- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 22.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Blood test
Dyspnoea
Electrocardiogram
Pulmonary thrombosis
Symptomtext
After a couple of week of being short of breath, I started monitoring my heart rate and my blood oxygen levels, on 11/11/2022 my oxygen level was staying between 82-96 and my pulse rate I could not get under 100 beats per minute. So I went tot he nearest emergency room, I had extensive blood work done, EKG, and the Dr. came in and advised that I had multiple blood clots in both of my lungs. I was admitted in the hospital where I underwent heparin therapy. I stopped the therapy on Sunday 11/13/2022 and they put me ELIQUIS, and I was discharged from the hospital at that time. I am now home recovering, my heart rate has come down, but I am still short of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- -
- Labordaten
- EKG 11/11/2022, blood work 11/11/2022, CT scan of lungs 11/22/2022, blood clots in both lungs.
- Aktuelle Erkrankungen
- COVID-19 09/19/2022 tested positive
- Vorgeschichte
- None
- Andere Medikamente
- Aspirin; citalopram; docusate sodium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 12.11.2022
- Impfdatum
- 12.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient fainted within a couple of minutes of receiving vaccine. she was nervous prior to, and woke up pretty quickly after she fainted. stated she felt okay after having her hang out for 5 minutes, color back to normal, no sweating or nausea. called grandmother later in the evening to check on her and grandmother stated that she was feeling great.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Symptomtext
Patient stated that she gets dizzy from sight of needles and passed out once at a younger age. After immunizing tech administered both shots the patient removed her mask and then passed out and rolled to the ground. Patient was light headed and dizzy for about 15 minutes. We applied ice packs and cold clothes to her face/neck and she began to feel better. She stayed in pharmacy area for about 30 minutes for observation before leaving with her husband. I will call her later this evening to follow up on her.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- NA
- Allergien
- none
- Vorherige Impfungen
- Patient stated she gets dizzy from sight of needles and passed out once a younger age
- Staat
- SD
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 12.11.2022
- Impfdatum
- 19.10.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 24,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Musculoskeletal stiffness
Pain
Pain in extremity
Product administered at inappropriate site
Symptomtext
Patient complains of sore arm that remains stiff and painful several weeks after receiving a flu vaccine. She stated that it was sore for a few days after receiving the vaccine and she thought it would get better but it has not. She also states that she has trouble lifting the arm past shoulder height due to pain. When asked, patient has not tried any over the counter treatments for the pain. Advised to try ibuprofen 200-400mg every 8 hours for a few days to see if the pain improves. Also recommended that patient see her primary care provider for further evaluation. I asked patient to point to where she received her vaccination and she pointed fairly high up on the arm, closer to the shoulder above the muscle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 20.03.2023
- Beginn
- 21.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site induration
Injection site pruritus
Injection site swelling
Symptomtext
At the right subcutaneous injection site where Varicella was administered there was a 3 inch area that was red, raised, hard, and itchy. Cortisone cream was recommended to treat the area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 07.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatitis acneiform
Rash erythematous
Symptomtext
Patient states they began to get a red pimple-like rash across different sections of the body, starting with the chest. He stated it looked like shingles compare to what he had seen online, but was not localized to a single area like shingles. He was unsure if the reaction was due to the shot or something else. He plans on following up at his next regular dermatology appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
PATIENT EXPERIENCED DIZZINESS AFTER THE FLU VACCINE. THIS WAS HER FIRST FLU VACCINE BUT SHE BELIEVES IT MAY HAVE BEEN DUE TO NOT EATING ANYTHING
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 21.10.2022
- Impfdatum
- 20.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Head titubation
Hypotonia
Symptomtext
AFTER ADMIN PATIENT WENT TO POST-ADMIN WAITING AREA. AFTER A FEW MINUTES HE FLAGGED ME SAYING HE FELT LIGHT-HEADED. I IMMEDIATELY WENT TO RENDER AID. PATIENT'S HEAD WAS BOBBING AND HE STARTED TO SLUMP IN CHAIR. I KEPT HIM IN CHAIR AND TALKED TO HIM TO GET HIM TO FOCUS AND REMAIN AWAKE. I UNZIPPED HIS OUTDOOR VEST AND APPLIED ICE PACK TO THE BACK OF HIS NECK. HE BEGAN TO FELL BETTER. ANOTHER ICE PACK WAS RETRIEVED AND ONE WAS PLACED UNDER EACH ARMPIT. HE BECAME MORE RESPONSIVE AND HIS COLOR RETURNED. I HAD HIM STAY SEATED AND REMAINDED WITH HIM FOR A FEW MINUTES MORE. HE FELT WELL ENOUGH TO LEAVE AT THIS POINT. HE WAS HERE WITH HIS SISTERSO I SUGGESTED SHE DRIVE HIME HOME. I CALLED HIM LATER THAT EVENING. HE SAID HE FELT BETTER AND THANKED ME FOR TAKING CARE OF HIM. IF FURTHER ISSES HE IS TO SEEK MEDICAL CARE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE ON REGULAR BASIS. OCCASSIONAL IBUPROFEN USE.
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Heart rate increased
Symptomtext
fast heartbeat and dizziness 30 minutes after the shot still dizzy hours later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 03.10.2022
- Impfdatum
- 02.10.2022
- Beginn
- 02.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Eye swelling
Pyrexia
Symptomtext
Patient said his eye swelled up within hours of the injections and later on that evening he had fever, chills and joint pain. Symptoms were better the following morning and all eye swelling gone 10/3/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- INFLAMMATORY ARTHRITIS
- Andere Medikamente
- TRLEPTAL, ZENPEP,, NEURONTIN, PLAQUINIL, AMLODIPINE
- Allergien
- EFFEXOR, DEPAKOTE, PENICILLIN, CIPRO
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 10.03.2023
- Impfdatum
- 08.03.2023
- Beginn
- 01.03.2023
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
No adverse reaction but vaccine given outside the recommended window of use. Primary COVID series not completed, and Booster administered..
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- no
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
PATIENT RECEIVED INFLUENZA VACCINE 11/10/2022. ANOTHER DOSE WAS DOCUMENTED AS RECEIVED ON 09/15/2022 BY ANOTHER FACILITY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 14.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
PT RECEIVED INFLUENZA VACCINE ON 11/14/2022. A HISTORICAL INFLUENZA VACCINE WAS RECORDED IN PATIENT'S CHART AS ADMINISTERED FOR 11/01/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- SULFA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 21.02.2023
- Impfdatum
- 08.02.2023
- Beginn
- 08.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Given third dose of influenza vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 0,5
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 17.02.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 15.02.2023
- Impfdatum
- 04.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
PATIENT RECEIVED INFLUENZA VACCINE ON 10/04/2022. PATIENT HAD PREVIOUSLY RECEIVED AN INFLUENZA VACCINE ON 09/20/2022 AT ANOTHER FACILITY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 22.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
The patient received 2 Flu shots within the same Flu season: 11/08/22 and 11/22/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient was given Moderna Bivalent vaccine when she should have received the Moderna Monovalent vaccine. She denies any adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- Yes
- Allergien
- Moxifloxacin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- 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
Gave wrong vaccine to patient. Gave a flu shot instead of a Tdap.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 11.11.2022
- Impfdatum
- 11.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
DTaP administered versus ordered Tdap. No adverse reaction reported. No treatment necessary.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Aspirin 81 mg
- Allergien
- No known allergy
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 3,0
- Geschlecht
- U
- Eingang
- 08.11.2022
- Impfdatum
- 17.03.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Symptomtext
Vaccine was out at room temperature 6 hours longer than the recommended time frame, administered to patient, with no reported adverse event; Initial information received from on 28-Oct-2022 regarding an valid non-serious case received from a consumer/non- healthcare professional (hcp). This case involves a 3-year-old and unknown gender patient, reported vaccine COVID-19 VACCINE and INFLUENZA VACCINE (QUADRIVALENT) was out at room temperature 6 hours longer than the recommended time frame, administered to patient, 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 suspect INFLUENZA VACCINE (QUADRIVALENT) produced by unknown manufacturer (strength, formulation, dose: unknown) (lot number: UT7751NA and expiry date: unknown) via intramuscular route in unknown administration site for Prophylactic Vaccination (Immunisation). On 17-Mar-2021, patient received a dose 1 of suspect COVID-19 VACCINE not produced by Sanofi Pasteur (lot number: EN6199 and expiry date: unknown) in the left deltoid. On 07-Apr-2021, the patient received dose 2 of the same vaccine (lot number: ER8737 and expiry date: unknown) in the left deltoid. On 10-Nov-2021 patient also received dose 3 of the same vaccine (lot number: FE3590 and expiry date: unknown) in the left deltoid as vaccine supplemental (Supplementation therapy). On an unknown date, a non-serious event reported, vaccine was out at room temperature 6 hours longer than the recommended time frame, administered to patient, with no reported adverse event (poor quality product administered) (unknown latency) following the administration of INFLUENZA VACCINE (QUADRIVALENT) and COVID-19 VACCINE. It was reported, Is Covid-19 Bivalent Vaccine a Pfizer product? Yes Covid-19 Bivalent Vaccine. Expiry Date of Covid-19 Bivalent Vaccine: 30 Nov 2023 Other Products: Calling regarding the Covid-19 vaccine bivalent that was administered past the timeframe. Was outside the time frame for 6 hours. Caller wanting to know when will it be safe for the patient to receive the bivalent vaccine again. They can give them another dose immediately, but to reach out to he manufacturer for guidance. Wanted to talk to Pfizer to see what the recommendation was. The vial was taken out of the fridge Friday, for 30 minutes drawn up into the syringes on Friday afternoon, 21Oct2022. Staff left Friday and didn't waste what wasn't used. The next shift came in today and an employee gave the injection from Friday to the patient. Went ahead and let the patient leave because she had already spent 20 minutes listening to the EUA recording. Vaccination Was Given: 9:48am. It is unknown if there were lab data/results available. Action taken with QUADRIVALENT INFLUENZA VACCINE (INFLUENZA VACCINE (QUADRIVALENT)) and COVID-19 VACCINE (COVID-19 VACCINE) was 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 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
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 24.10.2022
- Impfdatum
- 23.10.2022
- Beginn
- 23.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Insomnia
Symptomtext
Patient reported a increased heart rate and could not sleep that night. He mentioned that the increase in heart rate may have contributed to the lack of sleep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none listed
- Andere Medikamente
- unknown
- Allergien
- nkda
- Vorherige Impfungen
- -