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Reporte zur Charge U7665BA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

12Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
FL 2 TX 2 PA 2 GA 1 SC 1 OK 1 MO 1 NE 1 NY 1

VAERS 2620770

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

schwer
Staat
FL
Alter
59,0
Geschlecht
M
Eingang
25.04.2023
Impfdatum
25.04.2023
Beginn
25.04.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Discomfort Dizziness Fatigue Gait disturbance Seizure like phenomena Walking aid user

Symptomtext

PATIENT FELT HEAVY AND TIRED AFTER RECEIVING THE TETANUS VACCINE ALONG WITH THE SHINGLES VACCINE. THIS WAS THE SECOND DOSE OF THE SHINGLES VACCINE AND THERE WERE NO ISSUES WITH THE FIRST ONE. THEY DID TELL ME HE HAD A PREVIOUS PROBLEM WITH THE COVID VACCINE . THE PATIENTS REPRESENTATIVE (CARETAKER) CALLED HER SUPERVISOR AND SAID HE HAD NOT HAD THE TETANUS SHOT AND TO GO AHEAD AND GIVE IT. AFTER GIVING IT APPROX 45 MINUTES LATER I WAS CALLED TO AISLE WHERE HE WAS LIGHT HEADED AND UNABLE TO WALK AND NEEDED TO SIT. HE WAS VERY CONSCIOUS AND ANSWERED ALL OF MY QUESTIONS. CAREGIVER STATES HAS HAD THESE EPISODES BEFORE RANDOMLY AND USUALLY WILL GO HOME AND LIE FOR A WHILE AND FEEL BETTER. SHE DID NOT STATE HE WAS ON SEIZURE MEDS OR HAD SEIZURES WHEN ANSWERING QUESTIONAIRE BUT MENTIONED HE HAS BEEN TOLD THESE EPIDOSES ARE SEIZURE LIKE. THEY DID NOT WANT HELP LEAVING THE STORE AS WE HELPED HIM INTO A MOBILITY SCOOTER.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure like phenomena
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
NA
Vorgeschichte
HIGH BLOOD PRESSURE, CLOTS,
Andere Medikamente
LISINOPRIL 20 SIMVASTATIN 40
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2676356

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

mild
Staat
GA
Alter
52,0
Geschlecht
F
Eingang
24.08.2023
Impfdatum
22.08.2023
Beginn
24.08.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Pruritus

Symptomtext

Patient came in to get M-M-R II Live vaccine and Varivax at our pharmacy on 8/22/23. She called today and complained about her left arm being super itchy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
No medical tests and laboratory results related to the adverse event.
Aktuelle Erkrankungen
No other illness at the time of vaccination.
Vorgeschichte
Patient has a history of High blood pressure.
Andere Medikamente
No medication taken at the time .
Allergien
No history of allergies on profile .
Vorherige Impfungen
-

VAERS 2627899

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

mild
Staat
SC
Alter
47,0
Geschlecht
F
Eingang
07.05.2023
Impfdatum
04.05.2023
Beginn
06.05.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Urticaria

Symptomtext

Patient says has hives for past few days after receiving vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Diabetes, Thyroid, anemia
Andere Medikamente
unknown
Allergien
none stated
Vorherige Impfungen
-

VAERS 2626110

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

mild
Staat
OK
Alter
34,0
Geschlecht
F
Eingang
03.05.2023
Impfdatum
28.04.2023
Beginn
28.04.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Brain fog Chills Lethargy Nausea Pain Pyrexia Somnolence Vomiting projectile

Symptomtext

Night after shot was administered I woke up feeling really nauseous and starting projectile vomiting all night. The next day I had a fever, chills and body pain all over, in addition to nausea and extreme lethargy/sleepiness. The puking has stopped and chills went away after two days, but the nausea, extreme lethargy and mind fog has continued on for several more days and hasn't gotten better.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Migraines
Andere Medikamente
Fluoxotine 10mg/day Norethindrone 0.35mg/day
Allergien
None
Vorherige Impfungen
-

VAERS 2611561

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

mild
Staat
TX
Alter
62,0
Geschlecht
F
Eingang
07.04.2023
Impfdatum
05.04.2023
Beginn
07.04.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site nodule Injection site pain Injection site warmth

Symptomtext

Pt reports soreness at injection site, knot under skin approx size of a quarter or less, warmth to the touch and redness. redness is localized it is not spreading as of time of report

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
chronic pain syndrome
Andere Medikamente
cyclobenzaprine 10 mg, carvedilol 12.5 mg, pregabalin 100 mg,
Allergien
sulfa antibiotics, penicillin
Vorherige Impfungen
-

VAERS 2598276

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

mild
Staat
MO
Alter
48,0
Geschlecht
F
Eingang
16.03.2023
Impfdatum
13.03.2023
Beginn
13.03.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Decreased appetite Fatigue Headache Injection site erythema Injection site mass Injection site pruritus Injection site swelling Pain

Symptomtext

Moderate to severe fatigue and flu-like symptoms - including body aches, loss of appetite and severe headache 72hrs post-injection. Hard 2" lump at injection site 72hrs post injection with swelling, itching and redness at the injection site. Administering MD's office has been notified.

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

VAERS 2672427

GLAXOSMITHKLINE BIOLOGICALS · DTAP (INFANRIX) · Charge U7665BA

gering
Staat
PA
Alter
3,0
Geschlecht
F
Eingang
16.08.2023
Impfdatum
15.08.2023
Beginn
15.08.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Product availability issue Wrong product administered

Symptomtext

An order for Infanrix (DTAP) was placed by PA-C on 8/10/23. The patient arrived with her father on 8/15/23. The medical assistant collected ordered vaccines including PCV13 and Hep A. The MA grabbed Adacel (Tdap) without realizing the difference between DTAP and TDAP. The correct vaccine, Infanrix (DTAP) was not available at the time of incident. The patient was brought into the medical lab with her father for vaccine administration. After administering one vaccine, the MA came to the provider for assistance administering the other two vaccines. The provider inadvertently administered Adacel (TDAP) to the patient's right deltoid while the patient sat on her father's lap. The MA was also present in the lab at time of administration. The vaccine was partially administered as some of the vaccine was left in the syringe upon the patient pulling away. The mistake was realized when documenting the vaccines in the chart. The refrigerator was checked for the correct vaccine at which time the correct vaccine was not available. The provider informed the parent that the incorrect vaccine was administered and that the patient will need subsequent doses to complete the DTAP series. The parent and the provider agreed to administer the correct, needed vaccine at time of next visit after patient turns 4 years old.

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 2664891

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge U7665BA

gering
Staat
FL
Alter
49,0
Geschlecht
M
Eingang
02.08.2023
Impfdatum
19.05.2023
Beginn
19.05.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia

Symptomtext

Numbness to face and extremities one week after vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypoaesthesia
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
Dog Bite
Vorgeschichte
-
Andere Medikamente
None reported
Allergien
Ciprofloxacin (muscle pain, severe)
Vorherige Impfungen
-

VAERS 2650129

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

gering
Staat
PA
Alter
6,0
Geschlecht
F
Eingang
28.06.2023
Impfdatum
25.05.2023
Beginn
25.05.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age

Symptomtext

6 year old patient inadvertently received a dose of ADACEL, with no reported adverse event; Initial information received on 23-Jun-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 6 years old female patient who inadvertently received a dose of 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. On 25-May-2023, the patient received an unknown dose once of suspect diphtheria-2/tetanus/5 AC pertussis vaccine (Suspension for injection) (lot: U7665BA; expiry date: 04-Mar-2025; strength: standard) via intramuscular route in the left deltoid for Immunization. On 25-May-2023 the patient inadvertently received a dose of adacel, with no reported adverse event (product administered to patient of inappropriate age) (latency: same day). Action taken was 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 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2649094

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

gering
Staat
NE
Alter
28,0
Geschlecht
F
Eingang
23.06.2023
Impfdatum
09.06.2023
Beginn
09.06.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syringe issue

Symptomtext

Was attempting to take the needle cap off the needle and the syringe broke just under the base of the top of the vaccine syringe. Snapped completely off. NDC:49281-400-89 LOT: U7665BA EX: 04MAR25

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

VAERS 2639959

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

gering
Staat
TX
Alter
56,0
Geschlecht
F
Eingang
01.06.2023
Impfdatum
28.05.2023
Beginn
29.05.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Cellulitis Peripheral swelling

Symptomtext

PATIENT RECEIVED VACCINES ON 5/28. ON 5/29 SHE WOKE UP AND HER LEFT ARM WAS SWOLLEN IT KEPT GETTING WORSE THROUGHOUT THE DAY. ON 5/30 SHE CAME TO PHARMACY AND WAS ADVISED TO TAKE IBUPROFEN AND BENADRYL AND ICE HER ARM AND GO TO DR IF IT KEPT GETTING WORSE OR DID NOT RESOLVE. PATIENT WENT TO DR 6/1 AND WAS DIAGNOSED WITH CELLULITIS AND PRESCRIBED DOXYCYCLINE AND PREDNISONE

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cellulitis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
ASTHMA
Andere Medikamente
HCTZ, ALBUTEROL HFA
Allergien
-
Vorherige Impfungen
-

VAERS 2636033

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7665BA

gering
Staat
NY
Alter
63,0
Geschlecht
F
Eingang
24.05.2023
Impfdatum
22.05.2023
Beginn
22.05.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event

Symptomtext

No Adverse event. Tenivac was ordered by the provider and Adacel was administered. Patient and provider notified. This is being recorded as per my facilities policy. Patient tolerated vaccine well with NO ADVERSE REACTION.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-