- Staat
- FL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 14.07.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Myocardial infarction
Rheumatoid arthritis
Symptomtext
massive heart attack; Death; rheumatoid arthritis; This spontaneous case was reported by a consumer and describes the occurrence of MYOCARDIAL INFARCTION (massive heart attack), DEATH (Death) and RHEUMATOID ARTHRITIS (rheumatoid arthritis) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. Concomitant products included ADALIMUMAB (HUMIRA) for Rheumatoid arthritis. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced MYOCARDIAL INFARCTION (massive heart attack) (seriousness criteria death and medically significant), DEATH (Death) (seriousness criteria death and medically significant) and RHEUMATOID ARTHRITIS (rheumatoid arthritis) (seriousness criteria death and medically significant). The reported cause of death was massive heart attack. It is unknown if an autopsy was performed. No laboratory was not given. No treatment information was provided by reporter. According to, "The caller stated that she does not know if her brother?s friend received a Moderna, Pfizer or J&J vaccine." This a report of dead one day after the second dose of the product in a 55-year-old patient with concomitant Rheumatoid arthritis. Very limited information regarding the event has been provided for inferring causality. Further information has been request. Most recent FOLLOW-UP information incorporated above includes: On 08-Jul-2021: Follow Up information was received 08-JUL-2021 and added concomitant product and event verbatim; Sender's Comments: This a report of dead one day after the second dose of the product in a 55-year-old patient with concomitant Rheumatoid arthritis. Very limited information regarding the event has been provided for inferring causality. Further information has been request.; Reported Cause(s) of Death: massive heart attack
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- HUMIRA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Gait inability
Motor dysfunction
Muscle spasms
Pain
Seizure
Speech disorder
Tremor
Tunnel vision
Symptomtext
Severe rigors, to which I suspected I was having a seizure (first time in my life). Loss of motor function and shaking so vigorously that I experienced moderate-to-severe cramping in my neck, lower back, and hips. Unable to walk, difficulty speaking. Blacking out in peripheral vision (experiencing tunnel vision). Was in process of calling an ambulance, but after approximately 5 minutes, symptoms subsided. The following morning, I was sore, but largely asymptomatic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.06.2021
- Impfdatum
- 06.05.2021
- Beginn
- 09.05.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Influenza
Pain in extremity
Peripheral swelling
Thrombosis
Symptomtext
She had 2 blood clots in her right leg, and she was now on Eliquis; she had right leg swelling; she had right leg pain; flu; This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer. A female patient of an unspecified age received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in right arm on 06May2021 (Batch/Lot Number: Not Provided) as a single dose, for covid-19 immunisation, with first dose given 15Apr2021. Medical history and concomitant medications were not reported. The patient said she had the flu 3 days after getting her second COVID-19 Vaccine, had right leg swelling, right leg pain, and had 2 blood clots in her right leg. The patient said she was now on apixaban (ELIQUIS), and financial assistance, due to being on unemployment. The outcome of the events was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 19.05.2021
- Impfdatum
- 24.02.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody
Beta-2 glycoprotein antibody
Blood immunoglobulin A
Blood immunoglobulin G
Blood immunoglobulin M
Bone marrow failure
Bone marrow myelogram abnormal
C-reactive protein increased
COVID-19
Carbohydrate antigen 19-9
Chills
Culture
Cytomegalovirus test negative
Double stranded DNA antibody
Epstein-Barr virus antibody positive
Haptoglobin
Hepatitis viral test
Immune system disorder
Symptomtext
immune complex mediated response due to vaccine; portal vein thrombosis; experienced a 30 pound weight loss (over the past two months); night sweats; intermittent fever of unknown origin; chills; This is a spontaneous report from a contactable health care profession and follow up report from a contactable consumer via Pfizer-sponsored program. A 74-years-old male patient received the second dose bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; ), via an unspecified route of administration on 24Feb2021 (Batch/Lot Number: Not provided) as 2nd dose, single for covid-19 immunisation . Medical history included coronary artery, chronic obstructive pulmonary disease, chronic kidney disease, type II diabetes mellitus, hyperlipidaemia, hypertension. The patient's concomitant medications were not reported. The patient experienced immune complex mediated response due to vaccine, portal vein thrombosis, night sweats, intermittent fever, chills, experienced a 30 pound weight loss (over the past two months) on an unspecified date. The patient underwent lab tests and procedures which included ESR: 101 (elevated), CRP: 225 (elevated), White blood cell count elevated (18 today), Procalcitonin: 1.89 (elevated), Haptoglobin: 380, Quantitative IgG: 1,664 (elevated), Antinuclear Factor 1:320 ANA (at first came out negative then positive), Beta-2glycoprotein IgG: 33.4, Antiphospholipid panel: positive, Tumor marker CA 19-9: 46 (Mildly elevated) all on an unspecified date. Negative Lab results: Negative Cultures, Covid-19, RVP, TB, Hepatitis panel, dsDNA, EBV antigen, CMV, Lyme titers, quantitative IgA and IgM, beta 2 glyco IgA, venous duplex, white cell scan, nuclear scan of bone marrow, PNH panel all on an unspecified date. Reporter inquired Are there any reports on portal vein thrombosis after receiving both doses of the Pfizer Covid-19 vaccine? The clinical course was reported as follows Medical assistant stated that she has been treating a 74 year old male patient who received the first dose of the Pfizer Covid-19 vaccine on 02FEB2021 and the second dose on 24FEB2021 and after two weeks of receiving the second dose the patient started experiencing night sweats (2-3 times a night), intermittent fever of unknown origin and chills, he experienced a 30 pound weight loss (over the past two months) and portal vein thrombosis, at this point the differential includes an immune complex mediated response due to vaccine. He has been admitted for two weeks (admitted on 20APR2021) and performed rheumatology, oncology, hematology panels and ruled out infectious causes. It was also reported They did a full work up but nothing came up except that PRIVACY has a portal vein thrombosis. They are wondering if it is related to the vaccine and if there are some reports regarding this side effects. First dose of the vaccine was given 02Feb or 03Feb (reporter is not sure). Second dose of the vaccine was given 24Feb2021. The clinical outcome of the events was unknown
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Portal vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Test Name: ANA; Result Unstructured Data: Test Result:Negative; Comments: at first came out negative then positive); Test Name: ANA; Result Unstructured Data: Test Result:Poitive; Test Name: Antinuclear Factor; Result Unstructured Data: Test Result:1:320; Test Name: beta 2 glyco IgA; Result Unstructured Data: Test Result:Negative; Test Name: Beta-2glycoprotein IgG; Result Unstructured Data: Test Result:33.4; Test Name: IgA; Result Unstructured Data: Test Result:Negative; Test Name: Quantitative IgG; Result Unstructured Data: Test Result:1,664 (elevated); Test Name: IgM; Result Unstructured Data: Test Result:Negative; Test Name: PNH; Result Unstructured Data: Test Result:Negative; Test Name: PNH; Result Unstructured Data: Test Result:Negative; Test Name: nuclear scan of bone marrow; Result Unstructured Data: Test Result:Negative; Test Name: Tumor marker CA 19; Result Unstructured Data: Test Result:9: 46 (Mildly elevated); Test Name: Covid-19; Result Unstructured Data: Test Result:Negative; Test Name: CRP; Result Unstructured Data: Test Result:225 (elevated); Test Name: Negative Cultures; Result Unstructured Data: Test Result:Negative; Test Name: CMV; Result Unstructured Data: Test Result:Negative; Test Name: dsDNA; Result Unstructured Data: Test Result:Negative; Test Name: EBV; Result Unstructured Data: Test Result:Negative; Test Name: Haptoglobin; Result Unstructured Data: Test Result:380; Test Name: Hepatitis panel; Result Unstructured Data: Test Result:Negative; Test Name: Antiphospholipid panel:; Result Unstructured Data: Test Result:positive; Comments: Antiphospholipid panel:; Test Name: Reid Vapor Pressure; Result Unstructured Data: Test Result:Negative; Test Name: Lyme titers; Result Unstructured Data: Test Result:Negative; Test Name: Procalcitonin; Result Unstructured Data: Test Result:1.89 (elevated); Test Name: ESR; Result Unstructured Data: Test Result:101 (elevated),; Test Name: TB; Result Unstructured Data: Test Result:Negative; Test Name: venous duplex; Result Unstructured Data: Test Result:Negative; Test Name: WBC; Result Unstructured Data: Test Result:18 (today); Test Name: white cell scan; Result Unstructured Data: Test Result:Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Chronic kidney disease; COPD; Coronary artery disease; Diabetes mellitus; Hyperlipidemia; Hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 19.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Feeding disorder
Feeling abnormal
Fluid intake reduced
Migraine
Nausea
Pain in extremity
Photophobia
Skin warm
Symptomtext
Arm sore. Arm remained warm/hot to the touch for approx 36 hours. Headache started Friday pm (12 hours after Vacc). Ibuprofen ineffective. Saturday, 5 am (21 hours post vacc), migraine headache conditions: Sensitive to light, nauseous, unbearable headache. Ibuprofen ineffective. Could not eat or drink all day. Used ice packs on head. Sunday. Headache persisted throughout the day. Ibuprofen ineffective. Used ice packs. Was able to go outside and run errands. Started consuming drinks. Ate something at 1 pm. Monday morning, Woke up and headache was mild. Ibuprofen effective. went to work, able to eat and drink. Extremely tired and still feel muddle-headed. Forgot to bring ibuprofen, headache started reappearing at 1 pm. Arm soreness lasted approx 12 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin, omeprazole, Wellbutrin
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- -
- Beginn
- 03.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Fibrin D dimer
Muscle spasms
Myalgia
Tinnitus
Urticaria
Symptomtext
Narrative: 11/03/21 COVID vaccine dose #1 06/16/22 Pt reports to PCP history of reaction to COVID vaccine: "muscle cramps, cont with left leg cramp, had borderline D-dimer, not sure if it meant subclinical DVT or not, but no DVE dx. Chest pain, muscle pain, muscle cramps/pain, tinnitus and hives also reported by PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 03.04.2022
- Impfdatum
- -
- Beginn
- 06.01.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypertension
Injection site urticaria
Pruritus
Swelling
Urticaria
Symptomtext
patient received all 3 doses outside of hospital-no vaccine information provided Referred for evaluation of skin itch and swelling. Pt c/o 2-3 yr hx of intermittent itching, red, blotches, raised on her arms, face, legs, abdomen, legs. Warm to touch. Had episodes of eyelid swelling, no tongue swelling, no lip swelling, no throat tightness, no shortness, no dysphagia, occurs about couple times per month. Each lesion lasts less than 24 hours, no burning on painful lesions. When lesions resolve, skin is normal appearance. She takes loratadine when hives occur. Noticed 3 year hx of alcohol will make her have skin itching. Occurs within minutes of taking one sip of alcohol. Has been avoiding and hives until occur. She can take NSAIDs without any hives trigger. Does not notice any correlation. No correlation to any foods. All three Covid vaccine she developed hives throughout her body within a 15 minute and progressed to full body hives, lasted for two days. Covid vaccine, hives at injection site, Third dose, 1 week later developed hives and increased HTN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- -
- Beginn
- 15.12.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Hypoaesthesia
Pain
Pain in extremity
Paraesthesia
Symptomtext
Narrative: 04/08/21 COVID vaccine dose #1 (of1) ~12/2021 Received COVID booster at another location 01/20/2022 Patient calls, reports ~ 24 hours after his J&J booster he developed right hand tingling, pain and numbness that is starting to radiate up the arm; duration of 5 weeks no further information available at this time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 04.12.2021
- Impfdatum
- 01.09.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dyspnoea
Urticaria
Symptomtext
Narrative: 09/01 COVID (Pfizer) vaccine dose #1 09/02 pt reports "broke out in hives all over torso, some SOB (slight chest tightness trying to take a deep breath), self-treated with diphenhydramine 50 mg x2 doses with improvement after 2nd dose; hives remained until 9/04
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 02.04.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 112,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Cough
Diarrhoea
Dyspnoea
Exposure to communicable disease
Fatigue
Headache
Myalgia
Nausea
Painful respiration
Rhinorrhoea
SARS-CoV-2 test positive
Vomiting
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 03/12/21 COVID vaccine dose #1 04/02/21 COVID vaccine dose #2 07/23/21 Pt reports cough, headache, runny nose, and close exposure to illness; tested and sent home; COVID POSITIVE 07/24/21 Pt reports diarrhea, fatigue, muscle pain, chills; rx given for acetaminophen, DM/guaifenesin, loperamide 07/25/21 Pt reports low grade fever temp 99.1 07/28/21 Pt reports dry cough increasing in frequency, continuous fatigue, constant headache, occasional nausea, and generalize muscle pain; remains stable 07/29/21 Pt reports shortness of breath 07/30/21 Pt reports occasional coughing, vomiting, but is stable 08/01/21 Pt reports pain when taking deep breath 08/03/21 Pt reports decreased coughing, easier breathing 08/04/21 Pt reports nausea 08/05/21 Pt reports fatigue but is improving; isolation end
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 02/21/21 COVID NEGATIVE 07/23/21 COVID POSITIVE, VARIANT SEQUENCING PENDING
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 07.06.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 45,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Anosmia
COVID-19
Dyspnoea exertional
Exposure to SARS-CoV-2
Fatigue
Headache
Myalgia
Productive cough
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 06/07/21 COVID vaccine dose #1 07/22/21 Pt reports cough, muscle pain, and rhinorrhea x2 days; exposed to positive COVID church member; swab performed - COVID POSITIVE 07/23/21 Pt reports loss of taste/smell, cough, muscle pain, runny nose; rx given for DM/guaifenesin 07/24/21 Pt reports dry cough, frontal headache, muscle pain, rhinorrhea 07/25/21 Pt reports mild cough, returning loss of taste/smell, muscle pain, runny nose 07/26/21 Pt reports fatigue 07/27/21 Pt reports mild productive cough 07/28/21 Pt reports cough improving 07/29/21 Pt reports SOB on exertion, improving cough 07/30/21 Pt reports continued loss of taste/smell; isolation end
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- 07/22/21 COVID POSITIVE, DELTA VARIANT DETECTED
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 13.01.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 194,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest X-ray normal
Chest discomfort
Chills
Cough
Dyspnoea
Headache
Hypoaesthesia
Magnetic resonance imaging abnormal
Myalgia
Nasal congestion
Nausea
Nerve conduction studies abnormal
Oropharyngeal discomfort
Pain in extremity
Paraesthesia
Radiculopathy
Rhinorrhoea
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 12/21/20 COVID vaccine dose #1 01/13/21 COVID vaccine dose #2 02/02/21 Preop COVID test NEGATIVE 05/18/21 Pt reports numbness in right leg that feels like needle pricking; scheduled MRI and nerve conduction test 06/13/21 Pt reports severe pain in right leg; nerve conduction test reveals bilateral S1 radiculopathy and MRI reveals multilevel lumbar degenerative disease/degenerative disc disease with multiple levels of variable neuroforaminal stenosis: Community care consult to Neurosurgery placed 07/26/21 Pt presents to screening reporting chills, cough, muscle pain, nausea, runny nose, shortness of breath, vomiting x4 days; swabbed COVID POSITIVE 07/27/21 Pt presents to ED reporting headache, nausea, vomiting, chills, nasal congestion that started 5 days ago; has slight cough and dyspnea; discharged with rx for zinc, ascorbic acid 07/28/21 Pt reports dry cough with chest tightness after, headache, muscle pain; rx given for DM/guaifenesin 07/29/21 Pt reports going to medical facility for ongoing COVID care and plans to receive Regeneron 07/31/21 Pt reports diminished cough with use of benzonatate twice daily and cough syrup; improving and stable 08/02/21 Pt is improving and reports mild cough 08/04/21 Pt reports dry cough, throat discomfort, and nausea; requests medications recommended by medical facility Dr. (dexamethasone, azithromycin) be provided by agency but based on symptomology, pt does not have an indication for the medications; agency advised pt against the use and that he will need to obtain the meds outside the agency
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 07/26/21 COVID POSITIVE 07/27/21 CXR WNL
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 13.01.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 194,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest X-ray normal
Chest discomfort
Chills
Cough
Dyspnoea
Headache
Hypoaesthesia
Magnetic resonance imaging abnormal
Myalgia
Nasal congestion
Nausea
Nerve conduction studies abnormal
Oropharyngeal discomfort
Pain in extremity
Paraesthesia
Radiculopathy
Rhinorrhoea
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 12/21/20 COVID vaccine dose #1 01/13/21 COVID vaccine dose #2 02/02/21 Preop COVID test NEGATIVE 05/18/21 Pt reports numbness in right leg that feels like needle pricking; scheduled MRI and nerve conduction test 06/13/21 Pt reports severe pain in right leg; nerve conduction test reveals bilateral S1 radiculopathy and MRI reveals multilevel lumbar degenerative disease/degenerative disc disease with multiple levels of variable neuroforaminal stenosis: Community care consult to Neurosurgery placed 07/26/21 Pt presents to screening reporting chills, cough, muscle pain, nausea, runny nose, shortness of breath, vomiting x4 days; swabbed COVID POSITIVE 07/27/21 Pt presents to ED reporting headache, nausea, vomiting, chills, nasal congestion that started 5 days ago; has slight cough and dyspnea; discharged with rx for zinc, ascorbic acid 07/28/21 Pt reports dry cough with chest tightness after, headache, muscle pain; rx given for DM/guaifenesin 07/29/21 Pt reports going to medical facility for ongoing COVID care and plans to receive Regeneron 07/31/21 Pt reports diminished cough with use of benzonatate twice daily and cough syrup; improving and stable 08/02/21 Pt is improving and reports mild cough 08/04/21 Pt reports dry cough, throat discomfort, and nausea; requests medications recommended by medical facility Dr. (dexamethasone, azithromycin) be provided by agency but based on symptomology, pt does not have an indication for the medications; agency advised pt against the use and that he will need to obtain the meds outside the agency
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 07/26/21 COVID POSITIVE 07/27/21 CXR WNL
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 31.03.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 120,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Diarrhoea
Dyspnoea exertional
Ear infection
Ear pain
Exposure to SARS-CoV-2
Fatigue
Laboratory test
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Stool analysis
Symptomtext
Narrative: COVID infection following completion of COVID vaccine series 03/04/21 COVID vaccine dose #1 03/31/21 COVID vaccine dose #2 04/07/21 Pt reports diarrhea for 2.5 weeks with no improvement with ammonium and pepto 04/08/21 COVID NEGATIVE; lab orders and stool tests placed 04/21/21 Pt reports continuing diarrhea while on acidophilus, loperamide, and melatonin; tests came back positive for lactoferrin - GI consult placed 05/06/21 Pt presents to clinic for ear infection; rx given for hydrocortisone/neomycin/polymyxin ear drops 06/22/21 Pt presents to clinic reporting shortness of breath while walking short distances - Cardio consult placed given CAD history 07/22/21 Pt reports continuing ear pain 07/30/21 Pt presents to screening reporting close exposure to COVID positive person and fever of 101.1 on 07/29, temp at screening 100.9; COVID POSITIVE 07/31/21 Pt reports baseline cough, minimal fatigue, and fever of 101.1 on 07/29, temp at screening 100.9; COVID POSITIVE 07/31/21 Pt reports baseline cough, minimal fatigue, and fever (101.8); rx given for vitamin C, DM/guaifenesin, zinc 08/02/21 Pt reports fatigue, runny nose 08/04/21 Pt reports cough is nearly resolved but fatigue remains; improving
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- 07/30/21 COVID POSITIVE; VARIANT SEQUENCING PENDING
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 26.05.2021
- Beginn
- 28.06.2021
- Tage bis Beginn
- 33,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest X-ray normal
Chills
Cough
Diarrhoea
Dyspnoea
Dyspnoea exertional
Fatigue
Headache
Myalgia
Productive cough
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 05/26/21 COVID vaccine dose #1 (J&J) 07/03/21 Pt presents to screening reporting cough, congestion, and shortness of breath that started Monday (06/28)l; states he had close exposure to someone COVID positive; COVID POSITIVE 08/01/21 Pt reports chills, cough, fatigue, fever, muscle pain, runny nose, congestion, shortness of breath 08/03/21 Pt reports cough and shortness of breath upon exertion, improving 08/05/21 Pt is clinically resolved; reports fatigue and cough: using cough syrup 08/13/21 Pt presents to screening for retesting for work; denies symptoms and reports close exposure to COVID positive person; COVID POSITIVE 08/14/21 Pt reports chills, cough, occasional diarrhea, fatigue, headache, muscle pain, congestion, SOB upon exertion 08/16/21 Pt reports feeling fatigue, SOB, productive cough with clear sputum; he reports cough is worsening
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 06/24/21 CXR lungs clear 07/30/21 COVID POSITIVE, VARIANT SEQUENCING PENDING 08/13/21 COVID POSITIVE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 02.02.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 177,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Anosmia
COVID-19
Chills
Diarrhoea
Dysphagia
Dysphonia
Dyspnoea
Eating disorder
Fatigue
Headache
Myalgia
Oropharyngeal pain
Productive cough
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infection following completion of COVID vaccine series 01/12/21 COVID vaccine dose #1 02/02/21 COVID vaccine dose #2 07/14/21 Pt presents to clini c complaining of dysphagia, hoarseness, and increased mucus along with problems with liquids and solid: swallow test ordered and rx given for amoxicillin and DM/guaifenesin 08/01/21 Pt presents to screening reporting muscle pain, runny nose: temp 97.9; COVID POSITIVE 08/02/21 Pt reports chills x3 days, cough x4-5 days, mild headache, muscle pain (baseline), runny nose, shortness of breath (baseline), sore throat; rx given for cholecalciferol; DM/guaifenesin, fluticasone, throat lozenges 08/03/21 Pt reports productive cough, chronic fatigue, muscle pain, mild shortness of breath, sore throat 08/06/21 Pt reports loss of taste/smell, sore throat, and cough 08/07/21 Pt reports diarrhea upon coughing; denies blood in stool or abdominal pain 08/09/21 Pt reports dry cough that is improving rx given for benzonatate; clinically resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 08/01/21 COVID POSITIVE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 18.02.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 146,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Anosmia
COVID-19
Chest X-ray normal
Cough
Diarrhoea
Dyspnoea
Fatigue
Headache
Insomnia
Malaise
Nausea
Oropharyngeal pain
Paranasal sinus hypersecretion
Pollakiuria
Productive cough
Red blood cell sedimentation rate normal
Rhinorrhoea
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 01/21/21 COVID vaccine dose #1 02/18/21 COVID vaccine dose #2; pt reports "feeling like crap" - tiredness, nausea, fatigue, increased urination, insomnia 04/18/21 Preop COVID test for colonoscopy - COVID NEGATIVE 07/14/21 Pt reports upper respiratory infection with symptoms of sinus drainage and dry cough; COVID tested at outside facility - COVID POSITIVE 07/26/21 Pt reports cough, diarrhea, fatigue, headache, loss of taste/smell, nausea, runny nose, shortness of breath, sore throat that started 07/14; advised to go to ED due to SOB; CXR WNL; ED discharged her home with rx for albuterol, vitamin C, vitamin D, aspirin 07/28/21 Pt reports cough , runny nose, SOB, sore throat; rx given for benzonatate, vitamin D 07/30/21 Pt reports slight improvement in cough and intermittent SOB 08/01/21 Pt reports continued productive cough, fatigue, SOB, runny nose 08/03/21 Pt reports cough improving; clinically resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 04/18/21 COVID NEGATIVE 07/26/21 COVID POSITIVE 07/27/21 CXR WNL, troponin WNL, WBC WNL, ESR WNL,
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 30.11.2021
- Impfdatum
- 30.03.2021
- Beginn
- 25.07.2021
- Tage bis Beginn
- 117,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Cough
Diarrhoea
Dyspnoea
Exposure to communicable disease
Inflammatory marker increased
Malaise
Pain
Pneumonia
Pyrexia
Respiratory symptom
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infection following completion of COVID vaccine series 03/30/21 COVID vaccine dose #1 (J&J) 08/02/21 Pt presents to ED reporting exposure to patient with respiratory symptoms ~12 days ago (07/21); states he has symptoms of malaise, body aches, subjective fevers, cough, SOB, and 1-2 loose stools/day for the past 9 days (07/25); CXR bilateral pneumonia, inflammatory markers slightly elevated; admitted for COVID pneumonia; COVID POSITIVE 08/03/21 Treated inpatient with dexamethasone, remdesivir, albuterol/ipratropium 08/05/21 Pt requires oxygen on and off, mainly at night time 08/06/21 Pt discharged home with rx for famotidine, dexamethasone, and albuterol/ipratropium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- 08/02/21 CXR bilateral pneumonia 08/02/21 COVID POSITIVE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 06.04.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Asthenia
Chest pain
Diarrhoea
Dizziness
Headache
Illness
Malaise
Pain in extremity
Vaccination site pain
Symptomtext
does not feel a bit good; actually feels dizzy; sick at stomach; had a big case of diarrhea; sick and is you know hurting a little bit in chest; sick and is you know hurting a little bit in chest; has got an extreme headache; no energy, no energy; Arm every you know every couple of days or few days or something like that gets a real soreness in that arm and can feel it; Arm every you know every couple of days or few days or something like that gets a real soreness in that arm and can feel it; This is a spontaneous report received from a contactable consumer (patient). A 66-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number: not provided) (age at the time of vaccination was 66 years) via unspecified route of administration on 06Apr2021 as DOSE 2, SINGLE for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number: not provided) via unspecified route of administration on 16Mar2021 as DOSE 1, SINGLE for COVID-19 immunisation. It was reported that on an unknown date the patient does not feel a bit good, actually feels dizzy, sick at stomach, had a big case of diarrhea, sick and is you know hurting a little bit in chest, has got an extreme headache, no energy, no energy. Does not feel a bit good: began right after took that shot, within a week of the second shot. she explains she was worsened. Arm every you know every couple of days or few days or something like that gets a real soreness in that arm and can feel it: What caller was going to tell agent was that the arm caller took vaccine in, caller was told by person's up there at Rite Aid, where the vaccine was administered what they think it is. Caller's arm every you know every couple of days or few days or something like that gets a real soreness in that arm and can feel it. Actually, feels dizzy: Caller states this began the first week after receiving the second dose Pfizer Covid Vaccine. Caller was still dizzy. Caller just walked in a room to get vaccination card and is now laying down. Caller is laying down now and does not feel like agent knows. Caller states it was the same as it has been the last two or three days. Caller was still dizzy and still does not not have energy and caller begins to mention something about her stomach but stops and says it has been probably been 45 minutes to an hour and caller does not feel like too much more talking. The outcome of the events does not feel a bit good and actually feels dizzy was not recovered and unknown for other events. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 14.04.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 184,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest pain
Dyspnoea
Fibrin D dimer increased
SARS-CoV-2 test positive
Ventilation/perfusion scan
Symptomtext
SOB x2 weeks, to ED, + COVID test in fully vaccinated pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 14.04.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 184,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest pain
Dyspnoea
Fibrin D dimer increased
SARS-CoV-2 test positive
Ventilation/perfusion scan
Symptomtext
SOB x2 weeks, to ED, + COVID test in fully vaccinated pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 24.03.2021
- Beginn
- 01.03.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chest pain
Cough
Nasopharyngitis
Fatigue
Symptomtext
Really bad cough; Makes her so tired; Makes her chest hurt; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 24Mar2021 as dose 2, single for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. The patient has never had a Covid test. On 26Mar2021, 2 days later, the patient experienced really bad cough. On an unspecified date in Mar2021, the patient experienced makes her so tired and makes her chest hurt. The patient has been coughing ever since and was still coughing. The patient went to the doctor 7 days after the cough started and she started taking a cough medicine at night. The patient was still taking the cough medicine at night. The patient does not know what it was. It makes the patient so tired and makes her chest hurt. The patient called to check if this was a symptom of the vaccine. Therapeutic measures were taken as a result of really bad cough using Mucinex. The outcome of the event really bad cough was not resolved while other events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 01.12.2020
- Beginn
- 01.01.2021
- Tage bis Beginn
- 31,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Fatigue
Fibromyalgia
Gastrointestinal disorder
Joint dislocation
Myalgia
Symptomtext
her elbows came out; felt tired/ experienced chronic fatigue; achy all over; Fibromyalgia; More problems breathing; Problems with her intestines; This spontaneous case was reported by a consumer and describes the occurrence of FIBROMYALGIA (Fibromyalgia), DYSPNOEA (More problems breathing), GASTROINTESTINAL DISORDER (Problems with her intestines), FATIGUE (felt tired/ experienced chronic fatigue) and MYALGIA (achy all over) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Immunocompromised and Asthma (, she had problems with her lungs (sister has asthma but after second dose experienced more problems breathing). Sister also had problems with her intestines. ). In December 2020, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In January 2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 2 dosage form. In January 2021, the patient experienced FIBROMYALGIA (Fibromyalgia), DYSPNOEA (More problems breathing) and GASTROINTESTINAL DISORDER (Problems with her intestines). On an unknown date, the patient experienced FATIGUE (felt tired/ experienced chronic fatigue), MYALGIA (achy all over) and JOINT DISLOCATION (her elbows came out). At the time of the report, FIBROMYALGIA (Fibromyalgia), DYSPNOEA (More problems breathing), GASTROINTESTINAL DISORDER (Problems with her intestines), FATIGUE (felt tired/ experienced chronic fatigue), MYALGIA (achy all over) and JOINT DISLOCATION (her elbows came out) outcome was unknown. Sister was concerned about receiving full third dose and not half, as Moderna submitted FDA approval for 50 mcg dose now. she was worried that whether this dose will create any problem or not Concomitant medication use was unknown Treatment information was unknown Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma (, she had problems with her lungs (sister has asthma but after second dose experienced more problems breathing). Sister also had problems with her intestines.); Immunocompromised
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 25.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac discomfort
Dizziness
Dyspnoea
Feeling abnormal
Heart rate decreased
Symptomtext
pulse is low, around 45-50; feels like they are going to have a heart attack; strong dizziness; feels like their going to stop breathing; cannot explain what is happening to them.; This spontaneous case was reported by a consumer and describes the occurrence of HEART RATE DECREASED (pulse is low, around 45-50) and CARDIAC DISCOMFORT (feels like they are going to have a heart attack) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. notprovided) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 25-Aug-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Sep-2021, the patient experienced HEART RATE DECREASED (pulse is low, around 45-50), CARDIAC DISCOMFORT (feels like they are going to have a heart attack), DIZZINESS (strong dizziness), DYSPNOEA (feels like their going to stop breathing) and FEELING ABNORMAL (cannot explain what is happening to them.). At the time of the report, HEART RATE DECREASED (pulse is low, around 45-50), CARDIAC DISCOMFORT (feels like they are going to have a heart attack), DIZZINESS (strong dizziness), DYSPNOEA (feels like their going to stop breathing) and FEELING ABNORMAL (cannot explain what is happening to them.) outcome was unknown. No concomitant product was provided by the reporter. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 12.08.2021
- Impfdatum
- 16.02.2021
- Beginn
- 18.02.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Pyrexia
Tremor
Symptomtext
Chills; shaking really bad due to chills; Low grade 100.5F fever; A spontaneous report was received from a Healthcare Professional concerning a 82? Years-old male patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced events, chills, shaking really bad due to chills, and low grade 100.5f fever. The patient's medical history was included bypass surgery. Concomitant medications reported were not provided for drug use for unknown indication. On unknown date, prior to the onset of the events, the patient received their first of two planned doses of mRNA-1273 (lot batch: Not provided) intramuscularly for prophylaxis of COVID-19 infection. On 18 Feb 2021, the patient experienced the events, chills. shaking really bad due to chills, low grade 100.5f fever, term. Treatment details included ibuprofen. Action taken with mRNA-1273 in response to the events, chills, shaking really bad due to chills, and low grade 100.5f fever, was not reported. On an unknown date the outcome of events include, chills, shaking really bad due to chills, and low grade 100.5 f fever was not reported.; Reporter's Comments: This case concerns an 82 year old male patient, with history of bypass surgery, who experienced a non-serious unexpected event of tremor, and expected events of chills and pyrexia, 3 days after receiving second dose of mRNA- 1273 (Lot# Unknown). Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded. Further information has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: No adverse event (No reported medical history)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 14.07.2021
- Impfdatum
- 01.04.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blindness unilateral
Blood glucose
Chills
Cold sweat
Diabetes mellitus
Feeding disorder
Feeling abnormal
Gait disturbance
Headache
Hyperhidrosis
Lethargy
Neck pain
Pneumonia
Thirst
Symptomtext
Pneumonia; Losing vision in one eye/her vision is gone in one eye; Becoming diabetic; feeling funny; lethargic words; not being able to eat; thirsty; cold sweats; sweating profusely,; "drag his feet" which comes and goes all day; pain on the left side of her neck back on the head; hot chills; pain in left side of neck back on head; This spontaneous case was reported by a consumer and describes the occurrence of PNEUMONIA (Pneumonia), BLINDNESS UNILATERAL (Losing vision in one eye/her vision is gone in one eye) and DIABETES MELLITUS (Becoming diabetic) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Blood pressure high. Concomitant products included METFORMIN for Diabetes mellitus, AMLODIPINE for Hypertension, OXYMETAZOLINE HYDROCHLORIDE (CORICIDIN) and NYSTATIN (STATIN) for an unknown indication. In April 2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In May 2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced PNEUMONIA (Pneumonia) (seriousness criteria hospitalization and medically significant), BLINDNESS UNILATERAL (Losing vision in one eye/her vision is gone in one eye) (seriousness criterion medically significant), DIABETES MELLITUS (Becoming diabetic) (seriousness criterion medically significant), FEELING ABNORMAL (feeling funny), LETHARGY (lethargic words), FEEDING DISORDER (not being able to eat), THIRST (thirsty), COLD SWEAT (cold sweats), HYPERHIDROSIS (sweating profusely,), GAIT DISTURBANCE ("drag his feet" which comes and goes all day), NECK PAIN (pain on the left side of her neck back on the head), CHILLS (hot chills) and HEADACHE (pain in left side of neck back on head). The patient was hospitalized from 08-Jun-2021 to 14-Jun-2021 due to PNEUMONIA. The patient was treated with INSULIN for Diabetes mellitus, at a dose of 5 dosage form once a day. At the time of the report, PNEUMONIA (Pneumonia), BLINDNESS UNILATERAL (Losing vision in one eye/her vision is gone in one eye), DIABETES MELLITUS (Becoming diabetic), FEELING ABNORMAL (feeling funny), LETHARGY (lethargic words), FEEDING DISORDER (not being able to eat), THIRST (thirsty), COLD SWEAT (cold sweats), HYPERHIDROSIS (sweating profusely,), GAIT DISTURBANCE ("drag his feet" which comes and goes all day), NECK PAIN (pain on the left side of her neck back on the head), CHILLS (hot chills) and HEADACHE (pain in left side of neck back on head) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood glucose: 250 High. Patient stated that it affected the vision on her right eye and that "her vision was gone in one eye" Patient was still experiencing hot chills and sweating profusely, drag his feet which comes and goes all day, had pain on the left side of her neck back on the head. Treatment medication included Antibiotic (Unspecified name) for Pneumonia and 5 doses of insulin a day. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, further information is requested.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded. However, further information is requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- 7,0
- Labordaten
- Test Name: Blood Glucose
- Aktuelle Erkrankungen
- Blood pressure high
- Vorgeschichte
- -
- Andere Medikamente
- METFORMIN; AMLODIPINE; CORICIDIN; STATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 25.04.2021
- Impfdatum
- 26.02.2021
- Beginn
- 01.03.2021
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood pressure increased
Cardiac disorder
Chest pain
Feeding disorder
Gallbladder disorder
Loss of personal independence in daily activities
Nausea
Pain
Pancreatic disorder
Symptomtext
severe chest pain like severe heart burn attack/the doctors do not think it is heart burn/radiating pain into the right arm and lymp nodes; blood pressure was through the rood; severe pain; cardiac issues; GI issues/GI malfunction of the pancreas and gallbladder; GI issues/GI malfunction of the pancreas and gallbladder; can not eat, work, or engage in daily activities/She is unable to eat and is very weak; can not eat, work, or engage in daily activities/She is unable to eat and is very weak; can not eat, work, or engage in daily activities; nausea; This is a spontaneous report from a contactable consumer (patient). A 54-year-old female patient received the 1st dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 16Mar2021 09:45 (Batch/Lot Number: Unknown reported as either EN6205 or EM6205) as SINGLE DOSE for COVID-19 immunization; azithromycin (ZITHROMAX), via an unspecified route of administration from 26Feb2021 until 02Mar2021, at unspecified dose and frequency for dental care; and corticosteroid (CORTICOSTEROID), via an unspecified route of administration from an unspecified date with last dose shot on 23Mar2021 at unknown dose, once or twice a year for a couple of years for knee pain and joint pain . Medical history included dental procedure on an unknown date. Concomitant medications were not reported. On 25Mar2021 (9 days later), she developed severe chest pain like severe heart burn attack radiating pain into the right arm and lymph nodes, blood pressure was through the roof and was in severe pain. She was unable to eat, was very weak and also cannot work or engage in daily activities noted in Mar2021. The patient required emergency room and physician office visit due the events (including cardiac issue and GI issues/malfunction of the pancreas and gallbladder). She was hospitalized on 03Apr2021 and was just released on 04Apr2021. During hospitalization, doctors have ruled out cardiac issue and GI issues/malfunction of the pancreas and gallbladder and they cannot find out the cause. The patient received famotidine (PEPCID), omeprazole (PRILOSEC), pantoprazole (PROTONIX), acetaminophen (TYLENOL) as treatment. While in the hospital they gave her dicycloverine (BENTYL) which she thought was for nausea noted in 2021.She stated a week after she got the vaccine she got a corticosteroid shot which she was wondering if it can impact one's immune system and cause an adverse reaction with the vaccine. She also stated that a month prior to vaccine she took an azithromycin. She also was wondering with the combination of all these three things being close together if it may have caused a disruption in her body organic system. The action taken in response with the adverse event for azithromycin was post therapy while unknown for corticosteroid shot. The patient did not recover from chest pain while outcome of the remaining events were unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : PFIZER INC-2021376222 Pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Dental treatment
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pyrexia
Symptomtext
High fever= 103.6 Slept Fever resolved several hours later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 19.04.2021
- Beginn
- 21.04.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Symptomtext
Dizziness; Nausea; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A female patient received bnt162b2 (BNT162B2), administration date 19Apr2021 (Lot number: Not Provided) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DIZZINESS (non-serious) with onset 21Apr2021, outcome "unknown", described as "Dizziness"; NAUSEA (non-serious) with onset 21Apr2021, outcome "unknown", described as "Nausea". Additional information: Caller states she is calling for her sister regarding the Pfizer Corona Vaccine. States her sister is sleeping right now clarifies she is lying in bed. States we received the vaccine on Monday, 19Apr2021 however caller clarifies her sister received the vaccine on Monday 19Apr2021. Starting yesterday, 21Apr2021 the caller sister had dizziness and nausea. Now, her sister is lying down and complaining of nausea and dizziness. PSCC Communication: Referred caller to her sister healthcare professional for any treatment recommendations or medical advice. Caller makes the comment, so Pfizer has nothing this is ridiculous. Pfizer is giving this vaccine to the pharmacy, and you do not know if the pharmacy is keeping the vaccine in the refrigerator or handling it right. People are getting sick and when they call Pfizer Pfizer says go see your doctor. The thing is that Pfizer should not give this vaccine to the pharmacy. The pharmacy does not handle it well. Pfizer does not know if the pharmacy keeps it in the refrigerator or if the temperature is right or how long they are putting the product in the syringe and keeping it on their desk. She again states you do not know; you do not supervise you do not check. People are getting sick and when they call Pfizer is telling them to go see their doctor. The caller states Pfizer should have a doctor or somebody on the phone when people are having side effects so they can talk to a doctor. Pfizer should not say go and see a doctor. Pfizer is messing up people lives, and Pfizer does not even have a doctor on the phone to talk to people. Caller does not need information from medical information department. Pfizer is a big company, and they have to manage people who are having side effects so when these people call the company Pfizer should have a doctor on the phone so the people can ask the doctor what to do. Description of complaint: Caller states she is calling for her sister in regard to the Pfizer Corona Vaccine. Caller makes the comment, so Pfizer has nothing this is ridiculous. Pfizer is giving this vaccine to the pharmacy, and you do not know if the pharmacy is keeping the vaccine in the refrigerator or handling it right. People are getting sick and when they call Pfizer Pfizer says go see your doctor. The thing is that Pfizer should not give this vaccine to the pharmacy. The pharmacy does not handle it well. Pfizer does not know if the pharmacy keeps it in the refrigerator nor if the temperature is right or how long they are putting the product in the syringe and keeping it on their desk. She again states, you do not know, you do not supervise you do not check. People are getting sick and when they call Pfizer is telling them to go see their doctor. The caller states Pfizer should have a doctor or somebody on the phone when people are having side effects so they can talk to a doctor. Pfizer is messing up people live and Pfizer does not even have a doctor on the phone to talk to people. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 16.04.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Stepped in a hole, she did not fall, but now the bottom of her foot hurts.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received bnt162b2 (BNT162B2), administration date 16Apr2021 (Lot number: Not Provided) as dose 2, single 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: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "Stepped in a hole, she did not fall, but now the bottom of her foot hurts.". Additional information: She reports her dog Fraya, a large dog or granddaughter may have dug a hole. She reports she stepped in the hole while she was walking in her back yard to check on her tomatoes, she did not fall. She doesn't know what happened, if she bruised or pulled muscle in the bottom of her foot but, it hurts. She can't see it because its the bottom of her foot. It has been a little over a week since she had her last COVID vaccine and wants to know if it is safe to take something over the counter specifically, Ibuprofen, since she was previously told not to take it. She states she spoke to the hospital where she got the vaccine but, got no answer and a pharmacist but, again, got no answer. Caller does not think that she falling in or stepping in a hole has anything to do with getting the COVID vaccine. She reports everything with her COVID vaccines went a lot easier than she expected it to. Caller reports that she understands now why she did not get an answer to her question and does not need to be transferred because she has her answer. She states her answer came from the Regional Pharmacy Director she happens to know at the hospital she use to work for, it's all politics. She is not sure if the call-handler worked in a hospital before but, it is all politics. Its a long story doesn't its all related to politics especially if your non-clinical like she was. She now understands where the directive of no Ibuprofen comes from. She feels that she has answered her own question and does not want to continue on the call. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 02.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Urticaria
Symptomtext
Narrative: 11/02 COVID vaccine dose#1 11/03 seen in ED with c/o facial hives; no information provided regarding treatment, not admitted 11/12 seen by PCP, symptoms not mentioned, likely resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 10.04.2021
- Beginn
- 10.04.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fatigue
Rash
Rash pruritic
Urticaria
Symptomtext
Narrative: According to nursing note, Spoke with patient and reports receiving J&J vaccine approximately 3 weeks ago. Patient states she initially experienced fatigue and rash/hives on her body with the exception of her face or genitalia. Patient has attempted OTC Benadryl with minimal effects; switching to Allegra then topical cortisone with no relief. Patient reports no open lesions, but continues to experience urticaria with pruritic sensations. Patient is requesting for a medication to address the dermatological response." treated with oral predpak.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 13.04.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 245,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Cough
Headache
Nasal congestion
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Narrative: COVID infection following COVID vaccine series 03/19 COVID vaccine dose #1 04/13 COVID vaccine dose #2 12/14 pt presented to ED c/o scratchy throat x 1 day, chills last night head/nasal congestion, cough, dull headache; COVID positive; discharged from ED with rx for benzonatate: no further follow up noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- LAB RESULTS: Date Test Name Result 12/14/2021@12:45 COVID-19 PCR DETECTED
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 20.03.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 264,0
- Dosis
- 2
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
pt developed symptoms, tested positive for COVID and was admitted to the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- 12/9/2021- SARS-CoV-2 PCR Rapid Detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 23.05.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 60,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Cough
Exposure to SARS-CoV-2
Fatigue
Headache
Myalgia
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 04/17/21 COVID vaccine dose #1 05/23/21 COVID vaccine dose #2 07/21/21 Pt reports no symptoms but has had exposure to COVID positive wife; COVID POSITIVE 07/22/21 Pt reports chills, cough, fatigue, headache, fever, muscle pain; rx given for acetaminophen, DM/guaifenesin; adamantly denies receiving COVID vaccine despite records indicating vaccination - nurse contacted for assistance and requested correction for HIMS 07/23/21 Pt reports cough is improving: reports subjective fever and runny nose 07/24/21 Pt reports muscle pain, subjective fever 07/25/21 Pt reports other than feeling fatigue, he feels great and all other symptoms have resolved 07/26/21 Pt is improving and is to remain isolated until 7/30
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 07/21/21 COVID POSITIVE, DELTA VARIANT DETECTED
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 18.02.2021
- Beginn
- 20.07.2021
- Tage bis Beginn
- 152,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Fatigue
Headache
Malaise
Myalgia
Oropharyngeal pain
Productive cough
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sinus headache
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 01/2/21 COVID vaccine dose #1 02/18/21 COVID vaccine dose #2 07/20/21 Pt feels unwell 07/22/21 Onset of cough which progressed to fatigue 07/23/21 Pt progressed to fatigue coughing and congestion 07/24/21 Pt reports worsening symptoms, headache, and myalgia malaise 07/25/21 Pt reports headache, muscle pain, sore throat; COVID POSITIVE 07/26/21 Pt reports improved symptoms but continues to have fatigue, headache, coughing; rx given for benzonatate, cholecalciferol, zinc, ascorbic acid 07/27/21 Pt reports runny nose, muscle pain, improving dry cough, resolved headache 07/26/21 Pt reports improving each day, good appetite, no fever, intermittent headache 07/30/21 Pt reports productive cough with difficulty in expectorating, sinus headache 07/31/21 Pt denies symptoms, meets CDC criteria for resolution
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 07/25/21 COVID POSITIVE, VARIANT SEQUENING PENDING
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 09.03.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 136,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Cough
Diarrhoea
Fatigue
Headache
Oropharyngeal pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 02/15/21 COVID vaccine dose #1 03/09/21 COVID vaccine dose #2 07/23/21 Pt reports cough, low grade fever temp 99.4, O2 sat 98, runny nose; COVID POSITIVE 07/24/21 Pt reports chills, cough, diarrhea, fever, headache, sore throat, runny nose; rx given for acetaminophen, ascorbic acid, aspirin, cholecalciferol, DM/guaifenesin, famotidine, loperamide, throat lozenges, zinc 07/26/21 Pt reports improved runny nose; denies fever, cough 07/27/21 Pt reports he is feeling better and stable 07/29/21 Pt reports fatigue 07/30/21 Clinically resolved, isolation end
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 06/17/2021 T. VAGINALIS PCR POSITIVE 07/23/21 COVID POSITIVE, VARIANT SEQUENCING PENDING
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 24.02.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 150,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Fatigue
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 02/06/21 COVID vaccine dose #1 02/24/21 COVID vaccine dose #2 07/26/21 Pt presents to screening reporting of cough; COVID POSITIVE 07/27/21 Pt reports intermittent cough; rx given for vitamin C, zinc, vitamin D 07/28/21 Pt reports runny nose, fatigue 07/30/21 Pt reports minimal cough and resolved runny nose 08/01/21 Pt reports all symptoms have improved and is afebrile; states symptoms started 07/24; clinically resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 07/26/21 COVID POSITIVE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 15.05.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 70,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ageusia
Anosmia
COVID-19
Chills
Cough
Epistaxis
Exposure to SARS-CoV-2
Fatigue
Headache
Myalgia
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 04/27/21 COVID vaccine dose #1 05/18/21 COVID vaccine dose #2 07/29/21 Pt presents to screening reporting headache and runny nose for 2 days and reports close exposure to COVID positive person; COVID POSITIVE 07/30/21 PT reports chills, cough, fatigue, headache, muscle pain, runny nose, sore throat that started 07/24; rx given for acetaminophen, DM/guaifenesin, throat lozenges 07/31/21 Pt reports loss of taste/smell 08/01/21 Pt reports cough, headache, and runny nose but is stable 08/02/21 Pt reports dry cough, headache, muscle pain, and runny nose; states some bleeding while blowing nose - advised to not blow as hard and using salt water mist 08/03/21 Pt denies cough but reports muscle pain, runny nose, congestion, sneezing bu is improving 08/04/21 Pt reports fatigue and runny nose; clinically fesolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 27.02.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 151,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Exposure to SARS-CoV-2
Fatigue
Headache
Myalgia
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 02/06/21 COVID vaccine dose #1 02/27/21 COVID vaccine dose #2 07/29/21 Pt reports recent exposure to COVID positive person; COVID POSITIVE 07/30/21 Pt reports cough and muscle pain that started 07/28/07/31/21 Pt reports cough, fatigue, and is stable 08/01/21 Pt reports headache 08/02/21 Pt reports intermittent cough and improving muscle pain; no headache today 08/03/21 Pt continues to improve and cough is nearly resolved; clinically resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 07/29/21 COVID POSITIVE; VARIANT SEQUENCING PENDING
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain in extremity
Symptomtext
arm was hurting; elbow was hurting; This is a spontaneous report from a contactable consumer (patient friend). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: Not Provided), via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient experienced arm was hurting and elbow was hurting on unspecified date. The reporter stated that the patient had the shot about 50 days ago and her arm was hurting and then complained her elbow was hurting yesterday. She did not think it was related to the vaccine. The outcome of the events was unknown. No follow up attempts are needed. Information about lot/batch number cannot be obtained
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives; This is a spontaneous report from a contactable consumer (patient). A female patient of unknown age received first dose of BNT162B2 (PFIZER-BIONTECH m-RNA COVID-19 VACCINE, formulation: Solution for injection, batch number and expiry date were no reported) via an unspecified route of administration on an unspecified date as Dose 1 single for COVID-19 immunization. Medical history and Concomitant medications were not reported. The patient experienced hives that erupted 9 days (unspecified date) after the first shot. The patient was looking for advice on if she should get the second shot. Outcome of event was unknown at the time of reporting. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Pyrexia
Symptomtext
chills; fever; This is a spontaneous report from a contactable other hcp(nurse). A male patient of an unspecified age received bnt162b2 ((PFIZER-BIONTECH COVID -19 VACCINE, formulation: solution for injection, Batch/Lot Number: Not Provided, expiry date: unknown) via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date the patient experienced chills, and fever. Patient went to facility and is having adverse reactions to the COVID vaccine. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 28.01.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Therapeutic response unexpected
Symptomtext
sudden attack of pain in the same evening I received the vaccine; at night got a strong pain down into right hand; Very good side effect, Since the day after vaccination patient never had knuckle pains anymore; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (sudden attack of pain in the same evening I received the vaccine), PAIN IN EXTREMITY (at night got a strong pain down into right hand) and THERAPEUTIC RESPONSE UNEXPECTED (Very good side effect, Since the day after vaccination patient never had knuckle pains anymore) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. The patient's past medical history included Pain. Concomitant products included LEVOTHYROXINE, RIVAROXABAN (XARELTO) and VITAMINS NOS for an unknown indication. On 28-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced PAIN (sudden attack of pain in the same evening I received the vaccine), PAIN IN EXTREMITY (at night got a strong pain down into right hand) and THERAPEUTIC RESPONSE UNEXPECTED (Very good side effect, Since the day after vaccination patient never had knuckle pains anymore). At the time of the report, PAIN (sudden attack of pain in the same evening I received the vaccine), PAIN IN EXTREMITY (at night got a strong pain down into right hand) and THERAPEUTIC RESPONSE UNEXPECTED (Very good side effect, Since the day after vaccination patient never had knuckle pains anymore) outcome was unknown. No treatment information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Pain
- Andere Medikamente
- LEVOTHYROXINE; XARELTO; VITAMINS NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Influenza
Myalgia
Nausea
Symptomtext
body aches / same symptoms experienced by patient's boss; headache / same symptoms experienced by patient's boss; chills / same symptoms experienced by patient's boss; nausea; mini-flu / same symptoms experienced by patient's boss; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA (mini-flu / same symptoms experienced by patient's boss), MYALGIA (body aches / same symptoms experienced by patient's boss), HEADACHE (headache / same symptoms experienced by patient's boss), CHILLS (chills / same symptoms experienced by patient's boss) and NAUSEA (nausea) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced INFLUENZA (mini-flu / same symptoms experienced by patient's boss), MYALGIA (body aches / same symptoms experienced by patient's boss), HEADACHE (headache / same symptoms experienced by patient's boss), CHILLS (chills / same symptoms experienced by patient's boss) and NAUSEA (nausea). At the time of the report, INFLUENZA (mini-flu / same symptoms experienced by patient's boss), MYALGIA (body aches / same symptoms experienced by patient's boss), HEADACHE (headache / same symptoms experienced by patient's boss), CHILLS (chills / same symptoms experienced by patient's boss) and NAUSEA (nausea) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Medical history was not provided.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 29.09.2021
- Impfdatum
- 29.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cough
Fatigue
Feeling abnormal
Myalgia
Pain in extremity
Vaccination site reaction
Symptomtext
Extremely fatigued; Muscle pain in his quadriceps and muscles; Brain fog; Cough; Pain in his knees, arm, ankle, and joints; Pain in his knees, arm, ankle, and joints/arm tenderness; were just at the injection site /arm tenderness; This is a spontaneous report from a contactable consumer or other non hcp (Patient's wife). A 45-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: Not Provided), dose 2 via an unspecified route of administration on 29Mar2021 (at the age of 45-years-old) as DOSE 2, SINGLE for covid-19 immunisation; adalimumab (HUMIRA), via an unspecified route of administration from an unspecified date (Batch/Lot Number: Not Provided) to an unspecified date, for psoriatic arthropathy. The patient's medical history included psoriatic arthropathy (Psoriatic arthritis). The patient's concomitant medications were not reported. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: Not Provided), dose 1 via an unspecified route of administration on an unspecified date (at the age of 45-years-old) as DOSE 1, SINGLE for covid-19 immunisation. Caller calls on behalf of her husband. He had side effects after having the second shot of the Covid Vaccine 1 month ago on an unspecified date in 2021. Caller mentioned that for the last 7 days he experienced pain in his quads, a cough, fatigue, pain in his knees, arm, ankle, and joints, extreme fatigue, and brain fog. Her husband was also taking Humira for psoriatic arthritis. He was 45 years old with no underlying conditions. The caller mentioned that they got the second dose on 29Mar2021, and she and her husband experienced tiredness for 3 days and arm tenderness. Caller asks if there could be side effects a month after the vaccine. Caller comes on the line. She says that her symptoms were normal. Hers were just at the injection site and fatigue. She was more concerned about her husband. She had a hard time understanding the agent. She will just tell it again. She and her husband are 45 years old. They were both in good condition and healthier than most. Her husband has psoriatic arthritis and takes Humira. The arthritis was not always that bad. He doesn't take Humira at the regular dose. He takes it every 6 weeks, and it usually was supposed to be taken every 2 weeks. That was some background information on him. They had normal side effects after the second dose which were fine. They were good and everything was back to normal for 3 to 4 weeks. Now for the past 7 days he was extremely fatigued, has muscle pain in his quadriceps and muscles, and has brain fog. She was trying to figure out what was going on. She suggested that he get a Covid test. He had no breathing trouble and no fevers; it was just in his body. They were waiting for the results for the Covid test. She can't imagine it would be positive, but she hopes it was just to get to the bottom of this. She was wondering if his symptoms, when she reads about the symptoms that is kind of what he's having, but it's weird he was having them a month later. She was worried because she was online while she was talking, and it says Humira is an immune suppressant. That was how it works. Hopefully it doesn't conflict with the vaccine. She doesn't know how to really help him. What she was reading says taking something like Humira and the vaccine might not work. She would like to jump over to Medical Information now. She is slightly panicked and just wants to talk to them. Caller confirmed that her husband was extremely fatigued, had muscle pain in his quadriceps and muscles, and had brain fog and then wished to be transferred to Medical Information. Unable to confirm additional events with caller. While reporting an AE, caller mentioned that her husband got tested for Covid after receiving the Covid vaccine because they are concerned, he may have Covid. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Psoriatic arthritis (Verbatim: Psoriatic arthritis)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 29.09.2021
- Impfdatum
- 29.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cough
Fatigue
Feeling abnormal
Myalgia
Pain in extremity
Vaccination site reaction
Symptomtext
Extremely fatigued; Muscle pain in his quadriceps and muscles; Brain fog; Cough; Pain in his knees, arm, ankle, and joints; Pain in his knees, arm, ankle, and joints/arm tenderness; were just at the injection site /arm tenderness; This is a spontaneous report from a contactable consumer or other non hcp (Patient's wife). A 45-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: Not Provided), dose 2 via an unspecified route of administration on 29Mar2021 (at the age of 45-years-old) as DOSE 2, SINGLE for covid-19 immunisation; adalimumab (HUMIRA), via an unspecified route of administration from an unspecified date (Batch/Lot Number: Not Provided) to an unspecified date, for psoriatic arthropathy. The patient's medical history included psoriatic arthropathy (Psoriatic arthritis). The patient's concomitant medications were not reported. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: Not Provided), dose 1 via an unspecified route of administration on an unspecified date (at the age of 45-years-old) as DOSE 1, SINGLE for covid-19 immunisation. Caller calls on behalf of her husband. He had side effects after having the second shot of the Covid Vaccine 1 month ago on an unspecified date in 2021. Caller mentioned that for the last 7 days he experienced pain in his quads, a cough, fatigue, pain in his knees, arm, ankle, and joints, extreme fatigue, and brain fog. Her husband was also taking Humira for psoriatic arthritis. He was 45 years old with no underlying conditions. The caller mentioned that they got the second dose on 29Mar2021, and she and her husband experienced tiredness for 3 days and arm tenderness. Caller asks if there could be side effects a month after the vaccine. Caller comes on the line. She says that her symptoms were normal. Hers were just at the injection site and fatigue. She was more concerned about her husband. She had a hard time understanding the agent. She will just tell it again. She and her husband are 45 years old. They were both in good condition and healthier than most. Her husband has psoriatic arthritis and takes Humira. The arthritis was not always that bad. He doesn't take Humira at the regular dose. He takes it every 6 weeks, and it usually was supposed to be taken every 2 weeks. That was some background information on him. They had normal side effects after the second dose which were fine. They were good and everything was back to normal for 3 to 4 weeks. Now for the past 7 days he was extremely fatigued, has muscle pain in his quadriceps and muscles, and has brain fog. She was trying to figure out what was going on. She suggested that he get a Covid test. He had no breathing trouble and no fevers; it was just in his body. They were waiting for the results for the Covid test. She can't imagine it would be positive, but she hopes it was just to get to the bottom of this. She was wondering if his symptoms, when she reads about the symptoms that is kind of what he's having, but it's weird he was having them a month later. She was worried because she was online while she was talking, and it says Humira is an immune suppressant. That was how it works. Hopefully it doesn't conflict with the vaccine. She doesn't know how to really help him. What she was reading says taking something like Humira and the vaccine might not work. She would like to jump over to Medical Information now. She is slightly panicked and just wants to talk to them. Caller confirmed that her husband was extremely fatigued, had muscle pain in his quadriceps and muscles, and had brain fog and then wished to be transferred to Medical Information. Unable to confirm additional events with caller. While reporting an AE, caller mentioned that her husband got tested for Covid after receiving the Covid vaccine because they are concerned, he may have Covid. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Psoriatic arthritis (Verbatim: Psoriatic arthritis)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 09.04.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Urticaria
Symptomtext
She has a lot of allergies; Dermographia of the skin, commented she gets issues with getting hives and things like that.; This is a spontaneous report from a contactable consumer. This consumer (patient) reported for herself. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: Not reported), via an unspecified route of administration on 09Apr2021 as dose 1, single for covid-19 immunisation and fexofenadine hydrochloride (ALLEGRA), route of administration, start and stop date, batch/lot number and dose were not reported for an unspecified indication. The patient medical history included Dermographia of the skin from an unknown date and unknown if ongoing. The patient concomitant medications were not reported. On an unspecified date on Apr2021, the patient had a lot of allergies and dermographia of the skin (she got issues with getting hives and things like that). She has a lot of allergies and needs to take Allegra everyday. She already had the first dose, but she didn't take her medicine the day of the vaccine. However, she had to start taking it a day or two later. She confirmed she has not had a reaction as far as she knows. She has Dermographia of the skin, commented she gets issues with getting hives and things like that. The reporter asked will it interfere with the potency with vaccine, She also wanted to know if it will cause masking of symptoms if she should have an reaction or if anything to worry about. The outcome of events was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Dermographia (Verbatim: Dermographia of the skin)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 30.07.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Illness
Myalgia
SARS-CoV-2 test positive
Symptomtext
a week later became very sick; Sore arm; Tested positive for covid-19; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (Sore arm), ILLNESS (a week later became very sick) and SARS-COV-2 TEST POSITIVE (Tested positive for covid-19) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. notprovided) for COVID-19 vaccination. No Medical History information was reported. On 30-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Aug-2021, the patient experienced SARS-COV-2 TEST POSITIVE (Tested positive for covid-19). On an unknown date, the patient experienced MYALGIA (Sore arm) and ILLNESS (a week later became very sick). At the time of the report, MYALGIA (Sore arm), ILLNESS (a week later became very sick) and SARS-COV-2 TEST POSITIVE (Tested positive for covid-19) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications were not reported. Treatment information was not provided. Patient was born on the year 1984. Patient would like to know how long should they wait before getting their second dose. Patient stated they do not take any medication regularly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 08.09.2021
- Impfdatum
- -
- Beginn
- 01.04.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Myalgia
Nausea
Symptomtext
Brain fog; Nausea for weeks; Sore arm; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (Brain fog), NAUSEA (Nausea for weeks) and MYALGIA (Sore arm) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In April 2021, the patient experienced FEELING ABNORMAL (Brain fog), NAUSEA (Nausea for weeks) and MYALGIA (Sore arm). At the time of the report, FEELING ABNORMAL (Brain fog), NAUSEA (Nausea for weeks) and MYALGIA (Sore arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication was mentioned. No treatment medication was mentioned. This case was linked to MOD-2021-296133 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 27.08.2021
- Impfdatum
- 18.01.2021
- Beginn
- 10.02.2021
- Tage bis Beginn
- 23,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Urinary tract infection
Vertigo
Symptomtext
urinary tract infection; experiences vertigo "usually when I get up" / vertigo while sitting and throughout day; headache the day of receiving the vaccine; This spontaneous case was reported by a consumer and describes the occurrence of VERTIGO (experiences vertigo "usually when I get up" / vertigo while sitting and throughout day), URINARY TRACT INFECTION (urinary tract infection) and HEADACHE (headache the day of receiving the vaccine) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. Not provided and not provided) for COVID-19 vaccination. Concurrent medical conditions included Cancer. On 18-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 10-Feb-2021, the patient experienced HEADACHE (headache the day of receiving the vaccine). On 13-Feb-2021, the patient experienced VERTIGO (experiences vertigo "usually when I get up" / vertigo while sitting and throughout day). On an unknown date, the patient experienced URINARY TRACT INFECTION (urinary tract infection). At the time of the report, VERTIGO (experiences vertigo "usually when I get up" / vertigo while sitting and throughout day), URINARY TRACT INFECTION (urinary tract infection) and HEADACHE (headache the day of receiving the vaccine) outcome was unknown. No Treatment information was reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cancer
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Symptomtext
body ache; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (body ache) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. not provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced MYALGIA (body ache). At the time of the report, MYALGIA (body ache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant and treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Headache; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (Headache) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced HEADACHE (Headache). At the time of the report, HEADACHE (Headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.08.2021
- Impfdatum
- 29.01.2021
- Beginn
- 07.03.2021
- Tage bis Beginn
- 37,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Nausea
Pain in extremity
Pyrexia
Symptomtext
Pain in arm; Headache; Nausea; Low grade fever; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Pain in arm), HEADACHE (Headache), NAUSEA (Nausea) and PYREXIA (Low grade fever) in a 75-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. Concurrent medical conditions included Pulmonary fibrosis, Emphysema and COPD. On 29-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Mar-2021, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 07-Mar-2021, the patient experienced PAIN IN EXTREMITY (Pain in arm), HEADACHE (Headache), NAUSEA (Nausea) and PYREXIA (Low grade fever). At the time of the report, PAIN IN EXTREMITY (Pain in arm), HEADACHE (Headache), NAUSEA (Nausea) and PYREXIA (Low grade fever) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications with H/O pulmonary fibrosis, emphysema, and COPD. Treatment details included None. Action taken with mRNA-1273 in response to the events was not applicable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COPD; Emphysema; Pulmonary fibrosis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Nausea
Symptomtext
nausea; chills; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a consumer and describes the occurrence of NAUSEA (nausea) and CHILLS (chills) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced NAUSEA (nausea) and CHILLS (chills). At the time of the report, NAUSEA (nausea) and CHILLS (chills) outcome was unknown. No concomitant medication details were reported. No Treatment Medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
Really bad headache/Headache comes back every often and last for 3days; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (Really bad headache/Headache comes back every often and last for 3days) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced HEADACHE (Really bad headache/Headache comes back every often and last for 3days). At the time of the report, HEADACHE (Really bad headache/Headache comes back every often and last for 3days) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. No concomitant medication was mentioned. No treatment medication was mentioned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Symptomtext
extremely fatigued; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a consumer and describes the occurrence of FATIGUE (extremely fatigued) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced FATIGUE (extremely fatigued). At the time of the report, FATIGUE (extremely fatigued) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication details was reported. No treatment medication details was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 23.08.2021
- Impfdatum
- 28.05.2021
- Beginn
- 29.05.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pyrexia
Vomiting
Symptomtext
Vomiting; Temperature of 104; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 29-May-2021 and was forwarded to Moderna on 30-May-2021. This spontaneous case was reported by a consumer and describes the occurrence of VOMITING (Vomiting) and PYREXIA (Temperature of 104) in an 18-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No medical history was reported. On 28-May-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage form. On 29-May-2021, the patient experienced VOMITING (Vomiting) and PYREXIA (Temperature of 104). At the time of the report, VOMITING (Vomiting) and PYREXIA (Temperature of 104) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Treatment information was not reported. Reporter did not allow further contact; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the event, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was reported .
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- -
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 01.02.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Headache
Myalgia
Symptomtext
body discomfort; Arm pain,Body discomfort; A little of headache; This spontaneous case was reported by a consumer and describes the occurrence of DISCOMFORT (body discomfort), MYALGIA (Arm pain,Body discomfort) and HEADACHE (A little of headache) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided.) for COVID-19 vaccination. No medical history was provided by the reporter. In February 2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In March 2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced DISCOMFORT (body discomfort), MYALGIA (Arm pain,Body discomfort) and HEADACHE (A little of headache). The patient was treated with PARACETAMOL (PANADOL) for Muscle pain, at a dose of 1 UNK. At the time of the report, DISCOMFORT (body discomfort), MYALGIA (Arm pain,Body discomfort) and HEADACHE (A little of headache) outcome was unknown. concomitant drug include muscle pain medication eventof positive coronavirus antigen test
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Symptomtext
Experinced runs diarrhea after second dose.; This spontaneous case was reported by a patient and describes the occurrence of DIARRHOEA (Experinced runs diarrhea after second dose.) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced DIARRHOEA (Experinced runs diarrhea after second dose.). At the time of the report, DIARRHOEA (Experinced runs diarrhea after second dose.) outcome was unknown. Concomitant and treatment information provided. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 26.02.2021
- Beginn
- 26.02.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Decreased appetite
Fatigue
Pain in extremity
Somnolence
Weight decreased
Symptomtext
Pain that went down my leg to my foot, feeling it going down my thighs and knees; Pain started with one side of the hip then both; Tired; Sleepy; I have lack of appetite; lost 17 pounds; This spontaneous case was reported by a patient and describes the occurrence of PAIN IN EXTREMITY (Pain that went down my leg to my foot, feeling it going down my thighs and knees), ARTHRALGIA (Pain started with one side of the hip then both), FATIGUE (Tired), SOMNOLENCE (Sleepy) and DECREASED APPETITE (I have lack of appetite) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 26-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-Feb-2021, the patient experienced PAIN IN EXTREMITY (Pain that went down my leg to my foot, feeling it going down my thighs and knees), ARTHRALGIA (Pain started with one side of the hip then both), FATIGUE (Tired), SOMNOLENCE (Sleepy), DECREASED APPETITE (I have lack of appetite) and WEIGHT DECREASED (lost 17 pounds). At the time of the report, PAIN IN EXTREMITY (Pain that went down my leg to my foot, feeling it going down my thighs and knees), ARTHRALGIA (Pain started with one side of the hip then both), FATIGUE (Tired), SOMNOLENCE (Sleepy), DECREASED APPETITE (I have lack of appetite) and WEIGHT DECREASED (lost 17 pounds) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 09.03.2021
- Beginn
- 11.03.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Costochondritis
Gastrooesophageal reflux disease
Headache
Product dose omission issue
Symptomtext
Rib cage Pain/Costochondritis; acid reflux disease; Doctor advised patient not to take the second dose which was due on 6th April; Slight headache 4 days after Covid-19 injection administration; This spontaneous case was reported by a consumer and describes the occurrence of COSTOCHONDRITIS (Rib cage Pain/Costochondritis), GASTROOESOPHAGEAL REFLUX DISEASE (acid reflux disease), PRODUCT DOSE OMISSION ISSUE (Doctor advised patient not to take the second dose which was due on 6th April) and HEADACHE (Slight headache 4 days after Covid-19 injection administration) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. not provided) for COVID-19 vaccination. The patient's past medical history included Depression. Concomitant products included PARACETAMOL (TYLENOL). On 09-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Mar-2021, the patient experienced HEADACHE (Slight headache 4 days after Covid-19 injection administration). On an unknown date, the patient experienced COSTOCHONDRITIS (Rib cage Pain/Costochondritis), GASTROOESOPHAGEAL REFLUX DISEASE (acid reflux disease) and PRODUCT DOSE OMISSION ISSUE (Doctor advised patient not to take the second dose which was due on 6th April). At the time of the report, COSTOCHONDRITIS (Rib cage Pain/Costochondritis), GASTROOESOPHAGEAL REFLUX DISEASE (acid reflux disease), PRODUCT DOSE OMISSION ISSUE (Doctor advised patient not to take the second dose which was due on 6th April) and HEADACHE (Slight headache 4 days after Covid-19 injection administration) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Depression
- Andere Medikamente
- TYLENOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Symptomtext
Experienced minor muscle aches one day after first Covid-19 injection injection; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (Experienced minor muscle aches one day after first Covid-19 injection injection) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. not provided) for COVID-19 vaccination. Concurrent medical conditions included Hypertension. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced MYALGIA (Experienced minor muscle aches one day after first Covid-19 injection injection). At the time of the report, MYALGIA (Experienced minor muscle aches one day after first Covid-19 injection injection) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- 21.04.2021
- Beginn
- 07.05.2021
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse event following immunisation
COVID-19
Chills
Fatigue
Full blood count
Headache
Hyperhidrosis
Myalgia
Vomiting
Symptomtext
late reaction to the vaccine; deep sweating; very strong muscle pain; chills; tiredness; vomiting; headache; This spontaneous case was reported by a consumer and describes the occurrence of ADVERSE EVENT FOLLOWING IMMUNISATION, HYPERHIDROSIS, (deep sweating), MYALGIA (very strong muscle pain), CHILLS (chills) and FATIGUE (tiredness) in a 50-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. not provided) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included ASPIRIN [ACETYLSALICYLIC ACID], PENTOXIFYLLINE (TRENTAL) and HYDROCHLOROTHIAZIDE, IRBESARTAN (IRBESARTAN AND HYDROCHLOROTHIAZIDE) for an unknown indication. On 21-Apr-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage form. On 07-May-2021, the patient experienced ADVERSE EVENT FOLLOWING IMMUNISATION (late reaction to the vaccine), HYPERHIDROSIS (deep sweating), MYALGIA (very strong muscle pain), CHILLS (chills), FATIGUE (tiredness), VOMITING (vomiting) and HEADACHE (headache). The patient was treated with ACETAMINOPHEN at an unspecified dose and frequency and PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, ADVERSE EVENT FOLLOWING IMMUNISATION (rate reaction to the vaccine), HYPERHIDROSIS (deep sweating), MYALGIA (very strong muscle pain), CHILLS (chills), FATIGUE (tiredness), VOMITING (vomiting) and HEADACHE (headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, COVID-19: normal (normal) normal. On an unknown date, Full blood count: normal (normal) normal. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication include vintiasen 360.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: covid test; Result Unstructured Data: normal; Test Name: cbc; Result Unstructured Data: normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ASPIRIN [ACETYLSALICYLIC ACID]; TRENTAL; IRBESARTAN AND HYDROCHLOROTHIAZIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Symptomtext
pain after the second dose of the vaccine; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (pain after the second dose of the vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced MYALGIA (pain after the second dose of the vaccine). The patient was treated with IBUPROFEN at a dose of 1 dosage form. At the time of the report, MYALGIA (pain after the second dose of the vaccine) outcome was unknown. Patient was told to take Tylenol instead she took ibuprofen. Action taken with mRNA-1273 in response to the event was not applicable
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 21.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Illness
Pyrexia
Tooth infection
Symptomtext
Severe tooth infection; Sick; Fever; This spontaneous case was reported by a consumer and describes the occurrence of TOOTH INFECTION (Severe tooth infection), ILLNESS (Sick) and PYREXIA (Fever) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced TOOTH INFECTION (Severe tooth infection), ILLNESS (Sick) and PYREXIA (Fever). At the time of the report, TOOTH INFECTION (Severe tooth infection), ILLNESS (Sick) and PYREXIA (Fever) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant medications were reported. Treatment details included Antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 21.08.2021
- Impfdatum
- 13.02.2021
- Beginn
- 01.02.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Vertigo
Vomiting
Symptomtext
lightheadedness; vertigo; vomiting; nausea; This spontaneous case was reported by a consumer and describes the occurrence of NAUSEA (nausea), VOMITING (vomiting), DIZZINESS (lightheadedness) and VERTIGO (vertigo) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On 13-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In February 2021, the patient experienced NAUSEA (nausea), VOMITING (vomiting), DIZZINESS (lightheadedness) and VERTIGO (vertigo). The patient was treated with MECLIZINE [MECLOZINE] for Nausea, Vomiting, Lightheadedness and Vertigo, at an unspecified dose and frequency. At the time of the report, NAUSEA (nausea), VOMITING (vomiting), DIZZINESS (lightheadedness) and VERTIGO (vertigo) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient does not take concomitant medicines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 13.02.2021
- Beginn
- 13.02.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hot flush
Nasopharyngitis
Pain
Vaccination site pain
Symptomtext
Cold symptoms; arm is hot, face was very hot; sore at injection site; Light headed; Sore; A spontaneous report was received from a consumer concerning herself, a 68-years-old female patient, who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced light headed/dizziness, sore/pain, cold symptoms/nasopharyngitis, arm and face hot/hot flushes, sore at the injection site/vaccination site pain. The patient's medical history was not included . Concomitant products was not included. On 13 Feb 2021, prior to the onset of event the patient received first dose of their two planned doses of mRNA-1273 (Batch N0:not provided) in the left arm for prophylaxis of covid 19 infection. On 13 Feb 2021 the patient experienced light headed, and sore. On 21 Feb 2021 she began experiencing cold symptoms, arm is hot and sore at injection site. Face was very hot. Treatment information was not included. Action taken with mRNA-1273 in response to the events was not provided. The outcome of the events, light headed/dizziness, sore/pain were resolved on 13 Feb 2021, the outcome of the events, cold symptoms/nasopharyngitis, arm and face hot/hot flushes, sore at the injection site/vaccination site pain were resolved on 22 Feb 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: No adverse reaction (no reported medical history)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 15.08.2021
- Impfdatum
- 05.02.2021
- Beginn
- 10.02.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphonia
Pyrexia
Symptomtext
Has a fever; Started losing her voice; This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (Has a fever) and APHONIA (Started losing her voice) in an 82-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. The patient's past medical history included No adverse event. Concurrent medical conditions included Hypertension, High cholesterol and Diabetes. Concomitant products included OMEPRAZOLE. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Feb-2021, the patient experienced PYREXIA (Has a fever) and APHONIA (Started losing her voice). At the time of the report, PYREXIA (Has a fever) and APHONIA (Started losing her voice) had not resolved. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetes; High cholesterol; Hypertension
- Vorgeschichte
- Medical History/Concurrent Conditions: No adverse event
- Andere Medikamente
- OMEPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 15.08.2021
- Impfdatum
- 05.02.2021
- Beginn
- 06.02.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Symptomtext
Ache from the Moderna shot; This spontaneous case was reported by a patient and describes the occurrence of MYALGIA (Ache from the Moderna shot) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On 05-Feb-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Feb-2021, the patient experienced MYALGIA (Ache from the Moderna shot). At the time of the report, MYALGIA (Ache from the Moderna shot) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 25.06.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Therapeutic response unexpected
Symptomtext
sore arm; After the vaccine, she noticed an improvement of her Rheumatoid arthritis symptoms. She felt like she didn't have Rheumatoid Arthritis anymore.; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: Not Provided), via an unspecified route of administration on an unspecified date as 1st Dose, Single Dose and dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: Not Provided), via an unspecified route of administration on an unspecified date as 2nd Dose, Single Dose. The patient's Medical history included ongoing rheumatoid arthritis. She had to suspended all of her biological medications for her Rheumatoid Arthritis to get the vaccines. She has had Rheumatoid arthritis for a couple of years. She does have Rheumatoid arthritis, and after the COVID 19 vaccine , she noticed an improvement of her Rheumatoid arthritis symptoms. Concomitant medications included methotrexate (METHOTREXATE) taken for an unspecified indication, infliximab (REMICADE) taken for an unspecified indication. After both the doses of vaccination, the patient experienced sore arm. After the vaccine, she noticed an improvement of her Rheumatoid arthritis symptoms. She felt like she didn't have Rheumatoid Arthritis anymore.She doesn't know if it stimulated an immuno-regulation of the t suppresser cells or what. She hasn't felt this good even when she has flare ups, and is on steroids. She felt like she didn't have Rheumatoid Arthritis anymore. She had no joint hurting or stiffness. She felt good for about a week. Then her symptoms of Rheumatoid Arthritis came back. It was weird that she saw so much improvement for a week after the vaccine. It happened after both doses. The outcome for the events was Unknown. Information on the lot/batch number has been requested. Follow-up (16Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Rheumatoid arthritis (she noticed an improvement of her Rheumatoid arthritis symptoms. Verbatim: Rheumatoid arthritis/having a sore arm. She does have Rheumatoid arthritis, and after the COVID 19 vaccine , she noticed an improvement of her Rheumatoid arthritis symptoms. She doesn't know if it stimulated an immuno-regulation of the t suppresser cells or what.)
- Andere Medikamente
- METHOTREXATE; REMICADE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.06.2021
- Impfdatum
- 08.04.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
SARS-CoV-2 test
Symptomtext
arm soreness; This is a spontaneous report from contactable reporter(mother), reporting for her daughter (patient) A female patient of unknown age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: unknown), via an unspecified route of administration in left arm on 08Apr2021 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unknown date, the patient stated about Pfizer COVID-19 vaccine who says it was hard to figure out where to call. She said that they had their first dose April 8th. She says that they had a family member that passed away last Tuesday, and around that time was when they contracted and tested positive for COVID-19, for which they have been quarantined. She says that there had been a lot of people in and out of where they were after her mother in law passed, and some were wearing masks and some weren't. She says she and her son tested this past Tuesday which was positive, and they told her May 4th was when they could get their second dose after quarantining. She says that her husband was tested Monday and was positive and he was told it would be the 30th or something like that. Caller says that her son was tested Wednesday, and was told he was positive, and he also must be asymptomatic. She says all three of them tested positive out of the four that went, only her daughter was negative. She says that she needs to reschedule shots for the second dose that were scheduled for 24th of April, but she was not sure how to go about that. The patient says her husband went in related to his allergies to get tested. She says it was her mother-in-law that had passed, then Tuesday they all got tested and they were all negative. She says her husband started feeling like he had allergies Friday after he cut the grass, and her son is a crazy person about COVID, but he has asthma so he wanted them to all get tested again since allergies can be like COVID, and her husband's test was positive, so then she and her son got tested and they were positive, so they had three positives out of the four family members who got the first dose. She clarifies that her mother in law didn't get the vaccine, but she she had passed away Tuesday, and they contracted COVID during that time after she passed away at home. She says they contracted something from there, since they haven't been anywhere else and have stayed at home other than going there after her mother in law passed away. The patient says that they were all fine after they got the first dose of the vaccine, they had a sore arm that day that went away with no side effects. She says they all took the COVID-19 shot on April 8th. Caller says that her mother in law passed away on the 13th, and her husband had allergies kind of after, and she and her son had nothing. She says that they have no congestion, fever, none of that stuff. She says she was really shocked when they gave her the result that she was positive. The patient underwent lab tests and investigation results which included COVID-19 PCR test for which the result was negative. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained. No follow-up attempts are needed; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 PCR test; Result Unstructured Data: Test Result:negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.06.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Confusional state
Diarrhoea
Feeling abnormal
Gastrointestinal disorder
Headache
Malaise
Mental impairment
Nausea
Rectal haemorrhage
Suffocation feeling
Vision blurred
Symptomtext
Bleeding rectally for three days; couldn't think; Headache; Intestinal issues; Felt almost like she had COVID; Diarrhea; Nauseated; Felt like she was smothering; Felt foggy in her head like she couldn't think; Weak; Eye felt not right, blurry; Confused; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (BNT162B2), via an unspecified route of administration on an unspecified date (Batch/Lot Number: Not Provided) as 1ST DOSE, SINGLE for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced bleeding rectally for three days, headache, intestinal issues, felt almost like she had covid, diarrhea, nauseated, felt like she was smothering, felt foggy in her head like she couldn't think, weak, didn't feel right, just not herself, eye felt not right, blurry and confused on an unspecified date. The outcome of bleeding rectally, headache, intestinal issues, felt almost like she had covid, diarrhea, nauseated, felt like she was smothering, felt foggy in her head like she couldn't think, weak, didn't feel right, just not herself, eye felt not right, blurry and confused was unknown. Information on the lot/batch number has been requested
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 08.06.2021
- Impfdatum
- 23.02.2021
- Beginn
- 24.02.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Drug hypersensitivity
Malaise
Nasopharyngitis
Sneezing
Symptomtext
Allergy attack; Did not feel good, felt like they had a really bad cold; Did not feel good, felt like they had a really bad cold; sneezing and sneezing; This is a spontaneous report from a contactable Consumer (Patient). A female of unspecified age received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection; Lot number: not provided; Expiration date: Unknown), via unspecified route of administration on 23Feb2021 at 11:30 as first dose, single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On 24Feb2021, 23 hours after that dose was administered, patient started having like an allergy attack , she was sneezing and sneezing. She did not feel good, felt like she had a really bad cold all yesterday. She felt better today but did not know if she should or should not get the second dose of the Pfizer COVID-19 Vaccine relative to these events. The outcome of the events was resolving. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 02.06.2021
- Impfdatum
- 19.03.2021
- Beginn
- 08.04.2021
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Malaise
Symptomtext
not feeling well; Headache; This is a spontaneous report received from Pfizer sponsored program. A contactable male consumer reported for his wife. This is report 2 of 2. A 48-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: Not Provided), via an unspecified route of administration in Arm Left on 19Mar2021 at 16:30(at the age of 48 years old) as 1st dose, single dose for covid-19 immunisation. Medical history was reported none. Concomitant medication included vitamins (VITAMINS NOS). The patient experienced headache on 08Apr2021 and not feeling well on an unspecified date. Reporter stated as, "him and his wife had their first doses 19 mar 2021 second dose is today 9Apr2021, but they can't make it because both of them are not feeling well. he also said he is experiencing head cold symptoms now. Can they reschedule their second dose today and if not how can they set up their second dose, he also states that everything that they read said they shouldn't go if they are not feeling well. he wants to know if this is a reason not to have the shot and if he can go under these circumstances or not. He states his wife got Pfizer COVID-19 vaccine on 19 Mar 2021 at 1630. She has a headache that started last night. She has not taken anything for it". Outcome of the events headache was not recovered and unknown for malaise. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none, Comment: none
- Andere Medikamente
- VITAMINS NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 27.05.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Sore arm.; This is a spontaneous report from a Pfizer sponsored program support received from a contactable consumer reporting for her husband. A male patient of an unspecified age received BNT162B2 Pfizer-BioNTech COVID-19 mRNA Vaccine, via an unspecified route of administration on an unspecified date (Batch/Lot Number: not provided) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date the patient experienced sore arm. The event outcome was unknown at the time of the report. Information about lot/batch number has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 11.05.2021
- Impfdatum
- 20.04.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Fatigue
Symptomtext
Tiredness; left ear ache; This is a spontaneous report from a contactable consumer (patient's daughter). An 84-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in arm right on 20Apr2021 14:00 at the age of 84-years-old (Batch/Lot Number: Not Provided) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient had the vaccine yesterday on 20Apr2021 and was having side effects. She wanted to go over the side effects and what to do. It was for the Pfizer Coronavirus vaccine. Stated that this was her first dose. Stated that she was sleeping, having tiredness and ear ache in Apr2021. Stated that she got the vaccine at 2pm. Stated that she looked at list of symptoms and has never had ear aches. Wanted to know if ear aches was part of it and what to do about it. Stated that the ear ache was for her left ear. Stated that she received the vaccine on the right. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.05.2021
- Impfdatum
- 16.12.2020
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Vaccination site discomfort
Vaccination site joint movement impairment
Symptomtext
felt discomfort at the injection site; felt like she had to support her arm to lift it and it was painful; have some soreness; felt like she had to support her arm to lift it and it was painful; This is a spontaneous report from a contactable pharmacist (the patient). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number was not provided), via an unspecified route of administration on 16Dec2020 at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not provided. Patient reported she has experienced this with Flu vaccine (FLU ARIX) (GlaxoSmithKline). Patient does not have an NDC, Lot or expiration date, reporter stated she had the vaccine in September 2020 or the first of October 2020. On an unspecified date, the patient felt discomfort at the injection site, she felt like she had to support her arm to lift it and it was painful. Patient stated that vaccine is mandatory and she generally does have some soreness. Investigation assessment was not Provided. Patient stated that her Pfizer NDC number was the same as for the previous reports filed. The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- F
- Eingang
- 05.05.2021
- Impfdatum
- 28.03.2021
- Beginn
- 29.03.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Illness
Nightmare
Parosmia
Taste disorder
Symptomtext
faint putrid smell; Nightmare; Fatigue; smelling and tasting is bad; getting sick; This is a spontaneous report received from a contactable consumer(patient) reported for herself. A female patient of an unspecified age received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on 28Mar2021 (Batch/Lot Number: Not Provided) as SINGLE DOSE for covid-19 immunisation. Medical history included previous covid-19, reported as in November the patient and her husband both had covid, the patient's husband got over his fast. Neither the patient or the patient's husband had to be hospitalized. When the patient had covid she had symptoms of fatigue, awful smells, the patient thought she was a long hauler for covid. The patient kept getting bouts of where she can't function, has to stay in bed, her taste or smell was not good, the fatigue, her head felt heavy, her legs were like lead, dizzy, and didn't feel right. The patient's concomitant medications were not reported. The patient experienced faint putrid smell (non-serious) on an unspecified date with outcome of unknown nightmare(non-serious) on 29Mar2021 with outcome of unknown, fatigue (non-serious) on 29Mar2021 with outcome of unknown, smelling and tasting was bad (non-serious) on 29Mar2021 with outcome of unknown, getting sick (non-serious) on 29Mar2021 with outcome of unknown. Reported as after the first vaccine a day an a half later she had the same symptoms as covid and nightmares. Sunday, 18Apr2021, the patient was scheduled for her second dose of the vaccine. Monday the patient was fine, Tuesday and Wednesday she was down for the count again. Tuesday it started with a alight faint putrid smell and then she was down for the count. Sunday 28Mar2021 the patient had the vaccine. Monday night, 29Mar2021, the patient started getting sick, it was the same symptoms. The patient had a nightmare about trying to find her dead father, she wakes up shaking and crying sometimes. The patient also had the fatigue, smelling and tasting was bad. The patient wanted to know if she should get the second dose? Today was the first day she felt fine. The putrid smell she can't describe it, it smells like wet concrete. The patient saw that on tv some people say they have a complete recovery from their symptoms after the second dose, is that true? Is this normalcy? The patient's doctor doesn't have much information about the vaccine. No follow-up attempts are possible; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (symptoms of fatigue, awful smells, can't function, has to stay in bed...)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.05.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
sore arm; This is a spontaneous report from a contactable consumer (patient's parent). Report 4 of 4. This consumer reported for a patient (kid) received BNT162B2 on an unspecific date at single dose for COVID-19 immunization. Medical history and concomitant drug were not reported. Caller states that her three kids were complaining of sore arms. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021433532 same reporter/drug/event, different patient;US-PFIZER INC-2021433880 same reporter/drug/event, different patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 01.05.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal disorder
Pain in extremity
Symptomtext
both daughters are experiencing the same thing/pain in arms; couldn't move her arm; This is a spontaneous report from a contactable consumer (patient's mother) from a Pfizer sponsored program. The consumer reported similar events for three patients. This is the third of three reports. A female patient of an unspecified age received bnt162b2 (Pfizer BioNTech Covid 19 vaccine), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot Number: Not Provided) at single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Reporter was calling on behalf of her daughter that had the first dose of the COVID 19 vaccine and her daughter was experiencing pain in arms. Reporter stated she had three daughters and two received the COVID 19 vaccine and both were experiencing the same thing. Reporter stated the daughter (patient) yesterday had no pain, only at night she was complaining about having pain and then woke up this morning and the daughter said she couldn't move her arm she was in severe pain. Reporter stated the daughter did not work today but yesterday she worked and last night decided she would not be going because she has to use her arms at work and it was really difficult for her. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021423442 Same reporter/drug, different patients, similar AEs;US-PFIZER INC-2021425734 Same reporter/drug, different patients, similar AEs
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.04.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Symptomtext
Wicked tired; This is a spontaneous report from a contactable consumer. This consumer reported for a male patient that on an unspecified patient received his first dose of BNT162B2 (COMIRNATY, Formulation: Solution for injection, Lot number: unknown) on an unspecified route as a single dose for covid 19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date the patient was wicked tired. Outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 03.04.2021
- Impfdatum
- 01.04.2021
- Beginn
- 02.04.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Nausea
Pain
Pyrexia
Sensitive skin
Skin sensitisation
Symptomtext
Had left eye pain and skin sensitivity 20 minutes after the vaccine. Around hour 12, started with body aches and intense headache. Between hour 12 - 36, I had fevers up to 101.1, body aches, nausea, and headaches. All resolved by hour 36.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multi-vitamins
- Allergien
- adverse reaction to codeine
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 24.03.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood creatine phosphokinase increased
Myalgia
Symptomtext
Severe polymyalgias; CPKs very high at 80,000; This is a spontaneous report from a contactable physician. A 30-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot Not Provided, second dose) solution for injection intramuscular on an unknown date (at the age of 30-years-old) as a single dose for COVID-19 vaccination. Medical history included Cystic Fibrosis and Autoimmune Necrotizing Myositis. Concomitant medications were unknown. Historical vaccine included BNT162B2 (first dose) for COVID-19 vaccination on an unknown date with no adverse effect reported (tolerated first COVID-19 vaccine). The patient had no known allergies to medications, food, or other products. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Less than 24 hours after second COVID-19 vaccine injection, the patient had severe polymyalgia. CPKs checked very high at 80,000. The patient was currently admitted to the hospital. Unspecified treatment was provided for the events severe polymyalgias and CPKs very high. The outcome of the events severe polymyalgias and CPKs very high was unknown. Since the vaccination, the patient has not been tested for COVID-19. The patient was supposed to get RITUXAN as a regimen for his muscle disorder and was interested in Pfizer checking his neutralizing antibody level both pre and post Rituxan. The patient will receive RITUXAN shortly in the next week. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.; Sender's Comments: Based on chronological connection to the vaccine causality between events severe polymyalgia and CPKs checked very high and BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE0 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- Test Name: CPKs; Result Unstructured Data: Test Result:80,000; Comments: very high at 80,000
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Autoimmune myositis (Necrotizing); Cystic fibrosis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 06.03.2021
- Impfdatum
- 18.02.2021
- Beginn
- 24.02.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain lower
Abdominal wall haematoma
Computerised tomogram
Full blood count abnormal
Haemoglobin decreased
Lymphadenopathy
Scan with contrast
Symptomtext
Enlarged lymph left side in arm pit and neck, lower abdominal pain that resulted in Rectus Sheath Hematoma 6 days after second vaccine 2/24/2021. Treated for pain control and administered IV fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- 1,0
- Labordaten
- Admission to Emergency Room Hospital , confirmed by abnormal CBC low hemoglobin count and CT with contrast 2/24/2021.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Aspleenic, HBP, High Cholesterol, Neutropenia, Thrombocytosis, Asthma, Allergies, Bipolar, Herpes, Hypothyroid.
- Andere Medikamente
- Celebrex, Synthroid, Lisinopril, Lipitor, Prem-Pro, Valtrex, Singular, Seroquel, D3, Qnasal, Delura,
- Allergien
- Codeine, Vicodeine, Tape Adhesives, Bee Venom, Nickel
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.11.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Symptomtext
as if caller was hit by a truck; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 omi xbb.1.5 (COMIRNATY (2023-2024 FORMULA)), as dose number unknown, single (Lot number: Not Provided) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: FEELING ABNORMAL (non-serious), outcome "unknown", described as "as if caller was hit by a truck". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 16.05.2022
- Impfdatum
- 27.10.2021
- Beginn
- 16.05.2022
- Tage bis Beginn
- 201,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
Hospitalized with breakthrough COVID infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 05.03.2022
- Impfdatum
- 01.04.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product dose omission issue
Symptomtext
Missed second dose; This spontaneous case was reported by a patient and describes the occurrence of PRODUCT DOSE OMISSION ISSUE (Missed second dose) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. In April 2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1. On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (Missed second dose). At the time of the report, PRODUCT DOSE OMISSION ISSUE (Missed second dose) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product dose omission issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 27.05.2021
- Beginn
- 27.05.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product dose omission issue
Symptomtext
Missed second dose; This spontaneous case was reported by a patient and describes the occurrence of PRODUCT DOSE OMISSION ISSUE (Missed second dose) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On 27-May-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-May-2021, the patient experienced PRODUCT DOSE OMISSION ISSUE (Missed second dose). At the time of the report, PRODUCT DOSE OMISSION ISSUE (Missed second dose) had resolved. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product dose omission issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Erythema
Vaccination complication
Symptomtext
Very bad side effect; Red spots on her skin (all over her body, mostly on her arms); Feeling blisters on her back\ back blisters are "tiny grape" size; This spontaneous case was reported by an other health care professional and describes the occurrence of VACCINATION COMPLICATION (Very bad side effect), ERYTHEMA (Red spots on her skin (all over her body, mostly on her arms)) and BLISTER (Feeling blisters on her back\ back blisters are "tiny grape" size) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. Concomitant products included EMPAGLIFLOZIN (JARDIANCE) and ROSUVASTATIN. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (Very bad side effect), ERYTHEMA (Red spots on her skin (all over her body, mostly on her arms)) and BLISTER (Feeling blisters on her back\ back blisters are "tiny grape" size). At the time of the report, VACCINATION COMPLICATION (Very bad side effect), ERYTHEMA (Red spots on her skin (all over her body, mostly on her arms)) and BLISTER (Feeling blisters on her back\ back blisters are "tiny grape" size) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. This case was linked to MOD-2021-250591.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blister
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- JARDIANCE; ROSUVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 21.02.2022
- Impfdatum
- 19.08.2021
- Beginn
- 20.02.2022
- Tage bis Beginn
- 185,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccine breakthrough infection
Symptomtext
Hospitalized with breakthrough COVID infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Hypoaesthesia
Lethargy
Symptomtext
Weakness; Lethargy; hands and fingers are numb; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient received bnt162b2 (BNT162B2) (Lot number: Not Provided) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: ASTHENIA (non-serious), outcome "unknown", described as "Weakness"; LETHARGY (non-serious), outcome "unknown", described as "Lethargy"; HYPOAESTHESIA (non-serious), outcome "unknown", described as "hands and fingers are numb". Additional information included: Caller was calling about the Pfizer COVID 19 vaccine. She said she had the first one on Thursday seem to be ok after and Friday and Saturday but then she started feeling like she was having a reaction, she was having some weakness, lethargy and just today her hands were numb, her fingers were numb. She asked that, was something that had been reported with the vaccine. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 19.02.2022
- Impfdatum
- 06.04.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Taste disorder
Symptomtext
very bad taste in his mouth and numbness in his throat; very bad taste in his mouth and numbness in his throat; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), administration date 06Apr2021 (Lot number: Not Provided) as dose 1 single for covid-19 immunisation. Relevant medical history included: "bronchitis" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: TASTE DISORDER (non-serious), HYPOAESTHESIA (non-serious), outcome "unknown" and all described as "very bad taste in his mouth and numbness in his throat". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Bronchitis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropod sting
Symptomtext
spread like a bee sting; This is a spontaneous report received from a contactable reporter (Consumer). A female patient received BNT162B2 (BNT162B2) (Lot number: Not Provided) as dose number unknown, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: ARTHROPOD STING (non-serious), outcome "unknown", described as "spread like a bee sting". Additional Information: The patient stated kind of spread like a bee sting, if this get any bigger she was gonna have to name it. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021459675 same reporter/drug, different patient/event;US-PFIZER INC-2021459554 same reporter/drug, different patient/event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthropod sting
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.02.2022
- Impfdatum
- 23.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nasopharyngitis
Symptomtext
has cold symptoms since Sunday; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (159558). The reporter is the patient. A female patient received bnt162b2 (BNT162B2), administration date 23Mar2021 (Lot number: Not Provided) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: NASOPHARYNGITIS (non-serious), outcome "unknown", described as "has cold symptoms since Sunday". No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nasopharyngitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- -
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood urine present
Immunisation
Joint effusion
Joint swelling
Nephrolithiasis
Haemorrhage
Investigation
Urine analysis
Symptomtext
had to have 3 units of blood. All they could find after all kinds of tests were that it might be bleeding but, haven't found out anything.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A female patient received bnt162b2 (BNT162B2) (Lot number: Not Provided) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Manufacturer unknown), for COVID-19 immunization. The following information was reported: HAEMORRHAGE (medically significant), outcome "unknown", described as "had to have 3 units of blood. All they could find after all kinds of tests were that it might be bleeding but, haven't found out anything.". The patient underwent the following laboratory tests and procedures: investigation: haven't found out anything. Clinical course: Caller states she is calling regarding the Pfizer Covid vaccine booster. While caller was reporting on her experience after getting the booster, she mentioned that she does have customers that have had similar reactions to this. She had one lady who had to have 3 units of blood afterward. All they could find after all kinds of tests were that it might be bleeding but, haven't found out anything. The lot number for [BNT162b2], was not provided and will be requested during follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood urine present
- Hospital-Tage
- -
- Labordaten
- Test Name: tests; Result Unstructured Data: Test Result:haven't found out anything
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 26.01.2022
- Impfdatum
- 03.09.2021
- Beginn
- 25.01.2022
- Tage bis Beginn
- 144,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 RNA
Vaccine breakthrough infection
Symptomtext
Vaccine lot # was not provided Hospitalized with breakthrough covid infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 1/24/22- SARS-CoV-2 RNA present
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 14.11.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram pulmonary abnormal
Aortic dilatation
Atelectasis
Atrial fibrillation
Bronchial wall thickening
COVID-19
Chest X-ray normal
Pleural effusion
Pulmonary mass
Renal disorder
SARS-CoV-2 antibody test
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infection following COVID vaccine series 4/15 COVID vaccine dose #1 05/13 COVID vaccine dose #2 11/14 COVID vaccine dose #3 12/13 1st visit at new clinic, new onset afib, sent to ED due to afib/RVR, found to be COVID positive, admitted to hospital, CXR WNL 12/15 discharge from hospital, remained asymptomatic for COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angiogram pulmonary abnormal
- Hospital-Tage
- -
- Labordaten
- Date Test Name Result 12/15/2021#4:00:04 SARS-CoV-2 IgG 4.54 12/13/2021@14:10 COVID-19 PCR DETECTED CTA PE (12/13): Impression: 1. No evidence for pulmonary embolus. 2. Mild dependent atelectasis suspect trace bronchial thickening and debris. No convincing evidence for pneumonia this time. Trace bilateral pleural effusions. 3. 2 tiny pulmonary nodules. No specific follow-up the absence of risk factors for primary lung malignancy. If risk factors are present, one-year follow-up may be considered. 4. A tiny 6 mm exophytic focus at the lower pole left kidney is too small to characterize. Cannon be confidently attributed to tiny cyst however. Consider non emergent short interval renal mass protocol follow-up to exclude malignancy. 5. Ectatic ascending aorta up to 3.8 cm. Findings as above. CXR (12/13): Impression: No acute cardiopulmonary process.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 02.06.2021
- Beginn
- 17.05.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bacteraemia
Haematuria
Hypoaesthesia
Urine analysis
Symptomtext
Narrative: 05/06 UA shows bacteruria and hematuria, prescribed nitrofurantoin 05/12 COVID vaccine dose #1 05/17 pt reports having "numbness in face, legs and feet; stopping antibiotic" 06/02 COVID vaccine dose #2 no further complaints or treatment for complaint
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bacteraemia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 02.03.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 143,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asymptomatic COVID-19
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infections following completion of COVID vaccine series 03/22/21 COVID vaccine dose #1 07/23/21 Pt reports no symptoms; pre-op COVID swab performed - COVID POSITIVE 07/29/21 Pt remains asymptomatic, reports will isolate until 8/1 08/05/21 Pt rescheduled for COVID swab on 8/10
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- 07/23/21 COVID POSITIVE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 27.05.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 58,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asymptomatic COVID-19
SARS-CoV-2 test positive
Symptomtext
Narrative: COVID infection completion of COVID vaccine series 05/06/21 COVID vaccine dose #1 05/27/21 COVID vaccine dose #2 07/24/21 Pt denies any symptom; preop COVID swab -COVID POSITIVE 07/29/21 Pt remains asymptomatic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- 07/24/21 COVID POSITIVE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- -
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Respiratory disorder
Symptomtext
Respiratory Problems; This is a spontaneous report from a contactable consumer or other non hcp. This is report 2 of 2. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: Not Provided), via an unspecified route of administration on an unspecified date as dose number unknown, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced respiratory problems. The outcome of the event was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.10.2021
- Impfdatum
- 01.03.2021
- Beginn
- 01.03.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy to vaccine
Hypersensitivity
Symptomtext
a severe allergic reaction after eating grapes; body over reacted; This spontaneous case was reported by a consumer and describes the occurrence of HYPERSENSITIVITY (a severe allergic reaction after eating grapes) and ALLERGY TO VACCINE (body over reacted) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. not provided) for COVID-19 vaccination. No Medical History information was reported. In March 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In March 2021, the patient experienced HYPERSENSITIVITY (a severe allergic reaction after eating grapes) and ALLERGY TO VACCINE (body over reacted). At the time of the report, HYPERSENSITIVITY (a severe allergic reaction after eating grapes) and ALLERGY TO VACCINE (body over reacted) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications was not provided by the reporter Treatment information was not provided To whom it may concern- I am not sure if this is beneficial to forward this information to the appropriate channels. Patient received the Maderna vaccine in March. I have never had any type of food alergy. I have always eaten grapes. The other day I ate two small bundles of grapes with seeds in them and had a severe allergic reaction where I had to go to the ER and treated for the event. I feel there is a connection with how my immune system reacted having the vaccine and this event months later. Where my body over reacted this way. I feel this is is something to start following in future research and keep statistics on soon as these concerns and improving the issues that rollout.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Allergy to vaccine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- -
- Geschlecht
- M
- Eingang
- 23.09.2021
- Impfdatum
- 01.01.2021
- Beginn
- 01.01.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Swelling face
Weight
Weight increased
Symptomtext
Face looked extremely swollen; Thighs and arms were puffed up; Gained weight; This is a spontaneous report from a contactable consumer or other non hcp. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on unknown date in Jan2021 as dose 2, single for COVID-19 immunisation; botulinum toxin type a (BOTOX), via an unspecified route of administration from an unspecified date (Batch/Lot Number: Not Provided) to an unspecified date, at unspecified dose for an unspecified indication. The patient medical history and concomitant medications were not reported. The patient face looked extremely swollen, thighs and arms were puffed up, gained weight on an unknown date in Jan2021. The patient underwent lab tests and procedures which included weight: gained weight on unknown date in 2021. Outcome of the events was not recovered. The lot/batch number is not available despite the follow-up attempts made. Follow-up attempts completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- Test Name: Weight; Result Unstructured Data: Test Result:Gained weight; Comments: Gained weight
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 22.09.2021
- Impfdatum
- 27.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heavy menstrual bleeding
Symptomtext
ongoing menstrual cycle; This spontaneous case was reported by a consumer and describes the occurrence of HEAVY MENSTRUAL BLEEDING (ongoing menstrual cycle) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On 27-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced HEAVY MENSTRUAL BLEEDING (ongoing menstrual cycle). At the time of the report, HEAVY MENSTRUAL BLEEDING (ongoing menstrual cycle) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient informed that She is on birth control and has a very regular cycle. No treatment information was provided by the reporter. No Concomitant medicines were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heavy menstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination complication
Symptomtext
Side effects; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Side effects) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (Side effects). At the time of the report, VACCINATION COMPLICATION (Side effects) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medications was not provided by the reporter Treatment information was not provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination complication
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination complication
Symptomtext
Having bad symptoms; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Having bad symptoms) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (Having bad symptoms). At the time of the report, VACCINATION COMPLICATION (Having bad symptoms) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication was not provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination complication
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blindness
Symptomtext
Blindness; This spontaneous case was reported by a consumer and describes the occurrence of BLINDNESS (Blindness) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced BLINDNESS (Blindness) (seriousness criterion medically significant). At the time of the report, BLINDNESS (Blindness) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were provided by the reporter. No treatment information was provided by the reporter. Patient also reported "this temp" with no measurement or date given. Based on the current available information, a causal relationship cannot be excluded. Further information is not expected as reporter refused to be contacted. Reporter did not allow further contact; Sender's Comments: Based on the current available information, a causal relationship cannot be excluded. Further information is not expected as reporter refused to be contacted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blindness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient didn't get the second in 4 weeks and is 6 months past the first) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient didn't get the second in 4 weeks and is 6 months past the first). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient didn't get the second in 4 weeks and is 6 months past the first) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product use was not provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 27.08.2021
- Impfdatum
- -
- Beginn
- 25.04.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Ringing in the ears; This spontaneous case was reported by a consumer and describes the occurrence of TINNITUS (Ringing in the ears) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 25-Apr-2021, the patient experienced TINNITUS (Ringing in the ears). At the time of the report, TINNITUS (Ringing in the ears) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment information was provided Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 05.01.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Nasopharyngitis
Symptomtext
Cold; Covid-19; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of NASOPHARYNGITIS (Cold) and COVID-19 (Covid-19) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. not provided) for COVID-19 vaccination. No Medical History information was reported. On 05-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced NASOPHARYNGITIS (Cold) and COVID-19 (Covid-19). At the time of the report, NASOPHARYNGITIS (Cold) and COVID-19 (Covid-19) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, COVID-19: positive date - unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19; Test Result: Positive ; Result Unstructured Data: date - unknown
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 24.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Symptomtext
Shingles; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a patient and describes the occurrence of HERPES ZOSTER (Shingles) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) UNKNOWN. On an unknown date, the patient experienced HERPES ZOSTER (Shingles). At the time of the report, HERPES ZOSTER (Shingles) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. NO CONCOMITANT AND TREATMENT DRUGS WERE USED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 23.08.2021
- Impfdatum
- 05.05.2021
- Beginn
- 05.05.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Vaccination complication
Symptomtext
not feeling well after receiving his 1st dose; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (not feeling well after receiving his 1st dose) in a 51-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 immunisation. No Medical History information was reported. On 05-May-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-May-2021, the patient experienced VACCINATION COMPLICATION (not feeling well after receiving his 1st dose). On 27-May-2021, VACCINATION COMPLICATION (not feeling well after receiving his 1st dose) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, Blood test: inconclusive (Inconclusive) Inconclusive. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: blood test; Test Result: Inconclusive ; Result Unstructured Data: Inconclusive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation delayed
Menstruation irregular
Symptomtext
menstruation came sooner/menstruation came later; people who menstruated after 5 years of not doing so; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 03-Jun-2021 and was forwarded to Moderna on 03-Jun-2021. Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a nurse and describes the occurrence of MENSTRUATION IRREGULAR (menstruation came sooner/menstruation came later) and MENSTRUATION DELAYED (people who menstruated after 5 years of not doing so) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced MENSTRUATION IRREGULAR (menstruation came sooner/menstruation came later) and MENSTRUATION DELAYED (people who menstruated after 5 years of not doing so). At the time of the report, MENSTRUATION IRREGULAR (menstruation came sooner/menstruation came later) and MENSTRUATION DELAYED (people who menstruated after 5 years of not doing so) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown Route), the reporter did not provide any causality assessments. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation delayed
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
ringing in the ear; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a consumer and describes the occurrence of TINNITUS (ringing in the ear) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced TINNITUS (ringing in the ear). At the time of the report, TINNITUS (ringing in the ear) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medications were reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- 22.04.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
SARS-CoV-2 test
SARS-CoV-2 test positive
Symptomtext
tested positive to Covid virus after 1st shot of the Moderna Covid-19 Vaccine; This spontaneous case was reported by a patient and describes the occurrence of SARS-COV-2 TEST POSITIVE (tested positive to Covid virus after 1st shot of the Moderna Covid-19 Vaccine) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. not provided) for COVID-19 vaccination. No Medical History information was reported. On 22-Apr-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage form. On 20-May-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to dosage form. On an unknown date, the patient experienced SARS-COV-2 TEST POSITIVE (tested positive to Covid virus after 1st shot of the Moderna Covid-19 Vaccine). At the time of the report, SARS-COV-2 TEST POSITIVE (tested positive to Covid virus after 1st shot of the Moderna Covid-19 Vaccine) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: positive positive. No concomitant medication was reported , No treatment medication was reported . Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 virus test; Result Unstructured Data: positive; Comments: positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- 24.04.2021
- Beginn
- 26.04.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal stiffness
Symptomtext
Stiffness in neck and shoulder; This spontaneous case was reported by a patient and describes the occurrence of MUSCULOSKELETAL STIFFNESS (Stiffness in neck and shoulder) in a 53-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not Provided) for COVID-19 vaccination. The patient's past medical history included Colonoscopy (scheduled on 25-MAY-2021). On 24-Apr-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Apr-2021, the patient experienced MUSCULOSKELETAL STIFFNESS (Stiffness in neck and shoulder). On 02-May-2021, MUSCULOSKELETAL STIFFNESS (Stiffness in neck and shoulder) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. concomitant medications are not provided. Treatment information does not provided by the reporter. Reporter did not allow further contact; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal stiffness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Colonoscopy (scheduled on 25-MAY-2021)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 22.08.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administration error
Symptomtext
Administered Pfizer vaccine instead of moderna for the second dose; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 19-May-2021 and was forwarded to Moderna on 19-May-2021. This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTRATION ERROR (Administered Pfizer vaccine instead of moderna for the second dose) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. NOT provided) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) at an unspecified dose. On an unknown date, the patient experienced PRODUCT ADMINISTRATION ERROR (Administered Pfizer vaccine instead of moderna for the second dose). At the time of the report, PRODUCT ADMINISTRATION ERROR (Administered Pfizer vaccine instead of moderna for the second dose) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- 30.03.2021
- Beginn
- 30.03.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Missed 2nd dose of Moderna vaccine on recommended interval; This spontaneous case was reported by an other health care professional and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Missed 2nd dose of Moderna vaccine on recommended interval) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. Not provided) for COVID-19 vaccination. No Medical History information was reported. On 30-Mar-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Mar-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Missed 2nd dose of Moderna vaccine on recommended interval). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Missed 2nd dose of Moderna vaccine on recommended interval) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient had no symptom after first dose vaccine. No treatment medication were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 23.01.2021
- Beginn
- 01.02.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
COVID-19 diagnose after their first shot; This spontaneous case was reported by a consumer (subsequently medically confirmed) and describes the occurrence of COVID-19 (COVID-19 diagnose after their first shot) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. not provided) for COVID-19 vaccination. The patient's past medical history included No adverse event. On 23-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Feb-2021, the patient experienced COVID-19 (COVID-19 diagnose after their first shot). At the time of the report, COVID-19 (COVID-19 diagnose after their first shot) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: No adverse event
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- F
- Eingang
- 09.06.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Illness
Symptomtext
she got sick; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: Not Provided), via an unspecified route of administration on an unspecified date as 1ST DOSE, SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient got sick, will not be taking her second dose. Patient stated reports that her husband has been sick for months after getting the first Covid vaccine shot, she had her first dose as well and would not be taking her second dose since her husband has developed symptoms after getting the first dose and wanted to speak to someone to help her husband to heal. She had to get it, the company that she worked for said if she do not got it she would not get paid. She got sick but do not got as bad as him, symptoms lasted 3 days, then she was out of bed. The outcome of events she got sick was recovered on an unspecified date. Information about batch/Lot number has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Illness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- -
- Geschlecht
- M
- Eingang
- 08.06.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diabetes mellitus
Disease recurrence
Symptomtext
Diabetes came back after second dose of the Covid Vaccine; " Disease recurrence"; This is a spontaneous report from a Pfizer sponsored program from a contactable physician. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot Number: Not Provided) as single dose for covid-19 immunisation. Medical history included pancreatic transplant for diabetes, the patient was fine for 2 years. The patient's concomitant medications were not reported. The patient experienced diabetes came back after second dose of the covid vaccine on an unspecified date with outcome of unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.; Sender's Comments: -Based on the current limited available information a possible contributory role of the suspect product BNT162B2 to the development of event diabetes cannot be totally excluded "The impact of this report on the benefit-risk profile of the Pfizer productand on the conduct of the study 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 Committees, and Investigators, as appropriate."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diabetes mellitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes (Pancreatic Transplant for Diabetes, the patient was fine for 2 years); Pancreatic transplant (Pancreatic Transplant for Diabetes. the patient was fine for 2 years)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 02.06.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Sleep disorder
Symptomtext
Waking up multiple times throughout the night; This is a spontaneous report from a contactable consumer reported for a patient (mother in law). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: Not Provided), via an unspecified route of administration on an unspecified date as UNKNOWN, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Reportedly, his mother-in-law did get the Pfizer COVID vaccine in a different town, and she has had the same issue where she is waking up multiple times throughout the night but she is taking it like it is part of her new normal and she is not complaining about it. Probed if caller would like to complete a safety report for his mother in law and he declined. He said that he would let her know about this and he also did let her know about the VAERS system and he is just leaving it up to her if she wants to report on her own behalf. On an unspecified date, the patient experienced waking up multiple times throughout the night. Outcome of the event was unknown. Additional Context: Caller is a 43 y/o male. Reports he received his first Pfizer Covid vaccine dose on 27Mar2021. On 31Mar2021, he woke up with a shock in his chest and has woken up every night since then with a shock. He states he falls asleep and then wakes up an hour later every night. He also reports this "shock" sensation in his intestinal area. He reports his limbs have been twitching, he has a headache that feels like vibrating inside of his head. He also reports a vibrating sensation in his chest and abdomen. He did not receive the second dose of the vaccine. He reports a loss of sensation in his penis. He wants to know if these side effects have been reported before and what to do about them. Will e-transmit as duplicate AE. He reports his mother-in-law has also experienced wakefulness after receiving the Pfizer Covid vaccine. Response: Referred to HCP and spoke from attached document FACT SHEET FOR HCPs ADMINISTERING VACCINE; FULL EUA PI (v1.0) (LAB-1450-8.0 Revised: 10 May 2021) section 6.1 Clinical Trials Experience and from VR Consumer Inquiry Management (Off-Label or No Info) (v15.0). No follow-up attempts are needed; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sleep disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 15.05.2021
- Impfdatum
- 17.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
developed Covid after receiving the first dose; developed Covid after receiving the first dose; This is a spontaneous report from a contactable 71 year old male consumer (patient) who reported that: Dates for developed Covid after receiving the first dose: (From: Unspecified To: Unspecified) Reporter seriousness for developed Covid after receiving the first dose: Hospitalization Dates when patient was in hospital for developed Covid after receiving the first dose: Unspecified to Unspecified Additional Context: Caller received the first dose of the Covid-19 vaccine on 17Mar2021. He was supposed to have received the second dose on 02Apr2021. After receiving the first dose he developed Covid and was in the hospital. He is now negative. He is asking when can he get the second dose? Declines to provide email address. Declines to provide further details. initially provided date of birth but then requested that his birthdate be eliminated. Communication: PC filed. Is there a Product Complaint: Yes Description of Product Complaint: Description of complaint: developed Covid after receiving the first dose Product strength and count size dispensed: Covid 19 vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID; Result Unstructured Data: Test Result:developed Covid; Comments: After receiving the first dose .; Test Name: COVID; Test Result: Negative ; Comments: After hospitalization.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 11.05.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Exposure to SARS-CoV-2
SARS-CoV-2 test
Symptomtext
Tested positive for Covid after both Covid vaccines; Tested positive for Covid after both Covid vaccines; had a Covid exposure in another country; This is a spontaneous report received from a contactable physician. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration, first dose on an unspecified date (Lot Number: Not Provided), second dose on an unspecified date (Lot Number: Not Provided), both at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Physician stated she had a question about whether Pfizer was interested in tracking people who tested positive for the Covid virus after having the Covid vaccine. Physician stated she was calling on behalf of her Nephew. Patient tested positive for Covid twice, after both Covid vaccines. Patient travelled and had a Covid exposure in another country. Patient had two positive Covid tests. Outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the event Drug ineffective, COVID-19, exposure to SARS-CoV-2 and the suspect drug BNT162B2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: tested positive for Covid; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 01.05.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nasal disorder
Symptomtext
Problems with her nose; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Caller is calling in regards to the COVID vaccine. Her daughter took her second shot the Monday before last. A week later, so this past Monday (2 days ago), she went to the ENT. She clarifies her daughter was having problems with her nose, but it had nothing to do with the vaccine. So, whatever is going on with her nose, her daughter's doctor put her on 60mg of Prednisone for 5 days. She wasn't there with her daughter, but her husband was, and she is pretty sure he did tell them she had the second vaccine 2 days ago, and she wasn't done with the 2 week period. Caller is wanting to know is it okay for her daughter to be taking a steroid? Will it lessen the effect of the COVID vaccine if she is taking a steroid? Treatment received as Prednisone. Outcome was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nasal disorder
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 07.04.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Brain injury
Tinnitus
Symptomtext
have brain ringing and it is debilitating; have brain ringing and it is debilitating; This is a spontaneous report from a contactable consumer. This consumer reported similar events for three patients. This is the third of three reports. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot Number: Not Provided) as SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient stated that she have brain ringing and it is debilitating. Outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : PFIZER INC-2021313764 Same reporter/drug/events. different patient; PFIZER INC-2021330802 Same reporter/drug/events. different patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Brain injury
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 30.03.2021
- Impfdatum
- 19.03.2021
- Beginn
- 25.03.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Symptomtext
No sense of taste and minimal smell
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ageusia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- losartan 100mg
- Allergien
- none
- Vorherige Impfungen
- -