- Staat
- VT
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 11.12.2023
- Impfdatum
- 11.12.2023
- Beginn
- 11.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Hypoaesthesia
Loss of consciousness
Malaise
Mydriasis
Pallor
Symptomtext
Approx 7 to 10 min after vaccination I was alerted by someone waiting for their vaccine that patient wasn't doing well. I went out to see and he looked pale. He was having a hard time breathing, told me his arms felt numb. His pupils were dilated. He was sitting on the floor when I got out there. I immediately tried to get him to lie down and put his feet up on a chair. He passed out, I told Tech to call 911 and I went into phcy to get EpiPen. When I returned he was awake and wondered what had happened. EMTs arrived within 10 minutes, took my version of events and took over. They eventually transported him to the ED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Vitamin D
- Allergien
- n/a
- Vorherige Impfungen
- when he woke up he stated that he had to sit down while at restaurant the last time he got a covid vaccine, no mention of this o
- Staat
- IL
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 30.11.2023
- Impfdatum
- 29.11.2023
- Beginn
- 29.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site haemorrhage
Syncope
Symptomtext
Patient fainted after seeing blood at the site of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NO
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 02.11.2023
- Impfdatum
- 02.11.2023
- Beginn
- 02.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Presyncope
Syncope
Symptomtext
Patient after receiving Flublok and Adacel, fainted...appeared to have a vagal reaction after around 5 minutes. EMT's were called came and monitored patient until he had a stable blood pressure and released him under his wife's care who was with him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Previous history of fainting after getting vaccinations
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Passed out with a previous vaccination.
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 15.10.2023
- Impfdatum
- 15.10.2023
- Beginn
- 15.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
Patient received vaccines and then was asked to have a seat for 15minutes after receiving vaccines to watch for any kind of reaction. After a couples of minutes they passed out and the pharmacist immediately went out there to see if they were alright. They had already regained consciousness and stated they have passed out in the past 3 weeks. They believed it was related to anxiety from getting vaccines. They stayed for another 15minutes and then someone drove them home. They confirmed they were feeling better and were okay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 05.10.2023
- Beginn
- 01.10.2023
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
After the patient received two vaccinations, Comirnaty and Flublok. The patient fainted while still in the vaccination chair. I aroused the patient back to consciousness. I walked him to another chair then he fainted again. I aroused him again then laid him on the floor for 15 minutes. Had him stand slowly; he said he was fine; he appeared to be fine. He left the pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 06.10.2023
- Beginn
- 06.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Symptomtext
Patient fainted while sitting about 5 minutes after receiving both vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- fainted
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 30.09.2023
- Impfdatum
- 30.09.2023
- Beginn
- 30.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Loss of consciousness
Symptomtext
Patient was sitting in her seat and may have lost consciousness or zoned out for a minute after receiving her Flublok vaccine. She regained consciousness upon her name being called out. Her temperature initially was 97.8F and lowered to 96.8F within approximately 5 minutes and stated that she is experiencing some shortness of breath. After remaining in her seat and drinking some water, within 15 minutes, patient recovered and had no other issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None per patient
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 23.09.2023
- Impfdatum
- 16.09.2023
- Beginn
- 19.09.2023
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Malaise
Myalgia
Nasal disorder
Pain
Paralysis
Pyrexia
Symptomtext
Patient came in the pharmacy on 09/22/2023 at 10:00 to report his experiences: 09/18/2023 He was just laying in bed not feeling well. 09/19/2023 He got paralysis, fever, pain, muscle aches and nasal symptoms. (took Tylenol) 09/22/2023 He is fine now. He said the reactions are from the RSV Patient received Flublok in 08/30/2021 and 09/28/2022 without any complication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- FLUZONE HD
- Vorherige Impfungen
- FLUZONE HD 10/07/2016
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 05.12.2023
- 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
Injected limb mobility decreased
Pain in extremity
Symptomtext
Customer received the 2 vaccines on the left deltoid(Adacel and Flublok) and Shingrix on the right deltoid. He said that his arm was sore from the vaccines but he expected the pain/soreness to go away in a few days but that has not happened. Customer said his arm has been hurting since then. He said he finds it difficult to perform simple activities like putting on seatbelt and raising his hand over his head. He also said that he has gone to see a Doctor and a Chiropractor but the pain is still there. He plans to go for an XRAY to see if there is any damage to his arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.11.2023
- Impfdatum
- 14.10.2023
- Beginn
- 14.10.2023
- 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
Pain in extremity
Symptomtext
Patient received flublok and comirnaty together in left arm. Patient states it was really painful ,"like a cortisone shot/" when first shot, which was flu, was administered. She thinks it was administered too high in the arm. She had a really sore arm for 3 days and hasn't been able to lift her arm past her shoulder for 4 weeks now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- High blood pressure, high cholesterol
- Andere Medikamente
- Rosuvastatin, Metoprolol Succinate, Triamterene/Hctz
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 28.10.2023
- Beginn
- 29.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Eczema
Urticaria
Symptomtext
Patient received flu shot and Arexvy on Saturday and woke up with hives/eczema covering her face Sunday
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Patient reported h/o eczema
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 28.09.2023
- Impfdatum
- 21.09.2023
- Beginn
- 21.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Dizziness
Electrocardiogram normal
Feeling abnormal
Laboratory test normal
Pain in extremity
Symptomtext
after getting flublok, patient did not feel good, chest pain and arm pain , dizziness so he went to ER that night. They did ECG and other tests but all came normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- gabapentin, amlodipine, omeprazole, simvastatin,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 20.09.2023
- Impfdatum
- 20.09.2023
- Beginn
- 20.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dyspnoea
Heart rate increased
Symptomtext
The patient received his flu vaccine and left the pharmacy to do some shopping. The patient returned to the pharmacy 10-15 minutes later having shortness of breath, chest pain, and elevated heart rate. The patient said he had a heart stent placed on 9/14/2023. An ambulance was called and the patient was taken to the hospital by EMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Heart stent placed 9/14/2023
- Vorgeschichte
- COPD, T2DM, HTN, hyperlipidemia, neuropathy
- Andere Medikamente
- Albuterol HFA inhaler, clopidogrel, atorvastatin, losartan, pregabalin, klor-con, meloxicam, primidone, topiramate, tamsulosin, metformin, verapamil, cyclobenzaprine, pioglitazone, hydromorphone
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 04.10.2023
- Beginn
- 06.10.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Swelling
Symptomtext
swelling under my right rib; dizziness; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old female patient (not pregnant) received bnt162b2 omi xbb.1.5 (COMIRNATY (2023-2024 FORMULA)), on 04Oct2023 at 19:15 as dose 1, single (Lot number: HG4680) at the age of 57 years, in left arm for covid-19 immunisation; influenza vaccine rha 4v (baculovirus) (FLUBLOK QUADRIVALENT), on 04Oct2023 as dose 1, single (Lot number: U8058AA), in left arm for immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing); "HTN" (unspecified if ongoing); "NASH" (unspecified if ongoing); "TBI" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "Arthritis" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE; LOSARTAN; ZOLOFT; VYVANSE; PANTOPRAZOLE. Past drug history included: Gabapentin, reaction(s): "known allergies: Gabapentin", notes: known allergies: Sulfa, Gabapentin and immitrex; Imitrex, reaction(s): "known allergies: Imitrex", notes: known allergies: Sulfa, Gabapentin and immitrex. Vaccination history included: Covid-19 vaccine (DOSE NUMBER 3 (BOOSTER), SINGLE, Manufacturer: Unknown), for COVID-19 immunization; Covid-19 vaccine (DOSE NUMBER 2, SINGLE, Manufacturer: Unknown), for COVID-19 immunization; Covid-19 vaccine (DOSE NUMBER 1, SINGLE, Manufacturer: Unknown), for COVID-19 immunization. The following information was reported: DIZZINESS (non-serious) with onset 06Oct2023, outcome "not recovered"; SWELLING (non-serious) with onset 06Oct2023, outcome "not recovered", described as "swelling under my right rib". The events "swelling under my right rib" and "dizziness" required physician office visit. The information on the batch/lot number for bnt162b2 omi xbb.1.5 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis; Asthma; Hypertension; Hypothyroidism; NASH; Sulfonamide allergy; Traumatic brain injury
- Andere Medikamente
- LEVOTHYROXINE; LOSARTAN; ZOLOFT; VYVANSE; PANTOPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 21.10.2023
- Impfdatum
- 15.09.2023
- Beginn
- 18.09.2023
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
SHE SAID THAT 3 DAYS AFTER GETTING THE 2 ABOVE VACCINATIONS, SHE HAD A BULLSEYE RING RASH ON HER LOWER LEFT ABDOMEN AND A RASH ALL ACROSS HER ABDOMEN. SHE QUESTIONED IF IT WAS A TICK OR SPIDER BITE BUT WASN'T SURE. SINCE WE DON'T KNOW, I AM REPORTING IT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NONE YET, BUT I RECOMMENDED SHE FOLLOW UP WITH AN MD TO RULE OUT TICK BITE/LYME. SHE SHOWED ME A PHOTO AND IT WAS A DEFINITE BULLEYE RASH CLEAR IN MIDDLE WITH RING RASH.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NAPROXEN, MELOXICAM AND SULFA DRUGS
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 19.10.2023
- Impfdatum
- 14.10.2023
- Beginn
- 01.10.2023
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Peripheral swelling
Staphylococcal infection
Symptomtext
Pt claim that she developed a staph. infection due to the vaccines that was given to her on the right arm. She's currently on antibiotics prescribed by her doctor. She stated that her arm was swollen, throbbing and in pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Asthma
- Andere Medikamente
- unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 17.10.2023
- Impfdatum
- 15.10.2023
- Beginn
- 16.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain
Pruritus
Symptomtext
extreme soreness and redness. Very itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none listed
- Vorgeschichte
- non listed
- Andere Medikamente
- na
- Allergien
- none listed
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 09.10.2023
- Impfdatum
- 06.10.2023
- Beginn
- 06.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Pain in extremity
Pruritus
Symptomtext
Left arm swelling, redness including circle around vaccination site, high level of soreness/pain and itching of the left arm. Patient stated that they received two vaccines in the left arm, but that was not what was documented on file. Follow-up to occur with immunizer regarding this. Patient was told to consult doctor upon worsening symptoms and counseled that potentially Benadryl could assist with itching symptoms. This has occurred since receiving vaccination on Friday, October 6th, 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Maintenance medications on file at pharmacy, patient did not provide information on medications taken that day of vaccination.
- Allergien
- cephalosporins, opioids, sulfa products.
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 07.10.2023
- 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: nein
Injection site inflammation
Injection site swelling
Symptomtext
Severe swelling and inflamation at Injection site and shoulder. Possibly due to one of the components of the Vaccine or FMF auto-immune disease reaction according to physician per Patient. October 6th and 7th was the reaction to shot given on 10/4. Patient is to follow up with a Neurologist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site inflammation
- Hospital-Tage
- -
- Labordaten
- Follow up with Neurologist this week for further tests
- Aktuelle Erkrankungen
- FMF auto-immune disorder with flare ups after illnesses and vaccines
- Vorgeschichte
- FMF auto-immune disorder and severe allergies
- Andere Medikamente
- Nurtec, Ventolin hfa, Levofloxacin,Ondansetron,Adderall,tramadol
- Allergien
- Patient is allergic to everything and has FMF autoimmune syndrome and had a flare-up after covid shot at well
- Vorherige Impfungen
- Covid vaccine leading to Dizziness
- Staat
- IL
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 04.10.2023
- Impfdatum
- 21.09.2023
- Beginn
- 21.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
On 10-03-23 pt called about currently experiencing swelling and redness from the flu shot. She claims she can still see the "injection hole", but the area is not spreading, not warm to the touch, and does not hurt unless she lays on that side
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- un known
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.10.2023
- Impfdatum
- 08.09.2023
- Beginn
- 08.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Influenza like illness
Pain in extremity
Symptomtext
PT RECEIVED A 3RD DOSE OF SHINGRIX, THINKING SHE HAD ONLY RECEIVED 1 PREVIOUS DOSE. SHE HAD A SORE ARM, MILD FLULIKE SYMPTOMS THE NEXT DAY, BUT NO OTHER ISSUES. SHE STATED NO SIGNIFICANT ISSUES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- SMOKER HYPERLIPIDEMIA HIGH BLOOD PRESSURE RESTLESS LEGS ANXIETY DEPRESSION INCONTINENCE
- Andere Medikamente
- ROSUVASTATIN 20MG TAB ALPRAZOLAM 0.5MG TAB METFORMIN ER 500MG TAB TRULICITY 0.75/0.5 INJ OXYBUTYNIN ER 10MG TAB METOPROLOL ER 50MG TAB VENLAFAXINE ER 150MG CAP BUSPIRONE 10MG TAB ROPINIRole 1MG TAB
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 02.10.2023
- Impfdatum
- 28.09.2023
- Beginn
- 28.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Brain fog
Erythema
Injection site erythema
Injection site reaction
Lethargy
Peripheral swelling
Rash macular
Skin warm
Symptomtext
Most of left arm is swollen, red, warm to touch. Injection site is red and blotchy. Patient feels lethargic and mind feels foggy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- RENAL TUBULAR ACIDOSIS, JUVENILE ARTHRITIS, DIABETES
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 01.10.2023
- Impfdatum
- 22.09.2023
- Beginn
- 25.09.2023
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Rash
Urticaria
Symptomtext
Three days after receiving patient experiences a whole body reaction while on treadmill. Severe urticaria, hives. rash welts
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.10.2023
- Impfdatum
- 21.09.2023
- Beginn
- 22.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site rash
Injection site warmth
Symptomtext
Patient came to the pharmacy and reports a rash migrated 2" below the injection site. Patient came to the pharmacy and showed the rash and it was 2" below the injection site with 2" perimeter, round, and warm to the touch. Patient reported that it did not hurt, but felt warm. Recommended patient to put cold compress onto the area and report the emergency room if severe symptoms occur.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Vitamin D3, Melatonin, occasional Tylenol extra strength
- Allergien
- Sulfa based drugs
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.09.2023
- Impfdatum
- 29.09.2023
- Beginn
- 29.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Injection site erythema
Injection site warmth
Symptomtext
immediately after the injection-the pt states she experienced redness and warmth in the area
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 28.09.2023
- Impfdatum
- 19.09.2023
- Beginn
- 19.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Hives on one side per patient. Patient not sure which vaccine caused this because they got both on same day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 26.09.2023
- Impfdatum
- 20.09.2023
- Beginn
- 21.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Bone disorder
Chills
Feeling abnormal
Headache
Injection site haemorrhage
Pain
Peripheral swelling
Pyrexia
SARS-CoV-2 test negative
Symptomtext
so after injection on the left arm, it bled. Then Thursday morning she woke up and didn't feel right and by thur afternoon fever started lowe grade and then by 4pm it shot up to 103.6 degrees and at that time the patient had a massive headache, body aches, bones felt like cracking and chills, patient developed a huge not on left arm and each day the knot got bigger and bigger. cool and warm compress made left arm worse. pt took covid test and it was negative. right now it is blistery on top and knot at bottom of blister
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- pulmonary hypertension, osteoporosis, herniated and bulging disc
- Vorgeschichte
- pulmonary hypertension, osteoporosis, herniated and bulging disc
- Andere Medikamente
- No prescriptions or otc and etc in several days
- Allergien
- amoxicillin
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 26.09.2023
- 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
Erythema
Skin warm
Swelling
Vaccination site joint pain
Symptomtext
Redness, swelling, warm to touch, pain distal to injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site joint pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Augmentin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 23.09.2023
- Impfdatum
- 14.09.2023
- Beginn
- 14.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Patient received flu and shingles vaccines on 9/14/2023. Post vaccination, she experienced pain, swelling, redness on area of shingles vaccination (Left arm) that lasted 4-5 days. She has been experiencing dizziness that has not gone away and states she does not have any blood pressure or blood sugar problems when she checked.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- high blood pressure, high cholesterol, chronic pain of lumbar region
- Andere Medikamente
- Acetaminophen 500 mg tablets, diclofenac 50 mg, atorvastatin 10 mg, Hydrochlorothiazide 25 mg, Medroxyprogesterone 2.5 mg, Wegovy 0.25 mg, Baclofen 5 mg
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 22.09.2023
- Impfdatum
- 12.09.2023
- Beginn
- 12.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Injection site erythema
Symptomtext
REDNESS, LARGE BRUISING UNDER THE INJECTION SITE THE FOLLOWING MORNING.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HIGH BLOOD PRESSURE, COPD
- Andere Medikamente
- GABAPENTIN 300MG , CARVEDILOL 6.25MG TAB, CITALOPRAM 20MG TAB, ALLOPURINOL 100MG TAB, SPIRIVA RESPIMAT 2.5MCG SPR, FUROSEMIDE 20MG TAB, ALBUTEROL HFA 90MCG (9GM) AER, NITROGLYCER 0.4MG SUB, ALBUTEROL 0.083% 3ML NEB
- Allergien
- CODEINE, MORPHINE, BUPROPION
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.09.2023
- Impfdatum
- 15.09.2023
- Beginn
- 20.09.2023
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Rash erythematous
Symptomtext
A RED, ITCHY RAISED BUMP WITH THE SIZE OF THE PINKY FINGERNAIL , NOT PAINFUL HAS DEVELOPED AT THE INJECTION SITE ON THE FIFTH DAY AFTER GETTING THE VACCINE. SHE NOTICED IT WAS THERE AT 1:00PM, AND NO MORE ITCHY AT 4:53PM TODAY 9/20/23.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 18.09.2023
- Impfdatum
- 14.09.2023
- Beginn
- 15.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Symptomtext
patient reporting redness, hardness on skin around injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 16.09.2023
- Impfdatum
- 14.09.2023
- Beginn
- 15.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site nodule
Injection site swelling
Injection site warmth
Symptomtext
pt has warm, raised red nodule at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 15.09.2023
- Impfdatum
- 06.09.2023
- Beginn
- 12.09.2023
- Tage bis Beginn
- 6,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site induration
Injection site swelling
Injection site warmth
Symptomtext
PT RECEIVED SHINGRIX ON 9/6/23 IN LEFT ARM AND WHEN HER CALLED US ON 9/12 HE STATED A FEW DAYS AFTER THE INJECTION HIS LEFT ARM SWELLED UP WHERE THE SHOT WAS GIVEN AND GOT HARD AND WAS WARM TO THE TOUCH. HE TOOK BENADRYL AND PUT ICE ON HIS ARM AND WHEN HE CALLED ON 9/12 HE STATED HE FELT FINE NOW
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- THYROID,
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 18.12.2023
- Impfdatum
- 13.10.2023
- Beginn
- 14.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Symptomtext
Patient received flu shot on 10/13/23, received antibiotics for cellulitis on the 15th from an urgent care
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 21.10.2023
- Impfdatum
- 21.10.2023
- Beginn
- 21.10.2023
- 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
Underdose
Symptomtext
Patient moved while receiving a flu shot, and the full dose was not delivered, some of the flu shot spilled. The flu shot was administered by Certified pharmacy technician. Then a full dose of the same flu shot was administered by Pharmacist, to ensure patient received a full dose flu shot. Patient was satisfied with receiving a full dose flu shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- No adverse side effects
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.10.2023
- Impfdatum
- 30.09.2023
- Beginn
- 30.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysgeusia
Eye movement disorder
Symptomtext
patient had metallic taste in mouth when drinking pepsi about 1 hour after then later in the night noticed she cannot wink her right eye. Patient can close both eyes at the same time, can close left eye only, but can not close right eye only.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none per pt
- Vorgeschichte
- diabetes, copd
- Andere Medikamente
- gabapentin 300mg tid lovastatin 40mg qd cyclobenzaprine 10mg metforming 500mg bid claritin 10mg qd linzess 145 prn ciclopirox 8% triamcinolone 0.5% cream bid albuterol hfa yupelri performomist
- Allergien
- apiriin, penicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 27.09.2023
- Impfdatum
- 26.09.2023
- Beginn
- 26.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse event reported, However patient was below age approved for 18 years or older on vaccine. Followed up with patient's guardians did not report any events
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 26.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
excursion lasted for about 6 hours, in middle of night and the lowest temperature reached is 0C with no reported adverse event; 2 of the FLUBLOK vaccines have been administered since the excursion with no reported adverse event; Initial information received on 14-Sep-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 53-year-old male patient who experienced excursion lasted for about 6 hours, in middle of night and the lowest temperature reached is 0c and 2 of the flublok vaccines have been administered since the excursion with no reported adverse event while receiving vaccine Influenza Quadrivalent Recombinant Vaccine [Flublok QIV]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date the excursion lasted for about 6 hours, in middle of night and the lowest temperature reached is 0c with no reported adverse event (product storage error) (unknown latency). On an unknown date, the patient received a dose of suspect Influenza Quadrivalent Recombinant Vaccine post excursion (lot: U8058AA, Expiry date: 31-May-2024) with unknown strength, formulation via unknown route in unknown administration site for Immunization with no reported adverse event (poor quality product administered) (same day latency). Action taken: not applicable. At time of reporting, the outcome was Unknown for both the events. 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
- -
- Staat
- AZ
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 23.09.2023
- Impfdatum
- 23.09.2023
- Beginn
- 23.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse effect noted as of this time. The reason for this submission is to document that the patient was accidentally given Flublok, which is only indicated for patient 18 years of age and up. The patient is 15 years old.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 22.09.2023
- Impfdatum
- 22.09.2023
- Beginn
- 22.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient is 17 years old but accidentally received Flublok which is approved for 18 and over.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Adderall xr, prozac
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 19.09.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
FLUBLOK have been administered since the excursion with no reported adverse event; Initial information received on 14-Sep-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 48 years old female patient whom influenza quadrivalent recombinant vaccine [Flublok QIV] have been administered since the excursion with no reported adverse event. 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 Influenza Quadrivalent Recombinant Vaccine strength, dose: not reported lot U8058AA expiry date: 31-May-2024 via unknown route in unknown administration site for immunization. On an unknown date flublok have been administered since the excursion with no reported adverse event (poor quality product administered) on the same day following the administration of Influenza Quadrivalent Recombinant Vaccine. Action taken was not applicable. At time of reporting, the outcome was Unknown for the event flublok have been administered since the excursion with no reported adverse 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
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 6,0
- Geschlecht
- F
- Eingang
- 16.09.2023
- Impfdatum
- 16.09.2023
- Beginn
- 16.09.2023
- 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
no adverse events yet, told the mother I would call 9-18-23 to check in if any adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- UNKNOWN
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 13.09.2023
- 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: unbekannt
Erythema
Peripheral swelling
Symptomtext
Patient called the pharmacy to report adverse reactions after getting their flu shot. Patient's arm started getting red and swelled up 1 and 1/2 hours after getting their vaccine. Patient reported that it swelled up to 3x in size. It has come down today and has not spread further. The patient did report they have a history of reactions caused by an unknown cause. I told the patient to take ibuprofen and put ice on the area. They cannot take Benadryl. If they have worsening signs to seek emergency care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin, Prednisone, Azithromycin, Benadryl
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 07.09.2023
- Impfdatum
- 30.08.2023
- Beginn
- 31.08.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anger
Vaccination site cellulitis
Symptomtext
Pt came to the pharmacy angry because she thought that we gave her the wrong vaccine. The pharmacist had followed all the correct process and given the correct vaccine to the patient on 08/30/2023. Per the pharmacy manager, Pt has cellulitis just under the location where the vaccine was administered. Pt had gotten both these vaccines in the same left arm and the pharmacist had separated two vaccines by 1 inch. Rx manager referred her to go see her provider.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anger
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -