Does OSILODROSTAT Cause Condition aggravated? 27 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Condition aggravated have been filed in association with OSILODROSTAT (Isturisa). This represents 1.7% of all adverse event reports for OSILODROSTAT.
27
Reports of Condition aggravated with OSILODROSTAT
1.7%
of all OSILODROSTAT reports
4
Deaths
7
Hospitalizations
How Dangerous Is Condition aggravated From OSILODROSTAT?
Of the 27 reports, 4 (14.8%) resulted in death, 7 (25.9%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OSILODROSTAT. However, 27 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which OSILODROSTAT Alternatives Have Lower Condition aggravated Risk?
OSILODROSTAT vs OSIMERTINIB
OSILODROSTAT vs OSPEMIFENE
OSILODROSTAT vs OSPHENA
OSILODROSTAT vs OVINE DIGOXIN IMMUNE FAB
OSILODROSTAT vs OXACILLIN