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Reporte zur Charge EWU185

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
WA 1 CA 1

VAERS 1315982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EWU185

schwer
Staat
WA
Alter
49,0
Geschlecht
F
Eingang
01.07.2021
Impfdatum
13.05.2021
Beginn
13.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Anaphylactic reaction Blood pressure increased Heart rate increased Pharyngeal swelling Urticaria Condition aggravated Dissociation Dizziness Dysphonia Hypertension Immediate post-injection reaction Livedo reticularis Oropharyngeal pain Sensation of foreign body Tachycardia

Symptomtext

Anaphylaxis; This is a spontaneous report received from a contactable consumer or other non hcp. A 49-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number: EWU185) via an unspecified route of administration in left arm on 13May2021 at 19:00 (age at vaccination 49 years old, Pregnancy at time of Vaccination: No) as first dose, single for COVID-19 immunization. Medical history included Sjogren's syndrome, Reynauds, Ankylosis, Spondylitis and multi-nodular thyroid. Patient was allergic to Amoxicillin, Lamotrigine, Gabapentin, IV Contrast, peanuts, tree nuts and shellfish. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medication(s) included lithium (LITHIUM), cariprazine hydrochloride (VRAYLAR) and amfetamine aspartate monohydrate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (MYDAYIS). Since the vaccination, the patient had not been tested positive for COVID-19. The patient experienced anaphylaxis on 13May2021 at 19:00. The event resulted in Emergency room/department or urgent care. The patient received treatment for the adverse event in hospital. The patient was hospitalized for anaphylaxis on an unspecified date in 2021. The outcome of the event was recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic reaction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy to intravenous contrast media (known allergies: IV Contrast); Allergy to nuts (known allergies: Tree nuts); Ankylosis; Peanut allergy (known allergies: Peanuts); Raynaud's disease (Other medical history: Reynauds); Shellfish allergy (known allergies: Shellfish); Sjogren's (Other medical history: Sjogrens); Spondylitis; Thyroid nodular (Other medical history: multi-nodular thyroid)
Andere Medikamente
LITHIUM; VRAYLAR; MYDAYIS
Allergien
-
Vorherige Impfungen
-

VAERS 1470508

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EWU185

mild
Staat
CA
Alter
39,0
Geschlecht
F
Eingang
14.07.2021
Impfdatum
14.04.2021
Beginn
24.04.2021
Tage bis Beginn
10,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness postural Dysstasia Fall Gait disturbance

Symptomtext

I was unable to stand or walk. When trying to walk I was tripping over my feet and falling. I had to be held up. I could not walk or stand on my own and I was extremely dizzy when upright.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness postural
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Epilepsy
Andere Medikamente
Lamictal, Onfi, Zonisimide, Zoloft, Ambien CR, Red Yeast Rice, CQ10, Multi Vitamin
Allergien
Penicillin
Vorherige Impfungen
-