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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 Device power source issue? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Device power source issue have been filed in association with ILOPROST (AURLUMYN). This represents 0.1% of all adverse event reports for ILOPROST.

5
Reports of Device power source issue with ILOPROST
0.1%
of all ILOPROST reports
0
Deaths
4
Hospitalizations

How Dangerous Is Device power source issue From ILOPROST?

Of the 5 reports, 4 (80.0%) required hospitalization.

Is Device power source issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ILOPROST. However, 5 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 Device power source issue?

SOMATROPIN (1,219) PEGFILGRASTIM (486) TREPROSTINIL (299) CARBIDOPA\LEVODOPA (62) ETANERCEPT (54) BACLOFEN (50) GLYCOPYRROLATE (39) DEVICE (20) FOSCARBIDOPA\FOSLEVODOPA (14) INTERFERON BETA-1B (13)

Which ILOPROST Alternatives Have Lower Device power source issue Risk?

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

Related Pages

ILOPROST Full Profile All Device power source issue Reports All Drugs Causing Device power source issue ILOPROST Demographics