Does DUTASTERIDE Cause Product preparation issue? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Product preparation issue have been filed in association with DUTASTERIDE (Dutasteride). This represents 0.5% of all adverse event reports for DUTASTERIDE.
18
Reports of Product preparation issue with DUTASTERIDE
0.5%
of all DUTASTERIDE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Product preparation issue From DUTASTERIDE?
Of the 18 reports, 1 (5.6%) resulted in death, 5 (27.8%) required hospitalization.
Is Product preparation issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUTASTERIDE. However, 18 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 preparation issue?
ONABOTULINUMTOXINA (677)
COAGULATION FACTOR IX HUMAN\COAGULATION FACTOR VII HUMAN\COAGULATION FACTOR X HUMAN\PROTEIN C\PROTEIN S HUMAN\PROTHROMBIN (252)
HUMAN C1-ESTERASE INHIBITOR (238)
SOMATROPIN (200)
INCOBOTULINUMTOXINA (174)
STIRIPENTOL (129)
TESAMORELIN (119)
ABATACEPT (115)
INFLIXIMAB (101)
ABOBOTULINUMTOXINA (91)
Which DUTASTERIDE Alternatives Have Lower Product preparation issue Risk?
DUTASTERIDE vs DUTASTERIDE\TAMSULOSIN
DUTASTERIDE vs DUVELISIB
DUTASTERIDE vs DYDROGESTERONE
DUTASTERIDE vs EBASTINE
DUTASTERIDE vs ECALLANTIDE