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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 Wrong technique in device usage process? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Wrong technique in device usage process have been filed in association with ILOPROST (AURLUMYN). This represents 0.2% of all adverse event reports for ILOPROST.

9
Reports of Wrong technique in device usage process with ILOPROST
0.2%
of all ILOPROST reports
2
Deaths
7
Hospitalizations

How Dangerous Is Wrong technique in device usage process From ILOPROST?

Of the 9 reports, 2 (22.2%) resulted in death, 7 (77.8%) required hospitalization.

Is Wrong technique in device usage process 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 Wrong technique in device usage process?

ALBUTEROL (5,380) SOMATROPIN (4,746) EXENATIDE (3,255) FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,673) FLUTICASONE\SALMETEROL (2,259) FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (2,197) INSULIN GLARGINE (1,749) UMECLIDINIUM\VILANTEROL TRIFENATATE (1,531) BUDESONIDE\FORMOTEROL (1,481) BELIMUMAB (1,347)

Which ILOPROST Alternatives Have Lower Wrong technique in device usage process Risk?

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

Related Pages

ILOPROST Full Profile All Wrong technique in device usage process Reports All Drugs Causing Wrong technique in device usage process ILOPROST Demographics