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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ALPROSTADIL Cause Condition aggravated? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Condition aggravated have been filed in association with ALPROSTADIL (Edex). This represents 0.6% of all adverse event reports for ALPROSTADIL.

16
Reports of Condition aggravated with ALPROSTADIL
0.6%
of all ALPROSTADIL reports
0
Deaths
1
Hospitalizations

How Dangerous Is Condition aggravated From ALPROSTADIL?

Of the 16 reports, 1 (6.3%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALPROSTADIL. However, 16 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) 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)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which ALPROSTADIL Alternatives Have Lower Condition aggravated Risk?

ALPROSTADIL vs ALTEPLASE ALPROSTADIL vs ALTERNARIA ALTERNATA ALPROSTADIL vs ALTHIAZIDE ALPROSTADIL vs ALTHIAZIDE\SPIRONOLACTONE ALPROSTADIL vs ALUMINUM

Related Pages

ALPROSTADIL Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated ALPROSTADIL Demographics