Dimercaprol: Difference between revisions

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==Comments==
==Comments==
==Indications by Condition==
''The following table is automatically generated from disease/condition pages across WikEM.''
{{#ask:[[Has DrugName::Dimercaprol]]
|?Has Indication=Indication
|?Has Dose=Dose
|?Has Context=Context
|?Has Route=Route
|?Has Population=Population
|format=table
|headers=plain
|mainlabel=-
|sort=Has Indication
|limit=50
}}


==See Also==
==See Also==
*[[Toxicology (main)]]
*[[Heavy metals]]
*[[Antidotes]]
*[[Antidotes]]
*[[Arsenic]]
*[[Arsenic]]
*[[Lead toxicity]]
*[[Lead toxicity]]
*[[Mercury toxicity]]
*[[Mercury toxicity]]
==References==
==References==
<references/>
<references/>
[[Category:Pharmacology]]
[[Category:Pharmacology]]
[[Category:Toxicology]]

Latest revision as of 21:56, 20 March 2026

Administration

  • Type: Chelator, Antidote
  • Dosage Forms:
  • Routes of Administration: IM
  • Common Trade Names: British antilewisite (BAL)

Adult Dosing

  • Arsenic or gold toxicity, mild: 2.5 mg/kg IM 4 times per day x 2 days, BID on day 3, then daily x 10 days
  • Arsenic or gold toxicity, severe: 3 mg/kg IM q4 hours x 2 days, 4 times on day 3, then BID x 10 days
  • Mercury toxicity: 5mg/kg IM on day 1, then 2.5 mg/kg 1-2 times daily x 10 days
  • Lead poisoning, mild: 4 mg/kg IM for initial dose, then 3 mg/kg q4 hourr for 2-7 days in combination with edetate calcium disodium (EDTA)
  • Lead poisoning, severe: 4 mg/kg IM every 4 hr for 2-7 days in combination with edetate calcium disodium (EDTA)

Pediatric Dosing

  • Same as above

Special Populations

  • Pregnancy Rating: C
  • Lactation risk: Infant risk cannot be ruled out
  • Renal dosing: use at reduced dose and with caution
  • Hepatic dosing: contraindicated in hepatic insufficiency

Contraindications

  • Allergy to class/drug
  • Hepatic insufficiency (unless due to arsenic)

Adverse Reactions

Serious

  • Tachycardia, hypertension
  • Fever

Common

  • Fever
  • Bronchospasm, chest tightness
  • Headache, paresthesias, tremor
  • Blepharospasm, conjunctivitis

Pharmacology

  • Half-life:
  • Metabolism:
  • Excretion:

Mechanism of Action

  • Binds thiol group on heavy metals, preventing those groups from binding/inhibiting enzymes and allowing urinary excretion of metals

Comments

Indications by Condition

The following table is automatically generated from disease/condition pages across WikEM.

IndicationDoseContextRoutePopulation
Copper sulfate toxicity3-5mg/kg/dose IM q4hr x 2 days, then taper over 7-11 daysChelation, first-line for severeIMAdult
Lead toxicity50-75mg/m2 IM q4hr x 3-5 daysFirst-line if encephalopathy presentIMAdult
Mercury toxicity2.5-5mg/kg IM q6-12hrChelation, severe or inorganic mercuryIMAdult

See Also

References