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DƯỢC LÍ Goodman & Gilman's The Pharmacological Basis of Therapeutics 12th, 2010

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2012

INDEX

Churg-Strauss angiitis,

cyclophosphamide for,

1821

Chylomicronemia, drugs for, fibric

acid derivatives, 902

Chylomicron remnants, 879t, 881–882,

881f

Chylomicrons, 878–881, 879t

metabolism, 881f

CIALIS (tadalafil), 758–759, 1792

Cicatricial pemphigoid

dapsone for, 1823

mycophenolate mofetil for, 1823

Cicatricial pemphigopid,

cyclophosphamide for, 1821

Ciclopirox olamine, 1588

Ciclopirox topical, for onychomycosis,

1818

Cidofovir, 1596t, 1600–1601

for cutaneous viral infections, 1818

pharmacokinetics of, 1824t

Cilastatin, pharmacokinetics

of, 1851t

Ciliary body, 1774, 1776, 1776f

Ciliary ganglion, 173f

Cilostozol, 771–772

Cimetidine, 918

drug interactions with, 845

intravenous doses of, 1313t

metabolism of, 128t

for methemoglobinemia with

dapsone, 1824

pharmacokinetics of, 1816t

therapeutic uses of

for gastroesophageal reflux

disease, 1318t

for ulcers, 1319t

Cimex, 1818

Cinacalcet, 1297–1298, 1297f

pharmacokinetics of, 1825t

Cinchonism, 844

Cinnamates, 1827

Ciprofibrate

chemistry of, 901

and lipoproteins, 902

mechanism of action of, 902

structure of, 901f

Ciprofloxacin

for chancroid, 1842t

pharmacokinetics of, 1825t

SLC transporters and, 102t

therapeutic uses of, for

inflammatory bowel disease,

1352t

Ciproxifan, 925

Circulation

carbon dioxide and, 562

muscarinic antagonists and, 228

Cisapride, 1326–1327

arrhythmias caused by, 832

effects on bowel function, 1330t

polymorphisms and response to,

161t

therapeutic toxicity of, 79–80

Cisatracurium

characteristics of, 264t

dosing of, 265t

structure of, 259f

Cisplatin, 1668t–1670t, 1689

pharmacokinetics of, 1824t

SLC transporters and, 103t

toxicity of, extramedullary, 1682t

Citalopram

arrhythmias caused by, 832

disposition of, 409t

pharmacokinetics of, 1838t

potencies

at human transporters for

monamine neurotransmitters,

406t

at neurotransmitter receptors, 410t

nor 1

-Citalopram, potencies at human

transporters for monamine

neurotransmitters, 406t

nor 2

-Citalopram, potencies at human

transporters for monamine

neurotransmitters, 406t

Citrate, 853

c-jun oncogene, 730

CL-385004, 716t

Cladribine, 1668t–1670t, 1703–1704

Cladribine, SLC transporters

and, 102t

CLAFORAN (cefotaxime), 1496t

CLARINEX (desloratadine), 922t, 1816

Clarithromycin

pharmacokinetics of, 1825t

polymorphisms and response to,

161t

CLARITIN (loratadine), 922t, 1816

Classes of drugs, choosing within,

1802

Claudication, treatment of, 771–772

Clearance, 28–30

alterations of, to individual patient,

1806–1807

of common drugs, 1809t–1890t

creatinine, 1803

definition of, 29

hepatic, 29–30

Clearance (Cont.):

plasma, as pharmacodynamic

parameter, 1803–1804

renal, 30

Clemastine fumarate, 921t

CLEOCIN-T (clindamycin), 1817

Clevidipine

as antihypertensive agent, 774t

pharmacology of, 765

Clevudine, 1617

CLIMARA (estradiol), 1839t

CLIMARA PRO (estradiol/levonorgestrel),

1839t

Clindamycin

absorption of, 1535

for bacterial vaginosis, 1842t

distribution of, 1535

excretion of, 1535

gastrointestinal effects of, 1535

for malaria, 1390t

pharmacokinetics of, 1826t

therapeutic uses of, 1535

topical, for acne, 1817

untoward effects of, 1535

Clinical pharmacokinetics, 27–30

Clinical practice, pharmacogenetics in,

164–165

Clinical trials, 78–79

adverse reactions in, 10

conduct of, 7–9

ethical considerations in, 7

phase I, 8t, 9, 79

phase II, 8t, 9, 79

phase III, 8t, 9, 79

phase IV, 8t, 9

surrogate end points in, 9

CLINORIL (sulindac), 985

Clitocybe, 225

Clobazam, structure of, 459t

Clobenpropit, 925

Clobetasol propionate

cream, 1225t

ointment, 1225t

Clofarabine, 1704

Clofazimine, 1559

Clofibrate

adverse effects of, 902–903

chemistry of, 901

history of, 901

hypoglycemia and, 1248t

metabolism of, 128t

and statins, combination therapy

with, 898

structure of, 901f

therapeutic uses of, 903

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