Pharm: Basic Principles Flashcards

1
Q

Plasma proteins which bind basic protein

A

Orosomucoid

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2
Q

Excretion of amphetamine is facilitated by acidifying/alkalinizing urine? How about aspirin?

A

Excretion of a weak base such as amphetamine is faster in acidic urine. Excretion faster in weak acid such as ASA in alkaline urine.

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3
Q

Is retinoic acid for acne given as a topical preparation or a transdermal preparation?

A

Topical. Topical route includes application to skin or to mucous memorable of the eye, ear, nose, throat, airway or vagina for local effect. Transdermal route involves application to skin for systemic effect.

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4
Q

This parameter relates the amount of drug in the body to the concentration in the plasma

A

Volume of distribution

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5
Q

The concentrations of these three drugs decrease in a linear fashion over time

A

Zero order kinetics

Ethanol
Phenytoin
Aspirin

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6
Q

Identify which type of antagonism exists.

  1. Pralidoxime + malathion
  2. Secretin + gastrin
  3. Atenolol + dobutamine
A
  1. Chemical
  2. Physiologic
  3. Pharmacologic
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7
Q

T/F. The higher the therapeutic index, the safer the drug

A

True. Therapeutic index is the ratio of the TD50 to the ED50. A safe drug is expected to have a very large toxic dose and a much smaller effective dose.

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8
Q

Most common type of drug receptors in the body

A

G-protein coupled receptors

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9
Q

This describes the time required for the amount of drug in the body or blood to fall by 50%. For drugs eliminated by ____ kinetics, this number is a constant regardless of the concentration.

A

Half-life.

First-order kinetics

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10
Q

A 100 kg man takes in wonder drug X, a drug which is completely retained in the plasma compartment. In this instance, what is the volume of distribution.

A

4L.
Vd is equal to the plasma volume if the drug is completely retained in the plasma compartment. Plasma volume is about 4% of body weight.

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11
Q

What is the formula for half-life

A

(0.693 x Vd) / Cl

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12
Q

Quinacrine is a drug avidly bound in peripheral tissues. Do we expect the Vd of the drug to be greater or lesser than the physical body volume?

A

Greater. Drug would have a low plasma drug concentration.

Vd = (Amount in the body) / (plasma concentration)

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13
Q

How many half-lives of dosing at a constant rate are considered adequate to produce the effect to be expected at steady state?

A

3 - 4 half lives

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14
Q

What is the formula for maintenance dose? Loading dose?

A

Maintenance dose =
( Cl x desired concentration ) /
Bioavailability

Loading dose formula as above but change Cl to Vd

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15
Q

T/F. The therapeutic window is the safe range between the maximum therapeutic concentration and the minimum toxic concentration.

A

F. It is the difference between the MINIMUM therapeutic and toxic concentrations.

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16
Q

Inducers of CYP3A4 enzymes

A
Phenytoin
Carbamazepine
Corticosteroids
Efavirenz
Pioglitazone
Rifampin
Barbiturates
17
Q

Inhibitors of CYP3A4

A
Amiodarone
Azoles
Cimetidine
Clarithromycin
Cyclosporine
Erythromycin
FQs
Grapefruit
Protease inhibitors
Metronidazole
Quinine
Tacrolimus
SSRI
18
Q

Amine drugs that undergo N-acetylation

A

HIP
Hydralazine
Isoniazid
Procainamide

19
Q

Inhibitors of intestinal P-glycoprotein

A

Verapamil
Grapefruit
Mibefradil

20
Q

Drugs normally expelled by intestinal p-glycoprotein

A

Digoxin
Cyclosporine
Saquinavir

21
Q

In vivo test for mutagenicity? In vitro?

A

Ames test is an in vitro test; dominant lethal test is an in vivo test.

22
Q

Identify which phase of the clinical trial is described.

  1. Involves 100-200 patients with the disease in question.
  2. Determines whether the agent has the desired efficacy
  3. Pharmacokinetics of the drug is studied
  4. Rare toxicities hopefully identified
  5. Study benefits and toxicities of the drug under conditions of proposed clinical use
A
  1. Phase 2
  2. Phase 2
  3. Phase 1
  4. Phase 4
  5. Phase 3
23
Q

A few drugs are enzymes themselves like ___ which metabolizes uric acid

A

Pegloticase