Does PORACTANT ALFA Cause Condition aggravated? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Condition aggravated have been filed in association with PORACTANT ALFA (Curosurf). This represents 1.8% of all adverse event reports for PORACTANT ALFA.
10
Reports of Condition aggravated with PORACTANT ALFA
1.8%
of all PORACTANT ALFA reports
4
Deaths
2
Hospitalizations
How Dangerous Is Condition aggravated From PORACTANT ALFA?
Of the 10 reports, 4 (40.0%) resulted in death, 2 (20.0%) required hospitalization, and 6 (60.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PORACTANT ALFA. However, 10 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which PORACTANT ALFA Alternatives Have Lower Condition aggravated Risk?
PORACTANT ALFA vs PORFIMER
PORACTANT ALFA vs POSACONAZOLE
PORACTANT ALFA vs POTASSIUM
PORACTANT ALFA vs POTASSIUM, DIBASIC
PORACTANT ALFA vs POTASSIUM IODIDE