Does ILOPROST Cause Investigation? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Investigation have been filed in association with ILOPROST (AURLUMYN). This represents 0.2% of all adverse event reports for ILOPROST.
9
Reports of Investigation with ILOPROST
0.2%
of all ILOPROST reports
3
Deaths
9
Hospitalizations
How Dangerous Is Investigation From ILOPROST?
Of the 9 reports, 3 (33.3%) resulted in death, 9 (100.0%) required hospitalization.
Is Investigation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ILOPROST. However, 9 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 Investigation?
ARANESP (403)
NEULASTA (371)
XGEVA (115)
FLUTICASONE\SALMETEROL (96)
DARBEPOETIN ALFA (86)
ADVAIR (77)
DENOSUMAB (65)
ADVAIR HFA (51)
ALBUTEROL (51)
VENTOLIN (47)
Which ILOPROST Alternatives Have Lower Investigation Risk?
ILOPROST vs IMATINIB
ILOPROST vs IMBRUVICA
ILOPROST vs IMDEVIMAB
ILOPROST vs IMEGLIMIN
ILOPROST vs IMETELSTAT