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Suramin

Antiprotozoal · Antitrypanosomal

AntiprotozoalAntitrypanosomal
CDSCO approvedSchedule H
EXCRETION
not curated
INTERACTIONS
none in our sources
PREGNANCY
Embryotoxic in animal studies, avoid if
FDA category + note

Mechanism

Suramin is an antitrypanosomal drug primarily utilized for the treatment of early-stage Trypanosoma brucei rhodesiense infections. It is an antiparasitic agent that directly targets and inhibits the growth or survival of the Trypanosoma parasites.

Indications

Treatment of early-stage Trypanosoma brucei rhodesiense infection (sleeping sickness)Early-stage African trypanosomiasis caused by T. brucei rhodesienseFirst-stage T. b. rhodesiense HAT

Dosing

Adult
(thiabendazole) by mouth [all unlicensed] (available from ‘special-order’ manufacturers or specialist importing companies). Strongyloidiasis Adult Strongyloides stercoralis live in the gut and produce larvae which penetrate the gut wall and invade the tissues, setting up a cycle of auto-infection.…
Pediatric
4–5 mg/kg on day 1 followed by 5 weekly injections of 20 mg/kg (e.g., days 3, 10, 17, 24, 31). Maximal dose 1 g per injection, diluted in distilled water (IV).

Pharmacokinetics

Onset
binds to plasma proteins and persists at low levels for several weeks after infusion
Protein binding
99.7% serum protein bound (in blood plasma, not CSF or other compartments. It is a general systemic drug. Plasma protein binding is usually high.) This refers to serum protein binding. It is better to use 'serum protein bound' rather than 'plasma protein bound' as text specifies 'serum protein bound'. No. The text says 'plasma proteins'. So let's stick with that.…
Metabolism
negligible

Contraindications

  • Late-stage Trypanosoma brucei infection
  • Onchocerciasis (due to toxicity)

Side effects

Common
MalaiseNauseaFatigueVomitingDiarrheaStomatitisChillsAbdominal painEdemafeverurticariahypotensionexfoliative dermatitisparesthesiasphotophobiarenal dysfunctionPyrexiaNephrotoxicity (usually mild and reversible)
Serious
  • Toxicity (leads to its discontinuation for onchocerciasis)
  • Nausea (immediate reaction)
  • Vomiting (immediate reaction)
  • Shock (rare, ~1 in 2000 patients)
  • Loss of consciousness (rare, ~1 in 2000 patients)
  • Renal toxicity (most common problem after several doses, manifested by albuminuria)
  • Delayed neurological complications (headache, metallic taste, paresthesias, peripheral neuropathy)
  • nephrotoxicity
  • adrenal toxicity
  • optic atrophy
  • anaphylaxis

Pregnancy & lactation

Pregnancy

Embryotoxic in animal studies, avoid if

Related guidelines

Other Antiprotozoal drugs

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Sources: Goodman & Gilman 14e, Harrison 22e, BNF·Verified: 2026-05-13 · House clinical team