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Reporte zur Charge U024091

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
GA 3 WV 1 NC 1 NJ 1

VAERS 2324259

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U024091

mild
Staat
GA
Alter
0,2
Geschlecht
F
Eingang
20.06.2022
Impfdatum
03.06.2022
Beginn
03.06.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash

Symptomtext

Patient had a rash from head to toe for 48hrs after receiving the above vaccines

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2270972

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U024091

mild
Staat
WV
Alter
1,0
Geschlecht
M
Eingang
11.05.2022
Impfdatum
10.05.2022
Beginn
10.05.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Urticaria

Symptomtext

Developed few hives late in the evening after receiving vaccines. Seen in office aprox 24 hrs from vaccine-broken out head to toe in hives. Given oral benadryl 25 mg in office and 12 mg of Depo medrol with oral prednisilone to follow starting the following day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Hx of posterior urethral values-surgical repair. CKD Stage 1
Andere Medikamente
None
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2231250

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U024091

mild
Staat
NC
Alter
1,4
Geschlecht
F
Eingang
13.04.2022
Impfdatum
17.03.2022
Beginn
18.03.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Injection site erythema Injection site mass Injection site pain Injection site swelling

Symptomtext

17 month old infant presented on 3/17/22 to office for well-visit. MD ordered Pneumococcal conjugate vaccine 13-valent IM (PREVNAR 13), HiB PRP-OMP conjugate vaccine 3 dose IM (PedvaxHIB), and DTaP vaccine less than 7yo IM (INFANRIX) to be given during visit. CMA prepared and administered the following immunizations: Pneumococcal conjugate vaccine 13-valent IM (PREVNAR 13) IM to patient's right thigh (LOT #ER7046), HiB PRP-OMP conjugate vaccine 3 dose IM (PedvaxHIB) IM to patient's left thigh (LOT #U024091), and DTaP vaccine less than 7yo IM (INFANRIX) IM to patient's right thigh (LOT #23T73). On 1/11, parent sent message to office noting "pea-sized lump on patient's left thigh". Lump was non-tender and didn't seem to bother patient. Parent noted patient was afebrile, and no red streaks or marks noted. Parent encouraged to massage the area and to return to office if did not improve in 2 more weeks. Patient had received Hib vaccine in left thigh. Local injections site reaction including "Pain at injection site, erythema at injection site, swelling at injection site, tenderness at injection site".

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2645920

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U024091

gering
Staat
GA
Alter
0,4
Geschlecht
M
Eingang
15.06.2023
Impfdatum
09.06.2023
Beginn
09.06.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administration error

Symptomtext

On 6/9/23 at 10:30 am the patient was administered multiple vaccines. PCV20 and KINRIX were administered in error. The patient had no signs or symptoms of distress after vaccines were administered. The patient was monitored over 30 minutes after administration of the vaccines. Patient remained stable. No signs or symptoms of distress were noted.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NONE
Vorherige Impfungen
-

VAERS 2582572

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U024091

gering
Staat
GA
Alter
-
Geschlecht
U
Eingang
15.02.2023
Impfdatum
23.01.2023
Beginn
23.01.2023
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 reported; one dose of PEDVAXHIB was administered during an ongoing temperature excursion; This spontaneous report was received from a registered nurse and refers to a patient of unkonwn age and gender. The patient's pertinent medical history, current conditions, previous drug reactions or allergies and concomitant medications were not provided. On 23-JAN-2023, the patient was vaccinated with one dose of haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) intramuscular injection, at dose of 0.5 milliliter (lot number U024091 was verified to be a valid number, expiration date reported and established as 29-OCT-2023) administered for prophylaxis (strength, route of administration and anatomical location of vaccination were not provided); that underwent a temperature excursion of 34.8 Fahrenheit degrees for 144 hours, which started on 12-JAN-2023 (product storage error). There was a previous temperature excursion of 54.14 Fahrenheit degrees for 2 hours and 12 minutes. No additional adverse events were reported.

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

VAERS 2407951

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U024091

gering
Staat
NJ
Alter
-
Geschlecht
U
Eingang
11.08.2022
Impfdatum
01.07.2022
Beginn
01.07.2022
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 Adverse event; The medical assistant could not rule out that the imrpoperly stored vaccines, PEDAVX HIB, VAQTA and ROTATEQ were administered to patients.; This spontaneous report was received from a medical assistant and refers to an unspecified number of patients of unknown age and gender. The patients medical history, concurrent conditions and concomitant therapies were not reported. Between the week of 11-JUL-2022 and 15-JUL-2022, there was a temperature excursion with the lowest temperature at 0.92?C, of 11 hours and 30 minutes of the following vaccines: haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB), lot #U024091, expiration date: 29-OCT-2023, and lot#batch# W000458, expiration date: 17-JUN-2024 administered to prevent haemophilis influenza B infection (formulation, strength, and route of administration were not provided); rotavirus vaccine, live, oral, pentavalent (ROTATEQ) lot #1742419, expiration date: 23-JAN-2023, and lo#/batch# W004503, expiration date: 15-MAY-2023, administered to prevent rotavirus infection (formulation, strength, and route of administration were not provided); hepatitis a vaccine, inactivated (VAQTA) lot #U033212, expiration date: 07-NOV-2022, administered to prevent hepatitis A infection (formulation, strength, and route of administration were not provided); and hepatitis a vaccine, inactivated (VAQTA) lot #W002889, expiration date: 06-MAR-2023, administered to prevent hepatitis A infection (formulation, strength, and route of administration were not provided). The reporter could not rule out that the improperly stored vaccines were administered to patients on an unknown date in July 2022. (Improper storage of product in use). There were no additional adverse events reported (no adverse event). This is a non-valid case due to lack of patient's identifiers.

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