ReP USP - Resultado da busca

Artigo de periodico
Use of antidepressants and the risk of upper gastrointestinal tract bleeding: a case-control study (2023)
Forgerini, Marcela ; Schiavo, Geovana ; Urbano, Gustavo ; Nadai, Tales Rubens de ; Zapata-Cachafeiro, Maruxa ; Herdeiro, Maria Teresa Ferreira ; Mastroianni, Patrícia de Carvalho
Fonte: Clinical Therapeutics. Unidades: FOB, FMRP
Assuntos: FÁRMACOS, ANTIDEPRESSIVOS, HEMORRAGIA, SISTEMA GASTROINTESTINAL
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ABNT
FORGERINI, Marcela et al. Use of antidepressants and the risk of upper gastrointestinal tract bleeding: a case-control study. Clinical Therapeutics, v. 45, n. 7, p. e159-e166, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.clinthera.2023.04.010. Acesso em: 29 jun. 2025.
APA
Forgerini, M., Schiavo, G., Urbano, G., Nadai, T. R. de, Zapata-Cachafeiro, M., Herdeiro, M. T. F., & Mastroianni, P. de C. (2023). Use of antidepressants and the risk of upper gastrointestinal tract bleeding: a case-control study. Clinical Therapeutics, 45( 7), e159-e166. doi:10.1016/j.clinthera.2023.04.010
NLM
Forgerini M, Schiavo G, Urbano G, Nadai TR de, Zapata-Cachafeiro M, Herdeiro MTF, Mastroianni P de C. Use of antidepressants and the risk of upper gastrointestinal tract bleeding: a case-control study [Internet]. Clinical Therapeutics. 2023 ; 45( 7): e159-e166.[citado 2025 jun. 29 ] Available from: https://doi.org/10.1016/j.clinthera.2023.04.010
Vancouver
Forgerini M, Schiavo G, Urbano G, Nadai TR de, Zapata-Cachafeiro M, Herdeiro MTF, Mastroianni P de C. Use of antidepressants and the risk of upper gastrointestinal tract bleeding: a case-control study [Internet]. Clinical Therapeutics. 2023 ; 45( 7): e159-e166.[citado 2025 jun. 29 ] Available from: https://doi.org/10.1016/j.clinthera.2023.04.010
Artigo de periodico
Fixed-combination bimatoprost/brimonidine/timolol in glaucom: a randomized, masked, controlled, phase III study conducted in Brazil (2020)
Belfort Junior, Rubens; Paula, Jayter Silva ; Silva, Marcelo Jordão Lopes; Della Paolera, Mauricio; Kim, Thomas; Chen, Michelle Y.; Goodkin, Margot L.
Fonte: Clinical Therapeutics. Unidade: FMRP
Assuntos: GLAUCOMA, HIPERTENSÃO OCULAR, MEDICAMENTO
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ABNT
BELFORT JUNIOR, Rubens et al. Fixed-combination bimatoprost/brimonidine/timolol in glaucom: a randomized, masked, controlled, phase III study conducted in Brazil. Clinical Therapeutics, v. 42, n. 2, p. 263-275, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.clinthera.2019.12.008. Acesso em: 29 jun. 2025.
APA
Belfort Junior, R., Paula, J. S., Silva, M. J. L., Della Paolera, M., Kim, T., Chen, M. Y., & Goodkin, M. L. (2020). Fixed-combination bimatoprost/brimonidine/timolol in glaucom: a randomized, masked, controlled, phase III study conducted in Brazil. Clinical Therapeutics, 42( 2), 263-275. doi:10.1016/j.clinthera.2019.12.008
NLM
Belfort Junior R, Paula JS, Silva MJL, Della Paolera M, Kim T, Chen MY, Goodkin ML. Fixed-combination bimatoprost/brimonidine/timolol in glaucom: a randomized, masked, controlled, phase III study conducted in Brazil [Internet]. Clinical Therapeutics. 2020 ; 42( 2): 263-275.[citado 2025 jun. 29 ] Available from: https://doi.org/10.1016/j.clinthera.2019.12.008
Vancouver
Belfort Junior R, Paula JS, Silva MJL, Della Paolera M, Kim T, Chen MY, Goodkin ML. Fixed-combination bimatoprost/brimonidine/timolol in glaucom: a randomized, masked, controlled, phase III study conducted in Brazil [Internet]. Clinical Therapeutics. 2020 ; 42( 2): 263-275.[citado 2025 jun. 29 ] Available from: https://doi.org/10.1016/j.clinthera.2019.12.008
Artigo de periodico
Harmonization of pharmacovigilance regulation in Brazil: opportunities to improve risk communication (2019)
Varallo, Fabiana Rossi ; Forgerini, Marcela ; Herdeiro, Maria Teresa Ferreira ; Mastroianni, Patricia de Carvalho
Fonte: Clinical Therapeutics. Unidade: FCFRP
Assuntos: SEGURANÇA DO PACIENTE, FÁRMACOS, FARMACOVIGILÂNCIA, MEDICAMENTO
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ABNT
VARALLO, Fabiana Rossi et al. Harmonization of pharmacovigilance regulation in Brazil: opportunities to improve risk communication. Clinical Therapeutics, v. 41, n. 3, p. 598-603, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.clinthera.2019.01.013. Acesso em: 29 jun. 2025.
APA
Varallo, F. R., Forgerini, M., Herdeiro, M. T. F., & Mastroianni, P. de C. (2019). Harmonization of pharmacovigilance regulation in Brazil: opportunities to improve risk communication. Clinical Therapeutics, 41( 3), 598-603. doi:10.1016/j.clinthera.2019.01.013
NLM
Varallo FR, Forgerini M, Herdeiro MTF, Mastroianni P de C. Harmonization of pharmacovigilance regulation in Brazil: opportunities to improve risk communication [Internet]. Clinical Therapeutics. 2019 ; 41( 3): 598-603.[citado 2025 jun. 29 ] Available from: https://doi.org/10.1016/j.clinthera.2019.01.013
Vancouver
Varallo FR, Forgerini M, Herdeiro MTF, Mastroianni P de C. Harmonization of pharmacovigilance regulation in Brazil: opportunities to improve risk communication [Internet]. Clinical Therapeutics. 2019 ; 41( 3): 598-603.[citado 2025 jun. 29 ] Available from: https://doi.org/10.1016/j.clinthera.2019.01.013
Trabalho de evento-resumo periodico
Influence of verapamil on the pharmacokinetics of oxcarbazepine and 10-hydroxycarbazepine enantiomers in healthy volunteers (2013)
Antunes, Natalícia de Jesus; Wichert-Ana, Lauro; Coelho, Eduardo Barbosa; Pasqua, O. Della; Alexandre Júnior, V; Takayanagui, Osvaldo Massaiti; Lanchote, Vera Lúcia
Fonte: Clinical Therapeutics. Nome do evento: Conference of the European Association for Clinical Pharmacology and Therapeutics (EACPT). Unidades: FMRP, FCFRP
Assuntos: FARMACOCINÉTICA, FARMACOLOGIA, CONVULSÕES
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ABNT
ANTUNES, Natalícia de Jesus et al. Influence of verapamil on the pharmacokinetics of oxcarbazepine and 10-hydroxycarbazepine enantiomers in healthy volunteers. Clinical Therapeutics. Bridgewater: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 29 jun. 2025. , 2013
APA
Antunes, N. de J., Wichert-Ana, L., Coelho, E. B., Pasqua, O. D., Alexandre Júnior, V., Takayanagui, O. M., & Lanchote, V. L. (2013). Influence of verapamil on the pharmacokinetics of oxcarbazepine and 10-hydroxycarbazepine enantiomers in healthy volunteers. Clinical Therapeutics. Bridgewater: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Antunes N de J, Wichert-Ana L, Coelho EB, Pasqua OD, Alexandre Júnior V, Takayanagui OM, Lanchote VL. Influence of verapamil on the pharmacokinetics of oxcarbazepine and 10-hydroxycarbazepine enantiomers in healthy volunteers. Clinical Therapeutics. 2013 ; 35( 85): e76.[citado 2025 jun. 29 ]
Vancouver
Antunes N de J, Wichert-Ana L, Coelho EB, Pasqua OD, Alexandre Júnior V, Takayanagui OM, Lanchote VL. Influence of verapamil on the pharmacokinetics of oxcarbazepine and 10-hydroxycarbazepine enantiomers in healthy volunteers. Clinical Therapeutics. 2013 ; 35( 85): e76.[citado 2025 jun. 29 ]
Artigo de periodico
Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers (2010)
Silva, Marina de Freitas; Schramm, Simone Grigoleto; Kano, Eunice Kazue; Koono, Eunice Emiko Mori; Porta, Valentina ; Serra, Cristina Helena dos Reis
Fonte: Clinical Therapeutics. Unidade: FCF
Assuntos: BIOEQUIVALÊNCIA, FARMACOCINÉTICA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA
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ABNT
SILVA, Marina de Freitas et al. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers. Clinical Therapeutics, v. 32, n. 4, p. 758-765, 2010Tradução . . Disponível em: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf. Acesso em: 29 jun. 2025.
APA
Silva, M. de F., Schramm, S. G., Kano, E. K., Koono, E. E. M., Porta, V., & Serra, C. H. dos R. (2010). Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers. Clinical Therapeutics, 32( 4), 758-765. Recuperado de http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
NLM
Silva M de F, Schramm SG, Kano EK, Koono EEM, Porta V, Serra CH dos R. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers [Internet]. Clinical Therapeutics. 2010 ; 32( 4): 758-765.[citado 2025 jun. 29 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
Vancouver
Silva M de F, Schramm SG, Kano EK, Koono EEM, Porta V, Serra CH dos R. Bioequivalence evaluation of single doses of two tramadol formulations: a randomized, open-label, two-period crossover study in healthy Brazilian volunteers [Internet]. Clinical Therapeutics. 2010 ; 32( 4): 758-765.[citado 2025 jun. 29 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6VRS-4YYPPM6-H-1&_cdi=6242&_user=5674931&_pii=S0149291810001074&_orig=browse&_coverDate=04%2F30%2F2010&_sk=999679995&view=c&wchp=dGLzVzz-zSkzS&md5=39b0f577aa141d4e2b40edd118fdd7a3&ie=/sdarticle.pdf
Artigo de periodico
Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study (2008)
Serra, Cristina Helena dos Reis ; Koono, Eunice Emiko Mori; Kano, Eunice Kazue; Schramm, Simone Grigoleto; Armando, Yara Popst; Porta, Valentina
Fonte: Clinical Therapeutics. Unidade: FCF
Assuntos: BIOEQUIVALÊNCIA, ZIDOVUDINA (FARMACOCINÉTICA)
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ABNT
SERRA, Cristina Helena dos Reis et al. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study. Clinical Therapeutics, v. 30, n. 5, p. 902-908, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.clinthera.2008.05.003. Acesso em: 29 jun. 2025.
APA
Serra, C. H. dos R., Koono, E. E. M., Kano, E. K., Schramm, S. G., Armando, Y. P., & Porta, V. (2008). Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study. Clinical Therapeutics, 30( 5), 902-908. doi:10.1016/j.clinthera.2008.05.003
NLM
Serra CH dos R, Koono EEM, Kano EK, Schramm SG, Armando YP, Porta V. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study [Internet]. Clinical Therapeutics. 2008 ;30( 5): 902-908.[citado 2025 jun. 29 ] Available from: https://doi.org/10.1016/j.clinthera.2008.05.003
Vancouver
Serra CH dos R, Koono EEM, Kano EK, Schramm SG, Armando YP, Porta V. Bioequivalence and pharmacokinetics of two zidovudine formulations in healthy Brazilian volunteers: an open-label, randomized, single-dose, two-way crossover study [Internet]. Clinical Therapeutics. 2008 ;30( 5): 902-908.[citado 2025 jun. 29 ] Available from: https://doi.org/10.1016/j.clinthera.2008.05.003

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