Chapter 1-6 textbook Flashcards

1
Q

Vd formula

A

Amount in body/plasma drug concentration

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

Clearance formula

A

0.693(Vd)/half life

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

Water weight at birth

A

75-80%

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

Infant’s stomach pH

A

alkaline: >4

Decreased absorption of weakly acidic drugs and increased absorption of weakly basic drugs

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

Gastric emptying in infants

A

Prolonged

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

Percutaneous administration of meds in infants

A

Increased absorption due to decreased thickness of skin

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Pulmonary absorption in infants

A

Decreased due to lower tidal volumes and increased respiratory rates

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

Volume of distribution in infants

A

Increased due to increased total body water

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Metabolism in infants

A

Delayed–can cause increase in toxicities

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

Physiologic changes in pregnancy

A

Increased blood volume, increased CO, decreased systemic vascular resistance, increased pH of intestinal secretions, increased gastric emptying time, decreased gastric acid secretions, decreased intestinal motility, increased renal blood flow, increased GFR, increased uterine blood flow

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

Progesterone effects on GI

A

Decreased GI motility–delays absorption or orally administered drugs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Which drugs are more likely to cross placenta

A

Lipid soluble, nonionized, lower molecular weight, unbound and free drugs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

pharmacokinetic changes in elderly

A

Decreased blood flow to GI, increased gastric pH, delayed gastric emptying, decreased albumin and lean body mass, increased total body fat and decreased total body water, decreased liver blood flow and enzymes, decreased GFR and secretion

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

Pharmacokinetics

A

how the drug moves through the body

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

4 parts of pharmacokinetics

A

Absorption, distribution, biotransformation (metabolism), excretion/elimination

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

Bioavailability

A

how much of the drug reaches the site of action

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

F value

A

The fraction of the drug that reaches the systemic circulation
Depends on first pass metabolism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What routes will bypass first pass metabolism

A

IV and sublingual

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

Bioequivalent

A

Contains same active ingredient
Identical in strength, dosage, and route of administration
Same rate and extent of biovailability

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

Factors influencing absorption

A

Formulation, concentration, lipophillic, acidic vs basic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Distribution

A

Transport of drug in body fluid from site of absorption

Delivery of drug to various tissue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Factors to consider in distribution

A

Plasma protein binding, obesity, edema, tissue binding

Drug’s affinity for certain tissues

23
Q

What portion of drug is available to exert effects

A

Free drug–not protein bound

Someone with liver disease and decreased albumin will have less protein binding and can have more toxic levels of drug

24
Q

Biotransformation

A

Chemical inactivation of a drug through conversion to a water soluble compound that can be excreted

25
2 major organs of excretion
Liver and kidney (also fecal, respiration and breastmilk) | Kidney greater--depends on GFR which depends on cardiac and kidney function
26
Pharmacodynamics
How the drug affects the body
27
High affinity drug
Agonist
28
Low affinity drug
Antagonist
29
First order kinetics
If you give a drug, the same amount of drug will be eliminated over time depending on half life
30
Zero order kinetics
You excrete a constant amount of drug no matter how much you give Causes accumulation and receptor saturation--toxicity
31
Examples of drugs that undergo zero order kinetics
Phenytoin, alcohol, aspirin, dilantin, theophylline
32
Elderly have a decreased sensitivity to
Beta blockers and warfarin/heparin
33
Not recommended to give ____ to elderly due to fall risk
antihistamines
34
When do kidneys reach maturation in children
2 years old | Can reach toxic levels quickly prior to this
35
Metabolism in children
Slower--fewer liver enzymes
36
Examples of drugs that cross placenta easily
Acetaminophen, caffeine, cocaine, labetalol, morphine, penicillins, theophylline
37
Examples of drugs that do not cross placenta easily
Heparin and insulin
38
Category A medications
Studies in women showed no risk to fetus demonstrated in first trimester and no evidence of risk at later trimesters Ex. folic acid and thyroid hormone
39
Category B medications
Animal studies have not shown a fetal risk and no controlled studies have shown an adverse effect in first trimester and no evidence of risk in later trimesters Ex. Erythromycin and penicillin
40
Category C medications
Studies in animals have shown adverse effect on fetus and no controlled studies in women Only give drugs if benefits justifies risk Ex. Labetalol, nifedipine, ACE Inhibitors
41
Category D medications
There is positive evidence of human fetal risk but benefits may be acceptable despite risk Ex. Glyburide, diazepam, aspirin, ACEI
42
Category X medications
Studies in animals or humans have demonstrated fetal abnormalities Drug is contraindicated Ex. oral contraceptives, lovastatin, isotretinoin
43
MEC
Minimum effective concentration
44
MTC
Minimum toxic concentration
45
How to make urine more acidic
Cranberry juice, vitamin c, NH4Cl
46
How to make urine more alkaline
Aspirin
47
Phase 1 of drug metabolism
Modify drug by oxidation, reduction and hydrolytic reactions
48
Phase 2 of drug metabolism
Conjugation of drug molecule with transferase
49
Examples of general inducers of CYP450
``` Anti-seizure drugs (carbamazepine + phenytoin) Rifampin HIV drugs Chronic alcohol Glucocorticoids Barbiturates St Johns Wort ```
50
Therapeutic index
TD/ED
51
Examples of general inhibitors of CYP450
``` Proton pump inhibitors Azoles Macrolides Grapefruit juice SSRI's Acute alcohol Cimetidine Amiodarone Non-dihydropyridine calcium channel blockers Protease inhibitors ```
52
Gs protein
Stimulated protein; activates aneylyl cyclase which increases cAMP
53
Gi protein
Inhibitory; decreases cAMP
54
Gq protein
Activates phospolipase C; Activates DAG + IP3 which increases Ca