.2023
- Impfdatum
- 05.06.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 213,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Myocardial ischaemia
Symptomtext
ACUTE NON ST ELEVATION MI DEMAND ISCHEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 19.05.2023
- Impfdatum
- 28.06.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Generalised anxiety disorder
Hypotension
Septic shock
Urinary tract infection
Symptomtext
HYPOTENSION 10/27/2022 GENERALIZED ANXIETY DISORDER HYPOTENSION 10/27/2022 SEPTIC SHOCK HYPOTENSION 10/27/2022 UTI (URINARY TRACT INFECTION)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Septic shock
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 24.12.2022
- Impfdatum
- 17.06.2022
- Beginn
- 18.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Erythema
Pain in extremity
Symptomtext
Sore red arm day of vaccine Death the next day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UTI
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lovastatin Synthroid Qysemia
- Allergien
- None
- Vorherige Impfungen
- Sore arm
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 03.06.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 186,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Computerised tomogram head normal
Condition aggravated
Cystitis
Hypotension
Intensive care
Mental status changes
Nitrite urine present
SARS-CoV-2 test positive
Septic shock
Urine analysis abnormal
Symptomtext
Discharge Provider: Primary Care Provider: MD Admission Date: 12/6/2022 Discharge Date: Dec 9, 2022 COVID positive Date: 12/6/2022 PRESENTING PROBLEM: Hypotension [I95.9] Acute cystitis without hematuria [N30.00] Septic shock (HCC) [A41.9, R65.21] COVID-19 [U07.1] COVID-19 virus detected [U07.1] HOSPITAL COURSE: Per icu transfer summary 72 yo female with PMH significant for Alzheimer's and vascular dementia (lives at home with husband), COPD. She presented to the ED 12/6 for altered mental status. Husband provided history and told ER that the AMS began 12/6. CTH NEG, UA + nitrates, given Cefepime x1. Hypotensive despite 2L, was started on NE and admitted to ICU. 12/8 12/8 Hemodynamically stable to transfer out of the ICU On the general medical floor, patient was reportedly at baseline and was medically stable for discharge. Her symptoms were likely related to COVID infection and were expected to improve with conservative management in time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Septic shock
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD (chronic obstructive pulmonary disease) (HCC) Varicose veins of legs Mixed Alzheimer's and vascular dementia (HCC Hypotension Protein-calorie malnutrition, unspecified severity (HCC) Post menopausal problems; on HRT Panic; episodic bouts Current tobacco use Altered mental status
- Andere Medikamente
- DULoxetine (CYMBALTA) 30 MG delayed release capsuleDULoxetine; DULoxetine (CYMBALTA) 60 MG delayed release capsule estradiol (ESTRACE) 0.5 MG tablet galantamine (RAZADYNE ER) 16 MG 24 hr capsule LORazepam (ATIVAN) 1 MG tablet memantine ER (
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 13.07.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- 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
Intensive care
SARS-CoV-2 test positive
Symptomtext
Patient received Pfizer COVID vaccine on 2/23/21 (lot # EL3302), 3/16/21 (lot # EN6200), 8/18/21 (lot # FC3182), and 7/13/22 (lot # FM0173). Patient tested positive for COVID on 7/29/22 and 8/4/22. On 8/4/22, patient admitted with acute respiratory failure with hypoxia and COVID pneumonia. Patient was intubated on 8/7/22. As of today (8/9/22), patient is still intubated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 5,0
- Labordaten
- COVID status positive 7/29/22 and 8/4/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- with RA on cellcept/rinvoq, COPD, NIDDM2, CAD with 3 stents on plavix, HLD, HTN, hypothyroidism, OSA on cpap
- Andere Medikamente
- acetaminophen, amlodipine, vitamin c, bystolic, calcium/vitamin d3, cetirizine, clarithromycin, clopidogrel, ezetimibe, fenofibrate, folic acid, mvi, furosemide, levothyroxine, lisinopril, lorazepam, metformin, mometasone nasal sp, mycophen
- Allergien
- adhesive tape/silicones, carvedilol, cortisone, erythromycin, lincomycin, metoprolol, nitroglycerin, olmesartan, oxycodone, phosphorated carbohydrate, hydroxychloroquine, statins, streptomycin, sulfa, sulfamethoxazole/trimethoprim, isosorbide mononitrate
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 30.07.2022
- Impfdatum
- 30.06.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 16,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute myocardial infarction
Laboratory test
Symptomtext
STEMI heart attack; This is a spontaneous report received from contactable reporter (Consumer or other non HCP). A 68-year-old male patient received BNT162b2 (BNT162B2), on 30Jun2022 at 14:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 68 years, in left arm for covid-19 immunisation; atorvastatin calcium (LIPITOR), (Batch/Lot number: unknown) at low dose. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (1st vaccine 27Dec2020 Lot - unknown. Injected in left arm.), administration date: 27Dec2020, when the patient was 66-year-old, for Covid-19 immunization, reaction(s): "Covid-19"; BNT162b2 (2nd vaccine given on 20Jan2021, Lot EL9262, or EL9161 Expiration is unknown. Injected Left arm. ), administration date: 20Jan2021, when the patient was 66-year-old, for Covid-19 immunization, reaction(s): "Covid-19"; BNT162b2 (3rd dose , 1st booster, given on 09Oct2021 Lot FF8839 expiration of 31Dec2021, injected in left arm.), administration date: 09Oct2021, when the patient was 67-year-old, for Covid-19 immunization, reaction(s): "Covid-19". The following information was reported: ACUTE MYOCARDIAL INFARCTION (hospitalization) with onset 16Jul2022, outcome "recovered with sequelae", described as "STEMI heart attack". The patient was hospitalized for acute myocardial infarction (start date: 16Jul2022). The event "stemi heart attack" required emergency room visit. The patient underwent the following laboratory tests and procedures: Lab Test: (Apr2022) Normal. The action taken for atorvastatin calcium was unknown. Additional information: On 16Jul2022, he had a STEMI heart attack. He survived that. He had a complete blockage of LAD and has no prior history of heart disease. He survived because his collateral arteries were so good. He had no sign of heart disease. Is not hypertensive, and is on a low dose of Lipitor. Outcome: Recovered with lasting effects and it is somewhat unknown. An item of both. He was working for his former employer and this occurred on an airplane and he is pulmonary critical care. It depends on his heart remodels and his Ejection fraction and he is compromised. Procedure was that he had a stent placed in his LAD and it was on 16Jul2022. Reason why reporting is they had friend who was a gastroenterologist who had a cardiac event after receiving the COVID vaccine. She does not know if he reported. Neither one of them had any heart issues. He said that should not have happened to me. She did not wish to complete report for him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- Test Date: 202204; Test Name: Lab Test; Result Unstructured Data: Test Result:Normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 11.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Consciousness fluctuating
Dyspnoea
Loss of consciousness
Pulse absent
Respiratory arrest
Resuscitation
Symptomtext
Pt presented to clinic for 3rd dose of Covid vaccine. After pt received the vaccine, she left the room and went to the front desk to talk to the PCT. She talked to the PCT for approx. 1-2 minutes and the PCT notified this NP that the Patient was saying she was Short of breath. I went to the front desk and the patient was in and out of consciousness. This NP, eased patient to the floor once patient went unconscious. This Np, examined pt for pulse using stethoscope and pulse oximeter, with no pulse noted or breathing. Next, I started CPR and told the PCT to call 911. I continued to perform high quality CPR for 2-3 minutes and the patient regained Consciousness almost simultaneous as the police and fire department arrived. Pt was alert, oriented, and talking with the police and her father arrived to the store. The patient was confirmed to be breathing and noted to have a regular pulse prior to her being placed on a stretcher by the fire and police department.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory arrest
- Hospital-Tage
- -
- Labordaten
- Covid vaccine given 07/11/2022 at 5:28 p.m.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.09.2023
- Impfdatum
- 15.06.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 108,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram
Myocarditis
Symptomtext
Myocarditis; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 51-year-old female patient received bnt162b2 (BNT162B2), on 15Jun2022 as dose 2, single (Lot number: FM0173) at the age of 50 years for COVID-19 immunisation. The patient's relevant medical history included: "High Blood Pressure" (unspecified if ongoing), notes: she has had it for years. There were no concomitant medications. Vaccination history included: bnt162b2 (First Dose: 25May2022 Lot: FJ4989), administration date: 25May2022, when the patient was 50-year-old, for COVID-19 Immunization. The following information was reported: MYOCARDITIS (hospitalization) with onset Oct2022, outcome "not recovered". The patient was hospitalized for myocarditis (start date: Oct2022, discharge date: Oct2022). The patient underwent the following laboratory tests and procedures: Computerised tomogram: Unknown results; Unknown results. Therapeutic measures were taken as a result of myocarditis. Additional information: The reporter stated she developed, after she took the vaccine, myocarditis and was hospitalized. She got the vaccine in Jun2022, and shortly after that, she started having pains in her chest so then she thought she will watch it because sometimes maybe it is just pleuritic chest pain but then it kept going on and on and when she was walking outside, she would get short of breath with anything physical and she would be out of breath. She stated she couldn't understand how that would happen. One time she came to work, and it got harder to physically do stuff and then in Oct2022 she decided she was going to the ER (emergency room). She stated one Friday it got so bad, she said she was going to the hospital, so she went to the ER, and she got admitted and diagnosed with Myocarditis. She was hospitalized for 8 days. She also stated it hasn't resolved; it is ongoing. She was going about her business and going to work and coming home. She doesn't have a lot of activities and shopping and partying and all that stuff, she just goes to work and comes home. This year, in May2023, she ended up back in the hospital because of the same problems all over again. She went to the ER and it was the same thing again and she was admitted for 6 days in May2023. Even now she was having the same problems. It is persistent, she was just watching it. She is at work and at this point she has used up so much of her sick time, if she doesn't work, she won't get paid, she had to be watching it to see how long she can bear this. Treatment plan for the patient included hospitalization. They gave her a CAT scan and CT scan with dye, antibiotics, anti-Inflammatory in her IV (intravenous) line, pills, and they gave her medication in her IV. The reporter stated that the tests that they did at the hospital were done to come up with her diagnosis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Test Name: CAT scan; Result Unstructured Data: Test Result:Unknown results; Test Name: CT scan with dye; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (she has had it for years.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 01.08.2023
- Impfdatum
- 08.06.2022
- Beginn
- 07.01.2023
- Tage bis Beginn
- 213,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Symptomtext
ACUTE DVT OF BILAT LEGS, UNSPECIFIED VEINS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.07.2023
- Impfdatum
- 20.04.2020
- Beginn
- 20.04.2020
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Ageusia
Angina pectoris
Asthenia
Atrial fibrillation
Balance disorder
Computerised tomogram
Electrocardiogram
Electromyogram
Epistaxis
Eye pain
Fall
Gait disturbance
Guillain-Barre syndrome
Haemoptysis
Headache
Hypoaesthesia
Insomnia
Joint range of motion decreased
Symptomtext
Arm swollen pain, arm motion range couldn't lift arm, heart palpation nosebleed, spit up blood clotes fallen neuropathy, cane, thrombocytopenia, nerves attacted (AFib) heart pain musle loss Gullain Bar Syndrome Patient given Pfizer shot 4/2020. Patient began 1 1/2 hour later arm swollen legs num/needle pins in feet and legs. Coughing up bloot clots, lost muscle mas, weakness lost balance to walk, headaches, nauseous at stomach couldn't sleep heart paltation! Nosebleeds, arm range motion lost! Nerves attacted. Muscle mass lost, weight gain Brain to go blood clots in legs. Long Covid. Taste gone. Shots 4/16/21 Eye Sight low Pfizer Lot ER8732 5/07/21 Pfizer Lot EW0179 01/18/22 Pfizer Lot FD7218 7/04/22 PFR-BNT 30mcg/0.3mL Lot FM0173 11/15/22 Pfizer Bivalent 30mcg/0.3mL Lot GJ3277 Uptic Neuritis-Pain in eyes. I have Thrombocytopenia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- MRI 04/20/2023 EKG EMG, Ct
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Long Covid reaction to vaccine
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 02.08.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 105,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebellar stroke
Symptomtext
ACUTE STROKE OF CEREBELLUM, UNSPECIFIED TYPE AND ARTERY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebellar stroke
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 05.09.2022
- Impfdatum
- 23.06.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac monitoring
Electrocardiogram
Fatigue
Headache
Hypotension
Laboratory test
Syncope
Thirst
Vibratory sense increased
Symptomtext
Fatigue and headache Internal vibrations Syncope Extreme thirst Low blood pressure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Hospital ER 7/12/22 -several tests; 7/19/22 - BP 8/4/22 - consult 8/11/22 - EKG, Heart monitor Scheduled for Upstate Neurology 9/22/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.09.2022
- Impfdatum
- 11.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Back pain
Blood test
Fatigue
Feeling abnormal
C-reactive protein
Groin pain
Guillain-Barre syndrome
Magnetic resonance imaging
Muscle spasms
Musculoskeletal disorder
Pain
Hypersomnia
Inflammation
Mobility decreased
Memory impairment
Metabolic function test
Neuralgia
Symptomtext
CAN NOT LIFT LEGS, FATIGUE, PAIN, BRAIN FOG, MUSCLE SPASMS THROUGHOUT BODY, STARTED ONE WEEK AFTER RECEIVING 2ND BOOSTER PFIZER VACCINE. PT RECEIVED VACCINES PREVIOUSLY AND NO PREVIOUS ADRs REPORTED. CURRENTLY ON TREATMENT WITH HCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- ARMOUR THYROID 60 MG TABS PO ONCE DAILY
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.09.2022
- Impfdatum
- 11.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Back pain
Blood test
Fatigue
Feeling abnormal
C-reactive protein
Groin pain
Guillain-Barre syndrome
Magnetic resonance imaging
Muscle spasms
Musculoskeletal disorder
Pain
Hypersomnia
Inflammation
Mobility decreased
Memory impairment
Metabolic function test
Neuralgia
Symptomtext
CAN NOT LIFT LEGS, FATIGUE, PAIN, BRAIN FOG, MUSCLE SPASMS THROUGHOUT BODY, STARTED ONE WEEK AFTER RECEIVING 2ND BOOSTER PFIZER VACCINE. PT RECEIVED VACCINES PREVIOUSLY AND NO PREVIOUS ADRs REPORTED. CURRENTLY ON TREATMENT WITH HCP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- ARMOUR THYROID 60 MG TABS PO ONCE DAILY
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 9,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Computerised tomogram thorax abnormal
Condition aggravated
Cough
Deep vein thrombosis
Dyspnoea
Echocardiogram
Limb discomfort
Pain in extremity
Peripheral swelling
Pulmonary thrombosis
Ultrasound Doppler abnormal
Symptomtext
Leg pain in left leg began 08/17/2022 when kneeling, leg discomfort continued through 08/18/2022, sudden shortness of breath on 08/19/2022, diagnosed with blood clot in each lung and three DVTs in left leg, hospitalized overnight 08/19/2022-08/20/2022, Eliquis prescribed at time of discharge on 08/20/2022, shortness of breath and cough continue, as well as swelling in feet and lower legs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- 1,0
- Labordaten
- CT scan of lungs, ultrasound scans of legs, and echocardiogram.
- Aktuelle Erkrankungen
- Tension headaches, colonoscopy performed 07/11/2022 but no biopsies
- Vorgeschichte
- Mild mitral valve prolapse, migraine headaches and tension headaches, hypothyroidism, diverticulosis, two prior peripheral clots in right ankle (not DVT) more than 14 years ago, enlarged liver (cause unknown), mild sleep apnea, occasional positional dizziness
- Andere Medikamente
- Levothyroxin, furosemide, multi-vitamins, folate, calcium, vitamin d, vitamin e, melatonin, low dose aspirin, mometasone ointment
- Allergien
- Coconut
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 09.07.2022
- Beginn
- 11.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Ear discomfort
Electric shock sensation
Gingival pain
Headache
Maxillofacial pain
Nausea
Neck pain
Pain
Temperature intolerance
Thirst
Symptomtext
Electrical shocks and buzzing sensation in lower arms and legs- severe at onset, now mild. Lightheaded, heat intolerance, nausea, pain in maxilla and gums, ear fullness, excessive thirst, neck pain, and moderate to severe headache, all of which still persist. Pain treated with stretching, meditation, hot baths, ice, lidocaine gel to gums, hydration, OTC meds and supplements without great result. Headache has improved after a visit to the urgent care where a shot of toradol was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- erythromycin
- Vorherige Impfungen
- moderate arm swelling after a flu vaccine (brand name unk) 10 years ago
- Staat
- AZ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 05.07.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypotension
Loss of consciousness
Syncope
Symptomtext
Patient fainted when received vaccine. She was unconscious for about a minute. We placed patient on the floor and patient parent lifted patient legs. We called EMS and they were there within 5 minutes. They evaluated her and suggested to the parent that she either speak with her primary care immediately or go to the ER since her blood pressure was low. Patient parent decided to just go home and contact her primary care after the evaluation. Patient left about 45minutes after receiving the vaccine. Called to follow up with patient tonight, however no answer on the phone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- HPV - dizzy/faint
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 19.06.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Seizure like phenomena
Syncope
Symptomtext
Patient fainted & experienced seizure-like activity shortly after receiving vaccine. Event lasted approx 30 seconds. She was moved from sitting to laying on floor w/feet, elevated & began responding normally. 911 was called & EMT took her to ER. BP & P were WNL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Confusional state
Decreased appetite
Dizziness
Fall
Fatigue
Headache
Hyperhidrosis
Loss of consciousness
Malaise
Nausea
Palpitations
Retching
Vomiting
Symptomtext
Palpitations began at 9 pm after vaccination, i.e. approximately 9 hours later. About 1 am, severe nausea onset. Got up to go to the bathroom to vomit. After dry heaves, sat on toilet lid. Called out to husband was going to faint. Lost consciousness and fell. Returned to consciousness in less than 1 minute on the floor, some confusion lasting about 1 minute. Returned to bed with chills and sweating lasting into the next day until about 2 pm. Vomited at 9 am that same day. Dizziness persisting from onset the first evening until present time, 6/16 (4 days post-vaccination), worse when recumbent. Fatigue and headache also persistant from first night post vaccination to current. Loss of appetite, malaise from 1 day post vaccination to current.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Estradiol cream
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Deep vein thrombosis
Peripheral swelling
Ultrasound scan
Symptomtext
Leg swell Acute 6 - 05 - 2022 DVT Dx 6 - 06 - 2022 Traveled to state college for sports tournament. No other sick contacts Noticed DVT 6 - 5 - 22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Ultrasound , Blood test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling hot
Loss of consciousness
Nervousness
Syncope
Symptomtext
Pt was fine during vaccination. instructed pt to wait in waiting room for 15 min for observation. Within about 5 minutes pt had passed out. Another pt in the waiting room alerted us to it. I went out and pt came alert very quickly. I asked how he was feeling. He said shaky and a bit warm. I called 911 and also asked advice from Clinic. We put his feet up and gave him water. Pt was more alert and talkative. He then said it did happen once before as well. It appears pt had a vasovagal syncope. The fire dept came and checked him out. Mom and Dad came and took him home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None known of.
- Allergien
- None known of
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Feeling abnormal
Loss of consciousness
Vomiting
Symptomtext
Administered Covid 19 vaccine to patient informed mother to have a seat and wait 15 minutes as a precaution. After a few minutes gets my attention and states her daughter is not feeling good I went outside of the pharmacy and noticed patient looking dazed asked patient how she is feeling she said she felt dizzy I asked if she had any shortness of breath and she said no and lost consciousness for less than a minute asked her again if she was having any trouble breathing she said no then called 911. Before paramedics arrived patient vomited. Paramedics arrived and left with child and mother
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 15.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 12.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Agonal respiration
Amnesia
Cold sweat
Dizziness
Fatigue
Blood pressure decreased
Pulse absent
Resuscitation
Feeling abnormal
Hyperhidrosis
Hypotension
Irregular breathing
Loss of consciousness
Somnolence
Syncope
Symptomtext
My blood pressure began dropping about five minutes after the vaccination. Blood pressure was 100/68. The NP said my breathing was agonal. They could not find a pulse. they performed chest compressions for about 30 seconds. I remained lying on the floor for about 5 to 10 minutes before EMS came. Blood pressure was reassessed at that time and was 130/70. I have an appointment with a cardiologist on Tuesday, May 17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bipolar, M?ni?re?s disease
- Andere Medikamente
- Lamotrigine, Lorazepam, Sertraline, Gabapentin, Brimonidine Tartrate
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 08.11.2023
- Impfdatum
- 28.05.2022
- Beginn
- 06.06.2023
- Tage bis Beginn
- 374,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Atrial fibrillation
COVID-19
COVID-19 pneumonia
Condition aggravated
Cough
Febrile neutropenia
Left atrial appendage closure implant
Malaise
SARS-CoV-2 test positive
Symptomtext
Primary Care Physician at Discharge: MD Hematologist/Oncologist: Dr. Admission Date: 6/6/2023 Discharge Date: 06/10/2023 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Neutropenic fever [D70.9, R50.81] Pneumonia due to COVID-19 virus [U07.1, J12.82] DISCHARGE PROBLEM: COVID 19 Pneumonia CLL AFIB Warm autoimmune hemolytic anemia Left atrial appendage device closure PRESENTING COURSE: Patient is a 70 y.o. patient with a past medical history significant for warm hemolytic anemia, afib, chronic BLE swelling, and CLL currently on treatment with Gazyva and Venetoclax who presented to Health ED for symptoms of fever x 1 week and cough x 2 weeks. The patient started to not feel well on 5/20. He took a home Covid test and was positive on 5/23. HOSPITAL COURSE: Patient was admitted and started on IV Remdesivir in which he completed 5 days. He did require supplemental oxygen and was set up for home oxygen as well. He continued to improve and felt well enough to discharge home today with plans to complete 5 days of Paxlovid and 10 days of dexamethasone. He will hold his Venclexta while taking Paxlovid and will discuss restarting at follow up. He was educated on when to call with questions or concerns. He is stable and ready for discharge
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Primary hypertension Paroxysmal atrial fibrillation H/O bleeding disorder Chronic anticoagulation CLL (chronic lymphocytic leukemia) Pneumonia due to COVID-19 virus Acute hypoxemic respiratory failure Disorder of lung parenchyma
- Andere Medikamente
- acyclovir (ZOVIRAX) 400 mg tablet allopurinol (ZYLOPRIM) 300 MG tablet amLODIPine (NORVASC) 5 MG tablet aspirin 81 mg chewable tablet CALCIUM PO clopidogrel (PLAVIX) 75 mg tablet folic acid (FOLVITE) 1 MG tablet Magnesium 250 MG tablet pant
- Allergien
- NaproxenOther
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 31.07.2023
- Impfdatum
- 21.06.2022
- Beginn
- 28.01.2023
- Tage bis Beginn
- 221,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 13.07.2023
- Impfdatum
- 06.07.2022
- Beginn
- 13.04.2023
- Tage bis Beginn
- 281,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute sinusitis
Asthenia
Blood gases abnormal
Blood lactic acid
Blood pH increased
COVID-19
Chest X-ray normal
Cognitive disorder
Computerised tomogram head abnormal
Dysstasia
Electrocardiogram abnormal
Encephalopathy
Fall
Full blood count
Laboratory test
Lipase
Liver function test
Mental status changes
Symptomtext
Clinical Summary Patient is a 80 y.o. female with a history of Alzheimer's disease, hypertension and glaucoma who presented to hospital 4/13/2023 with fever and altered mental status. Patient found to have COVID 19, labs with BMP, CBC, BMP, HFP, lipase unrevealing. LA 1.1, UA without infection. Admit VBG with pH 7.4, pCO2 and pO2 stable. CXR non-acute. CT head with no acute intracranial findings, noted acute pansinusitis. 1. COVID 19 Infection: Presented as above. Vaccinated and boosted, denies prior COVID infections. Symptom onset 4/12/23. Admit CXR non-acute. Not requiring O2 on admit, therefore defer decadron or remdesivir. Consult to ID and started and completed course of paxlovid. Symptoms improved. 2. Sepsis: Met criteria with Temp 100.8, tachycardia on presentation. Secondary to COVID as above. CXR and UA without infection. CT head with pansinusitis. Procal negative. On Vanc/Zosyn in ED, held on further antibiotics on admit as suspect viral etiology or sepsis criteria with COVID. Given 1.5 L bolus in ED. Now dry lung strategy with COVID. Treat as discussed and monitor. 3. Acute Metabolic Encephalopathy on Chronic Dementia: Family describes 3-4 month cognitive and functional decline with history of Alzheimers dementia. Per family, prior baseline was alert and oriented with short term memory deficits. Recent baseline waxes and wanes, minimal short term memory. Family feels patient is at recent baseline on admit. Oriented to self, general location, month, year and family on admit. Continued home Remeron. Delirium precautions. 4. Oral thrush: Noted 4/15/23. Nystatin swish and spit continued. 5. Elevated Troponin: Admit Trop 19, second trop 17. Admit EKG with sinus tachycardia, no acute ischemic changes. No chest pain on admit. Suspect demand ischemia with above. No other ischemic eval planned. 6. Acute sinusitis: Diagnosed on admission. Completed Augmentin course 4/18/23. 7. Fall: Secondary to weakness at home. Unable to get off toilet and assisted to ground by family. Denied injuries or hitting head. PT/OT consulted, family interested in SNF on discharge. 8. Hypertension: Per history, continued home Cozaar with hold parameters. Monitor and titrate PRN. 9. Glaucoma: Per history, continued home eye drops.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 14.06.2023
- Impfdatum
- 09.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 12,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Amenorrhoea
Anxiety
Condition aggravated
Diarrhoea
Dysmenorrhoea
Dyspnoea
Feeling hot
Headache
Heavy menstrual bleeding
Nausea
Pain
Palpitations
Panic attack
Pyrexia
Symptomtext
Hair loss, frequent headaches, body aches, went from regular periods to no periods for 5 months and then extremely painful and heavy menstrual periods lasting anywhere from 3 weeks to 7.5 weeks, Felt internally hot to where I had to lay with ices packs all over my body just to get some relief, shortness of breath, Heart palpitations, increased anxiety and panic attacks, random fevers no higher than 102), Nausea, diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Major Depressive Disorder, Anxiety/Panic Disorder, PCOS
- Andere Medikamente
- Omeprazole 40mg Delayed release 1x daily, Alprazolam 0.25mg 3x daily prn
- Allergien
- Nickel
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 24.05.2023
- Impfdatum
- 17.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Alopecia
Autoimmune disorder
Ear pain
Head discomfort
Hypertension
Inflammation
Lichen planopilaris
Pain of skin
Tinnitus
Trigeminal neuralgia
Symptomtext
5/20/22 I started hearing crackling in my ear. Suddenly, I felt like my head was going to explode. It felt like I had firecrackers going off in my left ear. It hurt a lot. It finally subsided. Later that day, I went to urgent care. My blood pressure was very high. I was treated for a trigeminal neuralgia episode. I was given an anti-inflammatory shot. I went to a Neurologist who sent me to an Endodontist and checked my teeth and said nothing was going on with my teeth. I went to see my PCP and she said she thought it was a reaction to my vaccine three days earlier. This never happened again. In November, I started having issues with pain when you touched my skin. My scalp also began hurting when I would wash my hair. At the end of November, I went to the Dermatologist and was told I had an inflamed scalp, and my hair was falling out. I told him it also hurt to touch the inside of my ear. I felt like this was all related. I was treated for Lichen Planopilaris with doxycycline for two months and cortisone shampoo. Both auto immune diseases seem to have resolved. My hair is coming back in. It seemed very odd to me, that in 7 months I was diagnosed with two super rare immune auto diseases which have both resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Calcium; vitamin D; turmeric; CLARITIN
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 18.05.2023
- Impfdatum
- 01.11.2022
- Beginn
- 04.03.2023
- Tage bis Beginn
- 123,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Cough
Loss of personal independence in daily activities
Malaise
Mobility decreased
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
woke up on last day of a 7 night cruise with a sore throat. Drove home for 2 days with running nose and coughing. Treated with over the counter medicine and finally called the doctor on 6 after not getting any better. He told me to continue what I was doing as it was too late to treat for COVID. After another day or two went to a walk in clinic. Received a shot, and perscription for a steroid and cough medicine. Continued to take my medicine but was still sick with horrible cough and bad congestion. Was in bed about 2 1/2 weeks not able to do anything. After I was able to be up I continued to have no energy for about 2 months. I now feel back to normal and able to do the things I enjoy. I am NEVER sick and I think that is the reason it hit me so hard.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- at home covid test on March 6, 2023 - tested positive Went to walk in clinic and took another Covid test on March 10, 2023 - tested positive
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High blood pressure controlled with medicine High cholesterol controlled with medicine High pressure in eyes controlled with medicine
- Andere Medikamente
- Bupropion HCL XL 300 mg Lisinopril 40 mg tablet Estradiol 2 mg tablet Latanoprost 0.005% eye drops Atorvastatin 20 mg tablet Multi vitamin Calcium twice daily 800mg/800 vitamin D3 Glucosamine chondroitin 1500/1200 stool softener zinc 50 mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 06.07.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 93,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Brain fog
COVID-19
Computerised tomogram abnormal
Dyspnoea
Fatigue
Feeling abnormal
Malaise
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Scar
Symptomtext
In October 2022, after vacation, I began to feel bad on the plane home. I tested negative on October 7, 2022. I had a sore throat and body aches. At 3:00am I woke up with a 103 fever. I tested positive for COVID-19. I went to the clinic. Day two I had body aches and felt feverish. I was sick for about 8 days. My CT scan last month and I have scarring due to the COVID-19. My brain fog lasted until the end of December and remained short of breath and tired.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19, positive, 10082022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- COPD; Arthritis
- Andere Medikamente
- Vitamin E; Vitamin D3; Multi Vitamin; Flonase; Ibuprofen; Tylenol
- Allergien
- Tetracycline; Doxycycline
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 22.09.2022
- Beginn
- 15.03.2023
- Tage bis Beginn
- 174,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chronic obstructive pulmonary disease
Computerised tomogram
Illness
Investigation
Lung disorder
Pain in extremity
Pneumonia
Respiratory failure
X-ray
Symptomtext
First hospitalization 27Oct, I was respiratory failure with Pneumonia; I was hospitalized at the end of October with November, I am with Pneumonia for 6 days; Just recently hospitalized again with pneumonia is full-blown lung disease for 8 days since past week; second hospitalization. Reason of hospitalization: Pneumonia with Respiratory failure; full-blown lung disease; All of sudden now I have COPD; diagnosed with COPD and I never been sick a day in my life; second shot, I got sick; administered at the Right arm. Two weeks of pain, throbbing pain.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old female patient received BNT162b2 (BNT162B2), on 22Sep2022 as dose 2, single (Lot number: FM0173) at the age of 58 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "thyroid disease" (unspecified if ongoing). Concomitant medication(s) included: CALCIUM;VITAMIN D NOS oral taken for thyroid disorder. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: FM0773, in right arm), administration date: 01Sep2022, when the patient was 58-year-old, for COVID-19 immunization, reaction(s): "the first one go like my arm was going to fall off for 2 week the pain was unbelievable". The following information was reported: PNEUMONIA (hospitalization, medically significant) with onset 2022, outcome "unknown", described as "I was hospitalized at the end of October with November, I am with Pneumonia for 6 days"; PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "unknown", described as "administered at the Right arm. Two weeks of pain, throbbing pain."; ILLNESS (non-serious) with onset 2022, outcome "unknown", described as "second shot, I got sick"; PNEUMONIA (hospitalization, medically significant) with onset 15Mar2023, outcome "unknown", described as "Just recently hospitalized again with pneumonia is full-blown lung disease for 8 days since past week"; RESPIRATORY FAILURE (hospitalization, medically significant) with onset 15Mar2023, outcome "unknown", described as "second hospitalization. Reason of hospitalization: Pneumonia with Respiratory failure"; RESPIRATORY FAILURE (hospitalization, medically significant), outcome "unknown", described as "First hospitalization 27Oct, I was respiratory failure with Pneumonia"; LUNG DISORDER (non-serious), outcome "unknown", described as "full-blown lung disease"; CHRONIC OBSTRUCTIVE PULMONARY DISEASE (non-serious), outcome "unknown", described as "All of sudden now I have COPD; diagnosed with COPD and I never been sick a day in my life". The patient was hospitalized for pneumonia, respiratory failure (start date: 27Oct2022, discharge date: 03Nov2022, hospitalization duration: 8 day(s)); for pneumonia, respiratory failure (start date: 15Mar2023, discharge date: 24Mar2023, hospitalization duration: 10 day(s)). The patient underwent the following laboratory tests and procedures: Computerised tomogram: Unknown results; blood work: Unknown results; X-ray: Unknown results. Therapeutic measures were taken as a result of pneumonia, respiratory failure, pneumonia, respiratory failure, lung disorder, chronic obstructive pulmonary disease, illness, pain in extremity. The patient was treated in hospital with Rocephin, Doxycycline, Ceftin and Prednisone 120mg steroids, Nebulizer treatment, Albuterol and inhalers, and she was still on medication.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300135401 same reporter/patient/product, different dose/AE;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 8,0
- Labordaten
- Test Name: CAT scans; Result Unstructured Data: Test Result:Unknown results; Test Name: blood work; Result Unstructured Data: Test Result:Unknown results; Test Name: Xray; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Thyroid disorder
- Andere Medikamente
- CALCIUM;VITAMIN D NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 19.04.2021
- Beginn
- 27.09.2022
- Tage bis Beginn
- 526,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Fatigue
Pyrexia
SARS-CoV-2 test positive
Cough
Dyspnoea
Full blood count
Symptomtext
94y.o. male with a past medical history of AML with last round of chemo the day before admission, hypertension, hypercholesterolemia, and OSA. He presented to the emergency room with cough, difficulty breathing, and fever. Fever was noted during chemotherapy session. He was noted to be COVID-19 positive He was on Nc oxygen and able to be weaned. He was ofllowed by ID and had 5 days of remdesivir with clinical improvement On discharged he Continued acyclovir, cipro and diflucan He was followed by oncology for his history of AML and cbc was monitored He had CKD3 and we Monitored renal function. He was ambulatory and improved to room air Leukopeni improved and after discussing with ID , we felt stable for discharge home with a short course of steroids
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 6,0
- Labordaten
- 9/27 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 16.06.2022
- Beginn
- 18.09.2022
- Tage bis Beginn
- 94,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 pneumonia
Respiratory failure
Symptomtext
Hospitalization for acute hypercapni/hypoxic respiratory failure and COVID-19 pneumonia on dates 9/18/22- 9/30/22. Treated with dexamethasone, baricitinib, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- morphine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 20.06.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 124,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Alanine aminotransferase increased
Anion gap
Aspartate aminotransferase increased
Blood albumin decreased
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium decreased
Blood chloride normal
Blood creatine phosphokinase increased
Blood creatinine normal
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood thyroid stimulating hormone decreased
Blood urea normal
COVID-19
Chest X-ray abnormal
Computerised tomogram head normal
Symptomtext
COVID+ 10/22/22 Vaccination status - Pfizer x4 BRIEF OVERVIEW: Admission Date: 10/22/2022 Discharge Date: 10/23/2022 DETAILS OF HOSPITAL STAY: Clinical Narrative: Admitted after a fall and dehydration/mild rhabdomyolysis. Myoglobinuria. Did well with hydration. Renal functions stable. Incidental note of mild cough. Covid positive. See below discussion. Preferred home based care. See discussion. Home today. Please see the following problem-list oriented Hospital Course below: * Rhabdomyolysis Assessment & Plan Likely secondary to his fall and being down to the evening and early morning hours. He is also on a statin which will be held. Will hydrate. Recheck CK in a.m. CK a bit higher, as expected, but renal function normal and low enough that the Rhabdo will not be likely to impact renal function. Renal function stable. Push fluids at home. Stop Statin. The patient and his wife feel that the Statin has actually been contributing to his muscular discomfort (prior to the fall) and they will take a holiday from taking it. Type 2 diabetes mellitus with hyperglycemia Assessment & Plan Denies recent hypoglycemia. Was placed on a basal bolus regimen with glipizide on hold until further trends are available. A1C 7.2 Remained on bolus insulin back-up given the D5 solution. One time use. Improved off of the solution. Hypothyroidism Assessment & Plan Reports multiple recent adjustments in his thyroid. TSH was slightly low today though his free thyroxine level is 1.1. Recheck in 6 weeks. Dysphagia Assessment & Plan See above. Resolved, per patient report. No s/s during his time on the unit. Oropharyngeal cancer Assessment & Plan States he finished radiation therapy and chemotherapy summer of 2021. He does have a dry mouth and throat is result. He does have a history of dysphagia as well but states this had improved to the point were no other dietary consistency adjustments were required. He denies dysphagia to solids and liquids at present. It is somewhat unclear why he has been falling forward. His neurological exam seems relatively benign but will obtain CT head in a.m. 10/23 - CT head stable. F/u with PCP/Oncology. No evidence of recurrence. COVID-19 Assessment & Plan Mild cough of several days duration. Wife was enquiring about Paxlovid. This is a possibility. Will also check a film array. Chest x-ray clear. Recheck chest x-ray in a.m.. MDI as he has used this in the past. We did discuss the outpatient process for obtaining Paxlovid and will attempt to assist with this should it be needed and should the patient be discharged tomorrow. 10/23 - Discussed Paxlovid with Pharmacist. Discussed indications and dosing. Cr Cl > 65, recent symptoms onset, meets criteria. CXR with possible mild bibasilar infiltrates. O2 needs normal. Will discuss options with patient. He is at risk of other atypical infections. Film array pending. Add Azithromycin or Doxy. Discussed with patient and wife in detail. Functional status back to normal. States he "can do this at home". Remarkably few symptoms and CXR findings subtle. He prefers to not stay for Remdesivir and we discussed that if the Covid screen had not been positive we may not have done a CXR with his mild symptoms. He does want to consider Paxlovid and I discussed this with the pharmacist at the patient's retail pharmacy to ensure the ability to procure. I've discussed circumstances in which he should call me or return to the hospital/ED. His Oxygen needs are stable. He has no dyspnea or fever. Dehydration Assessment & Plan Hydrate. Recheck renal functions in a.m. Improved. Essential hypertension Assessment & Plan Will check orthostatic blood pressure and pulse. Follow-up. Home meds reviewed. - remained stable Penicillin allergy Assessment & Plan The patient does have a cough. Unclear if this was related to the positive COVID test or other etiology. A full film array will be obtained. Chest x-ray clear. No evidence of clear pneumonia or pulmonary infiltrates present. Penicillin allergy noted in the event that antibiotics required. Will provide Doxycycline on discharge. Hx of H/N Cancer and prior health-care exposures. - reviewed guidelines on drug interactions and doxycycline was not on any of the list of anti-infectives of concern. - he has no clinically significant hepatic dysfunction or insufficiency to require dose adjustment or concern. He will have repeat LFTs off of Crestor. INPATIENT PROCEDURES: CT Head without acute change.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- 1,0
- Labordaten
- Lab Results Component Value Date WBC 5.56 10/23/2022 RBC 4.20 (L) 10/23/2022 HGB 13.2 (L) 10/23/2022 HCT 38.4 (L) 10/23/2022 MCV 91.4 10/23/2022 PLATELET 125 (L) 10/23/2022 NEUTABSOLU 3.02 10/23/2022 Lab Results Component Value Date GLUCOSE 175 (H) 10/23/2022 SODIUM 139 10/23/2022 POTASSIUM 3.6 10/23/2022 CHLORIDE 104 10/23/2022 ANIONGAP 8 (L) 10/23/2022 BUN 13 10/23/2022 CREATININE 0.82 10/23/2022 CALCIUM 8.8 10/23/2022 TOTALPROTE 6.0 10/23/2022 ALBUMIN 2.9 (L) 10/23/2022 ALKALINEPH 73 10/23/2022 ASTP5P 110 (H) 10/23/2022 ALTP5P 39 10/23/2022 BILIRUBINT 0.3 10/23/2022 EGFR 89 10/23/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cancer Oropharyngeal - s/p XRT/Chemo ? Diabetes mellitus ? Hypertension ? Hypothyroidism, unspecified type likely secondary to radiation ? Mixed hyperlipidemia
- Andere Medikamente
- alpha lipoic acid 100 mg capsule Take by mouth 1 (one) time each day. ASTRAGALUS ROOT ORAL Take by mouth 1 (one) time each day. b complex vitamins capsule Take 1 capsule by mouth 1 (one) time each day. cholecalciferol (VITAMIN D-3) 50
- Allergien
- Aspirin Penicillins
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 04.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Fatigue
Migraine
Nausea
Pain
Symptomtext
I had fatigue and body aches for the first 2 days. I started to feel better then on the 3rd night I woke up with a migraine and nausea. The same thing happened after my 6th dose but vomiting instead of nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Kidney Transplant; Situational Asthma; Heart Condition; Gerd; Migraines
- Andere Medikamente
- Baclofen; Mycophenolate; Rosuvastatin; Propranolol; Omeprazole
- Allergien
- Morphine; Vicodin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 24.09.2022
- Impfdatum
- 23.07.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 58,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Cervical spinal stenosis
Fall
Fine motor skill dysfunction
Hypotension
Movement disorder
Spinal fusion surgery
Symptomtext
Patient had a sudden fall for the first time at 73 years old. He acquired cervical stenosis requiring a C3-C6 posterior decompression and fusion. He was also having severely low blood pressures requiring a levophed drip. Patient is currently unable to move his lower extremities as well as he has no hand and finger dexterity on either hand.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- CAD, HTN, HLD, DM type 2
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 09.09.2022
- Impfdatum
- 30.07.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
SARS-CoV-2 test positive
Walking distance test
Symptomtext
Patient up to date of COVID vaccines who admitted with COVID detected test and complications from COVID. Provider d/c note: "54-year-old female with past medical history significant for Mayer Rokitansky syndrome with solitary kidney and restrictive lung disease on 2 L of oxygen at night at home. She presented to the emergency department on 09/01/2022 with a chief complaint of shortness of breath and cough. She was diagnosed with COVID on arrival and did require nasal cannula. She was started on steroids and remdesivir. The patient continued to improve over the course of her stay and was on room air at time of discharge. Oxygen walk test was performed before discharge and she maintained at 98%. She completed her course of remdesivir and will be discharged home with the remainder of her Decadron. Patient was doing well, wanted to go home, had no further questions and was given strict return precautions to which she verbalized understanding."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 5,0
- Labordaten
- COVID detected PCR on 09/01/22 (after "not detected" result on 08/28/22).
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Essential hypertension (Chronic) 5/23/2016 Chronic intractable headache (Chronic) 5/23/2016 Thoracogenic scoliosis of thoracic region (Chronic) 5/23/2016 Allergic rhinitis (Chronic) 5/23/2016 Intrinsic atopic dermatitis (Chronic) 5/23/2016 Undiagnosed cardiac murmurs (Chronic) 5/23/2016 Mixed hyperlipidemia 3/9/2017 Mayer-Rokitansky-Kuster-Hauser syndrome (Chronic) 8/27/2021 Solitary kidney (Chronic) 8/27/2021
- Andere Medikamente
- -
- Allergien
- Bactrim Acetaminophen Sulfas Levonorgestrel-ethinyl Estrad
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 26.08.2022
- Impfdatum
- 11.07.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 42,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abscess drainage
Abscess limb
Blood culture negative
Bone abscess
COVID-19
Chest X-ray normal
Escherichia bacteraemia
Fatigue
Hypotension
Inflammatory marker increased
Intervertebral discitis
Laboratory test abnormal
Lethargy
Mental status changes
Osteomyelitis
SARS-CoV-2 test positive
Symptomtext
Discharge Provider: MD; Primary Care Provider: DO; Admission Date: 8/22/2022; Discharge Date: Aug 25, 2022 PRESENTING PROBLEM: COVID-19 [U07.1] HOSPITAL COURSE: Sixty-nine year old male with past medical history significant for obesity, nonambulatory at baseline, hypertension, hyperlipidemia, recent admissions for E coli bacteremia related to diskitis/osteomyelitis from L3-S1 as well as suspected vertebral abscess at the level of S1 that was drained. He was readmitted in May for altered mental status found to have large gluteal abscess was also drained. He presents to emergency department on 08/22 with worsening fatigue and lethargy. He is mildly hypotensive on admission and otherwise stable. Labs were notable for elevated inflammatory markers. He did test positive for COVID-19. His checks x-ray was normal. Admitted to Medicine Service further assessment and management. As far as COVID-19 goes, patient was treated supportively. He did not develop respiratory failure and did not require steroids or other treatments. Improved over the course of the days he was hospitalized. In regards to his hypotension, this resolved with IV fluids. We did switch his home Lasix to p.r.n. basis. Blood pressure normalized by the day of discharge. Patient was on Coumadin for history of DVT. This was continued in the hospital setting and started on a bridge with Lovenox which he will continue at his facility for infra-therapeutic INR. Interventional Radiology and surgical specialist evaluated patient is drains from prior diskitis/osteomyelitis and gluteal abscess. Blood cultures were obtained and remained negative. It did not feel there was any issue with the drains and recommended outpatient follow-up. Patient is discharged back to his facility in stable and improved condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Dysphagia; Obesity; Hypertension; DVT (Deep Venous Thrombosis); Hyperglycemia; Prostate cancer (HCC); History of DVT (deep vein thrombosis); Prediabetes; Atrial fibrillation, persistent (HCC); Morbid obesity (HCC); Mixed hyperlipidemia; Anticoagulated on Coumadin; Visit for monitoring therapy; Lymphedema of left lower extremity; Ambulatory dysfunction; Body mass index (BMI) of 38.0 to 38.9 in adult; Protein-calorie malnutrition, severe (HCC); Multiple comorbid conditions; Epidural abscess; COVID-19; BPH (benign prostatic hyperplasia); Hypotension
- Andere Medikamente
- Atorvastatin (LIPITOR); Calcium carbonate (TUMS); Cyclobenzaprine (FLEXERIL); Diclofenac sodium 1 % gel; Dofetilide (TIKOSYN); Enoxaparin sodium (LOVENOX); Furosemide (LASIX) Gabapentin (NEURONTIN); Hydrocodone-acetaminophen (NORCO); Hydro
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 03.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cardiac stress test
Computerised tomogram
Hypertension
Hypoaesthesia
Magnetic resonance imaging
Paraesthesia
Symptomtext
I experienced numbness and tingling down my left arm and it went all the way down to my leg and high blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- CT scan, MRI, Stress test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 04.08.2022
- Impfdatum
- 03.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dyspnoea
Nausea
Pruritus
Rash
Skin warm
Swelling
Symptomtext
Pt reported a rash with a bump. Stated it was warm and itchy but has since gotten better. Pt also reported difficulty breathing for a "couple minutes," nausea, and chills. Reaction occurred one hour after receiving vaccine. All reaction have resolved except rash.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 06.07.2022
- Beginn
- 06.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest pain
Dyspnoea
Eating disorder
Fatigue
Headache
Heart rate
Heart rate increased
Heart rate irregular
Illness
Insomnia
Maternal exposure during pregnancy
Myalgia
Oxygen saturation
Oxygen saturation decreased
Paraesthesia
Photophobia
SARS-CoV-2 test
Symptomtext
tested positive for Covid-19; sick; rapid heart beat; low O2 saturation; severe muscle pain; pins and needles sensation; chest pain; insomnia; irregular heartbeat; unable to eat without emesis; headache; extreme tiredness; light sensitivity; shortness of breath; unable to eat without emesis; I am pregnant; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 40-year-old female patient (pregnant) received BNT162b2 (BNT162B2), on 06Jul2022 at 12:00 as dose 1, single (Lot number: FM0173) at the age of 40 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Date of last menstrual period: 05Apr2022. The patient was 16 weeks pregnant at the time of exposure to BNT162b2. The patient was 16 weeks pregnant at the event onset. The patient is expected to deliver a baby(s) on 30Dec2022. There were no concomitant medications. The following information was reported: MATERNAL EXPOSURE DURING PREGNANCY (non-serious) with onset 06Jul2022 at 12:00, outcome "unknown", described as "I am pregnant"; CHEST PAIN (non-serious) with onset 07Jul2022, outcome "not recovered"; FATIGUE (non-serious) with onset 07Jul2022, outcome "not recovered", described as "extreme tiredness"; HEADACHE (non-serious) with onset 07Jul2022, outcome "not recovered"; INSOMNIA (non-serious) with onset 07Jul2022, outcome "not recovered"; HEART RATE IRREGULAR (non-serious) with onset 07Jul2022, outcome "not recovered", described as "irregular heartbeat"; PHOTOPHOBIA (non-serious) with onset 07Jul2022, outcome "not recovered", described as "light sensitivity"; OXYGEN SATURATION DECREASED (non-serious) with onset 07Jul2022, outcome "not recovered", described as "low O2 saturation"; PARAESTHESIA (non-serious) with onset 07Jul2022, outcome "not recovered", described as "pins and needles sensation"; HEART RATE INCREASED (non-serious) with onset 07Jul2022, outcome "not recovered", described as "rapid heart beat"; MYALGIA (non-serious) with onset 07Jul2022, outcome "not recovered", described as "severe muscle pain"; DYSPNOEA (non-serious) with onset 07Jul2022, outcome "not recovered", described as "shortness of breath"; ILLNESS (non-serious) with onset 07Jul2022, outcome "not recovered", described as "sick"; EATING DISORDER (non-serious), VOMITING (non-serious) all with onset 07Jul2022, outcome "not recovered" and all described as "unable to eat without emesis"; COVID-19 (non-serious) with onset 10Jul2022, outcome "not recovered", described as "tested positive for Covid-19". The events "tested positive for covid-19", "sick", "rapid heart beat", "low o2 saturation", "severe muscle pain", "pins and needles sensation", "chest pain", "insomnia", "irregular heartbeat", "unable to eat without emesis", "headache", "extreme tiredness", "light sensitivity" and "shortness of breath" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of covid-19, illness, heart rate increased, oxygen saturation decreased, myalgia, paraesthesia, chest pain, insomnia, heart rate irregular, eating disorder, headache, fatigue, photophobia, dyspnoea, vomiting. Additional information: Adverse event: I was vaccinated on 06Jul2022 and then tested positive for Covid-19 on 10Jul2022. I spent 2 weeks very sick with rapid heartbeat, increased resting heart rate, low O2 saturation (84-93), severe muscle pain, pins and needles sensation in every cell of my body, chest pain, irregular heartbeat, insomnia, unable to eat without emesis, headache, extreme tiredness, light sensitivity, shortness of breath and I am pregnant. Adverse event start date: 07Jul2022. Adverse event start time: 12:00 AM. Ae resulted in: [Doctor or other healthcare professional office/clinic visit] If patient recovered: Not recovered. If treatment ae: No
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220707; Test Name: heart rate; Result Unstructured Data: Test Result:increased; Test Date: 20220707; Test Name: O2 saturation; Result Unstructured Data: Test Result:84-93; Test Date: 20220711; Test Name: Binex; Test Result: Positive ; Comments: Nasal Swab; Test Date: 20220710; Test Name: COVID-19 Test; Test Result: Positive ; Comments: tested positive for Covid-19 on 10Jul2022
- 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
- IL
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 29.07.2022
- Impfdatum
- 28.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Lymphadenopathy
Musculoskeletal stiffness
Symptomtext
Bilateral lymph node swelling under the armpits and at the elbows. Neck stiffness. Chest soreness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 15.06.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Feeling abnormal
Headache
Impaired work ability
Pain
Paraesthesia
Productive cough
SARS-CoV-2 test positive
Vertigo
Symptomtext
I had body aches, headaches, and I felt like my head was spinning. I felt foggy and coughing up phlegm, I felt this way for a week. Afterwards, I tested positive for COVID-19. I continued to have a tingling sensation in my spine for two weeks, I have not returned to work. I was prescribed Paxlovid but I decided not to take it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- PCR COVID -19 Test= Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Hydrochlorothiazide; Telmisartan; Estroven; True Nature Probiotic
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 20.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: unbekannt
Back pain
Blood test normal
Chest X-ray normal
Chest discomfort
Chest pain
Computerised tomogram normal
Electrocardiogram normal
Flank pain
Immunisation reaction
Inflammation
Injection site pain
Pain
Scan with contrast normal
Symptomtext
I had my 2nd Covid Vaccine Booster (Pfizer) in my left arm on the afternoon of the 20th. The next morning I had a sudden sharp stabbing pain that went right through my chest and radiated to my left side and then back. The pain level was at a 10 and I was rushed to the ER thinking I was having a heart attack. The EKG was normal so I hate to wait for 2 hours to get back and receive pain medication. The doctor ordered blood work and did a chest x-ray which didn't show anything. I was sent home and told my body was more than likely having an inflammatory response to the vaccine. The next 3 days the pain and chest tightness continued and on a scale of 1-10 my pain continued to be at a 5-6. I continued to alternate between Ibuprofen and Tylenol to alleviate the pain. It really didn't help much. I was prescribed clonazepam and it helped some with the chest tightness. On the 4th day after the ER visit, I went to see my regular physician, at Medical Center. He prescribed me two weeks worth of Prednisone for inflammation. I felt better while on the Prednisone and my pain was tolerable. Within 48 hours after finishing the prescription of Prednisone my chest tightness, breast, and upper middle back slowly crept up from a 2 to a 5. All of the pain and tightness has been confined to the left upper body thorax region. There has been pain in left arm where the vaccine was administered. Four days after finishing the Prednisone I was back at the ER with chest tightness and upper back pain. The ER physician immediately ordered a CT SCAN with/and without contrast. He also ordered blood work. The CT scan came back normal as well as the EKG. The doctor prescribed me another 5 days of steroids and Percocet. I left the ER yesterday and started on the steroids today. My pain level is a 5-6 and the chest tightness continues. I believe all of my pain and suffering has been caused by my 4th Pfizer shot. I'm 51 years old. I'm reporting this on July 17th. It's been over 3 1/2 weeks since my vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- Percocet, Aleve, Prednisone
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 16.06.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Condition aggravated
Symptomtext
6:30 pm, June 19 until Monday morning, June 20: Started having Afib episode.. 150- 220 BPM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- Bad cold: May 31, 2022- June 2, 2022. 2 negative Covid tests
- Vorgeschichte
- Regular, irregular heart beat. First episode of AFib in November 2019 after returning from unspecified location in September 2019. Worst sickness I have ever had... awful cough for weeks, hi fever( 103.5+), aches, weakness...
- Andere Medikamente
- Arimidex, Metoprolol succinate, Xarelto, Ellura, Vitamin D3, Magnesium malate, Centrum multi- vitamin,
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 23.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Chest pain
Dyspepsia
Electrocardiogram
Feeding disorder
Gastrointestinal pain
Headache
Pyrexia
Reflux gastritis
Tremor
Weight decreased
Symptomtext
Woke up on the morning of 6/24/2022 with sharp chest pain, head pain rated a 10/10, and uncontrollable shaking with fever. This pain was constant and continued throughout the day. Unable to eat because of extreme pain upon eating and high production of stomach acid. On 6/25/2022, contacted Pharmacy, PCP, and nurse at medical school, was diagnosed with functional dyspepsia. Unable to eat for four days and feeling of extreme chest pain. Lost 6 lb body weight. On 6/27/2022, visited Urgent Care and was given an EKG and directed to take 20mg famotidine. Chest pain and disgestive pain persist, and patient has been in contact with PCP about this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG administered by Urgent Care on 6/27/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Zinc sulfate 60mg, vitamin d 5000mg, tylenol 1500mg
- Allergien
- Z-pac allergy
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 20.07.2022
- Impfdatum
- 09.07.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Condition aggravated
Decreased appetite
Extra dose administered
Fatigue
Injection site pain
Migraine
Somnolence
Symptomtext
More frequent and sever migraines normally I only take one injection monthly but after dose 4 I had to take 3 injections that month after the 2nd, also was wore out tired sleepy no energy and no appetite and soreness at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Fibromyalgia: Arthritis: Bone deterioration: Migraines: Diverticulitis: Anxiety
- Vorgeschichte
- Fibromyalgia: Arthritis: Bone deterioration: Migraines: Diverticulitis: Anxiety
- Andere Medikamente
- AJOVY: NURTEC
- Allergien
- Nut; seeds
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Erythema
Extra dose administered
Feeding disorder
Influenza like illness
Injection site pain
Mobility decreased
Nausea
Oedema peripheral
Peripheral swelling
Pyrexia
Skin warm
Symptomtext
Patient experienced injection site pain after COVID shot. On Sunday arm swelled significantly and was red and hot. The axilla swollen and hard to move. Patient had fever, nausea and dizziness. Symptoms resembled the flu and she was unable to eat
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Patient was initially evaluated by TLC nurse practioner who advised patient to be seen at Urgent Care. Urgent Care recommended patient be seen by Primary Care Physician
- Aktuelle Erkrankungen
- Patient considerably healthy
- Vorgeschichte
- None
- Andere Medikamente
- Low dose blood pressure medication
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 20.06.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Sleep disorder
Symptomtext
she had another episode the other night that it woke her up/then it woke her up again a couple nights ago, out of her sleep; she experienced pins and needles and tingling in hands for about a day and night after the shot; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A 43-year-old female patient received BNT162b2 (BNT162B2), on 20Jun2022 as dose 1, 0.3 ml single (Lot number: FM0173, Expiration Date: 12Aug2022) at the age of 43 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Migraine since she was a teenager" (ongoing). There were no concomitant medications. The following information was reported: PARAESTHESIA (medically significant) with onset 20Jun2022, outcome "unknown", described as "she experienced pins and needles and tingling in hands for about a day and night after the shot"; SLEEP DISORDER (non-serious), outcome "unknown", described as "she had another episode the other night that it woke her up/then it woke her up again a couple nights ago, out of her sleep". Clinical course: Caller stated she was calling about the gray cap Covid 19 vaccine, stated a patient had a reaction to first vaccine and was due for her second dose, explained she experienced pins and needles and tingling in hands for about a day and night after the shot. Clarifies she had another episode the other night that it woke her up. She had pins and needles and tingling that night; and then it woke her up again a couple nights ago, out of her sleep, with that. Caller wanted to know if it is safe for the patient to get her second dose.; Sender's Comments: Based on the current available limited information in the case provided, the causal association between the events paraesthesia and sleep disorder and the use of suspect product BNT162b2 cannot be fully excluded. The case will be reassessed once further information is available 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 RAs, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Migraine
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Body temperature
Erythema
Influenza like illness
Joint swelling
Clostridium difficile infection
Impaired work ability
Injected limb mobility decreased
Injection site joint pain
Injection site pain
Injection site swelling
Mobility decreased
Nausea
Pain
Pain in extremity
Pain in jaw
Peripheral swelling
Pyrexia
Symptomtext
Severe joint pain spread to include both hips, right knee,& left side of jaw.; Severe joint pain spread to include both hips, right knee,& left side of jaw.; swelling, & redness in both hands & wrists; swelling, & redness in both hands & wrists; swelling, & redness in both hands & wrists; severe joint pain spread to include both ankles & left wrist in addition to previously mentioned joints; immobilization/severe pain maintained since onset, esp. in hands; moderate all over joint pain/right shoulder/elbow/left shoulder; Severe joint pain in right shoulder resulting in inability to move shoulder/arm in any direction/immobilization; Flu-like symptoms approx 20 hrs after booster dose; nausea; low fever; body aches; pain at injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 26-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jun2022 at 17:45 as dose 3 (booster), single (Lot number: FM0173) at the age of 26 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Coconut" (unspecified if ongoing), notes: Known allergies: Coconut; "Allergy-induced asthma" (unspecified if ongoing), notes: Allergy-induced asthma; "Allergy-induced asthma" (unspecified if ongoing), notes: Allergy-induced asthma; "Anemia" (unspecified if ongoing); "ADHD" (unspecified if ongoing), notes: ADHD; "Chronic Depression" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Narcolepsy" (unspecified if ongoing); "sleep-wake disorder" (unspecified if ongoing), notes: sleep-wake disorder; "Known allergy:Almond" (unspecified if ongoing), notes: Known allergy:Almond; "Known allergy: Lavender" (unspecified if ongoing), notes: Known allergy: Lavender. The patient took concomitant medications. Past drug history included: Rx tramadol, reaction(s): "Known allergies: RX Tramadol", notes: Known allergies: RX Tramadol. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EW0175, Location of injection: Right arm), administration date: 21May2021, when the patient was 25-year-old, for COVID-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EW0175, Location of injection: Right arm), administration date: 30Apr2021, when the patient was 25-year-old, for COVID-19 Immunization. The following information was reported: INFLUENZA LIKE ILLNESS (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "Flu-like symptoms approx 20 hrs after booster dose"; PAIN (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "body aches"; PYREXIA (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "low fever"; NAUSEA (non-serious) with onset Jun2022, outcome "recovered" (2022); VACCINATION SITE PAIN (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "pain at injection site"; MOBILITY DECREASED (non-serious) with onset 30Jun2022, outcome "not recovered", described as "Severe joint pain in right shoulder resulting in inability to move shoulder/arm in any direction/immobilization"; ARTHRALGIA (non-serious) with onset 30Jun2022, outcome "not recovered", described as "moderate all over joint pain/right shoulder/elbow/left shoulder"; PAIN IN EXTREMITY (non-serious) with onset 30Jun2022 at 08:00, outcome "not recovered", described as "immobilization/severe pain maintained since onset, esp. in hands"; ARTHRALGIA (non-serious) with onset 03Jul2022, outcome "recovered" (05Jul2022), described as "severe joint pain spread to include both ankles & left wrist in addition to previously mentioned joints"; PERIPHERAL SWELLING (non-serious), JOINT SWELLING (non-serious), ERYTHEMA (non-serious) all with onset 06Jul2022, outcome "not recovered" and all described as "swelling, & redness in both hands & wrists"; ARTHRALGIA (non-serious), PAIN IN JAW (non-serious) all with onset 08Jul2022, outcome "recovered" (10Jul2022) and all described as "Severe joint pain spread to include both hips, right knee,& left side of jaw.". The events "flu-like symptoms approx 20 hrs after booster dose", "nausea", "low fever", "body aches", "pain at injection site", "moderate all over joint pain/right shoulder/elbow/left shoulder", "severe joint pain in right shoulder resulting in inability to move shoulder/arm in any direction/immobilization", "severe joint pain spread to include both ankles & left wrist in addition to previously mentioned joints", "swelling, & redness in both hands & wrists", "immobilization/severe pain maintained since onset, esp. in hands" and "severe joint pain spread to include both hips, right knee,& left side of jaw." required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of influenza like illness, nausea, pyrexia, pain, vaccination site pain, arthralgia, mobility decreased, arthralgia, peripheral swelling, joint swelling, erythema, pain in extremity, arthralgia, pain in jaw. Additional information: No other vaccine in four weeks, took other medications in two weeks. Unknown if covid prior to vaccination and not tested positive post vaccination. 2 days after injection (30Jun2022) moderate joint pain all over. 01Jul2022 moderate all over joint pain & severe joint pain in right shoulder. 02Jul2022 increased severity of joint pain in right shoulder resulting in inability to move shoulder/arm in any direction. 03Jul2022-05Jul2022 severe joint pain spread to include both ankles & left wrist in addition to previously mentioned joints. 06Jul2022 upon waking, severe joint pain, swelling, & redness in both hands & wrists, & severe joint pain w/o swelling in right shoulder and elbow, resulting in inability to use or move hands/fingers on either side. 07Jun2022 continued severe joint pain in previously mentioned areas, & now including left shoulder. 08Jun2022-10Jun2022 severe joint pain spread to include both hips, right knee, & left side of jaw. Swelling & immobilization/severe pain maintained since onset, esp. in hands.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Test Date: 202206; Test Name: Body temperature; Result Unstructured Data: Test Result:low fever
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: ADHD; Allergy (Allergy-induced asthma); Allergy to nuts (Known allergy:Almond); Allergy to plants (Known allergy: Lavender); Anemia; Anxiety; Asthma (Allergy-induced asthma); Chronic depression; Fruit allergy (Known allergies: Coconut); Narcolepsy; Sleep disorder (sleep-wake disorder)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Body temperature
Erythema
Influenza like illness
Joint swelling
Clostridium difficile infection
Impaired work ability
Injected limb mobility decreased
Injection site joint pain
Injection site pain
Injection site swelling
Mobility decreased
Nausea
Pain
Pain in extremity
Pain in jaw
Peripheral swelling
Pyrexia
Symptomtext
Severe joint pain spread to include both hips, right knee,& left side of jaw.; Severe joint pain spread to include both hips, right knee,& left side of jaw.; swelling, & redness in both hands & wrists; swelling, & redness in both hands & wrists; swelling, & redness in both hands & wrists; severe joint pain spread to include both ankles & left wrist in addition to previously mentioned joints; immobilization/severe pain maintained since onset, esp. in hands; moderate all over joint pain/right shoulder/elbow/left shoulder; Severe joint pain in right shoulder resulting in inability to move shoulder/arm in any direction/immobilization; Flu-like symptoms approx 20 hrs after booster dose; nausea; low fever; body aches; pain at injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 26-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jun2022 at 17:45 as dose 3 (booster), single (Lot number: FM0173) at the age of 26 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Coconut" (unspecified if ongoing), notes: Known allergies: Coconut; "Allergy-induced asthma" (unspecified if ongoing), notes: Allergy-induced asthma; "Allergy-induced asthma" (unspecified if ongoing), notes: Allergy-induced asthma; "Anemia" (unspecified if ongoing); "ADHD" (unspecified if ongoing), notes: ADHD; "Chronic Depression" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Narcolepsy" (unspecified if ongoing); "sleep-wake disorder" (unspecified if ongoing), notes: sleep-wake disorder; "Known allergy:Almond" (unspecified if ongoing), notes: Known allergy:Almond; "Known allergy: Lavender" (unspecified if ongoing), notes: Known allergy: Lavender. The patient took concomitant medications. Past drug history included: Rx tramadol, reaction(s): "Known allergies: RX Tramadol", notes: Known allergies: RX Tramadol. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EW0175, Location of injection: Right arm), administration date: 21May2021, when the patient was 25-year-old, for COVID-19 Immunization; BNT162b2 (Dose Number: 1, Batch/Lot No: EW0175, Location of injection: Right arm), administration date: 30Apr2021, when the patient was 25-year-old, for COVID-19 Immunization. The following information was reported: INFLUENZA LIKE ILLNESS (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "Flu-like symptoms approx 20 hrs after booster dose"; PAIN (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "body aches"; PYREXIA (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "low fever"; NAUSEA (non-serious) with onset Jun2022, outcome "recovered" (2022); VACCINATION SITE PAIN (non-serious) with onset Jun2022, outcome "recovered" (2022), described as "pain at injection site"; MOBILITY DECREASED (non-serious) with onset 30Jun2022, outcome "not recovered", described as "Severe joint pain in right shoulder resulting in inability to move shoulder/arm in any direction/immobilization"; ARTHRALGIA (non-serious) with onset 30Jun2022, outcome "not recovered", described as "moderate all over joint pain/right shoulder/elbow/left shoulder"; PAIN IN EXTREMITY (non-serious) with onset 30Jun2022 at 08:00, outcome "not recovered", described as "immobilization/severe pain maintained since onset, esp. in hands"; ARTHRALGIA (non-serious) with onset 03Jul2022, outcome "recovered" (05Jul2022), described as "severe joint pain spread to include both ankles & left wrist in addition to previously mentioned joints"; PERIPHERAL SWELLING (non-serious), JOINT SWELLING (non-serious), ERYTHEMA (non-serious) all with onset 06Jul2022, outcome "not recovered" and all described as "swelling, & redness in both hands & wrists"; ARTHRALGIA (non-serious), PAIN IN JAW (non-serious) all with onset 08Jul2022, outcome "recovered" (10Jul2022) and all described as "Severe joint pain spread to include both hips, right knee,& left side of jaw.". The events "flu-like symptoms approx 20 hrs after booster dose", "nausea", "low fever", "body aches", "pain at injection site", "moderate all over joint pain/right shoulder/elbow/left shoulder", "severe joint pain in right shoulder resulting in inability to move shoulder/arm in any direction/immobilization", "severe joint pain spread to include both ankles & left wrist in addition to previously mentioned joints", "swelling, & redness in both hands & wrists", "immobilization/severe pain maintained since onset, esp. in hands" and "severe joint pain spread to include both hips, right knee,& left side of jaw." required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of influenza like illness, nausea, pyrexia, pain, vaccination site pain, arthralgia, mobility decreased, arthralgia, peripheral swelling, joint swelling, erythema, pain in extremity, arthralgia, pain in jaw. Additional information: No other vaccine in four weeks, took other medications in two weeks. Unknown if covid prior to vaccination and not tested positive post vaccination. 2 days after injection (30Jun2022) moderate joint pain all over. 01Jul2022 moderate all over joint pain & severe joint pain in right shoulder. 02Jul2022 increased severity of joint pain in right shoulder resulting in inability to move shoulder/arm in any direction. 03Jul2022-05Jul2022 severe joint pain spread to include both ankles & left wrist in addition to previously mentioned joints. 06Jul2022 upon waking, severe joint pain, swelling, & redness in both hands & wrists, & severe joint pain w/o swelling in right shoulder and elbow, resulting in inability to use or move hands/fingers on either side. 07Jun2022 continued severe joint pain in previously mentioned areas, & now including left shoulder. 08Jun2022-10Jun2022 severe joint pain spread to include both hips, right knee, & left side of jaw. Swelling & immobilization/severe pain maintained since onset, esp. in hands.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- Test Date: 202206; Test Name: Body temperature; Result Unstructured Data: Test Result:low fever
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: ADHD; Allergy (Allergy-induced asthma); Allergy to nuts (Known allergy:Almond); Allergy to plants (Known allergy: Lavender); Anemia; Anxiety; Asthma (Allergy-induced asthma); Chronic depression; Fruit allergy (Known allergies: Coconut); Narcolepsy; Sleep disorder (sleep-wake disorder)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- 01.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse food reaction
Ageusia
Blood test
Chapped lips
Dry mouth
Dry eye
Oral discomfort
Oral pain
Dyspnoea
Eye irritation
Feeling abnormal
Hypophagia
Loss of personal independence in daily activities
Pain
Stomatitis
Thirst
Throat irritation
Tongue discomfort
Symptomtext
Dry eyes; Dry mouth; burning mouth; sores in mouth; Loss of taste; This case was reported by a consumer via call center representative and described the occurrence of eye dryness in a 62-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. In May 2022, the patient received the 1st dose of Shingrix (intramuscular) .5 ml. On an unknown date, several hours after receiving Shingrix, the patient experienced eye dryness, dry mouth, burning mouth, sore mouth and taste loss. On an unknown date, the outcome of the eye dryness, dry mouth, burning mouth, sore mouth and taste loss were not recovered/not resolved. It was unknown if the reporter considered the eye dryness, dry mouth, burning mouth, sore mouth and taste loss to be related to Shingrix. Additional Information: GSK Receipt Date: 05-JUL-2022 Reporter's Comments: The patient was self-reported case. The patient received first dose in Shingrix vaccine in right arm. The patient stated that few hours later, she started with dry eyes, dry mouth, burning mouth, sores in her mouth, and loss of taste. She stated that these symptoms had not gone away and had gotten worse since they started. She did not have any specific information about the vaccine itself. The reporter did not consent to follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Decreased appetite
Diarrhoea
Fatigue
Headache
Mobility decreased
Peripheral swelling
Vomiting
Symptomtext
7/14/headache, vomiting, swelling of left arm, left arm. side, breast started to swell. Unable to lift left side. Left breast 4 cups bigger, diarrhea, fatigue, no appwtite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- one a day vitamins
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Headache
Hypertension
Malaise
Palpitations
Symptomtext
Patient informed us that she wasn't feeling well within 5 minutes of getting the Pfizer vaccine (vaccine given at 11:16am PST). She stated that she had difficulty breathing, her heart was racing and she had a headache. We asked her if she wanted us to call 911 and she said yes. I called 911 and also grabbed her a bottle of water. She wanted to sit inside the counseling room while waiting for the medics to arrive. The paramedics arrived at 11:38am and they checked her vitals and consulted with the patient. After about 10 minutes, they informed me that the patients vitals were all normal except for her blood pressure being high. They also said her housemate will come by and pick her up and she was okay to go home. I told the patient she can wait in the counseling room for her housemate to arrive. Also asked if she needed anything else while she was waiting. She said she didn't need anything else. Her housemate came by and she left
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- latex
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 09.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray
Cough
Feeling cold
Influenza virus test negative
Lymphadenopathy
Malaise
Mobility decreased
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Sinus pain
Streptococcus test negative
Symptomtext
After vaccine I had extreme fever chills, I was freezing cold and could not get warm. I felt extremely sick. I ended up with the glands under my left arm severe swollen all the way to my breast. My fever was a bit over 100 and was barely able to get out of bed. This lasted about 4 days. I had these reactions to vaccines 2 and 3 the same but no where near as intense. My husband had the vaccine at the same time and he too had a fever and was extremely tired, but he was no where near what I was. On July 9th I woke up with symptoms of COVID and went to urgent care where I was tested positive. My current symptoms are extreme sore throat, pain in sinuses, a bit of fever, and cough. I went to urgent care again and they gave me a chest X ray to check my airway. It was fine. They gave me antibiotic in fear I was getting a severe sinus infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- COVID test with positive; tested for flu and strep with negative result; chest X ray
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamins
- Allergien
- Narcotics
- Vorherige Impfungen
- Influenza shots make me sick to my stomach.
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 14.06.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dyspnoea
Fear
Headache
Myalgia
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Salivary hypersecretion
Speech disorder
Throat irritation
Toothache
Symptomtext
I was at a conference last week and caught Covid-19 while there between 07/02/2022 and 07/08/222. Symptoms began on 07/09/2022 with a scratchy throat, muscle aches around 07:00PM. It just went down hill from there, by Sunday I was having difficulty breathing and a lot of congestion, headache, the roots of my teeth were throbbing, and I was salivating uncontrollably, and it would not stop, it was a very difficult, from the neck up. I was a respiratory therapist for 20 years and it was scary as I laid in bed one night and it felt like my air was blocked off. I felt like I was developing diphtheria. I was sleeping and I would wake up gasping for air. Monday morning, I called the doctor, and they scheduled a tele-visit Tuesday morning and they prescribed PAXLOVID and benzonatate and recommended MOTRIN and alternate with TYLENOL and take DAYQUIL and NYQUIL. Currently symptoms are ok, but I cannot talk well, I get very winded talking than anything else, I slept well last night. Congestion is still here and if I cough it feels like my head is going to pop off. The doctor said to go to hospital if I get a fever or oxygen stats go down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Home test with positive result.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; diabetic Type 2; high cholesterol
- Andere Medikamente
- Fish oil; losartan; metformin; baby aspirin; stool softener; beet root; PRESERVISION eye drops vitamin formula; resveratrol; LASIX; MOBIC; LIPITOR; metoprolol; vitamin D3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram abnormal
Palpitations
Supraventricular extrasystoles
Ventricular extrasystoles
Symptomtext
Palpitations/PACs/PVCs started about an hour to hour and a half after administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- ECGs via Apple Watch and Read My ECG June 18 and July 7. Echocardiogram and holter monitor pending.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamins, iron, vitamin D, omega-3a
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.07.2022
- Impfdatum
- 17.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Musculoskeletal chest pain
Symptomtext
Chest wall pain began all of a sudden two days after vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hashimoto thyroiditis, elevated blood pressure, osteoarthritis
- Andere Medikamente
- -
- Allergien
- Gluten sensitivity
- Vorherige Impfungen
- Extreme overall body soreness, at age 61, 1/18/2019 and 5/3/2019, Shingles shots, Shingrix.
- Staat
- KY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 30.06.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Cough
Feeling abnormal
Musculoskeletal chest pain
Oropharyngeal pain
Productive cough
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Starting 07/01/2022, I started getting a sore throat, chills, pain around the rib cage, fever and coughing up phlegm. On 07/02/2022, I kept feeling worse and continued to cough up more phlegm. On 07/03/2022, I went to urgent care and they tested me for COVID-19 which came back positive. I took everything I wasn't supposed to on Saturday to try to open up my throat because I was concerned (prednisone, doxy etc which is what I normally take when I have asthma/breathing issues) and the urgent care told me I shouldn't have. The urgent care called me in a rescue inhaler of albuterol and a new prescription for cough medicine. This is what I have been using every 6 hours. I am not doing to great but am okay as long as I don't cough. I'm still taking extra strength tylenol due to having a fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- COVID-19 test at urgent care (07/03/2022): Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; High Blood Pressure; Acid Reflux
- Andere Medikamente
- Metoprolol; Nexium; Pomicort; Flonase;
- Allergien
- Aspirin; Penicillin; NSAIDs and numerous others
- Vorherige Impfungen
- With the 1st booster (3rd dose), I had a fever for 4 days and chills one night.
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 04.07.2022
- Impfdatum
- 30.06.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lip swelling
Lymphadenopathy
Paraesthesia oral
Peripheral swelling
Symptomtext
Dose 1,2,3 were Moderna with no reaction Dose: 4 was Phizer with reaction Woke up with a very swollen and tingling lip. In addition, my right arm pit was severely swollen into my chest area as well all under my arm so lymph were inflamed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Night hypoxia, on 2L oxygen at night
- Andere Medikamente
- Meds:Synthroid, D3,Zinc,vitamin C, multivitamin,
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 27.06.2022
- Impfdatum
- 29.01.2021
- Beginn
- 26.06.2022
- Tage bis Beginn
- 513,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute left ventricular failure
Anaemia
Asymptomatic COVID-19
Chronic left ventricular failure
Chronic obstructive pulmonary disease
Dizziness
Dyspnoea
Pulmonary hypertension
Symptomtext
Pt has a PMH of diastolic congestive heart failure and complains of increased shortness of breath and dizziness. He has pulmonary hypertension, COPD, and is a former smoker. He was admitted for acute on chronic diastolic heart failure, acute on chronic anemia, and asymptomatic COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Paraesthesia oral
Symptomtext
Tingling lips and sweaty palms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Latex
- Vorherige Impfungen
- Flu vaccine 2 years ago caused muscle problems in left arm
- Staat
- IN
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 24.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Sleep disorder
Tinnitus
Symptomtext
No prior side effects with three prior shots and boosters. Within 90 minutes of the 4 injection, Patient had a sudden explosion of Tinnitus in his left ear only. The tinnitus is severe and constant and made sleeping almost impossible. He was able to sleep on his right side, but when he slept on the left side, the sound was unbearable. Patient has continued to experience extremely loud and constant ringing for the past 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- No further tests have been undertaken, but he will either have to see an ENT doctor or an audiologist if the left ear ringing continues.
- Aktuelle Erkrankungen
- Minor tinnitus
- Vorgeschichte
- No
- Andere Medikamente
- Atorvastatin 20 mg
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 13.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Dyspnoea
Palpitations
Poor quality product administered
Product administration error
Symptomtext
had a little bit of racing; feels like breathing harder than normally does; anxious feeling; the vials had been sitting there for over 48 hours and should had been thrown away; the vials had been sitting there for over 48 hours and should had been thrown away; 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 44-year-old male patient received BNT162b2 (BNT162B2), on 13Jun2022 at 10:20 as dose 3 (booster), single (Lot number: FM0173) at the age of 44 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1 , NDC: unknown, lot: EH9899, expiration: unknown, Route of administration: arm, unknown left or right), administration date: 07Jan2021, when the patient was 42-year-old, for COVID-19 immunization; BNT162b2 (Dose 2, NDC: unknown, lot: EL3302, expiration: Unknown, states 30May2021 is written on vaccine card but is unknown if this is expiration date. , Route of administration: Arm, unknown left or right arm), administration date: 28Jan2021, when the patient was 42-year-old, for COVID-19 immunization. The following information was reported: POOR QUALITY PRODUCT ADMINISTERED (non-serious), PRODUCT ADMINISTRATION ERROR (non-serious) all with onset 13Jun2022 at 10:20, outcome "unknown" and all described as "the vials had been sitting there for over 48 hours and should had been thrown away"; ANXIETY (non-serious) with onset 14Jun2022, outcome "unknown", described as "anxious feeling"; DYSPNOEA (non-serious) with onset 14Jun2022, outcome "unknown", described as "feels like breathing harder than normally does"; PALPITATIONS (non-serious) with onset 14Jun2022, outcome "not recovered", described as "had a little bit of racing". Additional information: Caller received a booster dose of the Pfizer COVID-19 Vaccine yesterday, and then was advised that the vials had been sitting there for over 48 hours and should had been thrown away. Caller wanted to know if there could be any safety concerns regarding this wrong administration. Caller mentioned not having an specific HCP. Caller complained that he was told to stay on hold 5 times and that he was on the phone during almost 2 hours just to be referred to an HCP and to receive the information he already knew. Caller also complained that it wasn't possible for "the other department" to send him the information he shared with them. Received booster dose Pfizer COVID-19 yesterday, 13Jun2022 from withheld. Was advised the booster dose Pfizer Covid 19 Vaccine administered to patient was supposed to have been tossed because was sitting out for over 48 hours. Wanted to know what needs to be done next?. Confirmed details provided by transfer agent. Booster dose Pfizer COVID-19 Vaccine received was supposed to have been tossed because was sitting out for over 48 hours: The withheld where received booster dose Pfizer COVID-19 Vaccine said to come back and receive another dose but caller said not getting another dose after the vaccine facility screwed up the caller's first booster dose Pfizer COVID-19 Vaccine. The main concern was what should patient be worried about, if Booster dose Pfizer COVID-19 Vaccine that was supposed to have been tossed because was sitting out for over 48 hours, was put in the body that was not supposed to be?. Since this morning, 14Jun2022, has had a little bit of racing and feels like breathing harder than normally does. Has had a little bit of racing: Clarifies can feel heart beat and just a little bit of, not really an anxiety type of person but has an anxious feeling. Feels like breathing harder than normally does: Does not know if improving, worsening or persisiting. Has had a little bit of racing: About the same, gets worse if sits down. Is caller going to get a copy of the report?. Caller would like a copy of the report. Caller asked DSU Agent for a copy of the recording. No vaccine administered at Military Facility. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s): No, any other vaccines were due in Dec2022. AE(s) following prior vaccinations: No, never and never had any allergies or anything. Patient's Medical History (including any illness at time of vaccination) was none. Relevant Tests were none. Is not being impatient, just feels like has to keep taking a big deep breath. Had a lot going through mind.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- 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
- RI
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 19.06.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Injection site hypoaesthesia
Injection site pain
Injection site paraesthesia
Paraesthesia
Vomiting
Symptomtext
Patient came in reporting pain at the injection site including numbness and tingling moving down her left arm to her fingertips. She reported the pain was so severe it caused her to vomit. She experienced these side effects for 3 days after the vaccination before coming in to report it. She self-treated with OTC Tylenol and ibuprofen which brought her pain down form an 8/10 to a 4-5/10.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- Latex gloves sumatriptan sulfa drugs morphine
- Vorherige Impfungen
- Similar symptoms with previous 2 Pfizer covid vaccines (full-body muscle aches, headaches) and was worse with the second dose of
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 17.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Condition aggravated
Middle insomnia
Neck pain
Symptomtext
For the last several years, I've had occasional pain in my right knee. After my second booster, the knee pain has increased; For the last several years, I've had occasional pain in my right knee. After my second booster, the knee pain has increased; It's been keeping me awake at night and still lingers today (18 days later); I developed pain in my left shoulder and left side of my neck (my shot was in my left shoulder).; I developed pain in my left shoulder and left side of my neck (my shot was in my left shoulder).; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP), Program ID: The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), on 24May2022 as dose number unknown (booster), single (Lot number: FM0173) for covid-19 immunization. The patient's relevant medical history included: "pain in my right knee" (unspecified if ongoing), notes: For the last several years, I've had occasional pain in my right knee. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose number -1, Manufacturer unknown), for covid-19 immunization; Covid-19 vaccine (Dose number -2, Manufacturer unknown), for covid-19 immunization; Covid-19 vaccine (Dose number -3, Manufacturer unknown), for covid-19 immunization. The following information was reported: ARTHRALGIA (non-serious), NECK PAIN (non-serious) all with onset 28May2022, outcome "unknown" and all described as "I developed pain in my left shoulder and left side of my neck (my shot was in my left shoulder)."; CONDITION AGGRAVATED (non-serious), ARTHRALGIA (non-serious), outcome "unknown" and all described as "For the last several years, I've had occasional pain in my right knee. After my second booster, the knee pain has increased"; MIDDLE INSOMNIA (non-serious), outcome "unknown", described as "It's been keeping me awake at night and still lingers today (18 days later)". Therapeutic measures were taken as a result of arthralgia, neck pain, condition aggravated, arthralgia. Additional Information: Patient never had a reaction to a Pfizer Covid shot until patient had 2nd booster on 24May2022. About four days after the second booster (Lot # FM0173), developed pain in left shoulder and left side of neck (shot was in patient left shoulder). It's been keeping patient awake at night and still lingers today (18 days later). Tylenol seems to help reduce the pain. For the last several years, patient had occasional pain in his right knee. After second booster, the knee pain has increased.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Pain knee (For the last several years, I've had occasional pain in my right knee.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 10.05.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
COVID-19
Cardiomyopathy
Chest X-ray abnormal
Dyspnoea
Electrocardiogram
Laboratory test
Palpitations
Pleural effusion
Troponin increased
Symptomtext
Patient was seen in ED due palpitations and dyspnea. She was recently diagnosed with COVID-19. She was COVID vaccinated and boosted. She presented with A. fib with RVR. Troponin was elevated at 116 and suspected to be myocardial strain from the underlying atrial fibrillation with rapid ventricular response. Diltiazem bolus and drip administered. chest x-ray note s small bilateral pleural effusions. Patient was admitted to hospital for further evaluation and treatment The Health department has no further information. No known outcome. Contact Provider for any additional information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Lab work ECG XRay chest
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- benign head tremor, anemia, hypertension, hyponatremia, hypomagnesemia,
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 16.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Electrocardiogram
Palpitations
Swelling
Symptomtext
Heart is beating pretty fast; It feels like her chest is like swollen like it is harder; Still feel like it's a lot of weight just being pushed on her chest; It feels like her chest is like swollen like it is harder; Still feel like it's a lot of weight just being pushed on her chest; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 29-year-old male patient received BNT162b2 (BNT162B2), on 04Jun2022 at 11:00 as dose number unknown, single (Lot number: FM0173) at the age of 29 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PALPITATIONS (non-serious) with onset Jun2022, outcome "unknown", described as "Heart is beating pretty fast"; CHEST DISCOMFORT (non-serious), SWELLING (non-serious) all with onset Jun2022, outcome "unknown" and all described as "It feels like her chest is like swollen like it is harder; Still feel like it's a lot of weight just being pushed on her chest". The events "heart is beating pretty fast" and "it feels like her chest is like swollen like it is harder; still feel like it's a lot of weight just being pushed on her chest" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient called to Pfizer because she was having side effects from the shot (Pfizer COVID-19 vaccine). The patient just feel like her heart was beating pretty fast and it felt like her chest was like swollen like it was harder, felt like 'if she pressed it just feel push on the chest'. Yes so she went to the doctor yesterday (09Jun2022) and she got a EKG and everything and they said everything was fine but she still felt like it's a lot of weight just being pushed on her chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220609; Test Name: EKG; Result Unstructured Data: Test Result:fine; Comments: got a EKG and everything and they said everything was fine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Nausea
Pain in extremity
Palpitations
Pyrexia
Symptomtext
lightheadedness, nausea, racing heart rate, fever, left arm soreness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- vitamins.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Pyrexia
Tremor
Symptomtext
PT REPORTED "SHAKING SO BAD THAT THE BED WAS SHAKING", CHILLS, AND FEVERISHNESS THE NIGHT AND NEXT MORNING OF THE VACCINE ADMINISTRATION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- ACETAMINOPHEN CARBAMAZEPINE PENICILLINS SALICYLATES
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 03.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Mobility decreased
Muscle tightness
Myalgia
Neck pain
Pain
Pain in extremity
Symptomtext
I had pzier vaccine, 4th shot, second booster on . I already have problems with my neck and shoulder muscles becoming so tight that I take several muscle relaxers everyday. After the shot, that night my shoulder muscles got so tight and hurt badly, even after I took multiple muscle relaxers that normally help. This time, nothing worked. I tried to sleep and woke up from the pain in my neck and shoulders, I was crying from the pain. pain radiated down my right arm (I was vaccinated on left arm) also. I stayed in bed the next day, still hurting quite a bit despite taking multiple doses of muscle relaxers. I went to bed that night, still hurting, but not as bad as the night before. I woke up the next morning and it was better. I?ve never experienced such pain before from my muscles without medicine or therapy at least lessening the pain until this vaccine. It felt like my muscles were glued together, and not in a good way.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Neck problems with shoulder muscles and migraines Pre-diabetic. High blood pressure. Sleep apnea.
- Andere Medikamente
- Yes
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- 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: ja
COVID-19
Fatigue
Headache
Immediate post-injection reaction
Malaise
Mobility decreased
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
I experienced immediate pain in the base of my throat when the shot was administered. I carry an epi pen for allergies and told my husband it was in my bag if I started having problem breathing. I began to feel unwell after we left the pharmacy with a bad headache. The next day I had body aches, headache and sinus congestion. It worsened over the next day and by Wednesday I had crushing fatigue, severe headache and a fever of 100.7 and body aches so badly I could barely get out of a chair. I went back to bed at 2:30 pm and slept for hours. Thursday morning I used a home rapid test and it was Positive for Covid. I had previously taken a home rapid test on Saturday, May 21 that was Negative. I was not experiencing any symptoms of Covid. I had wanted to make sure I did not have Covid prior to getting the Booster. When I went to the pharmacy for the Booster I felt perfectly well and had planned to go to dinner. I felt so unwell after getting the Booster, we did not have dinner that evening.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Covid home rapid test May 26, 2022 POSITIVE for Covid. Covid home rapid test May 29, 2022 POSITIVE for Covid.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Levothyroxine .75 mg
- Allergien
- Seasonal allergies for which I take weekly shots
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 22.06.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood magnesium normal
Eye disorder
Eye pain
Neurological examination
Pain
Pruritus
Symptomtext
12 hrs. after I got the vaccine, I was sleeping, woke up and saw in the mirror I had a spam and it lasted for three weeks, sometimes I saw it and feel it, a week later my right eye, started on the left and then the right eye. A month after the vaccine, I notice itching on my eyebrow and had pain it happens for a few weeks, after a few weeks, two months after, I still had eye pain, On December I saw a Neurologist, gave me an exam, she thought it was not the vaccine, but it was 12 hrs. after the vaccine, and it didn't have the before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- 13OCT2022 - Magnesium Test - Normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Synthroid; Baby Aspirin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Arthralgia
Fatigue
Myalgia
Pain in extremity
Symptomtext
I had soreness in my arm after receiving the vaccine for about a day. I have trouble with fatigue with muscle and joint soreness. I try to rest as much as I can and need to help with the symptoms. For a short time, I had hair loss but that has stopped. If I start with a good day and overdo it my symptoms are worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Atorvastatin; Herbal Teas; Vitamin D
- Allergien
- IV Contrast
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 21.06.2023
- Impfdatum
- 18.06.2022
- Beginn
- 01.05.2023
- Tage bis Beginn
- 317,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Sinusitis
Symptomtext
I had a sore arm for about a day after receiving the vaccine. I have a history of sinus infections in the spring and fall time frame. I had a sinus infection 05/2023. I contacted my doctor via telehealth visit, and I was put on an antibiotic, prednisone and cough suppression. As of today, I feel better with no lingering issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol; High Blood Pressure
- Andere Medikamente
- N/A
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 10.06.2023
- Impfdatum
- 18.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Asthenia
Burning sensation
Chills
Fatigue
Feeling cold
Headache
Hyperhidrosis
Influenza like illness
Nausea
Pain in extremity
Scarlet fever
Symptomtext
breaking into shivers like she was at the north pole and she could not get warm, it was like an internal earthquake; breaking into shivers like she was at the north pole and she could not get warm, it was like an internal earthquake; Then the heat turned on; for 4 hours she was burning up and sweating; Then the heat turned on; for 4 hours she was burning up and sweating / I would go in to sweat like a fever in sweat for another 4 hours; extremely tired; her arm hurts / soreness in the arm; had a headache that she had never had before unlike any other; nauseated; flu like discomfort; 4 hours like scarlet fever; Upset stomach; I would be weak; 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 female patient received BNT162b2 (BNT162B2), on 18May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 79 years for covid-19 immunisation. The patient's relevant medical history included: "I am over weight" (unspecified if ongoing), notes: I am over weight; "blood pressure" (ongoing), notes: I take blood pressure pill (Losartan); "reflux" (ongoing), notes: something for reflux, Omeprazole. Concomitant medication(s) included: LOSARTAN taken for blood pressure abnormal; OMEPRAZOLE taken for gastrooesophageal reflux disease. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot#: EN6202), administration date: 28Feb2021, when the patient was 78-year-old, for COVID-19 immunization, reaction(s): "her arm was sore", "a little fatigue"; BNT162b2 (DOSE 2, SINGLE, Lot: EN6206), administration date: 21Mar2021, when the patient was 78-year-old, for COVID-19 immunization, reaction(s): "her arm was sore", "a little fatigue"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot#: 3012SBA), administration date: 07Oct2021, when the patient was 78-year-old, for COVID-19 Immunization, reaction(s): "breaking into shivers like she was at the north pole and she could not get warm, it was like an internal earthquake", "breaking into shivers like she was at the north pole and she could not get warm, it was like an internal earthquake", "breaking into shivers like she was at the north pole and she could not get warm, it was like an internal earthquake", "Then the heat turned on; for 4 hours she was burning up and sweating", "Then the heat turned on; for 4 hours she was burning up and sweating", "extremely tired", "her arm hurts/soreness in the arm", "had a headache that she had never had before unlike any other", "Nauseated", "flu like discomfort", "suffered upset stomach", "Weak", "4 hours like scarlet fever". The following information was reported: CHILLS (non-serious), outcome "recovering", FEELING COLD (non-serious), outcome "unknown" and all described as "breaking into shivers like she was at the north pole and she could not get warm, it was like an internal earthquake"; BURNING SENSATION (non-serious), outcome "unknown", described as "Then the heat turned on; for 4 hours she was burning up and sweating"; HYPERHIDROSIS (non-serious), outcome "unknown", described as "Then the heat turned on; for 4 hours she was burning up and sweating / I would go in to sweat like a fever in sweat for another 4 hours"; FATIGUE (non-serious), outcome "unknown", described as "extremely tired"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "her arm hurts / soreness in the arm"; HEADACHE (non-serious), outcome "recovered", described as "had a headache that she had never had before unlike any other"; NAUSEA (non-serious), outcome "unknown", described as "nauseated"; INFLUENZA LIKE ILLNESS (non-serious), outcome "unknown", described as "flu like discomfort"; SCARLET FEVER (non-serious), outcome "unknown", described as "4 hours like scarlet fever"; ABDOMINAL DISCOMFORT (non-serious), outcome "unknown", described as "Upset stomach"; ASTHENIA (non-serious), outcome "unknown", described as "I would be weak". Therapeutic measures were taken as a result of headache, nausea. Additional information: The caller stated she had taken all of the Pfizer Covid vaccine shots, the primary and all the boosters. She stated it had been about 5 months since her last booster dose. She stated she was the only one her age that had her age that had the reactions she did and she read in the fact sheets and it said mild symptoms and she did not thought her symptoms were mild. Because of her reaction she was reluctant to take the next dose and wanted someone to tell her but the CDC and the doctors do not help. She stated she received the first two shots, no problem, the only major thing was a little fatigue and her arm was sore. She stated the booster dose, problem: She got the vaccine at noon and went and ran errands and at 10:00, she started breaking into shivers like she was at the north pole and she could not get warm, it was like an internal earthquake. Then the heat turned on; for 4 hours she was burning up and sweating. The next day the shivers and heat subsided and she was extremely tired and of course her arm hurts, it always hurts after. She had a headache that she had never had before unlike any other. She was also nauseated. Her headache subsided after she took Tylenol. The flu like discomfort lasted about a week. The next time (next booster dose)- she got the vaccine at noon, ran errands and at 10:00 almost to the point it all happened again. The third time (next booster dose), it happened again. She stated she does not consider 4 hours of shivering mild, 4 hours like scarlet fever. She had a healthy body. For her body to go into that state seemed rather extreme. She had read that fact sheet and all she was getting was okay thanks, for nothing. She wish some people at Pfizer would be like here were more severe side effects that may occur. After providing that there were some more severe side effects listed like allergic reactions she stated she did not see that in the fact sheet. The caller stated she already reported this and provided the previous agent with all the numbers for each vaccine and all of the information regarding this. The caller wanted to know if she should receive the next booster after all of this? She wanted someone to tell her whether these side effects were more than "mild." She wanted to know who can determine this for her? She doesn't know if there is a long term side effect or what it is doing to her body. The consumer stated that she had all her initial shots and all the boosters and so she thought it's then time she should get another one they say you get another one, right? You keep getting them if you are 80 but or do you stop getting them? The consumer stated that she got the Pfizer shot for the COVID- 19, she did not know what it's called. When paraphrased the concern, Consumer stated, Yes, correct. she wanted to know should she, number one? If I answer that question then I have a follow-up question which is the primary reason she was calling. Consumer was informed about the role of Pfizer Drug Safety and Pfizer Medical Information. Consumer stated, Okay, well now was she supposed to report that she had felt like she had adverse symptoms to this department? Because that's determining whether she wanted to take next one or not, for the last few shots she did know she had read all the reports about the have suffered a mild symptoms, she did not think her symptoms were mild, the first time she didn't notice it was going to happen, so the second, third time okay she thought she will be prepared with food and suffered upset stomach because the three time, 10 hours after she got the shot almost to the minute because she got the shot at noon and she went about doing her business and everything that happened at the time of shot was the soreness in the arm but at 10 o'clock that night for 3 times she would break out in the chills, she mean really bad chills like she was suffering from some disease and she would last about 4 hours, then the chills would stop and she would go in to sweat like a fever in sweat for another 4 hours, so then those with the side and she would be weak and nauseated and she had never had headache, she was in good condition, her vitals were good, she was over weight other than that I take blood pressure pill (Losartan) and something for reflux, Omeprazole and those are really 2 prescription she took for pretty good. Anyway for entire week she was just no good, she was disreg she don't consider, and then her friend through her age or little younger ones her age, the only symptoms they she was had soreness in the arm, now she had read that people say well it just means the shot was working, well it's having a hell of war with me so they must be working damn good to put her out for a week, she was wondering the next shot if she should take it if you understand because that was a week of her body going through (Incomplete sentence). When paraphrased the concern, Consumer stated, Yes because she know COVID is still around, she wear the mask and as much as possible if you go out to eat it was still going to be vulnerable to the people, you always going to take your mask on vacation. Consumer was informed about the role of Pfizer Drug Safety. Lot number for dose 4, Consumer stated that well she could not read that she would tell you what it looks it, she was going to give you her best guess, she could not tell it's F or P M0173. That's all she had. Consumer further stated, she had got another number but she don't know if this is a Pfizer product they have put it on COVID vaccination record but it got a different name and a lot number on 10Jun2022, she will give it to you but it look like BHAUERIC that's the name she guess. When she got it, she asked Pharmacist for a COVID card and this is what he wrote a Lot# but it doesn't say Pfizer on it she have been getting the Pfizer shot she thought but she can't really read the writing and then there is a number underneath it looks like the name and then it says GH9694, is that a Pfizer product? she told you she gave you those letters that's the first thing and then there is a number, she was giving you everything. she hope this is Pfizer (As consumer was unsure if the details were of Pfizer COVID Vaccine or any other vaccine, hence product details not captured in tab). Other Medical Conditions or Other Medications: Consumer stated, For blood pressure Losartan and Omeprazole, well she took a bunch of Vitamin supplements. Prior Vaccination (within 4 weeks): Consumer stated, The last vaccine she took a flu shot at the same time, she put her cards away but over the last day for the COVID vaccination which one she had the flu shot. Consumer stated that the day of the last COVID vaccine she gave you, she put the cards away. Consumer stated that tylenol and something for nausea but she did not remember she had chewable, Tums she think.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300214238 same patient and drug, different dose and event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure abnormal (I take blood pressure pill (Losartan)); Reflux esophagitis (something for reflux, Omeprazole)
- Vorgeschichte
- Medical History/Concurrent Conditions: Overweight (I am over weight)
- Andere Medikamente
- LOSARTAN; OMEPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 24.05.2023
- Impfdatum
- 18.05.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 206,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Fear
Feeling hot
Pyrexia
SARS-CoV-2 test positive
Somnolence
Symptomtext
I was fine but at ten at night I begin to feel tired and sleepy. I went to bed on 11DEC2022 at five aM I was very very hot and I was frighttend, I took my tenperature it was one hundred degrees I took Tylenol and went back to bed my fever upon waking up had spiked to onehundred one hundred and I was positive for COVID-19. A couple of hours later my fever continued to rise and my coughing started, a second test showed a clear positive result. A drive through PCR test also resulted in a positive. Fatigue for months was a factor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 12DEC2022 COVID-19 Test-Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin; Calcium; Omega 3 ; Vitamin D
- Allergien
- Avalox
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 28.05.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash pruritic
Symptomtext
Rash started to break out within 36-40 hours after taking the vaccine. It lasted 18-19 days after the vaccine. With a lot of itching and it looked like chicken pox.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- infected tooth
- Vorgeschichte
- -
- Andere Medikamente
- no
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 09.01.2023
- Impfdatum
- 10.08.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 139,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Fatigue
Headache
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I had the symptoms on 12/27/2022 which were headache, fatigue, tiredness and a little bit of chills and sore throat. I slept all night at took an at home test on 12/28/2022. I had a televisit with a physician's assistant 12/28/2022. I still have a little bit of fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 12/28/2022 COVID-19 test positive, 01/07/2022 COVID-19 test negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D; vitamin B12; iron
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 18.06.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Ageusia
Anosmia
COVID-19
Influenza A virus test positive
Productive cough
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Symptoms began with a fever as high of 102 that lasted for about 2 days, and I tested positive for COVID-19. On the second day my fever broke. I had some productive coughing and congestion. But I tested positive a second time on September 9, 2022. I lost my sense of taste and smell the first time I tested positive. This symptom lasted for about 3-4 weeks. I also tested positive for Influenza A on November 15, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 tests, positive, 092022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol; Acid Reflux
- Andere Medikamente
- Atorvastatin; Pantoprazole; Escitalopram
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 02.12.2022
- Impfdatum
- 02.06.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Injection site swelling
Pain
Pyrexia
Symptomtext
I had swelling at the injection site and minor pain. I had a low-grade fever, and sweating. This lasted for 2 days. I went to my doctor and spoke with him about it, but he did not prescribe any medications for this. I am not dealing with this at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetic; High Blood Pressure
- Andere Medikamente
- Losartan; Amlodipine; Humalog; Lantis; Klonopin
- Allergien
- Benadryl; Barium; Morphine; Contrast Dye
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 29.11.2022
- Impfdatum
- 21.06.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Computerised tomogram
Facial pain
Haemorrhage
Hyperhidrosis
Laboratory test
Lip pain
Malaise
Neuralgia
Neuropathy peripheral
Pain
Pain in extremity
Temperature intolerance
Urine analysis
Symptomtext
I had the booster on June 21, 2022, when I had peripheal nuropathy a few days later, I just thought it was anxiety as I was going through a stressful time with my husband?s eye cancer and our sons divorce. Dr. put me on Lexapro, it went back a few weeks later as it was so painful and it wasn?t working, she put me on Cymbalta, that worked better but still had low level pain. Went back again in the middle of August and she increased dosage. I finally got off it in September. I felt fine for about 5-6 weeks. I had another booster on 10/13 as we were traveling. Eleven days later I was back in intense pain. I didn?t connect it with the vaccine but then my son-in-law pointed out that some were having vaccine reactions that fit my symptoms. My Dr put me on gabapentin. I am getting better again but hoping to never get another vaccine. I had severe face/lip/limb pain, heat intolerance and breaking out in a sweat around my neck. It was so bad I thought I needed to go to the ER but did not go. It would come in waves, somedays better than others. Shooting pain in different parts of my body and when it was bad and overall malaize that just was horrible. I suffered!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial pain
- Hospital-Tage
- -
- Labordaten
- I was tested to make sure it wasn?t B12 deficienty, urine test as I had a bleeding incident. At my insistance my Dr. had a C-Scan done because I though I must have cancer or something is truly wrong. I am still suffering a low level of the all over nerve pain.
- Aktuelle Erkrankungen
- No illness but under a lot of stress so I attributed it to that
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin B, D3, Omega 3, multi-vitamin
- Allergien
- Cipro years ago
- Vorherige Impfungen
- There have been two
- Staat
- MI
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 11.11.2022
- Impfdatum
- 07.06.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 134,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cold sweat
Feeling abnormal
Feeling of body temperature change
Malaise
Nasal congestion
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
I went to my grandson's football game over the weekend. I started feeling like I was getting a cold on Tuesday, my daughter told me to test myself. I used a home COVID-19 test. It came back negative, I still felt bad on Wednesday, so I retested this time it came back positive. I did not want to believe it came back positive, so I retested on Thursday. This time I called my doctor and told her I had cold like symptoms, tested and it came back positive for COVID-19. She called me in prescription for PAXLOVID that I started taking that night. I had hot and cold sweats, stuffy nose, it felt like a head cold to me. By Sunday I was feeling better and testing negative for COVID-19. I thank God for PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Blood Pressure; COPD
- Andere Medikamente
- Metoprolol; hydrocodone; vitamin C; fludrocortisone; omeprazole
- Allergien
- No
- Vorherige Impfungen
- Pneumonia, my arm swelled up with a big lump on it.
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 09.05.2022
- Beginn
- 23.07.2022
- Tage bis Beginn
- 75,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
Not adverse as result of vaccine (as I told caller!) Contracted Covid in July 2 months after vaccine. Had usual symptoms and took Paxlavid as prescribed by Urgent Care. Tested negative 10 days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Tested positive for Covid on 7/24/22 at Urgent Care. Received Paxlavid and began treatment that night. Tested negative 10 days later.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma (mostly as a child)
- Andere Medikamente
- Estradiol patch (.25), Flonase, Premarin Cream (1gm), Multi Vitamin, Calcium + D, B-12 (1000mg), Biotin, Align
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 05.11.2022
- Impfdatum
- 02.07.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Pain in extremity
Wrong product administered
Symptomtext
The patient signed up for a shingles vaccine, second dose. He believed he was receiving the second shingles vaccine, but was given a covid-19 pfizer vaccine dose, 0.3 mL in L arm. Patient realized yesterday 11/4/22 as he was looking at his documentation that he was not given Shingles dose #2. He came into the clinic today to report this error and to receive his shingles vaccine. He reports after the pfizer vaccine, he had fatigue and a sore arm for a few days-1 week. No difficulty breathing, rash, chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 01.07.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 94,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Headache
Lymphadenopathy
Myalgia
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
Symptomtext
congestion, rhinorrhea, sore throat, myalgias, headaches, adenopathy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 27.10.2022
- Impfdatum
- 25.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Headache
Influenza like illness
Injection site reaction
Limb discomfort
Lymphadenopathy
Myalgia
Parosmia
Peripheral swelling
Skin swelling
Vomiting
Symptomtext
He got his vaccine, when he got the vaccine he got just a little bit of headache which went away. He smelled something chlorine smell when he got his vaccine and then it went away. Had no further symptoms and didn't feel anything. Then Wednesday night he went to bed and started getting muscle aches in his arms like he had the flu. He also then noticed a headache. He got up because he was feeling weird around 3:00 AM this morning, with the arm bothering him. He kept feeling on the outer arm where the shot was he could feel something. He raised his left arm up and he noticed that it was swelling under it. I thinks it was his lymph nodes in his armpit area. Then all of a sudden he laid back down and when he woke up all of the symptoms went away except for the armpit which is still a little puffy. He did not take anything for his symptoms. He did call his doctor and they told him that it was very normal for that to happen, that the lymph nodes swell up sometimes but should go away within 2 weeks. He then called his job and spoke with the nurse and he told her that he was having a reaction, and she told him that it was perfectly normal, and told him the same thing that his doctor told him. On Tuesday he ate dinner and he was talking his dog out for a walk, and he started throwing up like crazy outside. Then it just went away. It did not happen again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Thyroid caner with removal of thyroid, high blood pressure, asthma.
- Andere Medikamente
- Synthroid, Amlodipine, Calcium, Magnesium.
- Allergien
- Cashews (throat itching and vomiting), pistachio too.
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 06.06.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 96,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
congestion, headache, tired, coughing, O2 between 87 and 92 after fixing something to drink and walking across room
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Positive for Covid
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure controlled with med
- Andere Medikamente
- Losartan 100 mg, Cetirizine (generic allergy), senior multi-vitamin, baby asprin, calcium + D
- Allergien
- e-miacine, high blood pressure med that makes you cough, neosporin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 12.05.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 145,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Erythema
Rash
Symptomtext
Submitted per patient request- Pt presents to the clinic today for a rash to left arm. She reports that she had a Pfizer booster in May. She had previously not had a reaction. This was her fourth dose. She did have COVID-19 in August. She noticed the rash presented to the left side of the arm where she received her shot at the beginning of September. Denies any changes to soaps detergents, exposure to plants, environmental changes, or pain to the site. She states that it has decreased in size/ redness and has improved. Denies any fevers, chills, swelling, drainage or pustules, to the arm, hives, or systemic reaction, lymphadenopathy or changes in sensation. She is well today otherwise, just wants to be sure that she is OK and make sure that it is reported as a reaction. Does have a derm that she sees. Will send him a copy of this report and we will follow her reaction. Denies any systemic reaction after she received her last dose or any other doses. She has been using hydrocortisone OTC for her symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Small vessel disease Elevated Cholesterol
- Andere Medikamente
- Vitamin C Plavix Simvastatin Multi Vitamin- Women's one a day
- Allergien
- Shellfish Aspirin Wheat
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Pain
Vaginal ulceration
Symptomtext
Product was administered 19 days after refrigeration expiration date but before 1 year post manufacture expiration date. Patient states she developed vaginal ulcers 2-4 days after vaccine administration, saw a provider who prescribed an antibiotic, a narcotic for pain, and lidocaine for pain. The ulcers cleared up after 7 days from onset and denies any further issues or complications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 28.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
My arm is still sore; 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 58-year-old male patient received BNT162b2 (BNT162B2), on 28Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 58 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (First Dose, Lot Number: EN6201), administration date: 11Feb2021, when the patient was 56-year-old, for COVID-19 immunization; BNT162b2 (Second Dose, Lot Number: EN6025), administration date: 06Mar2021, when the patient was 56-year-old, for COVID-19 immunization; BNT162b2 (Third Dose/Booster Dose, he can barely read it on his card, reports Lot Number as FF8841), administration date: 11Oct2021, when the patient was 57-year-old, for COVID-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "not recovered", described as "My arm is still sore". Additional information: Caller mentioned that he got the Pfizer Booster Vaccine on 28Jun2022 and his arm is still sore from that booster. The caller stated that it has been three months and he has questions regarding this side effect. Caller stated that right after the vaccine it was the usual soreness like the other vaccines. It was really sore for a day or two. Since then, especially when he goes to the gym or golfs, he notices that it is more prevalent. Caller stated that he can also feel it if he sleeps the wrong way on his left arm. Stated that he feels it and its not like a bruise, it feels like it is inside of his arm. Caller stated that it has been ongoing and persistent. States that lately in his workouts he has been trying not to use his left arm as much. Then today he did use it, and now he was really feeling it. Patient did not receive any vaccinations within four weeks prior to the first administration date of the suspect vaccine. Caller denies any other medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- 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
- AZ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 14.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 16,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Muscular weakness
Symptomtext
Starting on 6/30 my elbow started to bother me a bit. I eventually began to experience sharp pain in my elbow that travelled up my arm. I began to use my left hand more because I felt the strength in my right arm/hand had gotten weaker. I developed shoulder pain sometime in July. I went to my doctor around July 20th and was prescribed a rehabilitation medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure; high cholesterol
- Andere Medikamente
- Atorvastatin; Lisinopril; Escitalopram; Vitamin E; Vitamin D3; Fish oil; Omeprazole; Fenofibrate;
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 03.06.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 53,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure to SARS-CoV-2
Fatigue
Headache
Pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case. Around family who tested positive for COVID-19. Started feeling really tired with body aches and a headache. Took a Home COVID-19 test, and it was positive. Had a telehealth visit with Dr. at the clinic and was prescribed PAXLOVID. Started feeling a little better about a week later. Took another COVID-19 test and tested negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test - positive. Home COVID-19 test - negative, 3 weeks later.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Naproxen sodium occasionally; calcium with vitamin D
- Allergien
- Penicillin; codeine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 26.07.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Impaired work ability
Interchange of vaccine products
Limb discomfort
Memory impairment
Muscle spasms
Pain in extremity
Symptomtext
Legs are giving out on me; Feeling very brain foggy; Actually interfering with my job; it is like I am in a zone, I hear what she says and then I don't even remember; weird leg cramps; Actually interfering with my job; it is like I am in a zone, I hear what she says and then I don't even remember; weird leg cramps/short pain; I did get the Pfizer instead of the Moderna this time because I got really sick with the Moderna; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34-year-old female patient received BNT162b2 (BNT162B2), on 26Jul2022 as dose number unknown (booster), single (Lot number: FM0173) at the age of 34 years for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: VITAMINS NOS; FISH OIL; IRON. Vaccination history included: Moderna, administration date: 2021, for covid 19 immunization, reaction(s): "got really sick ". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 2022, outcome "unknown", described as "I did get the Pfizer instead of the Moderna this time because I got really sick with the Moderna"; IMPAIRED WORK ABILITY (non-serious), MEMORY IMPAIRMENT (non-serious) all with onset Aug2022, outcome "unknown" and all described as "Actually interfering with my job; it is like I am in a zone, I hear what she says and then I don't even remember"; FEELING ABNORMAL (non-serious) with onset Aug2022, outcome "unknown", described as "Feeling very brain foggy"; LIMB DISCOMFORT (non-serious) with onset Aug2022, outcome "unknown", described as "Legs are giving out on me"; MUSCLE SPASMS (non-serious) with onset Aug2022, outcome "unknown", described as "weird leg cramps"; PAIN IN EXTREMITY (non-serious) with onset Aug2022, outcome "unknown", described as "weird leg cramps/short pain". Therapeutic measures were not taken as a result of limb discomfort, feeling abnormal, impaired work ability, muscle spasms, memory impairment, pain in extremity. Additional information: Patient stated, "The reason for my call ma'am, I just got done reaching out to the pharmacy and I am going to be honest with you, I don't know if it is from the vaccine. I know that I for sure that I do not have COVID, but I have noticed, I got my Pfizer last month at the end of the month. I believe it was 24Jul, I am not exact, but I did get the Pfizer instead of the Moderna this time because I got really sick with the Moderna, but I have been noticing, I have been having like weird leg cramps. They kind of come like a short pain, like come and go. It is like throughout the day and sometimes I am still like my legs are giving out on me since I got that booster, and I don't know if it just me in my head over thinking. I find it a little concerning. I never had this problem before. I am fairly young, I am only 34 years old, and I have been noticing this since, I got my Pfizer. So, I am not sure if this is a common side effects that people have been reporting but I also do feel I have been feeling very brain foggy since I got the vaccine too." Patient stated, "Yes, it is actually interfering with my job. I have been noticing it like throughout the day at work. There is sometimes like, I will be talking to my boss and I just totally, it is like, I am in a zone, I hear what she says and then I don't even remember, and I have been noticing this since I got the booster, and I did wait quite some time since I got my Moderna. It has been almost over a year." Patient started noticing side effects about two weeks after the vaccination. Any prior vaccinations (within 4 weeks): Patient stated, "No, I have only been waiting to get my flu shot until October."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- VITAMINS NOS; FISH OIL; IRON
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 01.06.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 82,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal discomfort
COVID-19
Cough
Diarrhoea
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Positive test and symptoms for Covid 19. High fever, malaise, sore throat, cough, intestinal distress, diarrhea. 8/22/2022 2-1/2 months after 2nd booster. 1,2, 1st booster were all Pfizer-biontech. 8/23/2022 telemedicine Dr who prescribed Paxlovin. Started dosage 7:30 PM 8/23 and continued 5 days. Felt better by 10PM 8/23 continuing for duration of prescription and following. Symptoms remaining are slight malaise, and strange stomach flutters. Wellness sched 9/6/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- (Was scheduled 9/1 but Dr rescheduled to 9/6). Covid-19 Home rapid 15min test on 8/22/2022. Wife tested pos Covid19 8/21/2022 also.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetic
- Andere Medikamente
- Metformin, atorivastin, glucosamine msm, centrum multi-vit,
- Allergien
- Chlorhexidine gluconate, seasonal allergies, mold
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 31.05.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 64,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody positive
Arthralgia
Myalgia
Red blood cell sedimentation rate increased
Symptomtext
Elevated Sedimentation Rate - repeated blood work, symptoms: pain in joints and muscles Positive ANA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 8/2/22 Sedimentation Rate - 53 8/16/22 Sedimentation Rate - 23 8/2/22 ANA - positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Rheumatoid Arthritis, Diverticulosis, Hypothyroidism
- Andere Medikamente
- Levothyroxin, Trintellix, omeprazole, fish oil, allegra, Flonase
- Allergien
- erythromycin, penicillin, bactrim, iodine dye, Wellbutrin, Levaquin, codeine, doxepin HCL, Zoloft, Gabapentin, tetanus-Diphtheria Toxoids
- Vorherige Impfungen
- Td- severe swelling and pain at injection site.
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 22.08.2022
- Impfdatum
- 22.05.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
On the day I tested positive for COVID-19 I had a scratchy throat and clear nasal discharge. The next day I woke up with a 102 fever, dry cough, and really tired. I called the doctor and she prescribed me Paxlovid. My symptoms lasted for 2-3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19- 07/22/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Melatonin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 18.05.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram abnormal
Exposure to SARS-CoV-2
Headache
Heart rate increased
Pyrexia
SARS-CoV-2 test negative
Symptomtext
I got out the shower and was getting ready for work and my smart watch went off and stated my heart was at a dangerously high rate. I sat down and drank water to see if it will go down, it did a little bit. But when I got up and walked it would go back up. Through the day it would fluctuate 121/100 so I called the doctor. I was also exposed to someone with covid-19 within the past week, I took a covid-19 test at the doctor and it was negative. At the doctor they checked my heart rate and it was 80 something while sitting down. When my heart rate went up initially I immediately got a headache and I have a history of migraines. I spoke to the nurse at my cardiologist office. Mid morning I was awaken to a headache and took my heartrate and it was 121. I called my Cardiologist who sent me for an EKG and when they did it yesterday they said I was also running a fever. They also did a COVID-19 test and it was negative and they told me I could have a virus that mimics Covid-19 but is not. They said hopefully it will clear up in a few days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- EKG, a little bit outside of normal. I'm waiting to see if there are any tests to do, COVID-19 - negative.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Lung disease MAI; Immunocompromised CREST
- Andere Medikamente
- Diacylamine; TOPAMAX; famotidine
- Allergien
- Azithromycin; codeine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 22.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Immunisation reaction
Pruritus
Urticaria
Symptomtext
Patient had vaccine on 7/22/22 and three days late, she breaks out in hives. these are generalized hives all over the body. the itch mildly. Patient has been to her primary care, OBGYN, allergist, dermatologist, perinatologist, Patient has not been given anything for these hives and there was no other cause attributed to the hives exception suspicions that the vaccine may be the cause. Patient had self-medicated with Benadryl but there have been no improvements. patient reports more hives keep appearing on her body and it's getting worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- done at the doctors' office.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- penicillin, cephalosporins
- Vorherige Impfungen
- Gardasil
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 28.06.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Pain
Pain in extremity
Panic attack
Symptomtext
Pulsation/pain in upper legs, swelling and burning in legs, started about 4 days after vaccine and comes and goes. Causes her to have panic attacks. Had symptoms with other dose(s) as well, Does have bad varicose veins, stents, pacemaker as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- She has a pacemaker and stents since 2001, very high cholesterol and HBP, diabetic.
- Vorgeschichte
- Same as above
- Andere Medikamente
- Cholesterol, HPB and diabetes meds.
- Allergien
- Did not provide any information.
- Vorherige Impfungen
- Pfizer BioNtech primary series (March/April, 2021) Age 67
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 21.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
On the same day at 11:30AM after my vaccine I started to feeling pain on the right side of my head with headache for about a week. I went to my doctor on 07/28/2022, she diagnosed me with mild - moderate migraine. She prescribed me sumatriptan 50 milligram 10 tablets. Am still taking the medication as of today 08/05/2022. I've never experienced anything like this with my other vaccines. Some times the head is so severe and sometime its moderate. I will consult with my doctor again since, it hasn't stopped yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D; B12
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 19.07.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood culture
Chest X-ray
Confusional state
Echocardiogram
Full blood count
Inflammatory marker increased
Injection site pain
Injection site swelling
Metabolic function test
Pain
Pyrexia
Urine analysis
Symptomtext
Directly after shot mild: swelling at the injection site and pain Starting 1 Week after vaccine date: Full body aches and pains, eventually turned to severe aches, pains, confusion, 104F fever, and elevated inflammation levels requiring hospitalization on 7/29/22 and was held in hospital until 8/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- 4,0
- Labordaten
- echocardiogram chest x ray blood cultures, cbc, metabolic panel, urinalysis
- Aktuelle Erkrankungen
- Teratology of Fallot inflammatory connective tissue disease Depression Anxiety
- Vorgeschichte
- Congenital Heart Defect Chronic Inflammation
- Andere Medikamente
- Vraylar Hydroxychloroquine Zoloft Klonopin Melatonin Theanine Probitotics Multivitamin
- Allergien
- Sulfa Drugs Psudafedrine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 02.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 17,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Amnesia
Headache
Laboratory test normal
Lymphadenitis
Oropharyngeal pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
Transient global amnesia
Symptomtext
I received my 2nd Covid booster and 1st Shingrix vaccination on the same day 07/02/2022, before taking a trip to visit family. My lymph nodes were inflamed, body aches and a fever for 2 days after the vaccines. 07/14/2022, I flew. 07/16/2022, my family tested positive for Covid. I have tested negative despite having a sore throat, runny nose and slight headache. 07/19/2022, I lost my memory for about 6 hours. I had no idea where I was, or why. I knew who I was but kept repeating myself. I went to the ER, they admitted me for two days to do extensive tests on my heart and brain. All test results were good. I was discharged 07/22/2022. Diagnosis was Transient Global Amnesia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Every test was done that you would expect from a leading hospital. And too many to list here.
- Aktuelle Erkrankungen
- seasonal allergies
- Vorgeschichte
- n/a
- Andere Medikamente
- Probioic, Vit D3, Calcium, Zyrtec
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 03.08.2022
- Impfdatum
- 17.07.2022
- Beginn
- 24.07.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Nasal congestion
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough Case of COVID-19; Nasal Congestion, Dry Cough, Low Grade Fever, Headache. I was given vitamin C and Zinc by the Dr.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR Test Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Asthma; Gout.
- Andere Medikamente
- Vitamin D; Vitamin E; Fish Oil; Hyzaar; Colchieine; Lipitor; Flomax; Norvasc; Singulir; Zyloprim.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 14.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Malaise
Rash
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Contracted Covid. Symptoms began on 6/28. I thought it was a reaction to prednisone, which I had just started for a severe rash. Scratchy throat. Progressed to congestion. Severe congestion developed on day 4 and cough for two weeks. Cough is still lingering one month later. I am not normally on prednisone, and since I had just started it, did not list it as a medication because it was only for two weeks? So I was taking prednisone while experiencing Covid symptoms. No fever. No fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Had PCR test on July 11. Still positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Acid reflux, where acid goes into lungs, not typical heartburn and causes coughing.
- Andere Medikamente
- Prevacid, Ramipril, Vitamin D
- Allergien
- Imodium, Doxycycline, contrast dye
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Discomfort
Fatigue
Hypoaesthesia
Symptomtext
Heavy Legs, Facial Burning, Numbness in legs, Exhaustion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- hypertension
- Andere Medikamente
- Olmesartan Amlodipine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 20.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Cough
Headache
Myalgia
Nasal congestion
Oropharyngeal pain
Pain assessment
Pyrexia
Retching
Symptomtext
Cough; Sore throat; Stuffy nose; Dry heaving; Fever; Muscle pain; Severe headache; 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 29-year-old female patient received BNT162b2 (BNT162B2), on 20Jul2022 at 14:00 as dose 1, 0.3 ml single (Lot number: FM0173, Expiration Date: 06Dec2022) at the age of 29 years intramuscular, in right arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PYREXIA (non-serious) with onset 26Jul2022, outcome "recovered" (27Jul2022), described as "Fever"; MYALGIA (non-serious) with onset 26Jul2022, outcome "unknown", described as "Muscle pain"; HEADACHE (non-serious) with onset 26Jul2022, outcome "not recovered", described as "Severe headache"; COUGH (non-serious) with onset 27Jul2022, outcome "not recovered"; RETCHING (non-serious) with onset 27Jul2022, outcome "not recovered", described as "Dry heaving"; OROPHARYNGEAL PAIN (non-serious) with onset 27Jul2022, outcome "not recovered", described as "Sore throat"; NASAL CONGESTION (non-serious) with onset 27Jul2022, outcome "unknown", described as "Stuffy nose". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient got first vaccine on 20Jul2022 and had really bad reactions the day before this report. The patient spent most of the day before this report from 4am-12 pm with a 102 fever and was in so much pain from muscle pain and headache.The fever started at 4am in the morning and broke the day before this report about 1 pm and then got another one that started last night and broke about 4am this morning. Still had headache and the fever broke around 2am in the morning on the day of reporting. The patient worked in animal medicine.There was no history of previous immunization with the Pfizer vaccine considered as suspect. No additional vaccines administered on Same Date of the Pfizer Suspect. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. There were no AEs following prior vaccinations. No family history relevant to AEs. There were no relevant lab tests. The events did not result in emergency room/physician visit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220726; Test Name: Fever; Result Unstructured Data: Test Result:102; Comments: spent most of yesterday from 4am-12 pm with a 102 fever; Test Date: 20220726; Test Name: Muscle pain; Result Unstructured Data: Test Result:11; Comments: muscles on a scale of 1-10 were an 11.
- 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
- AR
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 31.05.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chills
Cough
Decreased appetite
Gait inability
COVID-19
SARS-CoV-2 test
Vaccination failure
Hypoaesthesia
Influenza like illness
Nasal congestion
Nausea
Pain
Pain in extremity
Somnolence
Symptomtext
Tested positive; Tested positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 75-year-old female patient received BNT162b2 (BNT162B2), on 13Mar2021 at 14:00 as dose 1, single (Lot number: EN6200), in left arm, on 01Apr2021 at 15:00 as dose 2, single (Lot number: EP7534), in left arm, on 22Nov2021 at 23:00 as dose 3 (booster), single (Lot number: FH8030, Expiration Date: 28Feb2022), in left arm and on 31May2022 at 11:00 as dose 4 (booster), single (Lot number: FM0173) 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 02Jun2022 at 08:00, outcome "recovering" and all described as "Tested positive". She got her covid shot on 31May2022. She tested positive on 02Jun2022. She self-isolated and treated herself with old covid medicine and antibiotic from an old dental work. She stayed sick for the first part of Jun. She started feeling a little better around 14Jun2022. She was able to leave her house. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (02Jun2022) Positive, notes: I tested positive on 02Jun2022. 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
- Back pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220602; Test Name: Covid-19 Test; Test Result: Positive ; Comments: I tested positive on 02Jun2022
- 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
- 68,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 61,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Nasal congestion
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
Sneezing, cough, body aches, fever of 100.6, nasal and chest congestion, headache, fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Tested positive for COVID-19 on 07/20/2022 at 4:16 PM Pacific Daylight Time via On/Go self-administered at home COVID-19 test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HIV+ since 03/1985; Elite Controller of HIV; Antiretroviral Na?ve Hyperlipidemia Essential Hypertension IBS Arthritis Depression Insomnia IBS Hypothyroidism Anxiety Essential Hypertension Essential Hypertension Migraine 7.5 mg Dry mouth GERD Kidney stones Migraine Migraine HSV
- Andere Medikamente
- Amoxicillin 500 mg; Atorvastatin 40 mg; Chlorthalidone 50 mg; Celebrex 200 mg; Colestipol1 GM IBS desvenlafaxine er 50 mg; Eszopiclone 3 mg; Hyoscyamine ER .375 mg; Levothyroxine 75 mcg; Lorazapam 1 mg; Losartan 100 mg; Metoprolol 50
- Allergien
- Lactose intolerance Amlodipine allergy
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash macular
Symptomtext
RED BLOTCHES ON ARM, LEGS, AND FEET.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- NONE.
- Aktuelle Erkrankungen
- spine arthritis/vertigo
- Vorgeschichte
- spine arthritis/vertigo
- Andere Medikamente
- Fish Oil 1000mg 1 AM Vitamin E 400 IU 1 AM Calcium 600mg 1 AM Daily multi vitamin & mineral 1 AM Valtrex 500mg 1 AM Estradiol 0.0375 MB 1 x2 a week Atorvastatin 10 mg 1 AM Baclofen
- Allergien
- none
- Vorherige Impfungen
- RED BLOTCHES ON ARM LEGS FEET.
- Staat
- IL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Hypoaesthesia
Lymphadenopathy
Pyrexia
Swelling
Symptomtext
She got her vaccine, the next morning she had a swollen armpit. Then it progressed to her neck on the right side, same side as the vaccine was given. She took Tylenol for it and drank more water and Gatorade. It is still the same. After 2 days she put cold compresses to her armpit, which alleviates the numbness but she can still feel occasional numbness on the right arm/hand area. Her neck is swollen, bulging area and she feels like there is a lymph node that is inflamed. She also feels feverish, and had chills one night, but the following day it wore off. She did have swelling with the other vaccines in the armpit, but not in the neck area, which wore off in about 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Eggs, shellfish.
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 15.07.2022
- Beginn
- 15.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Eye pain
Myalgia
Peripheral swelling
Pruritus
Rash
Rhinalgia
Symptomtext
I received my 4th dose on 07/15/2022 and my adverse event started with in couple of hours of the vaccine, swollen arm; muscles aches; my joint hurts; rash on my back, face, and chest; itching; nose hurt; and eye hurts. I went to the rheumatologist who prescribed me steroids and then I went to my regular doctor gave me antibiotics and ALLEGRA. I was on the medication for 10 days. I am fine now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- 3 Types of arthritis; Brain aneurysm; Chronic migraine; Trigeminal neuralgia; Sipitor Neuroglia; Hypoglycemia
- Andere Medikamente
- PLAVIX; PLETAL; methotrexate; folic acid; RESTASIS; testosterone; estrogen patch; PREMARIN cream; brigatinib; EMGALITY; REYVOW; TYLENOL; palanquin; pantoprazole; MOTEGRITY; DULCOLAX; B12 injections per month; multivitamins; supplements.
- Allergien
- Drugs; morphine; codeine; DEMEROL; LEVAQUIN; ZOFRAN; HUMIRA; metformin; VICODIN; diiodine
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 21.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site discolouration
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Large red, warm, swollen circle at injection site slightly larger than a tennis ball with some itchiness. Spoke with physician due to past cellulitis reactions to vaccines in left arm and discussed concerns due to knee replacement in April 2022. Treatment included antihistamines, cold compresses, and a short course (7days) of prophylactic antibiotic Doxycycline to mitigate infection concern. Symptoms as of 7/26/2022 have largely resolved with only slight pink area at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site discolouration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma (excellent control) , high blood pressure (on medication and controlled)
- Andere Medikamente
- Montelukast Sodium 10mg 1xdaily Lostartan 50mg 1Xdaily, mulitvitamin, calcium 600mh, OsteoBi Flex Triple Strength, Fish oil 1000mg
- Allergien
- Allergies to Bactrim, Ceftin, Erythromycin, Relafen, Orudis, and peanuts. Allergy tested positive for allergy to Methyl Methacrylate, p-tert-Butylphenol Formaledhyde Resin, and Quaternium 15
- Vorherige Impfungen
- Cellulitis reaction to Pneumovax 23 and Tetanus, subsequent injections of same have occurred with no adverse event.
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- 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: nein
Discomfort
Myalgia
Pain
Pain in extremity
Symptomtext
She got her vaccine, she had soreness in the muscle part of the arm. The soreness is felt when there is arm movement up and down. The soreness is also felt when there is movement away from the body, swinging outward from the body. There is also discomfort when she is carrying a weight on that arm, like a 1# weight. There is also discomfort when trying to sleep on that arm at night. She keeps thinking it is going away, and now it's been 6 weeks now and there has been no improvement and perhaps getting worse. She has not taken anything for it other than ice on it the first day. Did not have any reaction to the other three previous Pfizer vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Prempro, Baclovir, Telmisartan, Amlodipine, Biotin, multivitamin, Omega 3, probiotic, elderberry, vital protein collagen peptide.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 22.07.2022
- Impfdatum
- 09.06.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Malaise
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I contracted COVID-19 on 07/10/2022 with symptoms of scratchy throat, fever of 100.6, headache, body aches, fatigue, sore throat, and shallow cough. I was not prescribed any medications. I was ill for 8 days before my symptoms began to resolve. I am still experiencing a lingering scratchy throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab ihome test was positive on 07/12/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- 5 Surgeries for injuries sustained in car wreck which included transfusions; Heart Event
- Andere Medikamente
- Multivitamin; Vitamin B Complex; Magnesium; Furosemide; Losartan; Metoprolol; Spironolactone
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 21.07.2022
- Impfdatum
- 25.05.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 54,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of personal independence in daily activities
Pain in extremity
Symptomtext
patient called the pharmacy on monday july 18 and complained on pain in his arm since the administration of the covid vaccine on may 25 2022 which is interfering with his daily activities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 17.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Urticaria
Symptomtext
hives and Swelling of the lips
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 17.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Constipation
Cough
Feeding disorder
Headache
Pain
Respiratory tract congestion
Retching
Symptomtext
Full body aches and pains. Slept for 4 days. Severe headache, dry heaves, constipation, coughing and congestion. Could not eat, only sip water. Equilibrium loss when walking to bathroom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Intestinal bleeding; hiatal hernia surgery to close 5 cm hole performed October of 2019; constant nasal congestion during weather changes; persistent cough; nerve flares in feet, hands and back with arthritis.
- Andere Medikamente
- None
- Allergien
- Penicillin, Pollen, Bee Stings, Pepperoni
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 01.06.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 36,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
Back pain
COVID-19
Diarrhoea
Fatigue
SARS-CoV-2 test positive
Symptomtext
07/07/2022, I went to work and felt so tired, like I had run a marathon. As the day went on, I was struggling to finish my day. My stomach was so woozy. I tried coke, food, closed the store at 9:30 pm, had a 30 minute drive home, back hurt, wasn't sure I would make it home. My husband said I needed to take a test. Temperature was 98.5. First COVID-19 test negative, I started to have very bad diarrhea. 07/08/2022, second COVID-19 test positive. I work in retail and I am very careful. Restrictions have relaxed in the stores. Doctor prescribed Paxlovid and it made me extremely sick. I had a very extreme migraine. I was feeling pain by my pancreas, my heart was beating fast. I thought I was having a heart attack. My vision was blurry. My husband placed an emergency call to the doctor and they told me to stop the Paxlovid right away. I felt like there was a coating on my tongue as though I was eating metal. Finally by 7/11/22 I could sleep and felt better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- 07/07/2022 COVID-19 home test- negative 07/08/2022 COVID-19 home test- positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Paxil
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 8,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Pain in extremity
Symptomtext
Patient received the adult pfizer 0.3ml instead of the children's dose per mom 7-14-22 child has no side effects except for a sore arm which has gone away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none aware of
- Vorgeschichte
- none aware of
- Andere Medikamente
- not aware of any
- Allergien
- none
- Vorherige Impfungen
- sore arm
- Staat
- GA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Dysphagia
Rash erythematous
Rash macular
Symptomtext
Patient reported "mild chest tightness" 2 hours after receiving vaccine, which subsided over the next 4 hours. Six hours after receiving vaccine, patient reports "mild difficulty swallowing" with blotchy red rash scattered across the face and upper body. Patient made her personal physician aware; was instructed to report her experience to facility that administered the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 31.05.2022
- Beginn
- 03.07.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Infusion
Malaise
Pain
Pain in extremity
SARS-CoV-2 test positive
Symptomtext
I had a slighter sore arm after receiving the vaccine. I tested positive for COVID-19 on 07/04/2022. My symptoms started on 07/03/2022 with minor aching and coughing. I did not have a temperature. I went to an urgent care center to be checked out. They gave me an infusion (don't remember the name of the medication). Prior to going to the urgent care center, I took TYLENOL for my symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Home test for COVID-19 on 07/04/2022 and it was positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure; cholesterol
- Andere Medikamente
- Yes declined to provide details
- Allergien
- ACE inhibitors; LIPITOR
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Fatigue
Gait disturbance
Heart rate increased
Pain
Pain in extremity
Sleep disorder
Symptomtext
He received his vaccine, everything was fine, waited the 15 minutes and left with no problems, did a few errands and came home. As the afternoon progressed, toward the later part he was feeling more and more exhausted, tired. He had to lay down and could not stay awake anymore. He did feel a more rapid heart beat, not pounding, but notable more rapid heart beat than normal. He got up around 6:00 for dinner, did not feel like eating much. He was going to bed, felt more body aches, and had a horrible night with body aches and pains all over, he could not roll over easily without the pains, and could not lay on the injection site arm. Earlier vaccines that he had had a more stronger localized pain or punch and that was it. He had a system wide reaction instead and the heart. He did have a fever around 99-100 and could not sleep at all, was up 6 times during the night and some staggering around. This morning he got up around 8:30 and got a little more sleep in the later hours of the morning and to get up and moving around he was dragging. He was able to eat breakfast, still feeling fatigued, and can feel localized pain on the arm, but nothing to complain about. It was mainly the severe reaction during the night and the fever, which he did not have with the other vaccines. Other vaccines the arm injection site pain disappeared within 3 days. His major concern in this regard is due to his health status with his health conditions, and people not wearing masks, etc., worries him as the virus continues to mutate and if this is his 4th vaccine with the same as the past 3 times then what's going to happen if he has to get more vaccines to cover other mutations if he's reacting this way. He is a microbiologist that has retired. He did have COVID back in January of 2022, and those symptoms happened about a month with the fatigue, ongoing hacking cough and malaise. Also had a runny nose but not like a cold. It started with a severe sore throat that disappeared and about a month later his cough disappeared. He does have a rising aortal aneurysm diagnosed in the past, which also concerns him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure, diabetes, asthma.
- Andere Medikamente
- Telmisartan/Amlodipine, Metoprolol ER succinate, Trasiba insulin, Lumigan eye drops, Dorzolamide HCL with Timolol maleate.
- Allergien
- Penicillin, Erythromycin, Sulfa, Ceftin, Relafen.
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 27.05.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 39,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Nasal congestion
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sinus headache
Symptomtext
Starting 07/05/2022, I had a very bad sinus headache and fever (the highest it ever went was 100.7). I tested positive with an at-home COVID-19 test that same day. Other symptoms that I experienced were fatigue, sore throat and cough. On 07/06/2022, I called the doctor and, after reviewing my symptoms, told me to just take some over the counter medications and told me, if it got worse, to call back. The fever started going down and was gone by 07/07/2022. I took Tylenol for it. The headache was gone by then. I was just left with a cough, nasal congestion and fatigue. Today, 07/12/2022, I still have fatigue, a mild cough and congestion. The last time I tested myself was 07/10/2022 which was positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (07/05/2022): Positive; At-home COVID-19 test (07/10/2022): Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Pravastatin; Ezetimibe; Restasis; Vitamin D3; Fish Oil; Multivitamin
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 11.07.2022
- Impfdatum
- 17.06.2022
- Beginn
- 06.07.2022
- 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
Headache
Pyrexia
SARS-CoV-2 test positive
Throat irritation
Symptomtext
07/6/2022 I started having symptom on 07/06 I had a scratchy throat and a headache. I also had a low-grade fever (100.3). 07/07 Tested positive for COVID-19 I contacted my doctor and he suggested me to go a clinic to get medication. I contacted them at 11:00 AM ET and I was helped. They gave me the bebtelovimab.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Rosuvastatin; Aspirin; Coenzyme Q-10; Vitamin D
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 11.07.2022
- Impfdatum
- 08.07.2022
- Beginn
- 09.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysmenorrhoea
Headache
Menstruation irregular
Myalgia
Pain
Symptomtext
Sore throat before vaccine. Muscle and body aches after the vaccine. Headache after the vaccine. Started second menstrual cycle the day after the vaccine. Last menstrual cycle was a week before the vaccine. Second menstrual cycle started the day after the vaccine. Heavy cramps, light to medium bleeding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sore throat day of vaccine
- Vorgeschichte
- -
- Andere Medikamente
- Levothyroxine
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 58,0
- Geschlecht
- U
- Eingang
- 08.07.2022
- Impfdatum
- 29.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Nasopharyngitis
Symptomtext
I am still very fatigue and tired.; I still have the headache.; I feel cold.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 58-year-old patient received BNT162b2 (BNT162B2), on 29Jun2022 as dose number unknown (booster), single (Lot number: FM0173) at the age of 58 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: TAMSULOSIN; PREDNISONE. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer), for Covid-19 immunization. The following information was reported: FATIGUE (non-serious), FATIGUE (non-serious) all with onset 29Jun2022, outcome "unknown" and all described as "I am still very fatigue and tired."; NASOPHARYNGITIS (non-serious) with onset 29Jun2022, outcome "unknown", described as "I feel cold."; HEADACHE (non-serious) with onset 29Jun2022, outcome "unknown", described as "I still have the headache.". Therapeutic measures were taken as a result of fatigue, headache, nasopharyngitis, fatigue. Additional information: The patient was receiving treatment with Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- TAMSULOSIN; PREDNISONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 07.06.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphoedema
Rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- lymphodema, 6/20/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- lisinopril hctz, multi vitamin, trilogy, vitamin d, vitamin d3
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal sensation in eye
Blood test
Feeling cold
Hypersomnia
Influenza like illness
Injection site erythema
Pain
Pruritus
Symptomtext
She got her vaccine, nothing at all for the rest of the day, felt energetic and good. Then she started feeling like she was coming down with the flu, eyes were warm, achy. About 2:30 AM she started feeling like she was freezing, went back to sleep and slept longer than usual and was then OK. Was outside and started feeling itchy and felt it spreading and her injection site was redder than her husband who also had a vaccine that day. She then started itching on her back and looked and then saw that her chest was covered, spread to her back, down to her buttocks region with radiation, lower back and all the way around her torso. She took Benadryl 5 ml which helped a little bit, and took Benadryl an hour before the vaccine as well. She did call her doctor and told her to take Benadryl or Zyrtec and were not able to see her. They told her to come in to do blood work before her next vaccine booster. She is still itching, and has not gone in to have allergy shots since the vaccine. She goes every 29-31 days for her shots. Has had allergic reactions to medications and vaccines in the past. She had a reaction to Shingrix and Pneumovax which were given at the same time and had a rather severe reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Pre-asthmatic.
- Andere Medikamente
- Women's gummy vitamin, Coenzyme Q10, Citracal calcium two a day, EyePromise eye vitamins, vitamin D.
- Allergien
- Shellfish, iodine, thimerosal, Propofal, OmniPaq 350, Erythromycin.
- Vorherige Impfungen
- Pneumovax vaccine and shingles vaccine, given at the same time and same arm. Had to get an injection from an UC to counteract
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 01.07.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Injection site pain
Injection site rash
Injection site warmth
Rash pruritic
Symptomtext
PATIENT GOT A GOLF BALL SIZED RASH WHICH IS ITCHY,WARM AND PAINFUL TO TOUCH AT THE INJECTION SITE. SHE GOT ELEVATED TEMPERATURE 100.07 AND RELIEVED BY TYLENOL. SHE WAS ADVISED TO TAKE BENADRYL FOR ITCHINESS. REPORT TO HER PCP, AND GO TO ER IF PROBLEM GOT WORSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- HIGH BLOOD PRESSURE, HIGH CHOLESTEROL
- Andere Medikamente
- NONE
- Allergien
- ENTEX
- Vorherige Impfungen
- SHE GOT LYMPH NODE SWEELING FOR 2 DAYS ONN THE PREVIOUS PFIZER SHOTS.
- Staat
- VA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Feeling abnormal
Headache
Musculoskeletal discomfort
Pain
SARS-CoV-2 test
Symptomtext
headache upset her stomach; stated that her left shoulder has been giving problems; second shot: felt achy (all over in all joints, back, shoulders); second shot: headache; second shot: felt bad just did not do much laid around; 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 female patient received BNT162b2 (BNT162B2), on 03Nov2021 as dose 2, single (Lot number: FM0173) at the age of 80 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "osteoporosis" (unspecified if ongoing), notes: Stated that she has very bad osteoporosis and arthritis. , Stated that she had this for 30 years prior to the Pfizer Covid shots and booster.; "arthritis" (unspecified if ongoing), notes: Stated that she has very bad osteoporosis and arthritis. , Stated that she had this for 30 years prior to the Pfizer Covid shots and booster.; "she has bad alpha-gal" (unspecified if ongoing), notes: Stated that she has bad alpha-gal which is if one gets bitten by a certain tick that she guessed that is what happened it causes one to has allergy to anything with any meat byproducts in it. Stated that she got this 3-4.5 years ago. Stated that the only meat that is safe is chicken, turkey and fish.; "heart attack symptoms" (unspecified if ongoing), notes: Stated that she had heart attack symptoms and ended up in the ER.; "Stated that they are environmental allergies" (unspecified if ongoing), notes: Stated that they are environmental allergies. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, single), for Covid-19 Immunization. The following information was reported: PAIN (non-serious) with onset 04Nov2021, outcome "recovered", described as "second shot: felt achy (all over in all joints, back, shoulders)"; FEELING ABNORMAL (non-serious) with onset 04Nov2021, outcome "recovered", described as "second shot: felt bad just did not do much laid around"; HEADACHE (non-serious) with onset 04Nov2021, outcome "recovered", described as "second shot: headache"; MUSCULOSKELETAL DISCOMFORT (non-serious) with onset 04Apr2022, outcome "not recovered", described as "stated that her left shoulder has been giving problems"; ABDOMINAL DISCOMFORT (non-serious), outcome "unknown", described as "headache upset her stomach". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pain, headache, musculoskeletal discomfort. Additional information: was achy all over in all joints, back, shoulders, had a bad headache and felt bad just did not do much laid around. Stated that her symptoms started the next day after the shot. Stated that it lasted for 2-3 days. Recovered completely. Stated after that she felt fine and resumed normal life. Stated that her headache lasted for a day. Stated that she recovered fine from that. Stated that she felt bad for a couple of days. Recovered completely. Treatment: Stated that she took an Excedrin for the headache. Stated that the headache upset her stomach. Stated that she had physical therapy for her shoulder that made it worst. Stated wanted to give her this injection that she wanted to find out if safe to take because of chemical makeup of it. Product details: Clarified that the second shot lot number was written on the card as FM0173. Stated that the second booster on 7Jun2022 had a lot number of UAG15344.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200902766 Same patient and drug, different event separated in time;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 2020; Test Name: Covid test; Test Result: Negative ; Comments: did test and they always came back negative (2 tests).; Test Date: 2020; Test Name: Covid test; Test Result: Negative ; Comments: did test and they always came back negative (2 tests).
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Alpha-gal allergy (she has bad alpha-gal. Stated that she got this 3-4.5 years ago.); Arthritis (had very bad osteoporosis and arthritis. this for 30 years); Environmental allergy (Stated that they are environmental allergies.); Heart attack (she had heart attack symptoms and ended up in the ER.); Osteoporosis (had very bad osteoporosis and arthritis. this for 30 years)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 17.06.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash maculo-papular
Symptomtext
developed macula-papular rash to extremities, torso, back, neck approx 48 hours after vaccination similar to prior rashes after Covid vaccines (Moderna and Pfizer vaccines). Resolved after approx 48 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash maculo-papular
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN, hypercholesterolemia
- Andere Medikamente
- Lisinopril, Simvistaton
- Allergien
- Moderna & Pfizer Covid vaccines: rash Shingrix vaccine: rash
- Vorherige Impfungen
- macular-papilar rash to torso, extermines after 2 prior Covid vaccines (Moderna #2 & Pfizer #1) and to prior Shingrix vaccine
- Staat
- OR
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 16.05.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 37,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Feeling abnormal
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Starting 06/22/2022, I tested positive for COVID-19. I had some sniffles but that's about it. I called my doctor the next day to see next steps. I was starting to feel poorly: nasal congestion and cough. On Friday 06/24/2022, I spoke to the doctor and they decided to prescribe me PAXLOVID. I have taken the full regimen as of this morning (06/29/2022) and I feel almost no symptoms. I am experiencing some mild runny nose intermittently but my fatigue has gone away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test (06/22/2022): positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Glaucoma
- Andere Medikamente
- Rosuvastatin; niacin XR; aspirin; dorzolamide/timolol eye drops; latanoprost eye drops; multivitamin; coQ10; vitamin B3; vitamin C
- Allergien
- Lisinopril; FLOMAX
- Vorherige Impfungen
- After shingles vaccine, I was lethargic and my arm was sore for a day or so.
- Staat
- TX
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 29.06.2022
- Impfdatum
- 17.05.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Decreased appetite
Fatigue
Malaise
Oropharyngeal pain
Productive cough
SARS-CoV-2 test positive
Sleep disorder
Throat irritation
Symptomtext
COVID-19 symptoms started 06/19/22 with scratchy throat first thing in the morning. 06/21/22 I had scratchy throat and severe sore throat when we started on a long trip. I tested positive on 06/22/22 with self test kit. The main thing was severe sore throat. I also felt tired but when I took the test, we decided to drive back home (15 hrs.) just in case we got worse and we would be home. I would say sore throat was the main symptom and fatigue as well and I was tired the night before but it could've been because I didn't sleep well. I had a cough and loss of appetite. I was able to drive back alternating with my wife and I was able to stay awake the whole time. When I got back, my doctor prescribed LAGEVRIO for 5 days, 4 in AM, 4 in PM. Other than that I didn't do anything but rest and social distance. I still have some phlegm and still feel tired although I could do well with normal activities and I've been staying put in our house. I went into the pharmacy yesterday to get the PCR test and I don't have the results yet but I thought that might tell me what type of COVID-19 I have experienced and get some evidence that I'm clear of symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19- positive- 06/22/22.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism; high cholesterol; hypertension; January 3 stents placed in arterial arteries; osteopenia
- Andere Medikamente
- Alendronate; aspirin; PLAVIX; ZETIA; levothyroxine; metoprolol; BENICAR HCT; pantoprazole; CRESTOR; tamsulosin; multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 26.06.2022
- Beginn
- 26.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Rash
Symptomtext
Patient was administered a Pfizer booster vaccine (4th) that was given SQ instead of IM on 6/26/2022. Developed a rash same day and rash has become larger as of today on 6/29/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Patient is a immuno-compromised patient
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 22.06.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Polymerase chain reaction
Pyrexia
Throat irritation
Symptomtext
I had a cough, scratchy throat & low grade fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- PCR
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- progesterone estrogen gel
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 14.05.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Hypersomnia
Malaise
Oropharyngeal pain
Pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Somnolence
Symptomtext
I felt sleepy and achy after the vaccine and slept a lot after the vaccine. I started feeling systems of Covid 19 on June 11. Prior to June 11th I felt very fatigue. I was traveling a lot and just felt like I over did it. I started feeling the sore throat and nasal drip. I took a home test for Covid 19 and it was positive on June 11. I took Flonase, Tylenol severe cold/night and alternated with Mucinex. Sore throat went away after two days. The congestion continues to today. The worst days was three and four days after tested positive. I had a telemedicine with a provider and they prescribed Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home test for Covid 19 and it was positive June 11, 2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Estriol, probiotic, multivitamin, potassium, omega 3, calcium/zinc/
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 11.05.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 39,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
COVID-19
Decreased appetite
Exposure to SARS-CoV-2
Fatigue
Headache
Insomnia
SARS-CoV-2 test positive
Symptomtext
I started to feel tired but I did not attribute it to COVID-19. A friend contacted me to advise that they tested positive. I then took an at home COVID-19 Test and it was positive. I contacted my doctor and asked for Paxlovid and I started taking it yesterday. I am having sleeplessness, headache, loss of appetite and taste.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19-Home Test-06-19-2022 Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Migraines
- Andere Medikamente
- Crestor, Lexapro, Bupropion, Clonazepam, Daily Multi-Vitamin, Fish Oil, Vitamin C, Zinc
- Allergien
- N/A
- Vorherige Impfungen
- Pfizer COVID-19-Breakthrough case of COVID-19
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 09.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Interchange of vaccine products
Joint swelling
Movement disorder
Off label use
SARS-CoV-2 test
Symptomtext
I have my right wrist and elbow have been swelled and are sore to touch, with limited movement; I have my right wrist and elbow have been swelled and are sore to touch, with limited movement; My left shoulder is sore and painful all the time; Fatigue is every night; DOSE 1, 2, 3 : Moderna and DOSE 4: BNT162B2; DOSE 1, 2, 3 : Moderna and DOSE 4: BNT162B2; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09May2022 at 16:45 as dose 4 (booster), single (Lot number: Fm0173) at the age of 60 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN; LOSARTAN; AMLODIPINE; PRAVASTATIN. Past drug history included: Morphine, reaction(s): "Known allergies: Morphine", notes: Known allergies: Morphine. Vaccination history included: moderna (DOSE 1; Lot number: 032H02A; Anatomical Location:Arm Left, Time of administration: 04:45 PM), administration date: 06Jan2021, when the patient was 58-year-old, for COVID-19 immunization; moderna (DOSE 2; Lot number: 032H02A; Anatomical Location:Arm Left, Time of administration: 04:45 PM), administration date: 03Feb2021, when the patient was 58-year-old, for COVID-19 immunization; moderna (DOSE 3; Lot number:939906; Anatomical Location:Arm Left, Time of administration: 04:45 PM), administration date: 04Nov2021, when the patient was 59-year-old, for COVID-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious), OFF LABEL USE (non-serious) all with onset 09May2022 at 16:45, outcome "unknown" and all described as "DOSE 1, 2, 3 : Moderna and DOSE 4: BNT162B2"; FATIGUE (non-serious) with onset 14May2022, outcome "not recovered", described as "Fatigue is every night"; JOINT SWELLING (non-serious), MOVEMENT DISORDER (non-serious) all with onset 14May2022, outcome "not recovered" and all described as "I have my right wrist and elbow have been swelled and are sore to touch, with limited movement"; ARTHRALGIA (non-serious) with onset 14May2022, outcome "not recovered", described as "My left shoulder is sore and painful all the time". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of joint swelling, movement disorder, arthralgia, fatigue. Additional information: The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has been tested for COVID-19. Device date was provided as 20Jun2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220520; Test Name: COVID test; Test Result: Negative ; Comments: COVID test type post vaccination: Nasal swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes
- Andere Medikamente
- METFORMIN; LOSARTAN; AMLODIPINE; PRAVASTATIN
- Allergien
- -
- 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
- 2
- 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
- TX
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Injection site pain
SARS-CoV-2 test positive
Symptomtext
Only slight soreness in the arm at the injection site. COVID infection about a week later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- Testing at doctor's office 6/13/2023, positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Buproprion, Atorvastatin, Escatalopram, Lisinopril, Mucinex 1200mg/twice daily
- Allergien
- No drug allergies, only grasses and pollen
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 22.06.2022
- Impfdatum
- 17.06.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site rash
Vaccination site warmth
Symptomtext
had rash and heat in the arm of the vaccine given location
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- high clolesterol, low thyriod
- Andere Medikamente
- no
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 98,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 23.05.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood sodium decreased
Decreased appetite
Discomfort
Dizziness
Electrocardiogram normal
Extra dose administered
Full blood count
Lipase normal
Metabolic function test
Platelet count decreased
SARS-CoV-2 test negative
Serum ferritin normal
Troponin
Urine analysis normal
Symptomtext
Dizziness, loss of appetite, generalized discomfort, and weakness started 1 week (on 5/30/22) after COVID-19 booster #2 (4th dose) on 5/23/22. Dizziness got worse prior to emergency room visit on 6/19/22, treated with normal saline IV 2 liters, magnesium sulfate 2 grams IV, and Tylenol 650 mg. Patient?s daughter had telephone appointment for ER follow-up on 6/22/22 with me and had requested that I report this adverse event, since patient also had prolonged dizziness after COVID-19 vaccine dose #2 on 4/4/2021 that started 6 days after COVID-19 vaccine and required hospitalization on 4/18/4/19/2021. Dizziness had resolved temporarily in June 2021, but then dizziness returned on July 2021 to December 2021. Patient did vestibular rehab via physical therapy and massage therapy of neck/upper back, which led to resolution of dizziness and patient doing well between December 2021 to May 2022. Patient also had dizziness for 2 days after COVID-19 vaccine dose #1 on 3/14. Patient did NOT have symptoms after COVID-19 booster #1 (dose 3) on 12/20/2021. Patient had Pfizer-BioNTech for all 4 doses of COVID-19 vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- On 6/19/2022 at ER visit: EKG with normal sinus rhythm and 1st degree AV block, CBC normal except platelets 127, CMP normal except sodium 135, lipase normal, urinalysis normal, troponin 0.05 and 0.06, SARS-COV-2 PCR negative, ferritin normal
- Aktuelle Erkrankungen
- No known acute illnesses in that timeframe
- Vorgeschichte
- CAD, mitral valve regurgitation, 1st degree AV block, Raynaud?s syndrome, iron deficiency anemia, osteoarthritis, history of vertebral fracture, osteoporosis, hearing loss, peripheral venous insufficiency
- Andere Medikamente
- Alendronate, amlodipine, clopidogel, ipratropium nasal spray, pravastatin, coenzyme Q10, glucosamine chondroitin, melatonin, vision-supporting vitamins
- Allergien
- Zinc topical, bacitracin zinc + polymyxin B sulfate
- Vorherige Impfungen
- COVID-19 vaccine #1 and #2 (please prior discussion of adverse event for more information)
- Staat
- AR
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 26.05.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Headache
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On 6-7-2022, I had a headache and runny nose. I used my allergy medication, TYLENOl and EMERGEN-C orange packets for symptoms. On 6-10, I began having a sore throat and chest congestion with a cough. I went to a walk in clinic and they performed a Covid test with positive results. They ordered POLY-TUSSIN DM, albuterol sulfate inhaler 2 puffs every 4-6 hrs. as needed and a Z-PAK dose pack. I did not take the Z-PAK but I did take the cough syrup and inhaler. I still have a lingering cough. I am reporting a breakthrough case of Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Covid test on 6-10-2022 - rapid antigen - positive result.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 Diabetes; Hyperlipidemia; Seasonal allergies
- Andere Medikamente
- Metformin; furosemide; lisinopril; ALIVE women's 50 plus multivitamin; generic ZYRTEC
- Allergien
- Codeine; PCN; aspirin; lidocaine; latex; shellfish; Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 21.06.2022
- Beginn
- 21.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Hypoaesthesia
Oropharyngeal discomfort
Symptomtext
ABOUT 5 MINUTES POST-VACCINATION PATIENT BEGAN TO FEEL LIGHT-HEADED AND DIZZY, AND COMPLAINED ABOUT NUMBNESS IN HER HANDS AND THAT HER THROAT FELT "THICK"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE PROVIDED
- Vorgeschichte
- NONE PROVIDED
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- PFIZER COVID 19, ONE YEAR PROIR AT AGE 46, ALSO DIZZINESS, FEELING NUMB, AND THROAT SWELLING
- Staat
- IL
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 10.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
he has got hives all over his body; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the parent. A 14-year-old male patient received BNT162b2 (BNT162B2), on 10Jun2022 as dose 2, single (Lot number: FM0173) at the age of 14 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 1, single), for COVID-19 immunization. The following information was reported: URTICARIA (non-serious) with onset Jun2022, outcome "unknown", described as "he has got hives all over his body". Therapeutic measures were taken as a result of urticaria. Additional information Reporter stated, my son got, he is 14, he got a second dose of the Covid vaccination on Friday and Saturday he has got hives all over his body. If wants to report or have any question: Reporter stated, I want to report. I was told to report it. My doctor told me to report it to you. Reporter stated, No I am the mother of my child. Medical conditions or Concomitant medications: Reporter stated, "Nothing (Further not appropriately clarified, hence tab left uncheckered). Treatment: Reporter stated, "Just Claritin like a you know, (voice overlapped). No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 20.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Rash
Urticaria
Symptomtext
pt had broken out in hives and rash. Pt went to the urgent care and took a steroid. Pt had hives and rash for 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 19.05.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 27,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Decreased appetite
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I started getting symptoms of a dry cough, tickle throat, and slight runny nose. Then today my symptoms have progressed to having chills also and a low grade fever 99.1. I have noticed that I don't have an appetite. I took a PCR test on 6/13/2022 and again on 6/14/2022, and 6/16/2022 which was negative. This morning I took a home COVID-19 test and it was positive and then a PCR test that is pending. I have contacted my doctor by email and I was prescribed PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoporosis; Arthritis
- Andere Medikamente
- Estradiol patch; vitamin D3; magnesium; vitamin B12
- Allergien
- REGLAN
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 15.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Dizziness
Nausea
Vertigo
Symptomtext
I woke up with vertigo, dizziness, and nausea. My neurologist told me to take MOTRIN. I tried to move my face and eyes, which seemed to help with the spinning and nausea. My condition has improved but my balance is still off but the dizziness and spinning are improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Tachycardia syndrome; sleep apnea; hyperlipidemia
- Andere Medikamente
- Atorvastatin; azelastine; baclofen; prochlorperazine; bupropion; methocarbamol; propranolol; fludrocortisone; pyridostigmine; aspirin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 17.06.2022
- Beginn
- 17.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Pyrexia
Skin warm
Symptomtext
Redness, hot to touch, no itching, fever and chills.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 11.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Balance disorder
Body temperature
Chills
Decreased appetite
Dizziness
Dysuria
Headache
Hypokinesia
Myalgia
Nausea
Oropharyngeal pain
Pyrexia
Vaccination site erythema
Vaccination site pain
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 89-year-old female patient received BNT162b2 (BNT162B2), on 11Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 89 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "High Blood Pressure" (unspecified if ongoing); "Acid Reflux" (unspecified if ongoing); "Neuropathy in the feet" (unspecified if ongoing); "Known allergies: mold" (unspecified if ongoing), notes: she is on medications for these allergies as well, but they are over the counter products.; "Known allergies: ragweed" (unspecified if ongoing), notes: she is on medications for these allergies as well, but they are over the counter products.; "Known allergies: leaves" (unspecified if ongoing), notes: she is on medications for these allergies as well, but they are over the counter products.; "Known allergies: grass" (unspecified if ongoing), notes: she is on medications for these allergies as well, but they are over the counter products. Concomitant medication(s) included: POTASSIUM. Past drug history included: Demerol, reaction(s): "Allergy". Vaccination history included: BNT162b2 (Dose 1: Lot EL3248. Administered in the Left Arm.), administration date: 10Feb2021, when the patient was 88-year-old, for Covid-19 immunization, reaction(s): "sick"; BNT162b2 (Dose 1: Lot EL3248. Administered in the Left Arm.), administration date: 10Feb2021, when the patient was 88-year-old, for Covid-19 Immunization, reaction(s): "weakness", "difficulty in being upright"; BNT162b2 (Dose 2, Expiry 30Apr2021. Lot number is documented starting with F dose 0.3mL. Administered in the Left Arm.), administration date: 30Apr2021, when the patient was 88-year-old, for Covid-19 Immunization, reaction(s): "weakness", "difficulty in being upright"; BNT162b2 (First Booster: Lot FF2588, Expiry 31May2021. There is also some number that states C00 then maybe a 6 and 19. Received 0.3mL. Administered in the Left Arm.), administration date: 13Sep2021, when the patient was 89-year-old, for Covid-19 Immunization, reaction(s): "felt like she was going to faint and had to lay down", "blood pressure and it was very high". The following information was reported: PYREXIA (non-serious), outcome "unknown", described as "running a temperature over a 100"; NAUSEA (non-serious), outcome "unknown"; HYPOKINESIA (non-serious), outcome "unknown", described as "wasn't even able to get up all night"; DECREASED APPETITE (non-serious), outcome "recovered", described as "wasn't able to eat"; HEADACHE (non-serious), outcome "not recovered"; OROPHARYNGEAL PAIN (non-serious), outcome "unknown", described as "sore throat"; DYSURIA (non-serious), outcome "unknown", described as "not able to urinate"; VACCINATION SITE PAIN (non-serious), VACCINATION SITE ERYTHEMA (non-serious), outcome "unknown" and all described as "redness at the injection site and soreness"; DIZZINESS (non-serious), outcome "unknown"; BALANCE DISORDER (non-serious), outcome "unknown", described as "balance problems"; MYALGIA (non-serious), outcome "unknown", described as "Muscle pain"; CHILLS (non-serious), outcome "unknown", described as "chills in her whole body"; ASTHENIA (non-serious), outcome "recovering", described as "weakness". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Reporter stated that she was calling about the Second Booster, caller further clarified that it was the Pfizer COVID vaccine. She wanted to report how bad the second booster was, if she knew it was going to be that bad then she wouldn't have taken it. She had the first dose and was sick but it was nothing close to this time. She had all the symptoms except a few, but it was very severe, she was running a temperature over a 100 which is high for her, she had nausea, she wasn't even able to get up all night, all she could do was lay there and moan, she felt horrible, she wasn't able to eat for 24 hours or more. Reporter retrieved her covid vaccine card. Reporter confirmed that all the covid vaccines she got were made by Pfizer. Reporter stated that after the first and second dose she had symptoms but she really doesn't recall what they were exactly, she does know that she had weakness and had to lay down because just felt as if she could not get up, however it was not for very long. She does remember she had difficulty in being upright. Outcome: At the moment she still has a bad headache and weakness, but is starting to get her appetite back. With the weakness she is not up and about, but she can be up compared to before, after the horrible night and yesterday afternoon, she wasn't able to be up, and could only be up for 2-3 minutes. Her Headaches are now slightly improved but it is still a problem, her weakness improved, and her appetite has improved. Getting back to her temperature, when she was finally able to get up at 11AM it was 100 degrees Fahrenheit, this temperature was taken yesterday 12Jun2022. Her Arm was sore for a few days, but this time, maybe it depends on the way the injection is given but its not as bad as the past injection with the soreness. Concomitant Medication: She is on her regular medications, caller declined to provide her medications stating that it would take too long, she is on 8 prescription. She is on medications for High Blood Pressure, Acid Reflux, and she is on Potassium. Medical Conditions: There is nothing she can think of right now, she has Neuropathy for which she takes medication, the Neuropathy is in the feet. She had no allergic reactions with the vaccines, but she is allergic to certain medications like Demerol and others that she cant think of. She is allergic to mold, ragweed, leaves, and grass, she is on medications for these allergies as well, but they are over the counter products. Caller states that she would like to add that the thing is that this reaction was so bad, that if she has to go through this every future injection then she would rather spend the rest of her life at home, just like how she has through most of this covid time period.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200838839 similar report from same reporter; US-PFIZER INC-202200838840 similar report from same reporter; US-PFIZER INC-202200838841 similar report from same reporter;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220612; Test Name: Temperature; Result Unstructured Data: Test Result:100 Fahrenheit; Comments: 100 degrees Fahrenheit
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Acid reflux (esophageal); Allergy to molds (she is on medications for these allergies as well, but they are over the counter products.); Allergy to plants (she is on medications for these allergies as well, but they are over the counter products.); Blood pressure high; Grass allergy (she is on medications for these allergies as well, but they are over the counter products.); Neuropathy; Ragweed allergy (she is on medications for these allergies as well, but they are over the counter products.)
- Andere Medikamente
- POTASSIUM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.06.2022
- Impfdatum
- 25.05.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 17,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Fatigue
Gait disturbance
Headache
Malaise
Peripheral swelling
Pyrexia
SARS-CoV-2 test negative
Vomiting
Symptomtext
I started feeling really tired and had a headache right after vx. Seemed to subside but then it came back really strong around 6/11/2022. I had a 102 fever with diarrhea and vomiting. One of my feet became so swollen that I could barely walk. I did a couple of at home COVID tests, and they were all negative. I still wasn't feeling well so I went to a lab for official testing and the test came back negative too. I saw 2 NP's at my regular Dr's office and they suspected I might have had COVID at some point, but they didn't do any further testing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol Inhaler, Symbicort, Flonase, Alendronate
- Allergien
- Animal dander, pollen, morphine, lortiab, percocet, codeine. Pretty much all narcotics
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 11.06.2022
- Beginn
- 12.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Pruritus
Symptomtext
Large red area surrounding injection site (2 1/2' in diameter) and itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Dicyclomine, multivitamins, cranberry tablets, zyrtec, cholestoff
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 15.06.2022
- Impfdatum
- 07.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cheilitis
Injection site erythema
Injection site nodule
Pyrexia
Rash
Symptomtext
Patient reported 102 degrees fever starting the day of vaccination that lasted about 3 days and resolved on its own. Reported red knot at injection site starting the day of vaccination, still ongoing but getting better. Patient reported rash on upper lip that extends up to his nostrils that started 2 days after vaccination. Patient received treatment from dermatologist. Dermatologist told patient she believed rash was caused by vaccine and prescribed treatment. Patient reported rash is getting better with treatment and starting to dry up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- sulfa drugs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 14.06.2022
- Impfdatum
- 12.06.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Erythema
Pain
Peripheral swelling
Skin warm
Symptomtext
patient came in for 4th shot of Pfizer 6/12/22 and today she has a swollen red arm that is hot to the touch, pain is radiating under armpit
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 03.06.2022
- Beginn
- 04.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pain
Symptomtext
Extreme muscle pain in left hip and thigh region; has worsened over the first three days; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old male patient received BNT162b2 (BNT162B2), on 03Jun2022 at 18:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 61 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN. Vaccination history included: Bnt162b2 (DOSE 3, SINGLE, Lot number: 32030BD, Anatomical location: Right arm), for Covid-19 immunization; Bnt162b2 (DOSE 2, SINGLE, Lot number: ER8734, Anatomical location: Left Arm), for Covid-19 immunization; Bnt162b2 (DOSE 1, SINGLE, Lot number: ER8727, Anatomical location: Right Arm), for Covid-19 immunization. The following information was reported: MYALGIA (non-serious) with onset 04Jun2022 at 07:00, outcome "not recovered", described as "Extreme muscle pain in left hip and thigh region"; PAIN (non-serious) with onset 04Jun2022 at 07:00, outcome "not recovered", described as "has worsened over the first three days". Therapeutic measures were not taken as a result of myalgia, pain. Additional information: The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID -19. The patient did not receive any other vaccine within 4 weeks of vaccination. Post vaccination, the patient had not been tested for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension
- Andere Medikamente
- LOSARTAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 09.06.2022
- Beginn
- 10.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint range of motion decreased
Lymphadenopathy
Pain
Skin warm
Symptomtext
Lymph node severely swollen under arm and breast. Hot to the touch. Can not move arm with out being in pain. Can not straighten arm out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood pressure
- Andere Medikamente
- -
- Allergien
- Penicillin, craw fish
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 08.06.2022
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Fatigue
Headache
Pain
Pyrexia
SARS-CoV-2 test positive
Sinus congestion
Vaccine breakthrough infection
Symptomtext
breakthrough infection 6/08/2022, fever, headache, body aches, sinus congestion, fatigue. Fever ended 6/9 morning. Began Paxlovid 6/10 evening. Symptoms abated; continued fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 6/8/2022 positive rapid test
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multivitamin, vitamin c, omega-3, lysine, elderberry
- Allergien
- mild allergy to mango
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 11.06.2022
- Impfdatum
- 08.06.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Dizziness
Dysstasia
Fall
Headache
Symptomtext
patient got up in the early morning hours of 6/11/22 to go to the bathroom. as he was walking to bathroom, he felt dizzy and started losing his balance and found it difficult to hold himself up. sought a safe landing and did fall. sat still for a few moments and patient returned to bed. awoke in morning around 8 am feeling better. patient states that on Friday, 6/10/22 he was experiencing a headache and took Tylenol before going to bed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- high blood pressure, stage 2 kidney disease
- Andere Medikamente
- fluoxetine, ativan, lisinopril, multiple vitamin/mineral, vit. d3, zinc
- Allergien
- penicillin as young adult (flushing, racing heart)
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 28.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Depressed level of consciousness
Dizziness
Fatigue
Feeling abnormal
Symptomtext
I experienced extreme fatigue, lightheadedness, and my boyfriend came home and found me on the floor where he was unable to rouse me. He stated it took around 5 minutes to rouse me. The symptoms of fatigue, lightheadedness, and brain fog lasted for 4 days before they abated. I have experienced mild lightheadedness off and on since dose 4 at random.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- Interstitial cystitis
- Vorgeschichte
- Interstitial Cystitis; Anxiety Disorder
- Andere Medikamente
- Lipitor Tranxene Protonix Vitamin E Vitamin D3 Iron Krill Oil Vitamin B12 Magnesium Zinc Calcium Norco Uribel
- Allergien
- Penicillin; sulfa; erythromycin; KEFLEX; LEVAQUIN; NEURONTIN; CIPRO; ESTRACE; tetracycline
- Vorherige Impfungen
- COVID-19 Pfizer Dose 1 at 61 years old, I felt like the room was spinning, heart was racing, felt faint and was transported to t
- Staat
- OH
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 04.06.2022
- Beginn
- 07.06.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Symptomtext
I got sudden onset inflammatory arthritis in both hands. Very painful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Dr visit
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Previous Breast Cancer
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 06.06.2022
- Impfdatum
- 06.06.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pyrexia
Throat tightness
Symptomtext
Patient received Johnson & Johnson and she reported that she had a fever for 2 days after - she received Pfizer 6/6/22 @ 4:30PM and reported 15 minutes later that she felt like her throat was constricting and getting tighter. She was offered benadryl but patient stated that she has many allergies including a gluten allergy so she did not want to take the benadryl. Epipen was prepared for administration but patient was still conscious and no shortness of breath was noticed so she denied the epipen and requested emergency to be called.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Patient states she has many allergies including gluten.
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 06.06.2022
- Impfdatum
- 05.06.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nausea
Pyrexia
Vomiting
Symptomtext
Nausea, vomiting, fever of 102?f
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- None yet
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 05.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Pain in extremity
Product administered to patient of inappropriate age
Product preparation issue
Symptomtext
The patient received the wrong formulation of Pfizer covid-19 vaccine. He was administered the adult dose instead of the pediatric dose. I notified the mother on 06/05/22 and she said that he has not had any adverse reaction to the vaccination except for soreness in the arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 05.06.2022
- Impfdatum
- 27.05.2022
- Beginn
- 29.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Blister
Herpes zoster
Pruritus
Rash
Symptomtext
Shingles flare up. Started with itching about 2 days after vaccine. Continued with bumps, blisters, pain on left side of body around abdomen. Had shingles previously in 1988.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chemical sensitivity
- Andere Medikamente
- Maca, fish oil, glucosamine, vitamin d, calcium.
- Allergien
- Zithromax
- Vorherige Impfungen
- Flu vaccine, in 1994
- Staat
- IN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 02.06.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Myalgia
Nausea
Pain in extremity
Vomiting
Symptomtext
Sore arm, headache, fatigue, muscle aches, nausea and vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, high blood pressure, diabetic, NASH, migraines
- Andere Medikamente
- Metformin, calcium, vitamins D, E, garlic, atorvastatin, arimedex, Lisinopril, dilteziam, gabapentin, aspirin, Claritin, baclofen
- Allergien
- Amoxicillin, demerol, erythromycin, doxycycline, singular, adhesive
- Vorherige Impfungen
- COVID vaccine
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 20.05.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Breast inflammation
Lymphadenopathy
Pain in extremity
Symptomtext
lymph nodes in my armpit were swollen; inflammation extended to my left breast.; Following day after I got the vaccine I had arm pain that became stronger at night.; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 20May2022 at 16:45 as dose 4 (booster), single (Lot number: FM0173) at the age of 57 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: INDERAL; LANSOPRAZOL; ROSUVASTATIN. Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Batch/Lot No: EW0151, Location of injection: Arm Left), administration date: 03Sep2021, when the patient was 56-year-old, for COVID-19 immunization, reaction(s): "little discomfort"; BNT162b2 (DOSE 2, SINGLE, Batch/Lot No: EL1284, Location of injection: Arm Left), administration date: 08Jan2021, when the patient was 56-year-old, for COVID-19 immunization, reaction(s): "little discomfort"; BNT162b2 (DOSE 1, SINGLE, Batch/Lot No: EH9899, Location of injection: Arm Left), administration date: 16Dec2020, when the patient was 56-year-old, for COVID-19 immunization, reaction(s): "little discomfort". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 21May2022 at 10:00, outcome "recovered" (May2022), described as "Following day after I got the vaccine I had arm pain that became stronger at night."; BREAST INFLAMMATION (non-serious) with onset 22May2022 at 10:00, outcome "recovered" (May2022), described as "inflammation extended to my left breast."; LYMPHADENOPATHY (non-serious) with onset 22May2022 at 10:00, outcome "recovered" (May2022), described as "lymph nodes in my armpit were swollen". Therapeutic measures were not taken as a result of pain in extremity, lymphadenopathy, breast inflammation. Additional information: The patient had not received other vaccine in 4 weeks. Reporter stated, following day after I got the vaccine, I had arm pain that became stronger at night. By morning noticed the lymph nodes in my armpit were swollen. Following day, the inflammation extended to my left breast. This was the first time that I got this side effects, the first three were great, just a little discomfort. The patient had not covid prior vaccination and covid tested post vaccination. Patient had no known allergies. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200765075 Same patient and drug, different event separated in time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- INDERAL; LANSOPRAZOL; ROSUVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 02.06.2022
- Impfdatum
- 10.05.2022
- Beginn
- 11.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bronchitis
Chest X-ray abnormal
Full blood count normal
Malaise
Pain
Pyrexia
Respiratory tract congestion
Symptomtext
I received my vaccine on 05/10/2022 at the pharmacy. 24 hours after dose I experienced malaise, achiness, chest congestion and fever. I went to urgent care on 5/17/2022 at 10 AM and was diagnosed with bronchitis. Symptoms continued and fever was getting worse. I made a second visit to urgent care on 05/31/2022 at 10 AM and during that visit I was prescribed doxycycline. As of today I am still having symptoms. I have had 5 Covid test which were all negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Chest x ray normal. CBC normal white count on higher end.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension; tachycardia; elevated cholesterol.
- Andere Medikamente
- Diltiazem extended release; losartan; Lipitor; metoprolol tartrate
- Allergien
- NSAIDA; aspirin; penicillin; contrast dye
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 31.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Dizziness
Dysstasia
Pyrexia
Visual impairment
Symptomtext
generalized weakness, hard time standing, fever, dizziness and sees black spots when trying to stand
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- no known
- Vorgeschichte
- adhd
- Andere Medikamente
- vyvanse during school year. last taken on 5/27/2022
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 24.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Malaise
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sinus congestion
Somnolence
Throat irritation
Symptomtext
I thought I was having allergies. I had lots of congestion and was more tired than normal. I had some nasal drainage and a throat tickle and a small cough. My son had tested positive on the day that I got my second booster which was the 24th. I have not been around him much and he has been able to stay away from the family. Through the weekend I got a stuffed-up head and I was even more tired and ended up napping because of being tired. The scratchy throat continued and has been bothering me still. Monday night I took a home test and it was positive and then I went to urgent care the next day and they did a COVID-19 PCR test which was positive. They gave me PAXLOVID if I wanted to use it but I have not taken it as this point because my symptoms have really been more like bad allergies. At this point my symptoms have not worsened and really stayed the same this far.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test; COVID-19 Rapid COVID Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Lisinopril; SINGULAIR; Azelastine; Vitamin D3
- Allergien
- PERCOCET; VIBRA-TABS; Tetracycline
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 26.05.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cellulitis
Extra dose administered
Injection site erythema
Injection site swelling
Symptomtext
red swollen at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Urgent care MD diagnosed with bacterial cellulitis
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- Atorvastatin Famotidine, nitroglycerine, omeprazole, simvastatin
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Balance disorder
Nausea
Symptomtext
Patient came in on 5-28-22 to state that she have been nauseated and could not keep her balance and could only attribute to the vaccine. She had the vaccine before but did not experience this reaction. Told patient to follow up with doctor if the symptoms continue or get worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 22.05.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood cholesterol
Heart rate
Pain in extremity
Vaccination site coldness
Vaccination site reaction
Symptomtext
her arm was just very hard today this morning and very sore; it feels hard at the injection site; the temperature of her injection arm is really cold; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID: (159558). The reporter is the patient. An 80-year-old female patient received BNT162b2 (BNT162B2), on 22May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 80 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "stents in the heart" (unspecified if ongoing); "Fast heart rate" (unspecified if ongoing); "High cholesterol" (unspecified if ongoing), notes: High Cholesterol is under control with medication; "Allergy" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: flu shot, administration date: 21Oct2021, when the patient was 79-year-old, for Immunization; BNT162b2 (DOSE 1, LOT: EN6201, ANATOMICAL LOCATION: LEFT ARM), administration date: 12Feb2021, when the patient was 78-year-old, for Covid-19 Immunization; BNT162b2 (DOSE 2, LOT: EN6199, ANATOMICAL LOCATION: LEFT ARM), administration date: 06Mar2021, when the patient was 78-year-old, for Covid-19 Immunization; BNT162b2 (DOSE 3, LOT: 30155BA, ANATOMICAL LOCATION: LEFT ARM), administration date: 22Oct2021, when the patient was 79-year-old, for Covid-19 Immunization. The following information was reported: VACCINATION SITE COLDNESS (non-serious) with onset 22May2022, outcome "recovering", described as "the temperature of her injection arm is really cold"; VACCINATION SITE REACTION (non-serious) with onset 23May2022, outcome "not recovered", described as "it feels hard at the injection site"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "her arm was just very hard today this morning and very sore". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Caller confirmed information provided by the transferring agent, stating that what she was experiencing was different than what she had experienced with her prior vaccines. Her first and second dose were the Pfizer covid vaccine, and then she got the booster, and then she had the flu shot. Yesterday afternoon she had the second booster, she got it because she was 80 years old with 2 stents in the heart as well as on Plavix. After getting the second booster yesterday, she was fine for the first hour, but then she noticed the arm got real cold, as if someone put ice on it, she said to herself that they have got to be kidding, maybe if she goes to bed the arm will get warm, however the arm got really hard not warm. This didnot bother her last night, but this morning it was still not red. Usually with her prior vaccines, around the injection site it gets red, even with the flu shot, and all vaccines, however this second booster her arm never turned red, it was still not red today, her arm was just very hard today this morning and very sore. It has got slightly warm today compared to yesterday. Caller confirms that the side effects she was experiencing are on the same arm that she received the second booster injection in. She asks if all this was normal, and why was her arm so cold. Caller states that she was just curious, this one was so much different than her other previous vaccines. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Name: Cholesterol; Result Unstructured Data: Test Result:High; Test Name: Heart rate; Result Unstructured Data: Test Result:134 beats/min; Comments: heart rate is around134 beats per minute
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy; Heart rate high; High cholesterol (High Cholesterol is under control with medication); Stent insertion NOS
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Injection site erythema
Injection site swelling
Injection site warmth
Symptomtext
Immediate injection site reaction - swelling (golf-ball sized lump) at injection site with redness and warmth
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- breast cancer 2020
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 25.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Full torso rash from navel to neck on front and entire back
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D, magnesium, zinc, vitamin B complex, fish oil, probiotics.
- Allergien
- Shrimp, gluten.
- Vorherige Impfungen
- Same reaction for dose #2, reported to VAERS
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 25.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
COVID-19
Cough
Malaise
Pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On 5/17 I was experiencing a slight cough, runny nose, and congestion the day before my vaccine. I also started feeling some body aches. On 5/18 I took an at home Covid test which was negative and the next two days I also tested negative. On Sunday, 5/22, I tried a different brand at home Covid test and that was positive but the older brand also was coming up positive at that point. My wife and I went to the pharmacy on 5/22 for a PCR test. My positive results came back 5/23. I also tested positive on 5/22 with a rapid test at another local pharmacy. I haven't spoken with my doctor since I have only had mild symptoms. I woke up this morning on 5/25, and have lost my sense of taste and smell. I've been treating my symptoms with over the counter medication and am doing well overall.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Covid tests-multiple days, mixed results.
- Aktuelle Erkrankungen
- Cough on 5/17/22
- Vorgeschichte
- None
- Andere Medikamente
- Omeprazole 20mg; amlodipine; rosuvastatin 20mg; sertraline 100mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 21.05.2022
- Beginn
- 22.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Vomiting
Symptomtext
VOMITTING AND NAUSEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Tree nuts
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyskinesia
Fatigue
Symptomtext
Pt called to states that he had a event of body jerking in the evening at bedtime. He did not experienced this with his previous doses. He states that he is okay the next day ,just tired but felt the body jerking was severe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 12.05.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Interchange of vaccine products
Lymphadenopathy
Pain of skin
Rash
Symptomtext
A few days after, my scalp erupted again and I had lymph node enlargements behind my ear and at the base of hairline. I had terrible pain on left side where blisters swarmed again so I seen a healthcare provider and they couldn't figure out what was going on except that they asked me if I had a vaccine or booster recently and I hadn't given it much thought the first time it happened but now that it happened again I wonder if it was tired to my booster shot. She thought that the scalp eruption presented itself like a shingles reaction but I've had the shingles vaccine before and in the past so I know what they can be like. My lymph nodes are still swollen but Doctor said to give that more time and to follow up in a few weeks if it's still present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain of skin
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin B, Vitamin D
- Allergien
- Coffee; almonds; watermelon; latex sensitivity; sodium lauryl sulfate
- Vorherige Impfungen
- Moderna Booster 2021
- Staat
- TN
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 18.05.2022
- Impfdatum
- 13.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
exanthematous rash noted to bilateral upper and lower extremities, torso and back, staring two hours prior to arriving to clinic-five days after receiving vaccine. He previously had three moderna Covid 19 vaccines. All vitals stable today etc.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- MI, 2019, anxiety
- Andere Medikamente
- warfarin, aspirin, atorvastatin, trazodone, escitalopram
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Immediate post-injection reaction
Unresponsive to stimuli
Symptomtext
Patient became dizzy as soon as the vaccine was given. She had pulse and was breathing, but did not respond.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No health conditions reported
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 29.12.2023
- Impfdatum
- 01.06.2022
- Beginn
- 20.07.2022
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment/Prior COVID infection 20Jul2022; COVID 19 Treatment/Prior COVID infection 20Jul2022; This is a spontaneous report received from a Consumer or other non HCP. A 65-year-old female patient received BNT162b2 (BNT162B2), on 01Jun2022 at 12:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 65 years intramuscular, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 25Feb2021 at 12:00 as dose 1, single (Lot number: EN6200), in left arm, on 18Mar2021 at 12:00 as dose 2, single (Lot number: EN6208), in left arm and on 10Nov2021 at 12:00 as dose 3 (booster), single (Lot number: EW0172), in left arm, all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "RNY Gastric bypass surgery", start date: 2008 (unspecified if ongoing), notes: RNY Gastric bypass surgery (2008); "morbid obesity", start date: 1998, stop date: 2012, notes: Roux-en-Y gastric bypass surgery. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 20Jul2022, outcome "unknown" and all described as "COVID 19 Treatment/Prior COVID infection 20Jul2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (20Jul2022) Positive, notes: Prior covid infection 20Jul2022 and also treated with Paxlovid. Therapeutic measures were taken as a result of vaccination failure, covid-19 (Paxlovid).; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300418417 Same patient/drug/event, different dose;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220720; Test Name: Covid infection; Test Result: Positive ; Comments: Prior covid infection 20Jul2022 and also treated with Paxlovid.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Morbid obesity (Roux-en-Y gastric bypass surgery); Roux-en-Y gastric bypass (RNY Gastric bypass surgery (2008))
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 06.12.2023
- Impfdatum
- 13.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy
Lipoma
Magnetic resonance imaging
Symptomtext
I have a large lipoma removed from my deltoid muscle at about the place where we injected the vaccine/ benign lipoma; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72-year-old male patient received bnt162b2 (BNT162B2), on 13May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 70 years intramuscular, in right deltoid for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing), notes: Hypertension. Concomitant medication(s) included: LISINOPRIL taken for hypertension. Vaccination history included: bnt162b2 (DOSE 1, SINGLE, Lot number: EN5318), administration date: 29Jan2021, when the patient was 69-year-old, for COVID-19 immunisation, reaction(s): "Lipoma"; bnt162b2 (DOSE 2, SINGLE, Lot number: EN6200), administration date: 19Feb2021, when the patient was 69-year-old, for COVID-19 immunisation, reaction(s): "Lipoma"; bnt162b2 (DOSE 3 (BOOSTER), SINGLE, Lot number: FF2590), administration date: 10Nov2021, when the patient was 70-year-old, for COVID-19 immunisation, reaction(s): "Lipoma". The following information was reported: LIPOMA (medically significant), outcome "unknown", described as "I have a large lipoma removed from my deltoid muscle at about the place where we injected the vaccine/ benign lipoma". The patient underwent the following laboratory tests and procedures: Biopsy: came up benign, notes: Biopsy which came up benign; Magnetic resonance imaging: large lipoma, notes: I have a large lipoma removed from my deltoid muscle at about the place where we injected the vaccine and the location can be confirmed through an MRI. Therapeutic measures were taken as a result of lipoma. Clinical course: Patient had a large lipoma removed from his deltoid muscle at about the place where injected the vaccine and the location could be confirmed through an MRI that was made and then the surgeon had a record and the biopsy which came up benign. So, those two three documentations about that item and he did not know if it was the problem with the vaccine or if it just happened but it was curious that it was all on the same area. The vaccine was injected all on the right deltoid, all the same and the lipoma was in that area also and the surgeon could explain that better than patient could certainly. But he was curious if they were related, he did not know but it was a record saying, he did not know why. However, was there any relationship in time and also in location. All of the vaccine that he received, were Pfizer's. Treatment: Consumer stated, "No, just removal. He mentioned again, they do had the documentation of the MRI and the surgeons report, and the biopsy and he did not know if any parts of it remained. So, it could be tested for something other than what she was looking for.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300354231 Same patient and product, Different dose and events;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy
- Hospital-Tage
- -
- Labordaten
- Test Name: biopsy; Result Unstructured Data: Test Result:came up benign; Comments: Biopsy which came up benign; Test Name: MRI; Result Unstructured Data: Test Result:large lipoma; Comments: I have a large lipoma removed from my deltoid muscle at about the place where we injected the vaccine and the location can be confirmed through an MRI
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension
- Andere Medikamente
- LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 08.11.2023
- Impfdatum
- 04.10.2022
- Beginn
- 09.01.2023
- Tage bis Beginn
- 97,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Nasopharyngeal swab
Limb mass
Muscle mass
Symptomtext
covid test result=Positive; covid test result=Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Oct2022 at 14:00 as dose 4 (booster), single (Lot number: GH9702) at the age of 70 years, in right arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 04Oct2022 (as reported) as dose 3 (booster), single (Lot number: FM0173) at the age of 70 years, in right arm for covid-19 immunisation; covid-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Penicillin allergies" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Naprosin, reaction(s): "Drug Allergy: Naproxen". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 09Jan2023, outcome "unknown" and all described as "covid test result=Positive". The patient underwent the following laboratory tests and procedures: Nasopharyngeal swab: (09Jan2023) Positive.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300354231 same patient/drug, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230109; Test Name: Nasal Swab; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 12.10.2023
- Impfdatum
- 25.09.2023
- Beginn
- 05.10.2023
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pityriasis rosea
Symptomtext
I have developed pityriasis rosea. It started on 10/04/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pityriasis rosea
- Hospital-Tage
- -
- Labordaten
- I saw my doctor 10/6/23 , he gave me an itching cream.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Just mental health, no physical ailments
- Andere Medikamente
- Lamictal, Celexa, Unisom, Omeprizole, Magnesium, calcium and zinc, Valtrex, Incassia
- Allergien
- Keflex
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 07.09.2023
- Impfdatum
- 21.11.2022
- Beginn
- 01.08.2023
- Tage bis Beginn
- 253,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 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 76-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Nov2022 as dose 4 (booster), single (Lot number: fm0173) 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: "Depression" (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 Aug2023, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Depression
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 25.07.2023
- Impfdatum
- 16.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
PATIENT WAS GIVEN PFIZER COVID 19 VACCINE FOR 11 AND UP AND PATIENT WAS 10YRS AND 10 MONTHES OLD. NO ADVERSE REACTION WAS NOTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 13.06.2023
- Impfdatum
- 02.06.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 272,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysphonia
Laryngitis
Laryngitis viral
No adverse event
Symptomtext
I had no reaction to the vaccine. In 03/2023, I was diagnosed with chronic laryngitis that lasted about 3 weeks. I saw a doctor and was advised that it was viral and treated as it was viral. I had chronic laryngitis in 12/2021 too. As of today, I am feeling better but my voice is still not the same.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysphonia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Omeprazole
- Allergien
- Milk; Dairy
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 24.05.2023
- Impfdatum
- 25.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; Vaccine brand other: Moderna; Vaccine brand: Pfizer/BioNTech; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Jun2022 as dose 4 (booster), single (Lot number: Fm0173) at the age of 68 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 28Dec2020 as dose 1, single (Lot number: 037k20a), in right arm, on 25Jan2021 as dose 2, single (Lot number: 041l20a), in right arm, on 13Nov2021 as dose 3 (booster), single (Lot number: 004f21a), in right arm and on 29Oct2022 as dose 5 (booster), single (Lot number: 052d22a), in right arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Past drug history included: Ceclor, reaction(s): "Known allergies: Ceclor". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 25Jun2022, outcome "unknown", described as "Vaccine brand other: Moderna; Vaccine brand: Pfizer/BioNTech"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) negative; (20May2023) positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: After testing negative and no symptoms, started showing symptoms 17May2023. Tested positive 20May2023. Product: COVID 19 Treatment: Paxlovid, Treatment start date: 09May2023 to Treatment stop date: 14May2023.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the events (DRUG INEFFECTIVE,COVID-19 ) and BNT162B2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20230520; 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, Comment: Other medical history: none
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 20.05.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 125,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy breast
Breast cancer female
Breast cancer stage I
Mammogram abnormal
Radiotherapy
Symptomtext
Cancer was discovered in the left breast during a routine mammogram. Doctor recommended a partial mastectomy. No Lymph node involvement, no chemo, just radiation. Cancer was stage 1B.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy breast
- Hospital-Tage
- -
- Labordaten
- 22September2022 routine mammogram 17Nov2022 Biopsy, undetermined result
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Hydrochlorothiazide; Clonidine; Zoloft; Amlodipine; Multivitamin
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 11.07.2022
- Beginn
- 01.04.2023
- Tage bis Beginn
- 264,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Drug ineffective; 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 76-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27Feb2021 as dose 1, single (Lot number: EN6198), in left arm, on 20Mar2021 as dose 2, single (Lot number: EP6955), in left arm, on 13Aug2021 as dose 3 (booster), single (Lot number: FH8028), in left arm and on 11Jul2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 75 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Marginal zone lymphoma" (unspecified if ongoing); "levaquin Allergy" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXIN; NORTRIPTYLINE; LATANOPROST; RHOPRESSA; TIMOLOL. The following information was reported: COVID-19 (medically significant) with onset Apr2023, outcome "unknown"; DRUG INEFFECTIVE (medically significant) with onset Apr2023, outcome "unknown". Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300157708 same reporter/patient, different drug/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergic reaction to antibiotics; Marginal zone lymphoma
- Andere Medikamente
- LEVOTHYROXIN; NORTRIPTYLINE; LATANOPROST; RHOPRESSA; TIMOLOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 04.04.2023
- Impfdatum
- 18.05.2022
- Beginn
- 08.07.2022
- Tage bis Beginn
- 51,0
- 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 1/21/21 Lot# EL3249; Pfizer 2/11/21 Lot# EM9810; Pfizer 10/25/21 Lot# FF8841; Pfizer 5/18/22 Lot# FM0173
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 15.03.2023
- Impfdatum
- 27.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood immunoglobulin A
Blood immunoglobulin G
Blood immunoglobulin M
Electromyogram
Therapeutic response unexpected
Symptomtext
Her IgG was 3050/It had been climbing; 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 79-year-old female patient received BNT162b2 (BNT162B2), on 27Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 78 years for covid-19 immunisation. The patient's relevant medical history included: "cancer" (unspecified if ongoing), notes: My cancer blood that pretty much takes me into normal range; "5 invasive heart procedures" (not ongoing); "4 strokes" (unspecified if ongoing); "4 different kinds of cancer" (unspecified if ongoing); "knee replacements" (not ongoing); "Myeloma" (unspecified if ongoing), notes: smoldering stage; "Polio", start date: 1951 (unspecified if ongoing) ; "totally paralysed" (unspecified if ongoing), notes: She has no residual paralysis except for the little bit she didn't recover from in the 1950s; "lost capability to breath" (unspecified if ongoing); "she even had to be revived" (unspecified if ongoing); "she was in iron lung" (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE , Batch\lot number: EL9264, at (withheld)), administration date: 29Jan2021, for COVID-19 immunisation, reaction(s): "Her numbers were climbing/reported them going down after her first vaccines"; BNT162b2 (DOSE 2, SINGLE , Batch\lot number: EN6198), administration date: 04Mar2021, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE , Batch\lot number: FE3592), administration date: 26Oct2021, for COVID-19 Immunization, reaction(s): "She has cancer and her readings are better". The following information was reported: THERAPEUTIC RESPONSE UNEXPECTED (non-serious), outcome "unknown", described as "Her IgG was 3050/It had been climbing". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: 79-year-old female stated, "About a year and a half ago, she had an hour long conversation with a nurse from Pfizer (withheld) regarding if it was possible if we were doing any clinical trials that had to do with the COVID vaccine reducing or improving cancer blood number results. She was supposed to get a call back and she never got a call. she let it go, however, she just had 2 eye shocking results with my cancer blood that pretty much takes her into normal range. The only thing that she can figure out is that she had her final booster. She called in originally because there was some kind of decline. She was wanting to see if she could now talk to someone in the area of clinical trials or research to follow-up. The numbers are significant. And she just could not believe they would be interested. She had the 3 shots, and then she had 1 booster. If it is true if this would have an affect." Reference number: #.Agency: Warm-transferred to (name withheld) Agency: #, Reportum: #. Duplicate AE e-transmitted. Response: Told caller we don't have a direct access line to speak to a researcher, however, told her there is the Clinical Trials Customer Service line which may provide information about clinical trials.Told caller no information found on the Agency regarding cancer benefits after receiving the vaccine and told caller Pfizer takes these reports very seriously. Told caller we are required to document and report any events whether positive or negative and take it very seriously in capturing these events. Offered to warm-transfer to safety to further report event. Warm transfer from (name withheld) Pfizer medical information: (withheld) Product: Pfizer COVID vaccine Bivalent for 12 years of age and older. About a year and a half of ago, she spoke with (name withheld) in this department. Reference: # After she received the vaccine, her cancer numbers started getting better. She was diagnosed with Myeloma and was just in the smoldering stage. She was not to the point of being treated. They had been monitoring her since 11Sep2020. Her numbers were climbing. She reported them going down after her first vaccines. Her first blood draw was 14Nov2022. When she first called in she was interested in convalescent therapy. She wanted to know if anyone had interest in her blood. She was in an Iron lung. She even had to be revived. She was totally paralyzed, and she lost capability to breath. She has been through a lot of critical health issues, but she was still her alive and kicking. She just hoped she could help others with her information. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202101689707 same reporter/patient/vaccine, different dose(3)/similiar event;US-PFIZER INC-202300102500 same reporter/patient/vaccine, different dose(5)/similiar event;US-PFIZER INC-202300103094 same reporter/patient/vaccine, different dose(1)/similiar event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood immunoglobulin A
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221114; Test Name: IgA; Result Unstructured Data: Test Result:44.0; Test Date: 20221114; Test Name: IgG; Result Unstructured Data: Test Result:3050; Comments: It had been climbing; Test Date: 20221114; Test Name: IgM; Result Unstructured Data: Test Result:26; Test Name: EMG test; Result Unstructured Data: Test Result:Unknown results; Comments: had an EMG test, and the neurologist said he was surprised she is still alive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Assisted ventilation; Cancer (My cancer blood that pretty much takes me into normal range); Cancer; Cardiac operation; Dyspnoea; Knee replacement; Myeloma (smoldering stage); Paralysed (She has no residual paralysis except for the little bit she didn't recover from in the 1950s); Polio; Resuscitation; Stroke
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 21.02.2023
- Impfdatum
- 22.10.2022
- Beginn
- 11.02.2023
- Tage bis Beginn
- 112,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Cough
Fall
SARS-CoV-2 test positive
Symptomtext
02/11/23 presents to ED for "cough, fall, generalized weakness". PMHx of "seizure disorder on AED, OSA (noncompliant with CPAP), CKD stage 3, PVD, known cervical spinal stenosis"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- 02/11/23 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 16.02.2023
- Impfdatum
- 08.07.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 146,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bone density abnormal
Osteopenia
Spinal osteoarthritis
Symptomtext
I didn't have any symptoms. I wanted to have a bone density test for a baseline. My results showed Osteoporosis in my L1-L4 vertebrae and Osteopenia in my hip and neck. The doctor prescribed 1500mg of calcium and 5000iu vitamin D3 per day. The doctor also put me on FOSAMAX, one pill per week, but it gave me heartburn and bone and joint pain. I stopped taking it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone density abnormal
- Hospital-Tage
- -
- Labordaten
- 12/2020 DEXA scan, Osteoporosis in my L1-L4 vertebrae and Osteopenia in my hip and neck
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cardiovascular Disease; Asthma; Celiac Disease
- Andere Medikamente
- Venlafaxine; rosuvastatin; BREO ELLIPTA; ALLERCLEAR; REGENEMAX PLUS; HELIOCARE ADVANCED; vitamin D3
- Allergien
- Seasonal; environmental; gluten
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 15.02.2023
- Impfdatum
- 20.05.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 127,0
- 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 1/19/21 Lot# EL3249; Pfizer 2/9/21 Lot# 9265; Pfizer 9/8/21 Lot# 30138A; Pfizer 5/20/22 Lot# Fm017
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 01.06.2022
- Beginn
- 10.01.2023
- Tage bis Beginn
- 223,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
tested positive for Covid; tested positive for Covid; 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), in Apr2021 as dose 1, single (Lot number: EW0153), in Apr2021 as dose 2, single (Lot number: EW0175), in Feb2022 as dose 3 (booster), single (Batch/Lot number: unknown) and in Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 56 years for covid-19 immunisation. The patient's relevant medical history included: "Crohn's disease" (unspecified if ongoing). Concomitant medication(s) included: APRISO, start date: Jul2022; FOLIC ACID. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 10Jan2023, outcome "unknown" and all described as "tested positive for Covid". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (10Jan2023) Positive, notes: tested positive for Covid on 10Jan2023; (15Jan2023) Negative, notes: tested negative on 15Jan2023 and 16Jan2023; (16Jan2023) Negative, notes: tested negative on 15Jan2023 and 16Jan2023; (19Jan2023) Positive, notes: tested positive on 19Jan2023 again. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient received COVID 19 Treatment with Paxlovid, Treatment start date was 11Jan2023, Treatment stop date was 15Jan2023. No Known allergies. The patient received other medication in 2weeks. Conclusion of Previously Completed Investigation for FM0173: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot FM0173 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 FM0173, fill lot FM0172, and the formulated drug product lot FM0147. 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/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. Conclusion of Previously Completed Investigation for EW0175: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EW0175 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 EW0175, fill lot EP8726, and the bulk formulated drug product lot EP8607. 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/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. Conclusion of Previously Completed Investigation for EW0153: The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EW0153 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 EW0153, fill lot EP8692 and the formulated drug product lot EW8071. 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/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. 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: 20230110; Test Name: Covid-19 test; Test Result: Positive ; Comments: tested positive for Covid on 10Jan2023; Test Date: 20230115; Test Name: Covid-19 test; Test Result: Negative ; Comments: tested negative on 15Jan2023 and 16Jan2023; Test Date: 20230116; Test Name: Covid-19 test; Test Result: Negative ; Comments: tested negative on 15Jan2023 and 16Jan2023; Test Date: 20230119; Test Name: Covid-19 test; Test Result: Positive ; Comments: tested positive on 19Jan2023 again.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Crohn's disease
- Andere Medikamente
- APRISO; FOLIC ACID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 29.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure increased
Blood test abnormal
Symptomtext
In July 2022, at a regular doctor's appointment I was told that my blood pressure was high. I don't remember the reading, but I was shocked to know how high. For many months now, we have tried several different medications to help with the blood pressure. I have had the following side effects that they attributed to each new medication, including edema and diarrhea and heart palpitations, massive fatigue, nausea but no vomiting. We are still monitoring multiple medications to help balance my blood pressure. I have been referred to a heart doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure increased
- Hospital-Tage
- -
- Labordaten
- Blood panels, abnormal, JULY2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diarrhea due to surgery; Osteoarthritis; Non-specific Neuropathy; High Blood Pressure
- Andere Medikamente
- Cholestyramine; SPIRIVA inhaler; loperamide; vitamin C; lutein; vitamin D3; probiotic; ibuprofen; acetaminophen
- Allergien
- Bees; hornet stings; sulfa drugs; phenobarbital; LASIX
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 23.05.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 183,0
- 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 1/2/21 Lot# EL9261; Pfizer 2/19/21 Lot# EM9810; Pfizer 9/27/21 Lot# FF8841; Pfizer 5/23/22 Lot# FM0173
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 99,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 21.07.2022
- Beginn
- 23.01.2023
- Tage bis Beginn
- 186,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case all Pfizer dose 1 2/18/21 EL9267 dose 2 3/12/21 EN6199 dose 3 10/14/21 FF2590
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ test on 1/23/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 23.06.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 77,0
- 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 2/26/21 Lot# EN6202; Pfizer 3/19/2 Lot# EN6204; Pfizer 9/28/2 Lot# FF2589; Pfizer 6/23/22 Lot# FM0173;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 13.06.2022
- Beginn
- 16.01.2023
- Tage bis Beginn
- 217,0
- 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 2 vaccines Pfizer 12/21/21 LOt# FJ8757; Pfizer 6/13/22 Lot# FM0173
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 14.07.2022
- Beginn
- 24.11.2022
- Tage bis Beginn
- 133,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Covid outbreak 11/24/2022 prescribed inhaler for cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Reactive Airways Disease
- Andere Medikamente
- Duloxatine
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 18.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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 65-year-old male patient received BNT162b2 (BNT162B2), on 22Feb2021 at 10:00 as dose 1, single (Lot number: EN6198), in left arm, on 15Mar2021 at 10:00 as dose 2, single (Lot number: EN6207), in left arm, on 28Sep2021 at 09:30 as dose 3 (booster), single (Lot number: EW0168), in left arm and on 18May2022 at 10:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 65 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing). Concomitant medication(s) included: VALSARTAN, start date: 01May2019; BYSTOLIC, start date: 14Jan2022. No known allergies reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive; negative, notes: home test on day 7; Positive, notes: positive on day 8. Therapeutic measures were taken as a result of vaccination failure, covid-19. Therapeutic measures were taken as a result of vaccination failure, covid-19 with paxlovid from 23Sep2022 to 27Sep2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: covid test; Test Result: Positive ; Test Name: covid test; Test Result: Negative ; Comments: home test on day 7; Test Name: covid test; Test Result: Positive ; Comments: positive on day 8
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high
- Andere Medikamente
- VALSARTAN; BYSTOLIC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 15.07.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 139,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 60-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 15Jul2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 59 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: "Osteoporosis" (unspecified if ongoing); "hypothyroidism" (unspecified if ongoing); "anxiety" (unspecified if ongoing). Concomitant medication(s) included: LEXAPRO, start date: 15Mar2002; LEVOTHYROXINE, start date: 15Jan2000; VITAMIN D [COLECALCIFEROL], start date: 15Jan2020. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Dec2022) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 with paxlovid from 19Dec2022 to 23Dec2022. Clinical Course: Patient was taking other medications/products within 2 weeks of starting COVID-19 treatment. Patient previously received a COVID-19 Vaccine. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on available information and the temporal association, a possible contributory role of Comirnaty vaccine cannot be excluded for the reported events of "DRUG INEFFECTIVE " and "COVID-19 .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202212; Test Name: COVID-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anxiety; Hypothyroidism; Osteoporosis
- Andere Medikamente
- LEXAPRO; LEVOTHYROXINE; VITAMIN D [COLECALCIFEROL]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 25.07.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 149,0
- 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
Viral test positive
Symptomtext
Five months after vaccine, tested positive for COVID-19; Doctor also said I tested positive for another virus as well, in addition to COVID-19. Don't remember the name of the virus; Was prescribed PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; High Cholesterol; Arthritis.
- Andere Medikamente
- Multivitamin; atorvastatin; fenofibrate; amlodipine; finasteride; fluticasone.
- Allergien
- SOMA COMPOUND
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 12.06.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 43,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Postmenopausal haemorrhage
Symptomtext
I am not sure if this is caused by the vaccine, but I think it is worth to mention that I didn't have my period for a over year (menopause) and since the last vaccine, I've had my period at least 5 times.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Postmenopausal haemorrhage
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no known medicines
- Vorgeschichte
- seasonal allergies
- Andere Medikamente
- Zyrtec
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 24.12.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Investigation
Paraplegia
Symptomtext
he tried to get out of bed he could not move from the waist down; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. An 83-year-old male patient received BNT162b2 (BNT162B2), on 19Jul2022 as dose 4 (booster), 0.3 ml single (Lot number: FM0173, Expiration Date: 30Sep2022) at the age of 83 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "Metastatic brain and lung cancer" (unspecified if ongoing), notes: My husband has metastatic brain and lung cancer.; "Metastatic brain and lung cancer" (unspecified if ongoing), notes: My husband has metastatic brain and lung cancer.; "Cholesterol" (unspecified if ongoing); "Immunocompromised" (unspecified if ongoing), notes: He has been on immunotherapy for two+ years with Opdivo. , He is immunocompromised and has been under immunotherapy for 2 years.; "Metastatic melanoma", start date: Aug2020 (unspecified if ongoing), notes: Metastatic melanoma Diagnosed latter part of Aug2020 had gamma knife treatment Sep2020. Concomitant medication(s) included: ATORVASTATIN oral taken for blood cholesterol abnormal; OPDIVO intravenous taken for immunodeficiency, start date: 2020, stop date: 2020. Vaccination history included: BNT162b2 (1st dose: Date: 09Feb2021. Time: Morning, she doesn't know specific time. , Anatomical Site of injection: arm, unknown which one. Route of Administration: intramuscular; Batch/Lot number: EK9231, EXP: Apr2021.), administration date: 09Feb2021, when the patient was 82-year-old, for COVID-19 immunization; BNT162b2 (2nd dose: Date: 02Mar2021, Time: Morning, unknown what time. , Anatomical Site of injection: unknown arm. , Route of Administration: intramuscular; Batch/Lot number: EL3246, EXP: Apr2021.), administration date: 02Mar2021, when the patient was 82-year-old, for COVID-19 immunization; BNT162b2 (he had the third dose in 26Aug2021., Time: Morning. Anatomical Site of injection: unknown arm. Route of Administration: intramuscular. , When he had the third, hours later when he tried to get out of bed he could not move from the waist down. In the morning he was fine.), administration date: 26Aug2021, when the patient was 82-year-old, for Covid-19 immunization, reaction(s): "he tried to get out of bed he could not move from the waist down"; Flu (He has had no other vaccines ever than typical Flu or pneumonia vaccines, which she can't remember when those were, they were not around the time of COVID-19 vaccines); Pneumonia vaccines (He got one of the pneumonia vaccines, she doesn't remember when.). The following information was reported: PARAPLEGIA (medically significant) with onset 19Jul2022, outcome "unknown", described as "he tried to get out of bed he could not move from the waist down". The patient underwent the following laboratory tests and procedures: Metastatic melanoma: (Aug2020) Metastatic melanoma. Clinical course: Reporter husband had metastatic brain and lung cancer. He had been on immunotherapy for two+ years with Opdivo. He had the first two vaccines for COVID. His oncologist recommended additional vaccines. So when he had the third, hours later when he tried to get out of bed he could not move from the waist down. In the morning he was fine. It also happened when he had the fourth. It had us concerned as to whether he should continue with boosters if this was a possible side effect from the third and fourth. Calling on behalf of her husband's booster doses. "When he had the first and second dose there was no problem. He was immunocompromised and had been under immunotherapy for 2 years. When he had the third dose in 26Aug2021, when we've gotten them before it was before noon. In the middle of the night, he went to the restroom and from the waist down he couldn't move his legs. When he got up in the morning, he was fine." Reporter stated she "brushed it off" and didn't call anyone. In Jul2022 he got "the fourth booster with the same side effect, in the middle of the night." When he went to have his immunotherapy treatment last week, she mentioned it because "they want him to keep getting boosters" due to his immunosuppression. They suggested they call the CDC or Pfizer to see if he should continue to take boosters in the concern that he may have a worse reaction the next time. Reporter was uncertain if he received the bivalent booster as his 4th dose. Jul2022 dose: Lot #FM0173. Question: Patient was uncertain if he received the bivalent booster as his 4th dose. Reporter calling about Pfizer COVID-19 vaccine for her husband whose birthday was [DOB withheld]. He was immunocompromised, he had metastatic melanoma to the brain and lung. When the vaccine first came out they got the first two doses in 2021, and then he had the third dose in Aug2021 per recommendation of his oncologist. For the third dose which they both got in the morning, in the middle of the night he got up to go to the rest room and he couldn't move his legs from the waist down, which put her in a panic mode. When he woke up the next day he was fine. Then in Jul this year he had another Pfizer booster and had the same effects on the fourth one. A little over a week ago they casually mentioned this to his oncologist and she said it was too coincidental for him to do that both times, and they should call Pfizer and find out if this is a possible side effect, and if it was, if he should get any more boosters. On his birthday, 09Feb2021, her husband had his first dose of the Pfizer COVID-19 vaccine. His legs didn't work after his third dose booster he got 26Aug2021, which he was 82, clarified to 81 years old. She clarified that it was the last two booster doses that he had the same side effects, which his oncologist suggested they contact Pfizer since she couldn't make that call if he should have any more boosters or not. She would hate for him to have another booster and have another side effect. They did no treatment, it was just that he wanted to get up to go to the restroom and he couldn't get out of bed. When he tried he almost fell, and she got him back in bed and they went back to sleep. When he woke up in the morning he was fine and walked to the kitchen and had breakfast. When she asked him that day how he was doing he said he was fine. This happened again after his fourth dose booster, the same. He tried to get up in the wee hours of the night and couldn't, then in the morning there was no problem when he got up, which they always get up between 7:30- 8:00AM. He walked to the kitchen and had breakfast and was his normal self the rest of the day, he was fine. Pfizer COVID-19 vaccine Indication: He was immunocompromised, and his oncologist wanted to make sure he was protected. She suggested since they are husband and wife and live together that she have it as well, so they both have been boostered. Concomitant Medications: The only prescription her husband took was Atorvastatin, which he had been on at least ten years. He also had immunotherapy, for a little over two years he had been on Opdivo immunotherapy. It was Sep or Oct2020 when he started Opdivo. He has had no other vaccines ever than typical flu or pneumonia vaccines, which she couldn't remember when those were, they were not around the time of COVID-19 vaccines. He got one of the pneumonia vaccines, she didn't remember when. He got the flu or pneumonia vaccines at [pharmacy name withheld]. She Could not read HCP or site name for his third dose, she wanted to say it might have been (pharmacy name withheld) because one time they went to (pharmacy name withheld) since they didn't have to make an appointment. His third dose information on the vaccine card only has the LOT number provided on the handwritten card. LOT Look like FE3181. Pfizer/BioNTech COVID-19 Vaccine Follow-up Questionnaire: Pfizer/BioNTech COVID-19 Vaccine Details: 1st dose: Date: 09Feb2021. Time: Morning, she doesn't know specific time, all boosters were in the morning. Anatomical Site of injection: arm, unknown which one. Route of Administration: intramuscular; Batch/Lot number: EK9231, EXP: Apr2021. HCP clinic site said (facility name withheld), this could be (facility name withheld). 2nd dose: Date: 02Mar2021, Time: Morning, unknown what time. Anatomical Site of injection: unknown arm. Route of Administration: intramuscular; Batch/Lot number: EL3246, EXP: Apr2021. HCP clinic site said [facility name withheld], this could be [facility name withheld] Cancer Specialists. 3rd dose: Date: Time: Morning. Anatomical Site of injection: unknown arm. Route of Administration: intramuscular. 4th dose: Date: 19Jul2022. He had it at [pharmacy name withheld], information for it printed a label put on the back of the vaccine card. NDC: LOT: FM0173. EXP: 30Sep2022. Dose: quantity 0.3mL, injected into his unknown arm. Complete if a 3rd or Subsequent dose was administered. Booster dose due to a weakened immune system: if the reason is a weakened immune system, please select one of the conditions below: Current or recent cancer. Prior Vaccinations (within 4 weeks): None. Her husband got no other vaccines the same day or the four weeks prior to his booster doses. Family Medical History Relevant to Adverse Events (AEs): None, she didn't have any side effects to the vaccines, she didn't even have a sore arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Investigation
- Hospital-Tage
- -
- Labordaten
- Test Date: 202008; Test Name: Metastatic melanoma; Result Unstructured Data: Test Result:Metastatic melanoma
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood cholesterol abnormal; Immunocompromised (He is immunocompromised and has been under immunotherapy for 2 years.); Lung metastases (My husband has metastatic brain and lung cancer.); Metastases to brain (My husband has metastatic brain and lung cancer.); Metastatic melanoma (Diagnosed latter part of Aug2020 had gamma knife treatment Sep2020)
- Andere Medikamente
- ATORVASTATIN; OPDIVO
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 21.06.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 66,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I had a scratchy throat and runny nose. They were both mild and felt like hay fever. I took PAXLOVID for the normal dose days. I felt better in a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID PCR test positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Omeprazole; rosuvastatin calcium; amlodipine valsartan; metformin HCL
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 10.12.2022
- Impfdatum
- 04.06.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Audiogram abnormal
Deafness
Symptomtext
Patient reported hearing loss. Patient had significant decline of hearing ability between 4/21/22 and 11/28/22. He started feeling his hearing loss around June 2022. The condition has persisted with no improvement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Audiogram abnormal
- Hospital-Tage
- -
- Labordaten
- Patient had audiogram on 4/21/22 and again on 11/28/22. The results on 11/28/22 showed a significant decline comparing to his results on 4/21/22. The results on 11/28/22 showed that he had moderate to severe hearing disability.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 28.11.2022
- Impfdatum
- 27.06.2022
- Beginn
- 27.11.2022
- Tage bis Beginn
- 153,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case dose 1 Pfizer 2/27/21 EN6202 dose 2 Pfizer 3/20/21 EN6207 dose 3 Pfizer 10/2/21 FE3592
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 11/27/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 12.05.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 81,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Biopsy skin
Symptomtext
Accelerated excessive hair loss in past three months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alopecia
- Hospital-Tage
- -
- Labordaten
- Scalp biopsy
- Aktuelle Erkrankungen
- Bouts of Vertigo
- Vorgeschichte
- None
- Andere Medikamente
- Lansoprazole 30 mg Advil Average 10/week Gaviscon OTC
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 27.05.2022
- Beginn
- 06.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Secretion discharge
Symptomtext
I received my vaccine on 05/27/2022 without any issues. The week of 06/06/2022, I started having this constant cough with excessive mucus. I have seen multiple doctors and they can't diagnose what is wrong. I have been on three rounds of antibiotics and two rounds of steroids. I have tried multiple over the counter medications, but nothing helps. I take ten to twenty-five cough a day. The ENT doctor recommended to see an allergist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Probiotic; multivitamin; vitamin B12; coQ10; biotin; CLARITIN
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 26.05.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 133,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 15.06.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 131,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID vaccine breakthrough case dose 1 Pfizer 1/26/21 EL9261 dose 2 Pfizer 2/25/21 EN6202 dose 3 Pfizer 10/3/21 FF2587
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ test on 10/24/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 27.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 64-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Mar2021 at 11:30 as dose 1, single (Lot number: EP7534), in left arm, on 03Apr2021 at 11:00 as dose 2, single (Lot number: EW0151), in left arm, on 25Oct2021 at 10:30 as dose 3 (booster), single (Lot number: FE3592), in left arm and on 27Jul2022 at 11:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 63 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Obesity" (unspecified if ongoing). Concomitant medication(s) included: PREMARIN (Brand: pharm), start date: 05Jul2010; GABAPENTIN (Brand: Aurobindo), start date: 01Apr2022, also reported as other medication in 2weeks. Past drug history included: Vicodin, reaction(s): "Known allergies: Vicodin"; Dilaudid, reaction(s): "Known allergies: dilaudid". 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) Positive, notes: COVID 19 Treatment; (18Oct2022) Negative; (20Oct2022) Positive, notes: Tested positive for COVID-19 48 hours after testing negative. Therapeutic measures were taken as a result of vaccination failure, covid-19 included Paxlovid, started on 10Oct2022 and stopped on 15Oct2022. Clinical course was reported as, Tested positive for COVID-19 on 20Oct2022 at 08:00, 48 hours after testing negative, 5 days after finishing full course of Paxlovid. Patient not received any treatment and was recovering.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 20221018; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20221020; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Tested positive for COVID-19 48 hours after testing negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Obesity
- Andere Medikamente
- PREMARIN; GABAPENTIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 22.10.2022
- Impfdatum
- 25.05.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 129,0
- 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 male patient received BNT162b2 (BNT162B2), on 08Mar2021 as dose 1, single (Lot number: EN6206), in left arm, on 30Mar2021 as dose 2, single (Lot number: ER8733), in left arm, on 06Oct2021 as dose 3 (booster), single (Lot number: FF2589), in left arm and on 25May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 66 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Oct2022, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: Patient took paxlovid for treatment of adverse events, Device timestamp: 19Oct2022. The patient had no Known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: none No known allergies
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- -
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 13.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- 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 contactable reporter(s) (Other HCP) from product quality group. The reporter is the patient. A 51-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Mar2021 as dose 1, single (Lot number: EN6207), on 13Apr2021 as dose 2, single (Lot number: ER8729), on 08Dec2021 as dose 3 (booster), single (Lot number: FJ8762) and on 13Jun2022 as dose 4 (booster), single (Lot number: FM0173) for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL, start date: 17Sep2021; MUCINEX, start date: 13Oct2022. 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". Therapeutic measures were taken as a result of covid-19 which included paxlovid from 15Oct2022 to 16Oct2022. Clinical course: The patient had no known allergies. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the current available limited information in the case provided, the causal association between the events and the use of suspect product BNT162B2 cannot be fully excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high
- Andere Medikamente
- LISINOPRIL; MUCINEX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 10.06.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID-19 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 female patient (not pregnant) received BNT162b2 (BNT162B2), on 04Oct2021 as dose 3 (booster), single (Lot number: FF2589), in left arm and on 10Jun2022 as dose 4 (booster), single (Lot number: FM0173) 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) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing). The patient had no known allergies. Concomitant medication(s) included: ATORVASTATIN, start date: 04Apr2022, stop date: 27Sep2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "unknown" and all described as "COVID-19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient was treated with Paxlovid. Clinical information: Other medication in 2 weeks product was Atorvastatin. Other medication in 2weeks brand was Generic for Lipitor. The patient was taking any other medications/products within 2 weeks of starting COVID-19 treatment. The patient previously received a covid-19 vaccine. No known allergies. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- ATORVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 13.05.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 111,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
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 54-year-old male patient received BNT162b2 (BNT162B2), on 14Mar2021 as dose 1, single (Lot number: 1802070), in right arm, on 28Oct2021 as dose 2 single (Lot number: Ff2593), in right arm and on 13May2022 as dose 3 (booster), single (Lot number: Fm0173) at the age of 53 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing), notes: High blood pressure; "high cholesterol" (unspecified if ongoing). The patient's concomitant medications were not reported. 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: (2022) Negative, notes: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; (2022) Negative, notes: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; (2022) Negative, notes: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; (2022) Negative, notes: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; (2022) Negative, notes: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; (10Oct2022) Positive, notes: tested positive again for COVID. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient was taking other medications/ products within 2 weeks of starting COVID-19 treatment. The patient previously received a COVID-19 Vaccine. The patient had no known allergies. After fever, sore throat, headache and overall feeling badly resolved with Paxlovid, cough and congestion continued. After testing negative for five consecutive days beginning on day 5 or 6 after symptom onset, tested positive again for COVID on 10Oct2022. This was a full 15 days after beginning Paxlovid. Adverse event was rebound COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 2022; Test Name: testing negative; Test Result: Negative ; Comments: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; Test Date: 2022; Test Name: testing negative; Test Result: Negative ; Comments: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; Test Date: 2022; Test Name: testing negative; Test Result: Negative ; Comments: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; Test Date: 2022; Test Name: testing negative; Test Result: Negative ; Comments: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; Test Date: 2022; Test Name: testing negative; Test Result: Negative ; Comments: testing negative for five consecutive days beginning on day 5 or 6 after symptom onset; Test Date: 20221010; Test Name: testing negative; Test Result: Positive ; Comments: tested positive again for COVID
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (High blood pressure); High cholesterol
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 06.06.2022
- Beginn
- 17.11.2021
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Interchange of vaccine products
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; Vaccine_brand=Pfizer / BioNTech, vaccine_brand_other=Moderna; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 19Mar2021 as dose 1, single (Lot number: ER2613), in left arm, on 12Apr2021 as dose 2, single (Lot number: ER8737), in left arm and on 06Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 52 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 17Nov2021 as dose 3 (booster), single (Lot number: OBF21A), in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: IBUPROFEN; LISINOPRIL; TYLENOL; OMEGA 3 FISH OIL [FISH OIL]. Past drug history included: Amoxicillin, reaction(s): "Known allergies: Amoxicillin", notes: Known allergies: Amoxicillin; Septra, reaction(s): "Known allergies: septrac", notes: Known allergies: septrac. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 17Nov2021, outcome "unknown", described as "Vaccine_brand=Pfizer / BioNTech, vaccine_brand_other=Moderna"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Oct2022) Positive; (Oct2022) Negative, notes: I had 2 negative tests that were taken 48 hours apart; (Oct2022) Negative, notes: I had 2 negative tests that were taken 48 hours apart. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: The patient has received Paxlovid for the treatment of Covid-19 from 28Sep2022 to 03Oct2022. 4 days after completing Paxlovid, and 24 hours after she had 2 negative tests that were taken 48 hours apart, her COVID symptoms returned and she had a positive test on 07Oct2022, it was not recovered. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202210; Test Name: Tests; Test Result: Positive ; Test Date: 202210; Test Name: Tests; Test Result: Negative ; Comments: I had 2 negative tests that were taken 48 hours apart; Test Date: 202210; Test Name: Tests; Test Result: Negative ; Comments: I had 2 negative tests that were taken 48 hours apart
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- IBUPROFEN; LISINOPRIL; TYLENOL; OMEGA 3 FISH OIL [FISH OIL]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 12.07.2022
- Beginn
- 01.07.2021
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Chest discomfort
Symptomtext
After receiving my fourth dose of Pfizer, I began to experience some chest pressure. I cannot remember the exact date, but it was a few days later. I went to see my PCP for a routine check-up and told him about my chest pain. He scheduled me with a cardiologist. I had an appointment with the cardiologist in September and I had a lot of blood drawn for testing. I have another appointment next month for a follow-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Prostate Cancer; Ulcer; High Blood Pressure; High Cholesterol
- Andere Medikamente
- Meloxicam; losartan; simvastatin; tamsulosin; omeprazole; LUMIGAN drops; temozolomide-dimolopsol; multivitamin
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 08.10.2022
- Impfdatum
- 23.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Interchange of vaccine products
Off label use
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; Interchange of vaccine products; Off label use; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old male patient received BNT162b2 (BNT162B2), on 11Feb2021 as dose 1, single (Lot number: EN6201), in left arm and on 23May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 70 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), 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. Concomitant medication included: PANTOPRAZOLE.. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19, the patient received the paxlovid on 31Aug2022.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201205965 Same reporter/patient, different drug, different event.;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19 Treatment; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PANTOPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 26.02.2021
- Beginn
- 03.10.2022
- Tage bis Beginn
- 584,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fall
Symptomtext
No COVID-19 symptoms reported. Case was admitted to hospital 10/03/2022 due to history of falling at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fall
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- history of falling
- Andere Medikamente
- None reported
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 29.06.2022
- Beginn
- 18.09.2022
- Tage bis Beginn
- 81,0
- 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) from product quality group. The reporter is the patient. A 52-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 51 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: "COPD" (unspecified if ongoing); "Asthma" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 18Sep2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18Sep2022) Positive, notes: On 18Sep I tested positive for COVID and started taking Paxlovid; (22Sep2022) Negative, notes: On 22Sep I tested negative for COVID with no symptoms; (26Sep2022) Positive, notes: This morning 26Sep I tested positive for COVID again with symptoms. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: No known allergies. No other medication in 2 weeks. Rebound covid. On 18Sep I tested positive for COVID and started taking Paxlovid. On 22Sep I tested negative for COVID with no symptoms. This morning 26Sep I tested positive for COVID again with symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220918; Test Name: COVID-19 test; Test Result: Positive ; Comments: On 18Sep I tested positive for COVID and started taking Paxlovid.; Test Date: 20220922; Test Name: COVID-19 test; Test Result: Negative ; Comments: On 22Sep I tested negative for COVID with no symptoms; Test Date: 20220926; Test Name: COVID-19 test; Test Result: Positive ; Comments: This morning 26Sep I tested positive for COVID again with symptoms
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 28.09.2022
- Impfdatum
- 24.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was given vaccine past beyond use date but did not experience any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 19.05.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 105,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 46-year-old male patient received BNT162b2 (BNT162B2), on 24Feb2021 at 12:00 as dose 1, single (Lot number: EN6202), in right arm, on 23Mar2021 at 13:15 as dose 2, single (Lot number: ER8727), in left arm, on 29Sep2021 at 17:15 as dose 3 (booster), single (Lot number: FF2588), in right arm and on 19May2022 at 17:30 as dose 4 (booster), single (Lot number: FM0173) at the age of 46 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 Sep2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure and covid-19 included Paxlovid (lot numberGE4606) from 14Sep2022 to 18Sep2022. Clinical course: It was unknown that the patient received other medications within 2 weeks to the COVID vaccine. Patient had a COVID-19 rebound and onset of symptoms from 24Sep2022 07:00 AM. Patient did not receive treatment for symptoms and not recovered from symptoms. The patient previously receive a COVID-19 Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 26.09.2022
- Impfdatum
- 14.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered to patient after the Beyond Use Date of 8/25/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 26.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered to patient after the Beyond Use Date of 8/25/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 26.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered to patient after the Beyond Use Date of 8/25/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 26.09.2022
- Impfdatum
- 26.08.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered to patient after the Beyond Use Date of 8/25/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.09.2022
- Impfdatum
- 26.01.2021
- Beginn
- 21.08.2022
- Tage bis Beginn
- 572,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
COVID-19
COVID-19 immunisation
Hypersomnia
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
Interchange of vaccine products; Revaccination with different COVID-19 vaccine; Slept a lot; Sick with COVID; This spontaneous case was reported by a consumer and describes the occurrence of HYPERSOMNIA (Slept a lot), COVID-19 (Sick with COVID), INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 048F21A, 011M20A and 027L0A) for COVID-19 vaccination. Co-suspect products included non-company products ADALIMUMAB (HUMIRA) for Rheumatoid arthritis and TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for COVID-19 vaccination. The patient's past medical history included Tobacco user (Stopped 1998.) in 1998. Concurrent medical conditions included Dizziness, Tuberculosis, Rheumatoid arthritis, Arthritis, Drug allergy (Statin allergy) and Abstains from alcohol. Concomitant products included MELOXICAM for Arthritis, MECLOZINE HYDROCHLORIDE (MECLIZINE [MECLOZINE HYDROCHLORIDE]) for Dizziness, LEFLUNOMIDE and FOLIC ACID for Rheumatoid arthritis, PREDNISONE, DILTIAZEM, CITALOPRAM, LISINOPRIL, TOPIRAMATE, PREGABALIN, ONDANSETRON, BENZONATATE, MONTELUKAST and PRAVASTATIN for an unknown indication. On 26-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Mar-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. In 2021, the patient started ADALIMUMAB (HUMIRA) (Subcutaneous) Citrate Free, 40mg/0.4ml, (40 mg,1 in 2 wk). On 10-Dec-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 26-Jun-2022, the patient received dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (Intramuscular) 1 dosage form. On 21-Aug-2022, the patient experienced HYPERSOMNIA (Slept a lot) and COVID-19 (Sick with COVID). On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) at an unspecified dose and frequency. On 28-Aug-2022, HYPERSOMNIA (Slept a lot) and COVID-19 (Sick with COVID) had resolved. At the time of the report, INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 21-Aug-2022, SARS-CoV-2 test: (Positive) Positive. On 28-Aug-2022, SARS-CoV-2 test: (Negative) Negative. On an unknown date, Body temperature: 99.8 99.8 F. It was unknown if patient was enrolled in a COVID-19 Vaccine Trial. The patient was treated with PAXLOVID and no further information was provided. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in. Company Comment: This is a spontaneous case concerning a 70-year-old female patient with no relevant medical history, who experienced the unexpected, non-serious adverse events of special interest of Hypersomnia and COVID-19, approximately 8 months after receiving the third dose of mRNA-1273 vaccine. The patient reported to have slept a lot and got sick with COVID (swab test positive) and was treated with Paxlovid. The events had resolved after 7 days. Revaccination with different COVID-19 vaccine and Interchange of vaccine products were also reported as the patient received a dose of other COVID-19 vaccine (Pfizer/Biontech) approximately 6 months after the third dose of mRNA-1273/2 months prior to the events of Hypersomnia and COVID-19. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2021-623654 (Patient Link).; Sender's Comments: This is a spontaneous case concerning a 70-year-old female patient with no relevant medical history, who experienced the unexpected, non-serious adverse events of special interest of Hypersomnia and COVID-19, approximately 8 months after receiving the third dose of mRNA-1273 vaccine. The patient reported to have slept a lot and got sick with COVID (swab test positive) and was treated with Paxlovid. The events had resolved after 7 days. Revaccination with different COVID-19 vaccine and Interchange of vaccine products were also reported as the patient received a dose of other COVID-19 vaccine (Pfizer/Biontech) approximately 6 months after the third dose of mRNA-1273/2 months prior to the events of Hypersomnia and COVID-19. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: 99.8 F; Test Date: 20220828; Test Name: Home test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220821; Test Name: Swab test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Abstains from alcohol; Arthritis; Dizziness; Drug allergy (Statin allergy); Rheumatoid arthritis; Tuberculosis
- Vorgeschichte
- Medical History/Concurrent Conditions: Tobacco user (Stopped 1998.)
- Andere Medikamente
- PREDNISONE; DILTIAZEM; MECLIZINE [MECLOZINE HYDROCHLORIDE]; LEFLUNOMIDE; MELOXICAM; FOLIC ACID; CITALOPRAM; LISINOPRIL; TOPIRAMATE; PREGABALIN; ONDANSETRON; BENZONATATE; MONTELUKAST; PRAVASTATIN; HUMIRA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 03.06.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 111,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 24.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event reported by patient but contacted the patient and informed them that the dose they received was given after the beyond use date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 24.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product storage error
Symptomtext
No adverse even reported by patient but we did inform patient that the vaccine had been administered after its beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse event was reported when we spoke to patient and informed them that their shot was received shot after the beyond use date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 23.08.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was given vaccine past beyond use date but did not experience any side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- ADHD
- Andere Medikamente
- None
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 14.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Mar2021 as dose 1, single (Lot number: En6205), in left arm, on 30Mar2021 as dose 2, single (Lot number: Er8733), in left arm, on 30Nov2021 as dose 3 (booster), single (Lot number: Fj8762), in left arm and on 14Jul2022 as dose 4 (booster), single (Lot number: Fm0173) at the age of 54 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Bactria" (unspecified if ongoing), notes: Known allergies: Bactria. There were no concomitant medications. Past drug history included: Augmentin, reaction(s): "Known allergies: Augmentin", notes: Known allergies: Augmentin; Clindamycin, reaction(s): "Known allergies: Clindamycin.", notes: Known allergies: Clindamycin. 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: (unspecified date) Positive, notes: COVID 19 Treatment; (Sep2022) Positive, notes: Testing positive again and bad symptoms 4 days after finishing initial treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. No other medication was received in 2weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 202209; Test Name: COVID-19 test; Test Result: Positive ; Comments: Testing positive again and bad symptoms 4 days after finishing initial treatment.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Bacterial allergy (Known allergies: Bactria)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 23.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
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 73-year-old male patient received BNT162b2 (BNT162B2), on 23Feb2021 as dose 1, single (Lot number: EN6201), in left arm, on 21Mar2021 as dose 2, single (Lot number: GP7534), in left arm, on 05Nov2021 as dose 3 (booster), single (Lot number: FF2590), in left arm and on 23May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Heart and vascular blockages with stents" (unspecified if ongoing), notes: Other medical history: Heart and vascular blockages with stents and a heart valve replacement; "Heart and vascular blockages with stents" (unspecified if ongoing), notes: Other medical history: Heart and vascular blockages with stents and a heart valve replacement; "a heart valve replacement" (unspecified if ongoing), notes: Other medical history: Heart and vascular blockages with stents and a heart valve replacement. Concomitant medication(s) included: XARELTO; CARVEDILOL; ATORVASTATIN; BABY ASPIRIN. The following information was reported: VACCINATION FAILURE (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: (unspecified date) positive, notes: COVID 19 Treatment; (Sep2022) faint line, notes: Tested on Monday (Labor Day) and at first it looked clear but looking closer, there was a very, very faint line; (Sep2022) positive, notes: Decided to test and the positive line was quicker to show up and darker than any previous tests. Therapeutic measures were taken as a result of vaccination failure, covid-19. Additional information: Sunday morning was last day of Paxlovid. Tested on Monday (Labor Day) and at first it looked clear but looking closer, there was a very, very faint line. No symptoms through Wednesday so I, thought I was clear. Thursday morning I started with a stuffy nose and thought it was allergies. Decided to test and the positive line was quicker to show up and darker than any previous tests. Putting our guard down, my wife was exposed more in the last couple of days. Symptoms are as bad or worse than the first, time around but got quick relief in a day the first time around. Follow up attempts are completed. 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; Test Date: 202209; Test Name: COVID-19 test; Result Unstructured Data: Test Result:faint line; Comments: Tested on Monday (Labor Day) and at first it looked clear but looking closer, there was a very, very faint line.; Test Date: 202209; Test Name: COVID-19 test; Test Result: Positive ; Comments: Decided to test and the positive line was quicker to show up and darker than any previous tests.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Coronary stent placement (Other medical history: Heart and vascular blockages with stents and a heart valve replacement); Heart valve replacement (Other medical history: Heart and vascular blockages with stents and a heart valve replacement); Vascular stent infection (Other medical history: Heart and vascular blockages with stents and a heart valve replacement)
- Andere Medikamente
- XARELTO; CARVEDILOL; ATORVASTATIN; BABY ASPIRIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 26.06.2022
- Beginn
- 21.08.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
COVID-19
Drug ineffective
Hypersomnia
SARS-CoV-2 test
Symptomtext
sick with COVID; sick with COVID; slept a lot; This is a solicited report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): 22K-163-4520987-00 (Agency). A 70-year-old female patient received BNT162b2 (BNT162B2), on 26Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 69 years intramuscular for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 26Jan2021 as dose 1, single (Lot number: 027L0A), on 04Mar2021 as dose 2, single (Lot number: 011M20A) and on 10Dec2021 as dose 3 (booster), single (Lot number: 048F21A), all intramuscular for covid-19 immunisation; adalimumab (HUMIRA), since 2021 (ongoing) (Lot number: 1164825) at 40 mg (40 mg, (citrate free (1 in 2 week)), subcutaneous for rheumatoid arthritis. The patient's relevant medical history included: "Tobacco use", stop date: 1998, notes: Tobacco use; "Abstains from Alcohol" (unspecified if ongoing); "Tuberculosis" (unspecified if ongoing). Concomitant medication(s) included: PREDNISONE; DILTIAZEM; MECLIZINE [MECLOZINE HYDROCHLORIDE] taken for dizziness; LEFLUNOMIDE taken for rheumatoid arthritis; MELOXICAM taken for arthritis; FOLIC ACID taken for rheumatoid arthritis; CITALOPRAM; LISINOPRIL; TOPIRAMATE; PREGABALIN; ONDANSETRON; BENZONATATE; MONTELUKAST; PRAVASTATIN. Past drug history included: Statin, reaction(s): "Statin allergy", notes: Statin allergy. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 21Aug2022, outcome "recovered" (28Aug2022) and all described as "sick with COVID"; HYPERSOMNIA (non-serious) with onset 21Aug2022, outcome "recovered" (28Aug2022), described as "slept a lot". The patient underwent the following laboratory tests and procedures: Body temperature: (unspecified date) 99.8 Fahrenheit; SARS-CoV-2 test: (28Aug2022) Negative; (21Aug2022) Positive. The action taken for adalimumab was dosage not changed. Therapeutic measures were taken as a result of drug ineffective, covid-19, hypersomnia. Clinical Course: Solicited report from a consumer of a 70-year-old female with events of non-serious slept a lot and sick with COVID with Humira 40mg/0.4ml (Adalimumab). On 21Aug2022, the patient experienced slept a lot and sick with COVID. On 28Aug2022, the slept a lot and sick with COVID resolved. Moderna COVID-19 vaccine (Elasomeran) and Pfizer BioNTech COVID-19 vaccine (Tozinameran) were also considered suspect. It was unknown if patient was enrolled in a COVID-19 vaccine trial. The patient was treated with Paxlovid. Causality for Humira 40mg/0.4ml (Adalimumab) The reporter's causality for the event(s) of slept a lot and sick with COVID with Humira 40mg/0.4ml (Adalimumab) was no reasonable possibility. On 25Aug2022, received updates to patient demographics, medical history, event information, reporter opinion of causality, suspect drug information, concomitant drug information, treatment drug information, laboratory/diagnostic procedures and narrative description. The event of "slept a lot" was added. The reporter considered "sick with covid" and "slept a lot" not related to BNT162b2. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Based on plausible dose -event relationship post vaccination and no other alternate explanation the causal role of BNT162B2 cannot be excluded for the reported covid-19, drug ineffective, hypersomnia.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: Test Result:99.8 Fahrenheit; Test Date: 20220828; Test Name: Home test; Test Result: Negative ; Test Date: 20220821; Test Name: Swab test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Abstains from alcohol; Tobacco user (Tobacco use); Tuberculosis
- Andere Medikamente
- PREDNISONE; DILTIAZEM; MECLIZINE [MECLOZINE HYDROCHLORIDE]; LEFLUNOMIDE; MELOXICAM; FOLIC ACID; CITALOPRAM; LISINOPRIL; TOPIRAMATE; PREGABALIN; ONDANSETRON; BENZONATATE; MONTELUKAST; PRAVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 26.06.2022
- Beginn
- 21.08.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
sick with COVID; sick with COVID; Moderna COVID-19 vaccine (Elasomeran) and Pfizer BioNTech COVID-19 vaccine (Tozinameran) were also considered suspect; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. Other Case identifier(s): 22K-163-4520987-00 (Agency). A 70-year-old female patient received BNT162b2 (BNT162B2), on 26Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 69 years intramuscular for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 26Jan2021 as dose 1, single (Lot number: 027L0A), on 04Mar2021 as dose 2, single (Lot number: 011M20A) and on 10Dec2021 as dose 3 (booster), single (Lot number: 048F21A), all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Dizziness" (unspecified if ongoing); "Rheumatoid arthritis" (unspecified if ongoing); "Arthritis" (unspecified if ongoing); "Tobacco use", stop date: 1998, notes: Tobacco use (stopped 1998); "Abstains from alcohol" (unspecified if ongoing); "Tuberculosis" (unspecified if ongoing); "Statin allergy" (unspecified if ongoing), notes: Statin allergy. Concomitant medication(s) included: PREDNISONE; DILTIAZEM; MECLIZINE [MECLOZINE HYDROCHLORIDE] taken for dizziness; LEFLUNOMIDE taken for rheumatoid arthritis; MELOXICAM taken for arthritis; FOLIC ACID taken for rheumatoid arthritis; CITALOPRAM; LISINOPRIL; TOPIRAMATE; PREGABALIN; ONDANSETRON; BENZONATATE; MONTELUKAST; PRAVASTATIN. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 2022, outcome "unknown", described as "Moderna COVID-19 vaccine (Elasomeran) and Pfizer BioNTech COVID-19 vaccine (Tozinameran) were also considered suspect"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 21Aug2022, outcome "recovered" (28Aug2022) and all described as "sick with COVID". The patient underwent the following laboratory tests and procedures: Body temperature: (unspecified date) 99.8 Fahrenheit; SARS-CoV-2 test: (28Aug2022) Negative; (21Aug2022) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. The reporter considered "covid" not related to BNT162b2. Clinical information: Solicited report from a consumer of a 70 year old female with events of non-serious slept a lot and sick with COVID with Humira 40mg/0.4ml (Adalimumab). On 21Aug2022, the patient experienced slept a lot and sick with COVID. On 28Aug2022, the slept a lot and sick with COVID resolved. Moderna COVID-19 vaccine (Elasomeran) and Pfizer BioNTech COVID-19 vaccine (Tozinameran) were also considered suspect. It was unknown if patient was enrolled in a COVID-19 vaccine trial. The patient was treated with Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: Test Result:99.8 Fahrenheit; Test Date: 20220828; Test Name: home test; Test Result: Negative ; Test Date: 20220821; Test Name: swab test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Abstains from alcohol; Arthritis; Dizziness; Drug allergy (Statin allergy); Rheumatoid arthritis; Tobacco user (Tobacco use (stopped 1998)); Tuberculosis
- Andere Medikamente
- PREDNISONE; DILTIAZEM; MECLIZINE [MECLOZINE HYDROCHLORIDE]; LEFLUNOMIDE; MELOXICAM; FOLIC ACID; CITALOPRAM; LISINOPRIL; TOPIRAMATE; PREGABALIN; ONDANSETRON; BENZONATATE; MONTELUKAST; PRAVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 10.09.2022
- Impfdatum
- 01.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 72-year-old male patient received BNT162b2 (BNT162B2), on 01Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 72 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: COVID-19 VACCINE taken for covid-19 immunisation as dose 1, single as dose 2, single as dose 3 (booster), single; ATORVASTATIN, stop date: 25Aug2022; TAMSULOSIN; SYNTHROID; VIT D3. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (02Sep2022) Negative, notes: tested negative 02Sep2022; (05Sep2022) Positive, notes: Paxlovid rebound, tested positive 05Sep2022,. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Known allergies was reported as none. Other medication in 2weeks were reported as yes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19 Treatment; Test Result: Positive ; Test Date: 20220902; Test Name: COVID 19 Treatment; Test Result: Negative ; Comments: tested negative 02Sep2022; Test Date: 20220905; Test Name: COVID 19 Treatment; Test Result: Positive ; Comments: Paxlovid rebound, tested positive 05Sep2022,
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- COVID-19 VACCINE; ATORVASTATIN; TAMSULOSIN; SYNTHROID; VIT D3
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 28.06.2022
- Beginn
- 04.09.2022
- Tage bis Beginn
- 68,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Nasopharyngeal swab
SARS-CoV-2 test
Vaccination failure
Symptomtext
Breakthrough COVID illness. Positive test result with home test kit. Reported symptoms are similar to a common cold.; Breakthrough COVID illness. Positive test result with home test kit. Reported symptoms are similar to a common cold.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Feb2021 as dose 1, single (Lot number: EN6202), on 28Mar2021 as dose 2, single (Lot number: EN6205), on 28Dec2021 as dose 3 (booster), single (Lot number: FE35Q4) and on 28Jun2022 as dose 4 (booster), single (Lot number: FM0173) 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 04Sep2022, outcome "recovering" and all described as "Breakthrough COVID illness. Positive test result with home test kit. Reported symptoms are similar to a common cold.". The patient underwent the following laboratory tests and procedures: Nasopharyngeal swab: (04Sep2022) Positive, notes: covid test type post vaccination=Nasal Swab covid test date=04Sep2022 covid test result=Positive; SARS-CoV-2 test: (unspecified date) Positive, notes: home test kit. Therapeutic measures were not taken as a result of vaccination failure, covid-19. Clinical information: Breakthrough COVID illness. Positive test result with home test kit. Reported symptoms are similar to a common cold. Dose received More than 3. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220904; Test Name: Nasal Swab; Test Result: Positive ; Comments: covid test type post vaccination=Nasal Swab covid test date=04Sep2022 covid test result=Positive; Test Name: home test kit; Test Result: Positive ; Comments: home test kit.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 10.09.2022
- Impfdatum
- 21.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old male patient received BNT162b2 (BNT162B2), on 21May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 62 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: "Diabetes" (unspecified if ongoing); "heart disease" (unspecified if ongoing); "Obesity" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), outcome "not recovered", COVID-19 (medically significant), 10 days after the suspect product(s) administration, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive; Comments: Treatment of COVID-19.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes; Heart disorder; Obesity
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 04.06.2022
- Beginn
- 04.06.2022
- 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
COVID 19 Treatment; COVID 19 Treatment; vaccine_brand=Pfizer / BioNTech;vaccine_brand_other=ModernaModerna; 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 received BNT162b2 (BNT162B2), on 04Jun2022 as dose 4 (booster), single (Lot number: FM0173) for covid-19 immunization; elasomeran (MODERNA COVID-19 VACCINE), on 24Feb2021 as dose 1, single (Lot number: 010A21A), on 24Mar2021 as dose 2, single (Lot number: 045A21A) and on 29Nov2021 as dose 3 (booster), single (Lot number: 013F21A) for covid-19 immunization. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Hashimoto's thyroiditis" (unspecified if ongoing); "GERD" (unspecified if ongoing); "osteoarthritis" (unspecified if ongoing); "kidney disease" (unspecified if ongoing); "obesity" (unspecified if ongoing). Concomitant medication(s) included: PRILOSEC [OMEPRAZOLE]; LEVOTHYROXINE. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 04Jun2022, outcome "unknown", described as "vaccine_brand=Pfizer / BioNTech;vaccine_brand_other=ModernaModerna"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "recovering" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (31Aug2022) Positive, notes: Finished the Paxlovid yesterday. Tested positive today. Therapeutic measures were taken as a result of drug ineffective, covid-19. with Paxlovid from 25Aug2022 to 30Aug2022. Clinical course: It was reported that paxlovid completed yesterday and again tested positive today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220831; Test Name: Tested; Test Result: Positive ; Comments: Finished the Paxlovid yesterday. Tested positive today.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; GERD; Hashimoto's thyroiditis; Kidney disorder; Obesity; Osteoarthritis
- Andere Medikamente
- PRILOSEC [OMEPRAZOLE]; LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 05.02.2021
- Beginn
- 26.08.2022
- Tage bis Beginn
- 567,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Hypoglycaemia
SARS-CoV-2 test positive
Symptomtext
08/26/22 presents to ED due to "hypoglycemia". "no significant PMH"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 08/27/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 03.09.2022
- Impfdatum
- 10.05.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 104,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old male patient received BNT162b2 (BNT162B2), on 10May2022 at 18:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 70 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: "Enlarged prostate" (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 Aug2022, outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Aug2022) Negative; (Aug2022) Negative; (Aug2022) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received Antiviral as COVID-19 Treatment from 22Aug2022 to 26Aug2022 for treatment of COVID-19. Patient received other medications/products within 2 weeks of starting COVID-19 treatment was Tamsulosin 4 mg (Lot: HAD0555a). patient previously received a COVID-19 Vaccine. Five days after finishing the Paxlovid regimen, and twice testing negative, Ithe patient was tested positive again after experiencing some mild symptoms. Patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202208; Test Name: COVID test; Test Result: Negative ; Test Date: 202208; Test Name: COVID test; Test Result: Negative ; Test Date: 202208; Test Name: COVID test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Enlarged prostate
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 01.09.2022
- Impfdatum
- 19.07.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 30,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old male patient received BNT162b2 (BNT162B2), on 19Jul2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 56 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: "HIV" (unspecified if ongoing). Concomitant medication(s) included: DOVATO; OLMESARTAN MEDOXOMIL. Past drug history included: Levaquin, reaction(s): "Known allergies: Levaquin", notes: Known allergies: Levaquin. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 18Aug2022 at 12:00, outcome "unknown" 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 drug ineffective, covid-19. Additional information: other medication details: other medication in 2weeks product: Dovato, Viiv, Olmestartan medixomil and Accord.
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: HIV disease
- Andere Medikamente
- DOVATO; OLMESARTAN MEDOXOMIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.09.2022
- Impfdatum
- 26.05.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 71,0
- 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
Reporting a Paxlovid Rebound: On 15Aug tested positive again & on 16Aug symptoms reoccurred. Restarted isolation/masking. Tested positive again 16Aug & 19Aug.; 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 71-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 26May2022 as dose 4 (booster), single (Lot number: FM0173) 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. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 05Aug2022, outcome "unknown" and all described as "COVID-19"; DISEASE RECURRENCE (medically significant) with onset 15Aug2022, outcome "unknown", described as "Reporting a Paxlovid Rebound: On 15Aug tested positive again & on 16Aug symptoms reoccurred. Restarted isolation/masking. Tested positive again 16Aug & 19Aug.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (05Aug2022) Positive; (10Aug2022) Negative; (13Aug2022) Negative; (15Aug2022) Positive; (16Aug2022) Positive; (19Aug2022) Positive; (22Aug2022) Negative; (25Aug2022) Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Therapeutic measures were not taken as a result of disease recurrence. Clinical course: Patient was double boosted & take precautions for Covid19 exposure. Tested positive for Covid19 on 05Aug2022 & began Paxlovid same day. By 09Aug2022 symptoms had resolved. Tested negative on 10Aug2022 and 13Aug2022. Reporting a Paxlovid Rebound: On 15Aug2022 tested positive again & on 16Aug2022 symptoms reoccurred. Restarted isolation/masking. Tested positive again 16Aug2022 & 19Aug2022. By 22Aug2022 symptoms began to lessen & tested negative. Tested negative again 25Aug2022. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220805; Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20220810; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20220813; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20220815; Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20220816; Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20220819; Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20220822; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20220825; Test Name: COVID-19 test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 31.08.2022
- Impfdatum
- 29.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
A vail had been left out from the previouse work day on 8/26/2022 and then administerd on 8/29/2022 patient was contacted and they said they were fine. I will follow up in the week. and advised them to call if anything came up
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- sertraline, atorvastatin, hydralazine, calcitol, levothyroxine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 30.08.2022
- Impfdatum
- 11.07.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 24,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Tinnitus
Vertigo
Symptomtext
Persistant severe vertigo, tinnitus, brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- Physical exam on 8/11/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia
- Andere Medikamente
- Lorsartan HCTZ 100-25, Amlodipine 10
- Allergien
- Amoxicillian
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- 27.04.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 96,0
- 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; COVID-19; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 64-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 14Jan2021 at 14:00 as dose 1, single (Lot number: EL3249), in right arm, on 04Feb2021 at 14:00 as dose 2, single (Lot number: EL3302), in right arm, on 05Oct2021 at 13:00 as dose 3 (booster), single (Lot number: FF2590), in right arm and on 27Apr2022 at 14:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 64 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: LIPITOR oral, start date: 02Mar2015, stop date: 06Aug2022. 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". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (19Aug2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19 with oral, Paxlovid from 06Aug2022 to 11Aug2022.; Sender's Comments: The vaccine efficacy varies from one patient to another and can be affected by different factors; however, a contributory role of the suspect vaccine BNT162B2 to the vaccination failure (LOE) cannot be ruled out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220819; Test Name: PCR; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
- Andere Medikamente
- LIPITOR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 18.08.2022
- Impfdatum
- 02.07.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 30,0
- 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 2/5/21 Lot# EL 9261; Pfizer 2/26/21 Lot# EM9810; Pfizer 12/15/21 Lot# 330268D; Pfizer 7/2/22 Lot# FM0173
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 15.07.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31Dec2020 at 16:00 as dose 1, single (Lot number: EK9231), in right arm, on 22Jan2021 at 16:00 as dose 2, single (Lot number: 162b2), in left arm, on 29Dec2021 at 16:00 as dose 3 (booster), single (Lot number: 320308D), in right arm and on 15Jul2022 at 17:30 as dose 4 (booster), single (Lot number: FM0173) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "Chronic Bronchitis" (unspecified if ongoing); "Known allergies: Shell fish" (unspecified if ongoing); "Known allergies: latex" (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 03Aug2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (03Aug2022) positive; (08Aug2022) Negative; (13Aug2022) positive, notes: Rebound on 13Aug with worsening symptoms. Therapeutic measures were taken as a result of covid-19. Clinical course: COVID positive 03Aug2022. Started Plaxlovid on 04Aug finished 09Aug. Mild to Moderate case. Negative test on Monday 08Aug. Rebound on 13Aug with worsening symptoms, and positive test.; Sender's Comments: Based on the information currently available, a causal association between the reported event and BNT162b2 cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220803; Test Name: COVID-19; Test Result: Positive ; Test Date: 20220808; Test Name: COVID-19; Test Result: Negative ; Test Date: 20220813; Test Name: COVID-19; Test Result: Positive ; Comments: Rebound on 13Aug with worsening symptoms
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Chronic bronchitis; Latex allergy; Shellfish allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 31.05.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), on 31May2022 at 14:30 as dose 4 (booster), single (Lot number: FM0173) at the age of 68 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: "Asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Trazadone, reaction(s): "allergies". 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". Therapeutic measures were taken as a result of drug ineffective, covid-19 including received Paxlovid from 19Jul2022 to 24Jul2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 13.08.2022
- Impfdatum
- 13.08.2022
- Beginn
- 13.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Product storage error
Symptomtext
BUD in refrigerator of 70 days was exceeded by 1 day. Expiration of product is 09/30/22 but 70 days under refrigeration was 08/12/2022. Vaccine was given 11:30am on 08/13/2022. No ADE from patient reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 13.08.2022
- Impfdatum
- 13.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body mass index
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). The reporter is the patient. A 50-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Jul2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 50 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 03May2021 as dose 1, single (Lot number: EW0176), in left arm, on 24May2021 as dose 2, single (Lot number: EW0187), in left arm and on 17Dec2021 as dose 3 (booster), single (Lot number: FE3594), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: latex" (unspecified if ongoing); "Known allergies: Wellbutrin, Benadryl" (unspecified if ongoing). Concomitant medication(s) included: TRETINOIN, start date: Apr2021; ALLERTEC [CETIRIZINE], start date: Jan2021; NEXIUM [ESOMEPRAZOLE MAGNESIUM], start date: May2022. The following information was reported: VACCINATION FAILURE (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: Body mass index: 29.5. Therapeutic measures were taken as a result of vaccination failure, covid-19. Treatment included Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body mass index
- Hospital-Tage
- -
- Labordaten
- Test Name: BMI; Result Unstructured Data: Test Result:29.5
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Drug allergy; Latex allergy
- Andere Medikamente
- TRETINOIN; ALLERTEC [CETIRIZINE]; NEXIUM [ESOMEPRAZOLE MAGNESIUM]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 13.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 13,0
- 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. A 43-year-old male patient received BNT162b2 (BNT162B2), on 27Jul2021 as dose 1, single (Lot number: fa7485), on 17Aug2021 as dose 2, single (Lot number: fc3183), on 19Jan2022 as dose 3 (booster), single (Lot number: fk5618) and on 13Jul2022 as dose 4 (booster), single (Lot number: fm0173) at the age of 43 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Esophageal Cancer" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing); "Hypertension" (unspecified if ongoing). Concomitant medication(s) included: CETIRIZINE; FAMOTIDINE; LOSARTAN POTASSIUM; OPDIVO; PANTOPRAZOLE; MULTIVITAMINS. Known allergies: nka. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 26Jul2022, outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (26Jul2022) Positive; (02Aug2022) Negative; (06Aug2022) 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: 20220726; Test Name: COVID-19; Test Result: Positive ; Test Date: 20220802; Test Name: COVID-19; Test Result: Negative ; Test Date: 20220806; Test Name: COVID-19; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Esophageal cancer; Hypertension; Hypothyroidism
- Andere Medikamente
- CETIRIZINE; FAMOTIDINE; LOSARTAN POTASSIUM; OPDIVO; PANTOPRAZOLE; Multivitamins
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 07.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 03Mar2021 at 13:45 as dose 1, single (Lot number: EL9261), in left arm, on 24Mar2021 at 13:45 as dose 2, single (Batch/Lot number: unknown), in left arm, on 12Oct2021 at 14:30 as dose 3 (booster), single (Lot number: FF8839), in left arm and on 07Jun2022 at 11:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "seasonal allergies" (unspecified if ongoing); "hypothyroid-senior citizen" (unspecified if ongoing). The patient has no known allergies. Concomitant medication(s) included: LEVOCETIRIZINE; SYNTHROID. 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: (unspecified date) Positive, notes: COVID-19 Treatment; (26Jul2022) Negative; (26Jul2022) Negative; (31Jul2022) positive again; (05Aug2022) still testing positive. Therapeutic measures were taken as a result of vaccination failure, covid-19 which included PAXLOVID. After treatment with PAXLOVID was completed on Thursday 26Jul2022, she had 2 negative tests and then symptoms returned around 31Jul2022 and tested positive again. On, 05Aug2022 and still testing positive. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Positive ; Comments: COVID-19 Treatment; Test Date: 20220726; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20220726; Test Name: COVID-19 Test; Test Result: Negative ; Test Date: 20220731; Test Name: COVID-19 Test; Result Unstructured Data: Test Result:positive again; Test Date: 20220805; Test Name: COVID-19 Test; Result Unstructured Data: Test Result:still testing positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Hypothyroidism; Seasonal allergy
- Andere Medikamente
- LEVOCETIRIZINE; SYNTHROID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- 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
COVID 19 Treatment; COVID 19 Treatment; COVID-19 VACCINE, unknown manufacturer administered as dose 1, 2, 3, and 4; BNT162B2 as dose 5 (booster); This is a spontaneous report received from a non-contactable reporter (Nurse). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 18May2022 as dose 5 (booster), single (Lot number: FM0173) at the age of 61 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing); "bronchiectasis" (unspecified if ongoing); "erosive arthritis" (unspecified if ongoing); "known allergies: sulfa" (unspecified if ongoing); "known allergies: Penicillin (pcn)" (unspecified if ongoing). Concomitant medication (in 2 weeks) included: SPIRONOLACTONE, start date: Jan2018. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 18May2022, outcome "unknown", described as "COVID-19 VACCINE, unknown manufacturer administered as dose 1, 2, 3, and 4; BNT162B2 as dose 5 (booster)"; DRUG INEFFECTIVE (medically significant), outcome "unknown", 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: patient was asymptomatic and tested negative after full course Paxlovid; Negative, notes: continued to test negative on day 6; Negative, notes: continued to test negative on day 7; Negative, notes: continued to test negative on day 8; Positive, notes: cough and sore throat returned day 9 and also tested positive day 9; Positive, notes: treatment of COVID-19. Therapeutic measures were taken as a result of covid-19. Additional information: COVID-19 treatment included Paxlovid, brand: Pfizer (Lot number: GE6376), administered orally from 28Jul2022 to 01Aug2022. The patient was asymptomatic and tested negative after full course Paxlovid. The patient continued to test negative on days 6, 7, 8. Cough and sore throat returned on day 9 and also tested positive on day 9. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the known safety profile and Limited information in the case report a casual association between LOE events and suspect drug BNT162B2 cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Negative ; Comments: patient was asymptomatic and tested negative after full course Paxlovid; Test Name: Covid-19 test; Test Result: Negative ; Comments: continued to test negative on day 6; Test Name: Covid-19 test; Test Result: Negative ; Comments: continued to test negative on day 7; Test Name: Covid-19 test; Test Result: Negative ; Comments: continued to test negative on day 8; Test Name: Covid-19 test; Test Result: Positive ; Comments: cough and sore throat returned day 9 and also tested positive day 9; Test Name: Covid-19 test; Test Result: Positive ; Comments: treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Bronchiectasis; Erosive arthritis; Hypertension; Penicillin allergy; Sulfonamide allergy
- Andere Medikamente
- SPIRONOLACTONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 07.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 06.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Swelling of lymph nodes in neck and arm pit on left side of body occurs next day after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- Prescription birth control pills (Vienva)
- Allergien
- N/a
- Vorherige Impfungen
- Same reaction after 2nd dose of Covid vaccine. 08/09/2021. Swelling of lymph nodes continued for 2 months. Pfizer vaccine lot FC
- Staat
- AZ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 22.05.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- 40,0
- 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 64-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 22May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 64 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: "known allergies: Sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Tetracycline, reaction(s): "Known allergies: Tetracycline". The following information was reported: COVID-19 (medically significant), DRUG INEFFECTIVE (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) Negative; (18Jul2022) Positive. Therapeutic measures were taken as a result of covid-19. Clinical course: Horrid taste while taking Paxlovid,went away when course was done. Covid recurrence (positive test) 7 days after previously negative test on last day of course. Still positive at present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202207; Test Name: COVID; Test Result: Negative ; Test Date: 20220718; Test Name: COVID; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Sulfonamide allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 30.07.2022
- Impfdatum
- 07.06.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 55-year-old male patient received BNT162b2 (BNT162B2), on 07Jun2022 at 15:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 55 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: "Gout" (unspecified if ongoing); "juvenile asthma" (unspecified if ongoing), notes: juvenile asthma; "Known allergies: Iodine contrast" (unspecified if ongoing), notes: Known allergies: Iodine contrast. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of drug ineffective, covid-19 with paxlovid.; Sender's Comments: Based on the known safety profile and Limited information in the case report a casual association between LOE events and suspect drug BNT162B2 cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19 Test; Test Result: Positive ; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (juvenile asthma); Gout; Iodine contrast media allergy (Known allergies: Iodine contrast)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 31.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 54-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31May2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 54 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: "history of ovarian cancer 2016", start date: 2016 (unspecified if ongoing). Concomitant medication(s) included: ESTROGEN; VITAMIN C [ASCORBIC ACID]; VITAMIN D NOS; ZINC; ZYRTEC [CETIRIZINE HYDROCHLORIDE]. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: COVID 19 Treatment; (19Jul2022) Negative, notes: previously tested negative; (26Jul2022) Positive, notes: tested positive again. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Rebound (tested positive again on 26Jul2022) previously tested negative on 19Jul2022. Mild congestion and sore throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 20220719; Test Name: COVID-19 test; Test Result: Negative ; Comments: previously tested negative; Test Date: 20220726; Test Name: COVID-19 test; Test Result: Positive ; Comments: tested positive again
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Ovarian cancer
- Andere Medikamente
- ESTROGEN; VITAMIN C [ASCORBIC ACID]; VITAMIN D NOS; ZINC; ZYRTEC [CETIRIZINE HYDROCHLORIDE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- -
- Geschlecht
- M
- Eingang
- 30.07.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac disorder
Symptomtext
Cardiac event; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 68-year-old male patient received BNT162b2 (BNT162B2), as dose number unknown, single (Lot number: FM0173) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: CARDIAC DISORDER (non-serious), outcome "unknown", described as "Cardiac event". Additional information: The reporter stated that the patient was her husband's friend who was a gastroenterologist, who also had a cardiac event after receiving the COVID vaccine. She does not know if he reported it. Neither one of them had heart issues. The patient said that should not have happened to him. They are approximately the same age and went to medical school.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 13,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Symptomtext
Shingles outbreak on face
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Sinusities
- Vorgeschichte
- None
- Andere Medikamente
- Zoloft Natur-Throid Vit D Calcium, Magnesium
- Allergien
- Ibuprofen
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Lymphadenopathy
Symptomtext
was given 12+ dose instead of 5-11 dose - guardian stated swollen lymph glands right arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient presented requesting second dose of Pfizer vaccine, Pfizer vaccine was given. Previous dose of Pfizer was given 07/01/2022. Upon reviewing chart patient had 2nd dose on 07/01/22 and 1st dose of Pfizer vaccine, last year. Making the Pfizer vaccine given the 3rd dose (booster); therefore making the 3rd (a booster) dose given to soon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 26.07.2022
- Impfdatum
- 26.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
9 YEAR OLD GIVEN PFIZER COVID VACCINE FOR 12 YEARS AND OLDER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 24.07.2022
- Impfdatum
- 03.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- 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
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 female patient (not pregnant) received BNT162b2 (BNT162B2), on 15Aug2021 at 11:30 as dose 3 (booster), single (Lot number: FC3181), in left arm, on 02Mar2022 at 13:00 as dose 4 (booster), single (Lot number: FJ6369), in left arm and on 03Jul2022 at 11:00 as dose 5 (booster), single (Lot number: FM0173) at the age of 62 years, in left arm for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 30Mar2022 at 08:45 as dose 1, single (Lot number: 020B21A), in left arm and on 27Apr2022 at 11:00 as dose 2, single (Lot number: 09C21A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Crohn's disease" (unspecified if ongoing); "Interchange of vaccine products" (unspecified if ongoing). Concomitant medication(s) included: CITRACAL [CALCIUM CITRATE], start date: May2020, stop date: 14Jul2022; OMEPRAZOLE, start date: Jan2021, stop date: 14Jul2022; B-12 NATURE MADE, start date: May2020, stop date: 14Jul2022; ACETAMINOPHEN, start date: 13Jul2022, stop date: 13Jul2022; IRON, start date: May2020, stop date: 14Jul2022. Past drug history included: Ampicillin, reaction(s): "known allergies: Allergic to ampicillin", notes: known allergies: Allergic to ampicillin; Vicodin, reaction(s): "known allergies: vicodin", notes: known allergies: vicodin. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED 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, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of drug ineffective, suspected covid-19. No follow-up attempts are possible. 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; Comments: Treatment of COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Crohn's disease; Interchange of vaccine products
- Andere Medikamente
- CITRACAL [CALCIUM CITRATE]; OMEPRAZOLE; B-12 NATURE MADE; ACETAMINOPHEN; IRON
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 16.07.2022
- Impfdatum
- 16.07.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Unresponsive to stimuli
Symptomtext
Patient became almost unresponsive after over 10 minutes of COVID-19 booster administration. Still in standing position but unaware of surroundings. Immediately taken to the clinic inside the store for better observation using store electric scooter. With the help of pharmacist, nurse practitioner and 911 phone instructions, patient started a bit of awareness and taken to the hospital after the 911 arrived. According to the wife, he is in total awareness now and in good condition waiting for further tests and monitoring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unresponsive to stimuli
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient was getting 1st booster vaccine (pfizer). After vaccine was given, the administrator noticed patient already got 1st booster and the shot she got today should be second booster. But second booster is not approved for non-immunocompromised patients. Informed mother of the mistake and she said it was okay. She said she can't remember that her daughter got the first booster and believes her daughter did not get the first booster shot even though it is on her vaccine card.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 09.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Ultrasound lymph nodes
Symptomtext
Enlarged lymph node appeared on right chest near collar bone after first injection of Pfizer BioNTech vaccination in November of 2021. After evaluation by his physician, he was advised to watch and wait through the month of December and be re-evaluated. At the second office visit he was advised to have ultrasound, as the enlarged node had not resolved. He did have the ultrasound, which was used to diagnose it as a "reactive lymph node." It has persisted without change for 7 months and is still present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- ultrasound, 01/2022
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- migraine
- Andere Medikamente
- rizatriptan, 10mg as needed naproxen, 500mg as needed
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 27.06.2022
- Beginn
- 02.07.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Unresponsive to stimuli
Symptomtext
Possible seizures, non-responsive spels
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unresponsive to stimuli
- Hospital-Tage
- -
- Labordaten
- Will get EEG
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 08.07.2022
- Impfdatum
- 15.06.2022
- Beginn
- 29.06.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Hyperhidrosis
Sleep disorder
Symptomtext
I was awaken about 3AM by profuse sweating my bed and covers was totally soaking wet. At first it was only happening at night and then it started happening happening throughout the day and I went to my Dr. and was put on an anti anxiety medication but, I only took 2 days worth because of the side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Amlodipine; vitamin C; iron; vitamin D3; vitamin E; flaxseed; probiotics; hydrochlorothiazide; turmeric
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 14.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 16,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
tested positive for covid this morning/GI symptoms/extreme fatigue/mental brain fog/headache/slight temperature of 99.8 degrees; tested positive for covid this morning/GI symptoms/extreme fatigue/mental brain fog/headache/slight temperature of 99.8 degrees; 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 51-year-old female patient received BNT162b2 (BNT162B2), on 03Mar2021 as dose 1, single (Lot number: EN6205, Expiration Date: 30Jun2021), on 24Mar2021 as dose 2, single (Lot number: EP7533, Expiration Date: Jul2021), on 22Nov2021 as dose 3 (booster), single (Lot number: FJ1620) and on 14Jun2022 at 08:00 as dose 4 (booster), single (Lot number: FM0173) at the age of 51 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension", start date: 2014 (ongoing), notes: hypertension which is controlled by medications. diagnosed with that probably in 2014; "Depression", start date: 2008 (ongoing), notes: Depression; "Anxiety", start date: 2008 (ongoing), notes: Anxiety; "IBS" (unspecified if ongoing). Concomitant medication(s) included: ACETAMINOPHEN. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 30Jun2022, outcome "unknown" and all described as "tested positive for covid this morning/GI symptoms/extreme fatigue/mental brain fog/headache/slight temperature of 99.8 degrees". The patient underwent the following laboratory tests and procedures: Body temperature: (22Jun2022) 99.8; SARS-CoV-2 test: (25Jun2022) Negative, notes: it was done on approximately 4:30pm; (30Jun2022) Positive, notes: Unit: Not Provided; (21Jun2022) Negative; (22Jun2022) Negative; (27Jun2022) Negative, notes: it was done on approximately 4:30pm. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Reporter states she started having symptoms last week but had three negative PCR tests and one negative home test and was about to go to work and tested again as she had two family members that had COVID last week; states she had some initial symptoms but her PCR came back negative and took a home test that popped right up. As reported patient did not visit to emergency room and physician office for AE. States she was going to do a phone appointment with her physician later today to talk about if she was a candidate for Paxlovid so she will be talking to her doctor. Prior Vaccinations (within 4 weeks) reported as None. Reporter states she started having GI symptoms and a lot of fatigue on 22Jun2022 and this is not ongoing and is slow mo COVID; states she had GI symptoms on the 22nd and then on the 23rd had extreme fatigue on the 23rd and 24th and had some mental brain fog on the 23rd and the 24th and then on the 25th and 26th she felt better and on the 27th she started noticing she had a headache and it prompted her to take the third PCR test. Reporter states her headache was about the same and seems to come on in the evenings and if she takes Tylenol she was fine and they go away; clarified it was 8 hour Tylenol for arthritis and lasts all night and her IBS symptoms have her stay away from NSAIDS; states she works for company and J&J and clarified the Tylenol is actually Pharmacy brand pain reliever Acetaminophen 650mg caplets and she took two and probably has taken it the last three nights; states she started noticing her headache on Sunday night and it started Sunday night but she might not have taken the Acetaminophen or was being stubborn if it was not bad enough to need to take it and she is stubborn about taking medication; states she self administered the PCR test and has the lab reports but all three PCR tests were negative and she kept getting them negative and thought are you kidding me. Reporter states she has a diagnosed of depression and anxiety and takes medications for those and was diagnosed in 2008 and while trying to state the date that was diagnosed states she thinks this was the mental fog she has. States she takes the medications Lexapro and Clonazepam and started those prior to the COVID vaccines and this was years prior to the vaccines and had not started on any medications since 2020 and if anything had come off of a few but nothing recently. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZERBIONTECH 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. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE INJECTABLE lot EP7533 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope was determined to be the reported finished goods lot EP7533, fill lot EP7531, and the bulk formulated drug product lot EP7527. 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. Conclusion of Previously Completed Investigation: The complaint for lack of effect of the PFIZERBIONTECH COVID-19 VACCINE INJECTABLE lot FJ1620 was investigated. The investigation included reviewing manufacturing and packaging batch records, deviation investigations, analytical release test results, and an analysis of the complaint history for the reported lot. The final scope was determined to be the reported finished goods lot FJ1620, fill lot FJ1606, and the bulk formulated drug product FJ8507. 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. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Body temperature
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220622; Test Name: temperature of 99.8 degrees; Result Unstructured Data: Test Result:99.8; Test Date: 20220625; Test Name: home covid test; Test Result: Negative ; Comments: it was done on approximately 4:30pm; Test Date: 20220630; Test Name: home covid test; Test Result: Positive ; Comments: Unit: Not Provided; Test Date: 20220621; Test Name: PCR Test; Test Result: Negative ; Test Date: 20220622; Test Name: PCR Test; Test Result: Negative ; Test Date: 20220627; Test Name: PCR Test; Test Result: Negative ; Comments: it was done on approximately 4:30pm
- Aktuelle Erkrankungen
- Anxiety (Anxiety); Depression (Depression); Hypertension (hypertension which is controlled by medications. diagnosed with that probably in 2014)
- Vorgeschichte
- Medical History/Concurrent Conditions: Irritable bowel syndrome
- Andere Medikamente
- ACETAMINOPHEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 28.06.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Blood pressure measurement
Feeling of despair
Lip swelling
Swelling face
Symptomtext
her whole face was swelling/ looked like she was paralyzed/left side of her face and cheek and nose was swollen; lips were all swollen; scared to death; blood pressure can get a little high; 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 received BNT162b2 (BNT162B2), on 28Jun2022 as dose 4 (booster), single (Lot number: FM0173) at the age of 73 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, Lot: EN6202, Expiry: Jun2021, site of administration: Left arm at 10:00), administration date: 04Mar2021, when the patient was 72-year-old, for Covid-19 immunization; BNT162b2 (DOSE 3, Lot: FC3183), administration date: 07Oct2021, when the patient was 73-year-old, for Covid-19 immunization; Bnt162b2 (DOSE 2 , Lot: EP6955), administration date: Mar2021, when the patient was 72 years old, for Covid-19 immunization.The following information was reported: BLOOD PRESSURE INCREASED (non-serious) with onset Jun2022, outcome "unknown", described as "blood pressure can get a little high"; FEELING OF DESPAIR (non-serious) with onset Jun2022, outcome "unknown", described as "scared to death"; SWELLING FACE (medically significant) with onset 29Jun2022, outcome "recovering", described as "her whole face was swelling/ looked like she was paralysed/left side of her face and cheek and nose was swollen"; LIP SWELLING (medically significant) with onset 29Jun2022, outcome "recovering", described as "lips were all swollen". The patient underwent the following laboratory tests and procedures: Blood pressure measurement: (Jun2022) blood pressure can get a little high, notes: blood pressure can get a little high so she takes the lowest dose of Lisinopril when it gets a little high which is 1 pill a day. Therapeutic measures were taken as a result of swelling face, lip swelling, blood pressure increased. Clinical Course: The patient woke up at 06:00 on 29Jun2022, and because her mouth was feeling swollen, she looked in the mirror and her lips were all swollen, up the left side of her face and cheek was swollen and looked like a big baseball. She did everything she could and got a washcloth and put ice on it. She kept that on most of the day. She did not feel bad, it was just all the swelling which seemed like it started going more toward her eyes on both sides and her whole face was swelling. She spoke to a pharmacist who suggested she see a doctor. She saw a Nurse Practitioner on 29Jun2022 at a clinic close to her house. She looked like a chimpanzee, even her nose was swollen by that time. While at the clinic she got a Dexamethasone steroid shot and today event is much better. She still has what looks like, on the left side, like she has a wad of chewing tobacco hanging down where her jawbone. It looked like she was paralysed. She has never had a reaction other than maybe a little bit of a sore arm before. After treatment or medical interventions, she was just given the Dexamethasone shot; and was given a prescription to take Prednisone. She had not even opened the Prednisone yet; she just picked it up today and was supposed to start Prednisone today; but she was not sure she was even to take the Prednisone because the only thing significant left was the lump on the left side of her cheek. If that was gone tomorrow, she may not take the Prednisone. She does not like to take drugs; she was an anti-drug person since having cared for her husband and mother for 12 years. She is going to try not to take the Prednisone; but if she sees that the swelling was starting to get worse then she will take it. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure increased
- Hospital-Tage
- -
- Labordaten
- Test Date: 202206; Test Name: Blood pressure; Result Unstructured Data: Test Result:blood pressure can get a little high; Comments: blood pressure can get a little high so she takes the lowest dose of Lisinopril when it gets a little high which is 1 pill a day
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 05.07.2022
- Impfdatum
- 05.07.2022
- Beginn
- 05.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysphonia
Pharyngeal swelling
Symptomtext
Patient received 1st dose of pfizer covid vaccine. During the 15 minute waiting period patient stated that he throat began to feel like it was swelling and he was getting horse. We called 911 and the paramedics attended to him and took him off. During this time pt was still able to breath and talk
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysphonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknonw/ none listed
- Andere Medikamente
- Unknown
- Allergien
- Shellfish/shrimp
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Patient received a dose of 30mcg instead of 10mcg for her age.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 30.06.2022
- Beginn
- 30.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
An intern had drawn up and injected 0.6 ml of the vaccine to the pt instead of 0.3 ml. Per pt, they are feeling fine. Caregivers were given instructions on side effects to watch out for and when to alert doctor or go to ER. Pt was waiting for about 15 to 20 minutes after vaccinations and did not report any issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Atrial fibrillation; Alzheimer's.
- Andere Medikamente
- Ropinirole; Atorvastatin; Digoxin; Warfarin; Metoprolol.
- Allergien
- Sulfa antibiotics.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 15.06.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SC / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Full blood count
Platelet count decreased
Symptomtext
the patient had been on of immunosuppressive dose of acyclovir for his herpes zoster in infection. He then went to the local pharmacy to have a shingles vaccine on June 6th or 7th of 2022 1 week later on 06/15/2022 the patient went to the Pharmacy and got the 3rd COVID vaccination which was his booster he then ended up in our emergency room with less than 2000 platelet counts.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Full blood count
- Hospital-Tage
- 5,0
- Labordaten
- Patient had CBC serial CBCs was seen in our emergency room on 6/25 /2022 and was given a dose of IV gammaglobulin at 0.5 milligrams/kilogram with Decadron at 20 mg IVPB q.12 hours. His platelet counts remained at 2000. He was given 2 additional doses of IV gammaglobulin at 1 gram/kilogram over 48 hours with the Decadron remaining at 20 mg IVPB. on 06/28/2022 his platelets rose to 21,000 as of 06/28/2022 the date of the reporting, the patient remains hospitalized
- Aktuelle Erkrankungen
- patient had suffered from herpes zoster that had started mid March of 2022. it affected the 5th cranial nerve distribution and the patient had lesions in the right periorbital area. He had been placed on acyclovir t.i.d. 1 g for 7 days but was continued on a chronic immunosuppressive dose.
- Vorgeschichte
- Hypertension obesity prediabetic
- Andere Medikamente
- Acyclovir losartan, Lipitor, Elavil, gabapentin, HydroDIURIL, hycosamine,, Xalatan, Zoloft, melatonin
- Allergien
- Ace inhibitors
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 24.06.2022
- Impfdatum
- 13.06.2022
- Beginn
- 15.06.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Symptomtext
Two to three days after the 3rd Pfizer COVID vaccine shot (or 'first booster'), she started her full period/menstruation. It's only been about a week and menstruation is still ongoing--which I think is normal. The timing may just be coincidental but I wanted to report it anyway. FYI, she's also had 'spotting' (or 'false starts' for better lack of the proper term) a few times over the past year, which I think is also normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- patent foramen ovale (PFO) heart condition
- Andere Medikamente
- daily multivitamin, magnesium vitamin, lactase pill (as needed for dairy)
- Allergien
- dairy (lactose)
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 22.06.2022
- Impfdatum
- 15.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Haematochezia
Symptomtext
Patient called our pharmacy and explained to us that the day following his vaccine and reported that he had blood in his stool that gradually got better over a few days but was concerned since it was the day after his vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Haematochezia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known other illnesses
- Vorgeschichte
- No chronic conditions
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 19.06.2022
- Impfdatum
- 19.06.2022
- Beginn
- 19.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Gave the wrong dose of 0.3ml or 30 ug Gray cap instead of 10 ug 0.2ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 17.06.2022
- Impfdatum
- 16.06.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
Patient came into the pharmacy to receive a HPV(Gardasil) vaccine but received a Covid 19 (Pfizer Biontech) instead. No adverse effects have been noticed yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No known
- Vorgeschichte
- No Known
- Andere Medikamente
- No known
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Nurse) from product quality group. The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 16Feb2022 as dose 2, single (Lot number: EL9266), in left arm and on 18May2022 as dose 3 (booster), single (Lot number: FM0173) at the age of 42 years, in left arm for Covid-19 immunisation; CoviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) for Covid-19 immunisation. The patient's relevant medical history included: "Autoimmune disorder" (unspecified if ongoing); "known allergies: Lime" (unspecified if ongoing), notes: known allergies: Lime. Concomitant medication(s) included: HUMIRA; CELEBREX. 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, notes: Treatment of COVID-19. Therapeutic measures were taken as a result of drug ineffective, Covid-19. Clinical course: Patient received Paxlovid from 31May2022 to 05Jun2022 for the treatment of COVID-19. 2 days after completion patient started experiencing worsening symptoms like first few days following Covid diagnosis. Extreme nausea, headache and body aches during treatment. Sender's Comments: Considering the nature of the reported events and product profile, a causal role of the suspect BNT162B2 cannot be denied for the reported events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19; Result Unstructured Data: Test Result: Unknown results; Comments: Treatment of COVID-19.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Autoimmune disorder; Fruit allergy (known allergies: Lime)
- Andere Medikamente
- HUMIRA; CELEBREX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 15.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 05.06.2022
- 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
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
I was suffering from nasal congestion the whole spring of 2022 and thought it was allergies. I was diagnosed with ear infection in May. After this 3 family members tested positive for Covid and then I tested positive on June 5, 2022. The only symptom I had during quarantine was a stuffy nose. My entire family received the vaccines and the boosters and we still got the Omicron variant. The family had a runny nose but no fever or any other symptoms. My husband had runny nose and a bit of a cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Nasal swab at home, drive thru doctor nasal swab - PCR.
- Aktuelle Erkrankungen
- Ear infection diagnosed May 10, 2022
- Vorgeschichte
- None
- Andere Medikamente
- BENADRYL; nasal spray; AMBIEN
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 11.06.2022
- Impfdatum
- 11.06.2022
- Beginn
- 11.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Vaccination error
Symptomtext
Patient and patient dad came in for COVID booster. Stated DOB and age 2x to 2 staff members. After found out patient and dad both lied about age to get adult Pfizer booster. Patient previously lied to pharmacy for first two shots, but said "correct" DOB of a year later to us. Thought suspicious but surprised patient lied so well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 11.06.2022
- Impfdatum
- 01.06.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No reaction on previous exposure to drug
Symptomtext
This was the 4th Pfizer Covid vaccine (2nd booster) and was administered on 6/1/22. No issues with prior Pfizer doses on 12/29/20, 1/22/21, or 9/29/21. Since I already had another script for prednisolone 1% and Atropine eye drops, I started treatment prior to seeing ophthalmologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Simple motor tics, vitamin D deficiency, HLA-B27 positive anterior uveitis (iritis), recently treated (March-April 2022) resolved in April 2022.
- Andere Medikamente
- Sertraline 37.5mg (1 & 1/2 of a 25mg tablet), Vitamin D3 5000 IU three times weekly.
- Allergien
- Itraconazole - rash
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 18.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 9,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Atrial fibrillation
Cardioversion
Symptomtext
I was asleep and my smart watch, it started clicking on my wrist and asked if I was having a heart event because it looked like I wasn't exercising. I used the watch to check my heart and it said I was in A-Fib. I went to the emergency room they confirmed I was in fact in A-fib. They gave me an amiodarone drip that did not work. They did give me a cardioversion that did work. I was given new prescriptions of amiodarone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Acetaminophen; alpha lipoic acid; amiodarone; ELIQUIS; LATISSE; biotin; calcium plus magnesium; chlor-trimeton; RESTATIS; duloxetine; ALLEGRA D; LANTUS; LYUMJEV; metformin; metoprolol succinate; minoxidil; multivitamin; oxycodone; potassiu
- Allergien
- Penicillin; codeine; statins; MULTAQ
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 13.05.2022
- Beginn
- 24.05.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
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 11 days after my 3rd dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home COVID test
- Aktuelle Erkrankungen
- I had a severe cold 2 weeks prior to the vaccine.
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 30.05.2022
- Impfdatum
- 30.05.2022
- Beginn
- 30.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Underdose
Symptomtext
Patient likely was administered 0.25 mls of adult pfizer vaccine rather than full 0.3 mls. Patient will be in Friday to repeat dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.05.2022
- Impfdatum
- 24.05.2022
- Beginn
- 25.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Induration
Local reaction
Swelling
Symptomtext
Local reaction, redness of ~6 cm in diameter with firm center. Slightly raised. Itching present. The symptoms improved after 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Cataract surgery.
- Vorgeschichte
- Hypothyroidism.
- Andere Medikamente
- Synthroid; Crestor; Aspirin; OsteoBiflex; Hydroeye; Restasis. Had Cataract surgery on 5/23 and was taking eye drops 4x daily: Prednisolone; Polymycin B; Ketorolac.
- Allergien
- Pennicillin; Cipro; Morphine.
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 28.05.2022
- Impfdatum
- 23.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Oral herpes
Symptomtext
Oral herpes after covid booster. I have never had a cold sore before. I woke up on the morning of May 27th with a swollen lip that apparently is a cold sore. This morning I have two little sores (not canker sores) in the inside of my lip. They look water filled. I'm single and I do not know how I would be getting this nor do I share anything (straws etc) with anyone. I researched side effects of the Pfizer vaccine and found that other people have reported getting oral herpes and shingles after getting the vaccine. I had the J&J vaccine 06/17/2021 and just got a sore arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- I haven't gone to the Dr but I will if needed. I did call my doctor and a prescription was called in.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 27.05.2022
- Impfdatum
- 27.05.2022
- Beginn
- 27.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
No adverse reactions reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type 1 Diabetes
- Andere Medikamente
- Novolog Flexpen, Glucagon 1mg Emergency Kit, Cyproheptadine 4mg.
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 21.05.2022
- Beginn
- 23.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Lymphadenopathy
Symptomtext
Swollen lymph nodes in the left armpit
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- pilopeptan woman
- Allergien
- none
- Vorherige Impfungen
- pain at the injection site
- Staat
- MD
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 20.05.2022
- Beginn
- 20.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 19.05.2022
- Beginn
- 19.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyskinesia
Symptomtext
Patient call to say that the evening of the shot , she experience extreme jerking of the body during the night . In the morning this condition stopped
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyskinesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 18.05.2022
- Beginn
- 18.05.2022
- 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
vaccine used was drawn up in syringe >12 hours prior to giving vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Multiple Sclerosis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 07.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary mass
Symptomtext
Her armpit, in the arm where she got her booster vaccine, was swollen/armpit lump; 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 47-year-old female patient received BNT162b2 (BNT162B2), on 07May2022 as dose 3 (booster), single (Lot number: FM0173) at the age of 47 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hyperthyroidism", start date: Oct2021 (ongoing), notes: Hyperthyroidism, Caller states she is not taking any medications for this condition. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Lot Number: EW0153, Route, Anatomical Location: left arm), administration date: 15Apr2021, when the patient was 46-year-old, for Covid-19 immunization; BNT162b2 (Dose 2, Lot Number: EW0169, Route, Anatomical Location: left arm), administration date: 06May2021, when the patient was 46-year-old, for COVID-19 immunization. The following information was reported: AXILLARY MASS (non-serious) with onset 09May2022, outcome "recovering", described as "Her armpit, in the arm where she got her booster vaccine, was swollen/armpit lump". Additional information: she got her booster on Saturday. Caller reports that yesterday, her armpit, in the arm where she got her booster vaccine, was swollen. Caller confirms as this was her first booster. Vaccine was not Administered at Military Facility. No prior Vaccinations (within 4 weeks) or any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) was reported. The caller is a 47-year-old female patient who previously called to report a previously called to report an "armpit lump" that appeared on Monday on the same arm where she received the on Monday on the same arm where she received the vaccine, after having received a booster shot on Saturday of the COVID vaccine for the Saturday booster shot of Pfizer's COVID vaccine. She mentions that "the little ball she does not know whether to consult with her primary care physician or what to do about it. to do about it. She provided the report number of ALKY87UD. She mentions that she had not spoken to anyone from Pfizer Medical Information. She also mentions that when the first vaccine was given to her she was given information about mild reactions, which included this lump as a secondary reaction, and asked if there would be a as a secondary reaction, and she asked if there would be any type of I additional information. During the call, the caller mentioned that her first dose was on 15Apr and the second on 06May, and that in October she started 06May, and that in October she started to feel sick so she went to see her doctor who diagnosed her with She went to see her doctor who diagnosed her with hyperthyroidism, for which she received treatment for a month and a half (6 weeks) and that she has and has returned to normal values since then. Without However, she knows of two other people who had similar thyroid problems after receiving similar thyroid problems after receiving the vaccine. She mentions that she finds it curious that it is transient, that she knows others with a similar other people with a similar problem and that she presented with no family history of hyperthyroidism. The caller asked if there was any information about thyroid effects after receiving the vaccine. The caller asks if she could receive the second booster of the vaccine after the reaction she had with the first booster. AE e-transmitted. Caller previously called and was given Reportum Number of ALKY87UD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary mass
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hyperthyroidism (Hyperthyroidism Caller states she is not taking any medications for this condition.)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 07.05.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
PT RECIEVED PFIZER FOR 12+ INSTEAD OF PEDIATRIC PFIZER DOSE FOR AGE 5-11. NO SIGNS/SYMPTOMS OUT OF THE ORDINARY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NOT KNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 09.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Pt under 50 and not eligible for 2nd booster but requested another shot of pfizer due to travelling to a Country and was inadvertently administered - primary series with J&J (4/6/21), initial booster with pfizer (12/4/21) and CDC has not made additional recommendations for this category
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 09.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Pt under 50 and not eligible for 2nd booster but requested another shot of pfizer due to travelling to a Country and was inadvertently administered - primary series with J&J (4/6/21), initial booster with pfizer (12/4/21) and CDC has not made additional recommendations for this category
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -