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Reporte zur Charge UJ507AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 2 MA 1 NJ 1

VAERS 1181858

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AA

moderat
Staat
MA
Alter
52,0
Geschlecht
F
Eingang
08.04.2021
Impfdatum
10.11.2020
Beginn
11.11.2020
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Hypopnoea Injected limb mobility decreased Injection site erythema Injection site pain Injection site swelling Lymphadenopathy Migraine Mobility decreased Muscle contracture Myalgia Rash

Symptomtext

A) Within 8 hours after injection: redness, swelling and pain at injection site (upper right arm); feeling tired. B) Overnight: swelling and redness continued to spread from neck to elbow. Swelling of lymph nodes under right arm and right side of neck. Muscle pain in arm, neck and shoulder, migraine. Rash. C) Over the following 2 days, symptoms continued to worsen: swelling of lymph nodes on both sides of the neck, under left and right arm (right more painful than left) and lymph nodes near pubic area - right side. Excruciating pain in all muscles of the body, particularly neck, head, right side of the torso and right arm. This affected my ability to breathe (shallow breath, unable to take a deep breath). Mobility extremely reduced for 24 hours (unable to switch from left to right side in bed, unable to sit, get up, walk and grab objects). I had to let myself fall off my bed, then crawled on all 4 to the kitchen to get a glass of water. Eventually, the muscles of my right arm contracted, bringing my right hand almost to the level of my right shoulder. I remained paralyzed in that position for the next 3 days. Symptoms started to disappear after 4 days. It took a total of 10 days to recover full mobility of my right arm. Traces of the rash are still visible 5 months after injection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
None. While I had the symptoms, I was unable to reach a phone and call anyone. Once they started to fade away, there was no point in calling anybody.
Aktuelle Erkrankungen
None.
Vorgeschichte
ADHD, Depression
Andere Medikamente
buPROPion XL 150 mg tablet; Claritin 10 mg tablet; cloNIDine 0.1 mg tablet; rosuvastatin 10 mg tablet; Vyvanse 70 mg capsule; WOMEN'S daily vitamin oral
Allergien
Allergy to pollen.
Vorherige Impfungen
-

VAERS 2608134

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AA

mild
Staat
-
Alter
34,0
Geschlecht
F
Eingang
26.02.2021
Impfdatum
03.11.2020
Beginn
03.11.2020
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Hypoaesthesia Pain Pain in extremity Pruritus Skin warm

Symptomtext

pain, itching in fingers,numbness Narrative: She reports reaction to injection.She states that her arm is very painful,warm to touch and is experiencing numbness and itching in her fingers. She denies difficulty breathing,CP.

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

VAERS 1008432

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AA

mild
Staat
NJ
Alter
35,0
Geschlecht
M
Eingang
06.02.2021
Impfdatum
27.01.2021
Beginn
27.01.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

Within 30 minutes of injection patient experiences hives on both arms. Hives spread over the mid section and legs over the next 24 hours. Reaction was treated with Prednisone, Benadryl, and Zyrtec. Hives reduced, but persisted for 8 days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
food allergies: Avocado , melon
Vorherige Impfungen
-

VAERS 1384808

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ507AA

gering
Staat
MI
Alter
-
Geschlecht
F
Eingang
09.06.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product storage error

Symptomtext

patient was given products that were exposed to highest temperature excursion at 49 fahrenheit and for 45 minutes/ No AE; Initial information received on 12-May-2021 regarding an unsolicited valid non-serious case received from a other health care professional via Agency. This case is linked to case 2021SA178936 (consumer case). This case involves an unknown age female patient who was given INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] pre-filled syringe lot number: UJ562AA expiration date: 30-Jun-2021, lot number: UJ507AA expiration date: 30-Jun-2021, lot number: UJ471AA expiration date: 30-Jun-2021, lot number: UT7073KA expiration date: 30-Jun-2021, lot number: UT7115KA expiration date: 30-Jun-2021, INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE QUADRIVALENT MULTIDOSE] lot number: UJ507AA expiration date: 30-Jun-2021, DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] lot number: U676AA expiration date: 31-Jul-2022, lot number: U6900AA expiration date: 18-Nov-2022, lot number: U6927AA expiration date: 28-Jan-2023, MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE [MENACTRA] lot number: U6827BB expiration date: 18-Feb-2022, lot number: U6827BA expiration date: 18-Feb-2022, IPV (VERO) [IPOL] MULTI DOSE VIAL lot number: T1D482N expiration date: 25-Jul-2022, DIPHTHERIA-15/TETANUS/5 HYBRID AC PERTUSSIS/IPV (MRC5) VACCINE [QUADRACEL] lot number: C5688AA expiration date: 26-Nov-2021 and DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] lot number: UJ529A expiration date: 22-Jul-2022 for prophylactic vaccination and was tested with TUBERCULIN TEST [TUBERSOL] lot number: C5804AA expiration date: 03-Feb-2023 for tuberculin test via an unknown route and administration site that was exposed to highest temperature excursion at 49 Fahrenheit and for 45 minutes (Product storage error). The patient's medical history, medical treatments, vaccinations, concomitant medications and family history were not provided. It was an actual medication error due to incorrect product storage (latency: same day). Description: Clinical coordinator called to report stability information of vaccines exposed to temperature excursion. On 09-Apr-2021, the highest temperature was at 49 Fahrenheit and the excursion lasted 45 minutes. On 23-Apr-2021, the highest temperature was at 48.7 Fahrenheit and the excursion lasted 30 minutes. Reason for excursion is that the fridge was not closed correctly, it did not shut all the way. Product used. At the time of report, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holders 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
TUBERSOL
Allergien
-
Vorherige Impfungen
-

VAERS 1022156

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE) · Charge UJ507AA

gering
Staat
MI
Alter
22,0
Geschlecht
F
Eingang
11.02.2021
Impfdatum
20.01.2021
Beginn
20.01.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Wrong product administered

Symptomtext

22 year old patient received FLUZONE HD/ NO AE; 22 year old patient received FLUZONE HD/ NO AE; a patient received FLUZONE QUAD and FLUZONE HD on same day/ NO AE; Initial information regarding an unsolicited valid non-serious case was received from a Pharmacist via Agency(Reference number- 00438020) via call-center and transmitted to Sanofi on 20-Jan-2021. This case involves a 22-years-old female patient who received 0.5 mL INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (batch number and expiry date not reported) in right deltoid and INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE] (batch number: UJ507AA and expiry date: 30-Jun-2021) in left deltoid on same day 20-Jan-2021 for prophylactic vaccination (extra dose administered, product administered to patient of inappropriate age and overdose). The patient's medical history, past medical treatment, vaccination, concomitant medication and family history were not provided. It was an actual medication error case due to extra dose administered, overdose and inappropriate age at vaccine administration (latency: same day). Patient received no other vaccines or medications. At the time of reporting, no adverse event was reported. 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 on the batch number for FLUZONE HIGH-DOSE QUADRIVALENT for this case.

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