7 -Meds and Pharm Flashcards

(65 cards)

1
Q

Do not pass through liver (no 1st pass metabolism)

A

Sublingual and rectal drugs

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2
Q

Absorption based on lipid solubility through epidermis

A

Skin absorption

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3
Q

Absorption restricted to non-ionized lipid-soluble drugs

A

CSF absorption

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4
Q

Largely responsible for binding drugs

A

Albumin

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5
Q

Drugs that will displace unconjugated bili from albumin in newborns

A

Sulfonamides (Bactrim, Sulfasalazine)

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6
Q

Causes kernicterus (brain damage) in newborns

A

Sulfonamides (Bactrim, Sulfasalazine)

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7
Q

Drug types (2) stored in bone

A

Tetracycline and Heavy metals

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8
Q

Constant amount of drug eliminated regardless of dose

A

0 (zero) order kinetics

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9
Q

Drug amount eliminated proportional to dose

A

1st order kinetics

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10
Q

Time for a drug to reach steady state

A

5 half lives

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11
Q

Amount of drug in body divided by amount in plasma/blood

A

Volume of Distribution

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12
Q

Drugs with high volume of distribution have higher concentrations in extravascular or intravascular compartment?

A

Extravascular (eg fat tissue)

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13
Q

Fraction of unchanged drug reaching systemic circulation known as

A

Bioavailabilityq

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14
Q

Drug level at which desired effect occurs in 50% of pts

A

ED50

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15
Q

Drug level at which death occurs in 50% of pts

A

LD50

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16
Q

Decline in potency with continued use

A

Tolerance

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17
Q

Effect at an unusually low dose

A

Hyperactive

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18
Q

Tolerance after only a few doses

A

Tachyphylaxis

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19
Q

Dose required for effect

A

Potency

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20
Q

Ability to achieve results without untoward effect

A

Efficacy

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21
Q

Responsible for drug metabolism

A

Smooth ER (Liver), P450 system

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22
Q

Demethylation, oxidation, reduction, hydrolysis metabolism phase

A

Phase 1

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23
Q

Metabolism Phase for glucuronic acid and sulfate attached to for water-soluble metabolite

A

Phase 2

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24
Q

Product of phase 2 metabolism that’s usually inactive and ready for excretion

A

water-soluble metabolite

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25
INHIBITORS of P450
``` MAMA bit (inhibit) VICK'S FACE MAOIs Amiodarone Metronidazole Alcohol (acute/binge-drinking) ``` ``` Verapamil Isonaizid Cimetidine Ketonzaole 'Sulfonamides ``` Flagyl Allopurinol Ciprofloxacin Erythromycin
26
INDUCERS of P450
``` CRAP GPS induces WAR Carbamazepines Rifampin Alcohol (Chronic) Phenytoin ``` Green and leafy veggies Phenobarb Smoking WARfarin
27
Most important organ for eliminating most drugs
Kidneys
28
How do the kidneys eliminate most drugs (2 ways)
Glomerular filtration | Tubular secretion
29
Water soluble drugs, more likely to be eliminated unaltered
Polar/Ionized Drugs
30
Fat soluble drugs, more likely to be metabolized before excretion
Nonpolar/Non-ionized Drugs
31
Negatively birefringent crystals that cause gout; End production of PURINE metabolism
Uric Acid
32
Gout affecting big toe joint
Podagra
33
Anti-inflammatory gout drug; binds TUBULIN and inhibit chemotaxis of WBCs
Colchicine
34
NSAID gout drug; inhibits prostaglandin synthesis (reversible COX)
Indomethacin
35
Xanthine oxidase inhibitor gout drug; blocks xanthine from forming uric acid
Allopurinol
36
Gout drug increasing renal secretion of uric acid
Probenecid
37
Gout drugs (4) and which for acute, which for chronic
``` I CAP the AC Indomethacin Colchicine Allopurinol Probenecid ``` Acute - Colchicine Chronic - Allopurinol
38
Binds bile acids in gut forcing body to resynthesize bile acids from cholesterol; can bind vitamin K, causing bleeding tendency
Cholestyramine
39
Lipid lowering drug that can cause liver dysfunction and rhabdo
HMG-CoA reductase inhibitors (Statins)
40
Lipid lowering drug that can cause flushing (Tx with ASA); inhibits cholesterol synthesis
Niacin
41
Prokinetic GI drug that inhibits dopamine receptors; increase gastric and gut motility
Metoclopramide (Reglan)
42
Prokinetic GI drug that binds and activates motolin receptor
Erythromycin
43
Prokinetic GI drug that acts as ANTAgonist to mu-opioid receptor
Alvimopan
44
GI drug that slows gut motility; AGONIST to mu-opioid receptor
Loperamide
45
GI drug that slows gut motility; AGONIST to opioid receptor and inhibits muscarinic receptors
Lomotil (Atropine/Diphenoxylate)
46
Antiemetic GI drug that inhibits dopamine receptors
Promethazine (phenergan)
47
Antiemetic GI drug that acts centrally to inhibit serotonin receptors
Ondansetron (zofran)
48
GI drug that is proton pump inhibitor; blocks H/K ATPase in stomach PARIETAL CELLS
Omeprazole
49
GI drug that blocks H2 receptors; decrease stomach acid
Cimetidine/Ranitidine
50
GI drug that acts as somatostatin analogue; decrease gut secretions
Octreotide
51
Cardiac drug that inhibits Na/K ATPase; increase myocardial Ca
Digoxin
52
Cardiac drug that is inotrope, slows AV conduction and NOT cleared with dialysis
Digoxin
53
Side effects of amiodarone (3)
Pulmonary fibrosis Hypothyroidism Hyperthyroidism
54
Used to treat torsades
Magnesium
55
Cardiac drug that causes transient interruption of AV node
Adenosine
56
Cardiac drug shown to be best single agent to improve survival in pts with CHF and prevent CHF after MI
ACE inhibitor
57
Cardiac drug that can prevent progression of renal dysfunction in pts with DM and HTN
ACE inhibitor
58
Cardiac drug shown to be best single agent to improve survival after MI
Beta-Blockers
59
Cardiac drug that is an acetylcholine antagonist, INCREASES heart rate
Atropine
60
Analogue of GnRH and LHRH
Leuprolide
61
Alpha-adrenergic receptor antagonist; BPH
Tamsulosin
62
PGE1 derivative; protective prostaglandin used to prevent peptic ulcer disease
misoprostol
63
Antipsychotic, inhibits dopamine receptors
Haldol
64
Most common side effect of iodine contrast
Nausea
65
ASA poisoning causes what metabolic conditions (2, it switches)
1st - respiratory alkalosis | 2nd - metabolic acidosis