Module 1-1 Flashcards

1
Q

what are the 6 rights of medication administration?

A

right drug, right dose, right time, right route, right patient, right documentation

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2
Q

define drug

A

Any chemical that affects the physiologic

processes of a living organism

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3
Q

define pharmacology

A

study or science of drugs

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4
Q

Chemical name

A

Describes the drug’s chemical composition and

molecular structure

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5
Q

Generic name (nonproprietary name)

A

Name given by the United States Adopted Name
3
Council

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6
Q

Trade name (proprietary name)

A

Brand name, The drug name has a registered trademark; use
of the name is restricted by the drug’s patent owner
(usually the manufacturer)

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7
Q

naming example:

A

chemical: 2-isbuphenyl blah blah
generic name: ibuprofen
trade name: Motrin

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8
Q

Pharmaceutics

A

The study of how various drug forms
influence pharmacokinetic and
pharmacodynamic activities

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9
Q

Pharmacokinetics

A
The study of what the body does to the drug
 Absorption
 Distribution
 Metabolism
 Excretion
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10
Q

Pharmacodynamics

A

The study of what the drug does to the body The mechanism of drug actions in living tissues

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11
Q

Pharmacotherapeutics

A

The use of drugs and the clinical indications

for drugs to prevent and treat diseases

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12
Q

Pharmacognosy

A

The study of natural (plant and animal) drug

sources ie. opium plant

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13
Q

drug abosorption-fastest to slowest

A

liquids elixirs and syrups, then suspension solutions, powders, capsules, tablets, coated tablets, enteric-coated tablets

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14
Q

Pharmacokinetics: Absorption

A

The rate at which a drug leaves its site of
administration, and the extent to which
absorption occurs. Includes bioavailability and bioequivalency

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15
Q

bioavailability

A

the percent of administered dose of unchanged drug that reaches systemic circulation. Impeded by complete absorption and first pass effect

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16
Q

bioequivalency

A

when two different formulations may have comparable bioavailability

17
Q

Factors That Affect Absorption

A

Absorption characteristics vary according to
the dosage form and route:
Food or fluids administered with the drug
Dosage formulation 
Status of the absorptive surface
Rate of blood flow to the small intestine
Acidity of the stomach
Status of GI motility

18
Q

Routes

A

A drug’s route of administration affects the
rate and extent of absorption of that drug Enteral (GI tract) - easy cheap
Parenteral - fastest
Topical - slower, longer duration, more localized

19
Q

Enteral route

A
The drug is absorbed into the systemic
circulation through the oral or gastric mucosa
or the small intestine
 Oral
 Sublingual
 Buccal
 Rectal
20
Q

First-Pass Effect

A

The metabolism of a drug and its passage
from the liver into the circulation
 A drug given via the oral route may be extensively metabolized by the liver before reaching the systemic circulation (high first-pass effect)
 The same drug—given IV—bypasses the liver, preventing the first-pass effect from taking place, and more drug reaches the circulation

21
Q

Parenteral Route

A
Intravenous (fastest delivery into the blood
circulation)
 Intramuscular
 Subcutaneous
 Intradermal
 Intraarterial
 Intrathecal - into spinal column
 Intraarticular - into a joint
22
Q

Topical Route

A
 Skin (including transdermal patches)
 Eyes
 Ears
     Nose
 Lungs (inhalation)
 Rectum - half has first pass effect has does not
 Vagina
23
Q

Distribution

A

The transport of a drug in the body by the
bloodstream to its site of action
 Protein-binding
 Water soluble vs. fat soluble - if lipid soluble it will penetrate cell membranes easier
 Blood-brain barrier - small lipid soluble get through easier
 Areas of rapid distribution: heart, liver,
kidneys, brain
 Areas of slow distribution: muscle, skin, fat

24
Q

Metabolism/Biotransformation

A
The biochemical transformation of a drug into
an inactive metabolite, a more soluble
compound, or a more potent metabolite
 Liver (main organ)
 Skeletal muscle
 Kidneys
 Lungs
 Plasma
 Intestinal mucosa
25
Q

Metabolism/Biotransformation

A

Biologic transformation of a drug into:
An inactive metabolite
 A more soluble compound
 A more potent metabolite

26
Q

Factors that decrease metabolism

A

Cardiovascular dysfunction
Renal insufficiency
 Starvation
 Obstructive jaundice - blockage in bile duct
 Slow acetylator
 Erythromycin or ketoconazole drug therapy- inhibit enzymes

27
Q

Factors that increase metabolism

A

Fast acetylator- genetically determined
Barbiturate therapy - phenylbarbitol
Rifampin therapy

28
Q

Delaying drug metabolism causes:

A

Accumulation of drugs
Prolonged action of the drugs ->drug toxicity, higher blood levels for longer periods of time
Stimulating drug metabolism causes:
Diminished pharmacologic effects

29
Q

Excretion

A

The elimination of drugs from the body
Metabolize drugs to make them more polar to be able to get rid of them
 Kidneys (main organ)
 Liver
 Bowel
 Biliary excretion
 Enterohepatic recirculation - break it down and it gets reabsorbed

30
Q
Half-life effectively removed after about 5 half-lives
1 half-life - 50% removed
2 half-lives - 75% removed
3 half-lives - 87.5% removed
4 half-lives - 93.75% removed
5 half-lives - 97% removed
A
The time it takes for one half 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
Most drugs considered to be effectively
removed after about five half-lives
Steady state - amount of drug removed via elimination = to amount absorbed. That is when the drug is at steady state, after about 4 to 5 half-lives
31
Q

Onset, Peak, and Duration

A

Onset
The time it takes for the drug to elicit a
therapeutic response
Peak
The time it takes for a drug to reach its
maximum therapeutic response
Duration
The time a drug concentration is sufficient to
elicit a therapeutic response

32
Q

Therapeutic Drug Monitoring

A

Peak level
Highest blood level- too high causes toxicity
Trough level (nadir)
Lowest blood level - too low inefficient

33
Q

Pharmacodynamics:

Mechanisms of Action

A

Receptor interactions
 Enzyme interactions
 Nonselective interactions

34
Q

Pharmacotherapeutics:

Types of Therapies

A

Acute therapy-short term, antibacterial cure
 Maintenance therapy- hypertension or schitzo
 Supplemental/replacement therapy- insulin
 Palliative therapy- make someone comfortable in terminal in terminal state opiods
 Supportive therapy-fluids and electrolytes ex. flu
 Prophylactic therapy-to prevent something ex. antibiotics prior to surgery or traveling
 Empiric therapy- clinical probability therapy antibiotic based on signs and symptoms

35
Q

Contraindications

A

Any characteristic of the patient, especially a disease state, that makes the use of a given medication dangerous for the patient. Liver damage, kidney disease
It is important to assess for contraindications!

36
Q

Monitoring

A

Therapeutic index
 Ratio of a drug’s toxic level to the level that
provides therapeutic benefits
Tolerance
 Decreasing response to repeated drug doses-
Dependence
 Physiologic or psychological need for a drug

37
Q

Monitoring (cont’d)

A

Interactions may occur with other drugs or food
 A drug interaction is the alteration of a drug’s action by:
 Other prescribed drugs
 Over-the-counter medications
 Herbal therapies

38
Q

Monitoring (cont’d)

A

Drug interactions
 Additive- 1+1=2
 Synergistic-1+1=3 diaretic and aceinhibitor
 Potentiation-one of the drugs does not have an effect
 Antagonistic- tetracycline and antacid
 Incompatibility- drugs cannot be mixed in an iv

39
Q

Drug Sources

A
Four main sources for drugs
 Plants- caffeine from coffee, nicotine from tobacco
 Animals- insulin, heparin, hormones
 Minerals- sodium chloride, 
 Laboratory synthesis- most drugs,