| Absorption | Bioavailability is 60 to 80% following oral administration. |
| Volume of distribution | Not Available |
| Protein binding | Not Available |
| Metabolism | |
| Route of elimination | Not Available |
| Half life | Not Available |
| Clearance | Not Available |
| Toxicity | Toxicity includes ventricular tachycardia or ventricular fibrillation, or progressive bradyarrhythmias, or heart block. LD50 = 7.8 mg/kg (orally in mice). |
| Affected organisms |
|
| Pathways | Not Available |
Acetyldigitoxin
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