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Reporte zur Charge GN2778

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

14Reporte angezeigt
0Todesfaelle
2Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
OK 2 MI 2 CO 2 TN 2 MD 1 PA 1 AZ 1 UT 1 NJ 1

VAERS 2699436

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

schwer
Staat
OK
Alter
-
Geschlecht
M
Eingang
20.10.2023
Impfdatum
21.08.2023
Beginn
22.08.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Abdominal X-ray Aspartate aminotransferase increased Endoscopy gastrointestinal normal Gastrointestinal pathogen panel Haematemesis International normalised ratio normal Melaena Metabolic function test abnormal Thrombosis Vomiting White blood cell count normal X-ray normal

Symptomtext

Vomiting bright red blood and clots on early AM 8/25; develop melena; Thrombosis; Vomited on day following vaccines (8/22) improved some within 2 days then vomiting bright red blood and clots on early AM 8/25, progressed to coffee ground emesis by 8am 8/25; Aspartate aminotransferase increased; Metabolic function test abnormal; Gastrointestinal pathogen panel; Abdominal X-Ray; Admitted on 8/25, endoscopy done and no source of bleeding; White blood cell count normal; X-Ray normal; International normalised ratio normal; This case was retrieved during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-OCT-2023 with the following VAERS primary ID 2683641-1. The original narrative from the sender is as follows: Vomited on day following vaccines (8/22) improved some within 2 days then vomiting bright red blood and clots on early AM 8/25, progressed to coffee ground emesis by 8am 8/25 and then developed melena. Admitted on 8/25, endoscopy done and no source of bleeding. Resolved within 1-2 days, discharged on 8/30. The reporter did not provide an assessment of the causal relationship between Vaxelis and the reported events Vomiting, Haematemesis, Melaena, and Thrombosis. The causal relationship between Vaxelis and the reported events Aspartate aminotransferase increased, Metabolic function test abnormal, Gastrointestinal pathogen panel, Abdominal X-Ray, Endoscopy gastrointestinal normal, White blood cell count normal, X-Ray normal, and International normalised ratio normal was assessed as not applicable, due to the nature of these events. No further information is expected. COMPANY COMMENT: Vomiting, Haematemesis, Melaena, and Thrombosis were assessed as serious due to hospitalization, whereas Aspartate aminotransferase increased, Metabolic function test abnormal, Gastrointestinal pathogen panel, Abdominal X-ray, Endoscopy gastrointestinal normal, White blood cell count normal, X-ray normal, and International normalised ratio normal were assessed as non-serious. Vomiting is listed, whereas Haematemesis, Melaena, Thrombosis, Aspartate aminotransferase increased, Metabolic function test abnormal, Gastrointestinal pathogen panel, Abdominal X-ray, Endoscopy gastrointestinal normal, White blood cell count normal, X-ray normal, and International normalised ratio normal are unlisted for Vaxelis as per the Reference Safety Information. Considering the current knowledge on Vaxelis (Vomiting is listed as per Regulatory Authority safety information) and the onset latency (events occurred 1 day after vaccination), and despite the co-suspect vaccines as confounding factors and lack of information in this case (no medical history of adverse events after the first vaccination with Vaxelis), the causal relationship between Vaxelis and the reported events Vomiting, Haematemesis, Melaena, and Thrombosis cannot be excluded and is assessed as related. The causal relationship between Vaxelis and the events Aspartate aminotransferase increased, Metabolic function test abnormal, Gastrointestinal pathogen panel, Abdominal X-ray, Endoscopy gastrointestinal normal, White blood cell count normal, X-ray normal, and International normalised ratio normal was assessed as not applicable, due to the nature of these events. This single individual case safety report does not modify the benefit/risk balance of this product. Therefore, no change in the label or other measures is recommended at this time. However, the company will continue to monitor all respective reports received and based on cumulative experience, will re-evaluate the available evidence on an ongoing basis.; Sender's Comments: Vomiting, Haematemesis, Melaena, and Thrombosis were assessed as serious due to hospitalization, whereas Aspartate aminotransferase increased, Metabolic function test abnormal, Gastrointestinal pathogen panel, Abdominal X-ray, Endoscopy gastrointestinal normal, White blood cell count normal, X-ray normal, and International normalised ratio normal were assessed as non-serious. Vomiting is listed, whereas Haematemesis, Melaena, Thrombosis, Aspartate aminotransferase increased, Metabolic function test abnormal, Gastrointestinal pathogen panel, Abdominal X-ray, Endoscopy gastrointestinal normal, White blood cell count normal, X-ray normal, and International normalised ratio normal are unlisted for Vaxelis as per the Reference Safety Information. Considering the current knowledge on Vaxelis (Vomiting is listed as per Regulatory Authority safety information) and the onset latency (events occurred 1 day after vaccination), and despite the co-suspect vaccines as confounding factors and lack of information in this case (no medical history of adverse events after the first vaccination with Vaxelis), the causal relationship between Vaxelis and the reported events Vomiting, Haematemesis, Melaena, and Thrombosis cannot be excluded and is assessed as related. The causal relationship between Vaxelis and the events Aspartate aminotransferase increased, Metabolic function test abnormal, Gastrointestinal pathogen panel, Abdominal X-ray, Endoscopy gastrointestinal normal, White blood cell count normal, X-ray normal, and International normalised ratio normal was assessed as not applicable, due to the nature of these events. This single individual case safety report does not modify the benefit/risk balance of this product. Therefore, no change in the label or other measures is recommended at this time. However, the company will continue to monitor all respective reports received and based on cumulative experience, will re-evaluate the available evidence on an ongoing basis.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Premature baby 26 to 32 weeks
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2683641

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

schwer
Staat
OK
Alter
0,3
Geschlecht
M
Eingang
19.09.2023
Impfdatum
21.08.2023
Beginn
22.08.2023
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Abdominal X-ray Aspartate aminotransferase increased Endoscopy gastrointestinal normal Gastrointestinal pathogen panel Haematemesis International normalised ratio normal Melaena Metabolic function test abnormal Thrombosis Vomiting White blood cell count normal X-ray normal

Symptomtext

vomited on day following vaccines (8/22) improved some within 2 days then vomiting bright red blood and clots on early AM 8/25, progressed to coffee ground emesis by 8am 8/25 and then developed melena. Admitted on 8/25, endoscopy done and no source of bleeding. Resolved within 1-2 days, discharged on 8/30.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
2,0
Labordaten
endosccopy-- no source of blood biofire GI panel-- negative CMP nl except AST of 62 WBC nl and INR nl AXR without pneumatosis
Aktuelle Erkrankungen
n/a
Vorgeschichte
ex 30 week infant
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 2720894

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

mild
Staat
MI
Alter
0,5
Geschlecht
F
Eingang
04.12.2023
Impfdatum
29.11.2023
Beginn
29.11.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Abdominal X-ray Barium swallow Chest X-ray Culture urine Differential white blood cell count Full blood count Influenza virus test Intussusception Metabolic function test Respiratory syncytial virus test SARS-CoV-2 test Ultrasound abdomen Urine analysis Vomiting projectile

Symptomtext

Patient received her 3rd Rotateq vaccine on 11/29 and around 9pm she began having episodes of projectile vomiting. She had 13 episodes of vomiting. Parents took her to the ER on 11/30 at 10:00pm. She was dxed w/ a small bowel intussusception. She was given IV fluids. Intussusception resolved w/o treatment in the ER.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vomiting projectile
Hospital-Tage
-
Labordaten
11/30/2023 Abdomen + chest xray, CBC w/ diff, CMP, Covid, flu, RSV tests, abdominal US, upper GT w/flat plate, UA + culture. Repeat abdominal US
Aktuelle Erkrankungen
Viral illness 2 wks before vaccination
Vorgeschichte
N/A
Andere Medikamente
Vitamin D Supplement
Allergien
NKA
Vorherige Impfungen
-

VAERS 2702597

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

mild
Staat
MI
Alter
0,3
Geschlecht
M
Eingang
26.10.2023
Impfdatum
31.08.2023
Beginn
03.09.2023
Tage bis Beginn
3,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Abdominal pain upper Diarrhoea Faeces discoloured Mucous stools

Symptomtext

Mucousy stool started 3 days after his vaccines. Stomach pains, diarrhea (green/liquid/mucousy) lasted for a little over a week.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Abdominal pain upper
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2686444

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

mild
Staat
-
Alter
0,4
Geschlecht
M
Eingang
26.09.2023
Impfdatum
19.09.2023
Beginn
19.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cold sweat Cough Feeling of body temperature change Injection site urticaria Urticaria Wheezing

Symptomtext

Hot and cold sweats for days. Developed a cough with light wheezing - lungs were clear upon additional appointment. Hives on both legs.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2678998

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

mild
Staat
CO
Alter
1,0
Geschlecht
F
Eingang
04.09.2023
Impfdatum
18.08.2023
Beginn
28.08.2023
Tage bis Beginn
10,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Body temperature increased Fatigue Injection site swelling Rash

Symptomtext

She was super tired, running a low grade temperature, broke out in a rash, and the injection site has started to swell. We took her to the pediatrician(for an unrelated checkup) who stated the rash could just be from a viral infection and to keep an eye on her.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
-
Andere Medikamente
Mylicon
Allergien
None
Vorherige Impfungen
-

VAERS 2673131

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

mild
Staat
MD
Alter
1,0
Geschlecht
F
Eingang
17.08.2023
Impfdatum
03.08.2023
Beginn
10.08.2023
Tage bis Beginn
7,0
Dosis
4
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash

Symptomtext

Rash on left lower extremity 7 days after administration of vaccines, then noticed four more on Bilateral leg. Seen in clinic as f/u rash on 8/12/2023

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

VAERS 2724498

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

gering
Staat
TN
Alter
0,2
Geschlecht
M
Eingang
15.12.2023
Impfdatum
04.12.2023
Beginn
10.12.2023
Tage bis Beginn
6,0
Dosis
1
Route/Site
SYR / LG
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Haematochezia Mucous stools Occult blood positive

Symptomtext

Patient noted to have blood and mucus in stool (with positive hemoccult). Spontaneous resolution

Weitere VAERSDATA-Felder
Praegender Schweregrund
Haematochezia
Hospital-Tage
-
Labordaten
Stool hemoccult (+) on 12/12/2023 (stool from 12/10/2023), Stool hemoccult (-) on 12/12/2023 (stool from 12/12/2023), and Stool hemoccult (-) on 12/15/2023
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Other vaccinations: Pentacel, Prevnar13
Allergien
none
Vorherige Impfungen
-

VAERS 2714974

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

gering
Staat
PA
Alter
0,5
Geschlecht
F
Eingang
17.11.2023
Impfdatum
16.11.2023
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect dose administered No adverse event

Symptomtext

No adverse event occured.We realized on 11/16/23 that we administered full vial instead of 0.25ml. Therefore, 0.5ml was given.

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

VAERS 2692350

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

gering
Staat
CO
Alter
0,2
Geschlecht
F
Eingang
06.10.2023
Impfdatum
06.10.2023
Beginn
06.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Swelling of eyelid

Symptomtext

Patient received Beyfortus (RSV mAb nirsevimab, 0.5mL) LOT: 2022829 in the Left thigh at 0900. Mother called post visit at 1600 and states she noticed eyelid swelling at 1500. No other symptoms reported. Mother was advised to have patient seen in urgent care.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Swelling of eyelid
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Unknown
Vorherige Impfungen
-

VAERS 2691740

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

gering
Staat
AZ
Alter
0,5
Geschlecht
F
Eingang
06.10.2023
Impfdatum
29.09.2023
Beginn
03.10.2023
Tage bis Beginn
4,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Petechiae Skin lesion

Symptomtext

Developed petechial lesions on bilateral lower legs Tuesday 10/3. Seen in clinic Thursday 10/5. Most lesions beginning to fade. No new lesions developing. No known trauma. Patient otherwise eating and playful.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Petechiae
Hospital-Tage
-
Labordaten
No labs ordered for same day. Asked mom to get CBC, pt, PTT drawn if new lesions developed- lab slip given in clinic
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2688865

PFIZER\WYETH · PNEUMO (PREVNAR20) · Charge GN2778

gering
Staat
UT
Alter
-
Geschlecht
U
Eingang
29.09.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Syringe issue

Symptomtext

got a Prevnar 20 syringe out of the box and tried to remove the cap on the end of the syringe and the end of the syringe broke off making the syringe unusable; The initial case was missing the following minimum criteria due to no adverse event reported. Upon receipt of follow-up information on 12Sep2023, this case now contains all required information to be considered valid. This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. A patient (no qualifiers provided) received pneumococcal 20-val conj vac (dipht crm197 protein) (PREVNAR 20), as dose number unknown, single (Lot number: GN2778, Expiration Date: Sep2025) for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DEVICE MALFUNCTION (non-serious), outcome "unknown", described as "got a Prevnar 20 syringe out of the box and tried to remove the cap on the end of the syringe and the end of the syringe broke off making the syringe unusable". The reporter considered "got a prevnar 20 syringe out of the box and tried to remove the cap on the end of the syringe and the end of the syringe broke off making the syringe unusable" not related to pneumococcal 20-val conj vac (dipht crm197 protein). Causality for "got a prevnar 20 syringe out of the box and tried to remove the cap on the end of the syringe and the end of the syringe broke off making the syringe unusable" was determined associated to device constituent of pneumococcal 20-val conj vac (dipht crm197 protein) (malfunction). The information on the batch/lot number for pneumococcal 20-val conj vac (dipht crm197 protein) has been requested and will be submitted if and when received.

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

VAERS 2681564

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge gn2778

gering
Staat
TN
Alter
0,5
Geschlecht
M
Eingang
13.09.2023
Impfdatum
31.08.2023
Beginn
31.08.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered

Symptomtext

Patient received the wrong dose of the COVID 19 vaccine. Patient was given 0.2ml of the vial containing the 0.2ml/10mcg dose instead of the 0.25ml/25mcg

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

VAERS 2675111

PFIZER\WYETH · PNEUMO (PREVNAR13) · Charge GN2778

gering
Staat
NJ
Alter
1,0
Geschlecht
M
Eingang
22.08.2023
Impfdatum
15.08.2023
Beginn
15.08.2023
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered No adverse event

Symptomtext

No adverse event occurred. The HIB vaccine was administered 2 days after the expiration date.

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