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Reporte zur Charge UT8104BA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

12Reporte angezeigt
0Todesfaelle
1Hospitalisiert
1Lebensbedrohlich
0Bleibende Schaeden
MI 3 WI 2 MN 1 NH 1 PA 1 NY 1 MA 1 WV 1

VAERS 2713266

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

schwer
Staat
MI
Alter
74,0
Geschlecht
F
Eingang
13.11.2023
Impfdatum
09.11.2023
Beginn
09.11.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Confusional state Endotracheal intubation Hypophagia Intensive care Lethargy Pyrexia

Symptomtext

Granddaughter describes patient having a high grade fever (104.2) within 24 hours of receiving vaccinations. Over the course of 3 days, patient became lethargic, stopped eating/drinking, and started to become mentally confused. Patient admitted to emergency care on 11/12/23 due to declining health and continual high grade fever.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
2,0
Labordaten
Unknown currently. Daughter reports patient in ICU. Daughter reports patient intubated and currently being evaluated for meningitis. Patient is currently still admitted to hospital per daughter.
Aktuelle Erkrankungen
no reported illnesses
Vorgeschichte
Long term health problems noted but which diseases specifically is not documented
Andere Medikamente
Unknown
Allergien
No reported allergies aside from ASA, morphine, and Morphine like related meds
Vorherige Impfungen
-

VAERS 2712122

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

mild
Staat
MN
Alter
67,0
Geschlecht
F
Eingang
09.11.2023
Impfdatum
09.11.2023
Beginn
09.11.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Fall Immediate post-injection reaction

Symptomtext

Patient was feeling a little dizzy and light-headed immediately after the vaccinations and sat down for around 10-15 minutes and had a piece of candy before she tried to head out of the store. Patient made it about 20 feet before she fell down from feeling faint. The patient never lost consciousness and did not hit her head during the fall do to her partner kind of holding her up breaking her fall. Patient was immediately attended to by one of the pharmacist's on duty. Patient's legs were elevated and an ice pack was placed on patient's head. After laying on the ground for about 30 seconds, patient was already saying she was feeling better. EMS was called immediately after she fell and paramedics came on scene to make sure she was okay and to check her blood pressure. Patient and paramedics determined that she did not need to be taken to the hospital and patient left under her own power with her significant other.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
Blood pressure test performed by paramedics, unsure on the results.
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Hyperlipidemia
Andere Medikamente
Simvastatin 40 mg Omeprazole 20 mg
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2696325

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

mild
Staat
NH
Alter
88,0
Geschlecht
F
Eingang
13.10.2023
Impfdatum
12.10.2023
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash Rash erythematous

Symptomtext

Resident noted to have a pink rash - Dime sized areas on bilateral upper extremities, rash improving

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Neomycin, Actonil, Bactrim, Calcium Channel Blackouts, Clams, oysters, Beauty products Seasonal
Vorherige Impfungen
-

VAERS 2695247

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UT8104BA

mild
Staat
-
Alter
74,0
Geschlecht
F
Eingang
12.10.2023
Impfdatum
06.10.2023
Beginn
06.10.2023
Tage bis Beginn
0,0
Dosis
6
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Discomfort Feeling abnormal Malaise Nasopharyngitis Oropharyngeal pain Respiratory symptom Respiratory tract congestion

Symptomtext

sore throat; head cold; respiratory symptoms; discomfort/ Within 2.5-3 hours her head became very congested/ 07Oct2023 as she felt very lousy the whole day; her head hurt and she got worse after that; fever; her head hurt and she got worse after that; all her joints became achy and she felt sick; This spontaneous case was reported by a consumer and describes the occurrence of OROPHARYNGEAL PAIN (sore throat), NASOPHARYNGITIS (head cold), RESPIRATORY SYMPTOM (respiratory symptoms), DISCOMFORT (discomfort/ Within 2.5-3 hours her head became very congested/ 07Oct2023 as she felt very lousy the whole day) and CONDITION AGGRAVATED (her head hurt and she got worse after that) in a 74-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024) (batch no. UT8104BA) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product INFLUENZA VACCINE (FLU VACCINE VII) for an unknown indication. Previously administered products included for Product used for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (1st dose, lot number EL9269) on 31-Jan-2021, PFIZER BIONTECH COVID-19 VACCINE (2nd dose, lot number EN6201) on 21-Feb-2021, PFIZER BIONTECH COVID-19 VACCINE (3rd dose, lot number FD8810) on 21-Oct-2021, PFIZER BIONTECH COVID-19 VACCINE (4th dose, lot number FK9896) on 04-Apr-2022, PFIZER BIONTECH COVID-19 VACCINE (5th dose, lot number GH9702) on 23-Sep-2022, Influenza vaccine and Flu. Past adverse reactions to the above products included No adverse event with Flu, Influenza vaccine, PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE, PFIZER BIONTECH COVID-19 VACCINE and PFIZER BIONTECH COVID-19 VACCINE. Concurrent medical conditions included Hypothyroidism. Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) for Hypothyroidism. On 06-Oct-2023, the patient received dose of INFLUENZA VACCINE (FLU VACCINE VII) (unknown route) 1 dosage form. On 06-Oct-2023 at 6:00 PM, the patient received sixth dose of mRNA-1273.815 (SPIKEVAX 2023-2024) (unknown route) .5 milliliter. On 06-Oct-2023, the patient experienced OROPHARYNGEAL PAIN (sore throat), NASOPHARYNGITIS (head cold), RESPIRATORY SYMPTOM (respiratory symptoms), DISCOMFORT (discomfort/ Within 2.5-3 hours her head became very congested/ 07Oct2023 as she felt very lousy the whole day), CONDITION AGGRAVATED (her head hurt and she got worse after that), PYREXIA (fever), HEADACHE (her head hurt and she got worse after that) and ARTHRALGIA (all her joints became achy and she felt sick). The patient was treated with PARACETAMOL (TYLENOL) at a dose of 500 milligram. On 08-Oct-2023, CONDITION AGGRAVATED (her head hurt and she got worse after that), PYREXIA (fever) and HEADACHE (her head hurt and she got worse after that) had resolved. At the time of the report, OROPHARYNGEAL PAIN (sore throat) and DISCOMFORT (discomfort/ Within 2.5-3 hours her head became very congested/ 07Oct2023 as she felt very lousy the whole day) was resolving, NASOPHARYNGITIS (head cold) and RESPIRATORY SYMPTOM (respiratory symptoms) had not resolved and ARTHRALGIA (all her joints became achy and she felt sick) outcome was unknown. For mRNA-1273.815 (SPIKEVAX 2023-2024) (Unknown), the reporter did not provide any causality assessments. Within three hours of vaccination she came down with sore throat, head cold, respiratory symptoms, Patient uses a CPAP machine. Patient got the Spikevax on 06Oct2023 around 6:00pm together with the flu shot as the vaccine provider said it was okay to take them together. Within 2.5-3 hours her head became very congested, all her joints became achy and she felt sick, She had sore throat, her head hurt and she got worse after that. She said that before she went to bed there was a lot of discomfort and she took Tylenol 500 mg. She lost the whole day of Saturday, 07Oct2023 as she felt very lousy the whole day. Next day, 08Oct2023, when she woke, she felt as if a "cloud has been lifted off". She did not have any temperature all along, no fever. At that time of the call she still did not feel herself but she is functioning. Most recent FOLLOW-UP information incorporated above includes: On 09-Oct-2023: Live FU with significant information accepted reporter details updated, new event, medical history, historical vaccine, concomitant medication and treatment were added. I- narrative was updated

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

VAERS 2694621

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

mild
Staat
PA
Alter
72,0
Geschlecht
F
Eingang
11.10.2023
Impfdatum
19.09.2023
Beginn
20.09.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Hypersomnia

Symptomtext

Patient got extremely fatigued about 12 hours after the vaccine. She was at another doctor's appointment and they were very concerned for her getting home. She arrived home but her neighbor found her sleeping in her running car. Luckily she was not injured but she slept for the rest of the afternoon and evening. She felt better after sleeping for 12 hours.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Patient takes Tramadol Er, Alendronate, Rosuvastatin, Ozempic, Metformin ER
Allergien
Codeine
Vorherige Impfungen
-

VAERS 2689048

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

mild
Staat
NY
Alter
69,0
Geschlecht
M
Eingang
30.09.2023
Impfdatum
19.09.2023
Beginn
20.09.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site vesicles

Symptomtext

PATIENT STATES THAT HE HAD SOME LOCALIZED BLISTERING AT SITE OF INJECTION(S) THAT BEGAN ON 9/20. HE STATES THAT IT HAS NOT WORSENED.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site vesicles
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
NSAIDS, GABAPENTIN, LYRICA, NORTRIPTYLINE, CONTRAST DYE
Vorherige Impfungen
-

VAERS 2725441

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

gering
Staat
MA
Alter
72,0
Geschlecht
M
Eingang
19.12.2023
Impfdatum
19.12.2023
Beginn
19.12.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Wrong product administered

Symptomtext

There was no adverse event. Patient requested a Flu and RSV vaccine and was given a Moderna Spikevax (Covid ) and RSV vaccine. Store contacted patient post immunization and patient returned to store on same day to receive flu vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
No tests or lab work completed
Aktuelle Erkrankungen
unknown
Vorgeschichte
None
Andere Medikamente
unknown
Allergien
no known allergies
Vorherige Impfungen
-

VAERS 2724159

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

gering
Staat
WV
Alter
65,0
Geschlecht
F
Eingang
14.12.2023
Impfdatum
25.11.2023
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Hypoaesthesia

Symptomtext

The patient came in yesterday, 12/13/2023, and stated that after her vaccination, she couldn't do anything with her hand. She couldn't even hold a cup of coffee. When I was initally giving her the vaccine on 11/25/23, she told me this happened to her a few years ago with another immunizer and flu shot. She stated she went to the doctor then and the doctor stated the immunizer must have hit the radial nerve. She did not go to the physician this time. She told me yesterday that her feeling had came back in her hand. She also stated it came back much sooner this time and that it took 3 months to come back last time this happened. I'm unsure how many years have passed since this happened to her the first time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypoaesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Diabetic
Andere Medikamente
Unknown
Allergien
Penicillin
Vorherige Impfungen
It was the same event that happened this time with a flu shot. I'm unsure of when it happened.

VAERS 2709404

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

gering
Staat
MI
Alter
56,0
Geschlecht
F
Eingang
03.11.2023
Impfdatum
03.11.2023
Beginn
03.11.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

Fifty-six year old patient received high-dose flu vaccine instead of the regular-dose flu vaccine indicated for her age. No side effects or adverse reaction noted at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
COPD, seizure disorder, opioid dependence, PTSD, rheumatoid arthritis, memory deficit, bipolar disorder, tremor, nicotine dependence, unsteady gait, and hypertension
Andere Medikamente
Clonazepam, quetiapine, ropinorole, Primidone, lidocaine cream, Trelegy Ellipta, Prozac, acetaminophen, ibuprofen, lisinopril, Haldol, methadone
Allergien
No known
Vorherige Impfungen
-

VAERS 2708216

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

gering
Staat
MI
Alter
64,0
Geschlecht
M
Eingang
01.11.2023
Impfdatum
01.11.2023
Beginn
01.11.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient was given a high dose flu vaccine when he should have had regular dose flu due to age. No adverse reactions or outcomes at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Hyperlipidemia Benign hypertension Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin
Andere Medikamente
allopurinoL (ZYLOPRIM) 100 MG tablet atorvaSTATin (LIPITOR) 80 MG tablet blood sugar diagnostic (ACCU-CHEK AVIVA) Strp colchicine (COLCRYS) 0.6 mg tablet dapagliflozin (FARXIGA) 10 mg tablet gabapentin (NEURONTIN) 300 MG capsule glimepiride
Allergien
Demerol [Meperidine]Nausea And Vomiting
Vorherige Impfungen
-

VAERS 2688271

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

gering
Staat
WI
Alter
60,0
Geschlecht
M
Eingang
28.09.2023
Impfdatum
22.09.2023
Beginn
22.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

FLUZONE HD was given instead of FLUBLOK with no reported adverse event; Initial information received on 22-Sep-2023 regarding an unsolicited valid non-serious case received from an Other health professional. This case is linked to case 2023SA294371(CLUSTER). This case involves a 60 years old male patient who experienced influenza quadrival A-B high dose hv vaccine [Fluzone high-dose quadrivalent] was given instead of influenza quadrivalent recombinant vaccine [Flublok] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included pneumococcal vaccine CONJ 20V (CRM197) (prevnar 20) for Immunisation. On 22-Sep-2023, the patient received 0.7 ml dose of suspect influenza quadrival a-b high dose hv vaccine (lot UT8104BA and expiration date- 31-Jun-2024) via intramuscular route in the left arm (strength: not provided) for Immunisation and received a dose of suspect influenza quadrivalent recombinant vaccine lot number not reported via unknown route in unknown administration site (dose, route, formulation, strength, lot/batch number and expiration date: not provided) for immunization (wrong product administered) 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
PREVNAR 20
Allergien
-
Vorherige Impfungen
-

VAERS 2688270

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8104BA

gering
Staat
WI
Alter
61,0
Geschlecht
F
Eingang
28.09.2023
Impfdatum
21.09.2023
Beginn
21.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

caller says that fluzone hd was given to patient instead of flublok with no reported adverse event; Initial information was received on 22-Sep-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case is linked to case 2023SA294386(CLUSTER). This case involves 61 years old female patient who reported that caller says that influenza quadrival a-b high dose hv vaccine [Fluzone HIGH-DOSE QUADRIVALENT] was given to patient instead of influenza quadrivalent recombinant vaccine [Flublok] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 21-Sep-2023, the patient received a dose of 0.7 ml of suspect influenza quadrival a-b high dose hv vaccine (lot UT8104BA, Expiry date : 30-Jun-2024, Frequency : once, formulation, strength was unknown) via intramuscular route in the left arm for Immunization and influenza quadrivalent recombinant vaccine (dosage, formulation, strength, expiry date, lot number not reported) via unknown route in unknown administration site for prophylactic vaccination (Immunization). . On 21-Sep-2023 the patient reported that caller says that fluzone hd was given to patient instead of flublok with no reported adverse event (wrong product administered) (latency : same day). Action taken was not applicable. At time of reporting, the outcome was Unknown for the event caller says that fluzone hd was given to patient instead of flublok 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
-