Medication Administration Flashcards

1
Q

Adverse event (AE)

A

Any undesirable experience associated with the use of a medical product in a patient. Usually described in terms of intensity.

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2
Q

Side effect

A

A nontherapeutic reaction to a drug. May be transient.

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3
Q

Allergic reaction

A

An acquired hyper response of body defenses to a foreign substance (allergen).

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4
Q

Anaphylaxis

A

A severe type of allergic reaction that involves the massive systemic release of histamine and other chemical mediators of inflammation that can lead to life-threatening shock.

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5
Q

What are the three checks of drug administration

A
  1. Checking the drug with the MAR
  2. Checking drug when preparing it, pouring it, etc.
  3. Checking the drug before administering it to the patient
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6
Q

The rate of dissolution

A

Determines how quickly the drug disintegrates and disperses into simpler forms

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7
Q

Distribution

A

Involves the transport of drugs throughout the body. The simplest factor determining distribution is the amount of blood flow to body tissues.

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8
Q

Metabolism (Biotransformation)

A

The process of chemically converting a drug to a form that is usually more easily removed from the body.

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9
Q

Hepatic microsomal enzyme system

A

As it relates to pharmacotherapy, liver enzymes that inactivate drugs and accelerate their excretion; sometimes called the P-450 system.

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10
Q

Prodrugs

A

Drugs that become more active after they are metabolized.

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11
Q

Enzyme induction

A

Process in which a drug changes the function of the hepatic microsomal enzymes and increases metabolic activity in the liver.

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12
Q

Minimum effective concentration

A

The amount of a drug required to produce a therapeutic effect.

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13
Q

Toxic concentration

A

The level of drug that will result in serious adverse effects

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14
Q

Therapeutic range

A

The dosage range or serum concentration that achieves the desired drug effects

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15
Q

Onset of drug action

A

Represents the amount of time it takes to produce a therapeutic effect after drug administration.

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16
Q

Peak plasma level

A

Occurs when the medication has reached its highest concentration in the bloodstream. Not necessarily associated with optimal therapeutic effect.

17
Q

Duration of drug action

A

The amount of time a drug maintatins its therapeutic effect

18
Q

Plasma half-life

A

The length of time required for the plasma concentration of a medication to decrease by one-half after administration.

19
Q

Loading dose

A

A higher amount of drug, often given only once or twice to “prime” the bloodstream with a sufficient level of drug.

20
Q

Maintenance doses

A

Given to keep the plasma drug concentration in the therapeutic range.

21
Q

Frequency distribution curve

A

A graphical representation of the number of patients responding to a drug action at different doses.

22
Q

Median Lethal Dose (LD50)

A

Often determined in preclinical trials, the dose of drug that will be lethal in 50% of a group of animals

23
Q

Median Effective Dose (ED50)

A

Dose required to produce a specific therapeutic response in 50% of a group of patients.

24
Q

Median toxicity dose (TD50)

A

Dose that will produce a given toxicity in 50% of a group of patients

25
Q

Graded dose-response

A

Relationship between and measurement of the patient’s response obtained at different doses of a drug.

26
Q

Potency

A

The strength of a drug at a specified concentration or dose

27
Q

Efficacy

A

The ability of a drug to produce a desired response

28
Q

Agonist

A

Drug that is capable of binding with receptors to induce a cellular response

29
Q

Antagonist

A

Drug that block the response of another drug

30
Q

Partial agonist (Agonist-antagonist drug)

A

Medication that produces a weaker, or less efficacious, response than an agonist

31
Q

Functional antagonists

A

Inhibit the effects of an agonist not by competing with the receptor but by changing pharmacokinetic factors

32
Q

Idiosyncratic response

A

Unpredictable and unexplained drug reaction