- Staat
- TN
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 09.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Febrile convulsion
Laboratory test
Symptomtext
Febrile seizure at 3:10 am lasting 2 minutes per dad report. Patient remained conscious, did not suffer from injury. Emergency medical services were called and patient's vitals were normal (values not known) per dad report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Febrile convulsion
- Hospital-Tage
- -
- Labordaten
- Seen in primary care clinic 8/10/22, neurological tests performed, patient was alert, awake, and oriented, happy and smiling. No laboratory or medical tests beyond physical examination or vital completed.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 1,4
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Urticaria
Symptomtext
All over body rash, described as hives
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- NAM
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Immediate post-injection reaction
Lip swelling
Mouth swelling
Nausea
Symptomtext
Nausea immediately after vaccine pt stated he drank some water and the nausea went away, roughly 5 minutes later he reported his mouth/lips started to feel hot and swollen. The patient was given Benadryl. vitals remained stable, no difficulty breathing or swallowing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- COMMON COLD
- Vorgeschichte
- NONE
- Andere Medikamente
- MUCINEX, FLONASE
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 5,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SC / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Culture throat
Headache
Streptococcus test negative
Tonsillar erythema
Tonsillar hypertrophy
Urticaria
Symptomtext
She developed a slight cough and slight headache on 3/17/22. She went to daycare today (3/18/22)and developed hives on her legs and neck. No known exposure to any food allergens. Her tonsils are red and swollen, she was tested for strep; the rapid strep is negative and throat culture is pending.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Atopic dermatitis, history of Kawasaki disease diagnosed February 2020
- Andere Medikamente
- Zyrtec
- Allergien
- Dairy, eggs,peanuts ,soy and wheat
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatitis diaper
Rash
Rash macular
Symptomtext
After patient awoke from daily nap, noted to have macular erythematous flat rash mostly on trunk, a little on extremities, diaper area also. No respiratory distress, no wheeze, no swelling of mucosal membranes, no scrotal swelling, no vomiting or diarrhea. Pulse ox was 97%.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Dad was COVID positive about 3 weeks prior, but patient tested negative. He had symptoms of cough and runny nose and mild fever.
- Vorgeschichte
- Eczema
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.07.2023
- Impfdatum
- 17.07.2023
- Beginn
- 17.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No Adverse Event; Nurse reports patient was accidently administered an expired dose of VARIVAX on Jul 17, 2023. Product expired on Jun 28, 2023. Product had no prior temperature excursions. No further information provided. No additional AE reported. No PQC reported.; This spontaneous report was received from a nurse refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 17-JUL-2023, the patient was vaccinated with one dose of varicella virus vaccine live (oka/merck)(VARIVAX) lot #U020238, expiration date: 28-JUN-2023 (exact dose, route of administration and anatomical location were not reported) for prophylaxis. The reporter informed that the was accidently administered an expired dose of vaccine (expired product administered). No prior temperature excursion had occurred. There were no additional adverse events reported (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 0,8
- Geschlecht
- M
- Eingang
- 26.01.2023
- Impfdatum
- 25.01.2023
- Beginn
- 25.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
Client received MMR and varicella vaccines too early at age 10 months. No adverse effects reported at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Down Syndrome
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- U
- Eingang
- 23.07.2022
- Impfdatum
- -
- Beginn
- 28.03.2022
- 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
No additional AE reported; HCP reported VARIVAX was administered to patient after a temperature excursion.; This spontaneous report was received from a nurse regarding a patient of an unknown age and gender. The patient's medical history, concurrent conditions, and concomitant therapies were not reported. On an unknown date, the patient was vaccinated with an improper storage dose of varicella virus vaccine live (oka/merck) (VARIVAX) subcutaneous injection, lot #U020238, expiration date: 28-JUN-2023 (dose regimen, route of administration and anatomical location were not provided), as prophylaxis (Product storage error). No adverse events (No adverse event) or product quality complains were reported. The improper storage lot # underwent a temperature excursion of -8.3 degrees Celsius (C) for about 1 hour and 1 minute without previous excursions. This is one patient of three received from the same reporter.; Sender's Comments: US-009507513-2207USA003330: US-009507513-2207USA003332:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 15.07.2022
- Impfdatum
- -
- Beginn
- 17.06.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Overdose
Symptomtext
Patient had no adverse effects or symptoms from this dose; A dose of PROQUAD and VARIVAX were both given to a patient on the same day; This spontaneous report has been received from a medical assistant regarding to a patient of unknown age and gender. The patient's concurrent conditions, medical history, drug/allergy reactions, and concomitant therapies, were not reported. On an unknown date (also reported as 17-JUN-2022), the patient was vaccinated with measles, mumps, rubella and varicella (oka-merck) virus vaccine live (rHA [recombinant human albumin]) (PROQUAD) (strength and route of administration not reported) (lot number U029320 with expiration date 19-MAR-2023) administered at a dose of 0.5 mL, once, for prophylaxis and varicella virus vaccine live (oka/merck) (VARIVAX) (strength and route of administration were not reported) (lot number U020238 with expiration date 28-JUN-2023) administered at a dose of 0.5 mL, once, for prophylaxis. The medical assistant reported that on the day of vaccination, both doses of measles, mumps, rubella and varicella (oka-merck) virus vaccine live (rHA [recombinant human albumin]) (PROQUAD) and varicella virus vaccine live (oka/merck) (VARIVAX) were administered to the patient (overdose). The patient did not have adverse effects (no adverse event) or symptoms from this dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prophylaxis
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 1,2
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient was supposed to receive MMR. Patient received MMRV, when staff realized that wrong vaccine was administered staff called parent to explain what happened and let mom know we will be monitoring the patient for the next 5 to 12 days. Patient at this time was asymptomatic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- -
- Geschlecht
- U
- Eingang
- 10.03.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No other concerns or issues noted; improperly stored VARlVAX had been administered; This spontaneous report was received from a customer and refers to a patient of unknown age and gender. No information about the patient's medical history, concomitant medications and concurrent conditions was reported. On 08-FEB-2022, the patient was vaccinated with improperly stored (41 degrees Fahrenheit for 45 minutes) varicella virus vaccine live (oka/merck) (VARIVAX) lot #U020238, expiration date: 28-JUN-2023 (dose, site and route of administration were not provided) for prophylaxis (product storage error). No other concerns or issues were noted (no adverse event).; Sender's Comments: US-009507513-2202USA003311: US-009507513-2202USA003391:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 1,0
- Geschlecht
- U
- Eingang
- 05.03.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No additional adverse events reported; incorrect product storage; This spontaneous report was received from other health professional and refers to 12-months-old patient of unknown gender. There were no information about the patient's concurrent conditions, concomitant therapies or medical history provided. On 26-JAN-2022, the patient was vaccinated with an improperly stored dose of varicella virus vaccine live (VARIVAX), lot #: U020238, expiration date: 28-JUN-2023, dose: 0,5 milliliter (route of administration and dose number were not reported) for prophylaxis (product storage error). Administered dose of vaccine experienced the temperature excursion between 6 degrees Fahrenheit (F) up to 14 degrees Fahrenheit (F) (13.8 F) for 1 hour, 45 minutes and between of 14 degrees Fahrenheit up to 46 degrees Fahrenheit for (14.4 F) for 25 minutes. There were no previous temperature excursions. No adverse event was reported (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 1,8
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Hib vaccine expired on 2/26/22 and was given on 3/1/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- -
- Geschlecht
- U
- Eingang
- 01.03.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
no other issues or concerns noted; improperly stored Varivax had been administered; This spontaneous report was received from a office manager and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 08-FEB-2022, the patient was vaccinated with an improperly stored dose of varicella virus vaccine live (Oka/Merck) (VARIVAX) lot #U020238, expiration date: 28-JUN-2023 (formulation, strength, dose, frequency, site and route of administration were not provided) for prophylaxis (product storage error). The vaccine experienced a temperature excursion of 41 degrees Fahrenheit for 45 minutes. No previous temperature excursions were reported. No other issues or concerns noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 1,0
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
No additional adverse events reported; dose of Improperly Stored VARIVAX has been administered to a patient; This spontaneous report as received from a registered nurse refers to a 12-month-old patient. No information regarding the patient's concurrent conditions, medical history, drug allergies and concomitant medications were provided. On 25-JAN-2022, the patient was vaccinated with varicella virus vaccine live (oka/merck) (VARIVAX) lot # U020238, expiration date 25-JUN-2023, dose: 0,5 milliliter (formulation, injection site and route of administration were not provided) for prophylaxis. The the vaccine was stored in inappropriate range of temperature. Temperature and time frame: 6 F (Fahrenheit) degrees up to 14 F degrees (13.8F) for 1 hour 45 minutes and 0 seconds; 14 F degrees up to 46 F degrees (14.4 F) for 0 hours 25 minutes and 0 seconds (product storage error temperature too high). There was no previous temperature excursion. No additional adverse event was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 1,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SC / RL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cough
Dysphonia
Rhinorrhoea
Stridor
Swelling face
Swelling of eyelid
Symptomtext
Significant coughing, inspiratory stridor, hoarseness, runny nose, (facial) swelling of the right upper eye lid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- No labs drawn after reaction
- Aktuelle Erkrankungen
- Positive COVID PCR test on 1/7/2022
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None Known
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 1,0
- Geschlecht
- U
- Eingang
- 14.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product storage error
Symptomtext
No additional adverse events reported.; Improperly Stored VARIVAX has been administered to a patient; This spontaneous report was received from a registered nurse referring to a 12 months old patient of unknown gender. The patient's concomitant medication, pertinent medical history and drug reactions/allergies were not reported. On 26-JAN-2022, the patient was vaccinated with a dose of improperly stored (later found supported) varicella virus vaccine live (oka/merck) (VARIVAX) (strength and route of administration were not reported, lot # U020238, expiration date was 28-JUN-2023) 0.5 ml for prophylaxis (product storage error). It was reported that the suspect vaccine was exposed to a temperature of 6 Fahrenheit (F) up to 14 F (13.8 F) for a time frame of 1 hours and 45 minutes and 0 seconds, 14 F up to 46 F (14.4 F) for 0 hours 25 minutes and 0 seconds. There were no previous temperature excursions. No further adverse event (AE) information was provided (no adverse event).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.02.2022
- Impfdatum
- 31.01.2022
- 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
Nurse reporting a dose of improperly stored VARIVAX; No additional adverse events reported; This spontaneous information was received from a registered nurse concerning a patient of unknown age and gender. Patient's concurrent conditions, medical history and concomitant medications were not provided. On 31-JAN-2022, the patient received an improperly stored dose of varicella virus vaccine live (oka/merck) (VARIVAX) 0.5 ml for prophylaxis, lot number: U020238 with expiration date on 28-JUN-2023 (strength, frequency, route of administration and anatomical location were not provided) (incorrect product storage). The varicella virus vaccine live (oka/merck) (VARIVAX) was stored at a temperature range of 6 degrees Fahrenheit (F) up to 14 degrees Fahrenheit (13.8F) for the time frame of 1 hour and 45 minutes and 0 seconds, and for the temperature range of 14F up to 46F (14.4F) for 0 hours 25 minutes and 0 seconds. There was no previous temperature excursion. No additional adverse events reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.02.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Varivax exposed to a temperature excursion was administered; This spontaneous report was received from a physician concerning a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant medications were not reported. On 21-DEC-2021 the patient was vaccinated with a dose of varicella virus vaccine live (oka/merck)(VARIVAX) lot # U020238 with expiration date: 28-JUN-2023, (dose, route of administration not reported) as prophylaxis, that had experienced a temperature excursion at 8.2 Fahrenheit degrees for 1 hour and 30 minutes. There were no previous temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 31.01.2022
- Impfdatum
- 23.12.2021
- Beginn
- 23.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Temperature 8.2F/ Time frame: 1 hours and 30 minutes; This spontaneous report was received from a physician referring to a patient of unknown age and gender. The patient's concomitant medications, concurrent conditions, medical history and drug reactions/allergies were not reported. On 23-DEC-2021, the patient received improperly stored varicella virus vaccine live (Oka/Merck) (VARIVAX) (lot # U020238, expiration date: 28-JUN-2023, strength, dose and route were unknown) for prophylaxis (product storage error). The vaccine was stored at 8.2 degrees Fahrenheit (F) for one hour and 30 minutes. There was no previous excursion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.01.2022
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Temperature 8.2F/ Time frame: 1 hours and 30 minutes; This spontaneous report has been received from a physician referring to a patient of unknown age and gender. The patient's pertinent medical history, concurrent conditions, concomitant therapies and previous drug reactions or allergies were not reported. On 21-DEC-2021, the patient was vaccinated with an improperly stored dose of varicella virus vaccine live (oka/merck) (VARIVAX) (dose, route of administration, anatomical site of vaccination and vaccine scheme were not reported; lot number U020238 has been verified to be valid, expiration date reported and established as 28-JUN-2023) as prophylaxis. The vaccine was exposed to a temperature excursion of 8.2 degrees Fahrenheit, during a time frame of 1 hour and 30 minutes (product storage error). There was no previous temperature excursion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -