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Reporte zur Charge U7004AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

23Reporte angezeigt
0Todesfaelle
2Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 6 TX 4 MO 3 OK 2 GA 1 AZ 1 NE 1 FL 1 MN 1 IN 1 LA 1 NV 1

VAERS 2246349

SANOFI PASTEUR · TDAP (ADACEL) · Charge u7004aa

schwer
Staat
GA
Alter
49,0
Geschlecht
M
Eingang
21.04.2022
Impfdatum
21.04.2022
Beginn
21.04.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fall Syncope

Symptomtext

The patient had syncope. He fell on the floor from a sitting position.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
asthma, he also stated he was immunocompromised
Vorgeschichte
asthma
Andere Medikamente
n/a
Allergien
none
Vorherige Impfungen
-

VAERS 1943185

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

schwer
Staat
CA
Alter
12,0
Geschlecht
F
Eingang
02.12.2021
Impfdatum
07.11.2021
Beginn
14.11.2021
Tage bis Beginn
7,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Computerised tomogram head Drug screen Electrocardiogram Laboratory test Seizure

Symptomtext

11/14/21 onset seizure. HAD TDAP VACCINE 8/23/2016

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
11/14/21 CT if head 11/14/21 Chemistry panel. ECG 11/14/21 urine tox screen
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
NKDA.
Vorherige Impfungen
No

VAERS 1520466

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

schwer
Staat
AZ
Alter
11,0
Geschlecht
F
Eingang
02.08.2021
Impfdatum
02.08.2021
Beginn
02.08.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Crying Immediate post-injection reaction Nervousness Rash macular Syncope

Symptomtext

syncope and collapse following vaccination. Occurred at the time of injection; patient seemed nervous at the time of vaccination. when provider came into the room, patient slumped - regained consciousness, and was crying afterwards. denied headache, denies sore nexk pain, no bruising at the site - still blotchy skinny from crying follow syncope episode.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
-
Vorherige Impfungen
-

VAERS 2488656

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

moderat
Staat
CA
Alter
14,0
Geschlecht
F
Eingang
25.10.2022
Impfdatum
26.05.2022
Beginn
26.05.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Heart rate increased Influenza A virus test negative Influenza B virus test Palpitations Respiratory syncytial virus test negative SARS-CoV-2 test negative Tachycardia

Symptomtext

Heart palpitations. Elevated heart rate, upwards of 140 BPM while sitting. Vaccine given around 3pm, noticed elevated heart rate around 7pm. Monitored at home for a while and heart rate was not decreasing so went to ER. ER Doctor and staff monitored her for several hours, sleeping heart rate was 115 BPM. ER diagnosis Tachycardia. Discharged from ER at 12:50am with a heart rate of 92 BPM.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
Influenza A, NAAT - Negative. Influenza B NAAT - Negative. RSV - Negative. SARS-CoV-2, NAAT (COVID 19) - Negative
Aktuelle Erkrankungen
Slight sore throat and lower mid back pain.
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2287310

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge U7004AA

moderat
Staat
MO
Alter
53,0
Geschlecht
M
Eingang
20.05.2022
Impfdatum
12.05.2022
Beginn
13.05.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Blood creatine phosphokinase increased Cellulitis Hypoglycaemia Hypotension Injection site erythema Injection site pain Injection site swelling

Symptomtext

Tdap and Covid 19 booster in left arm 5/12/22. Patient reported left arm pain to his family and was found down by them 5/13/22. He was noted to have left arm swelling, erythema, hypotension, hypoglycemia with elevated CPK. Diagnosis: Secondary cellulitis of left UE extending to left chest wall 2/2 vaccinations.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypotension
Hospital-Tage
5,0
Labordaten
CK 10,098
Aktuelle Erkrankungen
-
Vorgeschichte
Schizoaffective disorder
Andere Medikamente
divalproex DR, ferrous sulfate, folic acid, levothyroxine, paliperidone palmitate ER, ergocalciferol
Allergien
NKA
Vorherige Impfungen
-

VAERS 2265989

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

moderat
Staat
MO
Alter
56,0
Geschlecht
F
Eingang
06.05.2022
Impfdatum
27.04.2022
Beginn
27.04.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Decreased appetite Feeling abnormal Impaired work ability Injection site discolouration Mobility decreased Muscular weakness

Symptomtext

PATIENT INITIALLY HAD DISCOLORATION AROUND INJECTION SITE AND BACK OF LEFT ARM. DISCOLORATION PROGESSED DOWN LEFT SIDE SO PATIENT WENT TO ER. PATIENT WAS TOLD AT EVALUATION, REACTION TO SHINGRIX VACCINE AND ADVISED NOT TO RECEIVE SECOND DOSE. BLACK AND BLUE DISCOLORATION PROGRESSED ON LEFT SIDE INCLUDING HER EYE. AFTER RETURNING HOME FROM ER, AROUND MIDNIGHT PATIENT BEGAN TO FEEL MUSCLE WEAKNESS THAT PROGRESSED OVER THE NEXT 2 DAYS. PATIENT DESCRIBED AS FEELING PARALYZED ALTHOUGH SHE COULD STILL MOVE BUT THE EFFECTS WERE SUCH THAT SHE WAS UNABLE TO WORK FOR 2 DAYS AND JUST LAYED ON THE COUCH. SHE ALSO REPORTED FEELING "WEIRD" AND HAVING ANOREXIA. ON THE THIRD DAY THE PATIENT FELT BETTER AND RETURNED TO WORK

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
THYROID,, HEART
Andere Medikamente
LEVOTHYROXINE, DILTIAZEM, NP THYROID, HYDROXYZINE, B12 INJECTION, ADACEL VACCINE IN OPPOSING ARM
Allergien
CODEINE
Vorherige Impfungen
-

VAERS 1801187

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

moderat
Staat
CA
Alter
11,0
Geschlecht
F
Eingang
20.10.2021
Impfdatum
11.10.2021
Beginn
11.10.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Decreased appetite Dizziness Feeling abnormal Headache Heart rate decreased Hypotension Lethargy Nausea Pallor Pyrexia Tremor Visual impairment

Symptomtext

Within minutes of receiving vaccinations, child became dizzy, nauseous and pale. Said her vision was becoming dark. Sat child down and asked nurse to get a doctor and to take her blood pressure, pulse and blood sugar. Child was hypotensive with a low heart rate. Had child drink some juice. Within 10 minutes Childs color began to regain and child stated she was feeling better. Remained in doctors office for 2 hours until her blood pressure recovered to a more normal level. Less than 24hrs later child was complaining about being shaky and dizzy. Soon after she had a low grade fever (99-100 F), complained of a bad headache, no appetite, nauseous, lethargic which lasted 6 days. PCP is referring her to cardiologist for continued hypotension.

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

VAERS 2336512

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

mild
Staat
NE
Alter
35,0
Geschlecht
F
Eingang
27.06.2022
Impfdatum
24.06.2022
Beginn
25.06.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Fatigue Headache Injection site erythema Injection site pruritus Injection site swelling Injection site warmth Pain Pain in extremity

Symptomtext

Red, swollen, very hot, itch area approximately 3 inches around injection. Patient felt achy, fatigue, headache and sore arm lasting 3 days at time of reporting. Treatment with tylenol, benadryl cream and sleep. Previous bad reaction for patient with last tetanus shot (approximately 9 years ago...dime size swelling that popped & leaked oozing liquid)...possible patient allergy?

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None.
Vorgeschichte
Adrenal insufficiency.
Andere Medikamente
Ubrelvy, levothyroxine, fludrocortisone, meloxicam, prednisone, estradiol, sumatriptan, buproprion, calcium, womens one a day vitamin, probiotic, and i-caps
Allergien
None.
Vorherige Impfungen
-

VAERS 2316674

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

mild
Staat
TX
Alter
57,0
Geschlecht
F
Eingang
11.06.2022
Impfdatum
05.06.2022
Beginn
10.06.2022
Tage bis Beginn
5,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site pain Injection site swelling Limb discomfort

Symptomtext

FIVE DAYS AFTER RECIEVIENG THE VACCINE PATIENT DEVELOPED HEAVY ARM, PAIN, REDNESS AND SWELLING ABOVE INJECTION SITE. RECOMMENDED COLD COMPRESS , ACETAMINOPHEN AND ANTIHISTAMINE. PATIENT INFORMED OF SIGNS OF ANAPHYLAXIS. INFORMED TO CALL EMS IF NEEDED.

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

VAERS 2302148

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

mild
Staat
OK
Alter
27,0
Geschlecht
F
Eingang
30.05.2022
Impfdatum
27.05.2022
Beginn
30.05.2022
Tage bis Beginn
3,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Pruritus Skin mass Skin warm

Symptomtext

large, golf ball size, lump under skin, red hot and itching - not sure when the symptoms started exactly for the patient. She called me on 05/30/2022 at approximately 10:15am. I did refer her to go to a walk-in clinic due to she thought it was getting worse. I tried to call the patient when I started filling this form out but she did not answer. I do not know if patient did go to the walk in clinic or not.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
trazodone (only current medication I see on profile)
Allergien
sulfa, penicillin, latex
Vorherige Impfungen
-

VAERS 2273541

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

mild
Staat
FL
Alter
54,0
Geschlecht
M
Eingang
12.05.2022
Impfdatum
07.05.2022
Beginn
08.05.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site reaction

Symptomtext

A small, localized injection site reaction formed on arm the day after vaccinations.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site reaction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Seroquel, Zoloft, Metoprolol Tartrate, Lisinopril, Simvastatin, Doxazosin, Buspirone
Allergien
N/A
Vorherige Impfungen
-

VAERS 2252311

SANOFI PASTEUR · DTAP (DAPTACEL) · Charge U7004AA

mild
Staat
MO
Alter
32,0
Geschlecht
F
Eingang
26.04.2022
Impfdatum
04.04.2022
Beginn
06.04.2022
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pain Injection site swelling Injection site warmth Platelet count increased Weight bearing difficulty White blood cell count increased

Symptomtext

This is s Adacel T-dap vaccine: She got her vaccine at the clinic, she was fine initially. Two days after she had a swollen, sore arm at the deltoid at the site of injection with some warmth. No erythema, no purulence from the injection site. It seemed to improve after a week. Then it became again sore, swollen and it's been 3 weeks and she is still dealing with this. Her PCP told her to take ibuprofen with Tylenol alternating and warm compresses, conservative approach and to notify if it got worse. She spoke with her PCP a week ago and was reassuring and she called again today stating she still has the problem. Last week she said it was sore, her PCP offered her an anti-inflammatory. She then called today and said she noticed it was more sore with lifting weights, and was informed to stop lifting weights until symptoms improved that she may have a microtear.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
Her WBC was 12.7 and was going to do a repeat to see if it had gone down, platelets were 495. She reported no infectious process. This was routine labs. The reason for her initial visit was to resume medicine for her anxiety.
Aktuelle Erkrankungen
URI 2 weeks prior with negative COVID test.
Vorgeschichte
Anxiety, alopecia (unknown cause).
Andere Medikamente
Bupropion hydrochloride El 150 mg.
Allergien
Teen spirit deoderant (scratchy throat).
Vorherige Impfungen
-

VAERS 2242035

SANOFI PASTEUR · TDAP (ADACEL) · Charge u7004aa

mild
Staat
TX
Alter
47,0
Geschlecht
F
Eingang
19.04.2022
Impfdatum
15.04.2022
Beginn
16.04.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Injection site erythema Injection site swelling Injection site warmth Pruritus Urticaria

Symptomtext

pt called , stating she got adacel vaccine on April 15th, and then on 16th she started itching all over body , by 18th she got hives all over body and site on injection is little swollen, red and hot. advice to put icepack over swollen part. pt said she use Benadryl but not that helpful. no shortness of breath so far. pt on vacation and will visit urgent care for evaluation may need steroid.

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

VAERS 2218103

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

mild
Staat
TX
Alter
13,0
Geschlecht
M
Eingang
06.04.2022
Impfdatum
29.03.2022
Beginn
03.04.2022
Tage bis Beginn
5,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pruritus Injection site reaction Injection site urticaria Rash erythematous

Symptomtext

Patients Left deltoid where the vaccine was administered got very red splotchy hive-like rash, slightly itchy. The rash to the injection site did not appear until 4/3/22. Mom gave him Benadryl and applied over the counter hydrocortisone cream. Resolving.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pruritus
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
miralax
Allergien
N/A
Vorherige Impfungen
-

VAERS 1753997

SANOFI PASTEUR · DTAP (DAPTACEL) · Charge U7004AA

mild
Staat
CA
Alter
25,0
Geschlecht
F
Eingang
01.10.2021
Impfdatum
28.09.2021
Beginn
29.09.2021
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site pain Myalgia Vaccination site pain Vaccination site swelling

Symptomtext

24 hours after vaccine patient developed pain and swelling at vaccine site that peaked at 24 hours later (9/30/21) and then began to subside; has myalgias that were short lived but no fever. On exam, there is still redness, tenderess and alloydynia in a 6 X 5 cm area. patient is otherwise afebrile and well appearing.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
mild intermittent asthma
Andere Medikamente
Lessina
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1715371

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

mild
Staat
CA
Alter
21,0
Geschlecht
F
Eingang
20.09.2021
Impfdatum
14.09.2021
Beginn
15.09.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dry skin Injection site erythema Injection site swelling Injection site warmth

Symptomtext

The injection site of varicella @ left upper arm has redness, swollen, skin is rough , it is warm to touch, size 4.5cm x 5.0 cm, but no fever.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
no
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
No
Allergien
NKA
Vorherige Impfungen
-

VAERS 1663120

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

mild
Staat
MN
Alter
11,0
Geschlecht
M
Eingang
01.09.2021
Impfdatum
01.09.2021
Beginn
01.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Vomiting

Symptomtext

Patient vomited approx. 10 minutes after vaccination

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

VAERS 1582624

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

mild
Staat
IN
Alter
11,0
Geschlecht
M
Eingang
18.08.2021
Impfdatum
17.08.2021
Beginn
17.08.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Rash

Symptomtext

Was seen at ER on 8/17/2021 16:39. Patient is 11-year-old who presents with an allergic reaction. He just received his HPV, TDAP, MENINGITIS vaccine and he broke out in a rash primarily on his face. Denies any throat, tongue, or mouth swelling. No difficulty breathing, no wheezing, no nausea, or vomiting.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
Was treated at ER with Benadryl with his symptoms resolving. Was observed for some time, then was discharged home with a prescription of prednisone 20mg, 1.5 tab(s) oral every day for 7 days. 0 refills.
Aktuelle Erkrankungen
No
Vorgeschichte
Seasonal Allergies
Andere Medikamente
Ascorbic Acid (Vitamin C) 0.5 tab(s) chewed every day Multivitamin 1 tab oral every day.
Allergien
No
Vorherige Impfungen
-

VAERS 2653235

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

gering
Staat
OK
Alter
47,0
Geschlecht
F
Eingang
06.07.2023
Impfdatum
06.07.2023
Beginn
06.07.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

No signs or symptoms at this time. Vaccine was expired when given 27 APR23

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
-
Allergien
Benadryl Glucophage Byetta 10 MCG Pen Ibuprofen Iodine Morphine Sulfate Lasix Lortab MethylPREDNISolone (Pak) Demerol Lyrica Celebrex Penicillin Unstructured/Uncoded allergies will not be considered for drug-allergy warnings. Please remove and re-enter them in structured/coded format. Sulfa Unstructured/Uncoded allergies will not be considered for drug-allergy warnings. Please remove and re-enter them in structured/coded format. Gabapentin
Vorherige Impfungen
-

VAERS 2629486

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

gering
Staat
TX
Alter
42,0
Geschlecht
F
Eingang
10.05.2023
Impfdatum
04.05.2023
Beginn
04.05.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered No adverse event

Symptomtext

receiving an expired adacel with no reported adverse event; Initial information was received on 05-May-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves 42 years old female patient who receiving an expired 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 hepatitis b vaccine RHBSAG (YEAST) (Recombivax) for Prophylactic vaccination. On 04-May-2023, the patient received a dose 1 of 0.5 ml of suspect diphtheria-2/tetanus/5 ac pertussis vaccine (Suspension for injection) (lot U7004AA, Expiry date :27-Apr-2023) (strength : unknown) via intramuscular route in the left deltoid for immunization. On 04-May-2023 the patient developed a non-serious event of receiving an expired 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 with DIPHTHERIA, TETANUS and acellular pertussis vaccine (Adacel) was not applicable. At time of reporting, the outcome was Unknown for the event receiving an expired adacel with no reported 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 2276441

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

gering
Staat
LA
Alter
53,0
Geschlecht
F
Eingang
13.05.2022
Impfdatum
13.05.2022
Beginn
13.05.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Device breakage Syringe issue Underdose

Symptomtext

When I was screwing the needle to the prefilled syringe, I heard a clicking sound, but I did not think anything of it. When I went to inject the vaccine into the patient's arm, majority of the vaccine came out the side where it had cracked. I re-gave another dose of the vaccine with the patient's permission.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Device breakage
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
-
Allergien
N/A
Vorherige Impfungen
-

VAERS 2072088

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

gering
Staat
NV
Alter
76,0
Geschlecht
F
Eingang
28.01.2022
Impfdatum
26.10.2021
Beginn
27.10.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Fall Muscular weakness

Symptomtext

Patient stated that their legs fell out from under them the morning after receiving all four vaccines. Patient denies loosing consciousness or any symptoms of syncope or loosing consciousness. Patient was brought to the ER and was kept in the hospital for a three day stay. Stated that she the hospital was not able to determine the cause of her fall.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fall
Hospital-Tage
3,0
Labordaten
N/A
Aktuelle Erkrankungen
Patient denies any illness at time of vaccination.
Vorgeschichte
Type 2 diabetes
Andere Medikamente
Patient stated they do not take any OTC medications. Unknown prescription medication history.
Allergien
No known allergies.
Vorherige Impfungen
-

VAERS 1847611

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7004AA

gering
Staat
CA
Alter
58,0
Geschlecht
F
Eingang
05.11.2021
Impfdatum
05.11.2021
Beginn
05.11.2021
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Inappropriate schedule of product administration

Symptomtext

PATIENT RECEIVED A 2ND TDAP WHEN NOT NECESSARY WITHIN THE 10YEAR TIMEFRAME (PREVIOUS ADMINISTRATION DATE 05/26/2021). PATIENT ALSO RECEIVED A 4TH TWINRIX WHEN NOT NECESSARY (PREVIOUS ADMINISTRATION DATE 07/21/2010).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NONE KNOWN
Vorgeschichte
BREAST CANCER REMISSION
Andere Medikamente
LISINOPRIL ANASTRAZOLE
Allergien
NKDA
Vorherige Impfungen
-