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Reporte zur Charge EW0185 MUSC

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

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0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
SC 1

VAERS 1875882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0185 MUSC

moderat
Staat
SC
Alter
62,0
Geschlecht
F
Eingang
17.11.2021
Impfdatum
09.09.2021
Beginn
09.09.2021
Tage bis Beginn
0,0
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Alopecia Arthritis Back pain Condition aggravated Fatigue Hair disorder Headache Immunisation Influenza like illness Lymphadenopathy Off label use Product use issue Rash

Symptomtext

Current-Hair loss; Skin rash; intermittent left lower sharp back pain; swollen lymph node; headaches; arthritis pain worse; arthritis pain worse; tired; hair shedding; flue like Symptoms; Other vaccine same date vaccine date 09Sep2021; dose number=3; dose number=3; This is a spontaneous report from a contactable consumer or other non hcp. A 62-years-old female patient received bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Formulation: solution for injection, Batch/Lot Number: EW0185 MUSC), via an unspecified route of administration, administered in Arm Left on 09Sep2021 (age at vaccination 62-Years-old) as dose 3 (booster), single for COVID-19 immunization; SHINGRIX, via an unspecified route of administration from 09Sep2021 (Batch/Lot number was not reported) to 09Sep2021, at unspecified dose for an unspecified indication . Medical history included arthritis from an unknown date and unknown if ongoing , hypersensitivity from an unknown date and unknown if ongoing , blood cholesterol increased from an unknown date and unknown if ongoing , blood iron decreased from an unknown date and unknown if ongoing , seasonal allergy from an unknown date and unknown if ongoing , food allergy from an unknown date and unknown if ongoing. Concomitant medication(s) included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL); chorionic gonadotrophin (HTROP); colecalciferol (VIT D [COLECALCIFEROL]); calcium (CALCIUM) and fish/flack seed all taken for an unspecified indication, start and stop date were not reported. The patient previously took, niacin and experienced drug hypersensitivity, statins and experienced drug hypersensitivity. Patient previously received bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Formulation: solution for injection, Batch/Lot Number: EL1284), via an unspecified route of administration, administered in Arm Left on 06Jan2021 (age at vaccination 61-Years-old) as dose 1, single for COVID-19 immunization and bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Formulation: solution for injection, Batch/Lot Number: EL3249 MUSC), via an unspecified route of administration, administered in Arm Right on 26Jan2021 (age at vaccination 61-Years-old) as dose 2, single for COVID-19 immunization. on an unspecified date patient experienced current-Hair loss, Skin rash, intermittent left lower sharp back pain after vac- swollen lymph node, headaches, arthritis pain worse, tired, hair shedding, flue like Symptoms. HAIR LOSS is my biggest concern and 09Sep2021, other vaccine same date vaccine date 09sep2021, dose number=3. Patient did not received any treatment. The outcome events other vaccine same date vaccine date 09sep2021, dose number=3 was unknown and rest all was not received. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy; Arthritis; Food allergy; Grass allergy; High cholesterol; Iron low
Andere Medikamente
ADDERALL; HTROP; VIT D [COLECALCIFEROL]; CALCIUM
Allergien
-
Vorherige Impfungen
-