Does BEXAROTENE Cause Multiple organ dysfunction syndrome? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Multiple organ dysfunction syndrome have been filed in association with BEXAROTENE (Bexarotene). This represents 1.5% of all adverse event reports for BEXAROTENE.
11
Reports of Multiple organ dysfunction syndrome with BEXAROTENE
1.5%
of all BEXAROTENE reports
11
Deaths
11
Hospitalizations
How Dangerous Is Multiple organ dysfunction syndrome From BEXAROTENE?
Of the 11 reports, 11 (100.0%) resulted in death, 11 (100.0%) required hospitalization, and 8 (72.7%) were considered life-threatening.
Is Multiple organ dysfunction syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BEXAROTENE. However, 11 reports have been filed with the FAERS database.
What Other Side Effects Does BEXAROTENE Cause?
Drug ineffective (67)
Hypothyroidism (65)
Death (53)
Hypertriglyceridaemia (44)
Off label use (32)
Disease progression (28)
Blood cholesterol increased (27)
Malignant neoplasm progression (26)
Pruritus (24)
Nausea (22)
What Other Drugs Cause Multiple organ dysfunction syndrome?
TACROLIMUS (1,847)
CYCLOPHOSPHAMIDE (1,597)
MYCOPHENOLATE MOFETIL (1,566)
PREDNISONE (1,525)
DEXAMETHASONE (1,355)
METHOTREXATE (1,317)
METHYLPREDNISOLONE (1,278)
RITUXIMAB (1,188)
PREDNISOLONE (1,154)
CYCLOSPORINE (933)
Which BEXAROTENE Alternatives Have Lower Multiple organ dysfunction syndrome Risk?
BEXAROTENE vs BEZAFIBRATE
BEXAROTENE vs BEZLOTOXUMAB
BEXAROTENE vs BGB-11417
BEXAROTENE vs BICALUTAMIDE
BEXAROTENE vs BICTEGRAVIR