- Staat
- IL
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Aphasia
Condition aggravated
Fall
Muscle tightness
Seizure
Tremor
Symptomtext
Received Pfizer bivalent, was talking and discussing past side effects. Received flublok then stopped talking. Slumped in chair as if fainting. Intern held patient steady to avoid injury and called for backup. The patient began tensing up and shaking at this point, so pharmacist called EMS while the intern monitored the patient. He recovered and was responsive, but began to seize again once paramedics began to evaluate him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- history of seizure
- Andere Medikamente
- After the seizure, patient stated he takes Keppra for a seizure 2 years ago, but it is not filled at our pharmacy.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 04.12.2022
- Impfdatum
- 30.10.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mobility decreased
Pain in extremity
Symptomtext
Patient reported to pharmacy today, 34 days after injection, stating he has had a very abnormally sore arm, cannot lift his arm above his head and assumed that was not normal to still have. He was encouraged to be checked out by his physician as soon as possible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 26.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Pain
Pain in extremity
Peripheral swelling
Pruritus
Swelling
Swelling face
Symptomtext
Patient reported today that she took Flu vaccine on 9/26/22 and she develops swelling of arms, legs, face and stomach . In addition, she reported having body aches, whales all over her body, pain in the arms and legs and difficulty breathing. However, patient states she self administered Epi pen and took benadryl and now her symptom is improving. Denies SOB.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Recommend patient to go to ER but patient refused. None
- Aktuelle Erkrankungen
- Reports itchiness over whole body on 9/26/22, foot pain
- Vorgeschichte
- Rheumatoid arthritis, H/O renal insufficiency syndrome, nasal polyp, asthma, bipolar disorder
- Andere Medikamente
- acetaminophen (Tylenol Extra Strength) 500 mg tablet albuterol (PROVENTIL) 2.5 mg/3 mL nebulizer solution albuterol (PROVENTIL) 2.5 mg/3 mL nebulizer solution ascorbic acid, vitamin C, (vitamin C) 1000 MG tablet azelastine (ASTELIN) 137
- Allergien
- Allergies to Eggs, milk containing products, shellfish containing products, tea.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 04.01.2023
- Beginn
- 04.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Influenza like illness
Malaise
Pain
Symptomtext
Patient reported getting home after the vaccine and feeling not well. She reports flu like symptoms, feels body aches, and fatigue for the last week since vaccination. I advised the patient that since it would take approximately 2 week to have full immunity after the vaccine, she may have been exposed to the flu virus or another illness before and/or after the vaccine. I suggested she contact her doctor and if she could not get an appointment right away, to seek care at a walk in or urgent care facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- Patient states she has asthma
- Andere Medikamente
- none known
- Allergien
- none known
- Vorherige Impfungen
- felt sick after Moderna COVID vaccines
- Staat
- SD
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 31.12.2022
- Beginn
- 31.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
patient reported redness and swelling at the injection site, with pain running up to the shoulder starting 1/4/23
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 04.12.2022
- Impfdatum
- 01.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Pain in extremity
Symptomtext
Patient was administered flublok on 12/1 had sore arm that night, noticed redness, swelling and "heat" from injection site. Patient started using cold compresses. Patient presented at pharmacy on 12/4 and showed pharmacy a picture of her arm on 12/1 and her physical arm on 12/4 . Redness and swelling looks better but still tender per patient. Patient has dr's visit on 12/5 in AM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- blood pressure
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 31.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash pruritic
Symptomtext
Discovered itchy rash/spot on left hand after receiving flublok vaccine on 10/31. Applied alcohol and hydrocortisone to help relieve itchiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Throat tightness
Symptomtext
patient stated she felt dizzy and throat tightness. by time patient got back in room, throat no longer felt tight but still felt dizzy. patient did not experience swelling of face or tongue and was able to talk througout whole interaction, so administered benadryl. asked patient if she had anything to eat or drink yet. she said yes. offered crackers and water. she accepted water. monitored bp and hr, was within normal range. observed for 15 minutes in room. counseled pt on s/sx of allergic reaction and to contact 911 if experienced those s/sx at home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 22.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Pain in extremity
Product administered to patient of inappropriate age
Symptomtext
Patient was given vaccine indicated for people over the age of 18. We contacted patient's mother to notify of error and mother stated daughter had bruised, sore arm also.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Symptomtext
Patient received flu shot yesterday morning and reported to us this afternoon that she has red/raised slightly itchy spot where shot was given. Slight hot to touch. Assessed and reccommended to put ice packs on and keep and eye on. To report any changes to HC provider/ED if necessary.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
After one hour, patient returned to clinic with swelling, redness, and itching at injection site. We verified that she had received FluBlok because of reported egg allergy history. Patient took Benadryl to help with symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Allergy to eggs
- Vorherige Impfungen
- Fluzone
- Staat
- LA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Influenza like illness
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
. patient was administered flublok which is not approved for her age .had high fever and flu like symptoms. dad took her to the dr and gave her tylenol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 08.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Sore Arm
- Staat
- OK
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash pruritic
Symptomtext
Patient has rash on both arms and chest. She says it just itches a little bit. She has tried taking an antihistamine but rash has not cleared up. She said she will give it a few more days to see if it clears up and will let us know.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- No test have been done yet
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Unknown
- Allergien
- Penicillin, Lisinopril
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 24.09.2022
- Impfdatum
- 21.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Skin warm
Symptomtext
Per patient she received the shot on Wednesday 9/21/22 in her right arm. Didn't take a look at it until the next morning and noticed and injection site reaction. Arm was red and swollen about 2 1/2". Reported to pharmacist on duty on Thursday. Let the vaccine administrator know Friday night. Tried to follow up and left voicemail. Patient called back Saturday afternoon. Reported that redness/warmth has spread to about 7". Pt took aleve the night of and then an antihistamine Thursday. Tried cold compress as well. Recommended to follow up with a doctor to be safe, continue with anti-inflammatory and cold compresses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none yet
- Aktuelle Erkrankungen
- NO PER PATIENT
- Vorgeschichte
- NO PER PATIENT
- Andere Medikamente
- CALCIUM +VITAMIN D. TERBINAFINE
- Allergien
- STRONG REACTION TO DEMEROL.
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 19.11.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
given to a patient under 18 years of age with no reported adverse event; Initial information was received on 21-Nov-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 14 years old female patient who had given to a patient under 18 years of age with no reported adverse event after receiving influenza quadrivalent recombinant vaccine [Flublok]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. At the time of the event, the patient had ongoing Egg allergy. On 19-Nov-2022, the patient received 0.5 ml dose of suspect influenza quadrivalent recombinant vaccine (unknown formulation) (Frequency: once) (with lot: UJ909AA, expiry date: 30-Jun-2023) (strength was unknown) via intramuscular route in left deltoid site for Immunization. On 19-Nov-2022 the patient had a non-serious event given to a patient under 18 years of age with no reported adverse event (Product administered to patient of inappropriate age) (latency: same day) following the administration of influenza quadrivalent recombinant vaccine. Action taken: not applicable. It was not reported if the patient received a corrective treatment for the event. At time of reporting, the outcome was Recovered / Resolved in 2022 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
- Egg allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 22.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
administration of FLUBLOK to a pediatric patient with no reported adverse event; Initial information received on 24-Oct-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 13 years old female patient and there was administration of flublok (INFLUENZA QUADRIVALENT RECOMBINANT VACCINE) to a pediatric patient with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 22-Oct-2022, the patient received a dose of 0.5 ml of suspect INFLUENZA QUADRIVALENT RECOMBINANT VACCINE (formulation, strength: unknown) lot UJ909AA, expiration date: 30-Jun-2023 via intramuscular route in the left deltoid as Immunization. On 22-OCT-2022 there was an administration of flublok to a pediatric patient with no reported adverse event (product administered to patient of inappropriate age) same day following the administration of INFLUENZA QUADRIVALENT RECOMBINANT VACCINE. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (administration of FLUBLOK to a pediatric patient with no reported adverse event). 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
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tongue blistering
Symptomtext
Patient states approximately one to two weeks after receiving her Covid bivalent Pfizer booster she developed several tiny white blisters on her tongue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tongue blistering
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 22.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Vaccine was given to minor by mistake when vaccine is indicated for 18 years and older. Patient feels fine today 10/23 (24 hours later), but wanted reported in case of issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none listed
- Andere Medikamente
- none
- Allergien
- none known of
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 22.10.2022
- Impfdatum
- 22.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Recognized Flublok inadvertently given to patient under 18 years of age. No side effects noted per mom
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
patient was administered flublok which is not approved for her age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
patient was administered flublok which is not approved for her age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Flublock to be administered to people 18 years old - 64 year old's. This client is 77, with no reported effects from vaccination. This client has given NO report of any adverse effect at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Flublok given to patient under the age of 8
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 11.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Pt came in for yearly flu and Pfizer bivalent immunization; dose administered; pt called back asking to talk with pharmacy as she had received flu shot at physician's office 09/14/2022;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Mother unable to be reached at time of discovery
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 64,0
- 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
Induration
Mass
Swelling
Symptomtext
Immediate swelling, hard lump about the size of a golf ball
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Induration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none noted
- Vorgeschichte
- none noted
- Andere Medikamente
- none known
- Allergien
- prednisone
- Vorherige Impfungen
- -