leustatin - Drug Details
๐Ÿ“Š Estimates leustatin Dialyzability By Different_Modalities

leustatin

Complete Drug Information

Drug Name
leustatin
Trade Names
Leustatin, Litak, Mavenclad
Pregnancy Category
AU: D
Bioavailability
100% (i.v.); 37 to 51% (orally)
Routes of Administration
Intravenous, subcutaneous (liquid),Oral (tablet)
Protein Binding
25% (range 5-50%); up to 20% (orally)%
Metabolism
Mostly via intracellular kinases; 15-18% is excreted unchanged. Intravenous and subcutaneous bolus injection: 15-18% is excreted unchanged After oral administration, 25% (ยฑ21%) of dose is excreted unchanged in urine and 3.8% as a metabolite.
Elimination
Approximately 10 hours after both intravenous infusion and subcutaneous bolus injection ranging from 5.6 to 7.6 hours and 18.4 to 19.7 hours after oral administration, indicative of different elimination phases.
Excretion
Urinary
Formula
C10H12ClN5O3
Molar Mass
285.69
Volume of Distribution
C10H12ClN5O3

๐Ÿคฐ Pregnancy Category Information

Category: AU: D

Drugs which have caused, are suspected to have caused, or may be expected to cause an increased incidence of human fetal malformations or irreversible damage. These drugs may also have adverse pharmacological effects.