Does ALPROSTADIL Cause Product quality issue? 227 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 227 reports of Product quality issue have been filed in association with ALPROSTADIL (Edex). This represents 8.1% of all adverse event reports for ALPROSTADIL.
227
Reports of Product quality issue with ALPROSTADIL
8.1%
of all ALPROSTADIL reports
0
Deaths
10
Hospitalizations
How Dangerous Is Product quality issue From ALPROSTADIL?
Of the 227 reports, 10 (4.4%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALPROSTADIL. However, 227 reports have been filed with the FAERS database.
What Other Side Effects Does ALPROSTADIL Cause?
Drug ineffective (1,412)
Wrong technique in product usage process (510)
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 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 ALPROSTADIL Alternatives Have Lower Product quality issue Risk?
ALPROSTADIL vs ALTEPLASE
ALPROSTADIL vs ALTERNARIA ALTERNATA
ALPROSTADIL vs ALTHIAZIDE
ALPROSTADIL vs ALTHIAZIDE\SPIRONOLACTONE
ALPROSTADIL vs ALUMINUM