Does TENOFOVIR ALAFENAMIDE Cause Product storage error? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Product storage error have been filed in association with TENOFOVIR ALAFENAMIDE (VEMLIDY). This represents 1.3% of all adverse event reports for TENOFOVIR ALAFENAMIDE.
39
Reports of Product storage error with TENOFOVIR ALAFENAMIDE
1.3%
of all TENOFOVIR ALAFENAMIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product storage error From TENOFOVIR ALAFENAMIDE?
Of the 39 reports, 2 (5.1%) 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 TENOFOVIR ALAFENAMIDE. However, 39 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)
Product use issue (67)
Nausea (64)
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 TENOFOVIR ALAFENAMIDE Alternatives Have Lower Product storage error Risk?
TENOFOVIR ALAFENAMIDE vs TENOFOVIR DISOPROXIL
TENOFOVIR ALAFENAMIDE vs TEPLIZUMAB-MZWV
TENOFOVIR ALAFENAMIDE vs TEPOTINIB
TENOFOVIR ALAFENAMIDE vs TEPROTUMUMAB
TENOFOVIR ALAFENAMIDE vs TEPROTUMUMAB-TRBW