Does EMTRICITABINE Cause Hypertriglyceridaemia? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Hypertriglyceridaemia have been filed in association with EMTRICITABINE (Truvada). This represents 0.3% of all adverse event reports for EMTRICITABINE.
12
Reports of Hypertriglyceridaemia with EMTRICITABINE
0.3%
of all EMTRICITABINE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Hypertriglyceridaemia From EMTRICITABINE?
Of the 12 reports, 11 (91.7%) required hospitalization, and 2 (16.7%) were considered life-threatening.
Is Hypertriglyceridaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EMTRICITABINE. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does EMTRICITABINE Cause?
Foetal exposure during pregnancy (609)
Drug resistance (370)
Virologic failure (331)
Immune reconstitution inflammatory syndrome (262)
Exposure during pregnancy (212)
Drug ineffective (196)
Pathogen resistance (166)
Viral mutation identified (161)
Maternal exposure during pregnancy (160)
Death (154)
What Other Drugs Cause Hypertriglyceridaemia?
PEGASPARGASE (399)
VINCRISTINE (373)
METHOTREXATE (372)
DEXAMETHASONE (358)
CYTARABINE (244)
CYCLOPHOSPHAMIDE (191)
QUETIAPINE (181)
MERCAPTOPURINE (176)
PREDNISONE (161)
DAUNORUBICIN (143)
Which EMTRICITABINE Alternatives Have Lower Hypertriglyceridaemia Risk?
EMTRICITABINE vs EMTRICITABINE\RILPIVIRINE\TENOFOVIR ALAFENAMIDE
EMTRICITABINE vs EMTRICITABINE\RILPIVIRINE\TENOFOVIR DISOPROXIL
EMTRICITABINE vs EMTRICITABINE\TENOFOVIR
EMTRICITABINE vs EMTRICITABINE\TENOFOVIR ALAFENAMIDE
EMTRICITABINE vs EMTRICITABINE/TENOFOVIR DISOPROXIL