pharma Flashcards

1
Q

traditional drug definition

A
  • any substance that alters the physiology of the body
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2
Q

contemporary drug definition

A
  • any substance that alters the physiology of the body
  • NOT food
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3
Q

user intention for drugs

A
  • the intent on the usage matters
  • food is to fuel the body
  • drugs alter the body
  • this causes a grey area on the definition of drugs
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4
Q

the 4 names of drugs

A
  • chem
  • generic
  • trade
  • street
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5
Q

can intoxicating effects go up and down

A

yes

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6
Q

tolerance

A
  • tolerance to specific drug effects or events
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7
Q

primary v. secondary effects

A
  • prim: the main side effect
  • sec: other side effects from the drug
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8
Q

drug dosages

A
  • mg/kg
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9
Q

therapeutic index, ED, LD

A
  • TI = LD/ED
  • ED: effect dose (how much u give to see the effect)
  • LD: lethal dose (how much u can give before death)
  • ratio
  • look to see how much someone can get before a lethal dose and if it’s effective
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10
Q

potency

A
  • how much of that drug is needed
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11
Q

effectiveness

A
  • how effective the drug is
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12
Q

drug interactions

A
  • one drug that can cancel, increase, or decrease the effect of another drug
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13
Q

super added interaction

A
  • effects are greater than adding the 2 doses together
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14
Q

antaganizing interactions

A
  • stop or minimizes the effects of the drug
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15
Q

pharmacokinetics

A
  • pharam = relating to drugs
  • kintetic = relating to movement
  • how the drug is absorbed, how it moves around the system, what the body does
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16
Q

how the drug moves through the body

A
  • absorption
  • distribution
  • elimination
17
Q

administration

A
  • parenteral (outside the digestive tract)
  • intravenous (inside the vein)
  • intraperitoneal (within the peritoneal space)
  • intramuscular (in the muscle)
  • subcutaneous (under the skin)
  • inhalation
  • oral
  • dermal
18
Q

peritoneal space

A
  • the fluid filled space in and around organs
19
Q

distribution

A
  • how drugs move throughout the body
20
Q

important factors in distribution

A
  • lipid (fat) solubility (easily absorded and kept longer)
  • ionization (drug carries a charge and has a hard time travelling)
  • distribution to the central nervous system (blood ring barrier prevents non liquid soluable substances)
  • active and passive transport (p = right molecule can just go through, a = drug enters through a transporter)
  • protein binding
  • placental barrier (drugs pass very quickly)
21
Q

elimination

routes

A
  • exhalation
  • sweat
  • urine
  • feces
22
Q

elimination

liver

A
  • converts the drug molecules into another substance
  • 1st pass metabolism = before the drug can have a primary effect, it will be broken down
23
Q

elimination

kidney

A
  • filter the blood and only allow desired substance to remain
  • kidneys maintain the balance between salt and water in your bloodstream
  • nephrons will filter everything out
24
Q

elimination

rate of elimination

A
  • fast = drug isnt in system long
  • slow = drug is in system long
  • the curve of elimination is determined by half life
  • 1st order elimination = downwards curve slope and follows half lives
  • 0 order elimination = removes linearly, in a striaght line that does not follow the half life rule
25
Q

drug metabolism

key factors

A
  • species
  • age
  • gender
  • prior exposure to the drug
  • depression of an enzyme or enzymes
26
Q

can absorption, elimination, and distribution overlap?

27
Q

theraputeutic window

A
  • the point that finds balance between drug effectiveness and minimal side effects