Does OSILODROSTAT Cause Product administration interrupted? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product administration interrupted have been filed in association with OSILODROSTAT (Isturisa). This represents 0.8% of all adverse event reports for OSILODROSTAT.
13
Reports of Product administration interrupted with OSILODROSTAT
0.8%
of all OSILODROSTAT reports
0
Deaths
7
Hospitalizations
How Dangerous Is Product administration interrupted From OSILODROSTAT?
Of the 13 reports, 7 (53.8%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OSILODROSTAT. However, 13 reports have been filed with the FAERS database.
What Other Side Effects Does OSILODROSTAT Cause?
Off label use (272)
Fatigue (249)
Nausea (204)
Headache (111)
Adrenal insufficiency (97)
Death (97)
Asthenia (92)
Dizziness (91)
Decreased appetite (90)
Diarrhoea (90)
What Other Drugs Cause Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which OSILODROSTAT Alternatives Have Lower Product administration interrupted Risk?
OSILODROSTAT vs OSIMERTINIB
OSILODROSTAT vs OSPEMIFENE
OSILODROSTAT vs OSPHENA
OSILODROSTAT vs OVINE DIGOXIN IMMUNE FAB
OSILODROSTAT vs OXACILLIN