Tafenoquine, sold under the brand name Krintafel among others, is a medication used to prevent and to treat malaria.[4] With respect acute malaria it is used together with other medications to prevent relapse by Plasmodium vivax.[4] It may be used to prevent all types of malaria.[4] It is taken by mouth.[5]
Tafenoquine was approved for medical use in Australia and in the United States in 2018.[4][6] In the United States, as of 2019[update], a course of treatment costs about US$43.[7] Tafenoquine is related to primaquine.[8]
Tafenoquine may be used to prevent all types of malaria.[4] For this use 200 mg 3 days before travel then 200 mg per week until one week after travel is recommended.[8]
Tafenoquine is used for the treatment of the hypnozoite stages of Plasmodium vivax and Plasmodium ovale that are responsible for relapse of these malaria species even when the blood stages are successfully cleared. Primaquine for 14 days can also be used for this. The advantage of tafenoquine is that it has a long half-life (2–3 weeks) and therefore a single treatment is sufficient.[9] It is used with another medication, such as chloroquine, that kills the malaria in the blood.[10]
For prevention of malaria, it is taken as 200 mg per day for three days before being potentially exposed, than it is taken as 200 mg once per week including for 1 week after leaving the area with malaria.[11]
It is also used at a dose of 300 mg together with other antimalarials to treat P. vivax.[12][8]
Tafenoquine was approved for medical use in Australia and in the United States in 2018.[4][6] Tafenoquine was given an orphan drug designation and was granted breakthrough therapy status in 2013 in the United States.[13][14]
↑Elmes NJ, Nasveld PE, Kitchener SJ, Kocisko DA, Edstein MD (November 2008). "The efficacy and tolerability of three different regimens of tafenoquine versus primaquine for post-exposure prophylaxis of Plasmodium vivax malaria in the Southwest Pacific". Transactions of the Royal Society of Tropical Medicine and Hygiene. 102 (11): 1095–101. doi:10.1016/j.trstmh.2008.04.024. PMID18541280.