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Reporte zur Charge U002398

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MO 2 GU 1

VAERS 1837440

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U002398

mild
Staat
GU
Alter
8,0
Geschlecht
F
Eingang
02.11.2021
Impfdatum
09.10.2021
Beginn
21.10.2021
Tage bis Beginn
12,0
Dosis
1
Route/Site
SC / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Papule Rash

Symptomtext

Patient in for itchy red mostly papules and some vesicles on the face, trunk, upper and lower extremities for 2 days. Rashes are coming out not at the same time. She had her first Varicella vaccine on 10/09/2021 here at the clinic. No exposure to Varicella disease. The mother denies fever, cough, runny nose, fast or labored breathing, vomiting, diarrhea. No sick contacts. She saw Dr. yesterday because she was worried, but Dr. is not sure if it is chickenpox or a side effect of the Varicella vaccine. With 1 red papule on the forehead, 6 on the back, one on the right knee, one on the right leg; one vesicle on the right forearm and right cheek

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
If rashes open up and are noted not drying up with clear fluid or pus, apply Mupirocin Ointment.
Aktuelle Erkrankungen
She still has on and off whitish scales on her scalp. She was using Nizoral 2% Shampoo. Mother did not refill it yet but she has no more at home. She scratches her scalp on and off. Mother denies any cough, colds, fever, decrease of appetite, or decrease of activity.
Vorgeschichte
Mother was advised she has seborrhea capitis. Advised may give Ketoconazole 2% Shampoo every 3 to 4 days for up to 8 weeks alternate with regular shampoo.
Andere Medikamente
NONE
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2579324

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U002398

gering
Staat
MO
Alter
-
Geschlecht
U
Eingang
10.02.2023
Impfdatum
03.02.2023
Beginn
03.02.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

no additional AEs were reported; an expired VARIVAX dose was given to a patient; This spontaneous report has been received from a nurse referring to a patient of unknown age and gender. The information about the patient's concurrent conditions, concomitant therapies or medical history was not provided. On 03-FEB-2023, the patient was vaccinated with one dose of expired varicella virus vaccine live (oka/merck) (VARIVAX) lot # U002398, expiry date 22-JAN-2023 (route of administration and anatomical location were not provided) for prophylaxis (expired product administered). No additional adverse events (AEs) were reported (no adverse event).

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

VAERS 1919184

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U002398

gering
Staat
MO
Alter
-
Geschlecht
U
Eingang
03.12.2021
Impfdatum
26.11.2021
Beginn
26.11.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event Product preparation issue

Symptomtext

no additional AE reproted; Varivax was mixed with an expired diluent and administered to a patient; Varivax was mixed with an expired diluent and administered to a patient; This spontaneous report was received from a pharmacist, referring to a patient of unknown age and gender. The patient's medical history, concurrent conditions, drug reactions/allergies, and concomitant therapies were not reported. On 26-NOV-2021, the patient was vaccinated with varicella virus vaccine live (oka/merck) (VARIVAX) (dose, frequency, and route of administration were not reported, lot number U002398, expiration date 22-JAN-2023) for prophylaxis. The vaccine was mixed with an expired sterile diluent (lot number R009955, expiration date 24-JAN-2021) (expired product administered and product preparation issue). Both products were properly stored. No additional adverse event occurred. The outcome of the events was unknown.

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