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Sodium Thiosulfate

Sulfur-donor antidote

Sodium Thiosulfate

Sodium thiosulfate is a sulfur donor used principally in antidotal treatment of cyanide poisoning. Veterinary emergency applications include cyanogenic-plant exposure in ruminants. It also has selected specialist uses in toxicology and local tissue injury, although those applications have a smaller evidence base than its cyanide-detoxification role.

Group

Sulfur-donor antidote

Mechanism of Action

Thiosulfate supplies sulfur for sulfurtransferase pathways, including rhodanese-mediated conversion of cyanide to thiocyanate. This reduces cyanide available to inhibit mitochondrial cytochrome oxidase and permits recovery of cellular oxygen utilization. Thiocyanate is subsequently excreted. In selected local chemotherapy extravasations, chemical inactivation of reactive drug species provides a separate treatment rationale.

Dose Rates

Dogs

Use / stageDoseRouteScheduleInstructions
Cyanide antidote protocol413 mg/kgIVProtocol dose, not stand-alone prescription: slow IV after separately prescribed sodium nitrite with monitoring of oxygen delivery and methemoglobinemia. Complete antidote selection and timing must be specified.

Cats

Use / stageDoseRouteScheduleInstructions
Cyanide antidote protocol413 mg/kgIVProtocol dose, not stand-alone prescription: slow IV after separately prescribed sodium nitrite with monitoring of oxygen delivery and methemoglobinemia. Complete antidote selection and timing must be specified.

Cattle

Use / stageDoseRouteScheduleInstructions
Cyanide antidote protocol413 mg/kgIVProtocol dose, not stand-alone prescription: slow IV after separately prescribed sodium nitrite with monitoring of oxygen delivery and methemoglobinemia. Complete antidote selection and timing must be specified.
Alternative cyanide detoxification protocolReference onlyIVDescribed protocol uses sodium thiosulfate at least 500 mg/kg IV plus 30 g/cow PO for ongoing ruminal exposure. Select a complete emergency protocol; do not merge with the 413 mg/kg nitrite-following schedule.
Ruminal cyanide detoxification adjunctReference onlyPO30 g per cow orally has been described as an adjunct to the specified IV protocol. It does not replace systemic antidote therapy in a critically affected animal.
Alternative cyanogenic-plant poisoning regimen660 mg/kgIVOnceHistorical ruminant course using 30% solution. Rapid administration was described, while other instructions advise slow IV delivery; determine the actual rate in the complete emergency protocol before use.
Copper poisoning molybdate combinationReference onlyPOEvery 24 hUp to 21 days; 500 mg sodium thiosulfate plus 200 mg ammonium or sodium molybdate total orally daily for up to 3 weeks, with fluid replacement. This is a fixed combination course, not an automatic single-active prescription.
Arsenic poisoning oral adjunctReference onlyPOEvery 6 hUp to 4 days; 30–60 g total every 6 hours for 3–4 days has been suggested, with fluid/electrolyte support; efficacy is uncertain. A separate IV amount of 30–60 g as a 10–20% solution was described without a repeat interval.

Sheep

Use / stageDoseRouteScheduleInstructions
Cyanide antidote protocol413 mg/kgIVProtocol dose, not stand-alone prescription: slow IV after separately prescribed sodium nitrite with monitoring of oxygen delivery and methemoglobinemia. Complete antidote selection and timing must be specified.
Alternative cyanogenic-plant poisoning regimen660 mg/kgIVOnceHistorical ruminant course using 30% solution. Rapid administration was described, while other instructions advise slow IV delivery; determine the actual rate in the complete emergency protocol before use.
Copper poisoning molybdate combinationReference onlyPOEvery 24 hUp to 21 days; 500 mg sodium thiosulfate plus 200 mg ammonium or sodium molybdate total orally daily for up to 3 weeks, with fluid replacement. This is a fixed combination course, not an automatic single-active prescription.
Arsenic poisoning oral adjunctReference onlyPOEvery 6 hUp to 4 days; 30–60 g total every 6 hours for 3–4 days has been suggested, with fluid/electrolyte support; efficacy is uncertain. A separate IV amount of 30–60 g as a 10–20% solution was described without a repeat interval.

Goats

Use / stageDoseRouteScheduleInstructions
Cyanide antidote protocol413 mg/kgIVProtocol dose, not stand-alone prescription: slow IV after separately prescribed sodium nitrite with monitoring of oxygen delivery and methemoglobinemia. Complete antidote selection and timing must be specified.
Alternative cyanogenic-plant poisoning regimen660 mg/kgIVOnceHistorical ruminant course using 30% solution. Rapid administration was described, while other instructions advise slow IV delivery; determine the actual rate in the complete emergency protocol before use.
Copper poisoning molybdate combinationReference onlyPOEvery 24 hUp to 21 days; 500 mg sodium thiosulfate plus 200 mg ammonium or sodium molybdate total orally daily for up to 3 weeks, with fluid replacement. This is a fixed combination course, not an automatic single-active prescription.
Arsenic poisoning oral adjunctReference onlyPOEvery 6 hUp to 4 days; 30–60 g total every 6 hours for 3–4 days has been suggested, with fluid/electrolyte support; efficacy is uncertain. A separate IV amount of 30–60 g as a 10–20% solution was described without a repeat interval.

Horses

Use / stageDoseRouteScheduleInstructions
Arsenic poisoning adjunctReference onlyPO20–30 g total in 300 mL water orally with dimercaprol 3 mg/kg IM q4h has been described. Evidence for arsenic benefit is uncertain; timing and hydration require a complete toxicology plan.
Historical cyanide nitrite-following courseReference onlyIVAfter sodium nitrite 16 mg/kg IV (another course uses 10–20 mg/kg IV as a 20% solution), give sodium thiosulfate 30–40 mg/kg IV as a 20% solution. If repeated, give thiosulfate alone. This historical amount is much lower than other cyanide courses; do not merge the ranges.

Indications

Contraindications

Interactions

Adverse effects

Toxicity

Excessive or rapid administration can disturb circulation and acid-base balance; monitor and provide supportive care.

Preparations

PreparationFormStrengthRoute
Sodium thiosulfate injection 25% w/v
250 mg/mL for the specified medicinal formulation. Select a complete cyanide antidote protocol; do not assume compatibility with other antidotes.
Injection250 mg / mLIV
Sodium thiosulfate injection 10% w/v
100 mg/mL as pentahydrate; no assumed conversion to anhydrous salt.
Injection100 mg / mLIV

Monitoring and Administration

Provide airway, ventilation, oxygen and circulatory support while treating suspected cyanide exposure.

One veterinary protocol gives 413 mg/kg IV slowly after sodium nitrite. Another describes at least 500 mg/kg IV plus 30 g per cow orally to reduce ongoing ruminal cyanide release. These are different protocols and are not one broad dose range.

Nitrite use requires assessment of methemoglobinemia and oxygen delivery; some smoke-inhalation settings require a different antidote choice.

The older sheep study tested different thiosulfate/nitrite exposures; experimental doses are not substituted for a complete clinical protocol.

Monitor blood pressure and oxygenation. Store the described 250 mg/mL injection at 20–25°C, protected from light; do not freeze.

Large oral doses can cause profuse diarrhea. In arsenic or copper exposure, thiosulfate is an adjunct with uncertain arsenic efficacy; do not delay established poisoning management.

Human-derived extravasation approaches include a 2% SC solution with corticosteroids for anthracyclines, or 0.17 mol/L solution for cisplatin/carboplatin. A cited preparation combines 4 mL of 10% pentahydrate solution with 6 mL sterile water; 5 mL infiltration was described for carboplatin. These are not validated universal dog/cat protocols and must not be substituted for a drug-specific extravasation plan.

Historical ruminant withdrawal advice suggested 24 hours, but no current local authorization is inferred. Do not mix with cyanocobalamin; keep the already specified hydroxocobalamin incompatibility separate.

Veterinary use

For veterinary reference. Confirm the indication, dose, route, interval, product strength and any applicable withdrawal period before administration.