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Reporte zur Charge U6855AA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

11Reporte angezeigt
0Todesfaelle
1Hospitalisiert
0Lebensbedrohlich
2Bleibende Schaeden
VA 1 MD 1 IL 1 OH 1 NE 1 IN 1 KY 1 FL 1 TX 1

VAERS 1840378

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

schwer
Staat
VA
Alter
11,0
Geschlecht
F
Eingang
03.11.2021
Impfdatum
03.07.2021
Beginn
07.07.2021
Tage bis Beginn
4,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Cardiac stress test Dizziness Echocardiogram Electroencephalogram Electromyogram Fatigue Feeling abnormal Laboratory test Magnetic resonance imaging head Magnetic resonance imaging neck Syncope Tilt table test

Symptomtext

Her symptoms started with dizziness, fatigue, then became worsened with fainting, The dizziness, brain fog, fatigue is a daily problem that happens every time she in upright position. She has fainted now a handful of times.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Labwork October 2021 Stress test, Echocardiogram, EMG, EEG, Autonomic Test, Tilt table test all the week of October 11th- 15th Brain, head , neck MRI's 10-6-21 Fainted with ER visit late september 2021
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
penicillin
Vorherige Impfungen
-

VAERS 1382281

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

schwer
Staat
MD
Alter
24,0
Geschlecht
F
Eingang
30.06.2021
Impfdatum
02.06.2021
Beginn
04.06.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Chest discomfort Chest pain Computerised tomogram thorax normal Echocardiogram normal Exposure during pregnancy Myocarditis Inappropriate schedule of product administration Troponin increased

Symptomtext

Patient in 3rd trimester of pregnancy received TDAP and Covid vaccine on 6/2/21 in accordance with CDC guidelines. On 6/4/21 developed squeezing chest pain and work up revealed myocarditis. Patient hospitalized for 24 hours and discharged home following treatment with steroids.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
NKA
Vorherige Impfungen
-

VAERS 1917052

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

moderat
Staat
IL
Alter
31,0
Geschlecht
M
Eingang
02.12.2021
Impfdatum
25.05.2021
Beginn
25.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: unbekannt
Arthralgia Impaired work ability Injection site pain Limb discomfort Muscular weakness Neck pain Pain in extremity Paraesthesia Product administered at inappropriate site Wrong technique in product usage process

Symptomtext

See next page

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
vertigo
Vorgeschichte
-
Andere Medikamente
-
Allergien
House dust mite
Vorherige Impfungen
-

VAERS 1377977

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

moderat
Staat
-
Alter
11,0
Geschlecht
F
Eingang
07.06.2021
Impfdatum
04.06.2021
Beginn
04.06.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cyanosis Dizziness Dyspnoea Pallor Pyrexia Rash

Symptomtext

About 4 hours after patient received vaccine, she started feeling dizzy and short of breath. Mom states that she looked pale and the areas around her lips were cyanotic. She also developed a rash on her chest and face. Mom gave her benedryl twice. She also developed a subjective fever on the same day. Mom gave some Tylenol and it resolved. Has not come back.

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

VAERS 1260522

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

moderat
Staat
OH
Alter
40,0
Geschlecht
F
Eingang
26.04.2021
Impfdatum
23.04.2021
Beginn
25.04.2021
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Discomfort Grip strength decreased Hypoaesthesia Paraesthesia

Symptomtext

I received the vaccine around 3:45pm on Friday. Saturday night I went to bed and everything seemed fine. At 2am I woke up because my right hand was completely numb. I tried to "wake it up" by moving my wrist and my fingers. It took quite a while to eventually get the "pins and needles" feeling. That feeling lasted close to 30 minutes. My hand was uncomfortable the rest of the night. The next morning, Sunday, my right hand still had slight numbness around my thumb. The entire day my thumb was numb and I had the tingly feeling as I had experienced that night. All day today, Monday, I still have numbness in my right hand, mostly in and around my thumb. My grip isn't as strong as it usually is and holding a pen to write is slightly difficult.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
None yet.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Multi-vitamin, Omega 3, Ashwaghanda, Holy Basil
Allergien
Macrobid
Vorherige Impfungen
-

VAERS 1490809

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

mild
Staat
NE
Alter
12,0
Geschlecht
M
Eingang
21.07.2021
Impfdatum
14.07.2021
Beginn
15.07.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Rash erythematous Rash papular Rash vesicular Skin reaction

Symptomtext

significant localized skin reaction, erythematous, raised and almost appeared blister like. Provider instructed pt and mother to use ice and antihistamines. Parent verbalized understanding. On July 20th I spoke with mother and reaction had improved 90%.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash erythematous
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Takes Cetirizine 10mg daily,
Allergien
none
Vorherige Impfungen
2016 had a local reaction to fluzone

VAERS 1391267

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

mild
Staat
IN
Alter
-
Geschlecht
F
Eingang
11.06.2021
Impfdatum
28.05.2021
Beginn
02.06.2021
Tage bis Beginn
5,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inflammation Pain Pain in extremity Skin warm

Symptomtext

pain about an inch away from the injection site, radiating from the left upper deltoid to the lower deltoid; radiating from the left upper deltoid to the lower deltoid, with inflammation and warmth; Initial information received on 02-Jun-2021 regarding an unsolicited valid non-serious case received from a consumer. This case involves a 47 year old female patient who experienced pain about an inch away from the injection site, radiating from the left upper deltoid to the lower deltoid, with inflammation and warmth (pain) and (inflammation), while receiving vaccine DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL]. Medical history, medical treatment, concomitant medication, vaccination and family history were not provided. On 28-May-2021, the patient received a 0.5 ml dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U6855AA and expiry date: 25-Nov-2022) via an unknown route at an unknown administration site for prophylactic vaccination. On 02-JUN-2021, the patient developed a non-serious pain about an inch away from the injection site, radiating from the left upper deltoid to the lower deltoid, with inflammation and warmth (pain) and (inflammation), five days following the administration of DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE. It was also reported that the caller is calling on behalf of the patient who received the ADACEL vaccine on Sunday. The caller stated that the patient had pain not at the injection site, but an inch away from it. The pain travels from tricep to bicep and wanted to know if this was normal. That is the only description that was received. Reporter relationship: health care professional (HCP) Product used: used still using product: no Details of laboratory data not reported. It was not reported if the patient received a corrective treatment. At the time of reporting, the outcome of events was reported as unknown.

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

VAERS 1343076

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

mild
Staat
KY
Alter
52,0
Geschlecht
F
Eingang
24.05.2021
Impfdatum
21.05.2021
Beginn
22.05.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Axillary pain Back pain Body temperature increased Fatigue Flushing Hypokinesia Injection site mass Limb discomfort Lymphadenopathy Musculoskeletal stiffness Pain Pain in extremity Pain of skin

Symptomtext

Woke up on 5/22 with complaints of left arm stiffness and soreness, barely able to lift arm. Fatigue, total body aches, fever 100.8, back pain and stinging sensation on skin on back 5/23 large lump at injection site. no bruising or redness 5/24 lymph nodes under left arm enlarged and tingling sensation in armpit area, flushed feeling

Weitere VAERSDATA-Felder
Praegender Schweregrund
Axillary pain
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Biotin, saw palmetto, fish oil, vitamin E, hyaluronic acid
Allergien
PCN
Vorherige Impfungen
-

VAERS 1204658

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

mild
Staat
-
Alter
42,0
Geschlecht
M
Eingang
13.04.2021
Impfdatum
12.04.2021
Beginn
13.04.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Pyrexia

Symptomtext

patient self reported a fever of 107 taken with a temporal thermometer at 1700 the day of the vaccination. The patient used Tylenol a couple of times since the elevated fever. His fever initially reduced to below 102; he has not taken it recently and his temperature has been reduced to between 100.9 and 103.

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

VAERS 2524928

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

gering
Staat
FL
Alter
-
Geschlecht
M
Eingang
07.12.2022
Impfdatum
30.11.2022
Beginn
30.11.2022
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 Medication error No adverse event

Symptomtext

expired ADACEL vaccine being administered with no reported adverse event; Initial information received on 02-Dec-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves an unknown age male patient who had administered with expired DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (ADACEL) with no reported adverse event The patient's past vaccination(s) included TDAP with Caller states that it has been more than 10 years since the patient received a Tdap vaccine. The patient's past medical history, medical treatment(s) and family history were not provided. On 30-Nov-2022, the patient received a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE Suspension for injection lot U6855AA via intramuscular route in Left Arm, Dosage text 0.5 ml (milliliter) 1X (Total) , expiry date: 25-NOV-2022 ( strength, : unknown) for Immunisation On 30-NOV-2022 the patient who had administered ADACEL with expired with no reported adverse event (expired product administered) (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
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1306241

SANOFI PASTEUR · TDAP (ADACEL) · Charge U6855AA

gering
Staat
TX
Alter
15,0
Geschlecht
F
Eingang
11.05.2021
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration No adverse event

Symptomtext

ADACEL was given to the patient at age 11 and then ADACEL was given to the patient again at 15 years of age/no AE; Initial information was received on 23-Apr-2021 regarding an unsolicited valid non-serious case from a other health professional. This case involves a 15-year-old female patient was received DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] (lot U6855AA, expiry date-29-Nov-2022) via an intramuscular route in the left arm for prophylactic vaccination 16-Apr-2021 at the age of 11 years and then again at 15 years of age (inappropriate schedule of product administration). Medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included MENINGOCOCCAL VACCINE A/C/Y/W CONJ (DIP TOX) (MENACTRA) for Immunisation. It was a case of actual medication error due to inappropriate schedule of vaccine administered (latency same day). At the time of reporting, no adverse event was reported. 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
MENACTRA
Allergien
-
Vorherige Impfungen
-