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Reporte zur Charge U756AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 2 DC 1 WA 1

VAERS 2613149

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge U756AA

mild
Staat
TX
Alter
4,0
Geschlecht
M
Eingang
11.04.2023
Impfdatum
08.03.2023
Beginn
08.03.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Face oedema Vomiting

Symptomtext

WITHIN 1 HOUR OF VACCINES, DEVELOPED EDEMA OF THE FACE AND VOMITED ONE TIME.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vomiting
Hospital-Tage
-
Labordaten
3/8/23 ER- TREATED WITH EPINEPHRINE AND BENADRYL. REFERRED TO ALLERGIST
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
KEFLEX- HIVES AND SWELLING INSECT BITES- HIVES AND SWELLING
Vorherige Impfungen
-

VAERS 2611256

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U756AA

mild
Staat
TX
Alter
4,0
Geschlecht
M
Eingang
06.04.2023
Impfdatum
21.03.2023
Beginn
22.03.2023
Tage bis Beginn
1,0
Dosis
5
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site swelling

Symptomtext

Mom noticed swelling to area at injection site. No fever. Placed warm compress on it & administered Tylenol. Patient had a localized reaction to vaccine. Reddened area around injection site.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
reactive airway disease; eczema; Allergies
Andere Medikamente
Albuterol sulfate neb treatment; Albuterol HFA 90mcg; EpiPen
Allergien
Allergy to eggs
Vorherige Impfungen
-

VAERS 2583389

GLAXOSMITHKLINE BIOLOGICALS · TDAP (BOOSTRIX) · Charge U756AA

mild
Staat
DC
Alter
39,0
Geschlecht
M
Eingang
17.02.2023
Impfdatum
05.01.2023
Beginn
08.02.2023
Tage bis Beginn
34,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Headache Pruritus Rash Varicella zoster virus infection

Symptomtext

I had a rash on the left side of my torso that kept growing. I went into the doctor; they called in a dermatologist who immediately identified it as the zoster virus. I had very mild itching, slight headache. I was given a prescription that helped to clear it up and feel that I am doing much better.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
No
Aktuelle Erkrankungen
Flu like symptoms
Vorgeschichte
Asthma
Andere Medikamente
SINGULAIR
Allergien
No
Vorherige Impfungen
-

VAERS 2622871

SANOFI PASTEUR · DTAP + IPV (QUADRACEL) · Charge U756AA

gering
Staat
WA
Alter
10,0
Geschlecht
M
Eingang
28.04.2023
Impfdatum
06.04.2023
Beginn
06.04.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

administration of QUADRACEL to a patient that is 10 years old (with no reported adverse event); Initial information received on 24-Apr-2023 regarding an unsolicited valid non-serious case received via other health professional. This case involves a 10 years old male patient who was administred quadracel (with no reported adverse event) The patient's past medical history, medical treatment(s), concomitant(s) and family history were not provided. On 06-Apr-2023, the patient received suspect diphtheria-15/tetanus/5 hybrid ac pertussis/ipv (mrc5) vaccine Suspension for injection at dose of 0.5 ml (lot U756AA, Expiry date: 08-Nov-2024) (strength: unknown) via intramuscular route in the right deltoid for prophylactic vaccination (immunization). On 06-Apr-2023 the patient was given quadracel to a patient that is 10 years old (product administered to patient of inappropriate age) (same day latency) (with no reported adverse event) Action taken was not applicable. At time of reporting, the outcome was Unknown 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.

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