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Reporte zur Charge U014992

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

13Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 4 LA 2 WA 1 MD 1 KY 1 MS 1 AL 1 NC 1 MO 1

VAERS 2420134

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

mild
Staat
WA
Alter
3,0
Geschlecht
F
Eingang
25.08.2022
Impfdatum
23.08.2022
Beginn
23.08.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Lymphadenopathy Pyrexia

Symptomtext

Pt received vaccines on 23AUG2022; Pt reported back to the clinic 25AUG2022 with a swollen lymph node, red L thigh, and a fever. Pt was prescribed Ibuprofen and Augmentin. Pt was asked to return to clinic 26AUG2022 to see if the issue resolved itself.

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

VAERS 2098970

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

mild
Staat
MD
Alter
0,3
Geschlecht
M
Eingang
09.02.2022
Impfdatum
01.02.2022
Beginn
02.02.2022
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Arachnoid cyst Blood culture negative Fontanelle bulging Full blood count normal Irritability Lumbar puncture Magnetic resonance imaging head abnormal Procedural failure Pyrexia Urine analysis normal

Symptomtext

Patient presented the day after being given vaccines with fever , irritability and bulging fontanelle . Patient was admitted to Hospital for observation. CBC , blood culture and urine studies were normal. LP was attempted and failed . Ultrafast brain MRI was normal except for incidental arachnoid cyst - 11 mm in size. Patient defervesced without additional treatment and was discharged in stable condition after 24 hrs.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
1,0
Labordaten
see above
Aktuelle Erkrankungen
Covid -19 infection 1/2/222
Vorgeschichte
none
Andere Medikamente
None
Allergien
Milk protein
Vorherige Impfungen
-

VAERS 2579623

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
KY
Alter
1,7
Geschlecht
F
Eingang
10.02.2023
Impfdatum
09.02.2023
Beginn
09.02.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

This was a vaccine error. DTap (Infanrix) was expired by 2 days.

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

VAERS 2386666

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
MS
Alter
-
Geschlecht
U
Eingang
23.07.2022
Impfdatum
-
Beginn
08.07.2022
Tage bis Beginn
-
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; HCP reporting an improperly stored vaccine, PEDVAXHIB, was administered to a patient on 8Jul2022.; This spontaneous report was received from a certified medical assistant and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On 08-JUL-2022, the patient was administered an improperly stored dose of haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) intramuscular injection, lot # U014992, expiration date: 29-OCT-2023 (strength, dose, anatomical site, and route of administration were not provided) administered for prophylaxis (product storage error). Before being administered, the vaccine experienced a temperature excursion of 32 degrees Fahrenheit for 40 minutes. There were no previous temperature excursions. No additional adverse events reported (no adverse event).

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

VAERS 2362746

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge u014992

gering
Staat
AL
Alter
1,3
Geschlecht
F
Eingang
08.07.2022
Impfdatum
08.07.2022
Beginn
08.07.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered

Symptomtext

Patient Did not Have Adverse Reaction She Had Additional Unneeded Dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2325429

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
NC
Alter
0,2
Geschlecht
F
Eingang
21.06.2022
Impfdatum
20.06.2022
Beginn
20.06.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Diaphragmatic spasm Facial spasm Screaming

Symptomtext

Approximately 3 hours after receiving her 2mo vaccines, the patient developed what looked like diaphragmatic spasm that was occurring approximately every 0.5-3minutes as well as facial spasms that would last a few seconds and resolve resulting in her screaming, these episodes kept repeating every few minutes for approximately 5 hours. At around 5:50pm She received 2.5ml of benadryl and went to sleep and the episodes resolved.

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

VAERS 2242838

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
MI
Alter
1,0
Geschlecht
U
Eingang
20.04.2022
Impfdatum
11.03.2022
Beginn
11.03.2022
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 AE reported; improperly stored vaccines; This spontaneous report was received from a medical assistant and refers to a 12 months old of patient of unknown gender. No information regarding the patient's medical history, concurrent conditions or concomitant therapies was provided. On 11-MAR-2022, the patient was vaccinated with improperly stored haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) (lot #U014992 was confirmed to be valid, expiration date: 29-OCT-2023) and measles, mumps, and rubella (wistar ra 27-3) virus vaccine, live, (recombinant Human albumin (rHA)) (M-M-R II) (lot #U006488 was confirmed to be valid, expiration date: 26-FEB-2023) (dose, dose number, site and route of administration were not provided for both vaccines) for prophylaxis. Before the administration, from 23-FEB-2022, the vaccines were improperly stored at 8.7 Celsius degrees (C) for 1 hour and 36 minutes (product storage error). No additional adverse events were reported (no adverse event). This is one of several reports received from the same reporter.; Sender's Comments: US-009507513-2203USA005045: US-009507513-2204USA005825: US-009507513-2204USA005826: US-009507513-2204USA005827: US-009507513-2204USA005828:

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

VAERS 2242837

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
MI
Alter
0,2
Geschlecht
U
Eingang
20.04.2022
Impfdatum
10.03.2022
Beginn
10.03.2022
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 AE reported; improperly stored vaccines; This spontaneous report was received from a medical assistant and refers to a 9 week old patient of unknown gender. No information regarding the patient's medical history, concurrent conditions or concomitant therapies was provided. On 10-MAR-2022, the patient was vaccinated with improperly stored haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) (lot #U014992 was confirmed to be valid, expiration date: 29-OCT-2023) (dose, dose number, site and route of administration were not provided) for prophylaxis. Before the administration, from 23-FEB-2022, the vaccine was improperly stored at 8.7 Celsius degrees (C) for 1 hour and 36 minutes (product storage error). No additional adverse events were reported (no adverse event). This is one of several reports received from the same reporter.; Sender's Comments: US-009507513-2203USA005045: US-009507513-2204USA005825: US-009507513-2204USA005826: US-009507513-2204USA005827: US-009507513-2204USA005829:

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

VAERS 2242836

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
MI
Alter
0,2
Geschlecht
U
Eingang
20.04.2022
Impfdatum
04.03.2022
Beginn
04.03.2022
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 AE reported; improperly stored vaccines; This spontaneous report was received from a medical assistant and refers to a 11 weeks old patient of unknown gender. No information regarding the patient's medical history, concurrent conditions or concomitant therapies was provided. On 04-MAR-2022, the patient was vaccinated with improperly stored haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) (lot #U014992 was confirmed to be valid, expiration date: 29-OCT-2023) (dose, dose number, site and route of administration were not provided) for prophylaxis. Before the administration, from 23-FEB-2022, the vaccine was improperly stored at 8.7 Celsius degrees (C) for 1 hour and 36 minutes (product storage error). No additional adverse events were reported (no adverse event). This is one of several reports received from the same reporter.; Sender's Comments: US-009507513-2203USA005045: US-009507513-2204USA005825: US-009507513-2204USA005826: US-009507513-2204USA005828: US-009507513-2204USA005829:

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

VAERS 2242835

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
MI
Alter
0,2
Geschlecht
U
Eingang
20.04.2022
Impfdatum
02.03.2022
Beginn
02.03.2022
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 AE reported; improperly stored vaccines; This spontaneous report was received from a medical assistant and refers to a 9 week old patient of unknown gender. No information regarding the patient's medical history, concurrent conditions or concomitant therapies was provided. On 02-MAR-2022, the patient was vaccinated with improperly stored haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) (lot #U014992 was confirmed to be valid, expiration date: 29-OCT-2023) (dose, dose number, site and route of administration were not provided) for prophylaxis. Before the administration, from 23-FEB-2022, the vaccine were improperly stored at 8.7 Celsius degrees (C) for 1 hour and 36 minutes (product storage error). No additional adverse events were reported (no adverse event). This is one of several reports received from the same reporter.; Sender's Comments: US-009507513-2203USA005045: US-009507513-2204USA005825: US-009507513-2204USA005827: US-009507513-2204USA005828: US-009507513-2204USA005829:

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

VAERS 2225578

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
LA
Alter
-
Geschlecht
U
Eingang
11.04.2022
Impfdatum
21.03.2022
Beginn
21.03.2022
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 adverse event; products experienced supported temperature excursion; This spontaneous report was received from medical assistant and referred to a patient with unknown gender and age. The patient's medical history, current condition, concomitant therapy, drug allergy or reaction was not provided. On 21-MAR-2022, the patient was vaccinated with rotavirus vaccine, live, oral, pentavalent (ROTATEQ) VIAL 2, administered 2mL/once, oral (strength not provided) (lot # 1742464 with expiry date 20-SEP-2022) and haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) 0.5mL/once (strength and route not provided) (lot # u014992 with expiry date 29-OCT-2023) after products experienced supported temperature excursion (Incorrect product storage). Both vaccines for prophylaxis. There was no additional adverse event.

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

VAERS 2225113

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge u014992

gering
Staat
LA
Alter
-
Geschlecht
U
Eingang
09.04.2022
Impfdatum
-
Beginn
21.03.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

No additional AE.; patient was administered ROT ATEQ and PEDV AX HIB after products experienced supported temperature excursion; This spontaneous report was received from a medical assistant and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not provided. On 21-MAR-2022, the patient was vaccinated with improperly stored rotavirus vaccine, live, oral, pentavalent (ROTATEQ) 2ml at once orally, lot # 1742464, expiration date 20-SEP-2022; and haemophilus b conjugate vaccine (meningococcal protein conjugate) (LIQUID PEDVAXHIB) 0.5ml at once, lot # u014992, expiration date 29-OCT-2023 (exact route of administration was not provided) for prophylaxis (product storage error). No details about the temperature excursion was provided. It was unknown if digital data logger was involved. No additional adverse event was reporter (no adverse event).

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

VAERS 2217715

MERCK & CO. INC. · HIB (PEDVAXHIB) · Charge U014992

gering
Staat
MO
Alter
13,0
Geschlecht
M
Eingang
06.04.2022
Impfdatum
21.03.2022
Beginn
21.03.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

no additional AE reported; HCP reported that patient was accidently administered the wrong vaccine; This spontaneous report was received from a medical assistant and refers to a 13-year-old male patient. There was no information about patient's concomitant medications, concurrent conditions or pertinent medical history. On 21-MAR-2022, the patient was accidentally vaccinated with the wrong vaccine (wrong product administered), the patient received haemophilus b conjugate vaccine (meningococcal protein conjugate)(LIQUID PEDVAXHIB) lot number U014992 with expiration date 29-OCT-2023 (dose, route and anatomical location were not reported), but it was supposed to received meningococcal vaccine a/c/y/w conj (dip tox) (MENACTRA). 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
-