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Reporte zur Charge U7374AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

10Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NY 6 MA 2 TX 1 WI 1

VAERS 2695401

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
MA
Alter
-
Geschlecht
F
Eingang
28.12.2023
Impfdatum
28.07.2023
Beginn
28.07.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Decreased appetite Pallor Somnolence Hypophagia Sleep apnoea syndrome

Symptomtext

Mom stated baby was sleepy for 3D; Did not eat well; Mom reported today (10/5/23) at time of 2 mo. visit after receiving vaccines all extremities turned pale; This non-serious spontaneous safety report, with ID number: 2695401(VAERS ID 2695401-1), was received by a partner on 11-DEC-2023 and forwarded on 14-DEC-2023, from a HCP. The original narrative from the sender is as following: Mom reported today (10/5/23) at time of 2 mo. visit after receiving vaccines all extremities turned pale and stayed that way 5-10 min. Mom stated baby was sleepy for 3D and did not eat well. This incident was not documented in chart and nurse had no recollection of being notified no phone calls were received following. Mom refused vaccines at todays visit. The reporter did not provide an assessment of causal relationship between Vaxelis and the reported events "Mom reported today (10/5/23) at time of 2 mo. visit after receiving vaccines all extremities turned pale, Did not eat well, Mom stated baby was sleepy for 3D". No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypophagia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2695401

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
MA
Alter
-
Geschlecht
F
Eingang
28.12.2023
Impfdatum
28.07.2023
Beginn
28.07.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Decreased appetite Pallor Somnolence Hypophagia Sleep apnoea syndrome

Symptomtext

Mom stated baby was sleepy for 3D; Did not eat well; Mom reported today (10/5/23) at time of 2 mo. visit after receiving vaccines all extremities turned pale; This non-serious spontaneous safety report, with ID number: 2695401(VAERS ID 2695401-1), was received by a partner on 11-DEC-2023 and forwarded on 14-DEC-2023, from a HCP. The original narrative from the sender is as following: Mom reported today (10/5/23) at time of 2 mo. visit after receiving vaccines all extremities turned pale and stayed that way 5-10 min. Mom stated baby was sleepy for 3D and did not eat well. This incident was not documented in chart and nurse had no recollection of being notified no phone calls were received following. Mom refused vaccines at todays visit. The reporter did not provide an assessment of causal relationship between Vaxelis and the reported events "Mom reported today (10/5/23) at time of 2 mo. visit after receiving vaccines all extremities turned pale, Did not eat well, Mom stated baby was sleepy for 3D". No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypophagia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2688030

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
NY
Alter
-
Geschlecht
M
Eingang
28.12.2023
Impfdatum
01.09.2023
Beginn
01.09.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Extra dose administered; This case was retrieved during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-OCT-2023 with the following VAERS Primary ID 2688030-1. The original narrative from the sender is the following: N/A. Due to the nature of the event, the causal relationship between Vaxelis and the reported event "Extra dose administered" was not applicable. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2686500

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
NY
Alter
-
Geschlecht
F
Eingang
28.12.2023
Impfdatum
28.08.2023
Beginn
28.08.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration

Symptomtext

Inappropriate schedule of product administration; This case was retrieved during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-OCT-2023 with the following VAERS Primary ID 2686500-1. The original narrative from the sender is not provided. Due to the nature of the event, the causal relationship between Vaxelis and " Inappropriate schedule of product administration" was not applicable. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2658669

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
TX
Alter
-
Geschlecht
F
Eingang
28.12.2023
Impfdatum
19.07.2023
Beginn
19.07.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Circumstance or information capable of leading to medication error No adverse event Product administration error Product packaging confusion Wrong product administered Product label issue

Symptomtext

Pt received an HPV by accident; looked like Vaxneuvance and a box of HPV vaccine was misplaced into the box for Vaxneuvance; looked like Vaxneuvance and a box of HPV vaccine was misplaced into the box for Vaxneuvance; This was an error in administration.; No adverse reactions seen yet; This non-serious case was received during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-OCT-2023 with the following VAERS Primary ID 2644045-1. The original narrative from the sender is the following: "Pt received an HPV by accident since it looked like Vaxneuvance and a box of HPV vaccine was misplaced into the box for Vaxneuvance. This was an error in administration. No adverse reactions seen yet". Reporter assessed the causal relationship between Vaxelis and the events "Pt received an HPV by accident", " looked like Vaxneuvance and a box of HPV vaccine was misplaced into the box for Vaxneuvance"," looked like Vaxneuvance and a box of HPV vaccine was misplaced into the box for Vaxneuvance", " This was an error in administration." and " No adverse reactions seen yet" as not applicable due to the nature of this events. Of note, these events do not concern Vaxelis, but rather Vaxneuvance vaccine. Vaxelis should have been considered as a concomitant. However, the case was databased to mirror what was reported in VAERS. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Circumstance or information capable of leading to medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Tracheitis (Pt had tracheitis in past while she was in NICU); Upper respiratory infection (about 1 month ago.)
Vorgeschichte
Medical History/Concurrent Conditions: Arachnoid cyst ([not legible] mega cisterna magna vs. posterior fassa arachnoid cyst); Dependence on ventilator; Esotropia; Gastrostomy tube insertion; Myomectomy; Pyloric stenosis; Pyloromyotomy; Renal agenesis; Tracheostomy; Trisomy 18 (Trisomy 18, ex-36 6/7,); Valve-sparing root replacement (Right ventricle to [not legible] s/p VSO repair & ventricular,)
Andere Medikamente
ALBUTEROL HFA; POLYVISOL [ASCORBIC ACID;CYANOCOBALAMIN;ERGOCALCIFEROL;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL; ACETAMINOPHEN
Allergien
-
Vorherige Impfungen
-

VAERS 2719675

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
WI
Alter
-
Geschlecht
M
Eingang
30.11.2023
Impfdatum
21.09.2023
Beginn
18.10.2023
Tage bis Beginn
27,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Adenovirus test positive Failure to thrive Polymerase chain reaction positive Rotavirus infection Rotavirus test positive Weight gain poor

Symptomtext

Failure to thrive; Not gaining weight appropriately/ Unable to gain weight; HCP called to report that a 2-month-old infant has tested positive for the Rota Virus today, 10/19/2023/ Admin Rotateq on 09/21/23/ Tested positive for Rotavirus on 18-OCT-2023.; This serious spontaneous safety report with reference # (Interaction#) was received by a partner on 02-NOV-2023 and forwarded to agency on 28-NOV-2023 from a Health Care Professional. A male patient, with medical history of failure to thrive and a birth weight of 7 pounds 0.4 ounces, had been vaccinated with Vaxelis primary dose 1 on 21-SEP-2023 at the age of 2 months old (intramuscular route, Batch # U7374AA). Co-suspect vaccinations included RotaTeq (Batch# 1933912) and Vaxneuvance (Batch # V004289). No concomitant vaccinations or medications were reported. On 18-OCT-2023, the infant was hospitalized for being unable to gain weight. On 18-OCT-2023 (also reported as 19-OCT-2023), the patient tested positive for Rotavirus. The baby's stool was tested, with a PCR test, as part of routine testing related to the infant not gaining weight appropriately. On 19-OCT-2023, the infant also tested positive to adenovirus. It was reported that the infant had no other signs or symptoms and was not premature. On the same day, the infant was started on iron supplementation, he was not taking any other medications, or supplements. At time of this report, the outcome of the events "failure to thrive and not gaining weight appropriately/ unable to gain weight was unknown/not reported and that of event rotavirus infection was reported as resolved on an unknown date. The reporter did not provide an assessment of the causal relationship between Vaxelis and the reported events: Rotavirus infection, failure to thrive and not gaining weight appropriately/ unable to gain weight. FOLLOW UP information was received by agency on 28-Nov-2023 from the local affiliate. The correct day zero(0) for MCM-005491 is 02-NOV-2023, Initially it was incorrectly reported as 03-NOV-2023 by the local affiliate, hence the case MCM-005491 will be deactivated after submission, and the case MCM-005561 was created with a correct day 0(02-NOV-2023). Further information is expected. COMPANY COMMENT: Rotavirus infection, Failure to thrive and Weight gain poor were assessed as serious due to causing hospitalization. Rotavirus infection, Failure to thrive and Weight gain poor are unlisted for Vaxelis as per the Reference Safety Information. Considering the current knowledge on the vaccine, the co-suspect vaccines (RotaTeq, Vaxneuvance), the long onset latency (28 days after vaccination) and different etiology of events, the causal relationship between Vaxelis and Rotavirus infection, Failure to thrive and Weight gain poor is excluded and assessed as not related. This single individual case safety report does not modify the benefit/risk balance of this product. Therefore, no change in the label or other measures is recommended at this time. However, the company will continue to monitor all respective reports received and based on cumulative experience, will re-evaluate the available evidence on an ongoing basis.; Sender's Comments: Rotavirus infection, Failure to thrive and Weight gain poor were assessed as serious due to causing hospitalization. Rotavirus infection, Failure to thrive and Weight gain poor are unlisted for Vaxelis as per the Reference Safety Information Considering the current knowledge on the vaccine, the co-suspect vaccines (RotaTeq, Vaxneuvance), the long onset latency (28 days after vaccination) and different etiology of events, the causal relationship between Vaxelis and Rotavirus infection, Failure to thrive and Weight gain poor is excluded and assessed as not related. This single individual case safety report does not modify the benefit/risk balance of this product. Therefore, no change in the label or other measures is recommended at this time. However, the company will continue to monitor all respective reports received and based on cumulative experience, will re-evaluate the available evidence on an ongoing basis.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Adenovirus test positive
Hospital-Tage
-
Labordaten
Test Date: 20231019; Test Name: Adenovirus; Result Unstructured Data: Test Result:positive ;positive; Test Date: 20231018; Test Name: PCR test; Result Unstructured Data: Test Result:positive ;positive
Aktuelle Erkrankungen
Failure to thrive
Vorgeschichte
Medical History/Concurrent Conditions: Birth weight normal (7 lb 0.4 oz)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2683999

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
NY
Alter
0,6
Geschlecht
F
Eingang
20.09.2023
Impfdatum
25.08.2023
Beginn
25.08.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event

Symptomtext

n/a

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

VAERS 2683387

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
NY
Alter
2,0
Geschlecht
M
Eingang
18.09.2023
Impfdatum
30.08.2023
Beginn
30.08.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Unevaluable event

Symptomtext

n/a

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

VAERS 2683016

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
NY
Alter
1,8
Geschlecht
F
Eingang
18.09.2023
Impfdatum
30.08.2023
Beginn
30.08.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Unevaluable event

Symptomtext

n/a

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 2682488

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7374AA

gering
Staat
NY
Alter
0,6
Geschlecht
F
Eingang
15.09.2023
Impfdatum
18.08.2023
Beginn
18.08.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Unevaluable event

Symptomtext

n/a

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-