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Reporte zur Charge 301358a

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

7Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
PA 2 KY 1 IA 1 IL 1 NH 1 WA 1

VAERS 2467502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 301358

moderat
Staat
KY
Alter
19,0
Geschlecht
F
Eingang
03.10.2022
Impfdatum
03.09.2021
Beginn
10.09.2021
Tage bis Beginn
7,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Abdominal distension Abdominal pain upper Chest discomfort Diarrhoea Dyspnoea Eructation Fatigue Feeling abnormal Food allergy Headache Hot flush Inflammation Lethargy Nasal congestion Rhinorrhoea Throat tightness Vision blurred

Symptomtext

Severe food allergies After the first vaccine, I began belching. My baseline was almost never burping, so to begin belching was odd. After the second vaccine, after eating, I would get a substantial amount of drainage. After a few hours, it would slow, but I would wake up with a stuff nose, which was not my baseline normal. Then finally, after I got COVID, I had a whole aray of symptoms after eating: stomach aches, liquid stools, headaches, tightening of throat and chest making it difficult to breathe( especially after ingesting sugar), feeling fatigued and lathargic, bloating, hot flashes, blurred vision and fuzzy head, body wide inflammation, and the symptoms that arose after the vaccines.

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

VAERS 1776551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 301358

moderat
Staat
IA
Alter
30,0
Geschlecht
F
Eingang
11.10.2021
Impfdatum
08.10.2021
Beginn
09.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Burning sensation Drooling Lip swelling Pain in extremity Swelling face Swelling of eyelid Tachycardia

Symptomtext

Pt presenting to ER with reaction to COVID vaccine. She states she got the vaccine on Friday and noted a sore R arm with a burning sensation on Saturday. She then awoke at 0300 Sat morning with R sided facial swelling. Here R eye was swollen completely shut, she had upper and lower lip swelling, tongue swelling and a fire-like burning sensation to the R side of her body. She states she started taking benadryl. She states she was drooling which did improve with the benadryl. She has continued the benadryl and the swelling to the eye and lip improved. She is noted to have marked swelling to the R side of the face. She is able to speak and swallow without issues at this time. She is noted to have tachycardia and a temp of 100.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tachycardia
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Migraine
Vorgeschichte
Endometriosis, Dermatitis, Depression, Asthma, Anxiety, Environmental allergies
Andere Medikamente
Effexor, Inderal, Remeron, Clonazepam, Abilify
Allergien
Bee Venom
Vorherige Impfungen
-

VAERS 2311615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 301358

mild
Staat
IL
Alter
58,0
Geschlecht
F
Eingang
07.06.2022
Impfdatum
29.08.2021
Beginn
19.09.2021
Tage bis Beginn
21,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pruritus Sudden hearing loss Tinnitus

Symptomtext

Within a week of obtaining the 2nd vaccine, I had severe itching of hands, scalp, legs. On January 18, I awoke to Sudden Hearing Loss and severe Tinnitus.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
Benadryl was advised for the itching. Saw ENT for Tinnitus and hearing loss, did 2 rounds of oral steriods and 3 steriod shots in the ear. Dr, Ear, Nose, & Throat.
Aktuelle Erkrankungen
Celiac Disease
Vorgeschichte
Celiac Disease
Andere Medikamente
Lorazpam, Celexa, Vit B12 injection
Allergien
Celiac Disease, Wheat, Rye, Barley, Oats
Vorherige Impfungen
-

VAERS 1775385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 301358

mild
Staat
PA
Alter
19,0
Geschlecht
F
Eingang
10.10.2021
Impfdatum
15.09.2021
Beginn
10.10.2021
Tage bis Beginn
25,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Headache Nausea Pain SARS-CoV-2 test negative

Symptomtext

achiness headache and nausea

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
Covid negative
Aktuelle Erkrankungen
none
Vorgeschichte
depression
Andere Medikamente
Celexa 40mg daily, Birth control, Flagyl 2 BID
Allergien
none
Vorherige Impfungen
-

VAERS 2471450

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 301358

gering
Staat
NH
Alter
71,0
Geschlecht
M
Eingang
06.10.2022
Impfdatum
01.02.2021
Beginn
02.05.2021
Tage bis Beginn
90,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Unevaluable event

Symptomtext

None stated.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NA
Vorgeschichte
No
Andere Medikamente
Metoprolol; Losarten; clopedigrel; clorthaladone; atorvastatin; low dose aspirin, vitamin D; vitamin B.
Allergien
NA
Vorherige Impfungen
-

VAERS 2462764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 301358

gering
Staat
WA
Alter
67,0
Geschlecht
M
Eingang
28.09.2022
Impfdatum
08.09.2021
Beginn
-
Tage bis Beginn
-
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), on 08Sep2021 as dose 3 (booster), single (Lot number: 301358) at the age of 67 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment,. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: There was no other medication in 2weeks. Antiviral details: Product: Paxlovid, Treatment start date: 10Sep2022, stop date: 14Sep2022, Indication: Treatment of COVID-19. Rebound 5 days after finishing paxlovid course. Adverse event start date: 18Sep2022. If patient recovered: Recovering. If treatment ae: No. Known allergies: No.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment,
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2107307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 301358

gering
Staat
PA
Alter
59,0
Geschlecht
M
Eingang
12.02.2022
Impfdatum
02.10.2021
Beginn
03.10.2021
Tage bis Beginn
1,0
Dosis
3
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Swelling Vaccination site erythema

Symptomtext

Persistent redness right deltoid area (area of injection) more than 72 hours after injection; Redness tracks to right axilla; swelling and fullness in right axilla; This is a spontaneous report received from a contactable reporter(s) (Physician). The reporter is the patient. A 59 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 02Oct2021 14:15 (Lot number: 301358) at the age of 59 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: NAPROXEN. Vaccination history included: Bnt162b2 (Prev dose product: COVID 19, prev dose brand: Pfizer, prev dose brand unknown: False, prev dose lot number: EL9269, prev dose lot unknown: False,, prev dose administrator route: intramuscular, prev dose administration date: 05Feb2021, prev dose dose number:2, prev dose vaccine location:Right, arm.), administration date: 05Feb2021, when the patient was 59 years old, for Covid-19 immunization; Bnt162b2 (prev dose product: COVID 19, prev dose brand: Pfizer, prev dose brand unknown: False, prev dose lot number: EL3248, prev dose lot unknown: False,, prev dose administrator route: Intramusular, prev dose administration date: 15Jan2021, prev dose dose number 1, prev dose vaccine location: Right arm.), administration date: 15Jan2021, when the patient was 59 years old, for Covid-19 immunization. The following information was reported: VACCINATION SITE ERYTHEMA (non-serious) with onset 03Oct2021 02:30, outcome "not recovered", described as "Persistent redness right deltoid area (area of injection) more than 72 hours after injection"; ERYTHEMA (non-serious) with onset 03Oct2021 02:30, outcome "not recovered", described as "Redness tracks to right axilla"; SWELLING (non-serious) with onset 03Oct2021 02:30, outcome "not recovered", described as "swelling and fullness in right axilla". Therapeutic measures were not taken as a result of vaccination site erythema, erythema, swelling. Additional information: No known allergies, Post vaccination patient was not tested for COVID. Prior to vaccination patient had no COVID. Patient had no other medical history. Facility type Vaccine: Pharmacy or Drug Store. If other vaccine in four weeks: No No follow-up attempts are possible. No further information is expected. Follow-Up (13Oct2021): Follow-up attempts are completed. No further information is expected.

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