Does FINASTERIDE Cause Wrong technique in product usage process? 182 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 182 reports of Wrong technique in product usage process have been filed in association with FINASTERIDE (Finasteride). This represents 1.2% of all adverse event reports for FINASTERIDE.
182
Reports of Wrong technique in product usage process with FINASTERIDE
1.2%
of all FINASTERIDE reports
0
Deaths
38
Hospitalizations
How Dangerous Is Wrong technique in product usage process From FINASTERIDE?
Of the 182 reports, 38 (20.9%) required hospitalization, and 2 (1.1%) were considered life-threatening.
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 FINASTERIDE. However, 182 reports have been filed with the FAERS database.
What Other Side Effects Does FINASTERIDE Cause?
Erectile dysfunction (3,043)
Depression (2,530)
Anxiety (1,921)
Adverse drug reaction (1,902)
Sexual dysfunction (1,757)
Adverse event (1,399)
Loss of libido (1,353)
Suicidal ideation (1,301)
Insomnia (1,202)
Fatigue (1,184)
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 FINASTERIDE Alternatives Have Lower Wrong technique in product usage process Risk?
FINASTERIDE vs FINASTERIDE\TAMSULOSIN
FINASTERIDE vs FINERENONE
FINASTERIDE vs FINGOLIMOD
FINASTERIDE vs FINGOLIMOD LAURYL
FINASTERIDE vs FISH OIL