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Reporte zur Charge U6565AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NC 2 IL 1

VAERS 2659135

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge u6565aa

mild
Staat
-
Alter
20,0
Geschlecht
M
Eingang
06.01.2022
Impfdatum
01.02.2021
Beginn
02.02.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Arthralgia Chills Diarrhoea Dizziness Headache Pyrexia SARS-CoV-2 test negative

Symptomtext

Narrative: Pt had multiple immunizations yesterday, has headache minimal fever chills began last night one episode loose bm no blood no cough no sob no chest pain mild light headed no sore throat no rash mild right knee pain no swelling had negative covid

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

VAERS 977844

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6565AA

mild
Staat
-
Alter
19,0
Geschlecht
M
Eingang
27.01.2021
Impfdatum
27.01.2021
Beginn
27.01.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
SC / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

Urticaria 30 post vaccination

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

VAERS 948488

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6565AA

mild
Staat
NC
Alter
16,0
Geschlecht
F
Eingang
15.01.2021
Impfdatum
12.01.2021
Beginn
12.01.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia C-reactive protein increased Full blood count normal Headache Injection site swelling Joint dislocation Joint range of motion decreased Metabolic function test normal Nausea Pain Pain in extremity Pyrexia Tenderness

Symptomtext

Patient called on 1/13/2021 with reports of tactile fever/headache/nausea/body aches/right arm pain with limited range of motion/weakness limited by pain developing approximately 2-3 hours after vaccine administration. Findings on exam(1/13/2021): Right upper extremity with mild swelling at deltoid injection site without erythema but notable tenderness to touch. With displacement of right upper extremity at shoulder, pain 6/10 present with movement 30 degrees from vertical torso in anterior/posterior and right lateral abduction. Equivocal tenderness to palpation of soft <1cm x 3/4 cm shotty right axillary nodes that are mobile and non-erythematous. Screening labs - CBC w/diff, CMP, CRP

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
1/13/2021 CBC w/diff and CMP both WNL 1/13/2021 CRP elevated at 26.0 mg/L
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1255779

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6565AA

gering
Staat
NC
Alter
-
Geschlecht
U
Eingang
25.04.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient was administered an expired Menactra vaccine, no AE; Initial information regarding an unsolicited valid non-serious case was received from a pharmacist via Global Medical Information (GMI) (Reference number- 00555170) and transmitted to Sanofi on 09-Apr-2021. This case involves a patient (demographics unknown) who was administered an expired dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (lot U6565AA, expiry date: 28-Mar-2021) via unknown route in unknown administration site for prophylactic vaccination on an unknown date (Expired product administered) Medical history, medical treatment(s), vaccination(s), concomitant medications and family history were not provided. It was a case of an actual medication error due to expired vaccine used (latency same day) At the time of report, no adverse event was reported The reporter had an incident where a patient was given an expired Menactra vaccine in one of the clinics. They were looking for documentation on whether or not the patient needs to be revaccinated.. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. 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 marketing 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 1227983

SANOFI PASTEUR · MENINGOCOCCAL CONJUGATE (MENACTRA) · Charge U6565AA

gering
Staat
IL
Alter
16,0
Geschlecht
F
Eingang
19.04.2021
Impfdatum
29.03.2021
Beginn
29.03.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

expired Menactra was given to a patient/an expired 0.5ml dose of Adacel was administered in MT's right deltoid with no ae; Initial information received on 30-Mar-2021 regarding an unsolicited valid non-serious case from a other health professional (reference number :00540911). This case involves a 16 years old female patient who received expired 0.5 ml doses of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] (lot number and expiration date not reported via unknown route in the right deltoid) and MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] (lot U6565AA and expiration date:28-Mar-2021 via unknown route in an unknown administration site) for prophylactic vaccination on 29-Mar-2021 (expired product administered). And reporter wanted to know what to do. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included MEDROXYPROGESTERONE ACETATE (DEPO PROVERA, injection) on that same visit (that is on 29-Mar-2021). It was an actual medication error due to expired vaccine used (same day latency). It was not reported that the patient experienced any adverse event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. 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 marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. There will be no information available on the batch number of Adacel for this case.

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