Competency 1 Flashcards

1
Q

Pharmacodynamics

A

Pharmacodynamics is the study of the way drugs affect the body.

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2
Q

Dose response

A

Dose response is the relationship between the minimal versus the maximal amount of drug dose needed to produce the desired drug response.

  • Some patients respond to a lower drug dose
  • others need a high drug dose to get desired response.
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3
Q

Maximal efficacy

A
  • max drug effect
  • Ex. morphine and tramadol hydrochloride (Ultram) are prescribed to relieve pain.
  • The maximum efficacy of morphine is greater than tramadol hydrochloride, regardless of how much tramadol hydrochloride is given.
  • The pain relief with the use of tramadol hydrochloride is not as great as it is with morphine.
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4
Q

Onset of action

A

Onset of action is the time it takes to reach the minimum effective concentration (MEC) after a drug is administered.

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5
Q

Peak action

A

Peak action occurs when the drug reaches its highest blood or plasma concentration.

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6
Q

Duration of action

A

Duration of action is the length of time the drug has a pharmacologic effect.

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7
Q

Minimum effective concentration

A

the threshold level of a drug in plasma below which the efficiency of the drug as a treatment drops off sharply.

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8
Q

Drug interaction

A

A drug interaction is defined as an altered or modified action or effect of a drug as a result of interaction with one or multiple drugs.

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9
Q

Adverse drug reaction

A

An adverse drug reaction is an undesirable drug effect that ranges from mild untoward effects to severe toxic effects, including hypersensitivity reaction and anaphylaxis

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10
Q

Drug incompatibility

A

Drug incompatibility is a chemical or physical reaction that occurs among two or more drugs in vitro. In other words, the reaction occurs between two or more drugs within a syringe, IV bag, or other artificial environment outside of the body.

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11
Q

Drug-induced photosensitivity

A

A drug-induced photosensitivity reaction is a skin reaction caused by exposure to sunlight.

  • caused by the interaction of a drug and exposure to ultraviolet A (UVA) light, which can cause cellular damage.
  • two types:photoallergy and phototoxicity.
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12
Q

Enzyme inducers

A
  • drugs that promote induction of enzymes, by binding to it or activating
  • produce cascade effect of drug function
  • ex. Barbiturates like phenobarbital
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13
Q

Enzyme inhibitors

A

Ex . Anitulcer drug cimetidine ( Tagamet) , decreases metabolism of certain drugs like theophylline, causing increase plasma concentration of theophylline

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14
Q

Receptor theory

A

Drugs act through receptors by binding to the receptor to produce (initiate) a response or to block (prevent) a response. The activity of many drugs is determined by the ability of the drug to bind to a specific receptor. The better the drug fits at the receptor site, the more biologically active the drug is. It is similar to the fit of the right key in a lock.

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15
Q

Agonist

A

Drugs that produce a response

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16
Q

Antagonist

A

drugs that block a response

17
Q

Nonspecific drug effects

A

Drugs that affect various sites are nonspecific drugs and have properties of nonspecificity.
-effects may be either desirable or harmful. Drugs that evoke a variety of responses throughout the body have a nonspecific response.

18
Q

Nonselective drug effects

A

Drugs that affect various receptors are nonselective drugs or have properties of nonselectivity.
-Drugs that produce a response but do not act on a receptor may act by stimulating or inhibiting enzyme activity or hormone production

19
Q

Therapeutic index

A
  • therapeutic index (TI) estimates the margin of safety of a drug through the use of a ratio that measures the effective (therapeutic) dose (ED) in 50% of people (ED50) and the lethal dose (LD) in 50% of people (LD50)
  • The closer the ratio is to 1, the greater the danger of toxicity.
20
Q

Therapeutic drug range

A

The therapeutic range (therapeutic window) of a drug concentration in plasma is the level of drug between the minimum effective concentration in the plasma for obtaining desired drug action and the minimum toxic concentration (the toxic effect).

  • includes both protein-bound and unbound portions of the drug
  • If the therapeutic range is narrow, such as for digoxin (0.5 to 1 ng/mL), the plasma drug level should be monitored periodically to avoid drug toxicity.
21
Q

Protein bound drugs

A

As drugs are distributed in the plasma, many are bound to varying degrees (percentages) with protein (primarily albumin). Drugs that are greater than 89% bound to protein are known as highly protein-bound drugs

22
Q

Half-life

A

The half-life (1/2) of a drug is the time it takes for one half of the drug concentration to be eliminated.

23
Q

peak drug level

A

the highest plasma concentration of a drug at a specific time

24
Q

trough level

A

the lowest plasma concentration of a drug. The trough level measures the rate at which a drug is eliminated; levels are drawn immediately before the next dose of a drug is given.

25
Q

side effects

A

physiologic effects not related to desired drug effects

26
Q

drug toxicity

A

refers to how poisonous or harmful a substance can be. In the context of pharmacology, drug toxicity occurs when a person has accumulated too much of a drug in his bloodstream, leading to adverse effects within the body.Mar 7, 2016