These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
171 related articles for article (PubMed ID: 7820334)
1. A method for the evaluation of individual bioequivalence. Endrenyi L Int J Clin Pharmacol Ther; 1994 Sep; 32(9):497-508. PubMed ID: 7820334 [TBL] [Abstract][Full Text] [Related]
2. Asymmetry of the mean-variability tradeoff raises questions about the model in investigations of individual bioequivalence. Endrenyi L; Hao Y Int J Clin Pharmacol Ther; 1998 Aug; 36(8):450-7. PubMed ID: 9726700 [TBL] [Abstract][Full Text] [Related]
3. Bioequivalence evaluation of two brands of amoxicillin/clavulanic acid 250/125 mg combination tablets in healthy human volunteers: use of replicate design approach. Idkaidek NM; Al-Ghazawi A; Najib NM Biopharm Drug Dispos; 2004 Dec; 25(9):367-72. PubMed ID: 15495146 [TBL] [Abstract][Full Text] [Related]
4. A three-step procedure for assessing bioequivalence in the general mixed model framework. Vuorinen J; Turunen J Stat Med; 1996 Dec; 15(24):2635-55. PubMed ID: 8981677 [TBL] [Abstract][Full Text] [Related]
5. Types of bioequivalence and related statistical considerations. Hauck WW; Anderson S Int J Clin Pharmacol Ther Toxicol; 1992 May; 30(5):181-7. PubMed ID: 1592546 [TBL] [Abstract][Full Text] [Related]
6. A modified large sample approach in the assessment of population bioequivalence. Quiroz J; Ting N; Wei GC; Burdick RK J Biopharm Stat; 2000 Nov; 10(4):527-44. PubMed ID: 11104391 [TBL] [Abstract][Full Text] [Related]
7. Saquinavir 500 mg film-coated tablets demonstrate bioequivalence to saquinavir 200 mg hard capsules when boosted with twice-daily ritonavir in healthy volunteers. Bittner B; Riek M; Holmes B; Grange S Antivir Ther; 2005; 10(7):803-10. PubMed ID: 16312177 [TBL] [Abstract][Full Text] [Related]
8. Evaluation of the bioequivalence of capsules containing 150 mg of fluconazole. Porta V; Chang KH; Storpirtis S Int J Pharm; 2005 Jan; 288(1):81-6. PubMed ID: 15607260 [TBL] [Abstract][Full Text] [Related]
9. Comparison of the reference scaled bioequivalence semi-replicate method with other approaches: focus on human exposure to drugs. Karalis V; Symillides M; Macheras P Eur J Pharm Sci; 2009 Aug; 38(1):55-63. PubMed ID: 19524039 [TBL] [Abstract][Full Text] [Related]
10. A limited sampling approach in bioequivalence studies: application to long half-life drugs and replicate design studies. Mahmood I; Mahayni H Int J Clin Pharmacol Ther; 1999 Jun; 37(6):275-81. PubMed ID: 10395118 [TBL] [Abstract][Full Text] [Related]
11. Alternative confidence intervals for the assessment of bioequivalence in four-period cross-over designs. Quiroz J; Ting N; Wei GC; Burdick RK Stat Med; 2002 Jul; 21(13):1825-47. PubMed ID: 12111892 [TBL] [Abstract][Full Text] [Related]
12. Analysis of metabolites--a new approach to bioequivalence studies of spironolactone formulations. Vergin H; Mahr G; Metz R; Eichinger A; Nitsche V; Martens H Int J Clin Pharmacol Ther; 1997 Aug; 35(8):334-40. PubMed ID: 9266289 [TBL] [Abstract][Full Text] [Related]
13. [Bioequivalence and generic drugs. I. Studies of bioequivalence, considering the theoretical basis, design and use]. Zapater P; Horga JF Rev Neurol; 1999 Dec 16-31; 29(12):1235-46. PubMed ID: 10652753 [TBL] [Abstract][Full Text] [Related]
14. Bioequivalence evaluation of two brands of lisinopril tablets (Lisotec and Zestril) in healthy human volunteers. Tamimi JJ; Salem II; Alam SM; Zaman Q; Dham R Biopharm Drug Dispos; 2005 Nov; 26(8):335-9. PubMed ID: 16075412 [TBL] [Abstract][Full Text] [Related]
15. Assessment of individual and population bioequivalence using the probability that bioavailabilities are similar. Schall R Biometrics; 1995 Jun; 51(2):615-26. PubMed ID: 7662849 [TBL] [Abstract][Full Text] [Related]
16. Evaluation of the bioequivalence of zidovudine 100 mg capsules in healthy Thai male volunteers. Chompootaweep S; Poonsrisawat J; Xumseang P J Med Assoc Thai; 2006 Sep; 89 Suppl 3():S79-85. PubMed ID: 17722305 [TBL] [Abstract][Full Text] [Related]
17. A two one-sided tests procedure for assessment of individual bioequivalence. Liu J; Chow SC J Biopharm Stat; 1997 Mar; 7(1):49-61. PubMed ID: 9056588 [TBL] [Abstract][Full Text] [Related]
18. Extension to the use of tolerance intervals for the assessment of individual bioequivalence. Esinhart JD; Chinchilli VM J Biopharm Stat; 1994 Mar; 4(1):39-52. PubMed ID: 8019583 [TBL] [Abstract][Full Text] [Related]
19. [Applying multilevel models in evaluation of bioequivalence (I)]. Liu QL; Shen ZZ; Chen F; Li XS; Yang M Zhonghua Liu Xing Bing Xue Za Zhi; 2009 Dec; 30(12):1302-6. PubMed ID: 20193320 [TBL] [Abstract][Full Text] [Related]
20. Assessment of the bioequivalence of two formulations of clarithromycin extended-release 500-mg tablets under fasting and fed conditions: a single-dose, randomized, open-label, two-period, two-way crossover study in healthy Jordanian male volunteers. Alkhalidi BA; Tamimi JJ; Salem II; Ibrahim H; Sallam AA Clin Ther; 2008 Oct; 30(10):1831-43. PubMed ID: 19014838 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]