- Staat
- MN
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 28.11.2023
- Impfdatum
- 18.10.2023
- Beginn
- 22.11.2023
- Tage bis Beginn
- 35,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Death
Hypotonia
Unresponsive to stimuli
Symptomtext
11/20/23: significant change noted with resident: noted that resident was unusually weak, nurse noted that resident was completely flaccid and unresponsive. Admitted to hospice that evening. 11/22/23 resident found to be deceased. Date of death: 11/22/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No acute illnesses
- Vorgeschichte
- Parkinson's, DM 2, HTN, Thyroid disorder, Atherosclerotic heart disease, Anxiety, Depression
- Andere Medikamente
- Tylenol 500, Carvedopa-Levodopa, Celexa, Eliquis, Ferrous Sulf
- Allergien
- Lasix, Sulfa Antibiotics, Intuniv, Metformin, Vitamin D, K-tab, Levothyroxine, Lisinopril, Magnesium.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 09.11.2023
- 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
Blood test
Hypoaesthesia
C-reactive protein
Differential white blood cell count
Dysstasia
Fall
Full blood count
Gait inability
Immunisation reaction
Metabolic function test
Red blood cell sedimentation rate
Respiratory pathogen panel
Urine analysis
Syncope
Symptomtext
Injection occurred around 2:20pm on 9/30/2023. Symptoms of lower body numbness started later that day around 5pm. Pt went to emergency room and according to pt., he had blood work, blood pressure done and waited until 9:30 at which time he was discharged because they could not diagnose causation and told pt. to go to primary care provider as soon as possible. Pt contacted Dr and she referred him to another doctor. 3 days later pt saw Dr
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- unknown other than what was already reported by patient
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- diabetes, gout, uncontrolled hypertension, 3 stents, watchman pacemaker, severe neuropathy
- Andere Medikamente
- Losartan, allopurinol, atorvastatin, potassium citrate, metformin, sotalol, isosorbide, spironolactone
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 09.11.2023
- Impfdatum
- 30.09.2023
- Beginn
- 30.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Hypoaesthesia
C-reactive protein
Differential white blood cell count
Dysstasia
Fall
Full blood count
Gait inability
Immunisation reaction
Metabolic function test
Red blood cell sedimentation rate
Respiratory pathogen panel
Urine analysis
Syncope
Symptomtext
Injection occurred around 2:20pm on 9/30/2023. Symptoms of lower body numbness started later that day around 5pm. Pt went to emergency room and according to pt., he had blood work, blood pressure done and waited until 9:30 at which time he was discharged because they could not diagnose causation and told pt. to go to primary care provider as soon as possible. Pt contacted Dr and she referred him to another doctor. 3 days later pt saw Dr
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- unknown other than what was already reported by patient
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- diabetes, gout, uncontrolled hypertension, 3 stents, watchman pacemaker, severe neuropathy
- Andere Medikamente
- Losartan, allopurinol, atorvastatin, potassium citrate, metformin, sotalol, isosorbide, spironolactone
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 30.10.2023
- Beginn
- 31.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
PATIENT FAINTED THE FOLLOWING MORNING IN HER HOME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 16.11.2023
- Impfdatum
- 16.10.2023
- Beginn
- 17.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Mobility decreased
Muscular weakness
Symptomtext
Patient was very weak, had a hard time getting out of the bathtub the next morning. Could not turn over on the couch due to weakness. His legs felt rubbery. This all lasted one day and he felt 90% better the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetic type 2
- Andere Medikamente
- metformin, crestor, glipizide aspirin, latanoprost, fish oil, centrum silver, and super b complex
- Allergien
- shellfish, kidney dye
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 13.11.2023
- Impfdatum
- 13.10.2023
- Beginn
- 14.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropathy
Haematoma
Mobility decreased
Musculoskeletal disorder
Symptomtext
Patient developed hematoma size described as large. Patient has had joint issues since the shot and cannot fully use her left arm as she has in the past. It has become difficult to lift above 90 degrees.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 07.11.2023
- Impfdatum
- 03.11.2023
- Beginn
- 03.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Diarrhoea
Impaired work ability
Malaise
Mobility decreased
Pain
Pyrexia
Symptomtext
Ten hours after vaccine administration, patient experienced a fever of 103 degrees with accompanying shivering and chills and was unable to get out of bed for 2 hours. She treated the fever with alternating ibuprofen and acetaminophen for one and one-half days at which time it came down to 99 degrees. Ten hours later it was back to normal. She also had body aches, maiaise, and diarrhea during this time. She missed 2 days of work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Norco 10mg, Fluoxetine 20mg, Zolpidem 10mg, Lisinopril/HCTZ 10/12.5, cyclobenzaprine 10mg
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 23.10.2023
- Beginn
- 23.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Immunisation reaction
Peripheral swelling
Pharyngeal swelling
Symptomtext
Patient reported history of reaction with vaccine in past. 2 vaccines were administered in the same arm per patient request. Patient was monitored in the pharmacy area for 15 minutes post-vaccination with no reaction. Patient left the pharmacy area. In the evening, patient reported they had swelling of the arm. The following day, patient reported they had additional arm swelling and throat swelling with difficulty breating, when they went to the emergency room. Patient was admitted to hospital and treated for vaccine reaction, and discharged two days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Trazodone, Fluoxetine, Alprazolam, Atorvastatin,
- Allergien
- Tetracylcines
- Vorherige Impfungen
- Patient reported fainted/dizziness with prior vaccine administration, reported prior to vaccine administration 10/23/23. Patien
- Staat
- NJ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 23.10.2023
- Beginn
- 24.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mobility decreased
Pain in extremity
Symptomtext
patient has severe arm pain cant lift arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 22.10.2023
- Impfdatum
- 09.10.2023
- Beginn
- 10.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Dyspnoea
Palpitations
Peripheral swelling
Swelling
Swelling face
Symptomtext
Patient received Fluzone HD (first time eligible for the HD) at 9:30am 10/9/23. At 3:30pm, neck, face, feet and hands began to swell. Patient took 25mg of Benadryl and continued Benadryl Q6H. She also reports slight difficulty breathing that night with racing heart. In the morning, patient drove herself to the hospital. Hospital monitored her for about six hours and also gave her a dose of her metoprolol. About twenty four hours after the onset, she reports feeling much better and better quickly. Spoke to patient today 10/22/23 and seems to be fully recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 19.10.2023
- Impfdatum
- 15.09.2023
- Beginn
- 16.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Decreased appetite
Dyspnoea exertional
Fatigue
Injection site pain
Injection site swelling
Pain
Symptomtext
Patient reports extreme pain and swelling at injection sites for 4-5 days, dyspnea on exertion, extreme fatigue, loss of appetite, and body aches. Symptoms started the day after immunization and lasted 4-5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 05.10.2023
- 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
Fatigue
Palpitations
Symptomtext
Patient said he had heart palpitations that started after the vaccinations and continued the second day. Patient also felt very exhausted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- I encouraged patient to follow up with physician.
- Aktuelle Erkrankungen
- prostate cancer
- Vorgeschichte
- prostate cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 26.09.2023
- Impfdatum
- 24.08.2023
- Beginn
- 13.09.2023
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Allergy to vaccine
Blood test
Chest X-ray
Computerised tomogram
Dyspnoea
Dyspnoea exertional
Gait disturbance
Immediate post-injection reaction
Influenza virus test negative
Injection site pain
Injection site reaction
Laboratory test
Limb discomfort
SARS-CoV-2 test negative
Screaming
Somnolence
Sudden onset of sleep
Tendon rupture
Symptomtext
Patient has shortness of breath lasting for 3 weeks or more. Initially had localized reaction at the site of injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 16.09.2023
- Impfdatum
- 15.09.2023
- Beginn
- 15.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dyspnoea
Pyrexia
Tremor
Symptomtext
The immunizations were given at approximately 12:23 pm. The patient states he started having weakness, shaking, difficulty breathing, and fever later that night. As of the next morning 09/16/2023 the patient had not yet seeked medical treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Trazodone , Omeprazole, Warfarin, Methenamine, Risedronate, Losartan
- Allergien
- Penicillin, morphine
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 22.11.2023
- Impfdatum
- 13.11.2023
- Beginn
- 15.11.2023
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site pain
Skin warm
Symptomtext
Patient experienced erythema > 100mm along the left arm which was warm to the touch. Erythema first appeared approximately 16 hours after receiving vaccinations, with pain at injection site still present 2 days later, but improving from previous day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 27.10.2023
- Beginn
- 27.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Pain
Pain in extremity
Symptomtext
Patient described a shooting pain down to her elbow immediately after administration. Patient called the pharmacy the next day to report pain continued intermittently up to 5 times per day since receiving vaccine. RPh advised patient to contact PCP with any concerns. RPh called patient 11/1/23, patient reported issue resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- glaucoma
- Andere Medikamente
- latanoprost 0.005% ophth, timolol 0.5% ophth, ketoconazole 2% shampoo.
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 28.10.2023
- Impfdatum
- 27.10.2023
- Beginn
- 28.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Nausea
Pain
Symptomtext
pt stated achy, tired and nausated day after vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 14.10.2023
- Beginn
- 14.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Patient received both Spikevax covid booster and flu HD in left arm. she states the injection site was sore and below the injection site her arm was red and swollen for couple days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- high cholesterol, thyroid, high blood pressure
- Andere Medikamente
- levothyroxine, pravastatin, amlodipine
- Allergien
- no known allergy
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 23.10.2023
- Impfdatum
- 17.10.2023
- Beginn
- 23.10.2023
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pruritus
Symptomtext
Patient reports itching over her entire body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 22.10.2023
- Impfdatum
- 18.10.2023
- Beginn
- 19.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injection site erythema
Nausea
Pyrexia
Symptomtext
A red area about 5-6 inches long and 2.5-3 inches wide appeared on left arm about 4-5 inches below injection site. It took about 4 days to get to the point where it almost cleared up completely. She also had fever and felt fatigued and nauseated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- atorvastatin, trazodone, clobetasol shampoo, multivitamin, probiotic, Konsyl fiber powder, vitamin d3, CoQ10, famotidine
- Allergien
- shellfish base, betadine,
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 15.10.2023
- Impfdatum
- 21.09.2023
- Beginn
- 22.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Symptomtext
PT CLAIMS NEXT DAY REDNESS AT INJECTION SITE WHICH TRAVELED DOWN ARM IN RECTANGULAR FORM(NOT HEAT RADATING OFF AND NO FEVER)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- DIABETES
- Andere Medikamente
- N/A
- Allergien
- SULFA
- Vorherige Impfungen
- SAME/FLU SHOT/2022
- Staat
- CT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.10.2023
- Impfdatum
- 10.10.2023
- Beginn
- 11.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash pruritic
Symptomtext
pt presented with a rash aproximately palm sized. stated started the day after the vaccination and had shrunk in size and intensity over the next few days. reported as being itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- clonazepam, celecoxib, omeprazole
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 05.10.2023
- Impfdatum
- 02.10.2023
- Beginn
- 03.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Papule
Rash
Rash pruritic
Symptomtext
pruritic rash on left forearm and left side trunk: erythematous papules started the day after vaccine and worsening locally Treatment with triamcinolone topically; loratadine 10mg QD and famotidine 20mg BID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN Osteoarthritis Hyperlipidemai GERD Migraine Osteopenia Insomnia
- Andere Medikamente
- trazodone 50mg QHS pravastatin 20mg QD omeprazole 20mg QD norvasc 5mg QD meloxicam 15mg QD melatonin 3mg QHS fosamax 70mg qweek fish oil 1g QD imitrex 100mg prn
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 03.10.2023
- Impfdatum
- 30.09.2023
- Beginn
- 30.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Erythema
Injection site erythema
Injection site swelling
Night sweats
Symptomtext
Left arm red from shoulder to wrist, swollen at immunization site, raised red at immunization site, night sweats, dizziness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 30.09.2023
- Impfdatum
- 29.09.2023
- Beginn
- 30.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Pain in extremity
Vaccination site rash
Symptomtext
Patient has a flat rash on her upper arm where she received the 2 vaccines (she received them both in one arm due to her lymph nodes removed on her left arm) she also had a sore arm and headache that started last night
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- trazodone 50mg, furosemide 20mg, metoprolol er 50mg, levothyroxine 50mcg, simvastatin 40mg,
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.09.2023
- Impfdatum
- 26.09.2023
- Beginn
- 26.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Injection site swelling
Pruritus
Symptomtext
PATIENT REPORTS RASH AND SWOLLEN AT SITE ON INJECTION AND ITCHY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 28.09.2023
- Impfdatum
- 19.09.2023
- Beginn
- 21.09.2023
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
patient has developed swelling on the inner left arm toward the elbow; patient has developed redness on the inner left arm toward the elbow; Initial information was received on 21-Sep-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case is linked to case 2023SA291630 (CLUSTER). This case involves 71 years old male patient has developed swelling on the inner left arm toward the elbow and patient has developed redness on the inner left arm toward the elbow after receiving influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. No concomitant vaccines administered. On 19-Sep-2023, the patient received a dose of 0.7 ml of suspect influenza quadrival A-B high dose HV vaccine (Frequency : Total, lot U8130DA, strength, expiry date, formulation unknown) via intramuscular route in the left deltoid for Immunization. On 21-Sep-2023 the patient developed swelling on the inner left arm toward the elbow (peripheral swelling) and developed redness on the inner left arm toward the elbow (erythema) (latency : 2 days) following the administration of influenza quadrival A-B high dose HV vaccine. Reportedly "The reaction is on the same arm that the vaccine was given, but not technically at the injection site, but it is above the elbow on the same arm. A husband and wife have reported the same reaction. Patient has not experienced any fever." Action taken with quadrivalent influenza vaccine (fluzone high-dose quadrivalent) was not applicable. It was not reported if the patient received a corrective treatment for the events (patient has developed swelling on the inner left arm toward the elbow, patient has developed redness on the inner left arm toward the elbow). At time of reporting, the outcome was Not Recovered for the events patient has developed swelling on the inner left arm toward the elbow and patient has developed redness on the inner left arm toward the elbow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 28.09.2023
- Impfdatum
- 19.09.2023
- Beginn
- 21.09.2023
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
swelling on the inner right arm toward the elbow; redness on the inner right arm toward the elbow; Initial information received on 21-Sep-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case is linked to case 2023SA291592 (CLUSTER). This case involves a 71 years old female patient who had swelling on the inner right arm toward the elbow and redness on the inner right arm toward the elbow after receiving influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. No concomitant vaccines administered. On 19-Sep-2023, the patient received a total dose of 0.7 ml of suspect influenza quadrival A-B high dose HV vaccine prefilled syringe (lot U8130DA, expiry date- 30-JUN-2024) via intramuscular route in the right deltoid for Immunization. On 21-SEP-2023, (latency- 2 days), the patient developed swelling on the inner right arm toward the elbow (peripheral swelling) and redness on the inner right arm toward the elbow (erythema) following the administration of influenza quadrival A-B high dose HV vaccine. Reportedly, The reaction is on the same arm that the vaccine was given, but not technically at the injection site, but it is above the elbow on the same arm. Patient has not experienced any fever. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the outcome was Not Recovered / Not Resolved for both the events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 22.09.2023
- Impfdatum
- 20.09.2023
- Beginn
- 22.09.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site rash
Injection site warmth
Symptomtext
Patient presented to the pharmacy with a red rash around and below shingrix injection site. It was warm to the touch. Patient stated she first noticed this rash 9/22/23. She denied any other symptoms other than red appearance and hot to the touch. Denied fever, pain, itching or any other symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Hypothyroidism Diabetes Mellitus Type 2 Hyperlipidemia
- Andere Medikamente
- Quetiapine 25 mg Levothyroxine 88 mcg Atenolol 25 mg Metformin 500 mg Trazodone 50 mg Atorvastatin 80 mg Clopidogrel 75 mg
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.12.2023
- 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
Occupational exposure to product
Symptomtext
dose spilled onto the nurse's hands with no reported adverse event; Initial information received on 11-Oct-2023 regarding an unsolicited valid non-serious case received from other health professional. This case involves an unknown age and gender patient for whom influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent] dose spilled onto the hands 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 was exposed to 1 unit dose of suspect influenza quadrival A-B high dose HV vaccine, injection (strength, route: unknown) (Batch number: U8130DA; expiry date: 30-Jun-2024) (indication: immunization) as the dose spilled onto the hands with no reported adverse event (accidental exposure to product) (unknown latency). Reportedly, nurse was about to give a patient Fluzone High-Dose Quadrivalent and noticed that the plunger of the vaccine was crooked like it was tilted to the right. When the nurse tried to pull out the plunger, the medication spilled on to the nurse's hands. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 31.10.2023
- Impfdatum
- 19.10.2023
- Beginn
- 19.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
patient was given 2 doses of FLUZONE HD QIV 3 weeks apart with no reported adverse event; Initial information received on 19-Oct-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 74 years old female patient who was given 2 doses of influenza quadrival A-B high dose HV vaccine [Fluzone High-Dose Quadrivalent] 3 weeks apart with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included elasomeran (Spikevax) for Prophylactic vaccination. Patient received one dose 3 weeks ago, then On 19-Oct-2023, the patient again received a standard dose of suspect influenza quadrival A-B high dose HV vaccine (with an unknown formulation) at a dose of 0.7 mL total (lot U8130DA, expiry date- 30-JUN-2024) via intramuscular route in the right arm for Immunization. On 19-OCT-2023 the patient was given 2 doses of fluzone hd qiv 3 weeks apart with no reported adverse event (extra dose administered) (latency- same day) following the administration of influenza quadrival A-B high dose HV vaccine. Reportedly, Pharmacist called in asking for safety data and recommendations for FLUZONE HD QIV following its administration to a patient 3 weeks apart; patient did not remember that she already received one dose 3 weeks ago, and had another dose today 19Oct2023. Treatment: None 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
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- SPIKEVAX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.10.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
A Patient did not remember that FLuzone HD was already administered 3 weeks ago, and received additional dose today again with no reported adverse event; Initial information received on 19-Oct-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age and unknown gender patient where a patient did not remember that vaccine influenza quadrival a-b high dose hv vaccine [Fluzone high-dose quadrivalent] was already administered 3 weeks ago, and received additional dose today again 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 quadrival a-b high dose hv vaccine (lot U8130DA and expiration date- 30-Jun-2024) via unknown route in unknown administration site (dose, formulation, strength: not provided) for Immunisation (extra dose administered) Action taken- not applicable. At time of reporting, the outcome was Unknown for the event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 19.10.2023
- Impfdatum
- 19.10.2023
- Beginn
- 19.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dysstasia
Gait disturbance
Vertigo
Symptomtext
Patient received a high dose flu shot, then experienced vertigo when she tried to stand up. Patient is a resident at an assisted living facility and has a history of vertigo, as well as some level of disability. An aide from the facility was with her at the time of the vaccine and the adverse effects. We gave her a bottle of water and an ice pack to place on the back of her neck, which helped. After sitting for about 20 minutes, she was feeling a little better, but was still unable to stand and walk out on her own. She declined transport to the hospital, and the aide went out to the transport van to get a wheelchair to get her to the van and into the facility. She also called the facility nurse, who said that she would check the patient over when she gets back to the facility. The aide said that the patient is prone to dizziness and vertigo, and said that they would watch her closely for the rest of today. Patient was coherent and talking fine, moving fine, no shakiness, no fever, just vertigo. Patient was able to get into the wheelchair and left with the aide.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysstasia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.10.2023
- Impfdatum
- 11.10.2023
- Beginn
- 11.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient was given 2nd Fluzone HD dose. First dose was given on 9/20/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- asthma//diabetes
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 02.10.2023
- Impfdatum
- 02.10.2023
- Beginn
- 02.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
patient received a 2nd Fluzone HD dose for the year, 1st on Septmeber 18th 2023 . no reaction at this time will follow up with patient during the week
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- alprazalam.25, atorvastatin 10mg, amlodipine 5mg, tamsulosin .4mg, finesteride 5mg
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 24.09.2023
- Impfdatum
- 24.09.2023
- Beginn
- 24.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
Patient received an HD-flu shot and a Spikevax Moderna booster. Patient reported being in cancer remission, with lymph nodes removed, and requested we administer both shots in her left arm, which was done. Patient later called back to say she had misremembered and should have told us to administer the shots in her right arm, and was asking what she should do. Counseled patient about decreased efficacy and possible swelling, and to follow up with her doctor on Monday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO REPORTED ILLNESSES AT TIME OF VACCINATION. PATIENT REPORTED BEING 8 YEARS CANCER FREE.
- Vorgeschichte
- PATIENT REPORTED BEING 8 YEARS CANCER FREE
- Andere Medikamente
- ANASTRAZOLE, GABAPENTIN, LISINOPRIL
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 23.09.2023
- Impfdatum
- 22.09.2023
- Beginn
- 22.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
HIV test
Hepatitis A virus test
Hepatitis B virus test
Hepatitis C virus test
Injury associated with device
Symptomtext
accidental needle stick in provider after vaccination given .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- HIV test
- Hospital-Tage
- -
- Labordaten
- blood test for Hep a, b, c, and HIV
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- furosemide, atorvastatin, losartan
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 21.09.2023
- Impfdatum
- 20.09.2023
- Beginn
- 20.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Patient received an additional dose of influenza vaccine. She already received Fluad at her PCP office two days prior. No AE's reported by patient at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -