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Sulfadoxine/pyrimethamine, sold under the brand name Fansidar, is a combination medication used to treat malaria.[1][2] It contains sulfadoxine (a sulfonamide) and pyrimethamine (an antiprotozoal).[3] For the treatment of malaria it is typically used along with other antimalarial medication such as artesunate.[3] In areas of Africa with moderate to high rates of malaria, three doses are recommended during the second and third trimester of pregnancy.[4]
| Combination of | |
|---|---|
| Sulfadoxine | Sulfonamide |
| Pyrimethamine | Antiparasitic |
| Clinical data | |
| Pronunciation | peer-i-METH-a-meen/sul-fa-DOX-een[1] |
| Trade names | Fansidar, Fanlar, others |
| AHFS/Drugs.com | Consumer Drug Information |
| License data | |
| Pregnancy category |
|
| Routes of administration | By mouth |
| ATC code | |
| Legal status | |
| Legal status | |
| Identifiers | |
| CAS Number | |
| KEGG | |
| (verify) | |
Side effects include diarrhea, rash, itchiness, headache, and hair loss.[3][1] Rarely a severe allergic reaction or rash such as toxic epidermal necrolysis, may occur.[1] It is not generally recommended in people with a sulfonamide allergy or significant liver or kidney disease.[3] It works by blocking malaria's ability to use folinic acid.[1]
Sulfadoxine/pyrimethamine was initially approved for medical use in the United States in 1981.[1] It is on the World Health Organization's List of Essential Medicines.[5] It is not commercially available in the United States.[1]
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Malaria
It is approved in the United States as a treatment and preventive measure against malaria.[6] The combination is considered to be more effective in treating malaria caused by Plasmodium falciparum than that caused by P. vivax, for which chloroquine is considered more effective, though in the absence of a species-specific diagnosis, the sulfadoxine-pyrimethamine combination may be indicated.[7] Due to side effects, however, it is no longer recommended as a routine preventive,[8] but only to treat serious malaria infections or to prevent them in areas where other drugs may not work.[9] However, it is recommended by the World Health Organization (WHO) for seasonal preventative use in children when combined with amodiaquine.[10]
Other
It has also be used as a treatment and prophylactic measure for toxoplasmosis and Pneumocystis jiroveci pneumonia.[11][12][13][14][15][16]
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Adverse effects by incidence include:[6][11][17][18]
Common (>1% frequency):
- Hypersensitivity reactions (e.g. itchiness, contact dermatitis, and hives)
- Myelosuppression
- Gastrointestinal effects (e.g. nausea, vomiting, and diarrhoea)
- Headache
Rare (<1% frequency):
- Stevens–Johnson syndrome
- Toxic epidermal necrolysis
- Agranulocytosis
- Aplastic anaemia
- Disorder of haematopoietic structure
- Drug-induced eosinophilia
- Thrombocytopaenia
- Liver necrosis
- Hepatitis
- Jaundice
- Hepatomegaly
- Nephrotoxicity
Unknown frequency:
- Weight loss
- Abdominal cramps
- Hair loss
- Photosensitivity
- Fatigue
- Fever
- Polyneuritis
- Atrophic glossitis
- Gastritis
- Abnormal liver function test results (e.g. elevated serum ALT, AST, alkaline phosphatase, and bilirubin concentrations)
Contraindications
Use of this drug is contraindicated in:[6][17]
- Megaloblastic anaemia caused by folate deficiency
- Hypersensitivity to pyrimethamine, sulfonamides, or any ingredient in the formulation
- Repeated prophylactic (prolonged) use in patients with kidney or liver failure or blood dyscrasias
- Infants <2 months of age
- Prophylaxis in pregnancy at term
- Prophylaxis in nursing women
- Acute porphyria
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Sulfadoxine is a sulfonamide antibiotic that competes with p-aminobenzoic acid in the biosynthesis of folate.[6] Pyrimethamine serves as a selective inhibitor of protozoal dihydrofolate reductase, hence preventing the synthesis of tetrahydrofolate — the active form of folate.[6] A great degree of synergy occurs between the two drugs due to their inhibition of two different steps in the biosynthesis of tetrahydrofolate.[6]
| Pharmacokinetic parameter | Pyrimethamine | Sulfadoxine |
|---|---|---|
| Half-life | 111 hours | 169 hours |
| Cmax | 0.2 mg/L | 60 mg/L |
| Tmax | 4 hours | 4 hours |
| Protein bound | 87% | 90% |
| Excretion | Renal (16-30%) | Renal (30%) |
| Metabolism | Hepatic | Hepatic |
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