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Published on: January 17, 2011
Profuse oral secretions after propafenone administration in neonates
Fiammetta Piersigilli1, Cinzia Auriti, Massimo Stefano Silvetti
1Department of Neonatology, Bambino Gesù Children's Hospital, Rome, Italy. piersigilli@opbg.net
Insights
Oral propafenone can cause severe respiratory distress and excessive secretions in newborns, a previously unreported adverse effect. This finding necessitates careful monitoring and potential discontinuation of the drug in infants.
Area of Science:
- Neonatal pharmacology
- Pediatric cardiology
- Adverse drug reactions
Background:
- Propafenone is an antiarrhythmic medication commonly used for supraventricular tachycardias.
- Known adverse effects include proarrhythmic and systemic complications.
- The safety profile in neonates requires further investigation.
Observation:
- Three newborns experienced significant adverse events after receiving oral propafenone.
- The neonates presented with profuse oral secretions.
- Respiratory distress was observed, requiring medical intervention.
Findings:
- A novel adverse effect of oral propafenone in neonates is reported.
- The adverse events included excessive salivation and breathing difficulties.
- These reactions were severe enough to warrant stopping propafenone treatment.
Implications:
- This highlights a previously unrecognized risk associated with oral propafenone in the neonatal population.
- Clinicians should be vigilant for these specific adverse effects in infants treated with propafenone.
- Further research into neonatal propafenone dosing and adverse event profiles is warranted.
Abstract:
Propafenone, an antiarrhythmic drug that is effective for treating supraventricular tachycardias, can induce well-known proarrhythmic and systemic adverse effects. We describe a previously unreported adverse effect in 3 newborns: oral propafenone-induced profuse oral secretions and respiratory distress of sufficient severity to necessitate discontinuation of propafenone.
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