Does DUTASTERIDE Cause Product complaint? 35 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 35 reports of Product complaint have been filed in association with DUTASTERIDE (Dutasteride). This represents 0.9% of all adverse event reports for DUTASTERIDE.
35
Reports of Product complaint with DUTASTERIDE
0.9%
of all DUTASTERIDE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product complaint From DUTASTERIDE?
Of the 35 reports, 1 (2.9%) required hospitalization.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUTASTERIDE. However, 35 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 Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which DUTASTERIDE Alternatives Have Lower Product complaint Risk?
DUTASTERIDE vs DUTASTERIDE\TAMSULOSIN
DUTASTERIDE vs DUVELISIB
DUTASTERIDE vs DYDROGESTERONE
DUTASTERIDE vs EBASTINE
DUTASTERIDE vs ECALLANTIDE