- Staat
- GA
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 16.10.2023
- Impfdatum
- 12.10.2023
- Beginn
- 12.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Feeling abnormal
Intensive care
Vomiting
Symptomtext
The 3 vaccines were administered to patient on 10/12/2023 at 11:39 a.m. She was instructed on common side effects and asked to remain in waiting area for 15 minutes. Patient then left area with no issues. That evening, she began feeling bad and saw the facility nurse the next morning for vomiting. The nurse kept an eye non her until Saturday morning when she was sent to hospital and admitted to ICU. She then died sometime between then and Monday morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 11.11.2023
- Impfdatum
- 11.11.2023
- Beginn
- 11.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Vomiting
Symptomtext
Patient went to sit on the bench after receiving 3 vaccinations (Spikevax, Fluzon HD, Abrysvo.) After a few minutes, she threw up and fainted. A nurse that was in the store shopping came over to help. I ran over to check on the patient and called 911. While I was on the phone with 911, my tech-in-training saw EMS in the store shopping and flagged them down. EMS then took over. EMS stabilized the patient and checked her vitals in the IMZ booth for privacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 09.10.2023
- Beginn
- 09.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aberrant aortic arch
Angiogram cerebral abnormal
Aortic valve incompetence
Aphasia
Arteriogram carotid abnormal
Asthenia
Bacteriuria
CSF culture negative
Cerebral atrophy
Cerebral small vessel ischaemic disease
Chest X-ray abnormal
Computerised tomogram head abnormal
Confusional state
Contrast echocardiogram
Culture urine positive
Echocardiogram abnormal
Ejection fraction normal
Electrocardiogram normal
Symptomtext
WITHIN APPROXIMATELY FIVE HOURS OF RECEIVING FLUZONE HD QUADRIVALENT VACCINE, SINGLE DOSE SYRINGE, IM TO LEFT DELTOID ON 10/09/2023 AT 8:07AM AT THE DOCTOR'S OFFICE, PT'S HUSBAND NOTICED PT WAS DEMONSTRATING PERSONALITY CHANGES AND HAVING FULL BODY TREMORS. WITHIN MINUTES FROM THIS FINDING, PT BECAME APHASIC, CONFUSED AND DIAPHORETIC. SHE EXPERIENCED LOSS OF BLADDER CONTROL, MUSCULAR RIGIDITY AND GENERALIZED WEAKNESS. FAMILY MEMBERS ADMINISTERED CHEWABLE ASPIRIN 81MG X 3 PO TO PT THEN TRANSPORTED HER BY PERSONAL VEHICLE TO ER. PT WAS ADMITTED TO THE HOSPITAL ON 10/09/2023 AT 7:39PM. HER TREATMENT INCLUDED IV ANTIBIOTICS, ROCEPHIN & VANCOMYCIN, IV ANTIVIRAL, ACYCLOVIR, ANTIPYRETICS, IV FLUIDS, NS AT 75MLS PER HOUR, AND PT/OT/ST.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- 5,0
- Labordaten
- UA/URINE C&S, 10/09/2023, PSEUDOMONAS COMPLICATED UTI/BACTERIURIA; CT HEAD WITHOUT CONTRAST, 10/09/2023, DIFFUSE ATROPHY AND WHITE MATTER SMALL VESSEL ISCHEMIC CHANGES WITH NO EVIDENCE OF ACUTE INTRACRANIAL DISEASE; CTA HEAD AND NECK 10/09/2023, NO LARGE VESSEL OCCLUSIONS, CRITICAL STENOSES, VASCULAR MALFORMATIONS, OR ANEURYSMS, ANATOMIC VARIANT RIGHT SIDED AORTIC ARCH WITH ABERRANT LEFT SUBCLAVIAN ARTERY, INCIDENTAL LEFT UPPER LOBE PULMONARY NODULES; CXR, 10/09/2023, CENTRAL VASCULAR PROMINENCE, LEFT UPPER LOBE NODULAR DENSITIES; ECG 12-LEAD, 10/09/2023, WNL; MRI BRAIN WITH AND WITHOUT CONTRAST, 10/10/2023, NO ACUTE INTRACRANIAL ABNORMALITIES; FLUOROSCOPIC GUIDED XR LUMBAR PUNCTURE, 10/13/2023, WNL; CARDIAC ECHO, 10/10/2023, NEGATIVE BUBBLE STUDY, NORMAL LEFT VENTRICLE SIZE AND FUNCTION WITH SIGNIFICANT LEFT VENTRICULAR HYPERTROPHY WITH EJECTION FRACTION OF 55-60%. TRACE AORTIC REGURGITATION AND MILD TRICUSPID REGURGITATION; BEDSIDE SWALLOW EVALUATION, 10/10/2023, WNL; CULTURE CSF, 10/10/2023, WNL; USV DUPLEX VENOUS LOWER EXTREMITY, RIGHT, 10/11/2023, NO RIGHT LOWER EXTREMITY DVT; RESPIRATORY PANEL, 10/11/2023, WNL; MEINGITIS/ENCEPHALITIS PANEL, 10/13/2023, WNL; WEST NILE VIRUS AB LAB TESTS, 10/10/2023, WNL.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HYPOTHYROIDISM, DYSLIPIDEMIA, ALZHEIMER'S DISEASE, ANEMIA, SEASONAL ALLERGIES, HISTORY OF LEFT LOWER EXTREMITY AKA.
- Andere Medikamente
- SYNTHROID 75MCG PO QAM, LIPITOR 10MG PO DLY, NAMENDA 10MG PO; DLY, ARICEPT 5MG PO BID, ZYRTEC 10MG PO DLY PRN SEASONAL ALLERGIES, MULTIVITAMIN PO DLY.
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 09.10.2023
- Beginn
- 09.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram cerebral normal
Aphasia
Arteriogram carotid normal
Asthenia
Bacterial test
Bacterial test positive
Cerebral atrophy
Cerebral small vessel ischaemic disease
Chest X-ray
Computerised tomogram head abnormal
Decreased appetite
Echocardiogram
Fatigue
Hyperhidrosis
Lumbar puncture
Magnetic resonance imaging head
Nitrite urine absent
Tremor
Symptomtext
aphasia; sweating; loss of bladder control; tremors; diffuse atrophy and white matter; positive for bacteria; moderate leukocytes; small vessel ischemic change; fatigue; weakness; loss of appetite; Initial information was received on 16-Oct-2023 regarding an unsolicited valid serious case received from a other health professional. This case involves a 81 years old female patient who experienced aphasia, sweating, loss of bladder control, tremors, diffuse atrophy and white matter, small vessel ischemic change, positive for bacteria, moderate leukocytes, fatigue, weakness and loss of appetite 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. On 09-Oct-2023, the patient received a 0.7 ml dose of suspect influenza quadrival A-B high dose HV vaccine (unknown formulation) (lot UT8131DA, expiration date: 30-Jun-2024, unknown strength) via intramuscular route in the left deltoid for Immunization. On 09-Oct-2023 the patient had aphasia, sweating (hyperhidrosis), loss of bladder control (urinary incontinence), tremors (tremor), diffuse atrophy and white matter (atrophy), small vessel ischemic change (vasculitis), positive for bacteria (bacterial test positive), moderate leukocytes (white blood cell disorder), fatigue, weakness (asthenia), loss of appetite (decreased appetite) (Latency: same day) following the administration of influenza quadrival A-B high dose HV vaccine. Relevant laboratory test results included: Blood work: On an unknown date: [Unknown] Angiogram - On an unknown date: [no large vessel occlusions, no critical stenosis, no vascular malfunctions or aneurysms] Chest X-ray - On an unknown date: [Unknown] Computerised tomogram - On an unknown date: [Diffuse atrophy and white matter, small vessel ischemic change, no evidence of acute intracranial disease] Echocardiogram - On an unknown date: [Unknown] Lumbar puncture - On an unknown date: [Unknown] Magnetic resonance imaging - On an unknown date: [Unknown] Urine analysis - On an unknown date: [Positive for bacteria, moderate leukocytes, negative nitrites, culture pending] Action taken: not applicable. The patient was treated with acetylsalicylic acid (aspirin), ceftriaxone sodium (rocephin iv), ciprofloxacin and doxycycline, Neuro checks, seizure precautions, speech therapy, occupational therapy, physical therapy. At time of reporting, the outcome was Not Recovered / Not Resolved for the events. Seriousness Criteria: Hospitalization for all events except loss of appetite. (Hospitalization was from 09-Oct -2023 to 14-Oct-2023, duration: 5 days).; Sender's Comments: Sanofi Company Comment dated 22-Oct-2023: This case involves a 81 years old female patient who experienced aphasia, sweating, loss of bladder control, tremors, diffuse atrophy and white matter, small vessel ischemic change, positive for bacteria, moderate leukocytes, fatigue, weakness and loss of appetite after receiving influenza quadrival A-B high dose HV vaccine [Fluzone high-dose quadrivalent]. Further information on medical history, allergy history, family history, past or concomitant medication excluding alternative etiologies for the reported event are needed to fully assess this case. Based upon the limited reported information, the role of the individual suspect vaccine cannot be assessed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- 5,0
- Labordaten
- Test Name: CT angiogram of head and neck; Result Unstructured Data: no large vessel occlusions, no critical stenosis, no vascular malfunctions or aneurysms; Test Name: Chest X-ray; Result Unstructured Data: Unknown; Test Name: ct of the head; Result Unstructured Data: Diffuse atrophy and white matter, small vessel ischemic change, no evidence of acute intracranial disease; Test Name: Echocardiogram; Result Unstructured Data: Unknown; Test Name: Lumbar puncture; Result Unstructured Data: Unknown; Test Name: MRI head; Result Unstructured Data: Unknown; Test Name: urinalysis; Result Unstructured Data: Positive for bacteria, moderate leukocytes, negative nitrites, culture pending
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 09.10.2023
- Impfdatum
- 29.09.2023
- Beginn
- 30.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blindness
Blood pressure decreased
Dehydration
Dizziness
Symptomtext
Patient received the vaccine on Friday and Saturday morning while attending a football game patient became very dizzy, everything went dark, and her blood pressure kept dropping upon rising. Patient was taken by ambulance to the hospital. She was given a bag of fluids for dehydration and discharged
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- high cholesterol, high blood pressure
- Andere Medikamente
- Nebivolol 5mg, Simvastatin 10mg, Triamterene/HCTZ 37.5/25mg Tumeric, fish oil
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 17.11.2023
- Impfdatum
- 14.11.2023
- Beginn
- 16.11.2023
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site oedema
Injection site swelling
Symptomtext
Client developed an edematous, red-purple area distal to the injection site on her left arm and extending to her elbow. Based on a picture provided to this RN, it appeared to be roughly 8-12 cm in width (around the arm) and roughly 15-18 cm long (longitudinal toward her hand). Swelling was greater dependent to the injection site. Client was advised to seek medical attention of a physician or go to the ED of the local hospital urgently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None at this location
- Aktuelle Erkrankungen
- Denied
- Vorgeschichte
- None Stated
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 12.11.2023
- Impfdatum
- 11.11.2023
- Beginn
- 11.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Patient called back today 11/12/23 of severe arm pain. She's still able to move the arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 26.10.2023
- Impfdatum
- 25.10.2023
- Beginn
- 25.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Headache
Nausea
Pain
Symptomtext
BODY ACHES, HEADACHE, NAUSEA, SHOULDER PAIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 20.10.2023
- Beginn
- 20.10.2023
- 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 swelling
Symptomtext
Swelling and redness below injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- CHF, Anemia, Hypothyroidism
- Andere Medikamente
- Xarelto 20 MG Tablet 1 tablet with food Orally Once a day WALKER WITH WHEELS & SEAT DX: - - External - CPAP SUPPLIES one As directed DX: OSA ICD-9: 327.23 External q hs Multivitamin Adults - Tablet Orally Nadolol 40 MG Tablet 1 tablet Orall
- Allergien
- Bactrim and Penicillin
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 23.10.2023
- Impfdatum
- 20.10.2023
- Beginn
- 21.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Pain
Product administered at inappropriate site
Swelling
Symptomtext
VACCINE WAS ADMINISTERED TOO LOW ON THE ARM AND CAUSE PAIN, REDNESS, AND SWELLING.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 20.10.2023
- Impfdatum
- 11.09.2023
- Beginn
- 12.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Illness
Injection site erythema
Injection site irritation
Injection site swelling
Injection site warmth
Nasopharyngitis
Pyrexia
Symptomtext
PATIENT EXPEREINCED SWOLLEN, RED, HOT, AND IRRITATED AREA ON LEFT DELTOID 1 DAY POST INJECTION. CLAIMS SHE ALSO EXPEREINCED HIGH FEVER AND HAS BEEN SICK FOR APPROX. 5 WEEKS WITHOUT RESOLUTION. CAME TO PHARAMCY AND I DIRECTED HER TO GO TO MD AND BE ASSESSED. SHE RETURNED TO THE PHARMACY WITH AN RX FOR CEFDINIR FOR POSSIBLE CELLULITIS AND COLD LIKE SXS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- CLAIMS UNREMARKABLE
- Vorgeschichte
- DEPRESSION HTN ANX
- Andere Medikamente
- DULOXETINE WELLBUTRIN XL
- Allergien
- KNMA
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 20.10.2023
- 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: nein
Injection site erythema
Injection site rash
Injection site swelling
Symptomtext
Rash , redness and swelling aroundsite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- -
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 14.10.2023
- Impfdatum
- 13.10.2023
- Beginn
- 13.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Hot flush
Myalgia
Nausea
Vomiting
Symptomtext
Patient received flu shot and about 2 hours after vaccine was given patient experienced diarrhea, nausea, vomiting, hot flashes and muscle aches
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None listed
- Vorgeschichte
- None listed
- Andere Medikamente
- -
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 12.10.2023
- 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: unbekannt
Erholt: nein
Injection site bruising
Injection site erythema
Injection site swelling
Injection site warmth
Symptomtext
Patient noted bruising in her left arm at injection site and reddness and swelling in her lower left arm (about the size of an orange). The red area is also warm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- None noted
- Andere Medikamente
- Oxybutynin, Lisinopril, Lexapro, Amlodipine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 08.10.2023
- Impfdatum
- 18.09.2023
- Beginn
- 19.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry skin
Pruritus
Skin exfoliation
Symptomtext
He experienced severe itchy, flaky, dry skin on both arms that started the day after receiving the immunizations and has persisted since. He has applied moisturizers without much benefit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Charcot-Marie-Tooth disease,
- Andere Medikamente
- propranolol 40mg, acetaminophen/codeine 300/30mg
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 05.10.2023
- Impfdatum
- 28.09.2023
- Beginn
- 28.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Fear
Headache
Hyperhidrosis
Pyrexia
Symptomtext
Paralyzing weakness in bed; Headache; Chills, fever, and extreme sweating over a period of approximately 4 hours in total. Alone so could not leave bed safely to get to thermometer to take temperature. After around the 5th hour and after the sweating had subsided the temperature came in at 99.5 degrees. Sleep resumed and weakness continued until around 5:00 PM on the 29th. Slept well that night and felt stronger as of mid-morning on the 30th. Quite relieved because it was a scary experience. I feel it was the RSV because I have had Flu shots repeatedly over many years with no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Idiopathic Pulmonary Fibrosis (IPF), a type of Interstitial Lung Disease (ILD)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.10.2023
- 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: ja
Erholt: nein
COVID-19
Chest X-ray normal
Ear pain
Fatigue
Nausea
Pain
Productive cough
SARS-CoV-2 test positive
Vomiting
Symptomtext
Patient is a 67-year-old female with a past medical history of chronic cough, factor V Leiden (not on anticoagulation), anxiety, depression, bipolar 2, and PTSD presenting today for multiple concerns. Patient reports that 4 days ago she got both her fifth COVID shot as well as a "high-dose" flu shot. Since then she has been having multiple symptoms. She initially had some nausea and vomiting which has since subsided. She then developed severe throat pain radiating up to her ear. She is concerned she has otitis media. She has also developed a productive cough with thick white sputum and excessive sneezing. She is concerned that she has drainage dripping down and causing pneumonia. Has had body aches and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- Exam without evidence of otitis media, pharyngitis, or pneumonia. Her lungs are clear to auscultation bilaterally. COVID swab is positive which does correlate well with her symptoms. Chest x-ray without infiltrate to suggest pneumonia.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Lamictal ODT
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 29.09.2023
- Impfdatum
- 26.09.2023
- Beginn
- 27.09.2023
- 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 swelling
Injection site warmth
Symptomtext
Patient reports arm redness and swelling and warmth from injections site (deltoid) to elbow, wrapping around arm. No bumps or itching reported or observed. Symptoms first noticed the morning after vaccinations, on 9/27/23. When presented to pharmacy on 9/29/23, patient said symptoms were improving but were still present and observed. Instructed patient to report event to PCP. Patient declined recommendation to make an appointment with PCP or go to urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart problems, patient did not know specific diagnosis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 25.09.2023
- Impfdatum
- 25.09.2023
- Beginn
- 25.09.2023
- 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
Peripheral swelling
Skin swelling
Symptomtext
patient states her arm that got the flu shot starting puffing up and was super red at the site. she said it was as big as a golf ball. no other symptoms and it wasn't hurting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 16.09.2023
- Impfdatum
- 15.09.2023
- Beginn
- 16.09.2023
- 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 vesicles
Symptomtext
Patient came back today to show pharmacist her arm; it was red where she received the vaccinations, and it appeared to be a water blistered formed on her arm. Patient has been putting ice on it this morning. Per patient, the blister showed up this morning and has gotten bigger during the day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none noted on vaccine sheet
- Andere Medikamente
- celebrex, doxazosin, sertraline 50, crestor 20, lisinopril/hctz 20/12.5mg
- Allergien
- cephalosporins
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 13.09.2023
- Impfdatum
- 07.09.2023
- Beginn
- 08.09.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Diarrhoea
Erythema
Incorrect route of product administration
Pain in extremity
Symptomtext
Patient was given Arexvy subcutaneously instead of intramuscularly by mistake. The day after vaccination, patient had soreness, redness, joint aches in both arms and diarrhea off and on through Day3 after vaccination. As of Day 3 the redness, soreness and joint aches had resolved and only mild diarrhea was ongoing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Fibromyalgia, Rheumatoid Arthritis, heart disease
- Vorgeschichte
- Fibromyalgia, Rheumatoid Arthritis, heart disease
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 04.12.2023
- Impfdatum
- 02.12.2023
- Beginn
- 02.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
Patient received vaccine outside of our healthcare system. When admitted to the hospital, inadvertently received second influenza vaccine. No side effects noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 01.12.2023
- Impfdatum
- 22.11.2023
- Beginn
- 28.11.2023
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Symptomtext
Large amount of swelling in the arm that recieved both vaccines. Advised pt follow up with PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 26.11.2023
- Impfdatum
- 17.11.2023
- Beginn
- 26.11.2023
- Tage bis Beginn
- 9,0
- Dosis
- N/A
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye disorder
Ocular hyperaemia
Symptomtext
eye related side effect patient is also encouraged to report
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ocular hyperaemia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 15.11.2023
- Impfdatum
- 09.11.2023
- Beginn
- 12.11.2023
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Contusion
Skin discolouration
Symptomtext
Patient has a large purple bruising extending from deltoid muscle, across bicep muscle and down to elbow. There was not excess bleeding or pain at administration. The patient reported it was 3 days later when he started to notice a purple pooling/bruise on his arm and continued to enlarge for 2 days. It has since stopped enlarging and has some yellowing in the upper arm. Patient was seen by a prescriber and stated "they ran blood work and said I was fine".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test normal
- Hospital-Tage
- -
- Labordaten
- unknown to pharmacy
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 11.10.2023
- Impfdatum
- 10.10.2023
- Beginn
- 11.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Symptomtext
Patient's wife called this evening, stated her husband received his flu vaccine yesterday. He woke up this morning with cheeks, forehead, and nose red. It started to fade in early afternoon, but not has gotten redder again. He has eczema, but this is different and she thinks it may be from the flu vaccine. He has had the flu shot in the past, but never had a problem before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- eczema
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 11.10.2023
- Impfdatum
- 22.09.2023
- Beginn
- 02.10.2023
- Tage bis Beginn
- 10,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Gingival bleeding
Immune thrombocytopenia
Immunoglobulin therapy
Petechiae
Platelet count decreased
Platelet transfusion
Thrombocytopenia
Symptomtext
Patient developed severe thrombocytopenia to a level of 3K, whereas patient had previously normal level platelet count just 3 weeks prior. Patient presented with diffuse petechiae and bleeding from the gums. She was hospitalized and received platelet transfusion, diagnosed with ITP, followed by high-dose dexamethasone and IVIG, with resolution of platelet count.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gingival bleeding
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- No acute illnesses
- Vorgeschichte
- Hypertension, Stage 3b Chronic Kidney Disease, COPD, Prediabetes, Hyperlipidemia, History of Lung Cancer, Hypomagnesemia, History of iron deficiency anemia
- Andere Medikamente
- Tylenol, Albuterol inhaler, Aspirin, Atorvastatin, Diltiazem, Esomeprazole, Gabapentin, Hydrochlorothiazide, Lisinopril, Magnesium Oxide, Metformin
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 08.10.2023
- Impfdatum
- 07.10.2023
- Beginn
- 07.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Underdose
Symptomtext
Patient received pediatric dose of Pfizer Covid-19 vaccine instead of adult Comirnaty. Was first dose out of box and error was found when getting vaccine for next patient. Patient notified and reported no side effects. Most likely effect is insufficient protection from vaccine. Currently evaluating course of action in terms of timing for patient to receive correct vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Bug bite treated with antibiotic
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Opioid and Benzodiazepines
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 05.10.2023
- Impfdatum
- 02.10.2023
- Beginn
- 03.10.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Peripheral swelling
Symptomtext
Patient reported arm swelling the day after receiving the high dose fluzone injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Peripheral swelling
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 04.10.2023
- Impfdatum
- 04.10.2023
- Beginn
- 04.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 04.10.2023
- Impfdatum
- 04.10.2023
- Beginn
- 04.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Given high dose flu instead of regular flu
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 04.10.2023
- Impfdatum
- 21.09.2023
- Beginn
- 21.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
She was given the high dose but is not old enough. NO adverse event known.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.10.2023
- Impfdatum
- 14.09.2023
- Beginn
- 14.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
GIVEN AT AGE OF 61 YEARS. NO ADVERSE REACTION REPORTED/ASSESSED FROM PATIENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- denies.
- Vorgeschichte
- denies
- Andere Medikamente
- fish oil multivitamin
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 30.09.2023
- Impfdatum
- 30.09.2023
- Beginn
- 30.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
no adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- diabetes
- Andere Medikamente
- n/a
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.09.2023
- 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
administrating the product after experienced a temperature excursion with no reported adverse event; Initial information received on 11-Sep-2023 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age and unknown gender patient who experienced administrating the product Influenza Quadrival A-B High Dose HV Vaccine [Fluzone High-Dose Quadrivalent] after experienced a temperature 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 0.7 ml (frequency: once) suspect Influenza Quadrival A-B High Dose HV Vaccine lot UT8131DA, Expiry date: 30-Jun-2024) with unknown strength & formulation via intramuscular route in unknown administration site for Immunization after experienced a temperature excursion with no reported adverse event (poor quality product administered) (latency: same day) . Action taken: not applicable. At time of reporting, the outcome was Unknown. 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
- AL
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 17.09.2023
- Impfdatum
- 08.09.2023
- Beginn
- 08.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
Patient came in for flu and RSV vaccs and was administered flu and shingles (in error). No known adverse reaction occurred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Cancer
- Vorgeschichte
- Cancer
- Andere Medikamente
- Acyclovir 400mg, Doxazosin 4mg, Sertraline 50mg, Pantoprazole 40mg, Chemo drug, no known OTC
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 17.09.2023
- Impfdatum
- 08.09.2023
- Beginn
- 08.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
Patient came in for flu and RSV vaccines and was administer flu and Shingrix (in error). No known physical adverse reaction occurred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Heart
- Andere Medikamente
- Potassium 10mq ER, Atenolol 25mg. Rosuvastatin 20mg, Escitalopram 10mg, Triamtexine HCTZ 32.5/25mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 13.09.2023
- Impfdatum
- 13.09.2023
- Beginn
- 13.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Wrong product administered
Symptomtext
nothing known as of yet. pt has been contacted she was given two HD flu shots instead of one flu + one prevnar
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -