Zurueck zur Suche

Reporte zur Charge U1D222M

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

3Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 1 PA 1 MN 1

VAERS 2654265

SANOFI PASTEUR · RABIES (IMOVAX) · Charge U1D222M

kritisch
Staat
TX
Alter
24,0
Geschlecht
F
Eingang
10.07.2023
Impfdatum
07.05.2023
Beginn
07.05.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Coma scale Computerised tomogram head normal Electroencephalogram normal Eye movement disorder Laboratory test normal Loss of consciousness Magnetic resonance imaging normal Malaise Mental status changes Scan with contrast normal Seizure Seizure like phenomena Status epilepticus Tremor

Symptomtext

HPI: 24yo F with no known significant neurologic history with new onset seizures with initial status epilepticus. She had a potential rabies exposure on Wednesday 3 May and, having had prior rabies vaccinations x 2, underwent post exposure prophylaxis for rabies exposure with 2 dose series of rabies vaccine. Within 5 minutes of the second dose of the vaccine on day 3 after exposure she felt unwell, then became unconscious, and had seizure-like activity with rapid eye movements and rhythmic shaking of the left arm at about 1330. She remained unconscious with GCS 3 for the next 3 hours with frequent episodes every 2-20 minutes of recurrent seizure activity lasting 15 seconds to 3+ minutes. She was treated initially with midazolam in recurrent boluses of 2mg up to 12mg in total. She was loaded with levetiracetam 4500mg IV and given an additional 10mg IM diazepam. She underwent CT head with and w/o IV contrast which was negative. She had a total of over 23 seizure-like events over about 3 hours. Over the next week she had progressive improvement in mental status. She had no further large events after about 24hrs and had only 1 very brief event.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Coma scale
Hospital-Tage
6,0
Labordaten
Labs, EEG, MRI were all negative for seizure activity. Neurology consult ruled out seizure.
Aktuelle Erkrankungen
L sided ulnar nerve pain - possible ulnar nerve entrapment
Vorgeschichte
irritable bowel syndrome h/o depression
Andere Medikamente
occasional benzodiazepam for sleep/anxiety
Allergien
none
Vorherige Impfungen
-

VAERS 2666443

SANOFI PASTEUR · RABIES (IMOVAX) · Charge U1D222M

gering
Staat
PA
Alter
60,0
Geschlecht
F
Eingang
04.08.2023
Impfdatum
21.07.2023
Beginn
21.07.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

IMOVAX was administered to a patient/vaccine was out of its expiration date for 1 day, with no reported adverse event; Initial information was received on 01-Aug-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 60 years old female patient was received rabies (hdc) vaccine [Imovax rabies] and the vaccine was out of its expiration date for 1 day with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s), concomitant medications and family history were not provided. On 21-Jul-2023, the patient received a dose of suspect rabies (hdc) vaccine Powder and solvent for suspension for injection (strength: standard) at dose of 1 ml total once (lot number: U1D222M) vaccine was out of its expiration date for 1 day (expiration date: 20-Jul-2023) via unknown route in the right upper arm for Immunization (immunisation) with no reported adverse event (expired product administered) (latency: same day). No lab data reported. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event imovax was administered to a patient/vaccine was out of its expiration date for 1 day, with no reported adverse event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the authorization holder's compliance with the requirements set out in the guidelines. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2515286

SANOFI PASTEUR · RABIES (IMOVAX) · Charge U1D222M

gering
Staat
MN
Alter
24,0
Geschlecht
M
Eingang
23.11.2022
Impfdatum
17.11.2022
Beginn
17.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered at inappropriate site

Symptomtext

Rabies vaccine (Imovax) and Rabies Immune Globulin were given in same extremity (right arm).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered at inappropriate site
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-