The most commonly reported side effects of lucinactant include medical device complication, pneumothorax, and economic problem, based on 19 FDA adverse event reports from 2010 to 2025.
Percentages show how often each reaction appears relative to total reports for lucinactant.
These are voluntary reports and do not establish that lucinactant caused these reactions.
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Other drugs that appear in adverse event reports alongside lucinactant. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
36.8% of lucinactant adverse event reports involve female patients and 52.6% involve male patients. The largest age group is neonate at 62%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking lucinactant when the adverse event was reported.
Lucinactant is sold under the brand name Surfaxin.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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