An exact confidence interval from untransformed data for the ratio of two formulation means.
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Effect of altered gastric emptying and gastrointestinal motility on metformin absorptionA comparison of the Two One-Sided Tests Procedure and the Power Approach for assessing the equivalence of average bioavailabilityInference of bioequivalence for log-normal distributed data with unspecified variances.Absolute bioavailability of glimepiride (Amaryl) after oral administration.Dose linearity assessment of glimepiride (Amaryl) tablets in healthy volunteers.Pharmacokinetics and safety of a single dose of stavudine (d4T) in patients with severe hepatic impairment.Evaluation of possible drug-drug interaction between gadoxetic acid and erythromycin as an inhibitor of organic anion transporting peptides (OATP).In vitro dissolution and in vivo bioequivalence evaluation of two brands of trimetazidine tablets.Pharmacokinetics and comparative bioavailability of domperidone suspension and tablet formulations in healthy adult subjects.Pharmacokinetics and Bioequivalence Evaluation of 2 Loxoprofen Tablets in Healthy Egyptian Male Volunteers.A Novel Approach to Testing for Average Bioequivalence Based on Modeling the Within-Period Dependence Structure.A survey of the likelihood approach to bioequivalence trials.Pharmacokinetics and pharmacodynamics of irbesartan in patients with hepatic cirrhosis.Bioequivalence evaluation of two brands of cefaclor 500 mg capsules: quantification of cefaclor using solid phase extraction technique.B-domain deleted recombinant factor VIII preparations are bioequivalent to a monoclonal antibody purified plasma-derived factor VIII concentrate: a randomized, three-way crossover study.The effects of age and gender on the single dose pharmacokinetics of avitriptan administered to healthy volunteers.Comparative study of bioavailability and clinical efficacy of carbamazepine in epileptic patients.Bioequivalence evaluation of two brands of cefuroxime 500 mg tablets (Cefuzime and Zinnat) in healthy human volunteers.Bioequivalence evaluation of norfloxacin 400 mg tablets (Uroxin and Noroxin) in healthy human volunteers.On confidence limits associated with Chow and Shao's joint confidence region approach for assessment of bioequivalence.The assessment of individual and population bioequivalence.Fosinopril: pharmacokinetics and pharmacodynamics in Chinese subjects.Safety and pharmacokinetics of a single oral dose of gatifloxacin in patients with moderate to severe hepatic impairment.Lack of effect of food on the oral bioavailability of irbesartan in healthy male volunteers.The pharmacokinetics of venlafaxine when given in a twice-daily regimen.
P2860
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P2860
An exact confidence interval from untransformed data for the ratio of two formulation means.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
1984年论文
@zh
1984年论文
@zh-cn
name
An exact confidence interval f ...... atio of two formulation means.
@ast
An exact confidence interval f ...... atio of two formulation means.
@en
type
label
An exact confidence interval f ...... atio of two formulation means.
@ast
An exact confidence interval f ...... atio of two formulation means.
@en
prefLabel
An exact confidence interval f ...... atio of two formulation means.
@ast
An exact confidence interval f ...... atio of two formulation means.
@en
P356
P1476
An exact confidence interval f ...... atio of two formulation means.
@en
P2093
P2888
P304
P356
10.1007/BF01059558
P577
1984-12-01T00:00:00Z