Does DUTASTERIDE Cause Wrong technique in product usage process? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Wrong technique in product usage process have been filed in association with DUTASTERIDE (Dutasteride). This represents 1.4% of all adverse event reports for DUTASTERIDE.
55
Reports of Wrong technique in product usage process with DUTASTERIDE
1.4%
of all DUTASTERIDE reports
0
Deaths
13
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DUTASTERIDE?
Of the 55 reports, 13 (23.6%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DUTASTERIDE. However, 55 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DUTASTERIDE Alternatives Have Lower Wrong technique in product usage process Risk?
DUTASTERIDE vs DUTASTERIDE\TAMSULOSIN
DUTASTERIDE vs DUVELISIB
DUTASTERIDE vs DYDROGESTERONE
DUTASTERIDE vs EBASTINE
DUTASTERIDE vs ECALLANTIDE