- Staat
- AR
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Feeling hot
Loss of consciousness
Presyncope
Symptomtext
patient had been given a moderma booster 0.25 ml IM into right arm. I turned and was getting left arm ready and was giving Fluzone Hd into LA when patient suddenly said that she was hot and something was wrong.. Patient started fanning herself. I got a cold compress to apply to forehead. Her husband came in to see what was going on. She started to go in and out of consciousness. Paramedics were called during this time. An eppi pen administered. Pearamedics arrived within 10 minutes. The accessed her . She continued to lose consciousness while being moniter and finally came back. Her husband transported her to hiopital ER for follow up. When I talked to the husband later in day she was home and recovered. Drs told husband they thought she a vegal response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 24.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Confusional state
Fatigue
Lymph node pain
Lymphadenopathy
Mouth swelling
Rash vesicular
Symptomtext
After getting the high dose I had complete exhaustion confusion, mouth glands swollen, lymph nodes hurt shingles like feeling all over. loss of taste and smell.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 25.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Flushing
Head discomfort
Injection site erythema
Injection site swelling
Symptomtext
PT GOT VACCINATION AT AROUND 3:00 ON 9-25-21 AND REPORTED TO RPH ON 9-27-21. SHE DEVELOPED SYMPTOMS OVER THAT EVENING AND NEXT DAY OF REDNESS AND SWELLING AROUND INJECTION SIGHT AND IN SPOTS 2 TO 3 INCHES BELOW INJECTION SITE. SHE ALSO HAD FACIAL FLUSHING AND PRESSURE IN HER HEAD. PT STATES THIMERISOL ALLERGY, MFR PKGE STATES PRESERVATIVE FREE. SHE SAYS SHE WILL CONTINUE TO MONITOR HERSELF (PT IS A DR)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 16.09.2021
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Pain
Pyrexia
Symptomtext
FEVER, CHILLS AND BODY ACHES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NOT KNOWN
- Vorgeschichte
- -
- Andere Medikamente
- SIMVASTATIN, MELOXICAM, LISINOPRIL, LEVOTHYROXINE, TRAMADOL, AMLODIPINE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.09.2021
- Impfdatum
- 12.09.2021
- Beginn
- 12.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Pain
Pyrexia
Symptomtext
fever, dizziness, soreness, chills, fatigue,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, Hormone replacement therapy, anxiety
- Andere Medikamente
- nexium, singulair, atenolol, linzess, estradiol, lorazepam, niaspan, flonase
- Allergien
- Prevnar 13, sulfadrugs, nifedipine
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 19.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site swelling
Pyrexia
Symptomtext
redness , swelling at site, fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 11.11.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 25,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal wall operation
Colectomy
Colon cancer
Hepatectomy
Symptomtext
Malignant neoplasm of colon, unspecified part of colon. Admission for surgery - Open resection of transverse colon, abdominal wall, and portion left liver. Managed and recovered in hospital. Admission was within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal wall operation
- Hospital-Tage
- 12,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 29.10.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Bladder catheterisation
Bladder irrigation
Chromaturia
Coagulopathy
Computerised tomogram normal
Haematuria
Urinary tract infection
Urine analysis abnormal
Symptomtext
Patient in for persistent hematuria. Was discharged last week with hematuria that resolved with bedside irrigations. Foley catheter was removed at the time of his last discharge as urine was clear. Patient redeveloped clot retention. He was treated in the emergency department with CBI and again his urine cleared. CT scan shows no obvious source of bleeding such as large bladder mass. No large quantity of clots within the bladder. UA suggestive of persistent UTI. At the time of discharge his urine is amber. This is with CBI off for approximately 1 hour. Patient will discharge back to memory care unit with the indwelling Foley catheter in place. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bladder catheterisation
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 21.03.2022
- Impfdatum
- 12.10.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 31,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Fall
Hip arthroplasty
Hip fracture
Symptomtext
Patient off ladder on day of admission sustaining a left hip fracture. Admitted for management. optimized medically and taken to the operating room where patient underwent a left hip bipolar hemiarthroplasty for fracture. Patient tolerated the procedure well with no apparent complications. Patient was transferred to the floor where patient remained afebrile with stable vitals signs. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fall
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 16.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Affective disorder
Atrial fibrillation
Cognitive disorder
Conversion disorder
Crying
Screaming
Somatic symptom disorder
Symptomtext
Patient with history of depression, anxiety, hypertension, osteoarthritis and gout longstanding challenges with poorly controlled anxiety and panic presents with 2 weeks of multitude of somatic symptoms in addition to functional impairment from after mentioned suboptimally controlled mood. Upon seeing her in ED she was quite hysterical, crying out/calling out. Admitted her, discontinued benzodiazepines and BuSpar, scheduled low-dose Risperdal and continued paroxetine. During her short hospital course she improved back to baseline status. Additional ED visit for atrial fin wtih RVR; treated and released. ED visits and hospital admission were within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Affective disorder
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 08.10.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 39,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aortic stenosis
Aortic valve replacement
Cardiac valve prosthesis user
Symptomtext
Aortic stenosis, severe - operation: Transfemoral Transcutaneous Aortic Valve Replacement with aortic valve prosthesis of a 29 mm Evolut Pro+. Post procedure the patient did very well. Admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aortic stenosis
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 21.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Atrial fibrillation
Symptomtext
Atrial fibrillation with RVR, admitted to the telemetry floor for further management and continued on a diltiazem drip overnight with good control of heart rate. The morning of 10/23/21, the diltiazem drip was weaned off. Toprol XL 150 mg daily was restarted. Cardiologist recommended the addition of digoxin 0.125 mg daily for treatment of atrial fibrillation as well as the addition of aspirin 81 mg twice weekly for secondary prevention of stroke. The patient was stable for discharge and felt comfortable with this plan. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.03.2022
- Impfdatum
- 14.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Coronary artery bypass
Symptomtext
Coronary artery bypass grafting x4 on pump. The patient's oxygen was weaned to room air. He progressed well with physical and occupational therapy and was stable to be discharged to home with family support on POD #3. Hospital admission was within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coronary artery bypass
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 11.10.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 36,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Anaemia
Cardiac telemetry
Transfusion
Symptomtext
Acute on chronic anemia - Patient was admitted on telemetry started on Protonix drip and patient was given 3 unit blood transfusions. She has remained hemodynamically stable even at arrival, no further acute loss identified. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaemia
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 27.10.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Bradycardia
Diverticulum intestinal
Rectal haemorrhage
Symptomtext
ED visit for reported bradycardia - treated and released. Hospital admission after 3 episodes of bright red blood per rectum . Severe diverticulosis in the sigmoid and distal descending colon. Treated and discharged. ED visits and hospital admissions within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bradycardia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- 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 dose of Fluzone High-Dose Quadrivalent was administered to a patient, who had already received a high-dose flu shot this season at a pharmacy/ no AE; Initial information was received on 09-Nov-2021 regarding an unsolicited valid non-serious case from a physician via Global Media Information (under reference- 00850127) and transmitted to Sanofi on 09-Nov-2021. This case involves a 69-year-old female patient who administered INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] and she had already received a high-dose flu shot this season at a pharmacy, with no adverse event (Inappropriate schedule of product administration). Medical history, medical treatment(s), vaccination(s), concomitant medications and family history were not provided. On 08-Nov-2021, the patient received 0.7 mL dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [lot UJ715AB and expiry date 30-Jun-2022] via intramuscular route in unknown administration site for prophylactic vaccination. It was reported " Caller reporting patient is unsure of the exact date she received the flu shot, but it was in September 2021". It was a case of actual medication error due to Inappropriate schedule of vaccine administered (latency was on same day). At the time of reporting, patient had no adverse event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out by the regulatory authority. 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
- MO
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Feeling hot
Peripheral swelling
Symptomtext
SWOLLEN ARM, REDNESS, HOTNESS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 01.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cold sweat
Incorrect dose administered
Product preparation issue
Symptomtext
Patient was erroneously given undiluted vial of Pfizer COVID vaccine, equivalent to 5-6 doses. Was monitored in clinic for 1.5 hours afterward with stable q15m vitals. Patient felt clammy but otherwise no side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cold sweat
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- chronic DM, HTN, HLD, neuropathy, back pain
- Andere Medikamente
- aspirin, atenolol, dulcolax, fenofibrate, lasix, PRN neurontin, glimepiride, ketoconazole cream, lisiniopril, lovastatin, metformin XR, PRN nitroglycerin, omeprazole, zofran, K-dur, flomax, kenalog cream, maxzide
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 08.09.2021
- Impfdatum
- 08.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
High Dose vaccine (indicated for 65 year old plus) given to a 55 year old patient. Patient reported no symptoms. Patient contacted about mistake.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none provided
- Andere Medikamente
- none known
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 04.09.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Syringe issue
Underdose
Symptomtext
realized the syringe only had about 0.1 mL v. 0.7 mL of medication and reported she used a different syringe/ no AE; realized the syringe only had about 0.1 mL v. 0.7 mL of medication and reported she used a different syringe/ no AE; Initial information regarding an unsolicited valid non-serious case was received from other health professional and transmitted to Sanofi on 24-Aug-2021. This case involves an unknown age and gender patient while receiving INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (lot UJ715AB, expiry date not reported) then reported realized the syringe only had about 0.1 ml instead of 0.7 ml of medication and used a different syringe (underdose and syringe issue) via unknown route at an unknown administration site on an unknown date for prophylactic vaccination (latency was on same day). Medical history, past medical treatment, past vaccination, concomitant medication and family history were not provided. At the time of report, no adverse event reported. It was reported, "Caller reported there was no damage on the box or syringe, but the side was a little flimsy. Caller reported the other syringes look okay." It was not reported if the patient received any corrective treatment for the events. At time of reporting, the outcome was unknown for both the events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -