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Reporte zur Charge UJ879AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

12Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
MI 4 PA 2 GA 1 TX 1 OH 1 NH 1 OR 1

VAERS 2510763

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

schwer
Staat
PA
Alter
1,0
Geschlecht
M
Eingang
08.02.2023
Impfdatum
18.08.2022
Beginn
19.08.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Anaphylactic reaction Choking Cyanosis Dyspnoea Flushing Inappropriate schedule of product administration Vaccination site rash Hyperhidrosis Oedema peripheral Respiratory symptom Skin discolouration Skin warm

Symptomtext

Anaphylaxis; Inappropriate schedule of vaccine administered; Light rash in the site of the injection; This spontaneous case was reported by a patient family member or friend and describes the occurrence of ANAPHYLACTIC REACTION (Anaphylaxis) in a 1-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. AS1412B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product INFLUENZA VACCINE (FLU [INFLUENZA VACCINE]) for an unknown indication. The patient's past medical history included Hemangioma, Eczema and COVID-19 (Patient got COVID-19 when he was 3 months old at the end of Apr2022.) in April 2022. Previously administered products included for Hemangioma: Timolol (Hemangioma treated with Timolol (beta blocker).); for Eczema: Topical Hydrocortisone (Eczema treated with topical Hydrocortisone as needed.). Past adverse reactions to the above products included No adverse effect with Timolol and Topical Hydrocortisone. On 18-Aug-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Nov-2022, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 16-Nov-2022, the patient received dose of INFLUENZA VACCINE (FLU [INFLUENZA VACCINE]) (unknown route) 1 dosage form. On 19-Aug-2022, the patient experienced VACCINATION SITE RASH (Light rash in the site of the injection). On 16-Nov-2022, the patient experienced ANAPHYLACTIC REACTION (Anaphylaxis) (seriousness criterion medically significant) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL A) on 19-Aug-2022 at a dose of UNK, Frequency After; DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL A) on 16-Nov-2022 at an unspecified dose and frequency and EPINEPHRINE (EPIPEN [EPINEPHRINE]) on 16-Nov-2022 at an unspecified dose and frequency. At the time of the report, ANAPHYLACTIC REACTION (Anaphylaxis) and VACCINATION SITE RASH (Light rash in the site of the injection) had resolved and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Patient's caregiver stated that her son received 3 other vaccines on the same day of 1st dose of Moderna but she did not remembered the names. Patient had received other vaccines in the 4 weeks prior to COVID-19 vaccine. It was assessed if it should be appropriate to go to ER but it was not needed since there was no rebound. Company Comment: This spontaneous case concerns a 1-year-old male patient, with medical history of Hemangioma, Eczema and COVID-19 (Patient got COVID-19 when he was 3 months old at the end of Apr2022) and Co-suspect product INFLUENZA VACCINE who experienced the medically significant expected event of anaphylactic reaction, the unexpected event of Inappropriate schedule of product administration event in the context of 2nd. dose of mRNA- 1273 vaccine.As the SD information, there were more than 35 days between first two doses, then Inappropriate schedule of vaccine administration was noted in this case. The expected event occurred after the 1st. dose, and the serious event the same day of the second dose. The patient was treated with BENADRYL and EPINEPHRINE and the event was resolved. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report. Events seriousness was assessed based on medical judgement.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic reaction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: COVID-19 (Patient got COVID-19 when he was 3 months old at the end of Apr2022.); Eczema; Hemangioma
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2559204

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ879AA

mild
Staat
PA
Alter
15,0
Geschlecht
F
Eingang
12.01.2023
Impfdatum
10.01.2023
Beginn
12.01.2023
Tage bis Beginn
2,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site swelling

Symptomtext

red swelling at site of covid vaccine Covid vaccine given in lower portion of arm and flu vaccine given in upper portion of arm

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
none
Vorgeschichte
Advanced bone age BMI (body mass index), pediatric, greater than or equal to 95% for age Chronic otitis media of both ears Eczema ETD (eustachian tube dysfunction) Mild persistent asthma, uncomplicated PCOS (polycystic ovarian syndrome) Precocious sexual development Secondary amenorrhea Short stature
Andere Medikamente
none
Allergien
cefzil (cefprozil)
Vorherige Impfungen
-

VAERS 2535209

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

mild
Staat
GA
Alter
55,0
Geschlecht
F
Eingang
16.12.2022
Impfdatum
15.12.2022
Beginn
15.12.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Injection site erythema Injection site pruritus Injection site swelling

Symptomtext

FLU vaccine administered to client per RN to left deltoid. About 15 min after injection, client complaining of "severe itching" at site. Redness and swelling also noted at site. Client denies shortness of breath, headache, or any other complaints. Children's Liquid Benadryl 10ml given perRn to client. Client refused adult dose. Client stated "itching", along with redness had resolved about 15 after taking Benadryl. No other complaints voiced.

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

VAERS 2512657

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

mild
Staat
TX
Alter
16,0
Geschlecht
M
Eingang
17.11.2022
Impfdatum
28.10.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Injection site erythema Injection site pain

Symptomtext

Redness to L arm post inj. 3 days - > 2", tender to touch. pt was out of town - went to urgent care - Rx - Antibiotics Bactrim

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
PCN
Vorherige Impfungen
-

VAERS 2488256

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

mild
Staat
OH
Alter
6,0
Geschlecht
F
Eingang
25.10.2022
Impfdatum
21.10.2022
Beginn
22.10.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site reaction Injection site warmth Type III immune complex mediated reaction

Symptomtext

24-hours after vaccine administration, developed 5 inch diameter area of warmth and erythema. Appears to be consistent with Arthus-reaction versus injection site reaction unrelated to hypersensitivity. Lasted ~48-38 hours.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Acute otitis media
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2629148

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

gering
Staat
MI
Alter
4,0
Geschlecht
F
Eingang
09.05.2023
Impfdatum
05.05.2023
Beginn
09.05.2023
Tage bis Beginn
4,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Patient was given a private Flu vaccine instead of a private Polio vaccine. Parent was informed, child is doing well. Patient is scheduled to receive a Polio vaccine on 5/10/23 at no charge.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2613183

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

gering
Staat
-
Alter
56,0
Geschlecht
M
Eingang
11.04.2023
Impfdatum
28.12.2022
Beginn
01.12.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered No adverse event

Symptomtext

The patient requested flu vaccine and said that he had not received the flu vaccine for this season on the day of the visit. Patient returned the next day with wife and she was requesting a second dose of the flu vaccine. She did not receive the second dose and advised only one dose per season. The patient then stated that he had received one dose in our clinic and another at an outside clinic and that he has always received 2 flu vaccines per season because his primary physician recommended receiving 2 doses. Patient was educated that we could not provide a second dose. Patient did not experience any adverse reactions. Patient received flu vaccine 10/30/2022 at an outside clinic and then received a second dose of flu vaccine on 12/28/2022 from Health Department.

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

VAERS 2609288

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

gering
Staat
MI
Alter
1,3
Geschlecht
M
Eingang
04.04.2023
Impfdatum
31.03.2023
Beginn
01.03.2023
Tage bis Beginn
-
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

Patient was given adult dose of Hep A instead of the intended pediatric dose of Hep A

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

VAERS 2579961

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

gering
Staat
NH
Alter
30,0
Geschlecht
F
Eingang
11.02.2023
Impfdatum
06.02.2023
Beginn
06.02.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product storage error Wrong technique in product usage process

Symptomtext

medication error due to the inappropriate administration of FLUZONE QIV MDV that was no longer suitable for use post excursion with no reported adverse event; Initial information received on 07-Feb-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 30 years old female patient who experienced medication error due to the inappropriate administration of fluzone qiv mdv that was no longer suitable for use post excursion with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 06-Feb-2023, the patient received 0.5 ml (frequency: once) dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (lot number: UJ879AA and expiry date: 30-JUN-2023) (strength: standard) via intramuscular route in the deltoid (unsure which arm) for Immunization. On 06-FEB-2023 the patient had medication error due to the inappropriate administration of fluzone qiv mdv that was no longer suitable for use post excursion with no reported adverse event (product storage error) (latency: same day). Action taken: not applicable. At time of reporting, the outcome was Unknown for the 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2579531

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

gering
Staat
OR
Alter
51,0
Geschlecht
M
Eingang
07.02.2023
Impfdatum
01.02.2023
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

Hep B 1ml was administered past expiration date 1/25/23; notified patient

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
CHF, Cirrhosis, anemia
Vorgeschichte
CHF, cirrhosis
Andere Medikamente
carvedilol, ergocalciferol, lactulose, Bumetanide, spironolactone, trazodone, triamcinolone, xifaxan
Allergien
Penicillins
Vorherige Impfungen
-

VAERS 2502068

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

gering
Staat
MI
Alter
48,0
Geschlecht
F
Eingang
08.11.2022
Impfdatum
08.11.2022
Beginn
08.11.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

Gave 1.0 instead of 0.5 ml

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
N/A
Allergien
NKA
Vorherige Impfungen
-

VAERS 2494114

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ879AA

gering
Staat
MI
Alter
11,0
Geschlecht
F
Eingang
31.10.2022
Impfdatum
26.10.2022
Beginn
26.10.2022
Tage bis Beginn
0,0
Dosis
7+
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect product formulation administered No adverse event

Symptomtext

Pt. was given Pfizer Monovalent instead of Pfizer Bivalent. As far as I am aware pt. has not suffered any adverse events but just only given the wrong vaccine. Our office has filled out an incident report and have contacted the manufacturer for recommendations on when/if an additional dose is needed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect product formulation administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-