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Reporte zur Charge U7561AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

23Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
TX 4 OH 2 VA 1 IA 1 CA 1 GA 1 KS 1 NC 1 PA 1 MA 1 IL 1 AL 1

VAERS 2522515

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

schwer
Staat
VA
Alter
29,0
Geschlecht
M
Eingang
03.12.2022
Impfdatum
03.12.2022
Beginn
03.12.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Face injury Fall Syncope

Symptomtext

Patient fainted approximately 3-5 minutes after receiving the the shot..During the vaccine patient showed no signs of an adverse reaction. While walking away after the vaccine was administered patient fell onto the floor. Patient a had two minor injuries to the face. After being alerted, I rushed to the patient's side to assess the situation. Upon assessment, patient a had two minor injuries to the face, he was breathing and talking with no issues. I asked him if he was currently taking any medications or had any medical conditions, to which he responded no. I assisted him to his feet and supported his arms while he walked to our clinical services room. While there, I cleaned his wounds with peroxide and gave him an ice pack for his forehead. I then sat with him until he was stable and his mother came to pick him up.

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

VAERS 2685573

SANOFI PASTEUR · TDAP (ADACEL) · Charge u7561aa

mild
Staat
IA
Alter
38,0
Geschlecht
F
Eingang
23.09.2023
Impfdatum
18.09.2023
Beginn
23.09.2023
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 mass Injection site swelling

Symptomtext

Patient called 9/23/23 to report a adverse reaction from vaccine on 9/18/23. Patient states the side effect started the morning of 9/23/23 when she called. Patient complained of a swollen arm around the injection site and that the lump was about the size of 1/2-1 baseball. Patient stated it was not red or hot to the touch and that she was going to be icing it.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site mass
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
gastroparesis and migraines
Andere Medikamente
unknown
Allergien
none
Vorherige Impfungen
-

VAERS 2673560

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
CA
Alter
15,0
Geschlecht
F
Eingang
18.08.2023
Impfdatum
21.07.2023
Beginn
02.08.2023
Tage bis Beginn
12,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blister Pruritus Scab Scar

Symptomtext

Patient received MMR, IPV, Tdap and Varicella Vaccines on 8/21/2023. Mother reported that around August 2, 2023 around 9:00AM , 12 days after being vaccinated her daughter began to experience itching, and later noticed fluid filled vesicles to her upper torso that looked like she had chicken pox. No other symptoms reported by mother. Upon further assessment today, noted one dry crusty scar to mid upper umbilical region. No rashes, scars or other fluid filled vesicles noted.

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

VAERS 2650682

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
-
Alter
58,0
Geschlecht
M
Eingang
29.06.2023
Impfdatum
24.01.2023
Beginn
24.01.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Injection site erythema

Symptomtext

Reported Symptoms: 10022061:INJECTION SITE ERYTHEMA; 10022075:INJECTION SITE

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

VAERS 2636822

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
TX
Alter
12,0
Geschlecht
F
Eingang
25.05.2023
Impfdatum
22.05.2023
Beginn
23.05.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site pain Injection site swelling Local reaction

Symptomtext

Per mom they noticed swelling and slight redness on the left upper arm on 05/23/23. The following days the swelling began to worsen, pain on palpation, and the redness more defined and spreading. Mom scheduled an appt on 05/25/23 where the patient was diagnosed with a local reaction and prescribed Triamcinolone 0.1% apply small application to area bid and Zithromax 250mg 2 tabs on day 1, and 1 tab days 2 and 3. Advised to monitor and no follow up appt necessary at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
nkda
Vorherige Impfungen
-

VAERS 2631590

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
GA
Alter
50,0
Geschlecht
M
Eingang
12.05.2023
Impfdatum
11.05.2023
Beginn
12.05.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood pressure increased Headache

Symptomtext

Patient said the 3 imz he got yesterday gave him HighBloodPressure. Turns out he didn't take his bp med yesterday and then he woke with a headache this morning. Says he knows his bp is high when he has a HA so then he takes a bp pill. At one point he said he takes bp pill when he has HA and later he said he takes everyday. Not really clear but he didn't take it yesterday. Said his bp was elevated this morning. He took it again and it was still elevated but not as much. About an hour ago he decided to take a 2nd bp pill. HA and elevated bp/pulse were his only complaints. We advised him to sit for a bit (because he was currently on the clock and busy working) and then take bp again. I advised him to see his dr, urgentcare, or hospital if bp does not come down. He sat for a bit but then left.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none reported
Vorgeschichte
high blood pressure and diabetes
Andere Medikamente
unknown
Allergien
none
Vorherige Impfungen
-

VAERS 2627900

SANOFI PASTEUR · TDAP (ADACEL) · Charge u7561aa

mild
Staat
KS
Alter
53,0
Geschlecht
F
Eingang
07.05.2023
Impfdatum
04.05.2023
Beginn
04.05.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Hypersensitivity Injection site erythema Injection site pruritus Peripheral swelling

Symptomtext

had redness and swelling in both right and left arm, was more pronounced in the left arm which received two vaccine, she also had intense itching at the site of administration and significant erythema, was told to take benadryl for itching and allergic reaction and to seek medical care if she has facial swelling or trouble breathing or any worsening symptoms

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

VAERS 2619435

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
NC
Alter
63,0
Geschlecht
M
Eingang
23.04.2023
Impfdatum
14.01.2023
Beginn
14.01.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site pruritus

Symptomtext

redness and itching at site of the injection 4 months after the injection. Applied allergy cream and antibiotic ointment. I suggested hydrocortisone cream today and to contact his doctor Monday

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

VAERS 2606004

SANOFI PASTEUR · DTAP (DAPTACEL) · Charge u7561aa

mild
Staat
TX
Alter
41,0
Geschlecht
M
Eingang
29.03.2023
Impfdatum
24.03.2023
Beginn
29.03.2023
Tage bis Beginn
5,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain Pain in extremity Tenderness

Symptomtext

Nurse Received call from Employee at this time. Pt. states he is calling due to his "arm is quite sore." Pt. reports he was given a TDAP to the right arm on Friday 03/24/23. Pt. reports his arm is sore when he lifts it to turn on the light. Pt. denies redness, swelling, and/or bruising to right arm injection site at this time. Pt. reports pain as a "4" on a 1-10 pain scale at this time. Pt. reports taking Tylenol this morning. Pt. states, "tender when I push on it." Pt. denies taking Motrin as he reports having recent gastritis issues. Pt. was forwarded to the vaccine hotline for guidance. Nurse Received call from vaccine support hotline staff member stating she spoke with the pt. and counseled him to wait another two days to monitor site and "exercise it out." also reports she counseled the pt. to call back if it gets worse.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Pt denies taking Motrin as he reports having recent gastritis issues.
Vorgeschichte
Pt denies taking Motrin as he reports having recent gastritis issues.
Andere Medikamente
-
Allergien
N/A
Vorherige Impfungen
-

VAERS 2594795

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
PA
Alter
11,0
Geschlecht
F
Eingang
10.03.2023
Impfdatum
06.02.2023
Beginn
07.02.2023
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Myalgia Pyrexia

Symptomtext

Patient received adult dose of vaccine and experienced fever and myalgia on day one post vaccine. Patient's parent reported patient had good relief with Tylenol and no symptoms on day two post vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myalgia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Partial pacreatectomy
Andere Medikamente
-
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2557645

SANOFI PASTEUR · TDAP (ADACEL) · Charge u7561aa

mild
Staat
TX
Alter
11,0
Geschlecht
F
Eingang
11.01.2023
Impfdatum
27.12.2022
Beginn
28.12.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site induration Injection site urticaria Pyrexia

Symptomtext

erythematous wheal with induration on left arm( Menquadfi) site, 4"X4"TDaP site also with mild erythema and induration .

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
Started on amoxicilin due to fever - 12/29/2022
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
No
Allergien
No
Vorherige Impfungen
-

VAERS 2556732

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
OH
Alter
-
Geschlecht
U
Eingang
11.01.2023
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Headache Ocular discomfort Surgery Visual impairment

Symptomtext

suffering visual disturbances; requiring emergent surgery due to pressure in eyes; headache; Initial information received on 05-Jan-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age and unknown gender patient who experienced suffering visual disturbances, requiring emergent surgery due to pressure in eyes and headache 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. On an unknown date, the patient received a dose of suspect diphtheria-2/tetanus/5 ac pertussis vaccine Suspension for injection (unknown strength, dose, frequency) lot U7561AA, expiry date: 09-11-2024 via unknown route in unknown administration site for prophylaxis. On an unknown date the patient developed a non-serious suffering visual disturbances (visual impairment), requiring emergent surgery due to pressure in eyes (ocular discomfort), headache (unknown latency). Lab data was not reported. Action taken was not applicable. It was not reported if the patient received a corrective treatment for all the events. At time of reporting, the outcome was Unknown for all the events.

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

VAERS 2551516

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
-
Alter
46,0
Geschlecht
M
Eingang
05.01.2023
Impfdatum
25.12.2022
Beginn
26.12.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Burning sensation Discomfort Musculoskeletal stiffness Neuralgia Pain of skin Vision blurred Visual impairment

Symptomtext

Pt is a 46 yo M who presented for finger laceration from breaking glass window while on duty as a firefighter on 12/25. Pt stated his tetanus was not up-to-date and received a dose at the ED. Pt returned to the ED on 12/28 complained about R facial burning sensation and R visual disturbances. Symptom started on 12/26 AM with R paracervical neck stiffness, R parietal scalp pain/pressure, and R blurry vision, without improvement. 12/25 13:10 ? Presented to ED 12/25 14:04 ? Tdap given 12/25 14:30 ? Discharged from ED 12/28 07:15 ? Presented to ED 12/28 10:5 - Discharged from ED Pt received meds include diphenhydramine, fluorescein, ketorolac, prochlorperazine, and tetracaine, during 12/28 admission. Per clinical note, consulted with neuro and agreed presentation was likely neuropathic pain, but no other significant neuro issue. Neck muscle stiffness may be secondary to the Tdap but no local inflammation or pain with ROW with R shoulder/upper arm. Pain improved and blurry vision resolved at the time of discharge. Face sheet sent to ophthalmology clinic for further evaluation. It is not immediately clear if eye-related issue was associated with Tdap; it was not listed as a known side effect. Neck stiffness was likely a side effect to Tdap.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain of skin
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2547121

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
TX
Alter
26,0
Geschlecht
F
Eingang
30.12.2022
Impfdatum
23.12.2022
Beginn
23.12.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Magnetic resonance imaging Pain in extremity

Symptomtext

Pain in arm. I saw her in clinic a week after injection. No injection site abnormality. Pain in consistent part of arm. Shoulder joint itself does not appear involved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
MRI is pending
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
None; Tubersol
Allergien
Ibuprofen
Vorherige Impfungen
-

VAERS 2520973

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

mild
Staat
MA
Alter
37,0
Geschlecht
F
Eingang
01.12.2022
Impfdatum
29.11.2022
Beginn
01.12.2022
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site mass Injection site pain Muscle tightness Neck mass Tenderness

Symptomtext

I developed soreness and a lump at the injection site about 24 hours afterwards. About 40 hours after I received the vaccine I noticed the right side of my neck just above the collarbone was sore and tight. When I rubbed the area I noticed a marble sized lump on the side of my neck that is tender to the touch.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site mass
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Hypertension, anxiety/depression
Andere Medikamente
Spironolactone, venlafaxine, lisinopril, vitamin D, CoQ10, fish oil, berberine, turmeric, melatonin
Allergien
Morphine, latex
Vorherige Impfungen
-

VAERS 2655872

SANOFI PASTEUR · TDAP (ADACEL) · Charge u7561aa

gering
Staat
IL
Alter
71,0
Geschlecht
M
Eingang
13.07.2023
Impfdatum
11.07.2023
Beginn
11.07.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Product administered to patient of inappropriate age

Symptomtext

GIVEN TO PATIENT OUTSIDE AGE RANGE, DID NOT REPORT ANY ADVERSE EFFECTS, PER MFR MAY NOT BE AS EFFECTIVE AS BOOSTRIX FOR OVER 64

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
none
Vorgeschichte
hyperlipidemia
Andere Medikamente
zetia lipitor prilosec
Allergien
nkda
Vorherige Impfungen
-

VAERS 2641699

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

gering
Staat
-
Alter
17,0
Geschlecht
M
Eingang
06.06.2023
Impfdatum
01.06.2023
Beginn
01.06.2023
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Wrong product administered

Symptomtext

Patient received incorrect vaccine Tdap instead HPV due to ordering error.

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

VAERS 2634817

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

gering
Staat
AL
Alter
15,0
Geschlecht
M
Eingang
22.05.2023
Impfdatum
17.05.2023
Beginn
17.05.2023
Tage bis Beginn
0,0
Dosis
5
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Product administered to patient of inappropriate age Vaccination error

Symptomtext

5/22/2023 0955 Patient is 15 years old and was administered ProQuad(MMRV) SQ right arm on 5/17/2023. The patient should have been administered MMR and Varicella separately. ProQuad is not to be administered to patients 13 years or older. Patient tolerated the vaccines well and did not have any adverse reactions.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
None
Vorgeschichte
-
Andere Medikamente
-
Allergien
None
Vorherige Impfungen
-

VAERS 2613076

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

gering
Staat
IN
Alter
2,0
Geschlecht
M
Eingang
11.04.2023
Impfdatum
04.04.2023
Beginn
04.04.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

no adverse effects but gave to early

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2604999

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

gering
Staat
WY
Alter
1,0
Geschlecht
F
Eingang
28.03.2023
Impfdatum
27.03.2023
Beginn
27.03.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Wrong product administered

Symptomtext

Patient came to clinic 3/27/23 for 18 month well child check. She was due for Dtap and Hepatitis A. Family was in agreement to proceed with immunizations. I went back to nurse's station and accidentally grabbed a Tdap vaccine instead of Hepatitis A. I was not aware of this mistake until I was charting the vaccines in chart. I then notified the Vaccine Coordinator who helped me look up potential side effects and potential adverse reaction. Dr. was then notified of the error. She instructed me to contact family and let them know of the error. Family was notified today (3/28/23) and was instructed to watch for adverse reactions and side effects. They were also notified that patient could not receive another vaccine for 1 month. Patient is feeling well and had no symptoms at this time.

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

VAERS 2573195

SANOFI PASTEUR · TDAP (ADACEL) · Charge u7561aa

gering
Staat
NJ
Alter
31,0
Geschlecht
F
Eingang
01.02.2023
Impfdatum
31.01.2023
Beginn
31.01.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Wrong product administered

Symptomtext

TDAP adacel 0.5 mL administered IM in L deltoid. Pt tolerated well. Lot u7561aa Exp 11/09/2024 NDC 492140089. Tdap vaccine was given instead of the flu vaccine. NO adverse effects to patient or fetus at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
n/a
Vorgeschichte
-
Andere Medikamente
-
Allergien
no known allergies
Vorherige Impfungen
-

VAERS 2555114

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

gering
Staat
NY
Alter
54,0
Geschlecht
F
Eingang
10.01.2023
Impfdatum
29.12.2022
Beginn
29.12.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration No adverse event

Symptomtext

the patient received a booster dose of Adacel before the ten years of tenivac with no reported adverse event; Initial information received on 04-Jan-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 54 years old female patient who received a booster dose of diphtheria-2/tetanus/5 ac pertussis vaccine [adacel] before the ten years of tenivac 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 diphtheria vaccine toxoid, tetanus vaccine toxoid (tenivac) for Prophylactic vaccination. On 29-Dec-2022, the patient received a 0.5 ml dose once total of suspect diphtheria-2/tetanus/5 ac pertussis vaccine (Suspension for injection) (lot: U7561AA; expiry date: 09-Nov-2024; strength: standard) via intramuscular route in the right deltoid for Immunization. On 29-Dec-2022 the patient received a booster dose of adacel before the ten years of tenivac with no reported adverse event (inappropriate schedule of product administration) (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 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
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
TENIVAC
Allergien
-
Vorherige Impfungen
-

VAERS 2552829

SANOFI PASTEUR · TDAP (ADACEL) · Charge U7561AA

gering
Staat
OH
Alter
-
Geschlecht
U
Eingang
07.01.2023
Impfdatum
-
Beginn
30.12.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

excursion was due to the door being ajar. The temperature of the refrigerator reached 41.0-62.0 degrees Fahrenheit with no adverse event; Initial information received on 03-Jan-2023 regarding an unsolicited valid serious case received from a other health professional. This case involves an event of product storage error of MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE [MENQUADFI], DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] and DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL] (excursion was due to the door being ajar. the temperature of the refrigerator reached 41.0-62.0 degrees fahrenheit with no adverse event). On 30-Dec-2022, it was reported DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE (lot UJ680ABA), DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U7561AA) and MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE lot (U7576AD) (strength, formulation, dose, route and expiry date: unknown) to be used for immunization was exposed to excursion due to the door being ajar. the temperature of the refrigerator reached 41.0-62.0 degrees fahrenheit with no adverse event (product storage error) (unknown latency). Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events. 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
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-