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Reporte zur Charge UT7317LA

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

9Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
IL 2 ME 1 IN 1 PA 1 MA 1 NJ 1 MI 1 OH 1

VAERS 1968426

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge ut7317la

schwer
Staat
ME
Alter
24,0
Geschlecht
M
Eingang
21.12.2021
Impfdatum
21.12.2021
Beginn
21.12.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Loss of consciousness Seizure

Symptomtext

Patient had a seizure within a few minutes of receiving these vaccines. He was on his way to a bench to take a seat and collapsed against his partner. A pharmacy technician helped to clear the scene, paramedics were called, but the patient regained conciousness quickly and did not need further treatment.

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

VAERS 1872687

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7317LA

moderat
Staat
IN
Alter
60,0
Geschlecht
M
Eingang
16.11.2021
Impfdatum
23.09.2021
Beginn
24.09.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Pain in extremity Pneumonia Productive cough Retching

Symptomtext

Patient reported that he developed symptoms within 24 hours of vaccination. Symptoms included productive cough, shortness of breath, gagging, "questionable" pneumonia (per chest xray). Patient had arm pain for 3 weeks. He was seen at urgent care clinic after vaccination (unknown timeframe) and was prescribed albuterol, tessalon perles, steroid, and zithromax for COPD exacerbation. He followed up with primary care on 11/02/2021 where chest xray was ordered. No additional medication/treatment was given.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
chest xray on 11/2/21
Aktuelle Erkrankungen
lower abdominal pain, microscopic hematuria, sore throat
Vorgeschichte
diabetes, obesity, COPD, dysphagia, carotid artery stenosis, pulmonary hypertension, carpal tunnel syndrome, atherosclerosis, hyperlipidemia, hypertension, hypothyroidism, obstructive sleep apnea
Andere Medikamente
levothyroxine, Lantus, Jardiance, amlodipine, atorvastatin, carvedilol, metformin, Cozaar, hydrochlorothiazide, spironolactone, amitriptyline, Anoro, venlafaxine
Allergien
amoxicillin
Vorherige Impfungen
-

VAERS 1696365

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7317LA

moderat
Staat
PA
Alter
57,0
Geschlecht
M
Eingang
14.09.2021
Impfdatum
13.09.2021
Beginn
13.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Anxiety Dizziness Dyspnoea

Symptomtext

I gave him vaccine, he was light headed after so I gave him gatorade. Then he said he was having bad anxiety, then some breathing issues so patient took some of his albuterol. Pt didnt need epipen or benadryl from me. I asked if he wanted me to call 911 and he told me yes.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Patient did Herion the day prior, told me after the fact.
Vorgeschichte
Asthma, hip problems
Andere Medikamente
Patient I believe just took a Suboxone
Allergien
Amoxicillin
Vorherige Impfungen
-

VAERS 1943169

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7317LA

mild
Staat
MA
Alter
57,0
Geschlecht
M
Eingang
11.12.2021
Impfdatum
22.10.2021
Beginn
22.10.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Grip strength decreased Pain in extremity

Symptomtext

Pain in arm, having trouble holding items since vaccine has been given. Patient will probably seeking medical attention to help his arm feel better or for a diagnosis

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

VAERS 1832096

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7317LA

mild
Staat
NJ
Alter
64,0
Geschlecht
F
Eingang
31.10.2021
Impfdatum
16.09.2021
Beginn
17.09.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
C-reactive protein increased Pain in extremity Polymyalgia rheumatica X-ray limb normal

Symptomtext

Developed severe left arm pain and several days later it was both arms. Diagnosed with polymyalgia rheumaticus.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
10/12 CRP (non-cardiac) 17 Ref range 0-10 10/29 Shoulder xrays neg
Aktuelle Erkrankungen
NA
Vorgeschichte
arthritis,
Andere Medikamente
zoloft, nexium, zyrtec, biotin, calcium, colestipol
Allergien
dilaudid, codeine, methylchloraisothiazonoe
Vorherige Impfungen
-

VAERS 1766151

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7317LA

mild
Staat
IL
Alter
48,0
Geschlecht
F
Eingang
06.10.2021
Impfdatum
02.10.2021
Beginn
03.10.2021
Tage bis Beginn
1,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Blister Blister rupture Dermatitis contact Pain

Symptomtext

Patient came in on 10/4/21 regarding a potential adverse reaction to a flu and TDap vaccine. They were both given on the same day on 10/2 in the same arm. Patient requested to recieve both vaccines on the same arm. I advised the patient that she can get one on each arm since she seemed quite nervous about getting the vaccines. However, she said she was fine getting both vaccines in the same arm. She asked me if they interact with each other and I advised her that these two vaccines do not interact and that it is given often together. The patient came back on 10/4 to speak to the pharmacist on duty and was concerned because she had a small fluid filled blister off to side, same arm near the bandaid edge possibly (she already took the bandaids off) but it didn't look like it was at the actual injection area. She usually has no problems with the flu vaccine the past years she had recieved it. After giving her the vaccines, the bandaid got stuck to my gloves and I reapplied it to make sure it stuck onto her arm properly. There was no redness, no swelling, or warmth at the area. She didn't report any other allergies, itching or fever and also said it wasn't spreading or getting worse. She said she had soreness which the pharmacist on duty told her was normal especially with aftering getting the TDap vaccine (she also said she's had the vaccine in the past in 2009 and just been due since its been over 10 years since she got it). The pharmacist on duty did leave a message to her doctor's phone number she provided just in case and she would follow up as well. The pharmacist on duty gave the patient her opinion thought that it was most likely unrelated, if anything maybe a mild skin reaction, maybe due to the adhesive, but to keep an eye on it just in case. It didn't look like a normal hive or cellulistis blister, not spreading no redness or fever. She had Claritin at home that she might use. The pharmacist on duty told her to use Benadryl for anything severe. She would take Tylenol or ibuprofen if needed for the soreness. Patient states she does not have allergies to anything ( latex or medications). I called on her 10/6 to follow up with her and to see how she was doing. She said she originally saw the blister on 10/5. She also told me she had a Clinic appointment on 10/5 and spoke to a nurse practitioner there. The nurse there told her it is possibly an allergic reaction to latex - no mention of being allergic to the actual vaccine itself. Nurse also told her the rubber stopper of the TDap vaccine we used is made out of latex. However, again, the blister did not form on the site of injection. It was formed on the posterior upper part of her left arm (closer to her armpit) where the edge of the adhesive part of the bandaid might have touched. Patient showed me a picture and the blister was not near the injection site. Patient also mentioned that she had used her own Band-Aid at home and she showed me a picture of the outline of the adhesive (showed some sort of slight reaction to the Band-Aid). The bandaid we had was a store off-brand. She said she never had any problems with other bandages until now. She also informed me her blister ruptured the morning of 10/6. The nurse she spoke to told her to use gauze and tape to cover it up instead of a bandaid due to possibe allergic reaction to latex. Patient states she has a health appointment with a doctor on Monday, October 11th. I will follow up with her to see how the visit went and she will continue to monitor the area with the blister.

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

VAERS 1916146

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7317LA

mild
Staat
MI
Alter
15,0
Geschlecht
M
Eingang
30.09.2021
Impfdatum
22.09.2021
Beginn
23.09.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Musculoskeletal stiffness Neck pain Rash Vomiting

Symptomtext

1 Day after shot , pt complained of stiff neck and neck pain. 2 Day after , pt had vomited. 3 Day after, Rash all over body. 4 Day after , man took pt to ER to be examined.

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

VAERS 1713570

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7317la

mild
Staat
IL
Alter
60,0
Geschlecht
M
Eingang
18.09.2021
Impfdatum
05.09.2021
Beginn
06.09.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain in extremity

Symptomtext

sore arm for 2 weeks, no problems with mobility

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

VAERS 1813077

SANOFI PASTEUR · INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) · Charge UT7317LA

gering
Staat
OH
Alter
67,0
Geschlecht
M
Eingang
23.10.2021
Impfdatum
14.10.2021
Beginn
14.10.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event Wrong product administered

Symptomtext

The patient had requested Fluzone HD Quad and instead received the Fluzone Quad with no reported adverse event; Initial information received on 14-Oct-2021 regarding an unsolicited valid non-serious case received from other health professional, consumer/non health care professional and physician via media Information (under reference 00812641). This case involves a 67 years old male patient who requested INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] and instead received the INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (wrong product administered). The patient had no other vaccines. The patient's medical history, medical treatment(s), concomitant medication(s) and family history were not provided. 14-Oct-2021, the patient received a 0.5 mL dose of suspect FLUZONE QUADRIVALENT (Solution for injection, Total, lot number: UT7317LA and expiration date: 30-Jun-2022) via intramuscular route in the right deltoid for prophylactic vaccination. It was an actual medication error due to wrong vaccine administered (same day latency). It was reported "Pharmacy intern is asking how to go about giving a patient the FLUZONE HD when they received the FLUZONE QUAD yesterday?" At time of reporting, no adverse event 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
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-