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Reporte zur Charge UH949AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

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

VAERS 2066963

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge UH949AA

moderat
Staat
IL
Alter
27,0
Geschlecht
F
Eingang
26.01.2022
Impfdatum
01.11.2013
Beginn
13.11.2013
Tage bis Beginn
12,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Fatigue Fear Hypoaesthesia Somnolence Tremor

Symptomtext

After 30 minutes of receiving both the Tdap and flu vaccine, I started shaking, felt numb in my arms and legs, and very tired. I fell asleep immediately upon my arrival home, waking up the next day around 7am. Since I receive the flu shot annually, I did not suspect it being the catalyst. Also, I had not had a reaction to the Tdap vaccine as a baby/small child, so not sure if the combination caused the adverse reactions or there was a preservative in the Tdap vaccine. I did report it to my doctor (no longer in practice), but it was a foggy recollection. Since then, I have not received the Tdap vaccine, even when pregnant (2017-2018 and 2020) in fear of a similar reaction. Due to the COVID vaccine mandates and autoimmune diseases that have rectified during my pregnancies, I was motivated to figure out what caused my severe reaction/allergy. After speaking to my current primary doctor and a pharmacist, they both suspect a filler or preservative like polysorbate-80 had caused it, which is also found in the COVID vaccines. I did not seek treatment after the reaction because I did not recall more than the above-mentioned symptoms and didn't seem to be affected thereafter.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
Possibly a common cold
Vorgeschichte
Not at the time
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1401961

SANOFI PASTEUR · TDAP (ADACEL) · Charge UH949AA

gering
Staat
-
Alter
-
Geschlecht
M
Eingang
16.06.2021
Impfdatum
24.05.2021
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

Adacel was prepared on Friday and administered on Monday by another medical assistant, but the patient changed their mind with no adverse event; Initial information received on 27-May-2021 regarding an unsolicited valid non-serious case received from other health care professional. This case involves a 35-year old male patient who got DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] was prepared on Friday and administered on Monday by another medical assistant, but the patient changed their mind with no adverse event (product use issue) [lot number: UH949AA and expiration date: 18-Nov-2022] via intramuscular route in the left deltoid unknown route in unknown administration site for prophylactic vaccination. It was unknown if the patient had any medical history, concomitant disease or risk factor, past medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications were not reported. It was an actual medication error due to product use issue (latency: unknown). It was reported that he said that a needle was attached to the syringe and that they placed the syringe with the needle attached in the refrigerator. At the time of report, no adverse event was reported. It was unknown if there were lab data/results available. Disclaimer: 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. There will be no information available regarding batch number in this case.

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