- Staat
- OK
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Symptomtext
Bell's Palsey per Dr. appt 2-1-22 provided steroid shot and pills and should recover in next 2months to 1 year
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Had COVID 12-2021
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 12.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Paraesthesia
Symptomtext
I felt chest pain for 24 hours and pain full tingling in my arm and palm of mu hand for 48 hours and it's continuing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Lupus
- Vorgeschichte
- Lupus
- Andere Medikamente
- Hair-Vit
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Arm is a bit sore according to mom
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 28.09.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 80,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Oropharyngeal pain
Pyrexia
Rash
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID - sore throat started December 17, fever of 100.4 on December 19, rash, congestion, runny nose, cough, positive COVID test results December 21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Positive COVID results December 21
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- DVT depression/anxiety
- Andere Medikamente
- Warfarin Effexor Zyrtec Prozac Topamax Wellbutrin Trazadone
- Allergien
- none that I am aware of
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Adverse reaction
Injection site nodule
Muscular weakness
Nausea
Pain in extremity
Sleep disorder
Symptomtext
Per patient report: I wanted to report an adverse reaction to the flu shot. This is the first time I have ever had any type of reaction and it is getting progressively worse. Originally, I had a knot at the shot injection site which has completely gone away. I currently have ongoing pain in the arm from the injection location that radiates down to my fingers and into my shoulder creating both pain and loss of intermittent strength which I would classify as weakness. I have no redness, swelling, heat at site of injection, fever, hives, fast heartrate, headache or fatigue - I have felt oddly nauseous at times and the pain is affecting my sleep as it wakes me up. The feeling begins as a cramp at the the injection site then travels up and down. It has been two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site nodule
- Hospital-Tage
- -
- Labordaten
- Symptoms improving by time of pts report (2 weeks later)
- Aktuelle Erkrankungen
- 10/25/21 derm treatment: 55 year old female who presents for treatment of telengiectasia / rosacea. First session' Last seen: 9/27/2021 Consent form signed prior to beginning first treatment: Yes; ROS of the following were done and are negative: Constitutional, Eyes, Ears, Nose, Mouth, Throat, Cardiovascular, Respiratory, GI, Genitourinary, Musculoskeletal, Integument, Psychiatric, Endocrine, Allergic/Immunologic; Treatment #: 1 Areas treated include: face; Patient advised on risks and benefits of treatment including blistering, swelling, pain, scarring, failure to respond, hyper or hypopigmentation, need for repeat treatments. Yes; Laser used: 532nm KTP; Laser Settings: 532 nm 5 mm spot 8 joules/cm2 9 ms pulse width 0.8 Hz 1 pulses/lesion; Total number of lesions treated: cheeks, nose and chin; Skin was cooled with ice bags, cold clear ultrasonic jelly and 5 degree chiller plate
- Vorgeschichte
- Cardiovascular; Essential hypertension; Type 2 diabetes mellitus without complication, without long-term current use of insulin (HCC); Post-surgical hypothyroidism; Papillary thyroid carcinoma (HCC); IFG (impaired fasting glucose); telengiectasia / rosacea.
- Andere Medikamente
- Ascorbic Acid; Vitamin C 500 MG; Chew 500 mg; Glucose Blood (Strip); Lancets (Misc) OneTouch Delica Lancets 30G; Levothyroxine Sodium (Tab) 175 MCG; metFORMIN HCl; GLUCOPHAGE-XR 500 MG; Olmesartan Medoxomil; Benicar 40 MG
- Allergien
- Adhesive tape
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal sensation in eye
Eye pruritus
Eye swelling
Symptomtext
Around 6:30pm my eyes felt strange and itchy. Around 10:00pm I looked in a mirror and noticed they were swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Nasal congestion, runny nose, migraine. Tested negative for COVID (rapid test) 11/07/2021.
- Vorgeschichte
- Hypercholesterolemia, migraines.
- Andere Medikamente
- Crestor 40mg, Zetia, Fish Oil, Vitamin D, Nexletol, Allegra, ibuprophen
- Allergien
- Septra, niacin extended release, beeswax, nickel, gold, neomycin, grasses
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 2,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Swelling face
Symptomtext
Rash and facial swelling that started the evening of 11/7, worse the next morning. Discontinued amoxicillin when rash started. Rash improved by late morning 11/8
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Being treated for sinusitis with amoxicillin (as above) since 10/29
- Vorgeschichte
- -
- Andere Medikamente
- Amoxicillin
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Cough
Fatigue
Headache
Myalgia
Pyrexia
Symptomtext
Symptoms: fever overnight, chills, fatigue, headache, muscle pain, some coughing Treatment: Tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Both Covid Vaccine (Pfizer) Doses: 2/13/21 and 3/6/21 Age: 52 Symptoms: fever, chills. muscle pain, fatigue
- Staat
- PA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Macule
Rash macular
Symptomtext
After receiving Menactra in her left arm, she immediately started with swelling and erythema around the Menactra injection. I was called into the room by the medical assistant and patient was upset and crying that her arm hurt. She had an approx. 4 inch diameter area of erythema around the injection site and it was swollen. We immediately applied an ice pack. Then a few minutes later, mom noted three small red macules on her right forehead and a splotchy red rash on her chest. Her chest was clear, there were no respiratory symptoms, no mouth or facial swelling. Vitals were stable the entire time. She was given 300mg ibuprofen for the pain and 37.5mg benadryl for the rash. Even before giving the benadryl, the chest rash disappeared and the forehead rash started to improve. Patient was observed for approx. 45-50 minute after the vaccine and rash, swelling, and pain had completely resolved prior to leaving the office. Lungs were clear the entire time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Left discoid meniscus of knee, osteochondritis dissecans of left knee
- Andere Medikamente
- None
- Allergien
- Bee stings
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain lower
Dizziness
Hyperhidrosis
Malaise
Nausea
Symptomtext
Clinic Location: Facility Situation: Possible reaction to flu vaccine Name of Reactive drug/vaccine: Flulaval Time of Immunization Administration: 1207 Time of Reaction: symptoms reported to me by patient via telephone at approximately 1245 Subjective symptoms reported by patient: After vaccination, patient's coworker came to flu clinic and reported patient not feeling well. Coworker called patient on phone and I spoke to patient. Patient reported feeling sweaty, lightheaded, nauseous, and lower abdominal pain. Rated pain a 10/10 and was worsening. Patient told to call emergency services. Anaphylaxis: No Immediate nursing interventions: Advised patient to call EMS for transport to ED Was the Emergency Protocol for Anaphylaxis Initiated? No Patient response to interventions and additional details: Patient stated she would call emergency services
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 13.10.2021
- Impfdatum
- 11.10.2021
- Beginn
- 11.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Erythema
Eye pruritus
Injection site erythema
Injection site warmth
Symptomtext
Flushot was given at 0330. to right deltoid IM, 0530 the site was reddened and warm to touch, pharmacy was called and Loratadine was given. At 0540 redness was increasing and was spreading down her right side to her waist, across midback, and upper chest. She also developed itch eyes. She was taken to ER and seen by Dr and received treatment ( Pepcid IV 20 mg and Benedryl 50 mg IV and NS infusion. )
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- ADD Anemia Anxiety Depression Low Vit D HerpeSimplex
- Andere Medikamente
- Atorvastatin 40 mg daily Citalopram 20 mg daily Dextroamphetamine-Amphetamine 30 mg daily Diltiazem 180 mg daily Fluticasone Nasal sprays daily Valacyclovir 1 gm daily
- Allergien
- Codeine Lorcet
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 18.09.2021
- Impfdatum
- 18.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pallor
Vomiting
Symptomtext
The patient is a 13 y.o. female presents to the office for influenza vaccination. Vaccine Information Sheet given to patient. Vaccine screening questionnaire completed and reviewed Patient had emesis episode about 30-60 seconds post vaccine with pallor, no diaphoresis, no rash, no urticaria, no facial swelling or angioedema, no respiratory distress. Updated Dr. on patient's condition. No previous issues with vaccines and no known allergies. Patient's symptoms resolved with no continual emesis- waited in clinic for observation period. Patient stable on discharge with no complaints.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vomiting
- Hospital-Tage
- -
- Labordaten
- none indicated
- Aktuelle Erkrankungen
- no known
- Vorgeschichte
- ADHD
- Andere Medikamente
- no known
- Allergien
- no known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 14.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Administered expired (2021/2022) vaccine. Patient has reported no known symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 14.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Administration of an expired dose; This case was reported by a pharmacist via call center representative and described the occurrence of expired vaccine used in a female patient who received Flu Seasonal QIV (FluLaval Quadrivalent 2021-2022 season) (batch number N959G, expiry date 30th June 2022) for prophylaxis. Co-suspect products included flu seasonal qiv pre-filled syringe device (Flulaval Tetra Pre-Filled Syringe Device) injection syringe for prophylaxis. On 14th September 2022, the patient received FluLaval Quadrivalent 2021-2022 season and Flulaval Tetra Pre-Filled Syringe Device. On 14th September 2022, unknown after receiving FluLaval Quadrivalent 2021-2022 season and Flulaval Tetra Pre-Filled Syringe Device, the patient experienced expired vaccine used. On an unknown date, the outcome of the expired vaccine used was unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 21-Sep-2022 Reporter's Comments: The pharmacist reported the administration of an expired dose of Flulaval to a patient. Dose was given on 14th Sep 2022 and vaccine expiration date was June 30th 2022, The reporter give consent to follow up. Additional Supportive Information: The patient received expire vaccine which leads to expire vaccine used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 14.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Expired flu vaccine (intended for 2021/2022) was given for 2022/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 28.09.2022
- Impfdatum
- 19.09.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Exposure during pregnancy
Symptomtext
36 week pregnant patient received an expired dose; 6 week pregnant patient received an expired dose; This prospective pregnancy case was reported by a other health professional via call center representative and described the occurrence of vaccine exposure during pregnancy in a 39-year-old female patient who received Flu Seasonal QIV Quebec (FluLaval Quadrivalent 2022-2023 season) (batch number N959G, expiry date 30th June 2022) for prophylaxis. Co-suspect products included flu seasonal qiv quebec pre-filled syringe device (Flulaval Tetra Pre-Filled Syringe Device) injection syringe for prophylaxis. On 19th September 2022, the patient received FluLaval Quadrivalent 2022-2023 season and Flulaval Tetra Pre-Filled Syringe Device. The patient's last menstrual period was on an unknown date and estimated date of delivery was October 2022. The patient received FluLaval Quadrivalent 2022-2023 season at week 36 of the pregnancy. On 19th September 2022, unknown after receiving FluLaval Quadrivalent 2022-2023 season and Flulaval Tetra Pre-Filled Syringe Device, the patient experienced expired vaccine used. On an unknown date, the patient experienced vaccine exposure during pregnancy. On an unknown date, the outcome of the vaccine exposure during pregnancy and expired vaccine used were unknown. The pregnancy was ongoing. This report is made without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 19-SEP-2022 Reporter's Comment: The reporter was medical assistant. The reporter reported that, a 36 weeks pregnant patient received an expired dose of Flulaval, the vaccine expired on 30th June 2022. The consent for follow-up was not asked. Additional Supportive Information: A pregnant patient received an expired dose of Flulaval, which led vaccine exposure during pregnancy and expired vaccine used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 14.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
EXPIRED VACCINE ADMINISTERED (EXP 6/30/22). NO ADVERSE REACTIONS REPORTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 14.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
EXPIRED VACCINE ADMINISTERED (EXP 6/30/2022). NO ADVERSE REACTIONS REPORTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 14.09.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
EXPIRED VACCINE ADMINISTERED (EXP 6/30/22). NO ADVERSE REACTIONS NOTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 10.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
patient given pediatric covid vaccine dose instead of adult dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- ADHD
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 6,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Influenza vaccine administered instead of a Hepatitis B vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lymphadenopathy
Product preparation error
Symptomtext
The Registered Nurse that drew up the Phizer immunization forgot to use the Diluent. He received 0.3ML of straight Phizer. Once the medication error was found the client was contacted. He reported that he had swelling in his lymph nodes in his neck and clavical area but the same thing happened after his second immunization of Phizer. We asked him to notify us if he had any more adverse changes to his health.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart arrhythmia, only has one kidney from kidney cancer
- Andere Medikamente
- emgality injection same day
- Allergien
- none
- Vorherige Impfungen
- Client reports his lymph nodes in his neck and clavical area swelled after second Pfizer immunization