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DƯỢC LÍ Goodman & Gilman's The Pharmacological Basis of Therapeutics 12th, 2010
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880
SECTION III
MODULATION OF CARDIOVASCULAR FUNCTION
Table 31–2
Apolipoproteins
AVERAGE
CONCENTRATION MOLECULAR SITES OF
APOLIPOPROTEIN (mg/dL) CHROMOSOME MASS (kDa) SYNTHESIS FUNCTIONS
ApoA-I 130 11 ~29 Liver, intestine Structural in HDL; LCAT cofactor;
ligand of ABCA1 receptor; reverse
cholesterol transport
ApoA-II 40 1 ~17 Liver Forms –S–S–complex with apoE-2
and E-3, which inhibits E-2 and E-3
binding to lipoprotein receptors
ApoA-V <1 11 ~40 Liver Modulates triglyceride incorporation
into hepatic VLDL; activates LPL
ApoB-100 85 2 ~513 Liver Structural protein of VLDL,
IDL, LDL; LDL receptor ligand
ApoB-48 Fluctuates according 2 ~241 Intestine Structural protein of chylomicrons
to dietary fat intake
ApoC-I 6 19 ~6.6 Liver LCAT activator; modulates receptor
binding of remnants
ApoC-II 3 19 8.9 Liver Lipoprotein lipase cofactor
ApoC-III 12 11 8.8 Liver Modulates receptor binding of
remnants
ApoE 5 19 34 Liver, brain, Ligand for LDL receptor and receptors
skin, gonads, binding remnants; reverse
spleen
cholesterol transport (HDL with apoE)
Apo(a) Variable (under 6 Variable Liver Modulator of fibrinolysis
genetic control)
apo, apolipoprotein; HDL, high-density lipoproteins; IDL, intermediate-density lipoproteins; LCAT, lecithin:cholesterol acyltransferase; LDL, low-density lipoproteins; LPL, lipoprotein lipase;
VLDL, very-low-density lipoproteins.
880SECTION IIIMODULATION OF CARDIOVASCULAR FUNCTIONTable 31–2ApolipoproteinsAVERAGECONCENTRATION MOLECULAR SITES OFAPOLIPOPROTEIN (mg/dL) CHROMOSOME MASS (kDa) SYNTHESIS FUNCTIONSApoA-I 130 11 ~29 Liver, intestine Structural in HDL; LCAT cofactor;ligand of ABCA1 receptor; reversecholesterol transportApoA-II 40 1 ~17 Liver Forms –S–S–complex with apoE-2and E-3, which inhibits E-2 and E-3binding to lipoprotein receptorsApoA-V <1 11 ~40 Liver Modulates triglyceride incorporationinto hepatic VLDL; activates LPLApoB-100 85 2 ~513 Liver Structural protein of VLDL,IDL, LDL; LDL receptor ligandApoB-48 Fluctuates according 2 ~241 Intestine Structural protein of chylomicronsto dietary fat intakeApoC-I 6 19 ~6.6 Liver LCAT activator; modulates receptorbinding of remnantsApoC-II 3 19 8.9 Liver Lipoprotein lipase cofactorApoC-III 12 11 8.8 Liver Modulates receptor binding ofremnantsApoE 5 19 34 Liver, brain, Ligand for LDL receptor and receptorsskin, gonads, binding remnants; reversespleencholesterol transport (HDL with apoE)Apo(a) Variable (under 6 Variable Liver Modulator of fibrinolysisgenetic control)apo, apolipoprotein; HDL, high-density lipoproteins; IDL, intermediate-density lipoproteins; LCAT, lecithin:cholesterol acyltransferase; LDL, low-density lipoproteins; LPL, lipoprotein lipase;VLDL, very-low-density lipoproteins.
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viiiCONTENTS22. Treatment of Centra
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xiiCONTRIBUTORSBruce A. Chabner, MD
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xivCONTRIBUTORSJonathan M. Meyer, M
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xviCONTRIBUTORSRobert H. Tukey, PhD
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4SECTION IGENERAL PRINCIPLESbegan i
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16SECTION IGENERAL PRINCIPLESyears.
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18SECTION IGENERAL PRINCIPLESDRUGDO
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20SECTION IGENERAL PRINCIPLEScompou
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22SECTION IGENERAL PRINCIPLESgroups
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24SECTION IGENERAL PRINCIPLESphysic
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26SECTION IGENERAL PRINCIPLESdivers
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28SECTION IGENERAL PRINCIPLESphase
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30SECTION IGENERAL PRINCIPLESDivisi
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32SECTION IGENERAL PRINCIPLESconsis
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34SECTION IGENERAL PRINCIPLEStherap
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36SECTION IGENERAL PRINCIPLESMainte
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38SECTION IGENERAL PRINCIPLESThe ne
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42 signaling compounds are termed a
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44 receptors, but because the endog
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46 ligand-receptor complex, LR*. Th
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48 agonist plus an effective concen
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50SECTION IGENERAL PRINCIPLESPRESCR
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52 constrained by compartmentation
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54A. Activation by Ligand Binding o
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56 Second MessengersSECTION IGENERA
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58 markedly stimulates Ca 2+ flux,
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60 voltage-gated (Jegla et al., 200
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62SECTION IA(a) UnligandedreceptorI
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64 from the complex allowing the p5
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66 upon binding ligand. Other membe
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68 FADD/TRAF2, and caspase 8, which
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70 of cyclic GMP are also increased
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72 Vo NK, Gettemy JM, Coghlan VM. I
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74100ADeathSECTION I% of Population
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76SECTION IGENERAL PRINCIPLESisofor
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78SECTION IGENERAL PRINCIPLESantago
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80SECTION IGENERAL PRINCIPLESarrhyt
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82SECTION IGENERAL PRINCIPLESThe in
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84SECTION IGENERAL PRINCIPLESGastri
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86SECTION IGENERAL PRINCIPLESTable
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90TherapeuticeffectMetabolismTExcre
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92Clearance organs(liver, kidney)Co
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94Passive transport (downhill trans
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96SECTION IGENERAL PRINCIPLESNoncom
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Table 5-1Regulation of Transporter
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100ExtracellularSECTION IGENERAL PR
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Table 5-2Families in the Human Solu
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Table 5-3The ATP Binding Cassette (
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Table 5-4ABC Transporters Involved
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108SECTION IGENERAL PRINCIPLESIn th
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110SECTION IGENERAL PRINCIPLESthe u
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112SECTION IGENERAL PRINCIPLESOC +B
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114SECTION IGENERAL PRINCIPLEStrans
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116SECTION IGENERAL PRINCIPLESincre
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118SECTION IGENERAL PRINCIPLESHaseg
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120SECTION IGENERAL PRINCIPLESmulti
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124SECTION IGENERAL PRINCIPLESconst
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126SECTION IGENERAL PRINCIPLESorall
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Table 6-2Major Reactions Involved i
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130SECTION IGENERAL PRINCIPLESco-ad
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132SECTION IGENERAL PRINCIPLESreact
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134SECTION IGENERAL PRINCIPLESSN-38
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136SECTION IGENERAL PRINCIPLESnon-c
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Table 6-4Indications and Unwanted S
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140SECTION IGENERAL PRINCIPLESsyndr
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142SECTION IGENERAL PRINCIPLESthe t
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146SECTION IGENERAL PRINCIPLESstres
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148SECTION IGENERAL PRINCIPLESsubst
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150SECTION IGENERAL PRINCIPLESEthni
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152Monogenic traitMultigenic traitS
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154SECTION IGENERAL PRINCIPLESlikel
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15625060Common genetic formSECTION
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158AgeneCYP3A5*1 allele123456789101
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Table 7-3Examples of Genetic Polymo
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162warfarinCYP2C9hydroxywarfarin5SE
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164SECTION IGENERAL PRINCIPLESin a
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166SECTION IGENERAL PRINCIPLESBIBLI
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168SECTION IGENERAL PRINCIPLESRosne
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172 regulation of sacral parasympat
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174 third lumbar segment. The axons
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176 ganglia, the ratio of pregangli
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Table 8-1Responses of Effector Orga
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Table 8-1Responses of Effector Orga
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182 While these criteria are applic
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184 those vesicles in close proximi
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186HemicholiniumAcCoA + CholineChol
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188 in transmitter release comes fr
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190 Subtypes of Nicotinic Acetylcho
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Table 8-3Characteristics of Muscari
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194 and inhibition of excitable mem
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196SECTION IINEUROPHARMACOLOGYcorre
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Table 8-5Characteristics of Plasma
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200 by activation of β 2adrenergic
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202SECTION IIHOHOCH 3 OHOHOHHO H OH
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Table 8-6Characteristics for Adrene
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Table 8-7Representative Agents Acti
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208α 1A α 2A β 1NH 2NH 2NH 2SECT
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210 uncoupling of G-protein signali
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212 and atenolol, which antagonize
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214 to inhibit its own release. NPY
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216 Furchgott RF. Endothelium-deriv
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218 Nucleotides as Regulators of Ce
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220 M 1through M 5muscarinic recept
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222 difficult to observe with admin
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224 The difficulty in developing su
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226 neurotransmitter release, the p
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228 parasympathetic postganglionic
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230 sympathetic cholinergic fibers,
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Table 9-3Muscarinic Receptor Antago
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234 efficient, resulting in the del
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236 Chapple C, Khullar V, Gabriel Z
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240 In the 1950s, a series of aroma
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242 tertiary amine physostigmine ex
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Table 10-1Chemical Classification o
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246 The sites of action of anti- Ch
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248 tolerance reassessments, and re
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250 animals after long- term exposu
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252 When the diagnosis of myastheni
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254 Gallo MA, Lawryk NJ. Organic ph
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256 the inhibitory amino acids (γ-
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258 abundance in muscle, along with
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260 and the remainder of the muscle
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262SECTION IINEUROPHARMACOLOGYmyeli
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Table 11-2Classification of Neuromu
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266 Preventing Trauma During Electr
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268 reduced renal function (pancuro
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270 that are selective for M 1musca
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272 and its metabolites are elimina
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274 gastric emptying. Although the
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276 Volle RL. Nicotinic ganglion-st
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278Adrenergic AgonistsDirect-acting
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280SECTION IITable 12-1Chemical Str
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282 when both types of receptors ar
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284 falls (epinephrine reversal). A
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286 increase of 20-30% in oxygen co
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288 Therapeutic Uses and Status. NE
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290 may occur, particularly in pati
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292HONOHHNH 3 COCOOHNHC(CH 3 ) 3HOH
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294 agonist that has twice the pote
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296 these receptors is high, althou
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298 CNS. Amphetamine is one of the
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300 treatment of attention-deficit/
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302 syndrome and idiopathic autonom
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304 transient or may respond to adj
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306Alkylating agentCH 3OCH 2 CHNCH
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308 Syncopal episodes also have occ
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310 ingestion of tyramine-containin
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312OOOOHHNOOHHNOBISOPROLOLBETAXOLOL
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314 Billman, 2000; Brodde and Miche
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316 The β receptors mediate activa
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318 treatment for patients with all
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320 for an individual patient shoul
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322SECTION IINEUROPHARMACOLOGYTable
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324SECTION IINEUROPHARMACOLOGYTable
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326 nadolol is its relatively long
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328 or membrane-stabilizing activit
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330 and possibly papaverine-like re
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332 Gupta S, Wright HM. Nebivolol:
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336SECTION IINEUROPHARMACOLOGYNH 2N
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Table 13-1Serotonin Receptor Subtyp
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340SECTION IINEUROPHARMACOLOGY5-HT
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Table 13-3Some Actions of 5-HT in t
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344 suppressant in the management o
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346HNHNSECTION IICH 2H 3 CNHSO 2 CH
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Table 13-6Natural and Semisynthetic
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350 mCPP, an active metabolite of t
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352 Oby AADC, the same enzyme that
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354ND1 receptor familyD2 receptor f
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356SECTION IINEUROPHARMACOLOGYMesoc
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358 receptor agonist and a weak D 1
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360 Delgado PL, Charney DS, Price L
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364 system and integrate somatic an
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366 from the bloodstream into the b
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368A Ion channels α 1 subunits for
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Table 14-1Subtypes of Ca 2+ Channel
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372SECTION IINEUROPHARMACOLOGYselec
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374Presynapticneuron11 107Neurotran
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376SECTION IINEUROPHARMACOLOGYParav
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(including penicillin and pentylene
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380 (NMDA) receptors and non- NMDA
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Table 14-4Subtypes of Muscarinic Re
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384 thence to adenylyl cyclase. α
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386HistamineNH 2HNNSECTION IIH 1 H
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388β-LPHSignal peptideJP ACTH γ-L
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390 Oglutamate (NMDA)-mediated neur
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392 (e.g., ethanol) can exert relat
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394 Bleich S, Romer K, Wiltfang J,
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398 disease, especially myocardial
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400SECTION IINEUROPHARMACOLOGYTable
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402Table 15-1Antidepressants: Chemi
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404SECTION IINEUROPHARMACOLOGYanoth
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406SECTION IINEUROPHARMACOLOGYTable
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408 antipsychotics are synergistic
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410MAO to monoaminergic nerve termi
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412SECTION IINEUROPHARMACOLOGYDrug
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414SECTION IINEUROPHARMACOLOGYreupt
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418 glutamate receptor. Advances in
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420SECTION IINEUROPHARMACOLOGYPRESY
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SECTION IINEUROPHARMACOLOGY422 Schi
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424Table 16-1SECTION IINEUROPHARMAC
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426Table 16-1Chemical Structures, D
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428SECTION IINEUROPHARMACOLOGYantip
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430SECTION IINEUROPHARMACOLOGYDA re
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432SECTION IINEUROPHARMACOLOGYTable
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434SECTION IINEUROPHARMACOLOGYTable
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436 Absorption for most agents is q
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438 seen, although they are less pr
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440 health of the patient. Weight g
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442 increased risk of sudden death
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444 supporting data for certain anx
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446 treatment with both Li + and va
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448 therapeutic range (6-12 μg/mL)
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450 Li + intoxication. Li + freely
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452 Barten DM, Albright CF. Therape
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454 Mahmoud RA, Pandina GJ, Turkoz
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458 searches for agents with more s
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460 by barbiturates and volatile an
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462 a model in which benzodiazepine
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Table 17-2Major Metabolic Relations
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466SECTION IINEUROPHARMACOLOGYTable
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468SECTION IINEUROPHARMACOLOGYincid
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Table 17-4Structures, Trade Names,
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472SECTION IINEUROPHARMACOLOGYAbuse
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474SECTION IINEUROPHARMACOLOGYenzym
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476 Controversy in the management o
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478 BIBLIOGRAPHYSECTION IINEUROPHAR
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480 Twyman RE, Rogers CJ, Macdonald
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482 the existence of three main rec
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Table 18-1Actions and Selectivities
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486SECTION IINEUROPHARMACOLOGYNocis
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488 the receptor selectivity of the
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490SECTION IINEUROPHARMACOLOGY(Sork
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492SECTION IINEUROPHARMACOLOGYPrefr
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494SECTION IINEUROPHARMACOLOGYindir
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496SECTION IINEUROPHARMACOLOGYreser
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498Table 18-2SECTION IINEUROPHARMAC
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500SECTION IINEUROPHARMACOLOGYaFigu
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502SECTION IINEUROPHARMACOLOGYreact
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504 may not do so with meperidine;
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506 The use of fentanyl and sufenta
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508 doses of 20-25 mg morphine give
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510 of psychotomimetic side effects
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512 syndrome in patients dependent
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Table 18-3Epidural or Intrathecal O
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516 significantly (Du Pen et al., 1
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Routes of Administration Available.
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question the accuracy of the diagno
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522 Burkle H, Dunbar S, Van Aken H.
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524 McIntosh M, Kane K, Parratt J.
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528 asthmaticus with halothane and
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Table 19-1Properties of Inhalationa
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532 two-pore domain channels (Patel
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534Table 19-2Pharmacological Proper
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536 suppression of the EEG (Todd et
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SECTION IINEUROPHARMACOLOGY538 Etom
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Table 19-3Some Pharmacological Effe
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542 and side-effect profiles. Halot
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544 response to reduced blood press
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546 nonflammable and non-explosive
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548 anesthesia (Rasmussen et al., 2
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550 few side effects. However, succ
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552Table 19-4SECTION IINEUROPHARMAC
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554 effects on different organ syst
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556 potential to promote absorption
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558 CNS. Hypercarbia depresses the
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560 of other gases, resulting in a
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562 Grounds RM, Maxwell DL, Taylor
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564 Taylor DR, Pijnenburg MW, Smith
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566H 3 CO O CH 3C NOOC O H 2 NC OC
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568Aβ 1 subunitα subunitNI II III
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Table 20-1Susceptibility to Block T
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572 such as methylparaben that may
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574 complicates evaluation of the n
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576 amount of cream that can be app
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578 successful application of spina
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580 intravascular injection easier
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582 Yarov-Yarovoy V, McPhee JC, Ids
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therapy. More detailed information
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586SECTION IINEUROPHARMACOLOGYFigur
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588OpenInactivatedNa + Na +vigabatr
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590 The cellular electrophysiologic
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Table 21-3Interactions of Anti-Seiz
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594 These effects have been observe
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596 Oxcarbazepine is a prodrug that
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598 displacement of phenytoin from
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600 explain lamotrigine’s actions
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602 Pharmacological Effects and Mec
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604 should not be taken lightly, be
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606 of women with epilepsy have bee
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610 excitotoxic injury, regional va
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612SECTION IIPRESYNAPTIC TERMINALDi
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Treatment of Parkinson DiseaseCommo
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616 Levodopa therapy can have a dra
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618 of levodopa/carbidopa. The acti
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620 year to AD (Petersen et al., 20
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622 potentially vagotonic propertie
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624 designated IT15. It encodes a p
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626Extrafusalmuscle fibersUppermoto
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628 therapy for advanced Parkinson
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630 (the “proof” of an alcoholi
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632 methanol is taken along with et
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634 2006). Acutely, ethanol results
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636 atherogenesis (Chapter 31). Ano
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638 pancreatitis has been known to
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640 may occur with patients who app
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642 termed fetal alcohol effects (F
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644 metabolites of the drug, especi
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646 Lemoine P, Harousseau H, Bortey
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650 an addiction. These variables c
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652 paucity of other options for pl
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654 Withdrawal signs and symptoms o
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656SECTION IINEUROPHARMACOLOGYA sig
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658SECTION IINEUROPHARMACOLOGYTable
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660 crosses the blood-brain barrier
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662 high school students has declin
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664 developed and tested in control
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666 demonstrated in humans, the cer
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668 Mason BJ. Acamprosate and naltr
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672Glomerulus1111210139(Outer Strip
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674CCCCCCCCCCCCCBB1convectivesolute
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676 7. As water and solutes accumul
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Table 25-1Excretory and Renal Hemod
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680 However, even with a high degre
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682 Effects on Urinary Excretion. O
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684SECTION IIIMODULATION OF CARDIOV
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686 cardiac arrhythmias, particular
- Page 737 and 738:
Table 25-5Inhibitors of Na + -Cl -
- Page 739 and 740:
Thiazide diuretics decrease blood p
- Page 741 and 742:
692 Pentamidine and high-dose trime
- Page 743 and 744:
694ALATE DISTAL TUBULEAND COLLECTIN
- Page 745 and 746:
696 channels are expressed in IMCD.
- Page 747 and 748:
6981DIURETICSNa+ExcretionRateMABPMA
- Page 749 and 750:
700ChronicrenalfailureNephroticsynd
- Page 751 and 752:
702SECTION IIIMODULATION OF CARDIOV
- Page 753 and 754:
704SECTION IIIMODULATION OF CARDIOV
- Page 755 and 756:
706AVPAVPV 2β γα sAdenylylCyclas
- Page 757 and 758:
708 antidiuretic response to vasopr
- Page 759 and 760:
710 antidiuretic activity without i
- Page 761 and 762:
712SECTION IIIMODULATION OF CARDIOV
- Page 763 and 764:
714 Mild facial flushing and headac
- Page 765 and 766:
Table 25-9Vasopressin Receptor Anta
- Page 767 and 768:
718 Franse LV, Pahor M, Di Bari M,
- Page 769 and 770:
This page intentionally left blank
- Page 771 and 772:
722Angiotensinogen43 a.a. propeptid
- Page 773 and 774:
724AGTAng I43 amino acidpropeptideA
- Page 775 and 776:
726 in the locus p11.4 of the X chr
- Page 777 and 778:
728 state, AngII may increase, decr
- Page 779 and 780:
730 Normally, GFR is slightly reduc
- Page 781 and 782:
732SECTION IIIMODULATION OF CARDIOV
- Page 783 and 784:
734 metabolite, moexiprilat. Moexip
- Page 785 and 786:
736 effective. Once ACE inhibitors
- Page 787 and 788:
738 • ACE inhibitors may increase
- Page 789 and 790:
(75-300 mg) reductions in blood pre
- Page 791 and 792:
742 (LIFE): A randomized trial agai
- Page 793 and 794:
744 Wallukat G, Homuth V, Fischer T
- Page 795 and 796:
746Agents decreasing O 2 demandβ A
- Page 797 and 798:
Table 27-1Organic Nitrates Availabl
- Page 799 and 800:
750 consumption. An additional bene
- Page 801 and 802:
752 angina when a nitrate-free inte
- Page 803 and 804:
754 Transmucosal or Buccal Nitrogly
- Page 805 and 806:
Table 27-2Ca 2+ Channel Blockers: C
- Page 807 and 808:
758 increased modestly. After oral
- Page 809 and 810:
760 Exertional Angina. Ca 2+ channe
- Page 811 and 812:
Table 27-3Recommended Drug Therapy
- Page 813 and 814:
764 a Ca 2+ channel blocker may pro
- Page 815 and 816:
766 Hypertension is defined convent
- Page 817 and 818:
Table 27-6Hemodynamic Effects of Lo
- Page 819 and 820:
770 refractory to drugs that block
- Page 821 and 822:
772 promotes endothelial cell depen
- Page 823 and 824:
774 Methyldopa (α-methyl-3,4-dihyd
- Page 825 and 826:
776 result of the lack of sympathet
- Page 827 and 828:
778 normal renal function. However,
- Page 829 and 830:
780 expression of hypoxia-inducible
- Page 831 and 832:
782 ameliorated by a β receptor an
- Page 833 and 834:
784 Stop Hypertension (DASH) diet m
- Page 835 and 836:
786 Chaitman BR, Pepine CJ, Parker
- Page 837 and 838:
788 Pedersen ME, Cockcroft JR. What
- Page 839 and 840:
790 Congestive heart failure is the
- Page 841 and 842:
792NormalCongestivesymptomsototoxic
- Page 843 and 844:
794sympatheticstimulationBradykinin
- Page 845 and 846:
796SECTION IIIMODULATION OF CARDIOV
- Page 847 and 848:
798 counterproductive in symptomati
- Page 849 and 850:
800 CHF and may represent one mecha
- Page 851 and 852:
802 Mechanism of the Positive Inotr
- Page 853 and 854:
804 recognition of digoxin toxicity
- Page 855 and 856:
806Pressure (mm Hg)ESPVREDPVR(diast
- Page 857 and 858:
808 acid level reduction (over 24 w
- Page 859 and 860:
810 and management of end- stage CH
- Page 861 and 862:
SECTION IIIMODULATION OF CARDIOVASC
- Page 863 and 864:
This page intentionally left blank
- Page 865 and 866:
816Na +0 mV -90 mV4 mM 150 mM0 mV -
- Page 867 and 868:
818SA nodeAtriumAV nodePurkinje fib
- Page 869 and 870:
820 MECHANISMS OF CARDIACARRHYTHMIA
- Page 871 and 872:
822ADAD1accessorypathway2BEADSECTIO
- Page 873 and 874:
Table 29-2A Mechanistic Approach to
- Page 875 and 876:
826ABDecreasedphase 4slopeIncreased
- Page 877 and 878:
828 better characterized in a range
- Page 879 and 880:
830 nodal function permits a greate
- Page 881 and 882: 832 many arrhythmias than other β
- Page 883 and 884: 834 ANTI-ARRHYTHMIC DRUGSSECTION II
- Page 886: Table 29-5Pharmacokinetic Character
- Page 889 and 890: 838 Pharmacologic Effects. Digitali
- Page 891 and 892: 840 atrial fibrillation. However, d
- Page 893 and 894: 842 fall. To avoid this distributio
- Page 895 and 896: 844SECTION IIIMODULATION OF CARDIOV
- Page 897 and 898: 846 initially tolerating antiarrhyt
- Page 899 and 900: 848 Stewart RB, Bardy GH, Greene HL
- Page 901 and 902: 850Endothelial cellsPlatelets+COX-1
- Page 903 and 904: 852 formation of a superimposed thr
- Page 905 and 906: About 10-15 glycosaminoglycan chain
- Page 907 and 908: 856AUnfractionedheparinFactorXaPent
- Page 909 and 910: 858 For therapeutic purposes, hepar
- Page 911 and 912: 860 Bivalirudin contains the sequen
- Page 913 and 914: 862 with the functional level of pr
- Page 915 and 916: 864 inhibits platelet function. Eld
- Page 917 and 918: 866 Dabigatran etexilate is approve
- Page 919 and 920: 868 indications as aminocaproic aci
- Page 921 and 922: 870 for clopidogrel are to reduce t
- Page 923 and 924: 872 approved, ticagrelor is the fir
- Page 925 and 926: 874 has received anticoagulant or a
- Page 927 and 928: 876 Varmus H, eds. The Molecular Ba
- Page 929 and 930: 878 to as “small, dense LDL”) (
- Page 934 and 935: Another ACAT enzyme, ACAT-1, is exp
- Page 936 and 937: More than 900 mutations of the LDL
- Page 938 and 939: risk factors. This pivotal role of
- Page 940 and 941: Table 31-4Classification of Plasma
- Page 942 and 943: Table 31-6Assessing 10-Year Risk of
- Page 944 and 945: Can Cholesterol Levels Be Lowered T
- Page 946 and 947: catalyzes an early, rate-limiting s
- Page 948 and 949: Table 31-10Dose (mg) of Statins Req
- Page 950 and 951: and their active metabolites. Atorv
- Page 952 and 953: Mechanism of Action. The bile-acid
- Page 954 and 955: reversible side effects include tox
- Page 956 and 957: been reported to potentiate the act
- Page 958 and 959: American Heart Association; World H
- Page 960 and 961: and pravastatin across doses (STELL
- Page 962 and 963: Inflammation,Immunomodulation, andH
- Page 964 and 965: Histamine, Bradykinin, andTheir Ant
- Page 966 and 967: Table 32-1Characteristics of Histam
- Page 968 and 969: of acid, and moderate bronchospasm
- Page 970 and 971: receptor can elicit maximal vasodil
- Page 972 and 973: H 3 COCH 3CH 3H C O CH 2 CH 2 NH C
- Page 974 and 975: Table 32-2Preparations and Dosage o
- Page 976 and 977: Motion Sickness, Vertigo, and Sedat
- Page 978 and 979: Thioperamide was the first “speci
- Page 980 and 981: HMW-Kininogen927AngiotensinogenReni
- Page 982 and 983:
and kallidin from the kininogens ar
- Page 984 and 985:
inflammation appears to involve inc
- Page 986 and 987:
ACE inhibitors are widely used drug
- Page 988 and 989:
Slater EE, Merrill DD, Guess HA, et
- Page 990 and 991:
Lipid-Derived Autacoids:Eicosanoids
- Page 992 and 993:
dominates in the acute release of A
- Page 994 and 995:
of epidermal LOXs in normal skin fu
- Page 996 and 997:
COOH943OOHOOHO11-hydro-TxB 2dehydro
- Page 998 and 999:
can couple to both elevation of int
- Page 1000 and 1001:
at their sites of biosynthesis or t
- Page 1002 and 1003:
Cardiac output generally is increas
- Page 1004 and 1005:
aqueous humor outflow of the eye vi
- Page 1006 and 1007:
Analogous to the eicosanoids, PAF i
- Page 1008 and 1009:
Stomach. In addition to contracting
- Page 1010 and 1011:
Shinmura K, Tamaki K, Sato T, et al
- Page 1012 and 1013:
Anti-Inflammatory, Antipyretic,and
- Page 1014 and 1015:
IL-1 comprises two distinct polypep
- Page 1016 and 1017:
and analgesic but largely devoid of
- Page 1018 and 1019:
(CELEBREX) currently is the only CO
- Page 1021:
Sulindac Peak C p1-2 hours; 8 hours
- Page 1025:
Naproxen Peak C p1 hour 250 mg 5 mg
- Page 1029 and 1030:
and physical therapy, generally is
- Page 1031 and 1032:
might induce expression of COX-2. H
- Page 1033 and 1034:
PG-induced inhibition of both the r
- Page 1035 and 1036:
is related to the GI and hepatic pa
- Page 1037 and 1038:
ingestion of anti-inflammatory dose
- Page 1039 and 1040:
monitoring of serum salicylate leve
- Page 1041 and 1042:
It has been suggested that COX inhi
- Page 1043 and 1044:
Adverse Effects and Drug Interactio
- Page 1045 and 1046:
Absorption, Distribution, and Elimi
- Page 1047 and 1048:
oxide or aluminum hydroxide. Naprox
- Page 1049 and 1050:
dose-dependent relief from inflamma
- Page 1051 and 1052:
the chosen agent should be prescrib
- Page 1053 and 1054:
inflammatory mediators that lower t
- Page 1055 and 1056:
Drug Interactions. Allopurinol incr
- Page 1057 and 1058:
first presumes that the small secre
- Page 1059 and 1060:
Arber N, Eagle CJ, Spicak J, et al.
- Page 1061 and 1062:
current in rat sensory neurons: Who
- Page 1063 and 1064:
Immunosuppressants, Tolerogens,and
- Page 1065 and 1066:
of mAbs and the introduction of the
- Page 1067 and 1068:
H 3 CH 3 CHH 3 C2H 3 C CH 3 HO CHCH
- Page 1069 and 1070:
capsules and a 100-mg/mL oral solut
- Page 1071 and 1072:
component in whole blood and contri
- Page 1073 and 1074:
the treatment of polyomavirus nephr
- Page 1075 and 1076:
Toxicity. The major side effect of
- Page 1077 and 1078:
antagonists are in development and
- Page 1079 and 1080:
In a large phase II clinical trial,
- Page 1081 and 1082:
Interleukin-2. Human recombinant IL
- Page 1083 and 1084:
A CASE STUDY: IMMUNOTHERAPYFOR MULT
- Page 1085 and 1086:
Each of the agents mentioned in thi
- Page 1087 and 1088:
Opelz G, Vanrenterghem Y, Kirste G,
- Page 1089 and 1090:
PulmonaryPharmacologyPeter J. Barne
- Page 1091 and 1092:
1033Cigarette smoke(and other irrit
- Page 1093 and 1094:
Delivery DevicesSeveral ways of del
- Page 1095 and 1096:
1037Cellmembraneβ 2 agonistMethylx
- Page 1097 and 1098:
2Receptor Polymorphisms. Several si
- Page 1099 and 1100:
INFLAMMATORY CELLSCell number( apop
- Page 1101 and 1102:
Table 36-3Side Effects of Theophyll
- Page 1103 and 1104:
NORMALAChVagusnerveVagusnerveResist
- Page 1105 and 1106:
Chemistry. The adrenal cortex secre
- Page 1107 and 1108:
INFLAMMATORY CELLSEosinophilSTRUCTU
- Page 1109 and 1110:
Table 36-4Side Effects of Inhaled C
- Page 1111 and 1112:
AllergenCold air1053ExercisePAFAspi
- Page 1113 and 1114:
IL-4, IL-13FcεRIMast cellFcεRII/C
- Page 1115 and 1116:
frequency in vitro. Because inflamm
- Page 1117 and 1118:
Naloxone. Naloxone is a competitive
- Page 1119 and 1120:
which the inhibition of PDE5 prolon
- Page 1121 and 1122:
Hawkins G, McMahon AD, Twaddle S, e
- Page 1123 and 1124:
Szczeklik A, Stevenson DD. Aspirin-
- Page 1125 and 1126:
Hematopoietic Agents:Growth Factors
- Page 1127 and 1128:
ERYTHROPOIETIN1069SCF / FLTotipoten
- Page 1129 and 1130:
proliferation, and maturation are d
- Page 1131 and 1132:
daily for the 10 days preceding sur
- Page 1133 and 1134:
chemotherapy will increase granuloc
- Page 1135 and 1136:
intake, malabsorption, blood loss,
- Page 1137 and 1138:
Table 37-3Iron Requirements for Pre
- Page 1139 and 1140:
NormalIron DepletionIron-DeficientE
- Page 1141 and 1142:
Table 37-5Average Response to Oral
- Page 1143 and 1144:
Before initiating iron dextran ther
- Page 1145 and 1146:
common practice to describe megalob
- Page 1147 and 1148:
linked to a central cobalt atom and
- Page 1149 and 1150:
vitamins and minerals also can be g
- Page 1151 and 1152:
PteroylMonoheptaglutamate10933 6OCO
- Page 1153 and 1154:
Leucovorin should never be used for
- Page 1155 and 1156:
Clark SF. Iron deficiency anemia: D
- Page 1157 and 1158:
Sheridan WP, Begley CG, Juttner CA,
- Page 1159 and 1160:
Hormones and HormoneAntagonistsChap
- Page 1161 and 1162:
Introduction To Endocrinology:The H
- Page 1163 and 1164:
SON, PVN(AVP, OXY)HypothalamusAVP,O
- Page 1165 and 1166:
chromosome 17 (17q22), which also c
- Page 1167 and 1168:
HypothalamusAnteriorpituitaryTarget
- Page 1169 and 1170:
postnatal growth retardation is unr
- Page 1171 and 1172:
mixed GH- and prolactin-secreting a
- Page 1173 and 1174:
OHN1115NH 2CH 2OHOHDopamineNHNQuina
- Page 1175 and 1176:
incidence of leukemia. Despite this
- Page 1177:
Table 38-3Structures of Gonadotropi
- Page 1180 and 1181:
results from peripheral production
- Page 1182 and 1183:
Absorption, Distribution, and Elimi
- Page 1184 and 1185:
acids. It is synthesized as a large
- Page 1186 and 1187:
Gillam MP, Molitch ME, Lombardi G,
- Page 1188 and 1189:
Thyroid and Anti-Thyroid DrugsGrego
- Page 1190 and 1191:
6. recycling of the iodine within t
- Page 1192 and 1193:
residues, only two to five of which
- Page 1194 and 1195:
with a very high affinity (the equi
- Page 1196 and 1197:
DopamineGlucocorticoidsRetinoidsHig
- Page 1198 and 1199:
histone deacetylases and other prot
- Page 1200 and 1201:
which T 3enhances the velocity of c
- Page 1202 and 1203:
tablets and as a lyophilized powder
- Page 1204 and 1205:
commonly begun with a loading dose
- Page 1206 and 1207:
Table 39-4Anti-thyroid CompoundsPRO
- Page 1208 and 1209:
Measurements of the course of organ
- Page 1210 and 1211:
β Adrenergic receptor antagonists
- Page 1212 and 1213:
Table 39-6Commonly Used Iodine-Cont
- Page 1214 and 1215:
of 131 I therapy and only resumed 3
- Page 1216 and 1217:
Chemotherapy in Thyroid CancerAdvan
- Page 1218 and 1219:
thyroid-related hormones. J Clin En
- Page 1220 and 1221:
Sera N, Ashizawa K, Ando T, et al.
- Page 1222 and 1223:
Estrogens and ProgestinsEllis R. Le
- Page 1224 and 1225:
H 3 CH 3 C O16α-OHaseH 3 CH 3 C OO
- Page 1226 and 1227:
The gonadotropins (LH and FSH) regu
- Page 1228 and 1229:
ERα (Hewitt and Korach, 2003) and
- Page 1230 and 1231:
both coagulation and fibrinolytic p
- Page 1232 and 1233:
Besides co-activators and co-repres
- Page 1234 and 1235:
4-hydroxycatechols, are converted t
- Page 1236 and 1237:
content of the bile. Transdermal es
- Page 1238 and 1239:
of transcription factors in the two
- Page 1240 and 1241:
Agents Similar to Progesterone (Pre
- Page 1242 and 1243:
Group for the PEPI Trial, 1995); th
- Page 1244 and 1245:
If administered for one or several
- Page 1246 and 1247:
Progestin-Only Contraceptives. Seve
- Page 1248 and 1249:
with the long-acting preparations,
- Page 1250 and 1251:
BIBLIOGRAPHYAnderson GL, Limacher M
- Page 1252 and 1253:
Meis PJ, Klebanoff M, Thom E, et al
- Page 1254 and 1255:
AndrogensPeter J. SnyderTESTOSTERON
- Page 1256 and 1257:
have been identified: type I, which
- Page 1258 and 1259:
Other changes also may result from
- Page 1260 and 1261:
Testosterone(HISTERONE, others)OH12
- Page 1262 and 1263:
undesirable effects occur shortly a
- Page 1264 and 1265:
does not transiently increase sex s
- Page 1266 and 1267:
King DS, Sharp RL, Vukovich MD, et
- Page 1268 and 1269:
ACTH, Adrenal Steroids, andPharmaco
- Page 1270 and 1271:
ZonaGlomerulosaAng IIK +ACTHZonaeFa
- Page 1272 and 1273:
increases in the steroidogenic capa
- Page 1274 and 1275:
Cushing’s disease) and an ectopic
- Page 1276 and 1277:
HSP70SGRSGRHSP90SGRGRE GRECBGSIPTra
- Page 1278 and 1279:
CH 2 OH21CH 2 OHCH 2 OHCH 2 OH1219C
- Page 1280 and 1281:
to other vasoactive substances. Hyp
- Page 1282 and 1283:
synthetic congeners are administere
- Page 1284 and 1285:
Table 42-4Available Preparations of
- Page 1286 and 1287:
Cataracts. Cataracts are a well-est
- Page 1288 and 1289:
Traditional replacement regimens ha
- Page 1290 and 1291:
Studies with other forms of renal d
- Page 1292 and 1293:
Coombs test) are treated with predn
- Page 1294 and 1295:
Axelrod L. Perioperative management
- Page 1296 and 1297:
Endocrine Pancreas andPharmacothera
- Page 1298 and 1299:
proportion to the nutrient load ing
- Page 1300 and 1301:
The pancreatic α cell, which has c
- Page 1302 and 1303:
• Impaired glucose tolerance (IGT
- Page 1304 and 1305:
predominance of CD8+ cells (insulit
- Page 1306 and 1307:
glucose production and promote hepa
- Page 1308 and 1309:
Table 43-4Goals of Therapy in Diabe
- Page 1310 and 1311:
1 SAspLysSA chainGly21AsnSSArg Arg1
- Page 1312 and 1313:
abdomen currently is the preferred
- Page 1314 and 1315:
INSULIN SECRETAGOGUES AND ORALHYPOG
- Page 1316 and 1317:
may be more frequent in patients ta
- Page 1318 and 1319:
Absorption, Distribution, and Elimi
- Page 1320 and 1321:
patients in clinical trials and has
- Page 1322 and 1323:
exendin-4 causes glucose-dependent
- Page 1324 and 1325:
Therapeutic Uses. α-Glucosidase in
- Page 1326 and 1327:
Type 2 Diabetes1267AssessA1CDiabete
- Page 1329:
ParenteralInsulin a Glucose utiliza
- Page 1332 and 1333:
Glucose, mmol/L131211109876543Gluco
- Page 1334 and 1335:
Murphy R, Ellard S, Hattersley AT.
- Page 1336 and 1337:
Agents Affecting Mineral IonHomeost
- Page 1338 and 1339:
PhosphatePhosphate is an essential
- Page 1340 and 1341:
inhibits renin secretion). Simultan
- Page 1342 and 1343:
22128123 25119HO3 7provitamin D 3(7
- Page 1344 and 1345:
mucosal compartments. Thus, net cal
- Page 1346 and 1347:
Fibroblast Growth Factor 23 and Klo
- Page 1348 and 1349:
Stromal cell/osteoblastRANKLRANKOPG
- Page 1350 and 1351:
The amount of vitamin D necessary t
- Page 1352 and 1353:
(15-25 μg/kg of body weight) to mi
- Page 1354 and 1355:
Therapeutic Indications for Vitamin
- Page 1356 and 1357:
Pyrophosphate Bisphosphonate Medron
- Page 1358 and 1359:
Absorption, Fate, and Excretion. Ph
- Page 1360 and 1361:
% change lumbar spine BMD1614121086
- Page 1362 and 1363:
alendronate to PTH treatment provid
- Page 1364 and 1365:
Ballock RT, O’Keefe RJ. The biolo
- Page 1366 and 1367:
Okazaki M, Ferrandon S, Vilardaga J
- Page 1368 and 1369:
Drugs AffectingGastrointestinal Fun
- Page 1370 and 1371:
Pharmacotherapy of Gastric Acidity,
- Page 1372 and 1373:
PROTON PUMP INHIBITORSChemistry; Me
- Page 1374 and 1375:
mainstay in the treatment of pathol
- Page 1376 and 1377:
Pharmacokinetics. Misoprostol is ra
- Page 1378 and 1379:
In the hope of providing more rapid
- Page 1380 and 1381:
GERD and Pregnancy. Heartburn is es
- Page 1382 and 1383:
of acid-suppressant agents, usually
- Page 1384 and 1385:
Treatment of Disorders of BowelMoti
- Page 1386 and 1387:
achalasia of the esophagus (impaire
- Page 1388 and 1389:
1327OHHNNH 2OCH 3NNHNCH 3HCLCH 3OHN
- Page 1390 and 1391:
Rate(liters/day)Flow9.0H 2OUptake6.
- Page 1392 and 1393:
Table 46-3Classification and Compar
- Page 1394 and 1395:
effluent is clear. To avoid net tra
- Page 1396 and 1397:
visceral pain (Eutamene et al., 200
- Page 1398 and 1399:
In patients suspected of having bil
- Page 1400 and 1401:
et al., 2001). For patients with va
- Page 1402 and 1403:
NK 2receptors; it is not available
- Page 1404 and 1405:
Table 46-6Receptor Specificity of A
- Page 1406 and 1407:
Table 46-813455-HT 3Antagonists in
- Page 1408 and 1409:
R3Bile AcidCholic acidR12CH 3CH 3R3
- Page 1410 and 1411:
Sartor RB. Probiotic therapy of int
- Page 1412 and 1413:
Pharmacotherapy of InflammatoryBowe
- Page 1415 and 1416:
Intestinal lumenBacteriaAntibiotics
- Page 1417 and 1418:
sulfapyridine(metabolite)sulfasalaz
- Page 1419 and 1420:
(Greenberg et al., 1994; McKeage an
- Page 1421 and 1422:
improve significantly (generally wi
- Page 1423 and 1424:
Mesalamine and glucocorticoids are
- Page 1425 and 1426:
Chemotherapy of MicrobialDiseasesCh
- Page 1427 and 1428:
General Principles ofAntimicrobial
- Page 1429 and 1430:
of even polar drugs (Quagliarello a
- Page 1431 and 1432:
and liver dysfunction, which may le
- Page 1433 and 1434:
viability assay (Hanna and D’Aqui
- Page 1435 and 1436:
enzyme (Harshey and Ramakrishnan, 1
- Page 1437 and 1438:
suggest this approach may be as eff
- Page 1439 and 1440:
Resistance Due to Enhanced Excision
- Page 1441 and 1442:
Arion D, Kaushik N, McCormick S, et
- Page 1443 and 1444:
Wilson W, Taubert KA, Gewitz M, et
- Page 1445 and 1446:
Chemotherapy of MalariaJoseph M. Vi
- Page 1447 and 1448:
microenvironment. For the patient,
- Page 1449 and 1450:
1387Table 49-2Regimens for the Prev
- Page 1451:
Table 49-3Regimens for the Treatmen
- Page 1455:
Doxycycline P falciparum from Oral:
- Page 1459:
Quinine sulfate P. falciparum from
- Page 1463 and 1464:
Table 49-4Regimen for Presumptive S
- Page 1465 and 1466:
H 2 CCHHON1397H 3 COOHHCNNHF 3 CClC
- Page 1467 and 1468:
failures are rare. However, when at
- Page 1469 and 1470:
purine and pyrimidine synthesis. In
- Page 1471 and 1472:
MauritaniaSenegalPortugalMoroccoWes
- Page 1473 and 1474:
therapeutic doses, and thick smears
- Page 1475 and 1476:
based on patient age, severity of i
- Page 1477 and 1478:
for 3 months after mefloquine use b
- Page 1479 and 1480:
and teeth, tetracyclines should not
- Page 1481 and 1482:
Clinical suspicion of malariaor his
- Page 1483 and 1484:
and antimalarial drugs in discovery
- Page 1485 and 1486:
Krishna S, White, NJ. Pharmacokinet
- Page 1487 and 1488:
Chemotherapy of ProtozoalInfections
- Page 1489 and 1490:
recovered from all mammalian specie
- Page 1491 and 1492:
this infection (Bern et al., 2007;
- Page 1493 and 1494:
2007, Chappuis et al., 2005; Priott
- Page 1495 and 1496:
individuals with amebic colitis or
- Page 1497 and 1498:
microaerophilic bacteria such as He
- Page 1499 and 1500:
approved in India as the first oral
- Page 1501 and 1502:
and oocytes of C. parvum and inhibi
- Page 1503 and 1504:
lungs depends on both the size of p
- Page 1505 and 1506:
treatment of African trypanosomiasi
- Page 1507 and 1508:
Donnelly H, Bernard EM, Rothkotter
- Page 1509 and 1510:
Vöhringer HF, Arastéh K. Pharmaco
- Page 1511 and 1512:
Chemotherapy of HelminthInfectionsJ
- Page 1513 and 1514:
or with hookworms. In rare instance
- Page 1515 and 1516:
streams and rivers, O. volvulus inf
- Page 1517 and 1518:
been reported and higher doses of t
- Page 1519 and 1520:
inhibition of first-pass CYP-mediat
- Page 1521 and 1522:
general population; comparable stud
- Page 1523 and 1524:
Chemistry. Ivermectin exists as an
- Page 1525 and 1526:
Anthelmintic Action. After rapid an
- Page 1527 and 1528:
Therapeutic Uses. Pyrantel pamoate
- Page 1529 and 1530:
with onchocercal ocular involvement
- Page 1531 and 1532:
Sulfonamides, Trimethoprim-Sulfamet
- Page 1533 and 1534:
such a combination would yield syne
- Page 1535 and 1536:
treatment of an established deep in
- Page 1537 and 1538:
The synergistic interaction between
- Page 1539 and 1540:
Table 52-2Structural Formulas of Se
- Page 1541 and 1542:
concentrations in cerebrospinal flu
- Page 1543 and 1544:
Antimicrobial Activity. Enzymes cap
- Page 1545 and 1546:
Penicillins, Cephalosporins, andOth
- Page 1547 and 1548:
GlycopeptidepolymerNAMpenicillinsce
- Page 1549 and 1550:
1500 1000 1500 2000 2300Base pairsS
- Page 1551 and 1552:
microorganisms, including Clostridi
- Page 1553 and 1554:
Gonococcal Infections. Gonococci gr
- Page 1555 and 1556:
This is their valid clinical use. D
- Page 1557 and 1558:
Table 53-1Chemical Structures and M
- Page 1559 and 1560:
Untoward Reactions to PenicillinsHy
- Page 1561 and 1562:
toxic concentrations of procaine. I
- Page 1563 and 1564:
Table 53-2Names, Structural Formula
- Page 1565 and 1566:
the bile (neither is available in t
- Page 1567 and 1568:
manifest cross-reactivity to a memb
- Page 1569 and 1570:
Aztreonam generally is well tolerat
- Page 1571 and 1572:
Spratt BG. Resistance to antibiotic
- Page 1573 and 1574:
AminoglycosidesConan MacDougalland
- Page 1575 and 1576:
1507CHAPTER 54NEOMYCIN BAMINOGLYCOS
- Page 1577 and 1578:
consequently, gentamicin-resistant
- Page 1579 and 1580:
Table 54-2Algorithm for Dose Reduct
- Page 1581 and 1582:
ionic balance of the endolymph (Neu
- Page 1583 and 1584:
• To provide synergistic bacteria
- Page 1585 and 1586:
the infusion, which falls to ~20 μ
- Page 1587 and 1588:
Appel GB. Aminoglycoside nephrotoxi
- Page 1589 and 1590:
Protein Synthesis Inhibitorsand Mis
- Page 1591 and 1592:
Bacteroides spp., Propionibacterium
- Page 1593 and 1594:
Intra-abdominal Infections. Increas
- Page 1595 and 1596:
most anaerobic bacteria, including
- Page 1597 and 1598:
Drug Interactions. Chloramphenicol
- Page 1599 and 1600:
with the fully methylated ribosomal
- Page 1601 and 1602:
of acute exacerbations of chronic b
- Page 1603 and 1604:
These strains would not display a b
- Page 1605 and 1606:
which are more likely to be a probl
- Page 1607 and 1608:
membranes. The permeability of the
- Page 1609 and 1610:
of enterococci, primarily Enterococ
- Page 1611 and 1612:
Antimicrobial Activity. Daptomycin
- Page 1613 and 1614:
antibiotic in developing nations be
- Page 1615 and 1616:
Oliva ME, Rekha A, Yellin A, et al.
- Page 1617 and 1618:
Chemotherapy of Tuberculosis,Mycoba
- Page 1619 and 1620:
mRNA30SMycobacteriumRNA PolymeraseD
- Page 1621 and 1622:
Table 56-2Population Pharmacokineti
- Page 1623 and 1624:
pyrazinamide was administered for d
- Page 1625 and 1626:
AFastSlow15573BNumber of subjectsCp
- Page 1627 and 1628:
Lewis, 1999). The following species
- Page 1629 and 1630:
TMC-207 (R207910)TMC-207 is a diary
- Page 1631 and 1632:
Mechanisms of Resistance. Mutations
- Page 1633 and 1634:
employees of high-risk congregate s
- Page 1635 and 1636:
disease, which has early hypopigmen
- Page 1637 and 1638:
Diacon AH, Pym A, Grobusch M, et al
- Page 1639 and 1640:
Antifungal AgentsJohn E. BennettThe
- Page 1641 and 1642:
Table 57-1Pharmacotherapy of Mycose
- Page 1643 and 1644:
due to decreased production of eryt
- Page 1645 and 1646:
Table 57-3Interaction of Azole Anti
- Page 1647 and 1648:
bound to plasma proteins. Neither a
- Page 1649 and 1650:
the maintenance dose. There are no
- Page 1651 and 1652:
Extracellular spaceMannoproteinGluc
- Page 1653 and 1654:
Absorption, Distribution and Excret
- Page 1655 and 1656:
mild penile irritation. Cross-aller
- Page 1657 and 1658:
ButenafineButenafine hydrochloride
- Page 1659 and 1660:
terreus infection. Antimicrob Agent
- Page 1661 and 1662:
Antiviral Agents (Nonretroviral)Edw
- Page 1663 and 1664:
Aattachmentrelease1595buddingBuncoa
- Page 1665 and 1666:
ONHNH N N2 NOH CH 2OCH 2 CH 2ACYCLO
- Page 1667 and 1668:
The principal dose-limiting toxicit
- Page 1669 and 1670:
CNS or eye has not been well charac
- Page 1671 and 1672:
of foscarnet and ganciclovir synerg
- Page 1673 and 1674:
Ganciclovir therapy (5 mg/kg every
- Page 1675 and 1676:
NH H NH 2 3 C21607OAMANTADINEOHNCOO
- Page 1677 and 1678:
Table 58-3Pharmacological Character
- Page 1679 and 1680:
A B1uncoatingnucleus1golgi3glycopro
- Page 1681 and 1682:
IFN can cause myelosuppression and
- Page 1683 and 1684:
tubing with ribavirin. Techniques t
- Page 1685 and 1686:
Entecavir triphosphate is a weak in
- Page 1687 and 1688:
Therapeutic Uses. Tenofovir is appr
- Page 1689 and 1690:
Lai CL, Lim SG, Brown NA, et al. A
- Page 1691 and 1692:
Antiretroviral Agents andTreatment
- Page 1693 and 1694:
to occur at approximately three bas
- Page 1695 and 1696:
A reservoir of long-lived quiescent
- Page 1697 and 1698:
1. Triphosphate competeswith native
- Page 1700 and 1701:
Like all available antiretroviral d
- Page 1702 and 1703:
and cross-resistance. TAMs associat
- Page 1704 and 1705:
less potent and substantially more
- Page 1706 and 1707:
lamivudine, abacavir, and efavirenz
- Page 1708 and 1709:
Mechanisms of Action and Resistance
- Page 1710 and 1711:
DaughterDNA strand1641ParentRNA str
- Page 1712 and 1713:
Therapeutic Use. Nevirapine (VIRAMU
- Page 1714 and 1715:
efavirenz and nevirapine, and any p
- Page 1716:
Table 59-4Pharmacokinetic Propertie
- Page 1719 and 1720:
1649NONCONH 2OHNNO CH 2 CONH C(CH 3
- Page 1721 and 1722:
occurs less frequently at codon 84.
- Page 1723 and 1724:
6% of patients discontinued atazana
- Page 1725 and 1726:
high-fat meals (Bardsley-Elliot and
- Page 1727 and 1728:
HIV virusmembrane16571Nucleocapsidc
- Page 1729 and 1730:
vitro. The Y143C/H/R mutation has a
- Page 1731 and 1732:
Fischl MA, Stanley K, Collier AC, e
- Page 1733 and 1734:
Perelson AS, Neumann AU, Markowitz
- Page 1735 and 1736:
Chemotherapy ofNeoplastic DiseasesC
- Page 1737 and 1738:
General Principles of CancerChemoth
- Page 1739 and 1740:
Table 60-3Natural ProductsNONPROPRI
- Page 1741 and 1742:
6-MERCAPTOPURINE6-THIOGUANINEInhibi
- Page 1743 and 1744:
integrity. If a cell possesses norm
- Page 1745 and 1746:
Pullarkat ST, Stoehlmacher J, Ghade
- Page 1747 and 1748:
Cytotoxic AgentsBruce A. Chabner, J
- Page 1749 and 1750:
CyclophosphamideO1-triazeno)-imidaz
- Page 1751 and 1752:
Other repair enzymes are specific f
- Page 1753 and 1754:
CLINICAL PHARMACOLOGYNitrogen Musta
- Page 1755 and 1756:
Ethyleneimines and MethylmelaminesA
- Page 1757 and 1758:
disease. Almost 50% of the compound
- Page 1759 and 1760:
CisplatinAbsorption, Fate, and Excr
- Page 1761 and 1762:
new agents have greater capacity fo
- Page 1763 and 1764:
elements formed by amplification of
- Page 1765 and 1766:
Modification of BaseCYTOSINE(Capeci
- Page 1767 and 1768:
dUMPFdUMPthymidylatesynthaseN5-10me
- Page 1769 and 1770:
incorporation into DNA by DNA polym
- Page 1771 and 1772:
difluorodeoxyuridine (dFdU). Althou
- Page 1773 and 1774:
After rapid extracellular dephospho
- Page 1775 and 1776:
Deoxyadenosine also inactivates S-a
- Page 1777 and 1778:
sometimes resulting in colicky abdo
- Page 1779 and 1780:
Docetaxel causes greater degrees of
- Page 1781 and 1782:
The precise sequence of events that
- Page 1783 and 1784:
most potent antitumor agents known.
- Page 1785 and 1786:
echocardiography, which reveals abn
- Page 1787 and 1788:
H 2 N ONH 2NHNH 2 ON N OCH 3 H ON R
- Page 1789 and 1790:
and mitomycin must be discontinued
- Page 1791 and 1792:
L-ASP terminates the antitumor acti
- Page 1793 and 1794:
discontinuation. Corticosteroids an
- Page 1795 and 1796:
Asselin BL, Whitin JC, Coppola DJ,
- Page 1797 and 1798:
Heizer WD, Peterson JL. Acute myelo
- Page 1799 and 1800:
DNA following subchronic doxorubici
- Page 1801 and 1802:
Targeted Therapies: Tyrosine Kinase
- Page 1803 and 1804:
181614<2%2-10%>10%1733% of patients
- Page 1805 and 1806:
IGF-1kinase activity and ability to
- Page 1807 and 1808:
Metastatic Colon Cancer. Cetuximab
- Page 1809 and 1810:
aflibercept (VEGF Trap), a recombin
- Page 1811 and 1812:
classification as anti-angiogenics
- Page 1813 and 1814:
NNONHMechanism of Action. Bortezomi
- Page 1815 and 1816:
reduced to 5 mg daily for patients
- Page 1817 and 1818:
Table 62-2Dose and Toxicity of Mono
- Page 1819 and 1820:
complicate the patient’s course f
- Page 1821 and 1822:
Corbin AS, La Rosée P, Stoffregen
- Page 1823 and 1824:
Serafini P, De Santo C, Marigo I, e
- Page 1825 and 1826:
Natural Products in CancerChemother
- Page 1827 and 1828:
Table 63-1Clinical Uses for Anti-Es
- Page 1829 and 1830:
factor V Leiden mutation and tamoxi
- Page 1831 and 1832:
Aromatase activity is the product o
- Page 1833 and 1834:
Mechanism of Action. In contrast to
- Page 1835:
Table 63-2Structures of GnRH and De
- Page 1838 and 1839:
ketoconazole inhibits both testicul
- Page 1840 and 1841:
Sharifi N, Gulley JL, Dahut WL. And
- Page 1842 and 1843:
Special Systems PharmacologyChapter
- Page 1844 and 1845:
Ocular PharmacologyJeffrey D. Hende
- Page 1846 and 1847:
Table 64-1Autonomic Pharmacology of
- Page 1848 and 1849:
Table 64-2Effects of Pharmacologica
- Page 1850 and 1851:
for compounds with limited solubili
- Page 1852 and 1853:
Table 64-4Topical Antibacterial Age
- Page 1854 and 1855:
Table 64-5Antiviral Agents for Opht
- Page 1856 and 1857:
Use of Autonomic Agents in the EyeG
- Page 1858 and 1859:
• in patients who have an increas
- Page 1860 and 1861:
their chemistry and pharmacology ar
- Page 1862 and 1863:
Table 64-8Vitreous Substitutes aVIT
- Page 1864 and 1865:
necessary. Rifabutin, if used in co
- Page 1866 and 1867:
Table 64-9Ophthalmic Effects of Sel
- Page 1868 and 1869:
DarkLight1797[Ca 2+ ]DK [cGMP]LT [C
- Page 1870 and 1871:
the need for surgical intervention
- Page 1872 and 1873:
Morrow GL, Abbott RL. Minocycline-i
- Page 1874 and 1875:
Dermatological PharmacologyCraig Bu
- Page 1876 and 1877:
LamellarbodyTightjunctionScale desq
- Page 1878 and 1879:
Table 65-2Vehicles for Topically Ap
- Page 1880 and 1881:
to reserve this method for allergic
- Page 1882 and 1883:
as monotherapy or in combination wi
- Page 1884 and 1885:
Calcipotriene. Calcipotriene (DOVON
- Page 1886 and 1887:
ECP is used for cutaneous T-cell ly
- Page 1888 and 1889:
are irritants and may lead to micro
- Page 1890 and 1891:
HEXACHLOROCYCLOHEXANELindane has be
- Page 1892 and 1893:
gangrenosum, and Behçet’s diseas
- Page 1894 and 1895:
active derivative, inhibits the enz
- Page 1896 and 1897:
Table 65-10Biological Agents Common
- Page 1898 and 1899:
sepsis, tuberculosis), including le
- Page 1900 and 1901:
DRUGS FOR HYPERKERATOTICDISORDERSKe
- Page 1902 and 1903:
Barry BW. Breaching the skin’s ba
- Page 1904 and 1905:
Contraception andPharmacotherapy of
- Page 1906 and 1907:
Table 66-2Brand Names and Formulati
- Page 1908 and 1909:
Postcoital ContraceptionPostcoital
- Page 1910 and 1911:
Available routes of estrogen admini
- Page 1912 and 1913:
contraceptives containing progestin
- Page 1914 and 1915:
withdrawal in women who do not. If
- Page 1916 and 1917:
cavity, thorax, and even the perica
- Page 1918 and 1919:
Nursing mothers constitute a second
- Page 1920 and 1921:
β 2 agonistsNO donors1849β 2G s A
- Page 1922 and 1923:
rate then is reduced to 1-2 mL/minu
- Page 1924 and 1925:
Environmental Toxicology:Carcinogen
- Page 1926 and 1927:
human exposure. The most common mod
- Page 1928 and 1929:
InitiationPromotion1857MetabolicAct
- Page 1930 and 1931:
termination of the trial (William e
- Page 1932 and 1933:
Many of the toxic metals in the env
- Page 1934 and 1935:
impulsivity, short attention span,
- Page 1936 and 1937:
Exposure. Inorganic mercury cations
- Page 1938 and 1939:
Toxicity to the nervous system is t
- Page 1940 and 1941:
voluntarily replaced arsenic with o
- Page 1942 and 1943:
but has very little or no benefit i
- Page 1944 and 1945:
NaOONH 2(CH 2 ) 5NONR 2OCaexposure
- Page 1946 and 1947:
the FDA but is approved for use in
- Page 1948 and 1949:
Goldwater LJ. Mercury; a History of
- Page 1950 and 1951:
Principles of Prescription OrderWri
- Page 1952 and 1953:
to be equivalent to 5 mL and a “t
- Page 1954 and 1955:
shorter due to limits and pressures
- Page 1956 and 1957:
may be telephoned to a pharmacy onl
- Page 1958 and 1959:
Even the most carefully prepared pr
- Page 1960 and 1961:
ELECTRONIC PRESCRIBINGThe era of e-
- Page 1962 and 1963:
Design and Optimizationof Dosage Re
- Page 1964 and 1965:
percentage of the administered dose
- Page 1966 and 1967:
The time required to achieve a maxi
- Page 1968 and 1969:
estimated from the concentration of
- Page 1970:
Table AII-1Pharmacokinetic DataKey:
- Page 1974:
Alendronate a<0.7 b 44.9 ± 9.3 78
- Page 1978:
Ambrisentan a— b — 99 — c —
- Page 1982:
Aripiprazole a87 <1 >99 0.83 ± 0.1
- Page 1986:
Bicalutamide a— 1.7 ± 0.3 96 R:
- Page 1990:
Capecitabine a— 3 <60 145 (34%) L
- Page 1994:
CefdinirCap: 16-21 a 13-23 b 89 c 1
- Page 1998:
Cetirizine aRac: >70 b Rac: 70.9 ±
- Page 2002:
Cinacalcet a~20 — b 93-97 ~18 ~17
- Page 2006:
Clopidogrel a— b — Clo: 98 —
- Page 2010:
CyclosporineSI: 28 ± 18 a,b <1 93
- Page 2014:
Diazepam aPO: 100 ± 14 <1 98.7 ±
- Page 2018:
Donepezil a— b 10.6 ± 2.7 92.6
- Page 2022:
Duloxetine a42.8 (18.5-71.2) — >9
- Page 2026:
Entacapone a42 ± 9 b Negligible 98
- Page 2030:
Esomeprazole aEs: 89 (81-98) b Es/R
- Page 2034:
Felodipine a15 ± 8 <1 99.6 ± 02 1
- Page 2038:
5-Fluorouracil (5-FU)28 (0-80) a <1
- Page 2042:
Furosemide a71 ± 35 71 ± 10 98.6
- Page 2046:
Glipizide95 <5 98.4 0.52 ± 0.18 a
- Page 2050:
Hydroxychloroquine a79 ± 12 27 45
- Page 2054:
Imipenem/Cilastatin aImipenem 69 ±
- Page 2058:
Isoniazid a— b RA: 7 ± 2 c ~0 RA
- Page 2062:
Ivermectin a— <1 93.1 ± 0.2 2.06
- Page 2066:
Levofloxacin a99 ± 10 61-87 24-38
- Page 2070:
Lorazepam93 ± 10 <1 91 ± 2 1.1 ±
- Page 2074:
Mercaptopurine a12 ± 7 b 22 ± 12
- Page 2078:
Methylprednisolone82 ± 13 a 4.9 ±
- Page 2082:
Minocycline a95-100 11 ± 2 76 1.0
- Page 2086:
Moxifloxacin a86 ± 1 21.9 ± 3.6 3
- Page 2090:
Nitrofurantoin87 ± 13 47 ± 13 62
- Page 2094:
Oxcarbazepine a— O: <1 — O: 67.
- Page 2098:
ParoxetineDose dependent a <2 95 8.
- Page 2102:
Pramlintide a30-40% b - ~60 c Low:
- Page 2106:
Pregabalin a≥90 b 90-99 0 0.96-1.
- Page 2110:
Pseudoephedrine a~100 43-96 b — 7
- Page 2114:
Rabebrazole a52 b 0 b 95-98 4.2 ±
- Page 2118:
Remifentanil a— b Negligible 92 4
- Page 2122:
Rivastigmine a72 (22-119) b Negligi
- Page 2126:
Simvastatin a≤5 Negligible 94 7.6
- Page 2130:
Spironolactone a— b <1 c >90 d 93
- Page 2134:
Tamoxifen a— <1 >98 1.4 b,c 50-60
- Page 2138:
Tolterodine aEM: 26 ± 18 EM: Negli
- Page 2142:
Trimethoprim>63 63 ± 10 37 ± 5 1.
- Page 2146:
Vancomycin— a 79 ± 11 30 ± 11 C
- Page 2150:
Vincristine a— 10-20 Low 4.92 ±
- Page 2154 and 2155:
IndexInformation in figures and tab
- Page 2156 and 2157:
Adrenergic receptors (Cont.):beta,
- Page 2158 and 2159:
AMAPRYL (glimepiride), 1257tAmatoxi
- Page 2160 and 2161:
Angina pectoris (Cont.):variant (Pr
- Page 2162 and 2163:
Anticholinesterase agents (Cont.):s
- Page 2164 and 2165:
Aromatase inhibitors (Cont.):first
- Page 2166 and 2167:
Azelastine hydrochloride, 922, 922t
- Page 2168 and 2169:
Bile acids, 1346-1347Bile acid sequ
- Page 2170 and 2171:
Butorphanolactions and selectivitie
- Page 2172 and 2173:
Cardiovascular system (Cont.):opioi
- Page 2174 and 2175:
Cetuximab (Cont.):therapeutic uses
- Page 2176 and 2177:
CLOMID (clomiphene citrate),1841-18
- Page 2178 and 2179:
CPVT. See Catecholaminergicpolymorp
- Page 2180 and 2181:
DERMABOND (cyanoacrylate tissueadhe
- Page 2182 and 2183:
Diiodohydroxyquin (iodoquinol),1153
- Page 2184 and 2185:
Dose-response, 73-74, 74fDose-respo
- Page 2186 and 2187:
Electrocardiographic toxicitymanife
- Page 2188 and 2189:
Essential thrombocytosis, drugs for
- Page 2190 and 2191:
Felodipine (Cont.):cardiovascular p
- Page 2192 and 2193:
Fosinopril (Cont.):therapeutic uses
- Page 2194 and 2195:
GlutathioneABC transporters and, 10
- Page 2196 and 2197:
Hepatitisdrugs for, 1609-1617interf
- Page 2198 and 2199:
Hydralazine (Cont.):site of action
- Page 2200 and 2201:
Immunosuppression, 1006-1019biologi
- Page 2202 and 2203:
Iridocyclitis, 233viral, 1783tIrino
- Page 2204 and 2205:
β-Lactamase inhibitors, 1501Lactat
- Page 2206 and 2207:
Loop diuretics, 682-686, 683tabsorp
- Page 2208 and 2209:
Mefenamic acid, 989adverse effects
- Page 2210 and 2211:
Metoprolol, 777absortion, fate, and
- Page 2212 and 2213:
Multifocal atrial tachycardia, drug
- Page 2214 and 2215:
α-Neoendorphin, actions andselecti
- Page 2216 and 2217:
Nitrogen mustards, 1668t-1670t,1682
- Page 2218 and 2219:
Olanzapinedosage of, 425tmetabolism
- Page 2220 and 2221:
Oxygenases, 125tOxygenation, normal
- Page 2222 and 2223:
Persistent hyperinsulinemichypoglyc
- Page 2224 and 2225:
Pityrosporum ovale, 1830Pivoxicam,
- Page 2226 and 2227:
Prescription writing (Cont.):date i
- Page 2228 and 2229:
Proton pump inhibitors (Cont.):in c
- Page 2230 and 2231:
Receptors (Cont.):affinity and, 44-
- Page 2232 and 2233:
Riskadverse effects and publicaccep
- Page 2234 and 2235:
Serotonin-norepinephrine reuptakein
- Page 2236 and 2237:
SPORANOX (itraconazole), 1818SPRYCE
- Page 2238 and 2239:
Sympathomimetic amines (Cont.):for
- Page 2240 and 2241:
Thioridazinearrhythmias caused by,
- Page 2242 and 2243:
Transporters (Cont.):resistance and
- Page 2244 and 2245:
Valacyclovir (Cont.):mechanism of a
- Page 2246 and 2247:
Vitamin B 12(Cont.):folic acid and,
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