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Reporte zur Charge U019908

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NJ 2 MO 1 OH 1 PA 1

VAERS 2440819

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U019908

mild
Staat
MO
Alter
5,0
Geschlecht
M
Eingang
12.09.2022
Impfdatum
06.09.2022
Beginn
08.09.2022
Tage bis Beginn
2,0
Dosis
2
Route/Site
SC / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Body temperature increased Hypersensitivity Injection site erythema Injection site swelling Rash

Symptomtext

Mom called in to let us know that pt. had an allergic reaction to the vaccines he got at our office on 09/06/2022. It was his Right leg. mom states it was the vaccine given on the top of the thigh, not off to the side in the fatty part. starting Thursday, two days after, he had a red square shape red raised area around the injection site. Saturday he started with a 101 temp, forehead thermometer. Sunday he developed rash all over body. mom took to ED for evaluation and they said they believe he has had a reaction to a vaccine but he is ok and was discharged the same day. mom calling to just let us know and ask which vaccine it was. Let her know that the dtap and the polio where both in once shot and that was given on the top of his right thigh.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
no known
Aktuelle Erkrankungen
no known
Vorgeschichte
none
Andere Medikamente
none
Allergien
no known allergies
Vorherige Impfungen
-

VAERS 2626576

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U019908

gering
Staat
OH
Alter
2,4
Geschlecht
M
Eingang
04.05.2023
Impfdatum
29.12.2021
Beginn
11.01.2022
Tage bis Beginn
13,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Immunisation reaction

Symptomtext

Adverse effect of other vaccines and biological substances, initial encounter on 2022-01-11.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Immunisation reaction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Encounter for routine child health examination NOS; Need for immunization against single bacterial diseases
Vorgeschichte
-
Andere Medikamente
None
Allergien
-
Vorherige Impfungen
-

VAERS 2604300

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U019908

gering
Staat
NJ
Alter
-
Geschlecht
U
Eingang
28.03.2023
Impfdatum
24.02.2023
Beginn
24.02.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

No additional AE; TE on VARIVAX; This spontaneous report was received from a registered nurse and refers to a patient of unknown age and gender. Information regarding the patient's pertinent medical history, historical drugs, concurrent conditions, concomitant therapies, and previous drug reactions or allergies was not reported. On 24-FEB-2023, the patient was vaccinated with an improperly stored dose of varicella virus vaccine live (oka/merck) (VARIVAX) subcutaneous injection, 0.5 milliliter, lot #U019908, expiration date: 24-JUN-2023, administered for prophylaxis (strength, and route of administration were not provided). The vaccine was stored in a temperature of 7.2F/(6?F up to 14?F) for 1 hour 22 minutes. There was a previous temperature excursion of 10.9F/(6?F up to 14?F) for 1 hour 18 minutes 36 seconds. No additional adverse event/No PQC.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2485563

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U019908

gering
Staat
PA
Alter
6,0
Geschlecht
M
Eingang
21.10.2022
Impfdatum
20.10.2022
Beginn
20.10.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered No adverse event

Symptomtext

Child was vaccinated at clinic. Vaccinated based on records supplied by mother. After 2 hours of leaving, the mother called back in and said the school still wouldn't admit the child until a plan was made to receive 3rd HepB and 4th Dtap. I called the school nurse and while comparing dates, we discovered that we did not have the same records. School was given an entirely different record and after I received their record, I discovered child had received the necessary doses given on this date on March 1, 2022. The vaccines given at our clinic were not necessary. This was unknown by clinic staff, mother did not supply us with all of the child's records. No adverse effect or harm done to child.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
-
Andere Medikamente
-
Allergien
none
Vorherige Impfungen
-

VAERS 2335485

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U019908

gering
Staat
NJ
Alter
-
Geschlecht
U
Eingang
27.06.2022
Impfdatum
16.05.2022
Beginn
16.05.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

No additional AE reported; Nurse reporting that one patient was administered VARIVAX after experiencing a temperature excursion (Temperature: 6.6F); This spontaneous report was received from a nurse and referred to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 16-MAY-2022, the patient was vaccinated with varicella virus vaccine live (oka/merck) (VARIVAX) subcutaneous injection after experiencing a temperature excursion (temperature: 6.6F; time frame: 0 hours 5 minutes and 0 seconds) for prophylaxis (lot # U019908 is valid upon internal validation, expiration date: 24-JUN-2023; strength, dose, and route of administration were not provided) (product storage error). No additional adverse event was reported (no adverse event).

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