There are many things that can metabolize a drug, but the liver is the main one.
A pro-drug is a pharmacological inactive compound which becomes active through metabolism.
Drug Metabolism Reviews was created in 1972.
Pharmacokinetic phase: involves the absorption, distribution, metabolism, and elimination of the drug in the body. Pharmacodynamic phase: refers to the drug's interaction with its target receptors and the subsequent biochemical and physiological effects. Phase of termination: marks the decline of drug effects as the body clears the drug through metabolism and excretion.
Trimetazidine. A metabolic drug intefering and improving heart muscle oxygenation through better glucose metabolism and decrease fatty acid metabolism. Serve as an anti anginal. Can be added to nitrates therapy. No major side effects other than GI discomfort.
Drug metabolism primarily occurs in the liver, where enzymes break down drugs into metabolites that can be excreted from the body. Other organs, such as the kidneys and intestines, also play a role in drug metabolism to some extent.
The drug that you use!~
Drugs that slow drug metabolism include ciprofloxacin, erythromycin, fluoxetine, nefazodone, paroxetine, and ritonavir
How quickly a drug clears from the body is a function of its absorption, bioavailability, distribution, metabolism, and excretion properties.
Alcohol leaves the body through metabolism, respiration, urination, and perspiration.
First pass metabolism refers to the metabolism of a drug that occurs in the liver after it is absorbed from the gastrointestinal tract, before it enters systemic circulation. Phase 1 metabolism is the initial biotransformation of a drug, primarily carried out by enzymes such as cytochrome P450, to make the drug more polar and easier to eliminate from the body.
The drug that you use!~
The pharmacokinetic process consists of four main parts: absorption, distribution, metabolism, and excretion. Absorption refers to the process by which a drug enters the bloodstream, distribution describes how the drug spreads throughout the body tissues, metabolism involves the biochemical modification of the drug, primarily in the liver, and excretion is the elimination of the drug from the body, primarily through the kidneys. Together, these processes determine the drug's bioavailability, efficacy, and duration of action.