Does EFAVIRENZ Cause Intentional product use issue? 106 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 106 reports of Intentional product use issue have been filed in association with EFAVIRENZ (Efavirenz, Emtricitabine and Tenofovir Disoproxil Fumarate). This represents 1.3% of all adverse event reports for EFAVIRENZ.
106
Reports of Intentional product use issue with EFAVIRENZ
1.3%
of all EFAVIRENZ reports
72
Deaths
52
Hospitalizations
How Dangerous Is Intentional product use issue From EFAVIRENZ?
Of the 106 reports, 72 (67.9%) resulted in death, 52 (49.1%) required hospitalization, and 2 (1.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EFAVIRENZ. However, 106 reports have been filed with the FAERS database.
What Other Side Effects Does EFAVIRENZ Cause?
Virologic failure (916)
Foetal exposure during pregnancy (701)
Drug resistance (654)
Drug interaction (645)
Viral mutation identified (641)
Depression (602)
Pathogen resistance (567)
Maternal exposure during pregnancy (478)
Treatment failure (390)
Immune reconstitution inflammatory syndrome (301)
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 EFAVIRENZ Alternatives Have Lower Intentional product use issue Risk?
EFAVIRENZ vs EFAVIRENZ\EMTRICITABINE\TENOFOVIR DISOPROXIL
EFAVIRENZ vs EFAVIRENZ\LAMIVUDINE\TENOFOVIR DISOPROXIL
EFAVIRENZ vs EFFEXOR
EFAVIRENZ vs EFFIENT
EFAVIRENZ vs EFGARTIGIMOD ALFA