Does PORACTANT ALFA Cause Product complaint? 31 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 31 reports of Product complaint have been filed in association with PORACTANT ALFA (Curosurf). This represents 5.5% of all adverse event reports for PORACTANT ALFA.
31
Reports of Product complaint with PORACTANT ALFA
5.5%
of all PORACTANT ALFA reports
5
Deaths
9
Hospitalizations
How Dangerous Is Product complaint From PORACTANT ALFA?
Of the 31 reports, 5 (16.1%) resulted in death, 9 (29.0%) required hospitalization, and 2 (6.5%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PORACTANT ALFA. However, 31 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)
Infantile apnoea (30)
Pulmonary haemorrhage neonatal (27)
Product administration error (26)
What Other Drugs Cause Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which PORACTANT ALFA Alternatives Have Lower Product complaint Risk?
PORACTANT ALFA vs PORFIMER
PORACTANT ALFA vs POSACONAZOLE
PORACTANT ALFA vs POTASSIUM
PORACTANT ALFA vs POTASSIUM, DIBASIC
PORACTANT ALFA vs POTASSIUM IODIDE