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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 Intentional dose omission? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Intentional dose omission have been filed in association with DUTASTERIDE (Dutasteride). This represents 0.2% of all adverse event reports for DUTASTERIDE.

6
Reports of Intentional dose omission with DUTASTERIDE
0.2%
of all DUTASTERIDE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Intentional dose omission From DUTASTERIDE?

Of the 6 reports.

Is Intentional dose omission Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DUTASTERIDE. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does DUTASTERIDE Cause?

Dyspnoea (502) Asthma (329) Wheezing (329) Malaise (311) Condition aggravated (300) Sleep disorder due to a general medical condition (290) Dizziness (288) Fall (280) Insomnia (276) Fatigue (273)

What Other Drugs Cause Intentional dose omission?

DUPILUMAB (2,269) CERTOLIZUMAB PEGOL (1,253) ADALIMUMAB (845) TOFACITINIB (845) INFLIXIMAB (815) ABALOPARATIDE (623) ETANERCEPT (615) AMBRISENTAN (595) SODIUM OXYBATE (580) CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)

Which DUTASTERIDE Alternatives Have Lower Intentional dose omission Risk?

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

Related Pages

DUTASTERIDE Full Profile All Intentional dose omission Reports All Drugs Causing Intentional dose omission DUTASTERIDE Demographics