Does RILPIVIRINE Cause Product administration error? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Product administration error have been filed in association with RILPIVIRINE (EDURANT). This represents 0.7% of all adverse event reports for RILPIVIRINE.
50
Reports of Product administration error with RILPIVIRINE
0.7%
of all RILPIVIRINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From RILPIVIRINE?
Of the 50 reports.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RILPIVIRINE. However, 50 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 administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which RILPIVIRINE Alternatives Have Lower Product administration error Risk?
RILPIVIRINE vs RILUZOLE
RILPIVIRINE vs RIMABOTULINUMTOXINB
RILPIVIRINE vs RIMEGEPANT
RILPIVIRINE vs RIOCIGUAT
RILPIVIRINE vs RIPRETINIB