Does ALPROSTADIL Cause Wrong technique in product usage process? 510 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 510 reports of Wrong technique in product usage process have been filed in association with ALPROSTADIL (Edex). This represents 18.2% of all adverse event reports for ALPROSTADIL.
510
Reports of Wrong technique in product usage process with ALPROSTADIL
18.2%
of all ALPROSTADIL reports
0
Deaths
5
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ALPROSTADIL?
Of the 510 reports, 5 (1.0%) 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 ALPROSTADIL. However, 510 reports have been filed with the FAERS database.
What Other Side Effects Does ALPROSTADIL Cause?
Drug ineffective (1,412)
Product quality issue (227)
Penile pain (164)
Off label use (112)
Penile burning sensation (92)
Erection increased (75)
Penile haemorrhage (62)
No adverse event (60)
Injection site pain (57)
Expired product administered (52)
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 ALPROSTADIL Alternatives Have Lower Wrong technique in product usage process Risk?
ALPROSTADIL vs ALTEPLASE
ALPROSTADIL vs ALTERNARIA ALTERNATA
ALPROSTADIL vs ALTHIAZIDE
ALPROSTADIL vs ALTHIAZIDE\SPIRONOLACTONE
ALPROSTADIL vs ALUMINUM