Pharmacology Flashcards

1
Q

CYP450 3A4 inhibitors

A

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Sodium valproate
Isoniazid
Cyclosporin
Ketoconazole
Fluconazole
Alcohol
Clarithromycin (NOT Azithro or Roxithro)
Erythromycin
Ciprofloxacin
Omeprazole
Metronidazole

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2
Q

CYP450 3A4 inducers

A

CRAPGPS

Carbamazepine
Rifampicin
Alcohol
Phenytoin
Groselin
Phenybarbital
Sulphonylureas, St John Wart

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3
Q

P-glycoprotein inducers

A

SCRAPS

Steroids (mainly Dexmethasone)
Cyclosporin (is also a substrate and therefore can induce its own excretion), carbamazepine
Rifampicin
Aspirin
Phenytoin, paclitaxal
St Johns Wort

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4
Q

Abs dependent on time dependent Killing

A

Penicillins
Cephalosporins
Macrolides
Carbapenems
Lincosamides (clindamycin etc)

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5
Q

Abs dependent on concentration dependent killing

A

Aminoglycosides (Gentamicin, Tobramycin, Amikacin)

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6
Q

Abs dependent on total exposure

A

Vancomycin

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7
Q

Indapamide MOA

A

“Thiazide-like diuretic” which blocks NaCl at DCT & also has some action to inhibit peripheral vascular smooth muscle tone

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8
Q

Amioloride MOA

A

Blocks ENaC channels at the collecting duct to work in a similar way to Spironolactone (which indirectly blocks aldosterone to inhibit ENaC). Potassium sparing.

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9
Q

Acidic Drugs bind to which plasma protein

A

Albumin (Phenytoin, Digoxin, Warfarin, NSAIDS, Aspirin, Benzos)
Phenytoin will displace Warfarin and increase free Warfarin causing increased bleeding early - later Phenytoin will induce CYP and increase metabolism of Warfarin and effect

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10
Q

Lithium Clearance

A

100% renally cleared

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11
Q

Effect of Urine pH on drug clearance

A

Acidic drugs i.e Aspirin, Methotrexate, will have increased renal clearance in presence of alkali urine as this ionises the drug insist renal reabsorption. Only non-ionised drugs can cross renal membranes to be reabsorbed.
The opposite occurs for basic drugs

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11
Q

Ivabradine MOA

A

Works at the (I)f Na channels (funny-Na channels) in the pacemaker cells to prolong repolarisation and reduce heart rate, improving symptoms of angina

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12
Q

HLA mutation in Han Chinese causing increased allopurinol toxicity

A

HLAB5801

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13
Q

HLA mutation in Han Chinese causing increased carbamazepine toxicity

A

HLAB1502

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14
Q

HLA mutation causing increased hypersensitivity to Abacavir

A

HLAB5701

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15
Q

HLA mutation in Europeans/Japanese causing increased Carbamazepine toxicity

A

HLAB3101

16
Q

HLA mutation causing increased liver toxicity with Flucloxacillin

A

HLAB5701

17
Q

CYP required for Tamoxifen metabolism and interaction

A

CYP2D6 inhibited by SSRI (fluoxetine, Paroxetine) which decreases efficacy

18
Q

CYP involved in Clopdogrel action

A

CYP2C19 - metabolises clopidogrel (prodrug) to its active form. Decreased CYP219 leads to decreased clopidogrel efficacy. Can occur in presence of inhibitors such as omeprazole.

18
Q

CYP involved in Clopdogrel action

A

CYP2C19 - metabolises clopidogrel (prodrug) to its active form. Decreased CYP219 leads to decreased clopidogrel efficacy. Can occur in presence of inhibitors such as omeprazole.

19
Q

Diuretic that inhibits renal K secretion at the distal nephron by mineralocorticoid-independent mechanism

A

Amiloride

20
Q

Albumin bound drugs

A

Acidic drugs;
Aspirin
NSAIDs
Warfarin
Digoxin
Benzos
Phenytoin

21
Q

CYP 2C9

A

Metabolises Warfarin
Inhibited by Omeprazole, Amiodarone, Metronidazole, Cimetidine