Does BEXAROTENE Cause Hypertriglyceridaemia? 44 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 44 reports of Hypertriglyceridaemia have been filed in association with BEXAROTENE (Bexarotene). This represents 5.8% of all adverse event reports for BEXAROTENE.
44
Reports of Hypertriglyceridaemia with BEXAROTENE
5.8%
of all BEXAROTENE reports
14
Deaths
15
Hospitalizations
How Dangerous Is Hypertriglyceridaemia From BEXAROTENE?
Of the 44 reports, 14 (31.8%) resulted in death, 15 (34.1%) required hospitalization, and 5 (11.4%) 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 BEXAROTENE. However, 44 reports have been filed with the FAERS database.
What Other Side Effects Does BEXAROTENE Cause?
Drug ineffective (67)
Hypothyroidism (65)
Death (53)
Off label use (32)
Disease progression (28)
Blood cholesterol increased (27)
Malignant neoplasm progression (26)
Pruritus (24)
Nausea (22)
Blood triglycerides increased (20)
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 BEXAROTENE Alternatives Have Lower Hypertriglyceridaemia Risk?
BEXAROTENE vs BEZAFIBRATE
BEXAROTENE vs BEZLOTOXUMAB
BEXAROTENE vs BGB-11417
BEXAROTENE vs BICALUTAMIDE
BEXAROTENE vs BICTEGRAVIR