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Reporte zur Charge 5Y9N9

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

6Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IL 2 WV 1 GA 1 CA 1 OK 1

VAERS 2627114

GLAXOSMITHKLINE BIOLOGICALS · HIB (HIBERIX) · Charge 5Y9N9

kritisch
Staat
WV
Alter
0,3
Geschlecht
M
Eingang
03.05.2023
Impfdatum
28.03.2023
Beginn
28.03.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Brief resolved unexplained event Dyskinesia Electrocardiogram normal Electroencephalogram normal Erythema Hypopnoea Hypotonia Laboratory test normal Mental status changes Pallor Respiratory arrest Tension Unresponsive to stimuli

Symptomtext

A FEW HOURS AFTER VACCINES HE TENSED UP, TURNED RED, ARMS AND LEGS EXTENDED. LASTED 5-10 SECONDS. HE THEN WENT LIMP, PALE, UNRESPONSIVE, THEN STOPPED BREATHING ABOUT 20 SECONDS. BACK BLOWS GIVEN BUT NO CPR. BREATHING WAS THEN SHALLOW. WAS SEEN IN ER AND ADMITTED. LABS NORMAL. NO EKG CHANGES. CARDIOLOGY FELT IT WAS NOT HEART RELATED. VIDEO EEG WAS NORMAL. WAS DIAGNOSED WITH ALTERED MENTAL STATUS + B.R.U.E.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Respiratory arrest
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
NONE
Vorgeschichte
Per CARDIOLOGY: PRE-EXITATION, POSSIBLE WPW
Andere Medikamente
NONE
Allergien
NONE
Vorherige Impfungen
-

VAERS 2664223

GLAXOSMITHKLINE BIOLOGICALS · HIB (HIBERIX) · Charge 5Y9n9

mild
Staat
GA
Alter
0,8
Geschlecht
F
Eingang
01.08.2023
Impfdatum
06.10.2022
Beginn
07.10.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site bruising Injection site pain Injection site swelling

Symptomtext

Swollen and red area in my child's left thigh after 12 hours of injection, 3rd series - same brand. Area swollen bigger than 2 inch which has covered at least 60% of her thigh. 3rd day after injection area has worsen and tendered, contacted pediatricians and answered questions asked. 4th day swelling decreased and 5th day massive bruise occurred. It looked painful however child didn't seem to avoid using the leg and no fever noticed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site bruising
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
n/a
Allergien
-
Vorherige Impfungen
-

VAERS 2691038

GLAXOSMITHKLINE BIOLOGICALS · HIB (HIBERIX) · Charge 5Y9N9

gering
Staat
CA
Alter
0,3
Geschlecht
F
Eingang
05.10.2023
Impfdatum
26.09.2023
Beginn
26.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

Hiberix expired on 7/27/2023 and was administered today; This non-serious case was reported by a nurse via call center representative and described the occurrence of expired vaccine used in a 3-month-old female patient who received Hib (Hiberix) (batch number 5Y9N9, expiry date 27-JUL-2023) for prophylaxis. On 26-SEP-2023, the patient received the 1st dose of Hiberix. On 26-SEP-2023, an unknown time after receiving Hiberix, the patient experienced expired vaccine used (Verbatim: Hiberix expired on 7/27/2023 and was administered today). The outcome of the expired vaccine used was unknown. Additional Information: GSK Receipt Date: 26-SEP-2023 The reporter reported that the patient received Hiberix vaccine which was already expired, which led to expired vaccine used. The vaccine administration facility was the same as primary reporter The reporter consented to follow up via postal.

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

VAERS 2517543

GLAXOSMITHKLINE BIOLOGICALS · HIB (HIBERIX) · Charge 5Y9N9

gering
Staat
IL
Alter
0,5
Geschlecht
U
Eingang
28.11.2022
Impfdatum
13.10.2022
Beginn
-
Tage bis Beginn
-
Dosis
3
Route/Site
- / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Skin discolouration Vaccine positive rechallenge

Symptomtext

Grey dots on legs; This case was reported by a pharmacist and described the occurrence of skin discoloration in a infant patient who received DTPa-HBV-IPV (Pediarix) (batch number TS425, expiry date unknown) for prophylaxis. Co-suspect products included dtpa-hbv-ipv vaccine pre-filled syringe device (Pediarix Pre-Filled Syringe Device) injection syringe for prophylaxis, Hib (Hiberix) (batch number 5Y9N9, expiry date unknown) for prophylaxis and PNEUMOCOCCAL 13 VALENT CONJUGATE VACCINE (PREVNAR) for prophylaxis. Previously administered products included Pediarix with an associated reaction of skin discolouration (1st dose received on 08 June 2022, from batch number X9HS4 and refer case US2022AMR171034), Hiberix with an associated reaction of skin discolouration (1st dose received on 08 June 2022, from batch number EK5Y2 and refer case US2022AMR171034), Pediarix with an associated reaction of skin discolouration (2nd dose received on 11 Aug 2022 from batch number N7HL3 and refer case US2022AMR171039) and Hiberix with an associated reaction of skin discolouration (2nd dose received on 11 August 2022 from batch number BD27G and refer case US2022AMR171039). On 13th October 2022, the patient received the 3rd dose of Pediarix, Pediarix Pre-Filled Syringe Device and the 3rd dose of Hiberix. On an unknown date, the patient received PREVNAR. On an unknown date, less than 2 months after receiving Pediarix, Pediarix Pre-Filled Syringe Device and Hiberix, the patient experienced skin discoloration. On an unknown date, the outcome of the skin discoloration was unknown. It was unknown if the reporter considered the skin discoloration to be related to Pediarix, Pediarix Pre-Filled Syringe Device and Hiberix. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Linked case(s) involving the same patient: US2022AMR171034, US2022AMR171039 Additional Information: GSK Receipt Date: 16-NOV-2022 Reporter's Comments: The patient experienced the gray dots on right thigh that have been noted on patient's legs after receiving Pediarix and Hiberix. The reporter consented to follow up. Additional supportive information: This was 1 of 19 linked cases, reported by same reporter. It was unknown if the reporter considered the skin discoloration to be related to Prevenar.; Sender's Comments: US-GSK-US2022AMR171025:Same reporter US-GSK-US2022AMR171007:Same reporter US-GSK-US2022AMR148962:Same reporter US-GSK-US2022AMR171039:Same reporter US-GSK-US2022AMR171047:Same reporter US-GSK-US2022AMR149551:Same reporter US-GSK-US2022AMR171034:Same reporter US-GSK-US2022AMR171028:Same reporter US-GSK-US2022AMR171025:Same reporter US-GSK-US2022AMR171007:Same reporter US-GSK-US2022AMR149560:Same reporter US-GSK-US2022AMR148961:Same reporter US-GSK-US2022AMR149561:Same reporter US-GSK-US2022AMR148919:Same reporter US-GSK-US2022AMR171044:Same reporter US-GSK-US2022AMR171048:Same reporter US-GSK-US2022AMR171050:Same reporter US-GSK-US2022AMR171052:Same reporter US-GSK-US2022AMR171056:Same reporter US-GSK-US2022AMR171062:Same reporter

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

VAERS 2517039

GLAXOSMITHKLINE BIOLOGICALS · HIB (HIBERIX) · Charge 5Y9N9

gering
Staat
IL
Alter
0,3
Geschlecht
U
Eingang
25.11.2022
Impfdatum
11.10.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Skin discolouration

Symptomtext

Grey dots on legs; This case was reported by a pharmacist and described the occurrence of skin discoloration in a infant patient who received DTPa-HBV-IPV (Pediarix) (batch number TS425, expiry date unknown) for prophylaxis. Co-suspect products included dtpa-hbv-ipv vaccine pre-filled syringe device (Pediarix Pre-Filled Syringe Device) injection syringe for prophylaxis and Hib (Hiberix) (batch number 5Y9N9, expiry date unknown) for prophylaxis. Concomitant products included PEDIARIX and HAEMOPHILUS B CONJUGATE VACCINE (TETANUS) (HIBERIX). On 11th October 2022, the patient received Pediarix, Pediarix Pre-Filled Syringe Device and Hiberix. On an unknown date, less than 2 months after receiving Pediarix, Pediarix Pre-Filled Syringe Device and Hiberix, the patient experienced skin discoloration. On an unknown date, the outcome of the skin discoloration was unknown. It was unknown if the reporter considered the skin discoloration to be related to Pediarix, Pediarix Pre-Filled Syringe Device and Hiberix. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Linked case(s) involving the same patient: US2022AMR171025 Additional Information: GSK Receipt Date: 16-NOV-2022 Reporter's Comments: The patient experienced gray dots on skin after receiving Pediarix and Hiberix. The reporter was consented to follow up. Additional supportive information: This was 1 of 19 linked cases, reported by same reporter.; Sender's Comments: US-GSK-US2022AMR171025:Same reporter US-GSK-US2022AMR171007:Same reporter US-GSK-US2022AMR148962:Same reporter US-GSK-US2022AMR171047:Same reporter US-GSK-US2022AMR149551:Same reporter US-GSK-US2022AMR149560:Same reporter US-GSK-US2022AMR148961:Same reporter US-GSK-US2022AMR149561:Same reporter US-GSK-US2022AMR149551:Same reporter US-GSK-US2022AMR148962:Same reporter US-GSK-US2022AMR148919:Same reporter US-GSK-US2022AMR171034:Same reporter US-GSK-US2022AMR171039:Same reporter US-GSK-US2022AMR171042:Same reporter US-GSK-US2022AMR171044:Same reporter US-GSK-US2022AMR171048:Same reporter US-GSK-US2022AMR171050:Same reporter US-GSK-US2022AMR171052:Same reporter US-GSK-US2022AMR171056:Same reporter US-GSK-US2022AMR171062:Same reporter

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

VAERS 2449564

GLAXOSMITHKLINE BIOLOGICALS · HIB (HIBERIX) · Charge 5Y9N9

gering
Staat
OK
Alter
-
Geschlecht
U
Eingang
17.09.2022
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product preparation error

Symptomtext

Hiberix reconstituted with other diluent; This case was reported by a other health professional via call center representative and described the occurrence of wrong solution used in drug reconstitution in a patient who received Hib (Hiberix) (batch number 5Y9N9, expiry date 27th July 2023) for prophylaxis. On an unknown date, the patient received Hiberix. On an unknown date, unknown after receiving Hiberix, the patient experienced wrong solution used in drug reconstitution. On an unknown date, the outcome of the wrong solution used in drug reconstitution was unknown. Additional Information: GSK receipt date: 8-Sept-2022 Reporter's comment: The reporter consented to follow-up. Additional supportive information: The patient received Hiberix dose reconstituted with a diluent from another vaccine, which led to wrong solution used in drug reconstitution.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product preparation error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-