- Staat
- PR
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 14.07.2023
- Impfdatum
- 14.07.2023
- Beginn
- 14.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Syncope
Vision blurred
Symptomtext
The patient was vaccinated at 9:30 a.m. Mom left the office, I took him to a car and the patient expressed seeing cloudy vision and fainting on the pavement at 9:50 a.m.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Dyst. 176 B/P 102/59. 8-83
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- -
- Geschlecht
- M
- Eingang
- 28.12.2023
- Impfdatum
- 15.09.2023
- Beginn
- 15.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site swelling
Vaccination site erythema
Vaccination site swelling
Symptomtext
Patient was given MMR in the left thigh, the evening of the vaccine the vaccine site got red and swollen to the size of a quarter by the next day it was swollen to baseball size; Patient was given MMR in the left thigh, the evening of the vaccine the vaccine site got red and swollen to the size of a quarter by the next day it was swollen to baseball size; This case was retrieved during the Vaccines Adverse Event Reporting System (VAERS) monitoring on 12-OCT-2023 with the following VAERS Primary ID 2684685-1. The original narrative from the sender is the following: patient was given MMR in the left thigh, the evening of the vaccine the vaccine site got red and swollen to the size of a quarter by the next day it was swollen to baseball size. The reporter did not provide an assessment of the causal relationship between Vaxelis and the reported events "Vaccination site erythema and Vaccination site swelling". No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Eczema
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 25.11.2023
- Impfdatum
- 25.11.2023
- Beginn
- 25.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Nervousness
Pallor
Symptomtext
Pt felt nauseous and was looking pale after 2 vaccines were administered. He was extremely nervous and hadn't eaten lunch. Gave pt water and some chocolate. He started to feel better within minutes, and I was able to administer the rest of the vaccines. He was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 14.11.2023
- Impfdatum
- 09.11.2023
- Beginn
- 09.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site warmth
Symptomtext
Red area up to 6 cm and warm to touch noted around injection site of varicella (RUE) after 20 minutes. Area marked and receded after an additional 5 minutes. No difficulty breathing or rash. Pt then able to be DCd home. Refer to allergist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 27.09.2023
- Impfdatum
- 22.09.2023
- Beginn
- 22.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site reaction
Injection site urticaria
Rash
Urticaria
Vomiting
Symptomtext
Patient developed red whelps/urticaria on left arm, then left leg, then right arm and leg within 2-3 minutes after vaccines were administered. Benadryl was given po and rash began to resolve within 10 minutes. No further symptoms developed that day. 3 days after the vaccines, patient had vomiting that lasted a few hours .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 12.09.2023
- Impfdatum
- 31.08.2023
- Beginn
- 31.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Pharyngeal swelling
Rash macular
Sneezing
Erythema
Symptomtext
4 years On Moms way out of the office after vaccination ~5minutes patient returned with sneezing and red blotchy face No vomiting or increased WOB Pt given benadryl PO
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- TBI, epilepsy, developmental delay
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 12.09.2023
- Impfdatum
- 31.08.2023
- Beginn
- 31.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Pharyngeal swelling
Rash macular
Sneezing
Erythema
Symptomtext
4 years On Moms way out of the office after vaccination ~5minutes patient returned with sneezing and red blotchy face No vomiting or increased WOB Pt given benadryl PO
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- TBI, epilepsy, developmental delay
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 6,0
- Geschlecht
- F
- Eingang
- 29.08.2023
- Impfdatum
- 24.08.2023
- Beginn
- 24.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Vaccination site urticaria
Symptomtext
hives to the area vaccine was given, step mom gave her benadryl the next day
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 25.08.2023
- Impfdatum
- 19.08.2023
- Beginn
- 20.08.2023
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry skin
Rash erythematous
Skin abrasion
Skin exfoliation
Symptomtext
#non-specific rash erythematous, dry, scaly, excoriated rash, with regions of peeling appearing 1 day after varicella vaccine. pt denies itchiness, pain, burning, or systemic sx. Unclear etiology whether if rash 2/2 varicella vaccine or timing was coincidental. If were to treat with anti-viral, could stunt immune response to varicella vaccine. Given asx will do triamcinolone and have close f/u. -triamcionlone .1% BID -f/u in 1 week-- > if no improvement consider valacyclovir. -pt to send images to be imported in chart
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- triamcionlone 1% BID
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- skin problems- not specified
- Andere Medikamente
- none
- Allergien
- Cephalosporins, Penicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.07.2023
- Impfdatum
- 26.07.2023
- Beginn
- 27.07.2023
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pruritus
Urticaria
Symptomtext
21 hours after vaccine, developed hives and itching at injection site, wrist and torso (bra line). no other sx
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- none known
- Allergien
- shrimp, lemons, tomatoes, onions, barley, yeast, grapefruit
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 19.07.2023
- Impfdatum
- 18.07.2023
- Beginn
- 18.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Irritability
No adverse event
Pyrexia
Wrong product administered
Symptomtext
MMRV was given instead of MMR at the same time Varicella was given by mistake. No adverse reaction noted at this time. Mother states Patient has been fussy with low grade fever. She has given tylenol and motrin as need.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tylenol, Motrin, Clartin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 09.12.2023
- Impfdatum
- 09.12.2023
- Beginn
- 09.12.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exposure during pregnancy
Military service
Pregnancy test positive
Product use issue
Symptomtext
Patient inappropriately received the MMR and Varicella vaccines during a medical readiness event after testing positive with a urine hcg pregnancy test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- Urine hcg
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Prenatal Vitamins
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 29.11.2023
- Impfdatum
- 03.11.2023
- Beginn
- 03.11.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No adverse effect documented
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 13,0
- Geschlecht
- U
- Eingang
- 06.11.2023
- Impfdatum
- 01.07.2023
- Beginn
- 01.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
No additional AE; Physician calling to report a TE VARIVAX. HCP stated that the vaccines were administered to a patient on date of administration in July 2023.; This spontaneous report was received from a physician and referred to a 13-year-old patient of unknown gender. The patient's concomitant medication, pertinent medical history and drug reactions/allergies were not reported. On an unspecified date in July 2023, the patient was vaccinated with improperly stored vaccine of varicella virus vaccine live (oka/merck) (VARIVAX) injection (lot # X006981, expiry date: 07-MAR-2025), the second dose for the series (dose, strength and route of administration were not provided) for prophylaxis (Product storage error). The vaccine was exposed to 28 Fahrenheit (F)/14 F to 46 F for 15 minutes 0 seconds. There was no previous temperature excursion. No additional adverse event (AE) was reported. This is one of several reports received from the same reporter.; Sender's Comments: US-009507513-2309USA007382:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.09.2023
- Impfdatum
- 01.09.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
HCP reported VARIVAX was administered after a temperature excursion to patient. Date of administration is Sep 1, 2023. No further information provided. No additional AE reported. No PQC reported. Names of vaccines involved (including lot/exp): VARIV; No addtional AE; This spontaneous report was received from a nurse and refers to a male patient of unknown age. The patient's concurrent conditions, medical history, concomitant medications, drug reactions or allergies were not reported. On 01-SEP-2023, the patient was vaccinated with a dose of varicella virus vaccine live (oka/merck)(VARIVAX) (lot # X006981, expiration date: 07-MAR-2025), given once (dose, route of administration, anatomical location not provided) as prophylaxis, which underwent a temperature excursion at 6 Fahrenheit (F) during 20 minutes (product storage error). No additional adverse event (AE) reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.09.2023
- Impfdatum
- 01.09.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
HCP reported VARIVAX was administered after a temperature excursion to patient. Date of administration is Sep 1, 2023. No further information provided. No additional AE reported. No PQC reported. Names of vaccines involved (including lot/exp): VARIV; No additional AE reported; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's concurrent conditions, medical history, concomitant medications, drug reactions or allergies were not reported. On 01-SEP-2023, the patient was vaccinated with a dose of varicella virus vaccine live (oka/merck)(VARIVAX) (lot # X006981, expiration date: 07-MAR-2025), given once (dose, route of administration, anatomical location not provided) as prophylaxis, which underwent a temperature excursion at 6 Fahrenheit (F) during 20 minutes (product storage error). No additional adverse event (AE) reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 22.09.2023
- Impfdatum
- 22.09.2023
- Beginn
- 22.09.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient Recieved Varivax vaccine as well as MMRV vaccine during the same visit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 0,3
- Geschlecht
- F
- Eingang
- 18.08.2023
- Impfdatum
- 15.08.2023
- Beginn
- 15.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No signs or symptoms noticed at time of administration. There was no reaction to the given vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- U
- Eingang
- 14.08.2023
- Impfdatum
- 18.07.2023
- Beginn
- 18.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Overdose
Symptomtext
No Additional AE; HCP called to report that the patient was administered PROQUAD and VARIVAX in the same day. No Additional AE/PQC.; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. No information on patient's medical history, current conditions and concomitant medications was provided. On 18-JUL-2023 the patient was vaccinated with measles, mumps, rubella and varicella (oka-merck) virus vaccine live (PROQUAD) (albumin status: rHA) lot # w039840 and expiration date 12-JUN-2024, 0.5 milliliter for prophylaxis (dose number, route and site of administration were not provided) and varicella virus vaccine live (oka/merck)(VARIVAX) lot # x006981 (valid for varicella virus vaccine live (oka/merck)(VARIVAX)) and expiration date established as 07-MAR-2025, 0.5 milliliter for prophylaxis (dose number, route and site of administration were not provided) (overdose and no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 5,0
- Geschlecht
- M
- Eingang
- 14.08.2023
- Impfdatum
- 02.08.2023
- Beginn
- 02.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Somnolence
Unresponsive to stimuli
Urinary incontinence
Symptomtext
At 14:40 mom returns to clinic with child saying he is having a reaction to vaccines. Patient is awake but drowsy and talking. Mom states " he became unresponsive in drive thru line." Child also urinated on himself. Patient has 2-3 small red spots on chest and 2-3 small red spots on upper back. Does not have labored breathing and child states does not feel short of breath. Benadryl given per standing orders. BP at 14:45 was 130/82. rechecked BP at 15:00 it was 118/60. Patient becoming more active. Talking the whole time. Mom states history of febrile seizures. Last one 5 months ago. No new red spots appearing on body. Patient is alert and active. Encouraged mom to watch child closely. To ER if condition worsens. Mom verbalized understanding. Patient walked out with mom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- History of febrile seizures
- Andere Medikamente
- None
- Allergien
- PCN, Cephalosporins
- Vorherige Impfungen
- -