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Practical dosing of praziquantel for schistosomiasis in preschool-aged children
Piero L Olliaro1, Michel Vaillant2, Daniel J Hayes3
1UNICEF/UNDP/World Bank/WHO Special Programme for Research & Training in Tropical Diseases (TDR), Geneva, Switzerland.
Insights
Accurate praziquantel dosing for children with schistosomiasis is possible using current 600-mg tablets. Splitting tablets into quarters or halves allows for precise 40-60 mg/kg dosages in young children.
Area of Science:
- Tropical Medicine
- Infectious Diseases
- Pediatric Pharmacology
Background:
- Schistosomiasis affects preschool-aged children, posing unique dosing challenges for praziquantel.
- Current praziquantel formulations require adaptation for accurate pediatric dosing.
- Available 600-mg tablets can be split into 150-mg or 300-mg increments.
Purpose of the Study:
- To determine accurate praziquantel dosing schemes for children aged 3-72 months.
- To evaluate the feasibility of using existing praziquantel tablet formulations for pediatric schistosomiasis treatment.
- To establish weight-based dosing guidelines for young children using scored praziquantel tablets.
Main Methods:
- Examined dosing schemes for children aged 3-72 months (4-25 kg).
- Utilized weight-for-age growth references from sub-Saharan Africa and Brazil (n=106,230).
- Calculated accurate dosing within the target range of 40-60 mg/kg.
Main Results:
- Tablets divisible into four 150-mg quarters achieve adequate dosing for children ≥5 kg.
- Tablets divisible into two 300-mg halves are suitable for children ≥10 kg.
- Specific dosing regimens (e.g., ½ tablet for 5-7 kg, ¾ tablet for 8-10 kg) ensure 100% of subjects receive correct dosage.
Conclusions:
- Formulations divisible into four parts are preferred for children <11 kg.
- From 11 kg body weight, 600-mg praziquantel tablets divisible into quarters or halves can be used.
- These methods enable accurate praziquantel administration for pediatric schistosomiasis treatment.
Objective:
Schistosomiasis is known to occur in preschool-aged children, but achieving accurate dosing of praziquantel in its current form is challenging. While waiting for a paediatric formulation, there is a need to develop a means for using the available products to treat this age group. Current 600-mg tablets are differently scored to give units of 150 mg (a quarter of a tablet) or 300 mg (half a tablet).
Methods:
We examined several dosing schemes to dose accurately (40-60 mg/kg) children aged 3-72 months (weight range 4-25 kg, based on available weight-for-age growth references from sub-Saharan Africa and Brazil, n = 106,230).
Results:
Adequate dosing can be achieved with formulations that can be split into four 150 mg quarters for children weighing 5 kg or more, and with tablets than can be split into two 300 mg halves for children weighing 10 kg or more. Giving ½ tablet for 5-7 kg; ¾ tablet for 8-10 kg; 1 tablet for 11-15 kg; 1 ½ tablet for 16-21 kg; and two tablets for 22-25 kg will have 100% of subjects correctly dosed within the target 40-60 mg/kg range.
Conclusions:
Formulations that can be divided into four parts (to give 150 mg increments) are preferred for children weighing less than 11 kg; the same dosing can be applied with 600 mf praziquantel formulations that can be divided into four quarters or two halves from 11 kg body weight.
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