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Reporte zur Charge U035268

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

2Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OH 2

VAERS 2564843

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge U035268

gering
Staat
OH
Alter
-
Geschlecht
U
Eingang
21.01.2023
Impfdatum
-
Beginn
13.12.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event Product preparation error

Symptomtext

No additional AE reported; Pharmacist reports an expired dose of sterile diluent [U035268 11/9/2022] was used to reconstitute VARIVAX [U030161 9/28/2023] and it was administered to a patient on 13DEC2022. Caller confirmed sterile diluent was not involved in a temperature excur; Pharmacist reports an expired dose of sterile diluent [U035268 11/9/2022] was used to reconstitute VARIVAX [U030161 9/28/2023]; This spontaneous report has been received from a pharmacist and refers to a patient of unknown age and gender. There was no information regarding the patient's medical history, concurrent conditions and concomitant medications provided. On 13-DEC-2022, the patient was vaccinated with varicella virus vaccine live (Oka/Merck) (VARIVAX) subcutaneous injection, lot# U030161 confirmed to be valid with expiration date 28-SEP-2023 (exact dose, dose number, route of administration and anatomical location were not reported) for prophylaxis. The vaccine was reconstituted with an expired dose of sterile diluent, lot # U035268 confirmed to be valid with expiration date 09-NOV-2022 (exact dose was not reported) (expired product administered, product preparation error). The reporter confirmed that sterile diluent was not involved in a temperature excursion and was stored according to the recommended storage range until administration. There was no additional adverse event reported.

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

VAERS 2526041

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge U035268

gering
Staat
OH
Alter
42,0
Geschlecht
F
Eingang
08.12.2022
Impfdatum
03.12.2022
Beginn
03.12.2022
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

The patient has reported no adverse events to this reporter at this time; patient received an MMRII vaccine that was mixed with expired diluent; This spontaneous report has been received from a nurse practitioner, concerning a 42-years-old female patient. The patient's medical history, concurrent conditions, concomitant medications, previous drug reactions, and allergies were not provided. On 03-DEC-2022, the patient was vaccinated with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (recombinant Human albumin) (M-M-R II) subcutaneous injection, in her right arm as prophylaxis (lot number U013035 has been verified to be valid; expiration date reported and established as 23-APR-2023) (strength, dose, frequency, vaccination scheme, and route of administration were not provided), diluted with sterile diluent solution for injection (lot number U035268 has been verified to be valid; expiration date reported and established as 09-NOV-2022) (expired product administered). The patient had reported no adverse events.

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