標(biāo)題: Titlebook: Drugs Eicosanoids; Second Messengers. N John Fawcett Wilson Book 1995 Springer Science+Business Media Dordrecht 1995 Chloramphenicol.Methad [打印本頁(yè)] 作者: mandatory 時(shí)間: 2025-3-21 18:10
書目名稱Drugs Eicosanoids影響因子(影響力)
書目名稱Drugs Eicosanoids影響因子(影響力)學(xué)科排名
書目名稱Drugs Eicosanoids網(wǎng)絡(luò)公開度
書目名稱Drugs Eicosanoids網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Drugs Eicosanoids被引頻次
書目名稱Drugs Eicosanoids被引頻次學(xué)科排名
書目名稱Drugs Eicosanoids年度引用
書目名稱Drugs Eicosanoids年度引用學(xué)科排名
書目名稱Drugs Eicosanoids讀者反饋
書目名稱Drugs Eicosanoids讀者反饋學(xué)科排名
作者: LUDE 時(shí)間: 2025-3-22 00:13
Women Workers and The Family Wage in Canaday but with a bias towards sodium retaining effects. Fluorine or methyl substitutions at C6 also enhance potency. Typical examples of selective anti-inflammatory steroids are dexamethasone, betamethasone and triamcinolone which are 9-fluoro, 16-methyl or 16-hydroxy derivatives of hydro-cortisone with作者: Palatial 時(shí)間: 2025-3-22 01:49 作者: 青石板 時(shí)間: 2025-3-22 07:22 作者: 圍巾 時(shí)間: 2025-3-22 09:54 作者: cataract 時(shí)間: 2025-3-22 14:02 作者: cataract 時(shí)間: 2025-3-22 19:39
Corporate Training Investment Decisionsnext dose of > 10 μg/ ml. The therapeutic range in plasma is 15-25 μg/ml for peak concentrations and 4-6 μg/ml for the trough. Concentrations cannot be predicted accurately from dose, hence monitoring is used to avoid undertreatment and ensure safety.作者: Overstate 時(shí)間: 2025-3-23 01:00 作者: 搖曳 時(shí)間: 2025-3-23 03:52
Deborah E. Belle,Ruth F. Tebbets, whilst after single doses it is 18 to 65 hours. The therapeutic range in plasma is 4-12 μg/ml. Measurements of non-protein bound drug concentration in saliva and of the epoxide metabolite may be performed.作者: 交響樂 時(shí)間: 2025-3-23 09:08 作者: languid 時(shí)間: 2025-3-23 12:44 作者: filicide 時(shí)間: 2025-3-23 16:48
Corporate Training Investment Decisionserable inter-individual variation in metabolism, plasma half-life varying from 8 to 51 hours. The therapeutic range in plasma for treatment of endogenous depression is 0.1-0.2 μg/ml (combined amitriptyline and nortriptyline concentration).作者: 舊石器 時(shí)間: 2025-3-23 21:07
Corporate Training Investment Decisionsalf-life of 2 to 10 hours. The exception is in neonates where the hepatic enzymes are underdeveloped and much caffeine is excreted unchanged. The half-life is 36 to 144 hours in neonates. Toxic effects are associated with plasma concentrations > 15 μg/ml and fatalities with >80 μg/ml.作者: BRIDE 時(shí)間: 2025-3-23 22:29
Economies as an Antitrust Defense Revisitedative and antimuscarinic effects but more pronounced extrapyramidal side-effects as compared with chlorpromazine. After oral administration, some 75% of the dose is excreted in urine with < 1% as unchanged drug and the remainder in the faeces. The half-life in plasma is 2 to 3 hours.作者: jagged 時(shí)間: 2025-3-24 05:20 作者: 和平 時(shí)間: 2025-3-24 10:13
Cyclosporin A,phrotoxicity which occurs in approximately a third of patients. The concentration difference between possible transplant rejection and toxicity is small. It has been suggested that whole blood measurements of 0.25-1 μg/ml or plasma concentrations of 0.05-0.2 μg/ml produce satisfactory immunosuppression and minimize adverse effects.作者: 懶鬼才會(huì)衰弱 時(shí)間: 2025-3-24 13:52 作者: STERN 時(shí)間: 2025-3-24 18:31
Digoxin,s take 6 to 7 days to be achieved. Digoxin is excreted largely unchanged by the kidney hence clearance is prolonged by renal impairment. Therapeutic drug monitoring in hospitals has been shown to be cost-effective by reducing the incidence of side-effects and shortening in-patient stay.作者: 整體 時(shí)間: 2025-3-24 20:58
Acecainide (N-Acetylprocainamide),xcreted unchanged in urine. The half-life in plasma is 6-9 hours (procainamide 2.5-4 hours), increasing with renal impairment. Therapeutic concentrations in plasma have been proposed to be 10-30 μg/ ml for the sum of both procainamide and acecainide, or 4-10 μg/ml for procainamide and 6-20 μg/ml for acecainide.作者: thalamus 時(shí)間: 2025-3-25 00:40 作者: Spinal-Tap 時(shí)間: 2025-3-25 04:13
Bumetanide,centration reported after a 1 mg dose is 0.03 μg/ml. The drug is largely excreted in urine with some 10-15% in faeces. Most excreted drug is unchanged with small amounts of alcohol hydroxylation products present. The half-life in plasma is about 1-1.5 hours.作者: START 時(shí)間: 2025-3-25 09:55 作者: minaret 時(shí)間: 2025-3-25 15:11 作者: Lacunar-Stroke 時(shí)間: 2025-3-25 19:14 作者: 返老還童 時(shí)間: 2025-3-25 21:04
Acecainide (N-Acetylprocainamide),logical activity, a longer duration of action, and produces less frequent cardiac complications and hypersensitivity reactions than procainamide. The acetylation of procainamide is subject to genetic polymorphism with 30-40% being converted in fast acetylators. Up to 85% of a dose of acecainide is e作者: 擔(dān)心 時(shí)間: 2025-3-26 03:27 作者: lipids 時(shí)間: 2025-3-26 07:43
Amikacin,Excretion in urine by glomerular filtration is largely of unchanged compound with a plasma half-life of 2 to 3 hours. Ototoxicity and nephrotoxicity are minimized by avoiding peak plasma concentrations measured one hour after administration of > 30 μg/ml or trough concentrations measured before the 作者: 無(wú)底 時(shí)間: 2025-3-26 09:33
Amitriptyline,Amitriptyline is demethylated to nortriptyline and then by several other routes to metabolites excreted in urine. Genetic differences result in considerable inter-individual variation in metabolism, plasma half-life varying from 8 to 51 hours. The therapeutic range in plasma for treatment of endogen作者: overrule 時(shí)間: 2025-3-26 12:44
Boldenone,and produce behavioural changes of a masculinizing type in geldings and mares. Reproductive efficiency is impaired in both sexes. Metabolites appearing in urine in horses are 17α-hydroxy-epimers as glucuronic acid conjugates and unchanged drug with 17β-hydroxy compounds as sulphate conjugates.作者: Cursory 時(shí)間: 2025-3-26 20:32
Bumetanide, loop of Henle in the renal tubule. Use is in the treatment of pulmonary oedema in patients with heart or renal failure. The peak effect is within 30 minutes of intravenous or 1 hour of oral administration and diuresis complete within 6 hours. Oral absorption is rapid and complete. The mean peak con作者: Bereavement 時(shí)間: 2025-3-27 00:05 作者: 大笑 時(shí)間: 2025-3-27 02:31
Carbamazepine,te carbamazepine-10,11-epoxide retaining approximately one third of the antiepileptic activity of carbamazepine. Carbamazepine is a hepatic enzyme inducer of its own metabolism and of other drugs. The plasma half-life during chronic treatment is 10 to 30 hours in adults and 8 to 19 hours in children作者: AUGUR 時(shí)間: 2025-3-27 06:40
Corticosteroids,classes. The glucocorticoids are those compounds with relatively powerful activity on carbohydrate metabolism causing an elevation of circulating glucose concentration and liver glycogen stores. These compounds find wide clinical application as anti-inflammatory and immunosuppressive agents. The sec作者: 容易生皺紋 時(shí)間: 2025-3-27 09:27
Sodium Cromoglycate,of no value in the treatment of an acute attack of asthma but may prevent exercise-induced asthma if given half an hour before. The mode of action is not understood but has been associated with inhibition of a number of inflammatory mediators. Oral absorption is poor and < 10% of inhaled doses reach作者: 摻假 時(shí)間: 2025-3-27 16:29 作者: fallible 時(shí)間: 2025-3-27 18:03
Desipramine,s the principal active metabolite of imipramine. The plasma half-life varies from 10 to 35 hours as a result of inter-subject variability in metabolism. The therapeutic range in plasma is 0.07-0.2 μg/ml. Monitoring is valuable only in patients with a diagnosis of endogenous depression.作者: 業(yè)余愛好者 時(shí)間: 2025-3-28 00:53 作者: ureter 時(shí)間: 2025-3-28 05:11 作者: 珠寶 時(shí)間: 2025-3-28 09:35 作者: FLASK 時(shí)間: 2025-3-28 13:21 作者: 國(guó)家明智 時(shí)間: 2025-3-28 15:47
Ethosuximide,t 20% of unchanged drug. The plasma half-life is 40 to 60 hours in adults and approximately 30 hours in children. There is good correlation between plasma concentration and response. The therapeutic range in plasma is 40-100 μg/ml.作者: 比賽用背帶 時(shí)間: 2025-3-28 22:00
Etorphine,n morphine and its use carries some risk as it can be absorbed through human skin following accidental spillage. It is a drug of dependence but is said to produce less tolerance and respiratory depression than morphine.作者: Legend 時(shí)間: 2025-3-29 01:44 作者: Sedative 時(shí)間: 2025-3-29 04:32 作者: 替代品 時(shí)間: 2025-3-29 10:06 作者: 預(yù)兆好 時(shí)間: 2025-3-29 14:57
Alfentanil,ia. Prolonged use may lead to dependence. Biotransformation in the liver is to inactive metabolites which are excreted in urine. The half-life in plasma is about 1.5 hours. Plasma concentrations after a 50 μg/ kg intravenous dose have been measured as 0.54 μg/ml at 1 min falling to 0.038 μg/ml at 1 hour.作者: elucidate 時(shí)間: 2025-3-29 17:49 作者: CAMEO 時(shí)間: 2025-3-29 20:38 作者: Certainty 時(shí)間: 2025-3-30 01:38 作者: 工作 時(shí)間: 2025-3-30 07:00 作者: Cabinet 時(shí)間: 2025-3-30 10:00
Etorphine,n morphine and its use carries some risk as it can be absorbed through human skin following accidental spillage. It is a drug of dependence but is said to produce less tolerance and respiratory depression than morphine.作者: fidelity 時(shí)間: 2025-3-30 14:31 作者: 是剝皮 時(shí)間: 2025-3-30 20:23 作者: jabber 時(shí)間: 2025-3-31 00:29
Corporate Training Investment Decisionslogical activity, a longer duration of action, and produces less frequent cardiac complications and hypersensitivity reactions than procainamide. The acetylation of procainamide is subject to genetic polymorphism with 30-40% being converted in fast acetylators. Up to 85% of a dose of acecainide is e作者: 是比賽 時(shí)間: 2025-3-31 04:16
Corporate Training Investment Decisionsia. Prolonged use may lead to dependence. Biotransformation in the liver is to inactive metabolites which are excreted in urine. The half-life in plasma is about 1.5 hours. Plasma concentrations after a 50 μg/ kg intravenous dose have been measured as 0.54 μg/ml at 1 min falling to 0.038 μg/ml at 1 作者: ANTI 時(shí)間: 2025-3-31 06:55 作者: 弓箭 時(shí)間: 2025-3-31 11:30
Corporate Training Investment DecisionsAmitriptyline is demethylated to nortriptyline and then by several other routes to metabolites excreted in urine. Genetic differences result in considerable inter-individual variation in metabolism, plasma half-life varying from 8 to 51 hours. The therapeutic range in plasma for treatment of endogen作者: Cirrhosis 時(shí)間: 2025-3-31 16:17 作者: 引起 時(shí)間: 2025-3-31 20:12
Deborah E. Belle,Ruth F. Tebbets loop of Henle in the renal tubule. Use is in the treatment of pulmonary oedema in patients with heart or renal failure. The peak effect is within 30 minutes of intravenous or 1 hour of oral administration and diuresis complete within 6 hours. Oral absorption is rapid and complete. The mean peak con作者: 思想上升 時(shí)間: 2025-4-1 00:49 作者: Grandstand 時(shí)間: 2025-4-1 04:41
Deborah E. Belle,Ruth F. Tebbetste carbamazepine-10,11-epoxide retaining approximately one third of the antiepileptic activity of carbamazepine. Carbamazepine is a hepatic enzyme inducer of its own metabolism and of other drugs. The plasma half-life during chronic treatment is 10 to 30 hours in adults and 8 to 19 hours in children作者: Asseverate 時(shí)間: 2025-4-1 08:58 作者: 招致 時(shí)間: 2025-4-1 11:32 作者: 低三下四之人 時(shí)間: 2025-4-1 15:31
Women Workers and The Family Wage in Canadaive and antifungal activity used to minimize rejection following organ transplantation. Administration is via the parenteral or oral route. Absorption after oral administration is variable and incomplete. In blood it is found in erythrocytes (50%), leukocytes (10%), and bound to plasma proteins (40%
