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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\TAMSULOSIN Cause Product quality issue? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product quality issue have been filed in association with DUTASTERIDE\TAMSULOSIN. This represents 1.5% of all adverse event reports for DUTASTERIDE\TAMSULOSIN.

16
Reports of Product quality issue with DUTASTERIDE\TAMSULOSIN
1.5%
of all DUTASTERIDE\TAMSULOSIN reports
0
Deaths
2
Hospitalizations

How Dangerous Is Product quality issue From DUTASTERIDE\TAMSULOSIN?

Of the 16 reports, 2 (12.5%) required hospitalization, and 1 (6.3%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DUTASTERIDE\TAMSULOSIN. However, 16 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 quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which DUTASTERIDE\TAMSULOSIN Alternatives Have Lower Product quality issue Risk?

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

Related Pages

DUTASTERIDE\TAMSULOSIN Full Profile All Product quality issue Reports All Drugs Causing Product quality issue DUTASTERIDE\TAMSULOSIN Demographics