Does ENTECAVIR Cause Product dose omission? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product dose omission have been filed in association with ENTECAVIR (Entecavir). This represents 0.4% of all adverse event reports for ENTECAVIR.
18
Reports of Product dose omission with ENTECAVIR
0.4%
of all ENTECAVIR reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission From ENTECAVIR?
Of the 18 reports, 3 (16.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ENTECAVIR. However, 18 reports have been filed with the FAERS database.
What Other Side Effects Does ENTECAVIR Cause?
Drug resistance (312)
Death (298)
Drug ineffective (207)
Hepatitis b (166)
Off label use (129)
Maternal exposure during pregnancy (126)
Viral mutation identified (121)
Renal impairment (118)
Pathogen resistance (115)
Fatigue (108)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ENTECAVIR Alternatives Have Lower Product dose omission Risk?
ENTECAVIR vs ENTINOSTAT
ENTECAVIR vs ENTRECTINIB
ENTECAVIR vs ENZALUTAMIDE
ENTECAVIR vs EPCORITAMAB
ENTECAVIR vs EPCORITAMAB-BYSP