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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DUTASTERIDE Cause Condition aggravated? 300 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 300 reports of Condition aggravated have been filed in association with DUTASTERIDE (Dutasteride). This represents 7.6% of all adverse event reports for DUTASTERIDE.

300
Reports of Condition aggravated with DUTASTERIDE
7.6%
of all DUTASTERIDE reports
46
Deaths
251
Hospitalizations

How Dangerous Is Condition aggravated From DUTASTERIDE?

Of the 300 reports, 46 (15.3%) resulted in death, 251 (83.7%) required hospitalization, and 114 (38.0%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DUTASTERIDE. However, 300 reports have been filed with the FAERS database.

What Other Side Effects Does DUTASTERIDE Cause?

Dyspnoea (502) Asthma (329) Wheezing (329) Malaise (311) Sleep disorder due to a general medical condition (290) Dizziness (288) Fall (280) Insomnia (276) Fatigue (273) Cough (266)

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 DUTASTERIDE Alternatives Have Lower Condition aggravated Risk?

DUTASTERIDE vs DUTASTERIDE\TAMSULOSIN DUTASTERIDE vs DUVELISIB DUTASTERIDE vs DYDROGESTERONE DUTASTERIDE vs EBASTINE DUTASTERIDE vs ECALLANTIDE

Related Pages

DUTASTERIDE Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated DUTASTERIDE Demographics