Ch. 1 - Drug Action Flashcards

1
Q

Drug

A

any chemical substance that affects living systems by changing their structure or function

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

3 phases of drug action:

A
  1. ) Pharmaceutic phase
  2. ) Pharmacokinetic phase
  3. ) Pharmacodynamic phase
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

**Pharma(ceutic) phase****

A

(Dissolution)

  • Solid form: needs to disintegrate
    * Tablet > disintegration > dissolution
  • Liquid form
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Pharma(ceutic) phase: Enteric Coated

A
RESIST disintegration in STOMACH
-------------------------------------------------------------
DISINTEGRATES in the SMALL INTESTINE 
\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_\_
should NOT be crushed
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Pharma(ceutic) phase cont…

A

Food in GI tract:

 * may interfere 
 * may enhance
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

**Pharmaco(kinetic )Phase*****

A
  • kinetic* = means ‘movement’
  • process of drug movement to achieve drug action
    1. ) Absorption
    2. ) Distribution
    3. ) Metabolism (biotransformation)
    4. ) Excretion (elimination)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Pharmaco(kinetic )Phase: Absorption

A

Gastric absorption influnced by:
*food, gastric pH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Absorption cont.

A

bioavailability (subcategory)

  * % of drug dose that reaches the system       circulation 
  * Ex: taking it orally compared to intravenously
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Pharmaco(kinetic )Phase: (1) Distribution

A

drug becomes available to body fluids and body tissues

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Distribution (2)

A

Drug enters bloodstream –> rapidly carried to organs with blood supply

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Distribution (3)

A

Influenced by:

- blood flow
- drug's affinity to the tissue
- protein-binding effect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Pharmaco(kinetic )Phase: Protein-binding Effect

A
  • portion of the drug that is bound (to protein):
    * inactive (not available to receptors)
  • Unbound portion:
    * free (active) = pharmacologic effect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

3.) Metabolism (biotransformation):

A

IF NOT water soluble = biotransformation occurs to convert to a more water soluble form

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Metabolism (biotransformation): cont..

A

Age, hepatic disease = slow down ability
———————————————————-
Liver = primary source of metabolism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Half-Life:

A

-time it takes for 1/2 of drug to be eliminated from body
(Ex:)
Half-life: 4 hrs
{Every 4 hr interval drug conc. decreases 50%}
*Initial (8am) = 100% (500mg)
*After 4 hrs = 50% (250mg)
*After 8 hrs = 25% (125mg)
*After 12 hrs = 12.5% (62.5mg)
*After 16hrs = 6.25% (31.25mg)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

4.) Excretion (Elimination):

A

Kidney function affected by:
*age, kidney disease

17
Q

Pharmacodynamic phase**

A

drug concentration & its effects on the body

*Mechanism of action

18
Q

Drug Response: Primary or Secondary

A

diphenhydramine (Benadryl)

  • Primary effect:
    - treat symptoms of allergy
  • Secondary effect:
    - CNS depression –> drowsiness
19
Q

Onset:

A

time it takes to reach minimum effective concentration (occur)

20
Q

Peak:

A

drug reaches its highest blood concentration (level)

21
Q

Duration:

A

length of time drug has a pharmacologic effect

22
Q

Receptor Theory:

A
  • drugs most commonly form a chemical bond with specific receptors in the body
    * lock & key relationship
23
Q

Agonist:

A

interacts with receptor to produce a response

24
Q

Antagonist:

A

inhibits or prevents action of an agonist or blocks a response

25
Q

Therapeutic Range (Window):

A

Low Therapeutic Index (TI) = narrow margin of safety
———————————————————
High TI = wide margin of safety

26
Q

Peak level:

A

highest plasma concentration at a specific time —-(measures rate of absorption)

27
Q

Trough level:

A

lowest plasma concentration (measures rate of excretion)

28
Q

Loading Dose:

A

Large initial first dose when an immediate drug response is desired
**Ex: Z-pack = take 2 doses first day, then 1 dose after that

29
Q

Side effects:

A

acts on other tissues besides specific intended issue

30
Q

Adverse effects:

A

unpredictable (idiosyncratic) adverse effects
-allergic hypersensitivity d/t individuals immune system
————————————————————–
Severe allergic reaction > anaphylaxis > resp./circ. collapse > death

31
Q

Toxicity

A
  • ALL drugs are able to be toxic if dosage is high enough*

- related to dosage

32
Q

Teratogenic Effect:

A

congenital defect in fetus whose mom took drug during pregnancy

33
Q

Drug Tolerance:

A

resistance to effect of drug

-need higher dosage/frequency to produce desired effect

34
Q

Placebo Effect:

A

Psychological benefit from taking a chemical compound

- Persons feels that the pill will make them feel better