Does RILPIVIRINE Cause Wrong technique in device usage process? 98 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 98 reports of Wrong technique in device usage process have been filed in association with RILPIVIRINE (EDURANT). This represents 1.4% of all adverse event reports for RILPIVIRINE.
98
Reports of Wrong technique in device usage process with RILPIVIRINE
1.4%
of all RILPIVIRINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in device usage process From RILPIVIRINE?
Of the 98 reports, 1 (1.0%) required hospitalization.
Is Wrong technique in device usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RILPIVIRINE. However, 98 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 Wrong technique in device usage process?
ALBUTEROL (5,380)
SOMATROPIN (4,746)
EXENATIDE (3,255)
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673)
FLUTICASONE\SALMETEROL (2,259)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197)
INSULIN GLARGINE (1,749)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531)
BUDESONIDE\FORMOTEROL (1,481)
BELIMUMAB (1,347)
Which RILPIVIRINE Alternatives Have Lower Wrong technique in device usage process Risk?
RILPIVIRINE vs RILUZOLE
RILPIVIRINE vs RIMABOTULINUMTOXINB
RILPIVIRINE vs RIMEGEPANT
RILPIVIRINE vs RIOCIGUAT
RILPIVIRINE vs RIPRETINIB