if related to drug then
Absorption:
the amount of drug reaches the systemic circulation is called absorption.
Distribution:
the drug reversibly leaves the blood stream and enters into interstitial space or tissues.
Elimination:
irreversible removal of drug from body by excretion or metabolism of drug
If you currently need a pharmaceutical drug to manage the symptoms of a disease, don't put yourself at risk, or limit the effectiveness of your drug, by an interaction with common foods and herbs.
time when drug is fully available at the max (when the absorption rate and elimination rate of the drug equals)
absorption
§ Absorption: fully dissociated in aqueous solution at physiological pH. The components are rapidly and well absorbed by the oral route of administration. Absorption of Augmentin is optimized when taken at the start of a meal. § Distribution: Both clavulanate and amoxicillin have low levels of serum binding; about 70% remains free in the serum. § Metabolism: Elimination: All of these data indicate that the elimination pharmacokinetics seen in adults also apply to children with mature kidney function.
Pharmacokinetics refer to how the drug works through its mechanisms and how the drug interacts with the body. Absorption, distribution, metabolism, excretion and elimination of the drug from the body are all part of the pharmacokinetic phase of a drug trial. Pharmacists and industrial scientists are the foremost experts in this field. In a hospital or health clinic, pharmacists are involved in dosing drugs based on its pharmacokinetic profile in a patient - such as in babies and pediatric patients.
How quickly a drug clears from the body is a function of its absorption, bioavailability, distribution, metabolism, and excretion properties.
Digestion, absorption, and elimination.
ingestion, absorption, digestion and elimination
the more ionized the drug is the less absorption
Any medicine or drug that can interfere in absorption, distribution, metabolism and excretion of drugs and alter their original effect is call pharmacokinetic interactions.
Ingestion, digestion, absorption, and elimination.
The absorption, distribution, metabolism and excretion of drugs are the primary four parameters of pharmacokinetics.
Veterinary drug absorption is the uptake of a drug after administration so that it can cause some sort of alteration in the body.