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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 Condition aggravated? 177 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 177 reports of Condition aggravated have been filed in association with ILOPROST (AURLUMYN). This represents 3.6% of all adverse event reports for ILOPROST.

177
Reports of Condition aggravated with ILOPROST
3.6%
of all ILOPROST reports
75
Deaths
110
Hospitalizations

How Dangerous Is Condition aggravated From ILOPROST?

Of the 177 reports, 75 (42.4%) resulted in death, 110 (62.1%) required hospitalization, and 11 (6.2%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ILOPROST. However, 177 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 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 ILOPROST Alternatives Have Lower Condition aggravated Risk?

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

Related Pages

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