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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does HEPATITIS A VIRUS STRAIN 326F ANTIGEN Cause Product storage error? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product storage error have been filed in association with HEPATITIS A VIRUS STRAIN 326F ANTIGEN (VAQTA). This represents 26.1% of all adverse event reports for HEPATITIS A VIRUS STRAIN 326F ANTIGEN.

12
Reports of Product storage error with HEPATITIS A VIRUS STRAIN 326F ANTIGEN
26.1%
of all HEPATITIS A VIRUS STRAIN 326F ANTIGEN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product storage error From HEPATITIS A VIRUS STRAIN 326F ANTIGEN?

Of the 12 reports.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for HEPATITIS A VIRUS STRAIN 326F ANTIGEN. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does HEPATITIS A VIRUS STRAIN 326F ANTIGEN Cause?

No adverse event (23) Asthenia (10) Loss of personal independence in daily activities (8) Diarrhoea (7) Paraesthesia (7) Abdominal discomfort (6) Acute sinusitis (6) Cardiovascular disorder (6) Cognitive disorder (6) Coordination abnormal (6)

What Other Drugs Cause Product storage error?

INSULIN GLARGINE (7,743) EVOLOCUMAB (6,606) ETANERCEPT (3,653) DENOSUMAB (3,621) ERENUMAB-AOOE (2,958) DUPILUMAB (2,631) ALBUTEROL (2,474) ABATACEPT (2,101) DARBEPOETIN ALFA (1,619) INSULIN LISPRO (1,448)

Related Pages

HEPATITIS A VIRUS STRAIN 326F ANTIGEN Full Profile All Product storage error Reports All Drugs Causing Product storage error HEPATITIS A VIRUS STRAIN 326F ANTIGEN Demographics