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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 ILOPROST Cause Product use issue? 157 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 157 reports of Product use issue have been filed in association with ILOPROST (AURLUMYN). This represents 3.2% of all adverse event reports for ILOPROST.

157
Reports of Product use issue with ILOPROST
3.2%
of all ILOPROST reports
68
Deaths
81
Hospitalizations

How Dangerous Is Product use issue From ILOPROST?

Of the 157 reports, 68 (43.3%) resulted in death, 81 (51.6%) required hospitalization, and 2 (1.3%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ILOPROST. However, 157 reports have been filed with the FAERS database.

What Other Side Effects Does ILOPROST Cause?

Death (1,369) Dyspnoea (662) Headache (353) Cough (284) Pulmonary arterial hypertension (284) Hospitalisation (281) Fatigue (280) Dizziness (225) Pneumonia (224) Pulmonary hypertension (216)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which ILOPROST Alternatives Have Lower Product use issue Risk?

ILOPROST vs IMATINIB ILOPROST vs IMBRUVICA ILOPROST vs IMDEVIMAB ILOPROST vs IMEGLIMIN ILOPROST vs IMETELSTAT

Related Pages

ILOPROST Full Profile All Product use issue Reports All Drugs Causing Product use issue ILOPROST Demographics