Plugging In the Human Body: Hope, Hype, and Hidden Risks
December 3, 2025
Brand Name :
N/A
Synonyms :
diethylene triamine penta-acetic acid
Class :
Antidote
Dosage Forms & StrengthsÂ
SolutionÂ
200 mg/mlÂ
Take initial dose intravenously of 1 g daily
Take maintenance dose intravenously of 1 g daily
Dosing modifications
Renal Impairment
Dose modification not required
Hepatic impairment
Dose modification not required
Dosage Forms & StrengthsÂ
SolutionÂ
200 mg/ml Â
For <12 years:
Take initial dose on day 1 intravenously 14 mg/kg one time a day
Take maintenance dose on day 2 intravenously 14 mg/kg one time a day
Maximum daily dose not more than 1000 mg
For ≥12 years and Adolescents:
Take initial dose on day 1 intravenously 1000 mg one time a day
Take maintenance dose on day 2 intravenously 1000 mg one time a day
Start next day after the first dose administered
Refer to adult dosingÂ
Actions and SpectrumÂ
diethylene triamine penta-acetic acid (DTPA) acts as a chelating agent, meaning it forms stable complexes with metal ions. Â
It possesses a high affinity for certain metals, particularly divalent and trivalent cations such as iron, lead, and plutonium.Â
Frequency not defined Â
Gastrointestinal: Diarrhea, vomiting, nauseaÂ
Cardiovascular: Chest painÂ
Local: Injection site reactionÂ
Neuromuscular and skeletal: Muscle crampsÂ
Genitourinary: Pelvic painÂ
Central nervous system: Chills, dizziness, metallic taste, headacheÂ
Dermatologic: Dermatitis, pruritusÂ
Hypersensitivity: Hypersensitivity reactionÂ
Respiratory: Cough, wheezingÂ
Black Box WarningÂ
None
Contraindication/Caution:Â
Pregnancy consideration:Â
Pregnancy category: N/AÂ
Lactation: Excretion into human milk is unknown Â
Pregnancy Categories:        Â
Category A: well-controlled and Satisfactory studies show no risk to the fetus in the first or later trimester.Â
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women. Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.Â
Category N: There is no data available for the drug under this category.Â
Pharmacology Â
diethylene triamine penta-acetic forms multiple coordination bonds with metal ions, creating a stable chelate complex. This complexation reduces the toxicity of the metal ions and facilitates their elimination from the body.Â
PharmacodynamicsÂ
Limited information available Â
PharmacokineticsÂ
Absorption  Â
diethylene triamine penta-acetic is administered via intravenous (IV) injection to ensure its direct entry into the systemic circulation.Â
DistributionÂ
diethylene triamine penta-acetic distributes through the extracellular fluid compartment. Â
MetabolismÂ
diethylene triamine penta-acetic is minimally metabolized in the body.Â
Elimination and excretionÂ
diethylene triamine penta-acetic is primarily eliminated by renal excretion in the urine.
AdministrationÂ
diethylene triamine penta-acetic administered as an intravenous infusion or injection.
Patient information leafletÂ
Generic Name: diethylene triamine penta-aceticÂ
Why do we use diethylene triamine penta-acetic?Â
diethylene triamine penta-acetic acid (DTPA) is a chelating agent commonly used for its ability to bind to metal ions.  Â
It is primarily used for the treatment of heavy metal poisoning, particularly in cases of iron, lead, and plutonium toxicity. Â
DTPA is also used in lead poisoning cases. As it binds to lead ions and helps enhance their elimination through urine, reducing lead levels in the body. Â