Pharmacy Foundations: Drug interactions Flashcards

1
Q

Pharmacodynamics

A

effect or change that a drug has on the body or some other type of organism

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2
Q

pharmacodynamic drug interaction

A

When two or more drugs are given together, and their effects impact each other

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3
Q

Additive effects can be caused when….

A
  1. multiple drugs that are agonists at the same receptor are given together
    ie. 2 opioids given together, side effects (respiratory depression, sedation) can be increased
  2. multiple drugs have similar end effects through different mechanisms
    ie. Benzo = sedating w/ Opioids = sedating too
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4
Q

Synergism is when….

A

two drugs taken in combo have a greater effect than that obtained by simply adding the 2 individual effects

ie. taking Tylenol w/ opioid provides more effect than you’d expect if adding effect of opioid + Tylenol

A + B > A & B

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5
Q

Pharmacokinetics

A

effect or change that body has on a drug

ADME

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6
Q

ADME:

A

Absorption
Distribution
Metabolism
Excretion

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7
Q

Chelation is when….

A

drug binds to polyvalent cations in another compound, and cant be dissolved in gut fluid so will pass in stool

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8
Q

Drugs with polyvalent cations or other binding properties, should be separated from….

A

quinolones
tetracyclines
levothyroxine
oral bisphosphonates

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9
Q

Majority of Pharmacokinetic interactions occur during….

A

metabolism in the liver

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10
Q

CYP450 enzymes primarily expressed in the…

A

Liver

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11
Q

Prodrugs

A

Taken in inactive form, and converted by CYP450 enzymes into active from

can be used to extend dosing interval or prevent abuse

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12
Q

CYP enzyme inhibitors wil…

A

decrease enzyme function and ability to metabolize compounds

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13
Q

If drug is substrate for same CYP enzyme that is affected by an inhibitor then….

A

decreased rate of drug metabolism, leading to increased serum drug level

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14
Q

Common CYP inhibitors: GPACMAN

A

G = Grapefruit
P = protease inhibitors ie ritonavir
A = azole antifungals (fluc,itra,keto,posaco,voriconazole and isavuconazonium)
C = cyclosporine, cobicistate
M = macrolides (no azithromycin, just clarity/eryth)
A = amiodarone ( & dronedarone)
N = Non- DHP CCB (Dilt n Verapamil)

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15
Q

CYP enzyme inducers will…

A

increase enzyme production or activity

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16
Q

If drug is substrate for the same CYP enzyme that is affected by an inducer then….

A

increased rate of drug metabolism, leading to decreased serum drug level

17
Q

Common CYP inducers: PS PORCS

A

P = Phenytoin
S = smoking
P = Phenobarbital
O = Oxcarbazepine
R = Rifampin ( & rifabutin, rifapentine)
C = Carbamazepine (also auto-inducer)
S = St. Johns Wort

18
Q

“Lag” time for Enzyme Inducation

A

Induction often requires additional enzyme production, taking time. Full effect on drug levels not seen for up to 4 weeks, and when inducer stopped then can take 2-4 weeks for inducer effects to disappear

19
Q

P-gp inhibition will cause…..

A

drugs that are substrate of P-gp to have increased absorption and higher drug levelsC

20
Q

Common P-gp substrates

A

Anticoag = apixaban, edoxaban,rivarogaban and dabigatran
Cardiovascular = digoxin, diltiazem, carvedilol, ranolazine, verapamil
Immunosupressants = cyclosporine, sirolimus tacrolimus
HCV drugs = sofosbuvir

Others: colchicine, atazanavir, dolutegravir, posaconazole, raltegravir, saxagliptin

21
Q

Common P-gp inducers

A

Carbamazepine
Dexamethasone
Phenobarb
Phenytoin
rifampin
St. Johns Wort
Tipranavir

22
Q

Common P-gp inhibitors

A

anti-infectives = clarithromycin, itraconazole, posaconazole
Cardiovascular = amiodarone, carvedilol, conivaptan, diltiazem, dronedarone, quinidine, verapamil
HIV = cobicistat, ritonavbir
HCV = ledipasvir

Others = cyclosporine, fibanserin, ticagrelor

23
Q

Where are most drugs absorbed?

A

small intestine, entering portal vein and back to liver

24
Q

Enterohepatic Recycling

A

recycling of an already metabolized drug, which increases the duration of action of many drugs