Does ENTECAVIR Cause Intentional product use issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Intentional product use issue have been filed in association with ENTECAVIR (Entecavir). This represents 0.5% of all adverse event reports for ENTECAVIR.
21
Reports of Intentional product use issue with ENTECAVIR
0.5%
of all ENTECAVIR reports
0
Deaths
3
Hospitalizations
How Dangerous Is Intentional product use issue From ENTECAVIR?
Of the 21 reports, 3 (14.3%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ENTECAVIR. However, 21 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ENTECAVIR Alternatives Have Lower Intentional product use issue Risk?
ENTECAVIR vs ENTINOSTAT
ENTECAVIR vs ENTRECTINIB
ENTECAVIR vs ENZALUTAMIDE
ENTECAVIR vs EPCORITAMAB
ENTECAVIR vs EPCORITAMAB-BYSP