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Reporte zur Charge U7255A

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 2 NJ 1

VAERS 2620826

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7255A

schwer
Staat
TX
Alter
-
Geschlecht
F
Eingang
27.09.2023
Impfdatum
24.02.2023
Beginn
25.02.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Febrile convulsion Pyrexia

Symptomtext

Febrile convulsion; Parent reports fever 101.3 and staring episode the day after vaccine; This non-serious case was received during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-JUL-2023 with the following VAERS primary ID 2620826-1. The original narrative from the sender is as follows: Concomitant medication included Vitamin D for unknown indication. Parent reports fever of 101.3 and staring episode the day after vaccine,? febrile seizure. The reporter did not provide an assessment of causal relationship between Vaxelis and the event "patient reports fever of 101.3 and staring episode the day after vaccine,? febrile seizure.". No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Febrile convulsion
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
VITAMIN D3
Allergien
-
Vorherige Impfungen
-

VAERS 2620826

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7255A

schwer
Staat
TX
Alter
-
Geschlecht
F
Eingang
27.09.2023
Impfdatum
24.02.2023
Beginn
25.02.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
- / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Febrile convulsion Pyrexia

Symptomtext

Febrile convulsion; Parent reports fever 101.3 and staring episode the day after vaccine; This non-serious case was received during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-JUL-2023 with the following VAERS primary ID 2620826-1. The original narrative from the sender is as follows: Concomitant medication included Vitamin D for unknown indication. Parent reports fever of 101.3 and staring episode the day after vaccine,? febrile seizure. The reporter did not provide an assessment of causal relationship between Vaxelis and the event "patient reports fever of 101.3 and staring episode the day after vaccine,? febrile seizure.". No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Febrile convulsion
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
VITAMIN D3
Allergien
-
Vorherige Impfungen
-

VAERS 2591946

MSP VACCINE COMPANY · DTAP+IPV+HIB+HEPB (VAXELIS) · Charge U7255A

gering
Staat
NJ
Alter
-
Geschlecht
M
Eingang
26.06.2023
Impfdatum
03.02.2023
Beginn
02.03.2023
Tage bis Beginn
27,0
Dosis
UNK
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 Extra dose administered Vaccination site erythema

Symptomtext

Vaccination site erythema; Circumstance or information capable of leading to medication error; Extra dose administered; This case was retrieved during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-APR-2023 with the following VAERS Primary 2591946-1. The original narrative from the sender is as follows: Patient here for 12 month well child exam. Originally physician ordered Pentacel, Prevnar and Varivax but after chart review it was determined that child missed the 6 month well child exam and was in need of 3rd dose of Vaxelis. The consent form (paper) had been prepared based on the original orders of Pentacel, Prevnar and Varivax. When the medical assistant asked the MD to sign the order, the MD said (per the MA) we are giving VAXELIS, instead of Varivax. Per the MA, the MD watched the MA cross out VARIVAX and add VAXELIS as well as having the PENTACEL checked off. The MD then signed the order. MA administered the vaccines and upon documentation in the medical record, noted a different set of orders in the chart that DID NOT include the Pentacel but did include the Varivax. The MA did notify the physician and myself right away. The parent was notified of the event and was advised to monitor for increase in fever, irritability, or local reaction. I apologized for the experience and that I would be looking into how this occurred in spite of our careful attention to safety. I gave her my name to call for any additional questions. Parent did bring child to the ED for evaluation about 2 hrs after the incident. ED diagnosis of 'parental concern'. after the dual vaccinations received. Vital signs at that visit WNL with no fever. All other physical exam WNL except for '3 Vaccine sites notes with mild surrounding erythema but no tenderness'. The department on call physician was notified in case there were any further concern overnight which there were not. No subsequent calls were made to the office since then and no further ED evaluations noted. The reporter did not provide an assessment of the causal relationship between Vaxelis and the reported events. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Circumstance or information capable of leading to medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-