Does ILOPROST Cause Product dose omission? 40 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Product dose omission have been filed in association with ILOPROST (AURLUMYN). This represents 0.8% of all adverse event reports for ILOPROST.
40
Reports of Product dose omission with ILOPROST
0.8%
of all ILOPROST reports
8
Deaths
31
Hospitalizations
How Dangerous Is Product dose omission From ILOPROST?
Of the 40 reports, 8 (20.0%) resulted in death, 31 (77.5%) required hospitalization, and 1 (2.5%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ILOPROST. However, 40 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ILOPROST Alternatives Have Lower Product dose omission Risk?
ILOPROST vs IMATINIB
ILOPROST vs IMBRUVICA
ILOPROST vs IMDEVIMAB
ILOPROST vs IMEGLIMIN
ILOPROST vs IMETELSTAT