- Staat
- KS
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 30.10.2022
- Impfdatum
- 30.10.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Face injury
Facial bones fracture
Loss of consciousness
Symptomtext
Patient was given an fluzone quad and Tdap. He was in the waiting area and stood up to go to the bathroom approximately 2 min after receiving his vaccinations. He took about 5 steps and passed out, hitting his face on the concrete. He was out for a short period and when we woke, he was aware of his surroundings and could answer basic questions. I believe he experienced vasovagal syncope. He appeared to have a broken nose from hitting the concrete and his parents were going to take him to the ER. I will follow up with family tonight to see if any addition issues occurred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a at this time
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- unknown
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 03.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose
Dizziness
Loss of consciousness
Muscle rigidity
Musculoskeletal stiffness
Symptomtext
Patient arrived to the pharmacy requesting the covid vaccine (primary dose). After talking to the patient , he agreed to receive the influenza vaccine as well. Patient entered the immunization room with a friend. the 2 vaccines were administered to the patient in the right deltoid. Around half a minute of receiving the vaccine, patient said he was going to pass out and then he passed out. Patient was rigid (stiff) and his friend helped me placed the patient on the floor, while that was occurring I told my technicians to call EMS. After the patient was placed on the floor, he became awake and aware of his surroundings, that lasted less than 1 minute. He said that this always happens to him when he gets injections. EMS arrived and checked the patient and no signs of injury were observed. EMS pricked the patient finger to check his sugar and patient had the same reaction he had after receiving the vaccines. Patient then was cleared by EMS and left the pharmacy walking without need for assistance. The event was concluded to be due to his phobia to injections.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- Patient verbalized that he always have the same reaction to injections due to his fears to injections
- Staat
- MI
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 21.03.2023
- Impfdatum
- 27.02.2023
- Beginn
- 27.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Erythema
Hypoaesthesia
Injection site indentation
Injection site pain
Peripheral swelling
Injection site atrophy
Injection site pruritus
Injection site swelling
Sensitive skin
Symptomtext
Swelling of arm and redness, pain in injection site . Now a dent , sunk in spot on left upper arm, numbness that comes and goes , as well as pain very sensitive spot in arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site atrophy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Muscle tightness
Myalgia
Symptomtext
sore muscles/tightness around back and upper shoulders night of vaccination and continued for 2 days per patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- no spleen
- Andere Medikamente
- unknown
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 15.10.2022
- Beginn
- 16.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immunisation reaction
Symptomtext
Pt became light headed and dizzy the next morning upon rising. Pt went to ER with daughter that experienced same SE and were checked out and all other issues were ruled out. Pt was told it most likely related to vaccinations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none that contributed
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 18.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Child said he felt faint, told him to sit for 30 minutes and gave water
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 18.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Influenza A virus test negative
Influenza B virus test
Ocular hyperaemia
Pyrexia
Rhinorrhoea
Streptococcus test negative
Symptomtext
Mother of patient calling call center reported child was seen in clinic on 10/14/22 and states Saturday woke up with his eyes all red. States white of eyes have remained red since then and also has a little bit of runny nose and low-grade fever on Saturday. MOC states school nurse just called her to pick child up for red eyes and to take child to be seen by provider. Mother of child gave Motrin Patient was scheduled appointment with PCP where patient was tested for flu and strep. Medication as prescribed antibiotic Cefdinir, olopatadine solution, Cetirizine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- RAPID INFLUENZA A/B, -Negative (10/18/2022) STREP A- Negative (10/18/2022)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Feeling hot
Vomiting
Symptomtext
Patient post vaccinations c/o feeling warm and lightheaded, patient vomited x1 with resolution of symptoms. Patient was offered water and was continuously monitored. HR 76 strong/regular 1306 All symptoms resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 06.03.2023
- Beginn
- 06.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
PROQUAD ADMINISTERED TO 13 YEAR OLD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- UNKNOWN
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 19.12.2022
- Impfdatum
- 01.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 5,0
- Dosis
- N/A
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
On 12/6/22, patient received 1 dose of Trumenba and 1 dose of Bexsero, but he should have only received one or the other. There have been no known adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 01.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
The moderna dose that was administered on 11/21 was from a lot that had expired on 11/17. There have been no known adverse reactions. The manufacturer has been contacted for viability. The patient will continue the primary series as recommended, so he will receive his second dose in at least one month from 11/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 08.11.2022
- Impfdatum
- 03.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 19,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
an extra dose of FLUZONE QUADRIVALENT was accidently administer with no reported adverse event; Initial information received on 28-Oct-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 4 years old male patient had an extra dose of fluzone quadrivalent accidently administered with no reported adverse event while receiving vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR 3-COMPONENT, POLIO VACCINE INACT 3V (VERO), TETANUS VACCINE TOXOID (KINRIX) for Immunisation. On 03-Oct-2022, the patient received 0.5 mL dose of suspect INFLUENZA QUADRIVAL A-B VACCINE (formulation and strength not reported; lot UT7681LA) via intramuscular route in unknown administration site for prophylactic vaccination. On 22-Oct-2022 he also received 0.5 mL dose of the same vaccine (formulation and strength not reported; lot UT7695MA) via intramuscular route in unknown administration site for prophylactic vaccination. On 22-Oct-2022, the patient had an extra dose of fluzone quadrivalent was accidently administered with no reported adverse event (extra dose administered) (latency: same day of dose 2) following the administration of INFLUENZA QUADRIVAL A-B VACCINE. It was reported, a patient who received 2 doses of FLUZONE QIV syringe. 1st dose received on 03-Oct-2022 and 2nd dose was received on 22-Oct-2022. An extra dose of FLUZONE QUADRIVALENT was accidently administer to a patient. This situation is reported as a medication error due to the patient receiving 2 doses of the 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.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- KINRIX
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 0,3
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
fluzone qiv np being administered to a patient under 6 months of age with no reported adverse event; Initial information received on 26-Oct-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 3 months old female patient who recieved fluzone qiv np being administered to a patient under 6 months of age 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. Concomitant medications included DIPHTHERIA VACCINE TOXOID, HEPATITIS B VACCINE RHBSAG (YEAST), PERTUSSIS VACCINE ACELLULAR 3-COMPONENT, POLIO VACCINE INACT 3V (VERO), TETANUS VACCINE TOXOID (PEDIARIX) for Prophylactic vaccination; PNEUMOCOCCAL VACCINE CONJ 13V (CRM197) (PREVNAR 13) for Prophylactic vaccination; ROTAVIRUS VACCINE LIVE REASSORT ORAL 5V (ROTATEQ) for Prophylactic vaccination; and HIB VACCINE CONJ (OMPC) (PEDVAXHIB) for Prophylactic vaccination. On 26-Oct-2022, the patient received 0.5 mL total dose of suspect INFLUENZA QUADRIVAL A-B VACCINE once (formulation and strength not reported; lot UT7681LA and expiry date: 30-Jun-2023) via intramuscular route in the left thigh for prophylactic vaccination. On 26-Oct-2022, (latency: same day) the fluzone qiv np being administered to a patient under 6 months of age with no reported adverse event (product administered to patient of inappropriate age) 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.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PEDIARIX; PREVNAR 13; ROTATEQ; PEDVAXHIB
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 0,3
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient came to office for 3 month exam. Received all of her 3 month. Per provider mom requested flu vaccine as well. Flu vaccine administered into left thigh and tolerated it well. Pt remained in the office for 10 or so minutes following vaccination and showed no s/s of reaction. Mom notified that vaccine was given at 3 months instead of 6.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 02.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
SARS-CoV-2 test negative
Symptomtext
Patient came and complaint that the Saturday after getting the vaccine she ended up in the hospital. She had a lot of check ups done but everything came back negative. She thought that the Pfizer vaccine gave her Covid but the hospital said she was negative for COVID.She tells me that she has a chronic condition Bronchiostasis and also, thinks that the vaccine could of exacerbated it. Outcome she told that she was going to go to her medical doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- SARS-CoV-2 test negative
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Patient tells me she has a chronic condition called bronchiostasis.
- Andere Medikamente
- Lisinopril 10 mg Montelukast 10 mg Atorvastatin 10 mg paroxetine 30 mg
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Patient was given MMRV (proQuad) after the allowed time frame of the vaccine of 12 months to 12 years. The CDC was contacted and with regards to the vaccine being administered incorrectly. The representative stated that there according to testing from the manufacture there is no issue with the vaccine being administered after the suggested time frame as long as standard MMRV vaccination standards are being followed. Documentation was provided via Recommendations of the Advisory Committee on Immunization Practices (ACIP).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
COVID vaccine given 3 days post expiration date. No adverse event occured. PCP, dept of health notified and family notified. Awaiting advice from dept of health on validity of dose and subsequent dosing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Peripheral swelling
Symptomtext
PATIENT STATES ARM IS SWOLLEN AND RED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- DOXEPIN 10MG , LOTRONEX 0.5MG, XIFAXAN 550MG
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 15.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Wrong product administered
Symptomtext
Patient, was overdue for dose 2 of primary series for manufacturer Pfizer. First dose of Pfizer primary series given 1/20/22. Patient received Pfizer Bivalent booster on 9/15/22 instead of Pfizer monovalent/dose #2 of primary series. Medical provider, Dr. and Medical Officer, Dr. both made aware of situation. Mother of patient called and notified no harm done in patient receiving bivalent booster, which includes monovalent and variant. However, it still needs to be reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A, no adverse symptoms reported to date.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- ADHD, learning disability, flat foot
- Andere Medikamente
- N/A
- Allergien
- Penicillin and amoxicillin
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 15.09.2022
- Impfdatum
- 06.09.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Influenza like illness
Local reaction
Oxygen saturation decreased
Swelling
Symptomtext
After getting the shot, pt had a local reaction of redness and swelling, flu-like symptoms, and decreased oxygen levels. He is no longer having these side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
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