Does DUTASTERIDE\TAMSULOSIN Cause Product complaint? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product complaint have been filed in association with DUTASTERIDE\TAMSULOSIN. This represents 1.3% of all adverse event reports for DUTASTERIDE\TAMSULOSIN.
14
Reports of Product complaint with DUTASTERIDE\TAMSULOSIN
1.3%
of all DUTASTERIDE\TAMSULOSIN reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product complaint From DUTASTERIDE\TAMSULOSIN?
Of the 14 reports, 1 (7.1%) resulted in death, 1 (7.1%) 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\TAMSULOSIN. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does DUTASTERIDE\TAMSULOSIN Cause?
Dizziness (101)
Hypotension (82)
Urinary retention (80)
Drug ineffective (67)
Death (61)
Fall (47)
Gait disturbance (43)
Cerebral hypoperfusion (41)
Atrial fibrillation (39)
Prostate cancer (38)
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\TAMSULOSIN Alternatives Have Lower Product complaint Risk?
DUTASTERIDE\TAMSULOSIN vs DUVELISIB
DUTASTERIDE\TAMSULOSIN vs DYDROGESTERONE
DUTASTERIDE\TAMSULOSIN vs EBASTINE
DUTASTERIDE\TAMSULOSIN vs ECALLANTIDE
DUTASTERIDE\TAMSULOSIN vs ECONAZOLE