a-ß Arteether, a synthetic derivative of artemisinin.
A fast-acting blood schizonticide specifically indicated for the treatment of chloroquine-resistant P. falciparum malaria, including cerebral malaria.
Via intramuscular injection, specifically in the upper-external quadrant of the buttock.
The Central Drug Research Institute (C.D.R.I.) in Lucknow, India, and Themis Medicare Limited.
150 mg (1 ampoule) once daily for 3 consecutive days, or as directed by a physician.
3 mg/kg per day administered intramuscularly for 3 days, or as directed by a physician.
No.
Targets the erythrocytic stage of P. falciparum malaria. It concentrates in parasitized erythrocytes and inhibits parasite protein synthesis, alters ribosomal organization, and damages parasite membranes through lipid peroxidation.
Dihydroartemisinin, which has a half-life of more than 20 hours.
Neurotoxicity (gait disturbances, loss of spinal cord pain responses, incoordination, respiratory depression, convulsions, and cardio-respiratory arrest), nausea, dizziness, and depressed gastrointestinal activity.
Use with caution only if the potential benefits outweigh the potential risks to the fetus.
It is not known whether E MAL is excreted in human milk. Exercise caution when using E MAL while breastfeeding.
Does not interfere with the action of commonly used medications for the treatment of P. falciparum malaria, like quinine. Can be administered along with these drugs for severe malaria. Should not be administered with other artemisinin derivatives like Artesunate and Artemether.
Patients who are hypersensitive to artemisinin derivatives.
Below 30°C and protected from light.
High cure rate (nearly 100% in uncomplicated malaria and about 90% in complicated malaria). Most patients became afebrile within 36 hours and parasite-free within 72 hours. Recrudescence was less than 7%.
Lipophilic, leading to greater accumulation in brain tissue, making it suitable for the treatment of cerebral malaria. Exhibits gametocytocidal action, which helps to reduce the transmission of P. falciparum malaria. Well-tolerated and has a good compliance rate with minimal drug-related side effects.
Treatment of severe P. falciparum malaria, including cerebral malaria, and as a second-line treatment for chloroquine-resistant malaria. No cross-resistance with chloroquine has been detected.