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Reporte zur Charge UT8043CA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

32Reporte angezeigt
3Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 10 CO 5 WA 3 AZ 3 AK 2 OR 2 MN 1 NM 1 NV 1 ID 1 MT 1

VAERS 2684944

SEQIRUS, INC. · INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) · Charge UT8043CA

kritisch
Staat
CA
Alter
70,0
Geschlecht
M
Eingang
21.09.2023
Impfdatum
05.09.2023
Beginn
06.09.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / RA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Cough Death Pyrexia

Symptomtext

Received the vaccinations on 09/05/2023. Increased coughing less than 24 hours later, fever less than 24 hours. These symptoms lasted until 4 days after the vaccine when the patient was found deceased at home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
chronic obstructive pulmonary disease
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2683686

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

kritisch
Staat
-
Alter
102,0
Geschlecht
F
Eingang
19.09.2023
Impfdatum
12.09.2023
Beginn
12.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Death Pain

Symptomtext

Pt had chills and felt achy the same evening. Pt passed away on 9/14/2023

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

VAERS 2692474

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

schwer
Staat
WA
Alter
72,0
Geschlecht
F
Eingang
07.10.2023
Impfdatum
28.09.2023
Beginn
28.09.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest pain Echocardiogram abnormal Pericarditis

Symptomtext

PT STATES THAT AT 9 PM ON 9/28/23 CHEST PAIN BEGAN AND PERSISTED FOR DAYS. PT WAS SEEN IN THE ER ON 10/6/23. ECHO WAS PERFORMED AND SHOWED PERICARDITIS. PT WAS TOLD THERE WAS NO VIRAL ILLNESS PRIOR THAT COULD HAVE CAUSED THIS CONDITION. PT WAS STARTED ON COLCHICINE 0.6MG BID AND IBUPROFEN (UNKNOWN STRENGTH AND FREQ). PT WILL HAVE REPEAT ECHO IN 1 MONTH

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
-
Labordaten
ECHO- 10/6/23
Aktuelle Erkrankungen
-
Vorgeschichte
type 2 diabetes, hypertension, asthma, nerve disorder
Andere Medikamente
Ozempic, dicyclomine, metformin, amlodipine, spironolactone, pregabalin, losartan, atorvastatin, acyclovir
Allergien
nkda
Vorherige Impfungen
-

VAERS 2676144

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

schwer
Staat
CA
Alter
86,0
Geschlecht
M
Eingang
24.08.2023
Impfdatum
07.08.2023
Beginn
08.08.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Brain fog Computerised tomogram Electrocardiogram Fall Haemorrhage Head injury Injection site pain Loss of consciousness Skin abrasion X-ray

Symptomtext

He got his vaccine and the initial reaction on the first day and the beginning of the 2nd day was soreness in the area of the vaccine. About 9:00 AM the following morning he started feeling funny in his head. He was going to meet one of his son's at noon and he drove to where they were going to meet, and was in the parking lot where they were meeting, and about 11:15 his condition in his head got worse, and his son called him about 10 to noon and he told him he was almost there. He got out of his car, locked it up and leaned against the car and his head condition got worse and worse and he drove into the parking lot, but he was not aware of it, out of it, but still standing. Before his son got to him his son saw him fell over, he passed out he says. He fell on the parking lot asphalt and hit the side of his head on the parking lot stoppers. He struck his head and has a bump on the head on the left rear quadrant, and his fingers on his right hand are all skinned up, elbows skinned up, his knee on the left, and the palm of his hand on the right is skinned up as well. The first thing he recalls after passing out was his son leaning over him with his cell phone in his hand calling 911, and paramedics came and got him and he went to the ER. He went to Medical Center. He was still messed up in the head when he arrived there, his son explained to the paramedics what happened, and he does not know what the paramedics told the hospital staff. He was injured and bleeding. He had x-rays, a CT scan, EKG. He has a heart issue and has two cardiologist and an electrophysiology physician. After the EKG they thought that he was having a heart attack or something. They acted like it was heart related, and he told them that he had the flu vaccine, which they ignored that. After 2 hours they cleaned up his wounds, and bandage them. His hands had bled, and all his other areas were dressed. They wanted to keep him at the hospital and check out his heart well, he told them that he has 2 cardiologist and they did not need to check him for that. He had experienced the same reaction when he had the Azithromycin in June. He thought he was dying with that and called 911 himself. They checked his BP was 212/197 and was taken to the hospital. He was given Carvedilol and wanted him to stay in the hospital, and was released as he refused to stay. Discharge BP 199/119. later it was 138/82. He went home later that afternoon, and for the next 13 days he stayed at home dressing his wounds and recovering. He feels pretty good now, but is not completely over the consequences of the fall, and his head is still not really clear and back to normal.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
EKG's, CAT scan, x-rays.
Aktuelle Erkrankungen
None
Vorgeschichte
Atrial fibrillation, abdominal aortic aneurysm watching 4.6 cm now, (ascending aortic aneurysm surgery in 2009), Hyper
Andere Medikamente
Carvedilol, Flomax, Gas-X, Exlax, aspirin 81 mg.
Allergien
Many antibiotics, statin's, Morphine, Norco( He has a list).
Vorherige Impfungen
-

VAERS 2701495

UNKNOWN MANUFACTURER · INFLUENZA (SEASONAL) (NO BRAND NAME) · Charge UT8043CA

moderat
Staat
CO
Alter
70,0
Geschlecht
F
Eingang
24.11.2023
Impfdatum
25.08.2023
Beginn
26.08.2023
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anger Arthralgia Back pain Condition aggravated Confusional state Balance disorder Dysstasia Emotional distress Exercise tolerance decreased Depressed mood Discouragement Fatigue Frustration tolerance decreased Gait disturbance Gait inability Impaired quality of life Loss of personal independence in daily activities Mobility decreased

Symptomtext

she developed pain in her left knee that worsen the pain in the right knee/Knee pain; pain in her ankles and down the legs sometimes/ pain in right arm/feet pain; back pain is back; the vaccine is affecting my mentality; I'm having trouble in my daily basis/RSV (AREXVY) vaccine has totally ruined my quality of life; knee lock; neurological issue; nauseous nearly every, single morning and after eating; headaches; fatigue; body aches/bizarre pains coming out of nowhere all over my body; Although I still tried to walk, several times on each walk, I would nearly collapse from the pain; sometimes tingling; I was in the absolute best health I had been in for a very long time/Your RSV (AREXVY) vaccine has totally ruined my quality of life/My life has been awful; I am depressed; angry; Confused; disappointed/I feel like breaking the television every time I see your AREXVY ads of the seniors bragging about your vaccine; This non-serious case was reported by a consumer via call center representative and described the occurrence of knee pain in a 70-year-old female patient who received RSVPreF3 adjuvanted (Arexvy) (batch number 5 AN52, expiry date 20-OCT-2024) for prophylaxis. Co-suspect products included Influenza vaccine (batch number UT8043CA) for prophylaxis. The patient's past medical history included back pain. Concurrent medical conditions included cholesterol. Concomitant products included simvastatin. On 25-AUG-2023, the patient received Arexvy and Influenza vaccine. On 26-AUG-2023, 1 days after receiving Arexvy, the patient experienced knee pain (Verbatim: she developed pain in her left knee that worsen the pain in the right knee/Knee pain), leg pain (Verbatim: pain in her ankles and down the legs sometimes/ pain in right arm/feet pain), back pain (Verbatim: back pain is back), mental state abnormal (Verbatim: the vaccine is affecting my mentality), activities of daily living impaired (Verbatim: I'm having trouble in my daily basis/RSV (AREXVY) vaccine has totally ruined my quality of life), knee lock (Verbatim: knee lock), neurological disorder nos (Verbatim: neurological issue), postprandial nausea (Verbatim: nauseous nearly every, single morning and after eating), headache (Verbatim: headaches), fatigue (Verbatim: fatigue), general body pain (Verbatim: body aches/bizarre pains coming out of nowhere all over my body), gait disturbance (Verbatim: Although I still tried to walk, several times on each walk, I would nearly collapse from the pain), tingling (Verbatim: sometimes tingling), general physical condition decreased (Verbatim: I was in the absolute best health I had been in for a very long time/Your RSV (AREXVY) vaccine has totally ruined my quality of life/My life has been awful), depression (Verbatim: I am depressed), anger (Verbatim: angry), confusion (Verbatim: Confused) and frustration (Verbatim: disappointed/I feel like breaking the television every time I see your AREXVY ads of the seniors bragging about your vaccine). The patient was treated with cortisone. The outcome of the knee pain, leg pain, back pain, mental state abnormal, activities of daily living impaired, neurological disorder nos, postprandial nausea, headache, fatigue, general body pain, gait disturbance, tingling, general physical condition decreased, depression, anger, confusion and frustration were not resolved and the outcome of the knee lock was not reported. It was unknown if the reporter considered the knee pain, leg pain, back pain, mental state abnormal, activities of daily living impaired, knee lock, neurological disorder nos, postprandial nausea, headache, fatigue, general body pain, gait disturbance, tingling, general physical condition decreased, depression, anger, confusion and frustration to be related to Arexvy. It was unknown if the company considered the knee pain, leg pain, back pain, mental state abnormal, activities of daily living impaired, knee lock, neurological disorder nos, postprandial nausea, headache, fatigue, general body pain, gait disturbance, tingling, general physical condition decreased, depression, anger, confusion and frustration to be related to Arexvy. Additional Information: GSK Receipt Date: 06-NOV-2023 The reporter was the patient who states she received Arexvy and she was having the worse side effects. According to the reporter the morning after receiving the vaccine she got up with right knee locked up, the pain was very intense, terrible pain and got better after a walk but increased during the week. The reporter states the pain was constant and after month she developed pain in her left knee that worsen the pain in the right knee. The patient also reported pain in her ankles and down the legs sometimes, and yesterday she developed pain in her right arm. The reporter stated she had been on 3 different doctors and they did not had an explanation for the pain. The patient had no history of arthralgia, and doctors believed the pain was more a neurological issue. The reporter stated she tried Cortisone for a week without relief of the pain, also had X-rays and nothing showed there. The patient stated that her life was dramatic after she received the vaccine, my back pain was back. The reporter stated she received a Flu shot the same day she received Arexvy, lot UT8043CA (not a match in system). The patient stated that the vaccine was affecting her mentality, and she had trouble in daily basis. It was unknown if the reporter considered the knee pain, leg pain, back pain, mental state abnormal, activities of daily living impaired, knee lock and neurological disorder nos to be related to Flu vaccine. The reporter consented to follow up. Follow-up information received on 14-NOV-2023. The patient mentioned that GSK RSV (Arexvy) vaccine had totally ruined her quality of life. Since August 26, the day after she got the vaccine, her body had not been the same. The patient was in the absolute best health, she had been in for a very long time. In fact, for nearly 96 days in a row, she was walking from two to six miles. The GSK vaccine attacked patient's knees in a horrible way as the next day she had terrible knee pain in her right knee which would dissipate in a few minutes once she moved around. However, within a few weeks, that pain got worse and stuck around. Although, the patient still tried to walk, several times on each walk, she would nearly collapse from the pain. Then it let up a little, only to go to my left knee which was in so much more pain than the right one. In addition, the patient was nauseous nearly every, single morning and after eating, headaches, body aches, fatigue and bizarre pains coming out of nowhere all over her body. The patient had strange body pain, sometimes sharp, sometimes tingling. None of this was happening prior to getting the vaccine. The patient was depressed, angry, confused and disappointed that none of the doctors she had seen had been able to help her yet. The patient got this terrible vaccine. Even steroids did nothing. The patient's life had been awful and she felt like breaking the television every time she was GSK Arexvy ads of the seniors bragging about GSK vaccine. The reporter hoped that, others were not experiencing the horrible consequences from GSK vaccine that she had been experiencing. It was unknown if the company considered the knee pain, leg pain, back pain, mental state abnormal, activities of daily living impaired, knee lock, neurological disorder, postprandial nausea, headache, fatigue, general body pain, gait disturbance, tingling, general physical condition decreased, depression, anger, confusion and frustration to be related to Influenza vaccine. Summary of Changes: Patient initials, current condition, concomitant products, Arexvy vaccine batch number, Flu vaccine batch number and vaccination date updated. New events added postprandial nausea, headache, fatigue, general body pain, gait disturbance, tingling, general physical condition decreased, depression, anger, confusion and frustration with time to onset for all events 1 day and narrative updated.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
Test Date: 2023; Test Name: X-ray; Result Unstructured Data: (Test Result:nothing showed there,Unit:unknown,Normal Low:,Normal High:)
Aktuelle Erkrankungen
Cholesterol
Vorgeschichte
Medical History/Concurrent Conditions: Back pain
Andere Medikamente
SIMVASTATIN
Allergien
-
Vorherige Impfungen
-

VAERS 2684886

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

moderat
Staat
CA
Alter
66,0
Geschlecht
F
Eingang
26.10.2023
Impfdatum
31.08.2023
Beginn
31.08.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injected limb mobility decreased Injection site pain Joint range of motion decreased Mobility decreased Pain in extremity Peripheral swelling

Symptomtext

Profound pain with injection followed by 48 hours of intense pain and inability to move arm. Ongoing pain and decreased range of movement.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
asthma hypothyroidism depression osteoporosis hypercalciuria
Andere Medikamente
Multivitamin Calcium supplement Vitamin D Bupropion Lexipro levothyroxine chlorthalidone
Allergien
none
Vorherige Impfungen
-

VAERS 2684886

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut8043CA

moderat
Staat
CA
Alter
66,0
Geschlecht
F
Eingang
26.10.2023
Impfdatum
31.08.2023
Beginn
31.08.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injected limb mobility decreased Injection site pain Joint range of motion decreased Mobility decreased Pain in extremity Peripheral swelling

Symptomtext

Profound pain with injection followed by 48 hours of intense pain and inability to move arm. Ongoing pain and decreased range of movement.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
asthma hypothyroidism depression osteoporosis hypercalciuria
Andere Medikamente
Multivitamin Calcium supplement Vitamin D Bupropion Lexipro levothyroxine chlorthalidone
Allergien
none
Vorherige Impfungen
-

VAERS 2700234

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

moderat
Staat
WA
Alter
68,0
Geschlecht
M
Eingang
23.10.2023
Impfdatum
01.09.2023
Beginn
01.09.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injected limb mobility decreased Injection site pain Joint range of motion decreased Musculoskeletal stiffness Pain in extremity Product administered at inappropriate site

Symptomtext

WITHIN 1 WEEK OF VACCINE: -SORE LEFT ARM, THEN STIFFNESS; LEFT SHOULDER PAIN IN FLARES -VERY LIMITED RANGE OF MOTION OF LEFT ARM, UNABLE TO REACH ABOVE WAIST HEIGHT.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
I BELIEVE IT WAS 10/12/23- HAD AN MRI WITH ORTHOPEDICS, DR SAID HE COULD SEE THAT THE VACCINE WENT IN TOO HIGH/DEEP CORTISONE SHOT, TWICE DAILY ADVIL ROUND OF PREDNISONE STARTING 10/12/23. DX CODE T50.Z95A: Adverse effect of other vaccines and biological substances, initial encounter
Aktuelle Erkrankungen
NONE KNOWN
Vorgeschichte
NONE KNOWN
Andere Medikamente
none known
Allergien
NO KNOWN ALLERGIES
Vorherige Impfungen
-

VAERS 2683032

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

moderat
Staat
AZ
Alter
76,0
Geschlecht
M
Eingang
18.09.2023
Impfdatum
15.08.2023
Beginn
17.08.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood glucose abnormal Condition aggravated Diabetes mellitus

Symptomtext

Uncontrolled blood sugar 2 days after vaccination.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
home glucose monitoring
Aktuelle Erkrankungen
Unknown
Vorgeschichte
hypertension, diabetes, hyperlipidemia
Andere Medikamente
metformin, atorvastatin & metoprolol
Allergien
NKA
Vorherige Impfungen
-

VAERS 2724731

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

mild
Staat
CO
Alter
74,0
Geschlecht
M
Eingang
17.12.2023
Impfdatum
13.12.2023
Beginn
15.12.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site warmth

Symptomtext

red and hot around area vaccine was given

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
will go to medical doctor monday to check on it if still doing bad
Aktuelle Erkrankungen
a fib
Vorgeschichte
a. fib
Andere Medikamente
called pt and left message to call back. on file warfarin, tramadol, allopurinol
Allergien
nkda,
Vorherige Impfungen
-

VAERS 2723914

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

mild
Staat
MN
Alter
67,0
Geschlecht
F
Eingang
13.12.2023
Impfdatum
07.12.2023
Beginn
08.12.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Rash erythematous Rash pruritic

Symptomtext

rash/red/itching, patient applied clotrimazole topically - recommended this stop and to used hydrocortisone or Benadryl

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

VAERS 2704538

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
AK
Alter
79,0
Geschlecht
M
Eingang
27.10.2023
Impfdatum
20.10.2023
Beginn
24.10.2023
Tage bis Beginn
4,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Joint effusion Myalgia Swelling

Symptomtext

Four days after receiving vaccinations, patient developed fluid accumulation near elbow. Per patient, swelling is approximately size of lemon with no skin color or temperature changes. Area is not tender but deltoid muscle still sore to use.

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

VAERS 2694657

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
AK
Alter
78,0
Geschlecht
F
Eingang
12.10.2023
Impfdatum
04.10.2023
Beginn
05.10.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Pain in extremity Rash Rash erythematous Tenderness

Symptomtext

SORE TENDER ARM THAT HAD RED RASH AND NOW IS JUST PAINFUL

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

VAERS 2693930

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
CA
Alter
85,0
Geschlecht
M
Eingang
10.10.2023
Impfdatum
08.10.2023
Beginn
08.10.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain in extremity

Symptomtext

Patient came in on 10102023 at approximately 04:50 PM to let us know at the pharmacy what he had been feeling after getting both his RSV and Flu Vaccination(s). Patient stated that he felt mild pain on the back of his left hand after getting the vaccination and didn't think too much about it. When asking how he felt today, 10/10/2023, patient had stated that he felt fine overall but would like this to be documented.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none stated per signed consent form
Vorgeschichte
none stated per signed consent form
Andere Medikamente
none listed or identified in our system
Allergien
No Known Drug Allergies
Vorherige Impfungen
-

VAERS 2691436

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
CA
Alter
74,0
Geschlecht
F
Eingang
05.10.2023
Impfdatum
02.10.2023
Beginn
04.10.2023
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Head discomfort Injection site erythema Injection site swelling

Symptomtext

Patient reported possible side effect with vaccine. She noticed a large red swollen round spot on left bicep below where the shot was given . Patient took Alieve. It got a bit smaller today. Her head felt heavy the other day after getting the vaccine and she had to lie down at home. Patient has had flu and the first dose of shingles vaccines in the past without reaction but the only difference is that she both two vaccines in one day this time. Recommended patient to apply ice and continue Alieve. If symptom gets worse, patient is to contact medical doctor.

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

VAERS 2688940

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

mild
Staat
AZ
Alter
76,0
Geschlecht
M
Eingang
29.09.2023
Impfdatum
19.09.2023
Beginn
19.09.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Diarrhoea Headache Pyrexia

Symptomtext

Symptoms: Fever, headache, whole body joint pain, diarrhea. Time course: beginning same day of vaccines, symptoms consistent for 2 days then self resolved

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

VAERS 2685588

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
NM
Alter
79,0
Geschlecht
M
Eingang
23.09.2023
Impfdatum
11.09.2023
Beginn
12.09.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Fall

Symptomtext

PATIENT REPORTED DIZZINESS AND FALLING AT 4 AM THE NEXT DAY AFTER THE SHOTS

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

VAERS 2685557

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
CO
Alter
71,0
Geschlecht
F
Eingang
23.09.2023
Impfdatum
19.09.2023
Beginn
19.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Musculoskeletal stiffness Pain

Symptomtext

Spoke w/ patient. She received Fluzone HD and Prevnar20 on the same arm on 9/19. She wanted them in the same arm because she didn't want both arms to be sore. She says she began having soreness later that day and it progressed to a stiff neck (she's having trouble moving the neck). It's begun to get better, but she wasn't sure if it was related to the vaccination. We discussed that going forward, we should avoid more than 1 vaccine at a time and possibly consider Flublok or regular dose Fluzone instead of Fluzone HD. She said she just wanted to report it, is not seeking any compensation or further care.

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

VAERS 2683522

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

mild
Staat
CO
Alter
82,0
Geschlecht
M
Eingang
19.09.2023
Impfdatum
23.08.2023
Beginn
24.08.2023
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Inflammation Pain Pruritus Skin discolouration

Symptomtext

Patient came by pharmacy to report that after shot right arm became inflamed and itchy. This had been going on for over a month. Skin had discoloration down to wrist but had been receding from point of max inflammation. Patient states it is getting better and pain is lessoning.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
atorvastatin 40mg 1qd
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2683384

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
AZ
Alter
81,0
Geschlecht
F
Eingang
18.09.2023
Impfdatum
03.09.2023
Beginn
03.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Visual impairment

Symptomtext

Patient had extreme dizziness in the evening seeing checker board. She stated it lasted approximately 5 minutes

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
HTN and High Cholesterol
Andere Medikamente
Losartan, Pravastatin, Zetia
Allergien
Latex, Shellfish
Vorherige Impfungen
-

VAERS 2682292

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
NV
Alter
74,0
Geschlecht
M
Eingang
13.09.2023
Impfdatum
11.09.2023
Beginn
11.09.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Injection site pain Injection site swelling Injection site warmth Joint range of motion decreased Pain

Symptomtext

Rt. deltoid/immunization site area is red,swollen, warm, tender to touch. "Painful". Has good neuro-circ. as well as sensory perception to RUE. Strong radial pulse. Guarded R.O.M. D/T pain. Swelling from immunization site to Rt. elbow. Area is marked with surgical marker and dated. Patient will monitor area. Will try ice and Motrin. Will report to the ER ASAP if he develops any worsening/changing S/S.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
-
Vorgeschichte
Diabetes. High Cholesterolemia. Sleep Apnea. Bradycardia. HTN. Osteoarthritis. Hearing loss. Plantar Fascial. Sinusitis. Cataracts. B/L Cataract surgery.
Andere Medikamente
Rosuvastatin. Moxifloxacin eye drops. Dorzolamide eye drops. Cholocalcif .Artificial Tears eye drops. Lisinopril. Tafluprost eye drops. Zinc.
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2680684

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
-
Alter
76,0
Geschlecht
F
Eingang
09.09.2023
Impfdatum
06.09.2023
Beginn
06.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Erythema Fatigue Injection site erythema Injection site swelling Peripheral swelling Pyrexia

Symptomtext

Patient had significant swelling and redness in left arm after receiving the Arexvy. Said swelled up to lump the size of a golf ball and had redness the size of a tennis ball. Felt tired and feverish that evening. Flu shot injection site had some swelling and redness. Patient took Benadryl and wrapped left arm in a cold cloth when they went to bed that evening. Came in to pharmacy on 9/9 and right arm looked almost fully improved and left arm had some redness still but looked like it had improved a lot since 9/6.

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

VAERS 2676375

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

mild
Staat
CA
Alter
67,0
Geschlecht
F
Eingang
24.08.2023
Impfdatum
21.08.2023
Beginn
21.08.2023
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hyperhidrosis Lip swelling Pain

Symptomtext

PATIENT REPORTED ACHINESS AND SWEATS THE EVENING OF THE VACCINE AND LOWER LIP SWELLING THE FOLLOWING MORNING.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
AMLODIPINE, ATENOLOL, CICLOPIROX, ESCITALOPRAM, FUROSEMIDE, I
Allergien
-
Vorherige Impfungen
-

VAERS 2713573

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

gering
Staat
CO
Alter
32,0
Geschlecht
F
Eingang
13.11.2023
Impfdatum
13.11.2023
Beginn
13.11.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exposure during pregnancy Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Was given the wrong vaccine. pt is 32 and pregnant and was give HD Flu

Weitere VAERSDATA-Felder
Praegender Schweregrund
Exposure during pregnancy
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2709526

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

gering
Staat
ID
Alter
32,0
Geschlecht
F
Eingang
03.11.2023
Impfdatum
19.08.2023
Beginn
19.08.2023
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event Product administered to patient of inappropriate age

Symptomtext

The patient had no issues, the only problem was she isn't 65 and she didn't need the high dose.

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

VAERS 2697590

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

gering
Staat
CA
Alter
69,0
Geschlecht
F
Eingang
17.10.2023
Impfdatum
24.09.1954
Beginn
04.10.2023
Tage bis Beginn
25.212,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Peripheral swelling Skin exfoliation

Symptomtext

Her arm got swollen and the skin got scaly

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

VAERS 2690720

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge ut8043ca

gering
Staat
OR
Alter
68,0
Geschlecht
F
Eingang
04.10.2023
Impfdatum
03.10.2023
Beginn
01.10.2023
Tage bis Beginn
-
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Exposure via skin contact Immunisation Syringe issue

Symptomtext

When depressing vaccine into muscle the vaccine rolled down the arm. Looked like it came from the neck of syringe just below luer lock. Gave patient another dose Fluzone.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Exposure via skin contact
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2688361

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

gering
Staat
OR
Alter
23,0
Geschlecht
M
Eingang
28.09.2023
Impfdatum
28.09.2023
Beginn
28.09.2023
Tage bis Beginn
0,0
Dosis
1
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

Symptomtext

pt accidentally received fluzone HD instead of the age appropriate fluzone quadrivalent. pt seems to be doing fine so far.

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

VAERS 2686437

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

gering
Staat
MT
Alter
63,0
Geschlecht
M
Eingang
26.09.2023
Impfdatum
25.09.2023
Beginn
25.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient was mistakenly given high dose influenza vaccine, but patient is only 63 years old. No reported Adverse events from the vaccine itself.

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

VAERS 2682277

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

gering
Staat
CA
Alter
80,0
Geschlecht
F
Eingang
15.09.2023
Impfdatum
05.09.2023
Beginn
05.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Erythema Peripheral swelling

Symptomtext

Patient said extremely swollen and red arm. Never followed up with the pharmacy and didnt say how long after the shot. She was still in viscinity of pharmacy for 10 minutes after the immunization and did not mention any reaction to pharmacy.

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

VAERS 2681992

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

gering
Staat
WA
Alter
64,0
Geschlecht
M
Eingang
14.09.2023
Impfdatum
13.09.2023
Beginn
13.09.2023
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

Administered to a patient who was 64. Off on the date of birth by one month.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product administered to patient of inappropriate age
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2679181

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) · Charge UT8043CA

gering
Staat
CA
Alter
66,0
Geschlecht
F
Eingang
02.09.2023
Impfdatum
02.09.2023
Beginn
02.09.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Unevaluable event

Symptomtext

See additional information/continuation page

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