Does PORACTANT ALFA Cause Product quality issue? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product quality issue have been filed in association with PORACTANT ALFA (Curosurf). This represents 3.6% of all adverse event reports for PORACTANT ALFA.
20
Reports of Product quality issue with PORACTANT ALFA
3.6%
of all PORACTANT ALFA reports
4
Deaths
0
Hospitalizations
How Dangerous Is Product quality issue From PORACTANT ALFA?
Of the 20 reports, 4 (20.0%) resulted in death, and 2 (10.0%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PORACTANT ALFA. However, 20 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which PORACTANT ALFA Alternatives Have Lower Product quality issue Risk?
PORACTANT ALFA vs PORFIMER
PORACTANT ALFA vs POSACONAZOLE
PORACTANT ALFA vs POTASSIUM
PORACTANT ALFA vs POTASSIUM, DIBASIC
PORACTANT ALFA vs POTASSIUM IODIDE