- Staat
- ID
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 04.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood disorder
Cardiomegaly
Cerebellar stroke
Chest tube insertion
Condition aggravated
Decreased appetite
Diuretic therapy
Dyspnoea
Endotracheal intubation
Fungal infection
Gait disturbance
Intensive care
Joint swelling
Loss of personal independence in daily activities
Malaise
Pneumonia
Pulmonary oedema
Pulmonary thrombosis
Symptomtext
Client had swelling in his right ankle to his knee the following day. Did not feel well after the vaccinations. He thought his pneumonia had not resolved. Went to Area Health Center by ambulance on December 8, 2021 after collapsing. He was vomitting and unresponsive. His breathing had been getting progressively worse until this incident. He had no appetite prior. He was taken by ground ambulance to Hospital and then flown to other hospital for 6-7 days. He was diagnosed with blood clots in his right leg that traveled to his lungs. He was told his blood was as thick as motor oil. He had a thrombectomy and was diagnosed with an enlarged heart and 2 cerebellar strokes. He was discharged to home after 6-7 days because the hospital was so full with covid patients. He was told he was to sick to go home but to well to be in the hospital. He was discharged with pneumonia and had a fungal infection. He did receive PT at home. On January 23rd he was found nonresponsive by his wife again. She called 911 and he was transported to Hospital again and life flighted. He was in the ICU intubated and with chest tubes for 20 days. He was septic. He had a tracheotomy placed and was life flighted to an Hospital for 21 more days. His lungs were still filling with fluids. After 21 days he was transferred to a hospital for 3-4 days due to his lungs still being full of fluid. He was extubated then transferred to hospital still having pneumonia. He was there for a month getting extensive rehab learning to walk and perform ADL's. He is home now, recovering. He is still on oxygen continuously and taking diuretics daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebellar stroke
- Hospital-Tage
- 7,0
- Labordaten
- Thrombectomy-December 8, 2021 Cerebellar stroke-December 2021 Chest tubes-January 2022 Life flights times 3
- Aktuelle Erkrankungen
- Client had Pneumonia the prior to vaccinations. He had been treated with antibiotics and prednisone. He has a history of bronchitis and pneumonia.
- Vorgeschichte
- Bronchitis/pneumonia
- Andere Medikamente
- Unknown. He had finished a round of antibiotics and prednisone.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aspiration
Chest X-ray abnormal
Extra dose administered
Mydriasis
Pneumonia
Pulse absent
Sepsis
Urinary tract disorder
White blood cell count increased
Symptomtext
Patient was a resident on palliative plan of care after recent readmission from the hospital where he was found septic from urinary source. Patient had a medical history of CVA, Type 2DM,Tubulo-interstia nephritis with septic shock. On 11/03/2021 per nursing report the participant aspirated during meal. Patient stabilized requiring 2 L of Oxygen by nasal cannula. Chest X-ray revealed left lower lobe pneumonia and labs revealed elevated WBC. Patient started on Levofloxacin. Nurse reports the patient was doing well earlier in the evening. However, at 9pm participant found with no pulse with pupils dilated. Patient was a DNR. Medical record review identified that High Dose Quadrivalent Flu
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect route of product administration
Injected limb mobility decreased
Injection site pain
Injection site swelling
Swelling
Symptomtext
Patient came in today to report that her flu vaccine was administered too high. She said it didn't hurt at first, however that evening her shoulder progressed to swell and over night the swelling spread up the side of her left neck. She said she could not move her for the first 2 days, but range of motion has progressively come back. She iced it and took tylenol. She did not go in to the provider over the weekend, but waited until Monday and had her shoulder looked at by her PA. At this time, it is still a bit sore, but much better. She just wanted to let us know.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
Given a flu shot when he wanted his second covid shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 27.12.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Wrong product administered
Symptomtext
PATIENT WAS RECEIVING THREE VACCINES. COVID-19 VACCINE WAS ADMINISTERED FIRST AND THEN THE FLUZONE FOLLOWED IN THE SAME ARM. SHE WAS THEN TO RECEIVE THE ZOSTER VACCINE IN THE OTHER ARM. AS THE PHARMACIST WAS SPEAKING TO THE PATIENT HE DIDN'T NOTICE THAT HE GRABBED ANOTHER COVID-19 VACCINE. A SECOND COVID-19 VACCINE WAS ADMINISTERED DURING THE SAME VISIT. AFTER REALIZING WHAT HAPPENED THE PHARMACIST ADMINISTERED THE ZOSTER VACCINE AND HAD THE PATIENT WAIT 15 MINUTES. THERE WERE NO ADVERSE EFFECTS REPORTED BY THE PAITENT. THE PATIENT RECEIVED A THIRD AND FOURTH DOSE OF COVID-19 VACCINE AT SAME VISIT BY ACCIDENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
63 year old patient received Fluzone HD. She didn't report any adverse events yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Patient was given a high dose influenza at the age of 61 years old. No symptoms or adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- chronic sinusitis essential hypertension gastroesophageal reflux disease heart murmur Echo completed. Records requested history of osteoarthritis migraine Typically uses Excedrin but also has maxalt prn osteoarthritis of knee osteopenia seasonal allergy
- Andere Medikamente
- Celecoxib 200 mg fexofenadine 180 mg hydrochlorothiazide 12.5 mg losartan 25 mg maxal-mlt 10 mg multivitamin omeprazole 20 mg
- Allergien
- Penicillins
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
HIGH DOSE FLU VACCINE GIVEN TO PATIENT AGED 64 YEARS AT OFFSITE COMMUNITY CLINIC. DISCOVERED LATER WHEN PROCESSING PAPERWORK AT STORE LEVEL ON 11/24/21. SPOKE TO PATIENT AFTER THE DISCOVERY OF ERROR TO CHECK ON HER AND SHE STATES NO ILL EFFECTS AFTER VACCINE AND WAS GRATEFUL TO HAVE THE HIGH-DOSE FORMULATION.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE LISTED
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 1,3
- Geschlecht
- U
- Eingang
- 23.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
A patient received FLUZONE HD instead of FLUZONE QUADRIVALENT no AE; A patient under 65 years old received FLUZONE HD no AE; A patient under 65 years old received before realized it was FLUZONE HD no AE; Initial information regarding an unsolicited valid non-serious case was received from a physician via Medical Information (Reference number- 00850044) and transmitted to Sanofi on 09-Nov-2021. This case is linked to cases 2021SA378207 and 2021SA376763 (same reporter). This case involves a 15 month old patient (unknown gender) who was received before realized INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (product administered to patient of inappropriate age and accidental overdose) instead of INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (wrong product administered). The patient's medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included DIPHTHERIA VACCINE TOXOID, PERTUSSIS VACCINE ACELLULAR, TETANUS VACCINE TOXOID (DIPHTHERIA TETANUS ACELLULAR PERTUSSIS) and VARICELLA ZOSTER VACCINE LIVE (OKA/MERCK) (VARIVAX) for prophylactic vaccination On an unknown date, the patient received a 0.7 mL first dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (batch number: UJ773AC and expiry not reported, form: solution) via intramuscular route in left thigh for prophylactic vaccination instead of FLUZONE QUADRIVALENT. It was a case a case of actual medication error due to Wrong vaccine administered, Inappropriate age at vaccine administration and accidental overdose (latency same day). It was reported "Physician called to report that she ordered FLUZONE QUADRIVALENT but was sent FLUZONE HD instead. The FLUZONE HD was administered to three patients under 65 years old before she realized it was FLUZONE HD. Adverse events (AEs) were reported for all three patients with as much information as the caller was able to provide. The caller was in a hurry to obtain/provide information and return back to her practice." No other adverse event was reported. 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
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- DIPHTHERIA TETANUS ACELLULAR PERTUSSIS; VARIVAX [VARICELLA ZOSTER VACCINE LIVE (OKA/MERCK)]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Overdose
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
FLUZONE HD was administered to patient of less than 65 years age, no AE; FLUZONE HD was administered to patient instead of FLUZONE Quadrivalent, no AE; FLUZONE HD was administered to patient of less than 65 years age, no AE; Initial information received on 09-Nov-2021 regarding an unsolicited valid non-serious case received from a physician via the Agency (under the reference number 00850043). This case is linked to case 2021SA378207 and 2021SA378956 (cluster). This case involves a 15 months old female patient who was below 65 years age and was administered with INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] instead of INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (product administered to patient of inappropriate age) (wrong product administered) (overdose). The patient's past medical history, medical treatment(s), vaccination(s), concomitant medication(s) and family history were not provided. On an unknown date (was unable to obtain), the patient received 0.7 ml first dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (once in total, lot number UJ773AC and expiry date: the caller did not have this information available) via intramuscular route in the left leg for prophylactic vaccination instead of INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. It was a case of an actual medication error due to inappropriate age at vaccine administration and wrong vaccine administered. It was also a case of overdose (same day latency). It was reported "Physician called to report that she ordered FLUZONE QUADRIVALENT but was sent FLUZONE HD instead. The FLUZONE HD was administered to three patients less than 65 years old before she realized it was FLUZONE HD. Adverse Events were reported for all THREE patients with as much information as the caller was able to provide. The caller was in a hurry to obtain/provide information and return back to her practice." The physician was unaware of any treatment, emergency room (ER), or Doctor (DR) visit necessary post administration at the time of the call. At time of reporting, no adverse event reported. 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
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
Product administered to patient of inappropriate age
Product dispensing error
Wrong product administered
Symptomtext
ordered FLUZONE QUADRIVALENT but was sent FLUZONE HD instead with no reported adverse event; The FLUZONE HD was administered accidently instead of FLUZONE QUADRIVALENT with no adverse event; 13 years old patient recived FLUZONE HD with no reported adverse event; Initial information was received on 09-Nov-2021 regarding an unsolicited valid non-serious case received from a Physician via the Agency (under reference number - 00849976). This case is linked to cases 2021SA376763(CLUSTER) and 2021SA378956(CLUSTER). This case involves a 13-year-old female patient who was accidentally vaccinated with INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] instead of the INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] due to ordered FLUZONE QUADRIVALENT but was sent FLUZONE HD instead with no adverse event (product dispensing error) (wrong product administered) (product administered to patient of inappropriate age). The patient's medical history, past medical treatment(s), concomitant therapy, vaccination(s) and family history were not provided. On 28-Oct-2021, the patient received a 0.7ml dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot number UJ773AC and expiry date was not reported) via intramuscular route in the left arm for prophylactic vaccination. There were no laboratory data/results available. It was case of an actual medication error due to drug dispensing error, wrong vaccine administered and inappropriate age at vaccine administration (latency was on same day) At the time of report, no adverse events were reported. Event 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 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
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Erythema
Inappropriate schedule of product administration
Symptomtext
patient asked for 2 immunizations in the same arm, immunizer performed the task. A few days later patient developed redness and went to the local walk in to be evaluated on 11-3-21. She was diagnosed with cellulitis and given antibiotic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- NONE
- Allergien
- CEPHALOSPORINS, SSRI
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 01.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse events per patient via phone conversation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Technician was providing immunization. There were 2 people with the same name getting vaccinations at the time. The incorrect patient came in to the room and when asked if she was receiving the Moderna booster dose today, she confirmed it. However, this was incorrect as she was signed up for a flu shot. The patient reports "being in a haze" when the question was asked and "not hearing what was said" while she responded in the affirmative. Patient had already received a Moderna booster dose 1 week previously so we will monitor her for any adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 21.10.2021
- Impfdatum
- 20.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Interchange of vaccine products
Symptomtext
Patient received duplicate High dose flu vaccine on 10/7/2021 and 10/20/2021. Patient has also received duplicate COVID vaccines. He completed the Pfizer series( 1/20/21 and 2/10/21), Moderna series (2/26/21 and 3/26/21) and received a Pfizer booster (10/13/21).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -