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Pharm-week 2
| Question | Answer |
|---|---|
| Low Dose-Effect Curve | Measuring the response to the dose of the drug |
| Potency | the amount of drug required to produce an effect. |
| Efficacy | related to the maximal effect of a drug regardless of dose: is the maximum intensity of effect or response that can be produced by a drug |
| Therapeutic action/effect | the intended or desired results |
| Therapeutic range | range between the dose causing the minimum effect and the dose causing the minimum adverse effect. |
| Therapeutic index (TI) | number that determines the safety of a drug. ( the greater the TI, the safer the drug |
| Prophylactic | refers to measures or treatments designed to prevent disease or a condition before it occurs |
| Receptors | is a protein in or on a cell that a drug or natural substance binds to cause a specific effect in the body. |
| Agonist | is a drug that has an affinity for a receptor, combines with a receptor and produces an effect. |
| Antagonist | is a drug that binds to a receptor but does not activate it; instead, it blocks or reduces the effect of other substances. Counteracts the action of the agonist. |
| Renal | kidney |
| hepatic | liver |
| biotransformation | is the body's way of changing a drug so that it can be more easily excreted by the kidneys |
| toletance | the need for an increasingly large dose of the drug to obtain the same effects as the original dose |
| Duration | is the length of a drug's effect |
| half-life | the half-life of a drug is the amount of time that passes for its concentration to fall to half (50%) of its original blood level. |
| Median effect dose (ED50) | is the dose required to produce a desired clinical effect in 50% of test subjects. A low effective dose is preferred because it means less drug is needed to achieve the desired therapeutic effect. |
| Lethal Dose (LD50) | is the amount of a substance that causes death in 50% of a test population. A lower LD means the substance is more toxic. |
| Enteral | drugs are placed directly into the GI tract by oral or rectal administration |
| Parental | administered or occurring elsewhere in the body other than the mouth and alimentary canal |
| Absorption | is the process by which drug molecules are transferred from the site of administration to the circulating blood |
| metabolism | is the body's way of changing a drug so that it can be more easily excreted by the kidneys |
| distribution | the passage of drugs into various body fluid compartments such as plasma, interstitial fluids and intracellular fluids |
| Excretion | the elimination of a drug and its metabolites from the body |
| First-pass effect | The first-pass effect occurs when a drug is partially broken away by the liver before it reaches the bloodstream, reducing the amount of drug available to produce its effect. |