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Reporte zur Charge EN6193

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 1 CA 1 TN 1 WA 1

VAERS 2176986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6193

moderat
Staat
-
Alter
69,0
Geschlecht
F
Eingang
12.03.2022
Impfdatum
29.03.2021
Beginn
29.03.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Breast cancer female Chest discomfort Computerised tomogram Dyspnoea Mammogram Palpitations Positron emission tomogram Psoriasis Skin exfoliation

Symptomtext

Psoriasis; Skin exfoliation; Breast cancer female; Palpitation; Shortness of breath; Chest tightness; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (Not Provided). The reporter is the patient. A 69 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administration date 29Mar2021 (Lot number: EN6193) at the age of 69 years as dose 2, single for covid-19 immunisation; adalimumab (HUMIRA), subcutaneous, administration date Jul2012 (Batch/Lot number: unknown) as 40 mg (1 in 2 wk) and administration date 01Feb2022 (ongoing) (Batch/Lot number: unknown) as 40 (1 in 2 wk) for psoriasis. Relevant medical history included: "Hysterectomy" (unspecified if ongoing); "Tonsillectomy" (unspecified if ongoing); "Abstains from Alcohol" (unspecified if ongoing); "Tomato Allergy Manifestated by red spots on skin" (unspecified if ongoing); "Tomato Allergy Manifestated by red spots on skin" (unspecified if ongoing); "High Blood Pressure" (unspecified if ongoing); "High Cholesterol" (unspecified if ongoing); "Diuretic" (unspecified if ongoing); "had surgery to remove all the breast cancer on right side in July or Aug2021" (unspecified if ongoing), notes: had surgery to remove all the breast cancer on right side in July or Aug2021. Family history included: "Patient had two aunts with breast cancer on maternal side" (unspecified if ongoing). Concomitant medication(s) included: FUROSEMIDE taken for polyuria; LISINOPRIL; SIMVASTATIN taken for blood cholesterol increased; ISOSORBIDE MONONITRATE; ATENOLOL taken for hypertension. Vaccination history included: Bnt162b2 (DOSE 1, Route of Admin: Intra-muscular, Lot Number: EN6200), administration date: 08Mar2021, when the patient was 69 years old, for Covid-19 Immunization. The following information was reported: BREAST CANCER FEMALE (medically significant) with onset Jun2021, outcome "unknown", described as "Breast cancer female"; PSORIASIS (medically significant), outcome "unknown", described as "Psoriasis"; CHEST DISCOMFORT (medically significant) with onset 29Mar2021, outcome "recovered" (29Mar2021), described as "Chest tightness"; SKIN EXFOLIATION (non-serious) with onset 01Feb2022, outcome "recovered" (01Feb2022), described as "Skin exfoliation"; PALPITATIONS (non-serious) with onset 29Mar2021, outcome "recovered" (29Mar2021), described as "Palpitation"; DYSPNOEA (non-serious) with onset 29Mar2021, outcome "recovered" (29Mar2021), described as "Shortness of breath". The patient underwent the following laboratory tests and procedures: computerised tomogram: (Jun2021) breast cancer; mammogram: (Jun2021) breast cancer; positron emission tomogram: (Jun2021) breast cancer. The action taken for adalimumab was unknown. Therapeutic measures were taken as a result of breast cancer female. Clinical course: On an unknown date, the patient experienced top layer of skin fell on floor where psoriasis was/ psoriasis on 80 percent of body. On 29Mar2021, the patient experienced palpitation, shortness of breath and chest tightness. On 29Mar2021, the palpitation, shortness of breath and chest tightness resolved. In Jun2021, the patient experienced female breast cancer. On 01Feb2022, the patient experienced top layer of skin fell on floor where psoriasis was/ psoriasis on 80 percent of body. On 01Feb2022, the Top layer of skin fell on floor where psoriasis was/ psoriasis on 80 percent of body resolved. Pfizer BioNTech Covid-19 Vaccine (Tozinameran) was also considered suspect. The patient had no signs and symptoms of breast cancer. It was diagnosed in routine mammogram. She had radiation therapy and chemo therapy that started 01Dec2021. She had surgery to remove all the breast cancer on right side in July or Aug2021. She was admitted overnight. She had two aunts with breast cancer on her maternal side. She had psoriasis 80 percent of the body. The top layer of skin fell on floor where psoriasis was when she injected Humira. She did not have the expiry date of the Covid 19 vaccine because it was not written in the vaccination card. It was unknown if patient was enrolled in a COVID-19 Vaccine Trial. The patient was treated with TAXOL. Causality for Humira 40MG/0.4ML (Adalimumab) The reporter's causality for the event(s) of female breast cancer, palpitation, shortness of breath and chest tightness with Humira 40MG/0.4ML (Adalimumab) was no reasonable possibility. The reporter's causality for the event(s) of top layer of skin fell on floor where psoriasis was/ psoriasis on 80 percent of body onset 01Feb2022 and top layer of skin fell on floor where psoriasis was/ psoriasis on 80 percent of body unknown onset was not provided. Causality to Humira: 1) Breast cancer female (Breast cancer female), Action(s) taken with drug: Drug discontinued, Causality as per reporter (Drug/Vaccine): Not Related, Dechallenge: UNK 2) Skin exfoliation (Skin exfoliation), Action(s) taken with drug: Drug discontinued, Causality as per reporter (Drug/Vaccine): Not assessable, Dechallenge: Yes 3) Palpitation (Palpitations), Action(s) taken with drug: Drug discontinued, Causality as per reporter (Drug/Vaccine): Not Related, Dechallenge: Yes 4) Shortness of breath (Dyspnoea), Action(s) taken with drug: Drug discontinued, Causality as per reporter (Drug/Vaccine): Not Related, Dechallenge: Yes 5) Chest tightness (Chest discomfort), Action(s) taken with drug: Drug discontinued, Causality as per reporter (Drug/Vaccine): Not Related, Dechallenge: Yes 6) Psoriasis (Psoriasis), Action(s) taken with drug: Drug discontinued, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: UNK Drug: Pfizer Biontech Covid-19 Vaccine 1) Breast cancer female (Breast cancer female), Action(s) taken with drug: Not Applicable, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A 2) Skin exfoliation (Skin exfoliation), Action(s) taken with drug: Not Applicable, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A 3) Palpitation (Palpitation), Action(s) taken with drug: Not Applicable, Causality as per reporter (Drug/Vaccine): Probable, Dechallenge: N/A 4) Shortness of breath (Dyspnoea), Action(s) taken with drug: Not Applicable, Causality as per reporter (Drug/Vaccine): Probable, Dechallenge: N/A 5) Chest tightness (Chest discomfort), Action(s) taken with drug: Not Applicable, Causality as per reporter (Drug/Vaccine): Probable, Dechallenge: N/A 6) Psoriasis (Psoriasis), Action(s) taken with drug: Not Applicable, Causality as per reporter (Drug/Vaccine): Not Reported, Dechallenge: N/A No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
Test Date: 202106; Test Name: Computerized Tomography Scan of Breast; Result Unstructured Data: Test Result:Breast cancer; Test Date: 202106; Test Name: Mammogram; Result Unstructured Data: Test Result:Breast cancer; Test Date: 202106; Test Name: Positron Emission Tomography Scan of Breast; Result Unstructured Data: Test Result:Breast cancer
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Abstains from alcohol; Blood pressure high; Breast cancer; Diuretic effect; Food allergy; High cholesterol; Hysterectomy; Skin red; Surgery (had surgery to remove all the breast cancer on right side in July or Aug2021); Tonsillectomy
Andere Medikamente
FUROSEMIDE; LISINOPRIL; SIMVASTATIN; ISOSORBIDE MONONITRATE; ATENOLOL
Allergien
-
Vorherige Impfungen
-

VAERS 1299182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6193

moderat
Staat
PA
Alter
70,0
Geschlecht
M
Eingang
08.05.2021
Impfdatum
25.03.2021
Beginn
25.03.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Anaemia Blood glucose Blood glucose increased Body temperature Chills Dehydration Dysgeusia Headache Hepatic enzyme Hepatic enzyme abnormal Investigation Neutropenia Pyrexia SARS-CoV-2 test Thrombocytopenia

Symptomtext

dehydration; anemia; neutropenia; thrombocytopenia; abnormal liver enzymes; increased blood sugar level; dysgeusia; developed severe throbbing headache; fever (102-103 F); chills; This is a spontaneous report from a contactable physician (patient). A 70-year-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: EN6193), intramuscular, administered in Arm Left on 25Mar2021 08:30 as single dose for COVID-19 immunization in a hospital. Medical history included supraventricular tachycardia and NSTEMI (Non-ST Elevation Myocardial Infarction) both from an unknown date. No known allergies. No COVID-19 prior to vaccination. Concomitant medications included diltiazem hydrochloride (CARDIZEM CD) and asa (ASA) both taken for an unspecified indication, start and stop date were not reported. The patient previously received the first dose of bnt162b2 (lot number: EL9266) on 04Mar2021 in the left arm for COVID-19 immunization and experienced severe throbbing headache, fever and chills. On 25Mar2021 22:30, 14 hours after the second dose, the patient developed severe throbbing headache, fever, and chills lasting for 72 hours. On 08Apr2021, the patient was hospitalized for 1 day for dehydration, anemia, neutropenia, thrombocytopenia, abnormal liver enzymes, increased blood sugar level, dysgeusia. The patient again developed severe throbbing headache, fever (102-103 F), and chills. The patient underwent lab tests and procedures which included blood glucose: increased on 08Apr2021, body temperature: 102-103 fahrenheit on 08Apr2021, hepatic enzyme: abnormal on 08Apr2021, panel of lab tests: normal on 28Feb2021. The patient was tested for COVID-19 via nasal swab taken post vaccination with a negative result on an unspecified date. The patient was treated with IV fluids. The events required healthcare professional office/clinic and emergency room visit. The outcome of the events was recovering.; Sender's Comments: A possible contributory effect of suspect BNT162B2 on reported events 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
Dehydration
Hospital-Tage
1,0
Labordaten
Test Date: 20210408; Test Name: blood sugar; Result Unstructured Data: Test Result:increased; Test Date: 20210408; Test Name: body temperature; Result Unstructured Data: Test Result:102-103 Fahrenheit; Test Date: 20210408; Test Name: Liver enzymes; Result Unstructured Data: Test Result:abnormal; Test Date: 20210228; Test Name: Panel of lab tests; Result Unstructured Data: Test Result:normal; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Non ST segment elevation myocardial infarction; Supraventricular tachycardia
Andere Medikamente
CARDIZEM CD; ASA
Allergien
-
Vorherige Impfungen
-

VAERS 1083888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6193

moderat
Staat
CA
Alter
34,0
Geschlecht
F
Eingang
09.03.2021
Impfdatum
01.03.2021
Beginn
04.03.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Chills Fatigue Headache Lymphadenopathy Migraine Muscle spasms Nausea Pyrexia

Symptomtext

Swollen lymph node under armpit (left side), Fever, chills, migraine, muscle spasms, joint pain, headache, nausea, exhaustion

Weitere VAERSDATA-Felder
Praegender Schweregrund
Migraine
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Hypothyroidism
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1648548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6193

mild
Staat
TN
Alter
68,0
Geschlecht
F
Eingang
28.08.2021
Impfdatum
26.02.2021
Beginn
27.02.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Body temperature Chills Headache Lethargy Pyrexia Vaccination site pain

Symptomtext

Fever 101; Chills; lethargy; headache; arm soreness at vaccine site; This is a spontaneous report from a contactable consumer. A 68-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection. Batch/Lot Number: EN6193), dose 1 via an unspecified route of administration, administered in right arm on 26Feb2021 at 17:30 (at the age 68-years-old) as DOSE 1, SINGLE for COVID-19 immunization. Medical history included drug hypersensitivity (known allergies- Penicillin) from an unknown date and unknown if ongoing. Concomitant medication(s) included levothyroxine sodium (LEVOTHYROXINE SODIUM), fluticasone propionate (FLONASE [FLUTICASONE PROPIONATE]), pseudoephedrine hydrochloride (SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]) and montelukast (MONTELUKAST) taken for an unspecified indication, start and stop date were not reported received within 2 weeks. No other vaccine in four weeks. No COVID prior to vaccination. The patient was not pregnant at the time of vaccination. Facility type vaccine at Pharmacy or Drug store. On 27Feb2021 at 11:15 the patient experienced fever 101, chills, lethargy, headache, arm soreness at vaccine site. The patient underwent lab tests and procedures which included body temperature: 101 on 27Feb2021. COVID tested post vaccination reported as no. The outcome of the events were recovered on 20221. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
Test Date: 20210227; Test Name: Fever; Result Unstructured Data: Test Result:101
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Penicillin allergy (known allergies- Penicillin)
Andere Medikamente
LEVOTHYROXINE SODIUM; FLONASE [FLUTICASONE PROPIONATE]; SUDAFED [PSEUDOEPHEDRINE HYDROCHLORIDE]; MONTELUKAST
Allergien
-
Vorherige Impfungen
-

VAERS 1845423

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6193

gering
Staat
WA
Alter
-
Geschlecht
F
Eingang
05.11.2021
Impfdatum
21.02.2021
Beginn
01.03.2021
Tage bis Beginn
8,0
Dosis
2
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Musculoskeletal stiffness

Symptomtext

Slight stiffness after injection; This is a spontaneous report from a Pfizer-sponsored Program Pfizer from a contact-able consumer or other non hcp. Upon Fu date (08Mar2021) case was upgraded to valid. A 72-year-old female patient received second dose received from BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EN6193), via intramuscular route, administered in left arm on 21Feb2021 as dose 2, single for COVID-19 immunisation. Medical history included asthma from 01Aug1974 and ongoing no hospitalization or ER ever, cardiomyopathy Non-Ischemic Cardiomyopathy from 30May2008 and ongoing with angiogram- no blockage, atrial fibrillation from 04Oct2014 and ongoing (2 weeks after my husband died and stress related). The patient's concomitant medications were not reported. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EM9810), via intramuscular route, administered in right arm on 06Feb2021 at 14:00 as dose 1, single for COVID-19 immunisation. On an unspecified date on Mar2021, the patient experienced slight stiffness after injection 02. No noticeable rise in temperature, aches, pains, tiredness or headache after both shots (Last one almost 48 hours ago). The outcome of the event unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Musculoskeletal stiffness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Asthma (No Hospitalization or ER ever); Atrial fibrillation (2 weeks after my husband died. Stress related); Non-ischemic cardiomyopathy.
Vorgeschichte
Medical History/Concurrent Conditions: Angiogram (Angiogram- No blockage.)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-