General Principles of Pharmacology Flashcards

1
Q

Pharmacokinetics

A

Activity of a drug in the body over time (branch of pharmacology concerned with the movement of drugs within the body) study of the bodily absorption, distribution, metabolism, and excretion of drugs (how body effects drug)

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2
Q

Absorption

A

Refers to the way a drug is absorbed from a pharmaceutical formula into the blood stream, moving from its “site of delivery into the bloodstream,”
journey of a drug travelling from the site administration to the site of action

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3
Q

Distribution

A

Refers to the movement of a drug to and from the blood and various tissues of the body (process of transferring a drug from the bloodstream to tissues)

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4
Q

Metabolism

A

Is the chemical alteration of a drug by the body (breakdown of drug) break down and coverts medication into active chemical substance

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5
Q

First-pass effect

A

Drug gets metabolized at a specific location in the body that results in a reduced concentration of the active drug upon reaching its site of action

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6
Q

Therapeutic index

A

Is a ratio that compares the blood concentration at which a drug causes a therapeutic effect to the amount that causes death (margin of safety that exist between the dose of a drug that produces a desired effect and the dose that produces an unwanted side effect)

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7
Q

Half-life

A

the time it takes for the amount of a drugs active substance in the body to reduce by half

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8
Q

Pharmacodynamics

A

The relationship between drug concentration at the site of action and the resulting effect (what the drug dose to the body) how the drug effects the body

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9
Q

Agonist

A

A drug or substance that binds to a receptor inside a cell or on its surface and causes the same action as the substance that normally binds to the receptor

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10
Q

Antagonist

A

A substance that stops the action or effect of another substance (acts against and blocks and action)

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11
Q

Synergistic effect

A

Interaction of two or more drugs when their combined effect is greater than the sum of the effects seen when each drug is given alone ​

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12
Q

Therapeutic drug monitoring

A

Testing that measures the amount of a certain medicine in the blood (measuring of drug levels in the blood at timed intervals to maintain relatively constant levels

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13
Q

Adverse effects

A

Harmful or abnormal result

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14
Q

Toxicity

A

How poisonous or harmful a substance can be (occurs when person accumulated too much of a drug in the bloodstream, leading to adverse effects on the body)

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15
Q

Hepatotoxicity

A

The injury/ Liver damage caused by exposure to drugs

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16
Q

Nephrotoxicity

A

Rapid deterioration in the kidney function due to toxic effects of medications and chemical

17
Q

Anaphylactic reaction

A

Severe, potentially life-threatening allergic reaction

18
Q

Extrapyramidal symptoms

A

Commonly referred to as drug induced movement disorders (group of symptoms including tremor, slurred speech, anxiety, distress, paranoia etc.)

19
Q

Immunosuppression

A

suppression of the body’s immune system and its ability to fight infections an other diseases

20
Q

What role does albumin play in medication distribution

A

Albumin possesses specific sites for acidic and basic drug binding

It is a natural transport protein w/ multiple ligand bind sites

Most abundant plasma protein in he body

21
Q

What role does glycoprotein play in medication distribution

A

“Multi drug transport protein”
Transports a wide variety of drugs OUT of cells
KIDNEY- pumps drugs into urine for excretion
INTESTINE- transports drugs into the intestinal lumen, reducing drug absorption into the blood
BRIAN- pumps drugs into the blood theory limiting drug access to the brain

22
Q

Types of drug interactions

A

1) drug-drug: interaction between row or more prescriptions
2) drug- nonprescription: drug w/ other over the counter, herbs or vitamins
3) drug-food: food/beverage alters drug effect
4) drug-alcohol:
5) drug-disease:
6) drug- laboratory: some drugs can interfere w/ test

23
Q

Excretion

A

Movement of drugs and their metabolites out of the body

24
Q

The rate of absorption determines

A

How soon effects will begin

25
Q

The amount of absorption help determine

A

How intense effects will be

26
Q

Absorption includes

A

Rate of dissolution: must first be dissolve before absorbed (rate of dissolution determine rate of absorption)

Surface area: larger surface area, equals faster absorption

Blood flow: absorbed most rapidly from sites where blood flow is high (greater concentration gradient, more rapidly absorption will be)

Lipid solubility: highly lipid soluble drugs are absorbed more rapidly than drugs who’s lipid solubility is low (bc lipid soluble drugs cross membranes and low lipid soluble can not)

27
Q

Selectivity

A

Ability to elicit only the response for which the drug is given

The more selective a drug is the fewer side effects it will produce

Selective drug action is possible because drugs act through specific receptors

28
Q

Affinity

A

Refers to the strength of the attraction between a drug and its receptor

29
Q

Intrinsic activity

A

Ability of a drug the activate a receptor upon binding

30
Q

Consequences of drug-drug interactions

A

1) One drug may intensify the effect of the other
2) One drug may reduce the effect of the other
3) The combination may produce in the response not seen with either drug alone

31
Q

Drug-food interaction

A

Food decreases the rate of absorption and occasionally decreases the extent of exception

32
Q

Idiosyncratic effect

A

A uncommon drug response resulting from a genetic predisposition

33
Q

Paradoxical effect

A

Opposite of the intended drug response

34
Q

Iatrogenic disease

A

Disease resulting from medical care or treatment

35
Q

Teratogenic effect

A

Drug induced birth defect