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Reporte zur Charge U8041CA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

13Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 6 NM 3 WA 2 NV 1

VAERS 2699663

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

schwer
Staat
CA
Alter
9,0
Geschlecht
F
Eingang
20.10.2023
Impfdatum
20.10.2023
Beginn
20.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood pressure decreased Presyncope

Symptomtext

Influenza vaccine administered at 3:10, right deltoid, patient had a vasovagal reaction within 5 seconds. Team Alert called, patient moved to reclining chair, blood pressure and monitoring ensured. Team Alert team monitored patient, Patient transported to ED via ambulance about 20 minutes later due to dropping blood pressure.

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

VAERS 2688099

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

schwer
Staat
CA
Alter
15,0
Geschlecht
M
Eingang
28.09.2023
Impfdatum
27.09.2023
Beginn
27.09.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Analgesic drug level therapeutic Blood alcohol normal Blood electrolytes normal Chest X-ray normal Computerised tomogram head normal Electrocardiogram normal Foaming at mouth Resuscitation Seizure Toxicologic test normal Troponin normal Unresponsive to stimuli Vomiting

Symptomtext

Developed Seizure starting at 10:13 PM, had 6 witnessed convulsions lasting up to 30 seconds, resolved by 10:26 PM. Seizures were resolved after 13 minutes when Grandmother came and found him unresponsive and foaming at mouth. She performed CPR, causing him to vomit and breathe. Brought to the ED. Returned to baseline and had no seizures in the 16 hours since. Patient also on atomoxetine 18mg and clonidine 0.1 mg for ADHD; atomoxetine may be aswsociated with seizures.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
1,0
Labordaten
Had normal electrolytes, normal EtOH, tylenol, salicylate screen; normal CT head, EKG/Troponin and CXR. At 9/26, had negative urine toxicity.
Aktuelle Erkrankungen
9/26: Recent EtOH intoxication (first time), agitated, resolved without intervention that day
Vorgeschichte
ADHD
Andere Medikamente
Atomoxetine 18mg daily Clonidine 0.1mg daily
Allergien
none known
Vorherige Impfungen
-

VAERS 2715028

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

moderat
Staat
CA
Alter
48,0
Geschlecht
F
Eingang
17.11.2023
Impfdatum
03.10.2023
Beginn
03.10.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Injected limb mobility decreased Injection site pain

Symptomtext

Pt reports that deltoid area hurt unusually during vaccine and shortly after developed pain and decreased range of motion of L shoulder. We were advised of this by pt. 5 weeks post vaccine-- decreased range was still an issue and pain, particularly sleeping on Left side. Exam showed passive ROM limited to 90 degrees flexion and 90 degrees abduction, o/w normal at this time, with tenderness at lower deltoid insertion. Per pt report via email at 6 weeks post vaccination, both pain and range were improving.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2695370

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge U8041CA

moderat
Staat
NM
Alter
62,0
Geschlecht
F
Eingang
12.10.2023
Impfdatum
12.10.2023
Beginn
12.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Palpitations Paraesthesia

Symptomtext

Pt c/o tingling in bilateral hands and heart racing resolved within 5 minutes of the initial response; no complaints of any other symptoms; pt observed for 30 minutes Vitals Obtained: initial vitals B/P 140/72 HR=100-107, R=22, 02 sat 99-100 on Room air Final Vitals: HR=67 02 sat 98% on Room Air

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
Noe
Aktuelle Erkrankungen
None
Vorgeschichte
Hypertension, hyperlipidemia, prediabetes, allergies, hypothyroidism, hxo breast cancer
Andere Medikamente
Metformin 1000mg po daily, Losartan Potassium 50mg po daily, Levothyroxine Na 75mcg po daily, Crestor 20mg po daily, Allergra 180mg po at bedtime for allergies, Flonase 50mcg nasal prn for allergies, Benadryl 25mg po prn
Allergien
None
Vorherige Impfungen
-

VAERS 2712663

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

mild
Staat
CA
Alter
61,0
Geschlecht
M
Eingang
10.11.2023
Impfdatum
30.10.2023
Beginn
31.10.2023
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Magnetic resonance imaging Vision blurred

Symptomtext

Patient reported experiencing dizziness and blurry vision to both eyes the day after receiving the vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
MRI on Nov. 3, 2023
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
none noted
Vorherige Impfungen
-

VAERS 2707356

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

mild
Staat
NM
Alter
10,0
Geschlecht
M
Eingang
31.10.2023
Impfdatum
31.10.2023
Beginn
31.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Nausea

Symptomtext

Vaccine given at school vaccine clinic. Patient felt nauseated about 20-25 minutes after receiving the vaccine. No itching, swelling, hives of mouth, lips or tongue, or anywhere else. Pt did not vomit. VS stable. ER precautions reviewed with school nurse. Parents were called and pt will wait in nurses' office until they come to pick him up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Nausea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
No Known Allergies
Vorherige Impfungen
-

VAERS 2707351

GLAXOSMITHKLINE BIOLOGICALS · INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) · Charge U8041CA

mild
Staat
NM
Alter
12,0
Geschlecht
F
Eingang
31.10.2023
Impfdatum
27.10.2023
Beginn
27.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Abdominal pain Chills Nausea Vomiting

Symptomtext

Patient experienced nausea, abdominal pain, chills, emesis x1(unwitnessed) about 30 minutes post vaccine administration. Pt denies sudden weakness, SOB, hives, dizziness, changes in vision or speech. Pt reports she has experienced this with Covid vaccine and but not with Flu. School nurse present and evaluated patient immediately. VS taken and patient kept at nurses office for observation. See VS log. School nurse reports she will observe patient and update patient parent on incident. School nurse educated about call 911 if patient experiences difficulty breathing, swelling tongue, lips or throat, drop in blood pressure, increased HR.

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

VAERS 2696998

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge u8041ca

mild
Staat
CA
Alter
56,0
Geschlecht
F
Eingang
17.10.2023
Impfdatum
07.10.2023
Beginn
08.10.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Candida infection Diarrhoea Dizziness Fatigue Headache Nausea

Symptomtext

The day after flu vaccine 10/8/23 I woke up with headache, nausea, diarrhea, continue with headache, fatigue, dizziness, two days later developed thrush. Provider prescribed Nystatin oral suspension. As of today 10/17/23, feel little better. Two of my daughters also received the flu vaccine same day same one also developed thrush.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Diarrhoea
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
asthma
Andere Medikamente
none
Allergien
sulfa, sea food and nuts
Vorherige Impfungen
-

VAERS 2724889

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

gering
Staat
NV
Alter
53,0
Geschlecht
M
Eingang
18.12.2023
Impfdatum
14.12.2023
Beginn
14.12.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

duplicate dose

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
diabetes
Andere Medikamente
many
Allergien
-
Vorherige Impfungen
-

VAERS 2712273

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

gering
Staat
WA
Alter
71,0
Geschlecht
F
Eingang
09.11.2023
Impfdatum
11.10.2023
Beginn
11.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

inadvertently administered Fluzone qiv instead of the intended Fluzone high dose qiv with no reported adverse event; Initial information was received on 30-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 71 years old female patient who received inadvertently administered influenza quadrival a-b vaccine (fluzone qiv) instead of the intended influenza quadrival a-b high dose hv vaccine [Fluzone HIGH-DOSE QUADRIVALENT] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 11-Oct-2023, the patient received a unknown dose of suspect influenza quadrival a-b high dose hv vaccine (strength, expiry date, formulation, lot number not reported) via unknown route in unknown administration site and also received a dose of 0.5 ml of suspect influenza quadrival a-b vaccine (Suspension for injection) (lot U8041CA, Expiry date : 30-Jun-2024, strength was unknown) via intramuscular route in the arm not otherwise specified for all Immunization and inadvertently administered fluzone qiv instead of the intended fluzone high dose qiv with no reported adverse event (wrong product administered) (latency : same day). The information on batch number was requested. Action taken was not applicable. At time of reporting, the outcome was Unknown for the event inadvertently administered fluzone qiv instead of the intended fluzone high dose qiv with no reported 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.

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

VAERS 2700995

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

gering
Staat
CA
Alter
39,0
Geschlecht
F
Eingang
24.10.2023
Impfdatum
20.10.2023
Beginn
20.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Throat clearing Throat irritation

Symptomtext

within 10 minutes of administration c/o throat itching and clearing, given 10mg of claritin PO per MD, after 10 minutes still itching MD ordered 8mg of oral methylprednisolone, around 25 minutes throat feeling worse so EMS called and auto injector epi pen 0.3mg was self administered. Left via EMS at 1200.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Throat clearing
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
peanuts, tree nuts, coconuts, IV contrast, poinsettias, easter lilies.
Vorherige Impfungen
-

VAERS 2698511

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge U8041CA

gering
Staat
WA
Alter
44,0
Geschlecht
M
Eingang
19.10.2023
Impfdatum
19.10.2023
Beginn
19.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Vaccination site erythema Vaccination site haemorrhage Vaccination site induration Vaccination site swelling

Symptomtext

At time of vaccine administration, a small hard red bump formed and was approximately 2 cm across as well as minor bleeding that stopped after 1 min of direct pressure. The patient did not report any pain nor did they report any symptoms of anaphylaxis type symptoms (itching/swelling of the face/neck/throat). No treatments were provided for the bump that formed. I monitored the patient for 15 minutes and patient did not complain of any further issues surrounding the swelling/bump formation. I advised the patient to monitor and seek medical care if swelling increased, new pain develops or if any other concerning symptoms developed. Patient did not need any assistance to their vehicle and seemed in well when leaving the clinic.

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

VAERS 2689593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge U8041CA

gering
Staat
-
Alter
33,0
Geschlecht
F
Eingang
02.10.2023
Impfdatum
27.09.2023
Beginn
29.09.2023
Tage bis Beginn
2,0
Dosis
5
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Stomatitis

Symptomtext

Developed an oral mucositis two days after vaccination. Resolved a few days later.

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