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Reporte zur Charge U033046

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

19Reporte angezeigt
0Todesfaelle
0Hospitalisiert
0Lebensbedrohlich
0Bleibende Schaeden
CA 7 WA 5 FL 1 OH 1 TX 1 PA 1 UT 1 MI 1

VAERS 2408328

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

schwer
Staat
-
Alter
16,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
10.08.2022
Beginn
10.08.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Dizziness Pallor Syncope

Symptomtext

Approximately 5 minutes after vaccination, patient complained of feeling light-headed. His face appeared pale and he attempted to walk a couple of steps to get on the exam table and began to faint. He was caught by myself and his mother and guided to the floor without injury. The initial episode was very brief (seconds) and the patient was conscious and speaking by the time he was completely supine on the floor. He was provided a cool compress to the forehead for approximately 3 minutes until he felt able to stand to get to the table. Once flat on the table with legs raised, he was provided apple juice until he was able to sit and eventually stand and then walk to the car without light-headedness (approximately 20 minutes).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2632285

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

schwer
Staat
FL
Alter
8,0
Geschlecht
M
Eingang
01.07.2022
Impfdatum
09.06.2022
Beginn
09.06.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dizziness Poor peripheral circulation Posture abnormal Syncope

Symptomtext

30 min after vaccination patient felt dizzy and syncopal attack, became limp and had poor perfusion but regained normal status in 10 min

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2533236

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge u033046

mild
Staat
OH
Alter
1,0
Geschlecht
F
Eingang
15.12.2022
Impfdatum
02.12.2022
Beginn
13.12.2022
Tage bis Beginn
11,0
Dosis
1
Route/Site
SC / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Decreased appetite Dermatitis diaper Diarrhoea Influenza virus test Laboratory test Pyrexia Rash morbilliform SARS-CoV-2 test

Symptomtext

Morbilliform rash began on 12.13.2022. Fever started on 12.12.2022, diarrhea, decreased appetite, diaper rash

Weitere VAERSDATA-Felder
Praegender Schweregrund
Diarrhoea
Hospital-Tage
-
Labordaten
Flu, COVID and respiratory panels sent
Aktuelle Erkrankungen
NOne
Vorgeschichte
Tricuspid valve regurgitation, Patent foramen ovale,
Andere Medikamente
None
Allergien
NKDA, no known allergies
Vorherige Impfungen
-

VAERS 2449373

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

mild
Staat
TX
Alter
-
Geschlecht
M
Eingang
17.09.2022
Impfdatum
15.07.2022
Beginn
15.07.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect route of product administration Pain in extremity

Symptomtext

the patient stated that the first dose he received on 7/15/2022 was administered via intramuscular route; sore arm; This spontaneous report was received from a pharmacist and referred to an unknown age male patient. Pertinent medical history, concomitant medications and drug reactions/allergies were unknown. On 15-JUL-2022, the patient was vaccinated with the first dose of varicella virus vaccine live (oka/merck) (VARIVAX) subcutaneous injection, 0.5 milliliter, lot #U033046, expiration date: 21-OCT-2023, administered intramuscularly for prophylaxis (strength was not provided) (incorrect route of product administration). The patient reported having a "sore arm" following initial dose (unknown date in 2022). It was unknown if the patient sought a medical attention, received the treatment, or performed any lab diagnostics/studies. The therapy was not discontinued. On 17-AUG-2022, the patient was vaccinated with the second dose of varicella virus vaccine live (oka/merck) (VARIVAX) administered subcutaneously for prophylaxis (strength, dose, lot#, expire date was not provided). On 01-SEP-2022 an inbound telephone call, it was confirmed the patient received vaccine at a pharmacy. The outcome of sore arm was not reported. The causal relationship between sore arm and varicella virus vaccine live (oka/merck) (VARIVAX) was not reported.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2329433

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

mild
Staat
CA
Alter
4,0
Geschlecht
F
Eingang
23.06.2022
Impfdatum
20.06.2022
Beginn
20.06.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
SC / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site erythema Peripheral swelling

Symptomtext

SWOLLEN LEG, RED MARK AROUND THE AREA.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2314568

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge u033046

mild
Staat
CA
Alter
4,0
Geschlecht
F
Eingang
09.06.2022
Impfdatum
06.06.2022
Beginn
07.06.2022
Tage bis Beginn
1,0
Dosis
5
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pain Injection site swelling

Symptomtext

Left Upper Arm pain and swelling around site of injection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2566828

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
CA
Alter
1,1
Geschlecht
F
Eingang
21.02.2023
Impfdatum
20.01.2023
Beginn
20.01.2023
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event Product storage error

Symptomtext

No adverse effect; administered an expired dose of VAQTA; The involved VAQTA had also underwent a temperature excursion.; This spontaneous report was received from a nurse referring to a patient of unknown age and gender. Information regarding the patient's pertinent medical history, drug allergies/reactions, or concomitant medications was not provided. On 20-JAN-2023, the patient was vaccinated with an improperly stored and expired dose of hepatitis a vaccine, inactivated (VAQTA SYRINGE (DEVICE)) for prophylaxis (lot number W007375 had been verified to be a valid number; expiration date 16-JAN-2023, and upon internal validation established as the same date) (dosage, vaccination scheme, frequency, route of administration, and anatomical site of injection were not reported) (expired product administered and product storage error). The administered dose of the vaccine was stored at a temperature of 11.1 degree Celsius (C), for a time frame of 14 hours, as recorded by a data logger. There was no previous temperature excursion reported. There was no adverse effect reported. Follow-up information was received from the nurse on 14-FEB-2023. The report concerns to a 13-month-old female patient, who birth weight was 3.09 kilograms On 20-JAN-2023, the patient was also vaccinated with varicella virus vaccine live (oka/merck) (VARIVAX) subcutaneous injection, lot number U033046 was verified to be a valid number, expiration date 21-OCT-2023, administered subcutaneosly; mumps, and rubella (wistar ra 27-3) virus vaccine, live rHA (recombinant human albumin) (M-M-R II) subcutaneous injection, lot number U039664 was verified to be a valid number, expiration date 15-DEC-2023, administered subcutaneosly; influenza vaccine lot number 5M2H2, expiration date 30-JUN-2023, administered intramuscularly; and pneumococcal vaccine conj 13v (crm197) (PREVENAR 13) lot number FX0079, expiration date 30-NOV-2024, administered intramuscularly, all administered for prophylaxis (doses, strengths, anatomical injection sites and vaccination schemes were not reported). Hepatitis a vaccine, inactivated (VAQTA) was administered intramuscularly. It was reported that temperature excursion was on 12-JAN-2023, vaccines were used on 13-JAN-2023 (also reported as 20-JAN-2023, conflicting information). The vaccines were administered at private doctor's office/hospital with private funds. The reporter considered expired product administered related to hepatitis a vaccine, inactivated (VAQTA).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2580330

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
PA
Alter
4,0
Geschlecht
F
Eingang
13.02.2023
Impfdatum
27.07.2022
Beginn
27.07.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Wrong product administered

Symptomtext

There were NO adverse events or reactions. Kinrix was given when last DTap was Pentavalent therefore. Kinrix should not have been given. Per discussion with doctor, Kinrix administration was acceptable. All 7 previous dose of Polio were oral and given after 2016, so therefore did not count.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
NONE
Allergien
N/A
Vorherige Impfungen
-

VAERS 2561527

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge u033046

gering
Staat
WA
Alter
25,0
Geschlecht
F
Eingang
17.01.2023
Impfdatum
02.06.2022
Beginn
01.06.2022
Tage bis Beginn
-
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product storage error

Symptomtext

Improper storage of vaccine, was in vaccine refrigerator beyond 72hrs.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2561507

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge u033046

gering
Staat
WA
Alter
24,0
Geschlecht
F
Eingang
17.01.2023
Impfdatum
06.10.2022
Beginn
01.10.2022
Tage bis Beginn
-
Dosis
1
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product storage error

Symptomtext

Vaccine was improperly stored in vaccine fridge beyond the 72hrs time. Patient has been notified.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2561491

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge u033046

gering
Staat
WA
Alter
29,0
Geschlecht
M
Eingang
17.01.2023
Impfdatum
06.10.2022
Beginn
01.10.2022
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
No adverse event Product storage error

Symptomtext

Vaccine improperly stored, was kept in vaccine refridgerator beyond 72hrs. Patient did not indicate any reactions to the vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2561479

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge u033046

gering
Staat
WA
Alter
31,0
Geschlecht
F
Eingang
17.01.2023
Impfdatum
06.10.2022
Beginn
01.10.2022
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Product storage error

Symptomtext

Vaccine was improperly stored in vaccine refrigerator beyond the 72hrs prior to administration.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2561431

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
WA
Alter
14,0
Geschlecht
F
Eingang
17.01.2023
Impfdatum
17.01.2023
Beginn
17.01.2023
Tage bis Beginn
0,0
Dosis
2
Route/Site
SC / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

patient should have received Tdap but instead received Dtap.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2523563

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
CA
Alter
-
Geschlecht
U
Eingang
06.12.2022
Impfdatum
21.11.2022
Beginn
21.11.2022
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 AE; Medical assistant reports one dose of improperly stored VARIVAX was administered to one patient. ? ?; This spontaneous report has been received from a medical assistant, regarding to a patient of unknown gender and age. The patient's pertinent medical history, concurrent conditions, concomitant medications, and previous drug reactions or allergies were not reported. On 21-NOV-2022, the patient was vaccinated with an improperly stored dose of with improperly storage dose of varicella virus vaccine live (Oka/Merck) (VARIVAX)injection, for prophylaxis (lot number: U033046, which was determined to be valid, with an expiration date on 21-OCT-2023) plus an sterile diluent (strength, dose, vaccination scheme, route of administration, and anatomical site of injection were not reported). Administered doses were stored at a temperature of 14 degrees Fahrenheit (F) up to 46 degrees Fahrenheit, during a time frame of 5 hours and 20 minutes (product storage error). There was no previous temperature excursion. No additional adverse events were reported in the patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
STERILE DILUENT
Allergien
-
Vorherige Impfungen
-

VAERS 2428183

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
CA
Alter
1,0
Geschlecht
M
Eingang
02.09.2022
Impfdatum
01.09.2022
Beginn
01.09.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect route of product administration

Symptomtext

New MA inadvertently give MMR and Varicella IM rather than SQ

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect route of product administration
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2410150

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
UT
Alter
-
Geschlecht
U
Eingang
12.08.2022
Impfdatum
14.07.2022
Beginn
14.07.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Accidental overdose No adverse event

Symptomtext

no adverse event; Caller is a medical assistant who reports that PROQUAD and VARIVAX were inadvertently administered to a patient concomitantly today; This spontaneous report was received from a medical assistant and referred to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 14-JUL-2022, the patient was inadvertently vaccinated varicella virus vaccine live (oka/merck) (VARIVAX) (0.5 mL once, lot #U033046, expiration date: 21-OCT-2023) and measles, mumps, rubella and varicella (oka-merck) virus vaccine live(recombinant human albumin (rHA)) (PROQUAD) (0.5 mL, lot #U016976, expiration date: 24-NOV-2022) administered for prophylaxis (strength, anatomical location and route of administration were not provided) (accidental overdose) with sterile diluent (MERCK STERILE DILUENT). The patient had no adverse effects or symptoms from receiving these doses (no adverse event).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Accidental overdose
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
MERCK STERILE DILUENT
Allergien
-
Vorherige Impfungen
-

VAERS 2405747

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
CA
Alter
2,0
Geschlecht
M
Eingang
09.08.2022
Impfdatum
28.07.2022
Beginn
28.07.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Inappropriate schedule of product administration

Symptomtext

Patient received second Varicella Vaccine early. First dose was given 8/27/2021 and second dose given 7/28/22

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Unknown
Vorgeschichte
None
Andere Medikamente
Flouride, Albuterol
Allergien
Naproxen Sodium
Vorherige Impfungen
-

VAERS 2325044

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
CA
Alter
-
Geschlecht
U
Eingang
21.06.2022
Impfdatum
-
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 calling for TE evaluation on frozen products states products have been administered. Names of vaccines involved (including lot/exp) VARIVAX U033046 10/20/2023 ? Temperature 6?F up to 14?F (8F) for 0 hours 18 minutes 0 seco; No additional AE details.; This spontaneous report was received from a nurse referring to a 2-year-old. The patient's concurrent conditions, medical history and concomitant therapies were not reported. On an unknown date, the patient was vaccinated with an improperly stored dose of varicella virus vaccine live (oka/merck) (VARIVAX) lot #U033046, expiration date: 21-OCT-2023, administered for prophylaxis (strength, and route of administration were not provided); which was reconstituted with sterile diluent (STERILE DILUENT)(product storage error). The administered dose of the vaccine was stored with the lowest temperature of 6 degrees Fahrenheit up to 14 degrees Fahrenheit (mean of 8 degrees Fahrenheit) for 0 hours and 18 minutes 0 seconds; and with the lowest temperature of 14 degrees Fahrenheit up to 46 degrees Fahrenheit (mean of 18.4 degrees Fahrenheit) for 0 hours and 45 minutes 0 seconds. There was no previous temperature excursion. No additional adverse events.; Sender's Comments: US-009507513-2206USA002264: US-009507513-2206USA002231:

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Prophylaxis
Vorgeschichte
-
Andere Medikamente
STERILE DILUENT
Allergien
-
Vorherige Impfungen
-

VAERS 2320367

MERCK & CO. INC. · VARICELLA (VARIVAX) · Charge U033046

gering
Staat
MI
Alter
24,0
Geschlecht
M
Eingang
15.06.2022
Impfdatum
14.06.2022
Beginn
14.06.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Wrong product administered

Symptomtext

Provider had ordered Varicella, as well as a MMR vaccination. Patient was injected with a MMRV vaccination, already containing the Varicella vaccination, as well as a regular Varicella immunization. This was in error, as the incorrect MMR/MMRV was drawn up, resulting in the patient receiving a double dose of Varicella. Due to patient's age, provider stated that the possible side effects are flue like symptoms, and rash.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong product administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Latex
Vorherige Impfungen
-