Classes
DEA Class; Rx
Common Brand Names; Biltricide
- Anthelmintics
Description
Oral anthelmintic agent (trematodicide)
Used for schistosomiasis, clonorchiasis, and opisthorchiasis; also effective for certain cestode (tapeworm) infections
Alternative to albendazole for cysticercosis, but associated with higher incidence of side effects
Indications
Indicated for treatment for schistosomiasis caused by all species of Schistosoma
Indicated for clonorchiasis and opisthorchiasis caused by liver flukes (Clonorchis sinensis, Opisthorchis viverrini)
For the treatment of neurocysticercosis.
Contraindications
Hypersensitivity
Intraocular cysticercosis
Concomitant use with strong CYP450 inducers
Adverse Effects
- Appetite loss
- Dizziness
- Drowsiness
- Headache
- Malaise
- CSF reaction syndrome in patients treated for neurocysticercosis
- Abdominal pain
- Nausea
- Vomiting
- Diaphoresis
- Diarrhea
- Fever
- Itching
- Rash
- Urticaria
Warnings
Clinical deterioration may occur when treating schistosomiasis (eg, paradoxical reactions, serum sickness Jarisch-Herxheimer like reactions [sudden inflammatory immune response suspected to be caused by the release of schistosomal antigens]); reactions predominantly occur in patients treated during the acute phase of schistosomiasis
Can exacerbate CNS pathology due to schistosomiasis, paragonimiasis, or Taenia solium cysticercosis; consider whether to treat with praziquantel in patients with epilepsy or other CNS diseases; hospitalize patient for duration of treatment if infection found to be associated with cerebral cysticercosis
Evidence suggests treatment with praziquantel in the acute phase of infection may not prevent progression from asymptomatic infection to acute schistosomiasis, or from asymptomatic infection/acute schistosomiasis into chronic phase; may lead to potentially life-threatening events, for example, respiratory failure, encephalopathy, papilledema, and/or cerebral vasculitis
Bradycardia, ectopic rhythms, ventricular fibrillation, and AV blocks observed; monitor patients with cardiac arrhythmias during treatment
Reduced hepatic metabolism of praziquantel results in higher and sustained plasma concentrations of unmetabolized drug in patients with liver impairment; monitor for adverse reactions when administering the recommended dose to patients with hepatosplenic schistosomiasis who have moderate or severe liver impairment (Child-Pugh Class B or C)
Pregnancy and Lactation
Published studies have not identified association with use during pregnancy and major birth defects, miscarriage or adverse maternal or fetal outcomes
Limited data from published literature reports presence of drug in human milk at low concentrations; there is no information on effects of drug in breastfed infant or effects on milk production
Maximum Dosage
75 mg/kg/day PO.
75 mg/kg/day PO.
75 mg/kg/day PO.
75 mg/kg/day PO.
Safety and efficacy have not been established.
Safety and efficacy have not been established.
How supplied
Praziquantel
tablet
- 600mg