Clinical data | |
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Pronunciation | /ˌpɪrɪˈmɛθəmɪn/ |
Trade names | Daraprim, others |
AHFS/Drugs.com | Monograph |
MedlinePlus | a601050 |
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Routes of administration | By mouth |
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Pharmacokinetic data | |
Bioavailability | well-absorbed |
Protein binding | 87% |
Metabolism | Liver |
Elimination half-life | 96 hours |
Excretion | Kidney |
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ECHA InfoCard | 100.000.331 |
Chemical and physical data | |
Formula | C12H13ClN4 |
Molar mass | 248.71 g·mol−1 |
3D model (JSmol) | |
Melting point | 233 to 234 °C (451 to 453 °F) |
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Pyrimethamine, sold under the brand name Daraprim among others, is a medication used with leucovorin (leucovorin is used to decrease side effects of pyrimethamine; it does not have intrinsic anti-parasitic activity) to treat the parasitic diseases toxoplasmosis and cystoisosporiasis.[3][4] It is also used with dapsone as a second-line option to prevent Pneumocystis jiroveci pneumonia in people with HIV/AIDS.[3] It was previously used for malaria but is no longer recommended due to resistance.[3] Pyrimethamine is taken by mouth.[3]
Common side effects include gastrointestinal upset, severe allergic reactions, and bone marrow suppression.[3] It should not be used by people with folate deficiency that has resulted in anemia.[3] There is concern that it may increase the risk of cancer.[3] While occasionally used in pregnancy it is unclear if pyrimethamine is safe for the baby.[1] Pyrimethamine is classified as a folic acid antagonist.[3] It works by inhibiting folic acid metabolism and therefore the making of DNA.[3]
Pyrimethamine was discovered in 1952 and came into medical use in 1953.[3][5] It is on the World Health Organization's List of Essential Medicines.[6] It was approved as a generic in the United States in February 2020.[7]
FDA PR 20200228
was invoked but never defined (see the help page).