Does RILPIVIRINE Cause Condition aggravated? 131 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 131 reports of Condition aggravated have been filed in association with RILPIVIRINE (EDURANT). This represents 1.9% of all adverse event reports for RILPIVIRINE.
131
Reports of Condition aggravated with RILPIVIRINE
1.9%
of all RILPIVIRINE reports
3
Deaths
19
Hospitalizations
How Dangerous Is Condition aggravated From RILPIVIRINE?
Of the 131 reports, 3 (2.3%) resulted in death, 19 (14.5%) required hospitalization, and 1 (0.8%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RILPIVIRINE. However, 131 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which RILPIVIRINE Alternatives Have Lower Condition aggravated Risk?
RILPIVIRINE vs RILUZOLE
RILPIVIRINE vs RIMABOTULINUMTOXINB
RILPIVIRINE vs RIMEGEPANT
RILPIVIRINE vs RIOCIGUAT
RILPIVIRINE vs RIPRETINIB