Does ILOPROST Cause Incorrect dose administered by device? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Incorrect dose administered by device have been filed in association with ILOPROST (AURLUMYN). This represents 0.3% of all adverse event reports for ILOPROST.
14
Reports of Incorrect dose administered by device with ILOPROST
0.3%
of all ILOPROST reports
3
Deaths
9
Hospitalizations
How Dangerous Is Incorrect dose administered by device From ILOPROST?
Of the 14 reports, 3 (21.4%) resulted in death, 9 (64.3%) required hospitalization.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ILOPROST. However, 14 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 Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which ILOPROST Alternatives Have Lower Incorrect dose administered by device Risk?
ILOPROST vs IMATINIB
ILOPROST vs IMBRUVICA
ILOPROST vs IMDEVIMAB
ILOPROST vs IMEGLIMIN
ILOPROST vs IMETELSTAT