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Reporte zur Charge XN54L

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

1Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NC 1

VAERS 1533933

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) · Charge XN54L

schwer
Staat
NC
Alter
32,0
Geschlecht
F
Eingang
07.08.2021
Impfdatum
03.10.2017
Beginn
03.10.2017
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Anaphylactic reaction Dysphagia Dyspnoea Rash macular Speech disorder Urticaria

Symptomtext

Anaphylactic Reaction /ER Visit Required; red hive's spots; shortness of breath /could not breathe / could not talk; could not swallow; could not talk; This case was reported by a other health professional via call center representative and described the occurrence of anaphylactic reaction in a 32-year-old female patient who received Flu Seasonal QIV Dresden (Influenza vaccine Quadrivalent 2017-2018 season) (batch number XN54L, expiry date unknown) for prophylaxis. On 3rd October 2017, the patient received Influenza vaccine Quadrivalent 2017-2018 season. On 3rd October 2017, 10 min after receiving Influenza vaccine Quadrivalent 2017-2018 season, the patient experienced anaphylactic reaction (serious criteria GSK medically significant), erythema urticarial, shortness of breath, unable to swallow and speech disorder. The patient was treated with ambiguous medication nos (Epipen (Nos)), benadryl (nos) (Benadryl) and steroids nos (Steroids). On an unknown date, the outcome of the anaphylactic reaction was recovered/resolved and the outcome of the erythema urticarial, shortness of breath, unable to swallow and speech disorder were unknown. It was unknown if the reporter considered the anaphylactic reaction, erythema urticarial, shortness of breath, unable to swallow and speech disorder to be related to Influenza vaccine Quadrivalent 2017-2018 season. Additional details were provided as follows: The reporter was the patient. The patient received Flu vaccine without preservatives in left deltoid. She did not know the name of the vaccine, but known that it was manufactured by GSK. The patient had an anaphylactic reaction and had to be sent to the emergency room. The patient stated that in 10 minutes, she had red hives spots and after 20 minutes she had shortness of breath, where she could not breathe, could not swallow and could not talk. The patient was given an EpiPen, Benadryl and Steroids. The patient was provided with the date 27th July 2015. The reporter consented to follow up with health care professional.

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