- Staat
- VA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Abdominal distension
Blood creatine phosphokinase MB normal
C-reactive protein normal
Cardiac flutter
Condition aggravated
Cough
Diarrhoea
Dizziness
Electrocardiogram normal
Extra dose administered
Fatigue
Heart rate increased
Musculoskeletal chest pain
Palpitations
Platelet count increased
Red blood cell sedimentation rate increased
Tenderness
Symptomtext
Heart palpations started about one week after receiving the vaccine. Then, 3 weeks later I began coughing and noticed heart palpitations. Then, my heart began racing and felt like it was fluttering. My pulse was 144 and I feel dizzy and faint. I sat down and after about 3 minutes my pulse went down to 112. It remained 108-115 while at rest for the next 4 hours. Four hours later, my pulse went down to the 90s and a few hours later it went down to 80. The next day I felt tenderness in my left shoulder and left upper chest area, abdomen was swollen, upset stomach with diarrhea, mild heart palpitations, and felt tired. I visited my PCP the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- EKG was normal. An echocardiogram was ordered but not yet done. Platelets were high, sedimentation rate was high, and c reactive protein was high. CPK-MB was normal.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Zyrtec
- Allergien
- none
- Vorherige Impfungen
- heart palpitation after 1st and 2nd dose of Pfizer Covid 19 vaccine. Dose 1 was 1/8/2021, dose 2 was 1/25/21
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 21.10.2021
- Impfdatum
- 07.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Blood thyroid stimulating hormone normal
Brain natriuretic peptide increased
Dizziness
Electrocardiogram abnormal
Full blood count normal
Metabolic function test
Palpitations
Tachycardia
Ventricular arrhythmia
Symptomtext
10/14/21 0630: palpitations, tachycardia noted in AM and intermittently throughout the day. 10/14/21 1830: Increased tachycardia, lightheadedness, A fib noted on smartwatch 10/15/21: 1300: Saw cardiologist, prelim Dx of A. Fib, placed on Biotel patch monitor x 2 weeks. 10/21/21: Seen by second cardiologist/electrophysiologist: NOT A. fib but a left ventricular outflow tract-ventricular arrhythmia. (LVOT-VA). Plan to place on flecanide, consider ablation if Sx persist after data from monitor download reviewed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- 10/15/21: EKG--prelim dx atrial fibrillation 10/20/21: CBC, CMP, TSH all normal, mildly elevated BNP 10/21/21: EKG--LVOT-VA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- mild intermittent asthma hemochromatosis
- Andere Medikamente
- Nasacort B12 Vitamin D Omega 3 Elderberry
- Allergien
- Lodine (NSAID) Horse Serum
- Vorherige Impfungen
- Achilles tendon rupture 3 days after COVID Dose 1: Pfizer EJT1685 (previously filed VAERS)
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Headache
Vomiting
Symptomtext
Began getting a headache the next day which became progressively worse until she vomited and did not go away until after she went to bed and slept through the nigh. No history of headaches or migraines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Myalgia
Pain in extremity
Product preparation issue
Symptomtext
Patient received undiluted dose of Pfizer, 150mcg on 10/28/2021 (booster dose). On 10/29/2021, patient reported sore arm but otherwise felt well. Took ibuprofen 600-800mg every 8 hours as needed with good relief. 10/30/2021, patient reported diffuse muscle ache, but much improved from previous day. 11/2/2021, patient reported all symptoms completely resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HLD, history of SVT, pre-diabetic
- Andere Medikamente
- Vitamin C, Multivitamin, Fish oil
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 6,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Impetigo
Papule
Rash
Symptomtext
Mom insisted that he developed a papule that turned into Impetigo that has spread. I started him on antibiotics today. Mom was applying band aids and triple antibiotics and although it is spreading it seems to be healing x 24 hrs on meds. Rash is not pruritic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Cough Variant asthma
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 04.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Throat tightness
Urticaria
Symptomtext
large hive on neck and skin itchy and tightness in the throat within one hour of receiving the vaccine. Took a couple of Benadryl and 'eventually' subsided. No medical visit or treatment by physician, UR Or ED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 03.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
During a flu vaccine clinic for employees of facility, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
During a flu vaccine clinic for employees, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 03.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
During a flu vaccine clinic for employees, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
During a flu vaccine clinic for employees, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
During a flu vaccine clinic for employees, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
During a flu vaccine clinic for employees of facility, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
During a flu vaccine clinic for employeesof facility, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
During a flu vaccine clinic for employees at facility, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 02.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
During a flu vaccine clinic for employees of Behavioral Services at the Treatment Center, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
During a flu vaccine clinic for employees of Behavioral Services at the Treatment Center, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
During a flu vaccine clinic for employees of Behavioral Services at the Treatment Center, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
During a flu vaccine clinic for employees of Health Behavioral Services at the Treatment Center, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
During a flu vaccine clinic for employees of Behavioral Services at the Treatment Center, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
During a flu vaccine clinic for employees of at the Treatment Center, this employee was inadvertently given expired influenza vaccine. The vaccine administered was for the 2021-2022 season and expired on 6/30/2022. The employee was made aware of the this mistake, did not present with any adverse clinical reaction, and will be administered the influenza vaccine for the 2022-2023 season as soon as clinically appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 14.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
expired vaccine administered with no reported adverse event; Initial information received on 03-Oct-2022 regarding an unsolicited valid non-serious case received from a consumer/non-hcp. This case involves Adult and unknown gender patient who had expired vaccine administered with no reported adverse event while receiving vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 03-Oct-2022, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE Suspension for injection (formulation, strength, dose, route and administration site not reported) (lot UT7325MA and expiry date: 30-Jun-2022) for prophylactic vaccination. On 03-Oct-2022, (latency: same day) the patient had expired vaccine administered with no reported adverse event (expired product administered) following the administration of INFLUENZA QUADRIVAL A-B VACCINE. Action taken was 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.; Sender's Comments: 2022SA409871:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 13.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
expired vaccine administered with no reported adverse event; Initial information received on 03-Oct-2022 regarding an unsolicited valid non-serious case received from a other health professional. Linked to case- 2022SA409871. This case involves Adult and unknown gender patient who was administered expired INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QIV] vaccine with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 03-Oct-2022, the patient received a expired dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (formulation. dose, strength: unknown) (lot UT7325MA, exp: 30-Jun-2022) via unknown route in unknown administration site for prophylactic vaccination with no reported adverse event (expired product administered) (latency: same day) No lab data provided. 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.; Sender's Comments: US-SA-2022SA409871:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
expired vaccine administered with no reported adverse event; Initial information received on 03-Oct-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves Adult and unknown gender patient to whom expired vaccine administered with no reported adverse event for vaccine influenza quadrival A-B vaccine [Fluzone QIV]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 03-Oct-2022, the patient received an expired dose of suspect influenza quadrival A-B vaccine, suspension for injection, (strength: not reported) (lot UT7325MA; Expiry date: 30-Jun-2022) via unknown route in unknown administration site for immunization with no reported adverse event (expired product administered) (latency: on same day). Action taken : not applicable. Outcome: 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
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -