Chapter 1 Flashcards

1
Q

Study of science of drugs.

A

Pharmacology

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2
Q

Any chemical that affects the physiologic processes of a living microorganism.

A

Drug

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3
Q

3 drug names

A

Chemical
Generic
Trade

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4
Q

Describe the drug’s chemical composition and molecular structure

A

Chemical name

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5
Q

Name given by the United States Adopted Names Council.
Shorter than chemical name.
Used as official listing of drugs.

A

Generic name

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6
Q

Drug registered trademark.
Use of the name is restricted by the drug’s patent
owner or manufacturer.

A

Trade name

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7
Q

Drug is classified in 2 categories

A

Structure (ex. beta-adrenergic blockers) Therapeutic Use (ex. antibiotics, antihypertensive, antidepressants)

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8
Q

Pharmacologic principles

A

Pharmaceutics
Pharmacokinetics
Pharmacodynamics
Pharmacotherapeutics
Pharmacognosy
Pharmacoeconomics

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9
Q

The study of how various drug forms (ex. tablet, capsule, syrup, parenteral) influence the way in which the drug affects the body.

A

Pharmaceutics

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10
Q

Different drug dosage forms that hv different pharmaceutical properties
Dosage form determines the rate of dissolution

A

Pharmaceutics

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11
Q

It serves as a barrier to prevent the gastric acids in the stomach from dissolving or degrading drugs that are taken orally.

A

Enteric coated drugs

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12
Q

Prolongs drug absorption and duration.

A

Extended release forms
Prolongs drug absorption and duration.
 SR (Slow Release / Sustained Release)
 SA (Sustained Action)
 CR (Controlled Release)
 XL (Extended Length)
 XT (Extended Time)

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13
Q

Pharmaceutic phases

A

Tablet-disintegration-dissolution

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14
Q

Breakdown of a tablet into small particles.

A

Disintegration

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15
Q

 Dissolving of the smaller particles in the GI fluid before absorption.

A

Dissolution

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16
Q

The drug is absorbed into the systemic circulation through the oral, gastric mucosa, or the small intestine.

A

Enteral route

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17
Q

2 methods of administration of oral route

A

Applying topically to the mouth.
Swallowing for absorption along the GI tract into
system circulation.

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18
Q

is where the dosage form is placed under the tongue.
Rapidly absorbed by sublingual mucosa.

A

Sublingual route

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19
Q

is where the dosage form is placed between gums and inner lining of the cheek (buccal pouch).

A

Buccal route

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20
Q

Advantages:
 Used in children
 Little or no first-pass effect
 Used in vomiting / unconscious patient
 Higher concentrations rapidly achieved

A

Rectal route

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21
Q

Parenteral route

A

Intravenous
Intramuscular
Subcutaneous
Intradermal
Intra arterial
Intra articular

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22
Q

100% bioavailability.
 Desired blood concentration achieved.
 Large quantities.
 Used in patient with vomiting and diarrhea.
 Used in emergency situations.
 First pass avoided.

A

Intravenous

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23
Q

Absorption reasonably uniform.
 Rapid onset of action.
 Mild irritants can be given.
 First pass avoided.

A

Intramuscular

24
Q

Injected under the skin.
 Absorption is slow, so action is prolonged.

A

Subcutaneous

25
Drug is given within the dermis layer of skin.  Painful  Mainly used for testing sensitivity to drugs.
Intradermal
26
Injections of antibiotics and corticosteroids are administered in inflamed joint cavities by expert. Ex. hydrocortisone for rheumatoid arthritis
Intra-articular
27
 Rarely used  Drugs used for diagnosis of peripheral vascular diseases.
Intra-arterial
28
is the application of a drug directly to the surface of the skin.  Includes administration of drugs to any mucous membrane.  Skin (ex. transdermal patches, ointments)  Eye  Nose ( ex. sprays)  Ears  Lungs (ex. inhalation)  Vagina  Urethra  Colon
Topical administration / Topical route
29
Absorption of drug through skin.  Stable blood vessels
Transdermal
30
A drug’s time to onset of action,time to peak effect, and duration of action. Study of what happens to a drug from the time it is put into the body until the parent drug and all metabolites have left the body
Pharmacokinetics
31
The study of what the body does to the drugs.  Absorption  Distribution  Metabolism  Excretion
Pharmacokinetics
32
Is a phenomenon in which 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 or systemic circulation. It usually occurs in the stomach, small intestine, and liver. The first-pass effect happens most commonly when the drug is administered orally.
First-pass effect
33
Describes the way that a drug is released from its administered form.
Pharmacokinetics - Liberation
34
Various release types
Immediate: formulated to release the medicinal drug without delay. Delayed: formulated to release medicinal drug sometime after it is taken (usually orally). Extended: formulated to make the drug available over an extended period.
35
3 major processes for drug absorption through the gastrointestinal membrane are:
 Passive Absorption  Active Absorption  Pinocytosis
36
 The transport of a drug by the bloodstream to its site of action.
Distribution
37
Areas of rapid distribution: Areas of slow distribution:
heart, liver, kidneys, brain muscle, skin, fat
38
The biochemical alteration of a drug into an inactive metabolite, a more soluble compound, a more potent active metabolite, or a less active metabolite.
Metabolism
39
Factors that decreased metabolism: 
Cardiovascular dysfunction  Renal insufficiency  Starvation  Obstructive jaundice
40
Factors that increased metabolism: 
Barbiturate Therapy  Rifampin Therapy  Phenytoin Therapy
41
The elimination of drugs from the body.
Excretion Organs: Kidney, Liver, Bowel
42
The time it takes for one half (50%) of the original amount of a drug to be removed from the body.  A measure of the rate at which a drug is removed from the body.
Half life
43
The cellular processes involved in the drug and cell interaction
Drug action
44
 The time it takes for a drug to reach its maximum therapeutic response.
Peak
45
Require that drug products, both prescription and non-prescription, must be pure, effective, and safe.
Federal food, drugs, and cosmetics act of 1938
46
Allows FDA to set good manufacturing practices and mandates regular inspections of production facilities. Transferred to FDA control of prescription drug advertising.
Kefauver-Harris Amendment
47
Monitor, regulate, manufacture and marketing of drugs
1938: Food, Drug, and cosmetic act
48
Established two classes of drugs: RX legend and OTC.
Durham-Humphrey Amendment to the 1938 act
49
Prohibited the sale of misbranded or adulterated food and drugs.
Pure food and Drug Act
50
Federal legislation
2003: Health Insurance Portability and Accountability (HIPAA) 2003: Pediatric Research Equity Act 2007: Food and Drug Administration Amendments Act - mandate post marketing safety studies. 2009: Family Smoking Prevention and Tobacco Control Act - regulate cigarettes by various measures.
51
Components:  Quality, affordable healthcare for all Americans.  Improved quality and efficiency of health care.  Prevention of chronic disease and improved public health.  Improved access to innovative medical therapies.  Community living services and supports.
2010: Patient Protection and Affordable Care Act
52
shorten the time which new drugs could be developed and marketed.
1978: Drug Regulation Reform Act –
53
Negligence  Giving the wrong drug or dose that results in the patient’s death.
Misfeasance
54
Omission of a drug dose that results in the patient’s death.
Nomfeasance
55
Giving correct drug via wrong route.
Malfeasance