Pharmacology Flashcards

1
Q

Pharmacodynamics:def

A

‘What the drug does to the body’

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2
Q

Pharmacokinetics:def

A

‘What the body does to the drug’
The study of the time course of drug absorption (from the site of administration), distribution, metabolism and excretion

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3
Q

ADME acronym for?

A

Pharmacokinetics
The study of the time course of drug absorption (from the site of administration), distribution, metabolism and excretion

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4
Q

Administration of drugs routes

A

1 Oral (most common)
Convenient
Acceptable
No special skills
Variety of pharmaceutical solutions for different patients

2 p.o. = per os (by mouth)
3 Injection
4 IV (intravenous)
5 IM (intramuscular)
6 SC (subcutaneous) (…)
7 Inhalation (drugs for asthma, e.g., salbutamol)
8 Sublingual or buccal
9 Rectal (e.g., suppository)
10 Other epithelial surfaces (skin, cornea, vagina, nasal mucosa)

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5
Q

what is ‘First-pass’ metabolism and how does it affect drug administration?

(absorption)

A

Swallowed drug
(100%)
Digestive system
(enzymes)
Hepatic Portal System
Liver
(enzymes)
Rest of the body
(20%)

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6
Q

Distribution of drugs : define

A

Process by which a compound is transferred from the general circulation to other parts of the body and into the tissues

Most drugs bind to proteins esp. albumin

Compartment: Examples

Total body water: Small, water-soluble molecules (e.g. ethanol)

Extracellular water: Larger, water-soluble molecules (e.g. mannitol)

Blood plasma: Highly plasma protein-bound molecules, very large molecules, highly charged molecules (e.g. heparin)

Adipose tissue: Highly lipid-soluble molecules (e.g. diazepam)

Bone and teeth: Certain ions (e.g. fluoride)

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7
Q

What is drug Metabolism?

Where are the main sites?

A

The processes by which a drug is chemically altered in a way that facilitates its action OR enhances its elimination from the body

LIVER, kidney, GI tract, lungs, skin

Metabolites…

Inactive, less active, active, (therpeutic/toxic effects), Activated/pro-drug

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8
Q

What’s a pro-drug

A

Precursor of the active drug

Needs to be metabolised (in vivo) into pharmacologically active drugs

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9
Q

in Metabolism: what is Enzymatic Inhibition and Induction

A

Inhibition = slower metabolism Induction= Faster metabolism

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10
Q

What does excreation mean in relation to a drug?

A

The processes by which drugs or their metabolites are removed from the body

RENAL

biliary

respiratory

dermal

fecal

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11
Q

Summarise pharmacokinetics in the body

A
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12
Q

Summarise pharmacokinetics in the body

A
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13
Q

Summarise possible effects of Drug Action

1

2

3

4

A

1) Therapeutic: Intended biological effect (placebo?)
2) Side: Undesirable/unintended secondary effect - occurs in addition to the desired therapeutic effect after administration of a drug or combination of drugs under normal conditions / dose
3) Adverse: Harmful reaction after administration of a drug or combination of drugs under normal conditions of use
4) Toxic: Deleterious, undesired effect; following administration of a higher dose of the drug (medicine); e.g., drug poisoning

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14
Q

How do side effects happen at an appropriate dose?

Are they the same for all people?

A

Occur when the drug interacts with same type of receptor at different sites around the body

Or Interacts with more than one type of receptor

Most can be predictable by knowing the pharmacology of the drug

Not the same for all people - biology dependant

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15
Q

•What factors could influence drug response?

A

1 Age

2 Gender

3 Genetics

4 Body Composition

5 Previous exposure

6 Disease

7 Interactions (other medications)

AND

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16
Q
A
17
Q

•Describe the basic processes of drug-receptor interactions

A
18
Q
A
19
Q

Explain the dose-response relationship

A
20
Q

When does a full agonist achieve maximal response?

A

A full agonist achieves a maximal response when all its receptors are occupied