FINAL Flashcards

1
Q

Drug Names

A
  • Chemical: structure
  • Generic: original name for common understanding
  • Trade (brand) Name: assigned by pharmaceutical company
    > fillers/binders differ btwn brand & generic; may alter bioavailability
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1
Q
A
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2
Q

Therapeutic Classification

A
  • Usefulness in treating diseases or disorders
  • Pathology they intend to treat
  • Functional classification (Mosby’s)
  • EX: analgesics, antihypertensives
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3
Q

Pharmacologic Classification

A
  • Physiological effect at molecular/tissue lvl
  • Chemical classification (Mosby’s)
  • EX: calcium channel blocker
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4
Q

Factors Affecting Oral Absorption

A
  • Molecular Weight: too big, can’t pass membrane
  • Lipid Solubility: small & highly lipid soluble drugs rapidly through membrane (passive diffusion)
    > low lipid-soluble drugs: facilitated diffucion, active transport, pinocytosis
  • Surface area of gastrointestinal mucosa
  • Blood flow to gastrointestinal system
  • Rate of gastric emptying
  • Oral prep: disintegratable > liquid > suspension solutions > powders > capsules > tablets > coated tabs > enteric-coated tabs
  • Admin of multiple drugs simultaneously (interaction)
  • Foods & fluids admind w/ drugs
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5
Q

Factors Affecting Distribution

A
  • Blood flow to organs/tissues
    > areas of rapid perfusion/distribution: heart, liver, kidney, brain
    > areas of slow distribution: muscle, skin, fat
  • Ability to cross blood-brain barrier or fetal/placental barrier
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6
Q

Factors Affecting Distribution - Drug Properties

A
  • Protein Binding (albumin)
    > highly protein bound = less available for distribution
  • Water Solubility vs Lipid Solubility
    > highly water-soluble drugs stay in bloodstream; go more places
    > highly lipid-soluble drugs more readily pass lipid cell membranes & deposit in adipose tissue
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7
Q

Factors Influencing Drugs Effects

A
  • Age
  • Gender
    > men: more vascular muscles
    > women: more fat cells; slow release
  • Physiological Factors
    > hydration, acid-base, electrolytes
  • Pathological Factors
    > disorders change conditions for drugs (vascular, GI, liver, kidney disease)
  • Genetic Factors
    > lack enzymes, cultural differeneces
  • Psychological Factors
    > attitude: placebo effect, trust in HCP
  • Envir’t Factors
    > temp, relaxed envir’t
  • Tolerance
    > larger dose needed
  • Interactions
    > 2 or more drugs
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8
Q

Drug-Drug Interactions

alerts effectiveness

A
  • Site of Absorption
    > one drug prevents or accelerates absorp of another drug
  • During distribution/site of action
    > drugs compete for binding site of another; one drug gets bumped off
    > opposing mechanisms of action
    > drugs w/ similar AEs
  • During metabolism
    > 1 drug stims or blocks metabolism of another drug
  • During excretion
    > 1 drug competes for other to be excreted; leads to accumulation/toxicity
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9
Q

Drug-Food Interactions

A
  • Prevent absorp (oral route)
    > incrd acid production; speeds breakdown of drug
    > milk products: calcium binds drug; dcrd absorp
    > chemical reaction (iron binds w/ tetracycline)
  • Incrd or dcr drug’s effect (any route)
    > food affects liver enzyme
    > EX: grapefruit juice affects liver enzymes up to 48hrs after ingested; liver enzyme inhibitor; leads to toxic effects of some drugs
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10
Q

Drug Excretion

A
  • Kidneys are primary organ for excretion of drugs from body
  • Kidney Dysfunction: drugs not excreted effectively; reach toxic lvls
  • Nurse: monitor kidney func to avoid drug toxicity or AKI
  • Liver/bowel are secondary site for excretion
    > drugs processed by liver, released into bile, eliminated in feces
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11
Q

Drug Metabolism

A
  • Liver is primary site
    > hepatic microsomal enzyme system: inactivates/breakdown drug for excretion; some to active form
    > changes in hepatic microsomal enzymes can affect drug metabolism
  • Metabolic activity may be dcrd in some pts
    > infants & elderly, genetic disorders, severe liver disease
    > dosages reduced in dcrd liver func to prevent toxicity
  • Liver transforms some drugs to active form (prodrug)
  • Nurse:
    > liver disease is a caution/contra when adming certain drugs
    > monitor liver funcs to avoid drug toxicity or injury to liver
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12
Q

Enzyme Induction

A
  • Affects metabolism
  • Incrd activity of enzyme system by presence of 1st drug; speeds metabolism of 2nd drug using same enzyme system; cannot reach needed therapeutic lvls
  • Why some drugs cannot be taken together
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13
Q

Enzyme Inhibited

A
  • Affects metabolism
  • Some drugs inhibit enzyme system; make less effective
  • Drugs will not be broken down for excretion
  • Blood lvl of drug incrs to toxic lvl
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14
Q

Anaphylaxis

A
  • Adverse reaction
  • Involves massive systematic response (histamine)
  • Leads to bronchoconstriction, shock, & death
  • CMs:
    > hypotension
    > tachycardia
    > dyspnea
    > edema
    > hives
    > itching
    > resp or cardiac arrest
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15
Q

Agonist Drugs

A

Cholinergic Agonist: mimics acetylcholine
> cause same acitivity of natural chemicals would cause at tht site
- Incrs saliva production
- Slows HR
- Constricts bronchioles
- Stimulates digestive process
- Incrs urination

16
Q
A