VAERS Reports UJ807AA

VAERS 2666952

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ807AA

schwer

Staat: IL
Alter: 4,0
Geschlecht: F
Eingang: 07.08.2023
Impfdatum: 01.08.2023
Beginn: 01.08.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Crying Fall Hyperhidrosis Loss of consciousness Pallor Tongue injury

Symptomtext

After vaccines were administered, patient was sitting in a chair with mom's phone while sibling was being vaccinated. Patient was alert and oriented. Mom was holding sibling on her lap on exam table while myself and another nurse were each vaccinating and a third nurse was observing. This was approximately 3-4 minutes after patient's vaccines were administered. Patient reportedly lost consciousness and fell over into a cabinet then slumped down onto the floor. Within 10-15 seconds, patient was crying and alert. She was laid on exam table for a brief examination. She was aware of her surroundings, diaphoretic and pale. A slight amount of blood was noted on left side of tongue in mouth but no other injuries were noted or palpated on head or body. Patient denied any pain or injuries. Within another minute, patient's color retuned to normal and patient was asking to go home. Mom was instructed to report incident to physician and to continue monitoring patient. After approximately 15 minutes, Mom left with patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None listed per parent
Allergien: None
Vorherige Impfungen: -

VAERS 2603337

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge uj807aa

schwer

Staat: KY
Alter: 1,3
Geschlecht: M
Eingang: 24.03.2023
Impfdatum: 22.03.2023
Beginn: 23.03.2023
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Febrile convulsion Immunisation reaction Laboratory test normal Pyrexia

Symptomtext

Patient came into office on 3/22/2023 and received vaccines pentacel and prevanar at around 2:30PM. Mother states child started to get a fever early morning on 3/23/2023. Childs fever reached 104. Mother called EMS on 3/24/23 around 4 AM due to child having high fever and febrile seizure. Child was seen at local ED and all negative for everything. ED told mother that they feel it was immunizations and to increase PO intake and to f/u with pediatrician. Mother contacted pediatric office on 3/24/2023 after discharged from ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Febrile convulsion
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: infant tylenol
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2702320

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ807AA

gering

Staat: NY
Alter: 1,0
Geschlecht: M
Eingang: 26.10.2023
Impfdatum: 16.10.2023
Beginn: 16.10.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / RL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

expired dose of pentacel was administered to a 13 month old patient with no reported adverse event; Initial information received on 16-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 13 month old male patient and reporter reported that expired dose of diphtheria/tetanus/5 Hybrid Ac Pertussis/IPV(Vero)/Hib (PRP/T) Vaccine [Pentacel (Vero)] was administered to a 13 month old patient 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 Measles Vaccine Live (Enders-Edmonston), Mumps Vaccine Live (Jeryl Lynn), Rubella Vaccine Live (Wistar Ra 27/3), Varicella Zoster Vaccine Live (Oka/Merck) (Proquad) On 16-Oct-2023, the patient received a expired dose 4 at a dose of 0.5 ml of suspect diphtheria/tetanus/5 Hybrid Ac Pertussis/IPV(Vero)/Hib (PRP/T) Vaccine Suspension for injection (strength: unknown, expiry date: 01-Oct-2023 and lot UJ807AA) via intramuscular route in the right thigh (Vastus Lateralis) as immunization (expired product administered) (latency: 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: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PROQUAD
Allergien: -
Vorherige Impfungen: -

VAERS 2698180

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ807AA

gering

Staat: WI
Alter: 4,0
Geschlecht: F
Eingang: 19.10.2023
Impfdatum: 09.10.2023
Beginn: 09.10.2023
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

Expired vaccine administered , with no reported adverse event; Initial information received on 09-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 4 years old female patient whom expired vaccine diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (VERO)] 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 measles vaccine live (enders-edmonston), mumps vaccine live (jeryl lynn), rubella vaccine live (wistar RA 27/3), varicella zoster vaccine live (OKA/MERCK) (Proquad) for Prophylactic vaccination. On 09-Oct-2023, the patient received a dose 0.5 ml of suspect Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(VERO)/HIB(PRP/T) Vaccine Suspension for injection lot UJ807AA expiry date: 01-Oct-2023 via intramuscular route in the left deltoid for immunization. On 09-OCT-2023 the patient developed expired vaccine administered , with no reported adverse event (expired product administered) on the same day following the administration of Diphtheria/Tetanus/5 Hybrid AC Pertussis/IPV(VERO)/HIB(PRP/T) Vaccine. Reportedly, :Nurse mentioned that nurse misread the expiration date on a PENTACEL vaccine, nurse though the expiration date was 10Oct2023, but it was 01Oct2023, nurse was asking if they should repeat the dose Action taken was not applicable. At time of reporting, the outcome was Unknown for the event expired vaccine 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: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PROQUAD
Allergien: -
Vorherige Impfungen: -

VAERS 2696299

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ807AA

gering

Staat: TX
Alter: 0,5
Geschlecht: M
Eingang: 16.10.2023
Impfdatum: 09.10.2023
Beginn: 09.10.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

stated that the vaccine expired on 10/1 and was administered to a child today 10/9 with no reported adverse event; Initial information received on 09-Oct-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 6-months-old male patient who was administered diphtheria/ tetanus/ 5 hybrid AC pertussis/ IPV (vero)/ HIB(PRP/T) vaccine [Pentacel (Vero)] today (10/9) that had expired on 10/1 with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant: none. On 09-Oct-2023, the patient received 0.5 mL expired dose 3 of suspect diphtheria/ tetanus/ 5 hybrid AC pertussis/ IPV (vero)/ HIB(PRP/T) vaccine, suspension for injection (Strength: standard; Frequency: once) (batch number: UJ807AA; expiry date: 01-Oct-2023) via intramuscular route in the right thigh for Immunization with no reported adverse event (expired product administered) (same day latency). 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 2696026

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ807AA

gering

Staat: MD
Alter: 4,0
Geschlecht: M
Eingang: 14.10.2023
Impfdatum: 10.10.2023
Beginn: 10.10.2023
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

child had the first dose today at 4 years old with no reported adverse event; expiration date on the box of pentacel is Oct 1, 2023 with no reported adverse event; Initial information received on 10-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 4 years old male patient who was received first dose of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)] with no reported adverse event and expiration date on the box of pentacel was oct 1, 2023 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 VARICELLA ZOSTER VACCINE (VARICELLA VACCINE) and PNEUMOCOCCAL VACCINE CONJ (PNEUMOCOCCAL CONJUGATE VACCINE) for Prophylactic vaccination (Immunization). On 10-Oct-2023, the 4 years old male patient received 0.5 mL dose 1 of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE with no reported adverse event (inappropriate schedule of product administration) and expiration date on the box was oct 1, 2023 with no reported adverse event (expired product administered) (latency: same day)(Suspension for injection) (Frequency = once) (Strength = standard) (lot UJ807AA) via intramuscular route in the left deltoid for Immunization. Action taken: not applicable. Outcome: Unknown for both the events. 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 and Regulatory Authority 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: VARICELLA VACCINE; PNEUMOCOCCAL CONJUGATE VACCINE
Allergien: -
Vorherige Impfungen: -

VAERS 2663760

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ807AA

gering

Staat: NC
Alter: 0,6
Geschlecht: M
Eingang: 31.07.2023
Impfdatum: 20.07.2023
Beginn: 20.07.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / LL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

No adverse event Product preparation error

Symptomtext

administered with the PENTACEL liquid component alone without the Hib component with no reported adverse event; Initial information received on 25-Jul-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 7 months old male patient who was administered with the diphtheria/ tetanus/ 5 hybrid AC pertussis/ IPV (vero)/ HIB(PRP/T) vaccine [Pentacel (Vero)] liquid component alone without the hib component 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 B Vaccine and Pneumococcal Vaccine for Prophylactic vaccination. On 20-Jul-2023, the patient received 0.5 mL dose 3 of suspect diphtheria/ tetanus/ 5 hybrid AC pertussis/ IPV(vero)/ HIB (PRP/T) vaccine, suspension for injection (batch number: UJ807AA; expiry date: 01-Oct-2023) via intramuscular route in the left vastus lateralis for immunization with the pentacel liquid component alone without the hib component 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 with the pentacel liquid component alone without the hib component 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: HEPATITIS B VACCINE; PNEUMOCOCCAL VACCINE
Allergien: -
Vorherige Impfungen: -

VAERS 2633914

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ807AA

gering

Staat: NY
Alter: 15,0
Geschlecht: F
Eingang: 19.05.2023
Impfdatum: 15.05.2023
Beginn: 15.05.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Medication error No adverse event Product preparation error

Symptomtext

they used sterile water to mix it with the powder when they administered pentacel/reconstitution of vaccine using an improper diluent with no reported adverse event; Initial information was received on 15-May-2023 regarding an unsolicited valid non-serious case received from a physician. This case involves 15 months old female patient who reported they used sterile water to mix it with the powder when they administered pentacel/reconstitution of vaccine using an improper diluent with no reported adverse event after receiving diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine [Pentacel (VERO)]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, hepatitis b vaccine RHBSAG (YEAST), HIB VACCINE CONJ (MENIGOCOCCAL PROTEIN), PERTUSSIS VACCINE ACELLULAR 5-COMPONENT, POLIO VACCINE INACT 3V (VERO), TETANUS VACCINE TOXOID (Vaxelis) and pneumococcal vaccine CONJ 15V (CRM197) (Vaxneuvance) for Prophylactic vaccination. On 15-May-2023, the patient received a 0.5 ml once (dose 1) of suspect diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine Suspension for injection (lot:UJ807AA, expiry date: 01-Oct-2023) (Strength: Standard) via intramuscular route in unknown administration site for Immunization. On 15-May-2023 the patient had used sterile water to mix it with the powder when they administered pentacel/reconstitution of vaccine using an improper diluent with no reported adverse event (product preparation error) same day following the administration of diphtheria/tetanus/5 hybrid ac pertussis/ipv(vero)/hib(prp/t) vaccine. Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event. 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 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: Medication error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2633913

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ807AA

gering

Staat: NY
Alter: 1,3
Geschlecht: M
Eingang: 19.05.2023
Impfdatum: 15.05.2023
Beginn: 15.05.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Medication error No adverse event Product preparation error

Symptomtext

used sterile water to mix it with the powder when they administered pentacel with no adverse event; Initial information was received on 15-May-2023 regarding an unsolicited valid non-serious case received from a physician. This case involves a 15 months old male patient who used sterile water to mix it with the powder when they administered pentacel with no adverse event while receiving vaccine DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE [PENTACEL (VERO)]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, HEPATITIS B VACCINE RHBSAG (YEAST), HIB VACCINE CONJ (MENIGOCOCCAL PROTEIN), PERTUSSIS VACCINE ACELLULAR 5-COMPONENT, POLIO VACCINE INACT 3V (VERO), TETANUS VACCINE TOXOID (VAXELIS) for Prophylactic vaccination; and PNEUMOCOCCAL VACCINE CONJ 15V (CRM197) (VAXNEUVANCE) for Prophylactic vaccination. On 15-May-2023, the patient received 0.5 ml, once dose of suspect DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE (lot UJ807AA, expiry date: 01-Oct-2023), (strength: standard) via intramuscular route in unknown administration site for Immunization. On 15-May-2023, the patient had used sterile water to mix it with the powder when they administered pentacel with no adverse event (product preparation error) same day following the administration of DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(VERO)/HIB(PRP/T) VACCINE. Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event. 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 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: Medication error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2632953

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ807AA

gering

Staat: MA
Alter: 0,2
Geschlecht: M
Eingang: 17.05.2023
Impfdatum: 08.05.2023
Beginn: 08.05.2023
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

No adverse event

Symptomtext

MD ordered Pentacel and Ipol vaccines and both were given. Child has not had any adverse reactions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: one
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2629262

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge uj807aa

gering

Staat: IA
Alter: 0,2
Geschlecht: M
Eingang: 09.05.2023
Impfdatum: 08.05.2023
Beginn: 09.05.2023
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Wrong product administered

Symptomtext

Patient was due for the HIB vaccine, but when pulling the vaccines from the fridge, a combination vaccine that had HIB in it as well as DTAP, and IPV was pulled instead of a single dose of HIB being pulled. Patient received 2 doses of DTAP and IPV since he was given another vaccine with both of those as well. Patient mother was notified of the error and reports that patient has not had any reactions and seems completely fine at this point. No treatment necessary at this time

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2612468

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ807AA

gering

Staat: NY
Alter: 0,2
Geschlecht: M
Eingang: 10.04.2023
Impfdatum: 03.04.2023
Beginn: 04.04.2023
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LL

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Bed sharing Infant irritability Lethargy

Symptomtext

Mom put the baby in bed with her at midnight because he was fussy, Mom woke up in the morning and found the baby under the covers looking lethargic. She then called 911 and baby was taken to the emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bed sharing
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: reflux, infant acne
Vorgeschichte: none
Andere Medikamente: none
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2602293

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ807AA

gering

Staat: AR
Alter: 0,2
Geschlecht: M
Eingang: 23.03.2023
Impfdatum: 21.03.2023
Beginn: 21.03.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

No adverse event Wrong product administered

Symptomtext

Menveo vaccine given instead of Prevnar (which was due) The vaccine coordinator (which is I) noticed this mistake while entering vaccines into system, taking them out of inventory. Our clinic has a interface from our EMR to system that automatically sends the vaccines when they are entered into our EMR system. The vaccine coordinator brought this to nurses attention, then discussed with provider, clinic manager, notified vaccine rep., contacted communicable disease who verified child would be ok. Nurse contacted mother. Mother reports no signs, symptoms of reaction due to injection. She will continue to monitor patient and will report any change. Advised mother to bring child in for Prevnar immunization in 2-4 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2602280

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ807AA

gering

Staat: AR
Alter: 0,2
Geschlecht: M
Eingang: 23.03.2023
Impfdatum: 21.03.2023
Beginn: 23.03.2023
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

No adverse event Wrong product administered

Symptomtext

Menveo vaccine given instead of Prevnar (which was due) The vaccine coordinator (which is I) noticed this mistake while entering vaccines into system, taking them out of inventory. Our clinic has a interface from our EMR to system that automatically sends the vaccines to system when they are entered into our EMR system. The vaccine coordinator brought this to nurses attention, then discussed with provider, clinic manager, notified vaccine rep., contacted communicable disease who verified child would be ok. Nurse contacted mother. Mother reports no signs, symptoms of reaction due to injection. She will continue to monitor patient and will report any change. Advised mother to bring child in for Prevnar immunization in 2-4 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Famotidine 0.6 ml orally daily
Allergien: -
Vorherige Impfungen: -