Does PORACTANT ALFA Cause Product use issue? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product use issue have been filed in association with PORACTANT ALFA (Curosurf). This represents 1.1% of all adverse event reports for PORACTANT ALFA.
6
Reports of Product use issue with PORACTANT ALFA
1.1%
of all PORACTANT ALFA reports
2
Deaths
2
Hospitalizations
How Dangerous Is Product use issue From PORACTANT ALFA?
Of the 6 reports, 2 (33.3%) resulted in death, 2 (33.3%) required hospitalization, and 3 (50.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PORACTANT ALFA. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does PORACTANT ALFA Cause?
Neonatal hypoxia (118)
Off label use (71)
Ill-defined disorder (48)
Bradycardia neonatal (45)
Pulmonary haemorrhage (38)
Drug ineffective (34)
Endotracheal intubation complication (32)
Product complaint (31)
Infantile apnoea (30)
Pulmonary haemorrhage neonatal (27)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which PORACTANT ALFA Alternatives Have Lower Product use issue Risk?
PORACTANT ALFA vs PORFIMER
PORACTANT ALFA vs POSACONAZOLE
PORACTANT ALFA vs POTASSIUM
PORACTANT ALFA vs POTASSIUM, DIBASIC
PORACTANT ALFA vs POTASSIUM IODIDE