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Reporte zur Charge UJ877AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

11Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
NM 3 KS 1 OK 1 TX 1 GA 1 NY 1 PA 1 IL 1 MI 1

VAERS 2726311

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ877AA

mild
Staat
KS
Alter
1,0
Geschlecht
M
Eingang
21.12.2023
Impfdatum
11.12.2023
Beginn
12.12.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Ear infection Injection site mass Pyrexia Rash macular Viral infection

Symptomtext

Mother states that a day after vaccination, the pt was running a fever. 4 days after the vaccination occurred, mother took pt into PCP with c/o a fever off and on for past 3 days. The mother states that she has given the pt acetaminophen for the fever. The mother states that the pt was dx with an ear infection and prescribed amoxicillin. The mother states that there is a lump on the pt's left leg where vaccination occurred, and skin is red and splotchy all over the pt's body. The pt's PCP told the mother that "it was probably a viral infection".

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site mass
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Pt was dx with an ear infection 4 days after immunization and began taking amoxicillin for ear infection.
Vorgeschichte
NA
Andere Medikamente
Amoxicillin since 4 days after event.
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2722289

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ877AA

mild
Staat
OK
Alter
0,3
Geschlecht
F
Eingang
08.12.2023
Impfdatum
05.12.2023
Beginn
05.12.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Immediate post-injection reaction Rash Rash erythematous

Symptomtext

WITHIN A MINUTE AFTER THE ROTARIX AND VACINES WERE GIVEN, THE PATIENTS FACE STARTED BREAKING OUT IN RED PATCHES. HER CHEST AND ABDOMEN BROKE OUT AS WELL. THE RESIDENT, DR, CAME IMMEDIATELY TO CHECK VITALS, OBSERVE THE BABY, ASESS HER BREATHING AND WATCH HER. SHE ORDERED US TO ADMINISTER 2ML OF BENADRYL AND WATCH THE PT. THE RASH/RED PATCHES WENT AWAY WITHIN 10 MINUTES AND THE PT WAS NOT IN DSITRESS. DR ADVISED THAT SHE WILL BE IN HE ROOM FOR THE 6 MONTH OLF VACCINES, TO SIRECTLY OBSERVE THE PATIENT.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NONE
Vorherige Impfungen
-

VAERS 2712269

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ877AA

gering
Staat
TX
Alter
0,3
Geschlecht
F
Eingang
09.11.2023
Impfdatum
25.10.2023
Beginn
25.10.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event

Symptomtext

receiving an extra dose of PENTACEL with no reported adverse event; Initial information received on 30-Oct-2023 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This case involves a 4 months old female patient who was receiving an extra dose of 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 rotavirus vaccine for Prophylactic vaccination. On 25-Oct-2023, the patient received 0.5 ml (TOTAL) dose of suspect diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine Suspension for injection (lot- UJ877AA and expiration date- 22-Mar-2024) via intramuscular route in the right thigh (strength: not provided) for Immunisation (extra dose administered) (latency- same day). Patient inadvertently received 2 doses of IPOL and 2 doses of PENTACEL. All 4 doses received on the 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
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
ROTAVIRUS VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2710764

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ877AA

gering
Staat
NM
Alter
0,5
Geschlecht
F
Eingang
07.11.2023
Impfdatum
28.09.2023
Beginn
28.09.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product administered to patient of inappropriate age

Symptomtext

Patient received rotavirus vaccine at 6 months of age when child did not qualify for the vaccine. Child had never received a dose of rotavirus and was too old to receive it for the first time. Rotavirus should only be given to child before 15 weeks old. No symptoms or sign.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
No illnesses
Vorgeschichte
No long standing health conditions
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2708978

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ877AA

gering
Staat
NM
Alter
0,3
Geschlecht
M
Eingang
02.11.2023
Impfdatum
31.10.2023
Beginn
31.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal rigidity Crying Haematochezia Infant irritability Ultrasound abdomen normal

Symptomtext

Patient started to have flecks of blood in stool for about 24 hours and intermittent bouts of abdominal rigidity and irritability/crying. No emesis. No fever. Sent for STAT limited abdominal ultrasound, but no current sign of intussusception. Patient has had mucus in stools since birth, per mom, and frequent loose stools, but is being breastfed exclusively.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Abdominal rigidity
Hospital-Tage
-
Labordaten
Abdominal Ultrasound
Aktuelle Erkrankungen
frequent mucus in stool, loose stools
Vorgeschichte
-
Andere Medikamente
infant gas drops
Allergien
-
Vorherige Impfungen
-

VAERS 2701671

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ877AA

gering
Staat
NM
Alter
0,3
Geschlecht
M
Eingang
25.10.2023
Impfdatum
16.10.2023
Beginn
16.10.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age

Symptomtext

Patient received a flu vaccine at 4 months old. Flu vaccine is given for 6 month and older. Vaccine was administered to early. Notified mother and patient is fine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2694644

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ877AA

gering
Staat
GA
Alter
0,3
Geschlecht
F
Eingang
11.10.2023
Impfdatum
10.10.2023
Beginn
10.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Extra dose administered Infant irritability Wrong product administered

Symptomtext

Yesterday, 10/11/2023, patient received a vaccine by mistake. Patient was given Pentacel and PedvaxHib, 2 doses of Hib given. Patient was supposed to get Pentacel and Prevnar 13. Occurrence reported yesterday to RN/Practice manager. Occurrence reported today to patient's PCP and provider that saw patient yesterday, and to his nurse, MA who administered the vaccine yesterday. Patient's father was informed of occurrence, he verbalized understanding and accepted an apology. I inquired on patient, asked how she is doing, he verbalized that patient is well, acting her usual, was a little fussy yesterday after vaccines but not fussy today, overall well, eating and sleeping well, no fever. I advised patient's father to call us with any concerns or changes in patient's behavior. He was informed that patient should come in after 4 weeks to have Prevnar 13 administered, an appointment was scheduled. State notified today of occurrence.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
NONE
Allergien
none
Vorherige Impfungen
-

VAERS 2683320

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ877AA

gering
Staat
NY
Alter
1,5
Geschlecht
F
Eingang
18.09.2023
Impfdatum
08.09.2023
Beginn
08.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product preparation error

Symptomtext

administered pentacel, only the dtap/ipv component was given. caller with question on whether she could order the hib diluent in order to administer the hib portion of pentacel with no reported adverse event; Initial information received on 11-Sep-2023 regarding an unsolicited valid non-serious case received from a physician. This case involves a 1-year-old female patient who administered Diphtheria/Tetanus/5 Hybrid Ac Pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (Vero)], only the DTAP/IPV component was given 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 Influenza Vaccine for Prophylactic vaccination. On 08-Sep-2023, the patient received a dose of 0.5 ml (frequency: once) suspect Diphtheria/Tetanus/5 Hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine Suspension for injection of standard strength (lot: UJ877AA, Expiry date: 22-Mar-2024) via intramuscular route in the right thigh, only the DTAP/IPV component was given, the HIB diluent was not given and with question on whether she could order the HIB diluent in order to administer the HIB portion of Pentacel with no reported adverse event (product preparation error) (latency: same day). Action taken: not applicable. At time of reporting, the outcome was 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 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
INFLUENZA VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2667123

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ877AA

gering
Staat
PA
Alter
6,0
Geschlecht
M
Eingang
07.08.2023
Impfdatum
28.07.2023
Beginn
28.07.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

6-year-old received a dose of PENTACEL last week with no reported adverse event; Initial information was received from on 31-Jul-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 6 years old male patient who received a dose of diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine [Pentacel (vero)] last week with no reported adverse event. The patient's past vaccination(s) included measles vaccine;mumps vaccine;rubella vaccine;varicella zoster vaccine, hepatitis a vaccine, hepatitis b vaccine, Prevnar 13 and Pentacel. The patient's past medical history, medical treatment(s) and family history were not provided. Concomitant medications included pneumococcal vaccine conj 13v (crm197) (Prevnar 13) for prophylactic vaccination (immunisation); measles vaccine;mumps vaccine;rubella vaccine;varicella zoster vaccine (measles vaccine;mumps vaccine;rubella vaccine;varicella zoster vaccine) for prophylactic vaccination (immunisation); hepatitis b vaccine (hepatitis b vaccine) for prophylactic vaccination (immunisation); and hepatitis a vaccine (hepatitis a vaccine) for prophylactic vaccination (immunisation). Last week on 28-Jul-2023, a 6-year-old patient received dose 2 of suspect diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine Suspension for injection at dose of 0.5 ml once (lot number: UJ877AA, expiration date: 22-Mar-2024) via intramuscular route in the right deltoid for prophylactic vaccintation (immunisation) with no reported adverse event (product administered to patient of inappropriate age) (latency: same day). No lab data reported. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event 6-year-old received a dose of pentacel last week 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
PREVNAR 13; MEASLES VACCINE;MUMPS VACCINE;RUBELLA VACCINE;VARICELLA ZOSTER VACCINE; HEPATITIS B VACCINE; HEPATITIS A VACCINE
Allergien
-
Vorherige Impfungen
-

VAERS 2664386

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ877AA

gering
Staat
IL
Alter
0,3
Geschlecht
F
Eingang
01.08.2023
Impfdatum
26.07.2023
Beginn
26.07.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Medication error No adverse event Product preparation error

Symptomtext

administered half the dose of Pentacel only the diluent was administered, with no reported adverse event; Initial information received on 26-Jul-2023 regarding an unsolicited valid non-serious case received from a consumer. This case involves a 4 months old female patient who was administered half the dose of diphtheria/ tetanus/ 5 hybrid AC pertussis/ IPV(VERO)/ HIB(PRP/T) vaccine [Pentacel (Vero)] only the diluent was administered, 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 7V (CRM197) (Prevnar) and rotavirus vaccine live reassort ORAL 5V (Rotateq) for Prophylactic vaccination. On 26-Jul-2023, the patient received 0.5 mL dose 2 of suspect diphtheria/ tetanus/ 5 hybrid AC pertussis/ IPV (vero)/ HIB (PRP/T) vaccine, Suspension for injection (batch number: UJ877AA) (expiry date unknown) via intramuscular route in the right vastus lateralis for Immunization, half the dose of pentacel only the diluent was administered, with no reported adverse event (product preparation error) (same day latency). Action taken: was not applicable. At time of reporting, the outcome was Unknown for the event administered half the dose of pentacel only the diluent was administered, 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
Medication error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
PREVNAR; ROTATEQ
Allergien
-
Vorherige Impfungen
-

VAERS 2655478

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ877AA

gering
Staat
MI
Alter
5,0
Geschlecht
M
Eingang
12.07.2023
Impfdatum
07.07.2023
Beginn
07.07.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product administered to patient of inappropriate age

Symptomtext

9. Do you ever need help reading important papers or writing Yes

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-