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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 RILPIVIRINE Cause Product storage error? 174 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 174 reports of Product storage error have been filed in association with RILPIVIRINE (EDURANT). This represents 2.5% of all adverse event reports for RILPIVIRINE.

174
Reports of Product storage error with RILPIVIRINE
2.5%
of all RILPIVIRINE reports
0
Deaths
2
Hospitalizations

How Dangerous Is Product storage error From RILPIVIRINE?

Of the 174 reports, 2 (1.1%) required hospitalization.

Is Product storage error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RILPIVIRINE. However, 174 reports have been filed with the FAERS database.

What Other Side Effects Does RILPIVIRINE Cause?

Product dose omission issue (702) Injection site pain (640) Viral load increased (455) Virologic failure (404) Pathogen resistance (323) Pain (297) Off label use (274) Product use in unapproved therapeutic environment (234) Viral mutation identified (211) Blood hiv rna increased (205)

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)

Which RILPIVIRINE Alternatives Have Lower Product storage error Risk?

RILPIVIRINE vs RILUZOLE RILPIVIRINE vs RIMABOTULINUMTOXINB RILPIVIRINE vs RIMEGEPANT RILPIVIRINE vs RIOCIGUAT RILPIVIRINE vs RIPRETINIB

Related Pages

RILPIVIRINE Full Profile All Product storage error Reports All Drugs Causing Product storage error RILPIVIRINE Demographics