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Yakugaku Zasshi : Journal of the Pharmaceutical Society of Japan|March 4, 2016
[Evaluation of the Association of Hand-Foot Syndrome with Anticancer Drugs Using the US Food and Drug Administration Adverse Event Reporting System (FAERS) and Japanese Adverse Drug Event Report (JADER) Databases]Sayaka Sasaoka, Toshinobu Matsui, Junko Abe, et al.Plos One|October 11, 2016
Time-to-Onset Analysis of Drug-Induced Long QT Syndrome Based on a Spontaneous Reporting System for Adverse Drug EventsSayaka Sasaoka, Toshinobu Matsui, Yuuki Hane, et al.International Journal of Medical Sciences|March 7, 2017
Age-related trends in injection site reaction incidence induced by the tumor necrosis factor-α (TNF-α) inhibitors etanercept and adalimumab: the Food and Drug Administration adverse event reporting system, 2004-2015Toshinobu Matsui, Ryogo Umetsu, Yamato Kato, et al.Journal of Pharmaceutical Health Care and Sciences|July 22, 2017
Drug-induced gingival hyperplasia: a retrospective study using spontaneous reporting system databasesHaruna Hatahira, Junko Abe, Yuuki Hane, et al.Nursing Open|March 31, 2018
Contraceptives as possible risk factors for postpartum depression: A retrospective study of the food and drug administration adverse event reporting system, 2004-2015Megumi Horibe, Yuuki Hane, Junko Abe, et al.Plos One|July 22, 2017
Thromboembolic adverse event study of combined estrogen-progestin preparations using Japanese Adverse Drug Event Report databaseShiori Hasegawa, Toshinobu Matsui, Yuuki Hane, et al.Plos One|September 28, 2017
Comparison of the adverse event profiles of conventional and liposomal formulations of doxorubicin using the FDA adverse event reporting systemAkiho Fukuda, Kohei Tahara, Yuuki Hane, et al.Journal of Pharmaceutical Health Care and Sciences|June 23, 2016
Analysis of Stevens-Johnson syndrome and toxic epidermal necrolysis using the Japanese Adverse Drug Event Report databaseJunko Abe, Ryogo Umetsu, Kanako Mataki, et al.Pageof 1