Does TENOFOVIR ALAFENAMIDE Cause Product use issue? 67 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Product use issue have been filed in association with TENOFOVIR ALAFENAMIDE (VEMLIDY). This represents 2.2% of all adverse event reports for TENOFOVIR ALAFENAMIDE.
67
Reports of Product use issue with TENOFOVIR ALAFENAMIDE
2.2%
of all TENOFOVIR ALAFENAMIDE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product use issue From TENOFOVIR ALAFENAMIDE?
Of the 67 reports, 6 (9.0%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TENOFOVIR ALAFENAMIDE. However, 67 reports have been filed with the FAERS database.
What Other Side Effects Does TENOFOVIR ALAFENAMIDE Cause?
Death (217)
Product dose omission issue (153)
Off label use (96)
Drug ineffective (93)
Fatigue (92)
Headache (71)
Product dose omission (69)
Intentional dose omission (67)
Nausea (64)
Diarrhoea (60)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which TENOFOVIR ALAFENAMIDE Alternatives Have Lower Product use issue Risk?
TENOFOVIR ALAFENAMIDE vs TENOFOVIR DISOPROXIL
TENOFOVIR ALAFENAMIDE vs TEPLIZUMAB-MZWV
TENOFOVIR ALAFENAMIDE vs TEPOTINIB
TENOFOVIR ALAFENAMIDE vs TEPROTUMUMAB
TENOFOVIR ALAFENAMIDE vs TEPROTUMUMAB-TRBW