Zurueck zur Suche

Reporte zur Charge UJ613AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
GA 1 MO 1 CT 1 TN 1 TX 1 ME 1

VAERS 2379108

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ613AA

moderat
Staat
GA
Alter
0,3
Geschlecht
M
Eingang
22.07.2022
Impfdatum
21.07.2022
Beginn
21.07.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Blood magnesium normal Blood phosphorus normal Differential white blood cell count normal Full blood count normal Metabolic function test normal Musculoskeletal stiffness Tremor Unresponsive to stimuli

Symptomtext

1 hour after vaccines, child was sitting in his carrier when his arms and legs were stiff and shaking for approximately 3 minutes. unresponsive during episode.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
Labs done on 07/21/2022: CBC w/ diff, CMP, Magnesium, Phosphorus- all WNL
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
clindamycin palmitate HCI 75mg/mL oral solution
Allergien
none known
Vorherige Impfungen
-

VAERS 2515973

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ613AA

mild
Staat
MO
Alter
1,1
Geschlecht
M
Eingang
24.11.2022
Impfdatum
23.11.2022
Beginn
01.11.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Rash Urticaria

Symptomtext

Patient received vaccine at 1249 then proceeded to develop urticaria and welts to LE. By the following morning the rash involved the trunk, legs, neck, and face.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
Treated supportively with benadryl.
Aktuelle Erkrankungen
None
Vorgeschichte
Prematurity, trach and vent dependence, oral dysphagia, retinopathy of prematurity, hypothyroid
Andere Medikamente
Fluticasone inhaler, levothyroxine, MVI with iron, Synagis: last dose 11/3/2022
Allergien
None
Vorherige Impfungen
milder rash from influenza

VAERS 2409982

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ613AA

mild
Staat
CT
Alter
1,3
Geschlecht
M
Eingang
12.08.2022
Impfdatum
12.08.2022
Beginn
12.08.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Urticaria

Symptomtext

Acute urticaria; Benadryl

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

VAERS 2590722

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ613AA

gering
Staat
TN
Alter
1,0
Geschlecht
F
Eingang
03.03.2023
Impfdatum
27.02.2023
Beginn
27.02.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

she administered an expired vaccine to a patient with no reported adverse event; Initial information was received on 27-Feb-2023 and live follow up received on same date both were processed together regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 1 years old female patient who was treated with expired DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] 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 HEPATITIS A VACCINE (HEPATITIS A) ; MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE (MMR) for Immunisation; VARICELLA ZOSTER VACCINE (VARICELLA VACCINE); and PNEUMOCOCCAL VACCINE CONJ 13V (CRM197) (PREVNAR 13) for Immunisation. On 27-Feb-2023, the patient received total 0.5 ml of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE (lot UJ613AA and expiry 25-Feb-23) (expired product administered, latency same day) (strength: unknown) via intramuscular route in the left thigh for immunization. At time of reporting, the outcome was Unknown for the event she administered an expired vaccine 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
HEPATITIS A; MMR; VARICELLA VACCINE; PREVNAR 13
Allergien
-
Vorherige Impfungen
-

VAERS 2387934

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ613AA

gering
Staat
TX
Alter
-
Geschlecht
U
Eingang
25.07.2022
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 with no adverse event; Initial information received on 18-Jul-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case is linked to case 2022SA290846. This case involves a patient (unknown age and gender) who reported temperature excursion with no adverse event while receiving vaccines DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT [TENIVAC], DIPHTHERIA-15/TETANUS/5 HYBRID AC PERTUSSIS/IPV (MRC5) VACCINE [QUADRACEL], DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL], MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE [MENQUADFI], DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE [DAPTACEL], DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] and HIB (PRP/T) VACCINE [ActHIB]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a dose of suspect HIB (PRP/T) VACCINE lot number not reported via unknown route in unknown administration site, DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE llot C5873AA; Expiration: 30-Jun-2023 ), ODIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE, MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE (lot U7249AB; Expiration: 11-Mar-2024 ), DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE (lot UJ613AA; Expiration: 25Feb2023 ), DIPHTHERIA-15/TETANUS/5 HYBRID AC PERTUSSIS/IPV (MRC5) VACCINE , DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT l(strength, dose, formulation, route, lot number: not reported) all for immunization. On an unknown date the patient reported temperature excursion with no adverse event (product storage error) (unknown latency) following the administration of HIB (PRP/T) VACCINE, DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE, DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE, MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE, DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE, (DIPHTHERIA-15/TETANUS/5 HYBRID AC PERTUSSIS/IPV (MRC5) VACCINE and DIPHTHERIA-2/TETANUS-5 ADSORBED TOXOIDS NO PRESERVATIVE ADULT. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event temperature excursion with no 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
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2370764

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ613AA

gering
Staat
ME
Alter
1,3
Geschlecht
M
Eingang
15.07.2022
Impfdatum
15.07.2022
Beginn
15.07.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product administered to patient of inappropriate age

Symptomtext

6-month to 4-year-old COVID-19 vaccine (dose #1) pulled from the system and entered into the medical record incorrectly as Pfizer instead of Moderna, which patient received 6/25/2022. On this basis, given COVID-19 Pfizer dose #2 in office today. After receiving the vaccine, parent asked what the course of action was, whether they needed a dose 3 in the series or not. Advised parent I would call them once I could speak with the provider. Informed provider of what happened. Contacted CDC, Pfizer manufacturer and Moderna manufacturer to determine next steps. I was directed to CDC website, where instructions where found: "Children ages 6 months to 4 years who receive different mRNA products for the first 2 doses of an mRNA COVID-19 vaccine series should follow a 3-dose schedule. A third dose of either mRNA vaccine should be administered 8 weeks after the second dose to complete the 3-dose primary series." Relayed this information to patient's PCP, and per provider, called parent and scheduled for them to receive the Pfizer #3, 8 weeks from today.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
None needed.
Aktuelle Erkrankungen
-
Vorgeschichte
None
Andere Medikamente
Zyrtec (a few days prior, not currently)
Allergien
None
Vorherige Impfungen
-