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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 Hepatic function abnormal? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Hepatic function abnormal have been filed in association with ALPROSTADIL (Edex). This represents 0.3% of all adverse event reports for ALPROSTADIL.

8
Reports of Hepatic function abnormal with ALPROSTADIL
0.3%
of all ALPROSTADIL reports
2
Deaths
4
Hospitalizations

How Dangerous Is Hepatic function abnormal From ALPROSTADIL?

Of the 8 reports, 2 (25.0%) resulted in death, 4 (50.0%) required hospitalization, and 1 (12.5%) were considered life-threatening.

Is Hepatic function abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALPROSTADIL. However, 8 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 Hepatic function abnormal?

NIVOLUMAB (1,131) PEMBROLIZUMAB (1,079) METHOTREXATE (1,054) CABOZANTINIB S-MALATE (912) CYCLOPHOSPHAMIDE (824) BEVACIZUMAB (769) PACLITAXEL (603) LENVATINIB (528) ATORVASTATIN (520) CYCLOSPORINE (508)

Which ALPROSTADIL Alternatives Have Lower Hepatic function abnormal Risk?

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

Related Pages

ALPROSTADIL Full Profile All Hepatic function abnormal Reports All Drugs Causing Hepatic function abnormal ALPROSTADIL Demographics