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

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Olanzapine

dosage of, 425t

metabolism of, 433t

pharmacokinetics of, 1869t

potencies at neurotransmitter

receptors, 427t

for pruritus, 1828t

side effects of, 425t

Olfactory bulb, beta adrenergic

receptors in, 204t

Olfactory nucleus, beta adrenergic

receptors in, 204t

Olmesartan

as antihypertensive agent, 774t,

785–786

pharmacokinetics of, 1870t

Olmesartan medoxomil, 745

Olmessartan medoxomil, structure of,

737f

Olopatadine hydrochloride,

921t, 922

for ophthalmic use, 1789

Olsalazine, structure of, 977f

Omapatrilat, 932

Omeprazole

CYP2C19 and, 157

esomperazole and, 1802

metabolism of, 128t

pharmacology of, 1311–1312

polymorphisms and response to,

159t

therapeutic uses of

for gastric cytoprotection, 952

for gastroesophageal reflux

disease, 1318t

for ulcers, 1319t

Onchocerciasis, 1447, 1455–1456

Ondansetron, 1341–1343

pharmacokinetics of, 1870t, 1871t

therapeutic uses of, for nausea and

vomiting, in cancer

chemotherapy, 1344t

Online Mendelian Inheritance in Man,

153t

ONTAK (denileukin difitox), 1745,

1750, 1827

Onychomycosis, 1818

therapy for, 1816t

OPC-21268, 715t

OPC-31260, 716t

OPC-41061, 716t

OPC-51803, 709t, 717

Ophthalmia neonatorum, prophylaxis,

1781t

Opioid antagonists, 513–515

Opioid antidote, 86t

Opioid receptor antagonists, for

pruritus, 1828t

Opioid receptors, 486–490

delta, 485t

kappa, 485t

mu, 485t

Opioids

abuse and addiction, 523, 658–661

actions and selectivities of, 485t

analgesia due to, 491

mechanism and sites, 492–493

antidiuretic hormone and, 495

biliary tract and, 498

bladder and, 498

cardiovascular system and, 496–497

for chronic pain, guidelines for, 520t

comibination therapy, 521–522

constipation with, 1335

cough with, 496

for diarrhea, 1337

dosage of, 519

for dyspnea, 522–523

effect profile, 491–498

endogenous, 484, 485t–486t

esophagus and, 497

gastrointestinal tract and, 497

growth hormone and, 495

immune system and, 498

inhalation of, 518

intestine and, 497

miosis and, 495

mood alterations and rewarding

properties of, 493–494

nauseant and emetic effects, 496

nerve injury and, 491

neuroendocrine effects with,

495–496

non-analgesic therapeutic uses of,

522–523

oxytocin and, 495

prolactin and, 495

rectal administration of, 518

respiration and, 493–494

rotation of, 521

routes of administration, intraspinal

infusion, 500t

sedation with, 494–495

sex hormones and, 495

skin and, 498

stomach and, 497

therapeutic uses of, 518–522

tissue injury and, 491

tolerance, 521

toxicity, 523–524

transnasal administration of, 518

types of, 499

Opioids (Cont.):

uterus and, 498

variables modifying therapeutic

response to, 519–520

and vasopressin secretion, 704

Opioid toxidrome, 83t

Opisthorchis infections, 1449

Oprelvekin, 1075

Optic nerve, 1774, 1776f, 1778

systemic agents affecting, 1792

Optic neuropathy, toxic, agents

causing, 1792

OPTIVAR (azelastine), 922, 1789

ORAGALUTRAN (ganirelix), 1119t

Oral administration, 20–21

Oral bioavailability

of common drugs, 1809t–1890t

hepatic disease and, 1802

as pharmacodynamic parameter, 1802

Oral contraceptives, 1185–1186. See

also Estrogen(s); Progestins

brand names, 1835t–1836t

cancer and, 1187

cardiovascular effects, 1187

combination

adverse effects and side effects of,

1834

biphasic, 1833

brand names, 1835t

formulations, 1835t

contraindications to, 1834

estrophasic

brand names, 1836t

formulations, 1836t

extended-cycle, 1833

brand names, 1836t

formulations, 1836t

monophasic, 1833

brand names, 1835t

formulations, 1835t

one-year failure rate, 1834t

therapeutic uses of, 1834

triphasic, 1833

brand names, 1835t

formulations, 1835t

and dyslipidemia, 890t

for endometriosis, 1840

formulations, 1835t–1836t

for hirsutism, 1840

mechanism of action, 1186

metabolic effects, 1187–1188

polymorphisms and response to,

161t

progestin-only, 1836

brand names, 1836t

formulations, 1836t

2055

INDEX

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