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Reporte zur Charge KN3J4

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

11Reporte angezeigt
2Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IL 1 ME 1 OH 1 VA 1 PA 1 FL 1 RI 1 NJ 1 NM 1 CT 1 MI 1

VAERS 1959021

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

kritisch
Staat
IL
Alter
0,3
Geschlecht
M
Eingang
17.12.2021
Impfdatum
13.12.2021
Beginn
16.12.2021
Tage bis Beginn
3,0
Dosis
1
Route/Site
PO / MO
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Cardiac arrest Death Echocardiogram Resuscitation Unresponsive to stimuli Vomiting

Symptomtext

Morning of 12/16 family found him unresponsive in bed and noted emesis in bed. Parents started CPR. Paramedics arrived and in full arrest. Resuscitation attempted in ER for 1 hour. No cardiac activity, and resuscitation attempts stopped.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
-
Labordaten
Discussed with coroner and cause of death still pending. Autopsy had not been performed yet.
Aktuelle Erkrankungen
RSV diagnosed on 11/24/21 in the ER. He was seen twice in the ER, and admitted on 11/26 to the hospital. Required HFNC initially and discharged home 11/29/21.
Vorgeschichte
none
Andere Medikamente
Vitamin D 400 IU drops
Allergien
none
Vorherige Impfungen
-

VAERS 1939585

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

kritisch
Staat
ME
Alter
0,2
Geschlecht
M
Eingang
10.12.2021
Impfdatum
12.11.2021
Beginn
12.11.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
PO / MO
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Autopsy Death Sudden infant death syndrome

Symptomtext

Patient passed away a few days later. at the time of the 2 mo wcc patient was well and no concerns noted, patient had been ill with cold sx on 11/04/2021 and at that time flu, rsv and covid negative

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
11/04/2021 and at that time flu, rsv and covid negative waiting on autopsy report- believed to have been from SIDS
Aktuelle Erkrankungen
cold sx
Vorgeschichte
no
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 1833486

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

moderat
Staat
OH
Alter
0,1
Geschlecht
F
Eingang
01.11.2021
Impfdatum
31.10.2021
Beginn
31.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
PO / MO
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal rigidity Abdominal wall operation Aspiration Chest X-ray abnormal Condition aggravated Crying Culture Diarrhoea Faeces discoloured Frequent bowel movements Gastric aspiration procedure Gastrointestinal sounds abnormal Haematochezia Intra-abdominal pressure increased Laparoscopic surgery Nothing by mouth order Pneumatosis Pneumoperitoneum

Symptomtext

Patient inconsolable for 30 minutes. RN at bedside to assess prior to DC and pt presented with round-taunt abdomen. Bowel sounds hypoactive. Stooling x4 watery yellow/brown stools. Temp 97.5F. X-ray with pneumatosis, no free air on decub. Has been having watery stools. Emesis 10 ml. OG placed with aspiration of 30 ml feculent fluid. Bloody stool in diaper. Later decubitus film confirms small amount of free air. Will proceed with ex lap. Patient returned from OR. Surgical team noted that they did not find any perforation or ischemic bowel. No resection was performed and the abdomen was closed. Plan to extubate in AM, continue NPO, begin zosyn x 7 days and gentamicin x 2 days (if cultures remain negative).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
congenital gastroschisis -- silo placed on DOL 1 and then a sutureless closure was done on DOL 4. Patient was set to be discharged on 10/31 but then became inconsolable shortly after enteral vaccine was given.
Andere Medikamente
multivitamins with iron 0.5 ml daily
Allergien
nkda
Vorherige Impfungen
-

VAERS 2115590

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

mild
Staat
VA
Alter
0,2
Geschlecht
M
Eingang
16.02.2022
Impfdatum
09.02.2022
Beginn
09.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
PO / MO
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Immediate post-injection reaction Incorrect dose administered Vomiting projectile

Symptomtext

Projectile vomiting; Vomited prior to swallowing the complete dose; This case was reported by a nurse via call center representative and described the occurrence of vomiting projectile in a 2-month-old male patient who received Rota (Rotarix lyophilized formulation) (batch number KN3J4, expiry date 29th June 2023) for prophylaxis. Co-suspect products included rotavirus vaccine oral applicator device (Rotarix Oral Applicator Device) oral applicator for prophylaxis. On 9th February 2022, the patient received the 1st dose of Rotarix lyophilized formulation (oral) and Rotarix Oral Applicator Device. On 9th February 2022, immediately after receiving Rotarix lyophilized formulation and Rotarix Oral Applicator Device, the patient experienced vomiting projectile and incomplete dose administered. On 9th February 2022, the outcome of the vomiting projectile was recovered/resolved. On an unknown date, the outcome of the incomplete dose administered was unknown. It was unknown if the reporter considered the vomiting projectile to be related to Rotarix lyophilized formulation and Rotarix Oral Applicator Device. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional details were provided as follows: The patient was given the dose of Rotarix vaccine by Medication Technician, and he projectile vomited prior to swallowing the complete dose, which led to incomplete dose administered. The reporter stated that, they believed the patiet might have been overfed and the patient did not appear to be ill. Till the time of reporting, the patient had not been re-dosed. The Vaccine administration facility was the same as Primary reporter. The reporter consented to follow up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vomiting projectile
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2075926

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

mild
Staat
PA
Alter
0,2
Geschlecht
F
Eingang
31.01.2022
Impfdatum
04.10.2021
Beginn
04.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
PO / MO
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect route of product administration Injection site nodule Irritability

Symptomtext

Patient received an intramuscular dose of an oral vaccine. Patient recovered well without incident; she was just fussy on the day of receipt of 4 IM injections (instead of 3 with 1 oral dose) with a small knot on both sides where the injections were administered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site nodule
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Poly-Vi-Sol
Allergien
None
Vorherige Impfungen
-

VAERS 1971324

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

mild
Staat
FL
Alter
-
Geschlecht
F
Eingang
22.12.2021
Impfdatum
07.12.2021
Beginn
07.12.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
PO / MO
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Injection site pain Product administered to patient of inappropriate age Sleep disorder

Symptomtext

Vaccines were given early, during the 1 month visit. Baby was crying and fussy as per parents after the vaccines. Parents were informed by phone call, from our office, of the early vaccine dosages on the same date of administration, 12/07/2021. Father called us on 12/14/2021 to inform that baby has been fussy and not sleeping well. Father took baby to the ER on that date. Mother called on 12/15/2021 that we didn't get back to her on a call from 12/14/2021, but we did speak with father on that date. Left mother a voicemail. On 12/16/2021 Dr. called and left a voicemail for parents, in order for us to check on baby and to call us back as needed. On 12/21/2021 mother had a concern about fussiness and not sleeping, some leg pain as well. 3-way call was done and Dr. advised mother to bring in baby to our office 12/22/2021 in the morning. Also advised mother to take videos of what mother is concerned about to show the doctor during her office visit.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
Father took infant to ER on 12/14/2021, as per his reporting. Multiple phone calls were done in between vaccination date and follow up office visit on 12/22/2021. Follow up visit on 12/22/2021 at 8:30 AM showed that baby was calm, sleeping, and not crying in mother's arms during the examination. No abnormalities noted.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1944497

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge Kn3J4

mild
Staat
RI
Alter
0,3
Geschlecht
F
Eingang
13.12.2021
Impfdatum
06.12.2021
Beginn
06.12.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
PO / MO
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pyrexia Rash

Symptomtext

fever (100-102 F) 12/6-12/9, then developed rash on body 12/10

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
vitamin d
Allergien
-
Vorherige Impfungen
-

VAERS 1880287

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

mild
Staat
NJ
Alter
0,3
Geschlecht
M
Eingang
18.11.2021
Impfdatum
17.11.2021
Beginn
17.11.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
PO / MO
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash erythematous Urticaria

Symptomtext

almost immediately after all vaccines were given to patient he develop urticaria/red erythematous patches like lesions only in bilateral Lower extremities. No other lesions were noted above trunk region. No respiratory issues. No swelling. Patient was given benadryl in office and rash began to subside after monitoring patient for 15 min in the office.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash erythematous
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
unknown, infant is exclusively breastfeeding
Vorherige Impfungen
-

VAERS 1843790

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

mild
Staat
NM
Alter
0,3
Geschlecht
F
Eingang
04.11.2021
Impfdatum
04.11.2021
Beginn
04.11.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / OT
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Urticaria

Symptomtext

PATIENT DEVELOPED URTICARIA OF THE CHIN IN 15 MIN AFTER RECEIVING VACCINES. NO SWELLING OF LIPS, SHORTNESS OF BREATH, COUGH. LUNG SOUNDS ARE CLEAR BILATERALLY WITH OXYGEN LEVELS AT 100%. HIVES DID NOT SPREAD TO OTHER AREAS OF THE BODY. PATIENT WAS PROVIDED WITH DOSE OF PREDNISOLONE IN THE OFFICE. MOTHER WAS ADVISED TO PROVIDE 2 ADDITIONAL DAYS OF PREDNISOLONE STARTING TOMORROW. REVIEWED SIGNS OF ANAPHYLAXIS, MOTHER WAS ADVISED TO SEEK URGENT MEDICAL ATTENTION SOONER IF NEEDED FOR CONCERNING SIGNS AND SYMPTOMS. HIVES RESOLVED PRIOR TO PATIENT LEAVING OFFICE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
PRELONE 15MG/5ML LIQUID TAKE 2 MLS PO ONCE DAILY X 2 DAYS
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2041959

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

gering
Staat
CT
Alter
0,3
Geschlecht
M
Eingang
18.01.2022
Impfdatum
28.12.2021
Beginn
28.12.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
PO / MO
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered Product preparation issue

Symptomtext

This case was reported by a other health professional via call center representative and described the occurrence of inappropriate preparation of medication in a 4-month-old male patient who received Rota (Rotarix lyophilized formulation) (batch number kn3j4, expiry date 29th June 2023) for prophylaxis. Co-suspect products included rotavirus vaccine oral applicator device (Rotarix Oral Applicator Device) oral applicator for prophylaxis. On 28th December 2021, the patient received Rotarix lyophilized formulation (oral) and Rotarix Oral Applicator Device. On 28th December 2021, unknown after receiving Rotarix lyophilized formulation and Rotarix Oral Applicator Device, the patient experienced inappropriate preparation of medication and inappropriate dose of vaccine administered. On an unknown date, the outcome of the inappropriate preparation of medication and inappropriate dose of vaccine administered were unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional details were provided as follows: The reporter stated that the patient received only the diluent component of Rotarix vaccine, which led to inappropriate preparation of medication and Inappropriate dose of vaccine administered. The reporter denied consent to follow-up.

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

VAERS 1974766

GLAXOSMITHKLINE BIOLOGICALS · ROTAVIRUS (ROTARIX) · Charge KN3J4

gering
Staat
MI
Alter
0,2
Geschlecht
M
Eingang
23.12.2021
Impfdatum
20.12.2021
Beginn
01.12.2021
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Product administered to patient of inappropriate age

Symptomtext

MMR vaccine administered at 2 month well child visit. No known adverse outcomes.

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