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Reporte zur Charge UJ765AB

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

11Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
ID 2 KS 2 MT 1 WA 1 OR 1 ND 1 MD 1 NJ 1

VAERS 2192830

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

mild
Staat
MT
Alter
77,0
Geschlecht
F
Eingang
22.03.2022
Impfdatum
02.02.2021
Beginn
30.12.2021
Tage bis Beginn
331,0
Dosis
7+
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Cough Fatigue Influenza Influenza A virus test positive Malaise Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

SICK ON 12-30-2021 WITH CHEST CONGESTION, FATIGUE AND COUGH. TESTED POSITIVE FOR COVID-19 AND INFLUENZA A ON 01-01-2022. ADMITTED TO SHC ON 01-01-2022 DISCHARGED 01-05-2022

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
5,0
Labordaten
TESTED POSITIVE FOR COVID-19 AND INFLUENZA A ON 01-01-2022. PCR
Aktuelle Erkrankungen
UNKNOWN
Vorgeschichte
ASTHMA, HYPERTENSION, ARTHRITIS
Andere Medikamente
ASCORBIC, VIT B-12, VIT D3, LUTEIN, CRANBERRY PO, DIFLUCAN, FLORASTOR, BENICAR HCT, SINGULAIR, MICRO-K, DITROPAN-XL, BREOELLIPTA, VENTOLIN, ESTRACE VAGINAL, EPINEPHRINE PEN, TYLENOL
Allergien
ADHESIVES, CELERY OIL, CHOCOLATE, TOMATO, TRAMADOL, ASPRIN, AUGMENTIN, CORN, CORN REMOVER ADV, DARVOCET, DOXYCYCILIN, LATEX, LUBE-IDE, MACROBID, NEOSPORIN, NUT-FOOD, SULFA DRUGS
Vorherige Impfungen
-

VAERS 1889152

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UJ765AB

mild
Staat
WA
Alter
76,0
Geschlecht
M
Eingang
22.11.2021
Impfdatum
12.10.2021
Beginn
01.11.2021
Tage bis Beginn
20,0
Dosis
1
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood lactic acid Blood magnesium Body temperature increased C-reactive protein Cardiac ablation Chills Fatigue Fear Fibrin D dimer Full blood count Hyperhidrosis Laboratory test abnormal Metabolic function test Myalgia Pain Pain in extremity Red blood cell sedimentation rate Rheumatoid factor

Symptomtext

11/01/2021 thru 11/11/2021.. Daily sore muscles, mostly upper legs and calves, but could also be shoulders and forearms. Eventually required Tylenol 1000mg every 6 hours and Lidocaine gel. This daily pain increased daily until I feared standing or walking because this would intensify the pain. After several days, I developed chills/shakes and severe sweating. Temp ranged from normal up to 101.8. ER visit on Saturday, 11/6 and sent home after labs done. Saw PCP on 11/9, labs ordered. Cardiac ablation (scheduled) done on 11/11. Prednisone started 11/12 per PCP for abnormal lab. Aching muscles was gone until prednisone X 5 days done, then returned but more mild in forearms and upper legs. Now also severe fatigue. No temps.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
11/6: UA, Lactic acid, Blood culture, Troponin, CMP, CBC 11/09: Vit D, Sed rate, Total creatine kinase, Quant. CRP 11/11: CBC, BMP, HFP 11/14: BNP, CRP, CBC, CK total & MB, CMP, D-dimer, mag, sed rate, Troponin 11/15: CBC, CMP, CRP & rheumatoid tests
Aktuelle Erkrankungen
Cardiac arrythmia
Vorgeschichte
Cardiac arrythmia HTN Cholesterol
Andere Medikamente
Metoprol CoQ10, Vit C, Vit D3, Omega 3, Turmeric, MVI, Glucosomine, Mag Digoxin Atorvastatin Xarelto HCTZ
Allergien
Bees
Vorherige Impfungen
-

VAERS 2576879

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

gering
Staat
ID
Alter
79,0
Geschlecht
M
Eingang
07.02.2023
Impfdatum
02.02.2023
Beginn
02.02.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

expired dose of fluzone high-dose quadrivalent was administered to a patient with no reported adverse event; Initial information was received on 02-Feb-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 79 years old male patient who experienced expired dose of fluzone high-dose quadrivalent was administered to a patient with no reported adverse event while receiving vaccine influenza quadrival a-b high dose hv vaccine [Fluzone HIGH-DOSE QUADRIVALENT]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 02-Feb-2023, the patient received a Dose 1 dose of 0.7 ml of suspect influenza quadrival a-b high dose hv vaccine lot UJ765AB via intramuscular route in the left deltoid for Immunization. On 02-Feb-2023 the patient developed a non-serious event of expired dose of fluzone high-dose quadrivalent was administered to a patient with no reported adverse event (expired product administered) following the administration of influenza quadrival a-b high dose hv vaccine. Action taken not applicable. It was not reported if the patient received a corrective treatment for the event (expired dose of fluzone high-dose quadrivalent was administered to a patient with no reported adverse event). At time of reporting, the outcome was Unknown for the event expired dose of fluzone high-dose quadrivalent was administered to a patient 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2128194

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

gering
Staat
OR
Alter
-
Geschlecht
U
Eingang
19.02.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

temperature excursion due to the refrigerator door being left opened; Initial information received on 31-Jan-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case is linked to case 2022SA036034. This case involves Adult and unknown gender patient who experienced temperature excursion due to the refrigerator door being left opened while receiving vaccines influenza quadrival a-b high dose hv vaccine [fluzone high-dose quadrivalent], diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult [tenivac] and ipv (vero) [ipol] and while treated with caffeine, chlorphenamine maleate, dextromethorphan hydrobromide, ginger powder, hesperidin, licorice extract, methylephedrine hydrochloride, paracetamol [s. tac general] and althaea officinalis root, cinnamomum camphora essential oil, citrus aurantium oil, eucalyptus globulus leaf essential oil, mentha x piperita essential oil ([gardisil) The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient started taking S. TAC GENERAL (CAFFEINE, CHLORPHENAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, GINGER POWDER, HESPERIDIN, LICORICE EXTRACT, METHYLEPHEDRINE HYDROCHLORIDE, PARACETAMOL) Film-coated tablet dosage unknown (with an unknown batch number) and GARDISIL (ALTHAEA OFFICINALIS ROOT, CINNAMOMUM CAMPHORA ESSENTIAL OIL, CITRUS AURANTIUM OIL, EUCALYPTUS GLOBULUS LEAF ESSENTIAL OIL, MENTHA X PIPERITA ESSENTIAL OIL) formulation unknown dosage unknown (with an unknown batch number). On an unknown date, the patient received a dose of suspect IPV (VERO) lot T1D481M. On an unknown date, the patient received a dose of suspect DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT lot U6603AA.Exp.date: 05MAR2022 On an unknown date, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE lot UJ765AB. On an unknown date the patient developed a non-serious event " temperature excursion due to the refrigerator door being left opened" (product temperature excursion issue) (unknown latency) following the first dose intake CAFFEINE, CHLORPHENAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, GINGER POWDER, HESPERIDIN, LICORICE EXTRACT, METHYLEPHEDRINE HYDROCHLORIDE, PARACETAMOL, (unknown latency) following the first dose intake of ALTHAEA OFFICINALIS ROOT, CINNAMOMUM CAMPHORA ESSENTIAL OIL, CITRUS AURANTIUM OIL, EUCALYPTUS GLOBULUS LEAF ESSENTIAL OIL and MENTHA X PIPERITA ESSENTIAL OIL and following the administration of IPV (VERO), (unknown latency) ,DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT and (unknown latency) and of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. it was reported " reporting a temperature excursion due to the refrigerator door being left opened resulting in the blower operating continuously causing a low temperature excursion. Caller reporting FLUZONE HIGH-DOSE QUADRIVALENT, GARDISIL, IPOL, and TENIVAC at a low of 0.5C for 405 minutes. Caller unsure if any opened IPOL MDVs. See related case #: 00957378TENIVAC Lot#: U6603AA, Exp.date: 05MAR2022 No further information provided by the reporter. This is reported as potential AE because of temperature excursion. To be evaluated. Reporter relationship : HCP Product used : Not Applicable" Action taken with poliomyelitis vaccine (inactivated) (ipol), diphtheria and tetanus toxoids (tenivac), althaea officinalis root, cinnamomum camphora essential oil, citrus aurantium oil, eucalyptus globulus leaf essential oil, mentha x piperita essential oil (gardisil) and quadrivalent influenza vaccine (fluzone high-dose quadrivalent) was unknown. action taken with caffeine, chlorphenamine maleate, dextromethorphan hydrobromide, ginger powder, hesperidin, licorice extract, methylephedrine hydrochloride, paracetamol (s. tac general) was not applicable. It was not reported if the patient received a corrective treatment for the event (temperature excursion due to the refrigerator door being left opened). At time of reporting, the outcome was Unknown for the event temperature excursion due to the refrigerator door being left opened.

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

VAERS 1909225

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

gering
Staat
ND
Alter
62,0
Geschlecht
F
Eingang
30.11.2021
Impfdatum
17.11.2021
Beginn
17.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product administered to patient of inappropriate age

Symptomtext

Patient received a high dose fluzone vaccine and is not 65 or older.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1890281

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

gering
Staat
KS
Alter
63,0
Geschlecht
F
Eingang
22.11.2021
Impfdatum
25.10.2021
Beginn
25.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

High Dose Flu Vaccine given to patient that was only 63y/o

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Unsure
Andere Medikamente
Unknown
Allergien
None
Vorherige Impfungen
-

VAERS 1833391

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

gering
Staat
MD
Alter
64,0
Geschlecht
F
Eingang
01.11.2021
Impfdatum
29.10.2021
Beginn
30.10.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

NO ADVERSE REACTION WAS REPORTED

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

VAERS 1801060

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge uj765ab

gering
Staat
KS
Alter
63,0
Geschlecht
F
Eingang
20.10.2021
Impfdatum
08.10.2021
Beginn
08.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age Wrong product administered

Symptomtext

pt received fluzone HD and based on age should have received fluarix quadrivalent

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1798965

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

gering
Staat
ID
Alter
72,0
Geschlecht
F
Eingang
19.10.2021
Impfdatum
19.10.2021
Beginn
19.10.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chest discomfort Musculoskeletal discomfort

Symptomtext

Approximately 2 minutes after receiving the vaccine, patient reported feeling chest tightness and back discomfort. Patient was given a bottle of water and asked to remain seated for 15 minutes. Her symptoms resolved and patient was able to leave the premises.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest discomfort
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None listed.
Vorgeschichte
None listed,
Andere Medikamente
-
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1795223

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

gering
Staat
NJ
Alter
63,0
Geschlecht
F
Eingang
18.10.2021
Impfdatum
09.10.2021
Beginn
09.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

Patient was not 65 at time of dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1767949

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UJ765AB

gering
Staat
-
Alter
65,0
Geschlecht
M
Eingang
07.10.2021
Impfdatum
06.10.2021
Beginn
06.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered Syringe issue

Symptomtext

Administration error, an incomplete influenza vaccination was given due to syringe failure, most of the vaccine exited the hub and ran down patient's arm. The dose was repeated during the same visit, in the same arm, 1 inch away, so that patient would receive a complete dose

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