Zurueck zur Suche

Reporte zur Charge UJ641AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

4Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
ND 1 NV 1 IL 1 DE 1

VAERS 2121134

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ641AA

moderat
Staat
ND
Alter
1,3
Geschlecht
M
Eingang
17.02.2022
Impfdatum
16.02.2022
Beginn
16.02.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Erythema Lethargy Pallor Rash macular Respiratory rate increased Retching Skin discolouration Tremor Vomiting

Symptomtext

After receiving his vaccine, patient took a nap. When he woke up at 4:00 PM he was shaking, his hands and feet were purple in color, and he had rapid breathing. While we were preparing to take him to the emergency room, he began vomiting repeatedly until he was dry heaving. He then became pale, lethargic, and we observed a redness on his limbs with a blotchy webbing pattern. We took him to the emergency room and explained he was having an allergic reaction to a vaccine he received. They tried to tell us it was normal. They never checked his vitals. They gave him anti-nausea medicine, Benadryl, and Tylenol. They discharged us after 1 hour and we continued to monitor him at home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Dairy and eggs
Vorherige Impfungen
-

VAERS 2245978

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ641AA

mild
Staat
NV
Alter
1,2
Geschlecht
F
Eingang
21.04.2022
Impfdatum
10.03.2022
Beginn
15.03.2022
Tage bis Beginn
5,0
Dosis
4
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Pyrexia Rash Rash macular Rash papular Rash vesicular

Symptomtext

Five days post vaccine patient developed macular, papular, vesicular rash over entire body. mom reports started on the patients face. mom also reports fever with the onset of rash.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
None ordered
Aktuelle Erkrankungen
none reported
Vorgeschichte
None
Andere Medikamente
None
Allergien
No know allergies
Vorherige Impfungen
-

VAERS 2192089

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ641AA

mild
Staat
IL
Alter
0,3
Geschlecht
F
Eingang
22.03.2022
Impfdatum
16.03.2022
Beginn
17.03.2022
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Activated partial thromboplastin time shortened Blood culture negative Blood fibrinogen normal Eosinophil count normal Eosinophil percentage Haematocrit normal Haemoglobin normal International normalised ratio normal Lymphocyte count increased Lymphocyte percentage increased Mean cell haemoglobin concentration normal Mean cell haemoglobin normal Mean cell volume normal Monocyte count Monocyte percentage Neutrophil count decreased Neutrophil percentage decreased Petechiae

Symptomtext

Fever to 103 the following day. Patient developed thrombocytopenia with a petechial rash on 3/19/22. Lowest platelet count was 38K. Platelets recovered to 106K 2 days later. Further evaluation pending

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
3/19/22 RBC 4.30 3.10 - 4.50 mil/mcL HGB 12.3 9.0 - 14.0 g/dL HCT 36.2 29.0 - 41.0 % MCV 84.2 74.0 - 108.0 fl MCH 28.6 26.0 - 34.0 pg MCHC 34.0 29.0 - 37.0 g/dL RDW-CV 12.1 11.0 - 15.0 % RDW-SD 36.8 35.0 - 47.0 fL PLT 38 (LL) 140 - 450 K/mcL Prothrombin Time Result Value Ref Range Prothrombin Time 11.4 9.3 - 11.7 sec INR 1.1 Partial Thromboplastin Time Result Value Ref Range PTT 29 23 - 32 sec Fibrinogen Activity Result Value Ref Range Fibrinogen 234 140 - 411 mg/dL Blood Culture Specimen: Blood Result Value Ref Range Culture, Blood or Bone Marrow No Growth <24 hours 3/21/22 Results for patient as of 3/22/2022 09:51 3/21/2022 10:19 WBC: 12.5 RBC: 4.33 HEMOGLOBIN: 12.3 HCT: 35.5 MCV: 82.0 MCH: 28.4 MCHC: 34.6 PLATELET COUNT: 106 (L) RDW: 11.8 NUCLEATED RBC%: 0.2 (A) ABSOLUTE NUCL RBC: 0.0 SEGMENTED NEUTROPHIL: 6 (L) LYMPH: 88 (H) MONO: 2 (L) EOSIN: 4 ABSOLUTE NEUT: 0.8 (L) ABSOLUTE LYMPH: 11.0 ABSOLUTE MONO: 0.2 ABSOLUTE EOS: 0.5 # CELLS COUNTED: 100
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2289165

SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ641AA

gering
Staat
DE
Alter
1,3
Geschlecht
M
Eingang
21.05.2022
Impfdatum
16.05.2022
Beginn
16.05.2022
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

16 month old was given 2 doses of Hib. He was given ACTHIB when he already got a dose of PENTACEL (with no reported adverse event); Initial information received on 16-May-2022 regarding an unsolicited valid non-serious case received from healthcare professional. This case involves a 16 months old male patient who was given 2 doses of hib he was given acthib when he already got a dose of pentacel (with no reported adverse event) while receiving vaccine diphtheria/tetanus/5 hybrid ac pertussis/ipv(mrc5)/hib(prp/t) vaccine [Pentacel]. 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 hib vaccine conj (tet tox) (Acthib) for prophylactic vaccination. On 16-May-2022, the patient received 0.5 ml dose of suspect diphtheria/tetanus/5 hybrid ac pertussis/ipv(mrc5)/hib(prp/t) vaccine [Pentacel] (lot UJ641AA and expiry date 28-Feb-2023 via intramuscular route in the right thigh) (strength, formulation: unknown) for immunization. On 16-May-2022 the patient developed a non-serious event "16-month-old was given 2 doses of hib. he was given acthib when he already got a dose of pentacel (with no reported adverse event) (extra dose administered) same day following the administration of diphtheria/tetanus/5 hybrid ac pertussis/ipv(mrc5)/hib(prp/t) vaccine [Pentacel]." 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
PREVNAR; ACTHIB
Allergien
-
Vorherige Impfungen
-