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Reporte zur Charge U5856AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

5Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
FL 4 CA 1

VAERS 2670362

GLAXOSMITHKLINE BIOLOGICALS · TDAP (BOOSTRIX) · Charge u5856aa

moderat
Staat
CA
Alter
55,0
Geschlecht
F
Eingang
12.08.2023
Impfdatum
28.08.2019
Beginn
28.08.2019
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Mobility decreased Pain in extremity Pyrexia

Symptomtext

s/p Shingrix IZ in 2019 she had fever, L arm pain, and her L arm has never felt the same, still has normal strength, no tingling/numbness, but feels she has to be more delicate with it and flexibility is less, demonstrates normal ROM of L shoulder as she discusses; she thinks she has an injury from her IZ

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
none
Vorgeschichte
hyperlipidemia, lower back pain, prediabetes and overweight, presbyopia
Andere Medikamente
n/a
Allergien
-
Vorherige Impfungen
-

VAERS 2418177

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U5856AA

gering
Staat
FL
Alter
-
Geschlecht
M
Eingang
23.08.2022
Impfdatum
05.08.2022
Beginn
05.08.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

got doses out of the box of expired Tenivac single-dose syringes with no reported adverse event; Initial information received on 15-Aug-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case is linked to case 2022SA340295. This case involves a 25 years old male patient who got dose out of the box of expired DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT [TENIVAC] single-dose syringes with no reported adverse event while receiving vaccine The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 05-Aug-2022, the patient got a dose from out of the box of expired suspect DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT, single dose syringe (expired product administered) (latency: same day) , (dose:0.5ml) (frequency: once) ( lot: U5856AA ; expiry date: 26-Jan-2020) via intramuscular route in the left deltoid for immunization. There was no other event reported Action taken : not applicable. Outcome: unknown 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 guidelines. 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 2418176

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U5856AA

gering
Staat
FL
Alter
73,0
Geschlecht
F
Eingang
23.08.2022
Impfdatum
25.07.2022
Beginn
25.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

expired TENIVAC was administered with no reported adverse event; Initial information received on 15-Aug-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case is linked to case 2022SA340295(CLUSTER). This case involves a 73 years old female patient to whom expired diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult [Tenivac] was administered with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 25-Jul-2022, the patient received a expired 0.5 ml dose of suspect diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult, suspension for injection, once, (strength: unknown) (lot U5856AA: expiry date: 26-Jan-2020) via intramuscular route in the right arm for Immunization was administered with no reported adverse event (expired product administered) (latency; same day) Action taken : not applicable. Outcome : Unknown. 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 guidelines. 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 2415729

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U5856AA

gering
Staat
FL
Alter
27,0
Geschlecht
M
Eingang
19.08.2022
Impfdatum
05.08.2022
Beginn
05.08.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

got doses out of the box of expired tenivac single-dose syringes with no adverse event; Initial information received on 15-Aug-2022 regarding an unsolicited valid non-serious case received from a pharmacist. Agency Inquiry Number: 01235545 This case involves a 27-year-old male patient who got doses out of the box of expired Diphtheria-2/Tetanus-5 Adsorbed Toxoids No Preservative Adult [Tenivac] single-dose syringes with no adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. This case is linked to cases 2022SA342354, 2022SA341716, and 2022SA340696. On 05-Aug-2022, the patient received suspect Tenivac single-dose syringes at dose 0.5ml once via intramuscular route in the left deltoid (lot U5856AA, expiry date: 26-Jan-2022) for immunization (expired product administered) same day latency. No adverse event was reported. 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2415727

SANOFI PASTEUR · TD ADSORBED (TENIVAC) · Charge U5856AA

gering
Staat
FL
Alter
43,0
Geschlecht
M
Eingang
19.08.2022
Impfdatum
25.07.2022
Beginn
25.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

got doses out of the box of expired tenivac single-dose syringes with no reported adverse event; Initial information received on 15-Aug-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 43 years old male patient who got dose out of the box of expired diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult [Tenivac] single-dose syringes with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 25-Jul-2022, the patient received 0.5 mL dose of suspect diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult single-dose syringes (lot U5856AA, expiry date: 26-Jan-2020) via intramuscular route in the left deltoid for immunization. On 25-Jul-2022, the patient got dose out of the box of expired diphtheria-2/tetanus-5 adsorbed toxoids no preservative adult single-dose syringes with no reported adverse event (expired product administered). It was reported, "would like to verify an expiration date on a box of TENIVAC SINGLE-DOSE SYRINGES that was confusing. Pharmacist states that the expiration date is 26Jan20. Pharmacist asking about the follow-up and if someone should get another dose if they were to get an expired dose of the vaccine. Pharmacist states that four people got doses out of the box of expired TENIVAC SINGLE-DOSE SYRINGES". Action taken was 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-