Does DAROLUTAMIDE Cause International normalised ratio increased? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of International normalised ratio increased have been filed in association with DAROLUTAMIDE (NUBEQA). This represents 0.2% of all adverse event reports for DAROLUTAMIDE.
6
Reports of International normalised ratio increased with DAROLUTAMIDE
0.2%
of all DAROLUTAMIDE reports
1
Deaths
2
Hospitalizations
How Dangerous Is International normalised ratio increased From DAROLUTAMIDE?
Of the 6 reports, 1 (16.7%) resulted in death, 2 (33.3%) required hospitalization, and 1 (16.7%) were considered life-threatening.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DAROLUTAMIDE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does DAROLUTAMIDE Cause?
Fatigue (384)
Death (361)
Hot flush (203)
Asthenia (173)
Prostatic specific antigen increased (156)
Off label use (133)
Neuropathy peripheral (127)
Diarrhoea (122)
Dizziness (122)
Rash (116)
What Other Drugs Cause International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which DAROLUTAMIDE Alternatives Have Lower International normalised ratio increased Risk?
DAROLUTAMIDE vs DARUNAVIR
DAROLUTAMIDE vs DARUNAVIR ETHANOLATE
DAROLUTAMIDE vs DARUNAVIR\RITONAVIR
DAROLUTAMIDE vs DASABUVIR
DAROLUTAMIDE vs DASABUVIR\OMBITASVIR HEMINONAHYDRATE\PARITAPREVIR\RITONAVIR