- Staat
- CA
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 14.11.2022
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
General physical condition abnormal
Syncope
Symptomtext
Patient received the Pfizer COVID booster and then the high dose senior flu shot. After getting the flu vaccine, the patient looked off but insisted that he was fine. After taking a few steps out the vaccination room, he collapsed. Patient was offered water and EMS was contacted. EMS offered to take him to the ER but patient refused. Pharmacy staffed called and left message at 1500 to check on the status of the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Contusion
Diarrhoea
Dystonia
Electric shock sensation
Eye pain
Hypoaesthesia
Muscle spasms
Neuralgia
Pain in extremity
Paraesthesia
Tremor
Symptomtext
9/9/2022 2:32pm Shingrix Vaccine administered 9/9/2022 5:30pm I was lying on bed, reading. Sudden unusual aching and pain appeared on bottoms of both feet, ankles, then spreading up to both knees. Rubbing them did not aleviate discomfort. Walking around a bit seemed to help, but this strange aching returned as soon as I was sitting or lying down. (This symptom is still ongoing, however, and now added 2 episodes of foot cramping and foot dystonia which began on 9/27/2022) Numbness + tingling ongoing since 9/9/2022 9/11/2022 Sudden overall body weakness, followed by quick, stabbing, "electrical shock" pains along distal edge of right hand, followed by left hand about an hour later, This symptom continued while sleeping for 3 nights, Hand issue has since subsided. 9/13/2022 Sharp pain R temple followed by deep bruising pain behind right eye. Painful to touch and when moving eyes. Aspirin helped. 9/15/2022 Sclera of R eye became blood red still very painful move or touch. 9/17/2022 12:00pm Office visit with APRN. Suggested that Shingrix vaccine was creating autoimmune reaction related to having Sjogrens. Prescribed Gabapentin for nerve pain, which I have NOT taken (I'm very afraid of any medications). 9/17/2022 2:12pm Office visit with Ophthalmologist. Indicated that this was autoimmune reaction to Shingrix vaccine because of Sjogrens. Prescribed Prednisolone ACE 1% Eye drops. This medication quickly helped R eye. 9/18/2022 Same pain/redness sequence of symptoms began in left eye. Used Prednisolone Eye Drops to resolve. 9/24/2022 Sudden onset of body weakness and trembling (?) Hand "electrical shocks" and severe surprise "diarrhea". Rest and lots of water helped. 9/28/2022 Contact Dr (my rheumatologist for Sjogrens) to let him know of these Shingrix/Sjogrens developments.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Sjogrens Celiac
- Andere Medikamente
- Levothyroxine 12.5 mcg
- Allergien
- Gluten
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 13.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Abdominal pain
Back pain
Biopsy pancreas
Blood test
Chest pain
Endoscopic ultrasound normal
Lipase increased
Pancreatitis acute
Pancreatitis relapsing
Symptomtext
Severe abdominal pain, chest and back. Pain was the worse I ever had. When pain persisted through the next days, I went to hospital and was admitted with acute pancreatitis. This happened in September and then flared up in October, resulting in another trip to ER and another hospital stay
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 5,0
- Labordaten
- Blood tests, various, 10/1/22: Lipase was 17,600 Endoscopic ultrasound with fine needle aspiration by Dr. Test showed no cancer
- Aktuelle Erkrankungen
- NONE: with the hep of medicines noted above, my body was working fine
- Vorgeschichte
- GERD, anxiety, high blood pressure,
- Andere Medikamente
- Atorvastin 40 mg, Flonase, hyoscamine .125, Lorazepam 0.5, Losartin 50 mg, Pantoprazole 40 mg, Venlafaxine, metamucil
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Symptomtext
On Nov 28th, patient reported that his arm is still sore and he has pain lifting arm above the shoulder level. Deep ache all the time since the vaccinations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no known
- Vorgeschichte
- unknown
- Andere Medikamente
- gabapentin 600mg, and tadalafil 5mg
- Allergien
- sulfa and codeine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.11.2022
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Fall
Pain
Pyrexia
Vomiting
Symptomtext
Symptoms started 3 hours after vaccine. Severe chills, fever, vomiting, body aches and weakness. PT fell in bedroom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none noted
- Vorgeschichte
- ostomy 2008, 2' fecal incontinence CKD 3 thyroid dysfunction, hypothyroidism dg 39yo Multiple sclerosis, diagnosed age 16 yo COPD dry eye depression neurogenic bladder, self catheterizes hypothyroidism low back pain Barrets Esophogus
- Andere Medikamente
- Taking amLODIPine Besylate 5 MG Tablet, Sig: 1 tablet Orally Once a day Taking busPIRone HCl 5 MG Tablet, Sig: 1 tablet Orally Three times a day Taking Trospium Chloride 20 MG Tablet, Sig: 1 tablet Orally At Bedtime Taking traZODone HCl
- Allergien
- Substance: SULFA. Reaction: anaphylaxis, vomit. Type: Allergy. Status: Active. Substance: Amoxicillin. Reaction: vomit. Type: Side Effects. Status: Active. Substance: Duricef (Cefadroxil). Reaction: vomit. Type: Allergy. Status: Active. Substance: Adhesive Tape. Reaction: rash. Type: Allergy. Status: Active. Substance: Latex Gloves. Reaction: rash. Type: Allergy. Status: Active. Substance: Macrobid. Reaction: rash. Type: Allergy. Status: Active.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 25.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Peripheral swelling
Skin discolouration
Injection site bruising
Symptomtext
Patient came the second day with a big bruise on her left arm, the bruise was at the injection site and extends down to her elbows. The bruise was purple to blue in color
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Benadryl 25mg cap
- Allergien
- Sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 25.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Peripheral swelling
Skin discolouration
Injection site bruising
Symptomtext
Patient came the second day with a big bruise on her left arm, the bruise was at the injection site and extends down to her elbows. The bruise was purple to blue in color
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Benadryl 25mg cap
- Allergien
- Sulfa antibiotics
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Injection site pain
Injection site swelling
Symptomtext
Per pt, she had red, swollen, tender left arm from below injection site to just above elbow that lasted 4 days. She took Benadryl to relieve symptoms. Symptoms got better each day and resolved by day 4.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHRONIC PAIN, MOOD DISORDER, ARTHRITIS
- Andere Medikamente
- SUMATRIPTAN, OXYCODONE, CELECOXIB, ESCITALOPRAM, LEUCOVORIN, METHOTREXATE
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 25.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hyperhidrosis
Vomiting
Symptomtext
Patient went to restroom and starting feeling lightheaded, after 15 minutes, patient said feeling ok to go home. Patient called the Pharmacy on Sunday September 25th, stating was sweating a lot at night, felt faint, and vomiting. During conversation patient said no breathing problems,, or any allergic type reactions, told patient should go see or call provider if condition worsens.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension, hypothyroidism
- Andere Medikamente
- none
- Allergien
- Sulfa, Metronidazole, Penicillins
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 03.09.2022
- Beginn
- 03.09.2022
- 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 pruritus
Injection site swelling
Symptomtext
Site: Itching at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Patient states has been applying benadryl 2% cream to the injection site and will try hydrocortisone 1% cream as well for the itching. She will take benadryl once she gets home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 10,0
- Geschlecht
- M
- Eingang
- 23.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental exposure to product
Medication error
No adverse event
Product use issue
Symptomtext
10-year-old patient was inadvertently administered fluzone high-dose QIV with no reported adverse event; The 10-year-old patient was inadvertently administered Fluzone High-Dose QIV with no reported adverse event; Initial information was received on 16-Nov-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 10 years old male patient who had inadvertently administered fluzone high-dose qiv with no reported adverse event 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. Concomitant medications included COVID-19 vaccine for COVID-19 immunization. On 15-Nov-2022, the patient received 0.7 ml dose of suspect influenza quadrival A-B high dose HV vaccine (unknown formulation) (lot: UJ895AC) (frequency: total) (expiry date, strength was unknown) via intramuscular route in the left deltoid for Immunisation. On 15-Nov-2022 the patient had a non-serious event 10-year-old patient was inadvertently administered fluzone high-dose qiv with no reported adverse event (product use issue) and (Accidental exposure to product) (latency: same day) following the administration of influenza quadrival A-B high dose HV vaccine. Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the outcome was Unknown for 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
- Accidental exposure to product
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- COVID-19 VACCINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Off label use
Symptomtext
52-year-old female receiving Fluzone Quadrivalent High-Dose, with no reported adverse event; Initial information received on 13-Oct-2022 regarding an unsolicited valid non-serious case received from a healthcare professional. This case involves a 52-year-old female patient who was receiving INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT], with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 10-Oct-2022, the patient received 0.7ml dose total of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (strength, formulation: unknown) (lot number: UJ895AC and expiry date: 30-Jun-2023) via intramuscular route in the left arm for Immunization and 52-year-old female was receiving fluzone quadrivalent high-dose, with no reported adverse event (off label use; latency: same day). It was reported, the Nurse reported that the error was due to the order was given verbally; that the provider misspoke thinking the consumer was over 65-years; and the age of the patient was not checked prior to administration. Action taken was not applicable. At time of reporting, the outcome was Unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 13.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Erythema
Peripheral swelling
Skin warm
Tenderness
Symptomtext
Arm hot, red, Swollen, tender to the touch, Swollen left breast.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast swelling
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lupus, Malignant neoplasm of the breast, anemia, chronic pain, Insomnia
- Andere Medikamente
- Pregabalin, Calcium Vitamin D, Multi vitamin with minerals, DULoxetine, Ondansetron, Melatonin, MS Contin, buPROPion HCl ER, Senna, CeleBREX, Prazosin, oxyCODONE, Levothyroxine, MiraLax, Diclofenac
- Allergien
- Reglan, Bee venom, Tape
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
patient received the product FLUZONE QUADRIVALENT HIGH DOSE, but the patient is less than 65 years old, with no reported adverse event; Initial information received on 30-Sep-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 58 years old male patient who received the product fluzone quadrivalent high dose(INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE), but the patient is less than 65 years old, with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 30-Sep-2022, the patient received a dose of 0.7 ml of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (formulation, strength: unknown) lot UJ895AC, expiration date:30-Jun-2023 via intramuscular route in the left deltoid as Immunization On 30-SEP-2022 the patient received the product fluzone quadrivalent high dose, but the patient is less than 65 years old, with no reported adverse event (product administered to patient of inappropriate age) same day following the administration of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (patient received the product FLUZONE QUADRIVALENT HIGH DOSE, but the patient is less than 65 years old, with no reported adverse event). 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 guidelines. 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
- TX
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Pt received the high Dose Influenza vaccine. Notified patient. pt has no reaction or no symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Asthma, Gerd
- Andere Medikamente
- -
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Peripheral swelling
Symptomtext
Patient reported that her whole arms were swollen and red starting a few hours after getting the shots
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- osteoporosis
- Andere Medikamente
- N/A
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
PATIENT RECEIVED FLU VACCINE AT DR OFFICE EARLIER IN THE DAY. CAME IN FOR COVID BOOSTER AND FLUZONE HD WAS ADMINISTERED BY MISTAKE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- 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
Wrong product administered
Symptomtext
NO ADVERSE EVENTS, PATIENT RECIEVED FLUZONE HD INSTEAD OF FLUBLOK, PHARMACIST NOTICED AFTER PATIENT LEFT THE PHARMACY, NO SIDE EFFECTS WERE REPORTED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- RA
- Andere Medikamente
- methotrexate (reported by patient)
- Allergien
- none
- Vorherige Impfungen
- -