test 1 Flashcards

(40 cards)

1
Q

Chemical name

A

– chemical structure of drug

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2
Q

Generic name

A

– nonproprietary name

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3
Q

Trade/Brand name

A

– name owned and marketed by a pharmaceutical company

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4
Q

Contraindications

A

Contains warnings as to particular patients or situations in which the drug should not be used

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5
Q

Drug Interactions

A
  • Modification of the effect of a drug when given with another drug
  • Results in either a decrease or increase in the action of the drug
  • Beneficial (Drug combination therapy)
  • Harmful (Adverse side effects)
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6
Q

Three Types of Drug Interactions

A
  • Additive interactions
  • Synergistic interactions
  • Potentiation interactions
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7
Q

Additive Drug Interactions

A

-sum of the effects of two drugs given together is equal to each of them given separately but at the same time

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8
Q

Synergistic Drug Interactions

A

-summation of each individual drug’s activity exceeds the sum of the two individual drugs

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9
Q

Potentiation Drug Interactions

A

-One drug (which has no direct effect) increases the response of the other drug, which normally has a lesser effect

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10
Q

Adverse Drug Reactions (ADR)

A

•Unintended side effects from a drug
•At least 5% of hospitalizations are the result of an adverse drug reaction
– tremors, bronchospasms, headaches, vomiting, photosensitivity etc.
•Not all ADRs are allergies

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11
Q

Drug Allergy

A
  • Drug allergies are immune-mediated and induce a hypersensitivity reaction (Mild-hives, Severe-anaphylactic shock)
  • Drug allergies are only one example of an ADR
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12
Q

Pharmacokinetics

A
  • what the body does to a drug

- Absorption, distribution, metabolism, and elimination

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13
Q

Pharmacodynamics

A

-what the drug does to

the body

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14
Q

Absorption

A

How a drug moves from its site(s) of administration into plasma

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15
Q

absorption of the drug is based on

A
  • size of the drug (smaller the easier)
  • ionization of the drug (non-ionized pass through membrane easier)
  • lipid solubility (lipophilic easier to pass through than hydrophilic)
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16
Q

Distribution (pharmacokinetics)

A

-The dissemination of a drug throughout the body, such as plasma, tissues, or organs
•Bloodstream is the major vehicle for distribution

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17
Q

Distribution Influenced by

A
  • Blood flow
  • Fat or water solubility
  • Protein binding
18
Q

Metabolism (pharmacokinetics)

A

-The biotransformation of a drug into other secondary components called metabolites
•Preparing drug for elimination
•Drug becomes more water soluble to enhance elimination

19
Q

Elimination (pharmacokinetics)

A
  • The processes that remove a drug from the body in urine, bile, or feces
  • Drugs can also be excreted via the pulmonary system, skin, hair, saliva, and expired air
20
Q

routes of administration determined by

A
  • Determined by property of drug (Water or lipid soluble, Ionization)
  • Desirability of a rapid onset
  • Need for long-term treatment
  • Restriction of delivery to a local site
21
Q

Enteral (through digestive tract) Administration

A
  • Administering drug by mouth (Swallowed, Under tongue (sublingual), Between gums and cheek (buccal))
  • Most common
  • Most convenient
  • Most economical
  • Safest
22
Q

Oral Administration

A
•Easily self administered
•Toxicities/overdoses may be overcome with
antidotes
•Low gastric pH inactivates some drugs
•MOST COMPLICATED DRUG ABSORPTION ROUTE
23
Q

Oral Preparations: Enteric coated

A
  • Chemical coating that protects drug from stomach acid
  • Drug dissolves in the intestine (less acidic)
  • Useful for drugs that are acid unstable
24
Q

Extended-Release Preparations

A
  • Drugs contain special coatings or ingredients that control drug release
  • Allows slow absorption
  • Prolonged duration of action
  • Can be dosed less frequently
  • Improves patient compliance
  • Useful for drugs with short half-lives
25
Sublingual/Buccal Administration
•Drug diffused directly into systemic circulation
26
Sublingual/Buccal Administration advantages
* Bypasses gastrointestinal (GI) environment * Ease of administration * Rapid absorption
27
Parenteral Administration
•Drug introduced directly into systemic circulation
28
Parenteral Administration advantages
* Useful for drugs poorly absorbed by GI tract * Useful for patients unable to take oral medications * Circumstances that require rapid onset of action * Highest drug bioavailability * Avoids harsh GI environment * Most control over drug dosage
29
Parenteral Administration Disadvantages
* Irreversible * Causes pain and fear * Local tissue damage * Potential for infections
30
Routes of Administration (Parenteral)
* Intravenous (IV) * Intramuscular (IM) * Subcutaneous (SC)
31
Intravenous (IV)
* Administration into a vein * Most common parenteral route * For drugs not absorbed orally * Rapid effect * Maximum control of drug dose
32
Intravenous (IV) Disadvantages
* Potential for infection * Hemolysis * No drug recall * Cause adverse drug reaction
33
Intramuscular (IM)
``` •Administration into a muscle •Aqueous solutions -Absorbed rapidly •Specialized depot preparations -Suspension of drug in nonaqueous vehicle (polyethylene glycol) -Absorbed slowly ```
34
Subcutaneous (SC)
``` •Administration in the subcutaneous tissue of the skin •Absorption via diffusion •Slower drug onset than IV route •Provides constant, slow, sustained effects ```
35
Oral/Nasal Inhalation
* Administration via the airways and lungs * Rapid delivery of drug * Gases and aerosolized drugs * Convenient for patients with respiratory disorders * Direct drug delivery to site of action
36
Intrathecal/Intraventricular
* Administration directly into cerebrospinal fluid * Rapid delivery of drug * Needed to bypass blood-brain barrier
37
Topical
* Administration of drug to the skin | * Used when desire a local effect
38
Transdermal
``` •Administration of drug via the skin •Achieves systemic circulation of drug •Rate of absorption -Skin -Lipid solubility of drug •Sustained delivery of drug ```
39
Rectal
* Administration via the rectum * Prevents destruction of drug by stomach acid * Ideal if drug causes vomiting
40
Rectal Disadvantages
* Drug absorption is erratic and variable * Irritate rectum * Not a well accepted route