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Reporte zur Charge U6702AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

12Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
FL 5 TX 3 KS 1 PA 1 NY 1 VA 1

VAERS 1484909

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

moderat
Staat
KS
Alter
55,0
Geschlecht
F
Eingang
19.07.2021
Impfdatum
28.06.2021
Beginn
28.06.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Chest pain Chills Hepatic enzyme abnormal Myalgia Painful respiration Platelet count Platelet count decreased Pyrexia White blood cell count White blood cell count decreased

Symptomtext

Patient had high fever, muscle aches, and chills the evening of the vaccination (approx 6 hours later). The next day, she went to the ER with chest pain and painful breathing. At the ED, her liver enzymes were found to be elevated while her white blood cell and platelet counts were low.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
6/29/2021: liver enzymes elevated, white blood cell count low, platelet count low
Aktuelle Erkrankungen
none known
Vorgeschichte
hypothyroidism
Andere Medikamente
levothyroxine, omeprazole, estradiol
Allergien
none known
Vorherige Impfungen
-

VAERS 1263733

SANOFI PASTEUR · DTAP (DAPTACEL) · Charge U6702AA

moderat
Staat
PA
Alter
67,0
Geschlecht
F
Eingang
27.04.2021
Impfdatum
18.08.2020
Beginn
18.08.2020
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal pain upper Condition aggravated Diarrhoea Fibromyalgia Lymphadenopathy Myalgia Tremor

Symptomtext

Imediately upon driving home a large lump appeared under left side of ear along jaw line(lymp node swollen) another lump node swelling on left elbow and another smaller one on right elbow. Pain in the stomach with violent diarhea. Muscle aches with increased fibromyalia pain and tremor worst at night. Fibromyalgia symptoms which have been less for years have increased and not going back to normal. Tremor has increased in actiivity. Due to Dr. going to a VIP doctor, cannot get into see him notified him of this the swelling in left arm in December 2020. Due to Covid cannot get in to new doctor till August 2021. The fibromyaliga increase in pain is something I thought I had to put up with, but thought this should of been told because if people with these types of illnesses should not get certain vaccines. I am now petrified to get the Covid vaccine due to my pain. Will discuss with my heart doctor and new doctor when I get in.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
fibromyalgia/mild benign tremor
Andere Medikamente
Losartan
Allergien
Certain Antibiotics and fillers in prescriptions
Vorherige Impfungen
-

VAERS 2277722

SANOFI PASTEUR · TDAP (ADACEL) · Charge u6702aa

mild
Staat
NY
Alter
63,0
Geschlecht
F
Eingang
14.05.2022
Impfdatum
14.05.2022
Beginn
14.05.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Anxiety Dizziness Nausea

Symptomtext

A few mins after the patient received her shingrix and adacel vaccines, pt said she felt dizzy, lightheaded and nauseous. She said she felt a little anxious because she's afraid that the vaccines would give her pain. She stated that it's probably in her head. About 8 mins later, she said she felt ok and she left the pharmacy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
N/Z
Aktuelle Erkrankungen
N/A
Vorgeschichte
6 months post kidney transplant
Andere Medikamente
N/A
Allergien
Macrolides
Vorherige Impfungen
-

VAERS 1460350

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

mild
Staat
VA
Alter
23,0
Geschlecht
F
Eingang
09.07.2021
Impfdatum
09.07.2021
Beginn
09.07.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Flushing Immediate post-injection reaction Injection site haemorrhage

Symptomtext

Pt had gushing of blood from the arm immediately as soon as needle made its way out of the arm. In addition, the patient started feeling dizzy and flushed upon going to the sitting area, whereas she had to turn back around and come back to the vaccine admin area to be closely monitored

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
Blood pressure was checked 3 times ranged from 90/60 to 119/62
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1112575

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

mild
Staat
TX
Alter
53,0
Geschlecht
F
Eingang
18.03.2021
Impfdatum
16.03.2021
Beginn
16.03.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Diarrhoea Fatigue Headache Nausea Somnolence Vomiting

Symptomtext

Headache, nausea, vomiting, diarrhea, tired, sleepy

Weitere VAERSDATA-Felder
Praegender Schweregrund
Diarrhoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
hypertension
Andere Medikamente
Metaprolol
Allergien
-
Vorherige Impfungen
-

VAERS 1073242

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

mild
Staat
TX
Alter
18,0
Geschlecht
M
Eingang
04.03.2021
Impfdatum
20.11.2020
Beginn
20.11.2020
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Headache Hypersomnia Lethargy Pain Pyrexia

Symptomtext

Patient felt tired and lethargic the day of the shot, and went to bed early. He wok up the next day with a fever just under 102F. He had a splitting headache, body aches, and exhaustion. He spent the day sleeping, drinking water and eating soup. The following day (3rd day) he woke up with a lesser headache which dissipated throughout the day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Daily Vitamins - Omegas/fish oil, multivitamin
Allergien
None
Vorherige Impfungen
Nausea, Meningococcal MCV4, Sanofi Pasteur, lot U645CA

VAERS 1888527

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

mild
Staat
FL
Alter
11,0
Geschlecht
F
Eingang
22.02.2021
Impfdatum
18.02.2021
Beginn
18.02.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dysphagia Oral pruritus Oropharyngeal pain

Symptomtext

Sore throat & itchines of mouth 1 min. after administration but not told to medical staff. at 3:30am Pt awoke c/o sore throat, trouble swallowing. Given EpiPen, called 911. Seen at ER & given Benadryl, Pepcid AC & steroids. Pt home & doing well.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Oral pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Vyvanse 30mg capsule Multivitamin
Allergien
PCN, Mold, sesame seed oil, Peanuts, Tree nuts
Vorherige Impfungen
-

VAERS 2408506

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

gering
Staat
FL
Alter
25,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
21.06.2022
Beginn
22.06.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered

Symptomtext

Expired vaccine was given. Patient did not have any adverse effects.

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

VAERS 2363941

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

gering
Staat
FL
Alter
11,0
Geschlecht
M
Eingang
09.07.2022
Impfdatum
27.06.2022
Beginn
27.06.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

inadvertently administered an expired dose of the Adacel with no reported adverse event; Initial information received on 29-Jun-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 11 years old male patient who had inadvertently administered an expired dose of the DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] 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 HPV VACCINE VLP RL1 4V (YEAST) (GARDASIL); and MENINGOCOCCAL VACCINE A/C/Y/W CONJ (DIP TOX) (MENACTRA). On 27-Jun-2022, the patient received a 0.5ml dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U6702AA and expiry date: 20-Jun-2022) via intramuscular in right deltoid for Immunization. On 27-Jun-2022 the patient developed a non-serious inadvertently administered an expired dose of the adacel with no reported adverse event (expired product administered, Latency: same day) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. Action taken : not applicable. Outcome: Unknown 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2363940

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

gering
Staat
FL
Alter
11,0
Geschlecht
F
Eingang
09.07.2022
Impfdatum
29.06.2022
Beginn
29.06.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Medication error No adverse event

Symptomtext

patient was inadvertently administered an expired dose of the Adacel single-dose vial with no adverse event; Initial information was received on 29-Jun-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 11 years old female patient who experienced patient was inadvertently administered an expired dose of the adacel single-dose vial with no adverse event while receiving vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included HPV VACCINE VLP RL1 4V (YEAST) (GARDASIL) and MENINGOCOCCAL VACCINE A/C/Y/W CONJ (DIP TOX) (MENACTRA) for Immunisation. On 29-Jun-2022, the patient received 0.5 ml of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U6702AA, expiry-20-JUN-2022) (formulation, and strength: unknown) via intramuscular route in unknown administration site for Immunization. On 29-JUN-2022 the patient developed a non-serious patient was inadvertently administered an expired dose of the adacel single-dose vial with no adverse event (expired product administered) (latency same day) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event patient was inadvertently administered an expired dose of the adacel single-dose vial with no 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 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2356760

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

gering
Staat
FL
Alter
25,0
Geschlecht
M
Eingang
03.07.2022
Impfdatum
21.06.2022
Beginn
21.06.2022
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 dose of ADACEL was administered to a patient with no reported adverse event; Initial information received on 22-Jun-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 25 years old male patient who was administered expired dose of Adacel with no reported adverse event, after receiving vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 21-Jun-2022, the patient received a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U6702AA and expiration date:20-Jun-2022) at a dose of 0.5ml via intramuscular route in the left deltoid as prophylactic vaccination. On 21-Jun-2022(latency: same day), the patient was administered expired dose of adacel with no reported adverse event (expired product administered) following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS 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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1683361

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6702AA

gering
Staat
TX
Alter
50,0
Geschlecht
F
Eingang
08.09.2021
Impfdatum
08.09.2021
Beginn
08.09.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Patient said that she was told by the doctor to come and get a Tetanus Shot, so we obliged. Then when she asked for a shot record, we realized she had the immunization 28 days prior.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
unknown
Vorgeschichte
depression, anxiety, diabetes
Andere Medikamente
Janumet 50-100, Seroquel XL, Gabapentin, Cymbalta,
Allergien
nkda
Vorherige Impfungen
-