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atcel
100

A drug that binds to and stimulates the activity of one or more receptors in the body

Agonist

100

The physiologic state in which the amt of drug removed via elimination is equal to the amt of drug absorbed with each dose

Steady state

100

In pharmacokinetics, the time required for half of an administered dose of a drug to be eliminated by the body, or the time it takes for the blood level of a drug to be reduced by 50%

Half life

100

A drug that binds to and inhibits the activity of one or more receptors in the body 

Antagonist

100

Substances that catalyze nearly every biochemical reaction  in a cell

Enzymes

200

A measure of the extent of drug absorption for a given drug and route:

Bioavalibility

200

The study of what happens to a drug from the time it is put int othe body until the drug has left the body

Pharmacokinetics

200

The study of biochemical and physiologic interactions of drugs at their sites of activity

Pharmacodynamics

200

Transport of a drug by the bloodstream to it's site of action

Distribution

200

Ration between the toxic and thereapeutic concentrations of a drug: 

Therapeutic index

300

One or more biochemical reactions involving a parent drug. Occurs mainly in the liver

Biotransformation

300

THe time required for a drug to elicit a therapeutic response after dosing

Onset of action

300

Maximum concentration of a drug in the body after administratino, usually measured in a bold sample of therapetic drug monitoring

Peak level

300

Length of a time the concentration of a drug in the blood or tissues is sufficient to elicit a response: 

Duration of actions

300

Barrier restricting the passage of various chemicals and microscopic entities (Bacteria, viruses) between the bloodstream and CNS. Still allows for the passage of essential substances such as oxygen

Blood brain barrier

400

The lowest concentration of drug reached in the body after it falls from it's peak level

Trough level

400

Initial metabolism in the liver of a drug absorbed from the GI tract before the drug reaches systemic circulation through the bloodstream

1st pass effect

400

Drug interactions in which effect of a combo of 2+ drugs with similar actions is equivalent to the sum of individual effects of the same drugs given alone. FOr example 1+1=2

Additive effects

400

Desired or intended effect of a particular medication

Therapeutic effect

400

Time required for a drug to reach its maximum therapeutic response in the body

peak effect

500

Drug interactions in which the effect of a combination of 2 or more drugs with similar actions is greater than the sum of the individual effects of the same drugs given alone. 1+1>2

Synergistic effects

500

The process by which solid forms of drugs disintegrate in the GI tract and become soluble before being absorbed into the circulation 

Dissolution

500

Movement of a drug from it's site of administration into bloodstream for distribution to the tissues

absorption

500

Elimination of drugs from the body: 

excretion

500

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