Does ILOPROST Cause Wrong technique in product usage process? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Wrong technique in product usage process have been filed in association with ILOPROST (AURLUMYN). This represents 0.6% of all adverse event reports for ILOPROST.
30
Reports of Wrong technique in product usage process with ILOPROST
0.6%
of all ILOPROST reports
6
Deaths
18
Hospitalizations
How Dangerous Is Wrong technique in product usage process From ILOPROST?
Of the 30 reports, 6 (20.0%) resulted in death, 18 (60.0%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ILOPROST. However, 30 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 product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which ILOPROST Alternatives Have Lower Wrong technique in product usage process Risk?
ILOPROST vs IMATINIB
ILOPROST vs IMBRUVICA
ILOPROST vs IMDEVIMAB
ILOPROST vs IMEGLIMIN
ILOPROST vs IMETELSTAT