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Updated: May 29, 2026

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
[Neonatal intoxication with pyrimethamine: risk due to the absence of pediatric formulation?]
M Genuini1, C Freihuber, I Girard
1Service de néonatologie, hôpital Armand-Trousseau, faculté de médecine, AP-HP, université Pierre-et-Marie-Curie, 26, avenue du Dr-Arnold-Netter, 75571 Paris cedex 12, France.
Insights
A newborn experienced seizures and cholestasis after a 100x pyrimethamine overdose for congenital toxoplasmosis. This case highlights the need for pediatric formulations and careful dosing of pyrimethamine in infants.
Area of Science:
- Pediatric Pharmacology
- Infectious Diseases
- Clinical Toxicology
Background:
- Congenital toxoplasmosis treatment relies on pyrimethamine and sulfonamides.
- Existing treatments lack pediatric-specific formulations, posing dosing challenges.
- Accurate dosing is critical, especially in neonates.
Observation:
- A newborn with asymptomatic congenital toxoplasmosis received a pyrimethamine dose 100 times the recommended amount.
- The infant developed partial seizures 48 hours post-overdose.
- Symptoms included appetite loss and vomiting, with spontaneous resolution within 5 days.
Findings:
- The overdose resulted in moderate, self-resolving cholestasis.
- Seizures were a key adverse event linked to the pyrimethamine toxicity.
- Clinical presentation and laboratory findings indicate a need for vigilant monitoring.
Implications:
- This case underscores the critical need for pediatric-friendly pyrimethamine formulations.
- It emphasizes the importance of precise prescription and administration protocols for neonates.
- Further research into safe dosing ranges and management of pyrimethamine toxicity in infants is warranted.
Abstract:
Curative treatment of congenital toxoplasmosis is based on the association of pyrimethamine and sulfonamide. There is currently no pediatric galenic formulation. We report the case of a newborn child affected by asymptomatic congenital toxoplasmosis who received an overdose of pyrimethamine. The patient received a dose of pyrimethamine 4 times, equal to 100 times the recommended dose, due to an error in the prescription. He had partial seizures 48 h after the last medicinal absorption. We noted a lack of appetite and vomiting, with a favorable progression in 5 days. Blood analysis showed isolated, spontaneously regressive moderate cholestasis. We propose a pharmacological clarification on the treatment of congenital toxoplasmosis.
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