This study is a regulatory post-marketing surveillance in Japan, and it is a local prospective and observational study of patients who have received Julina for postmenopausal osteoporosis. The objective of this study is to assess safety and efficacy of using Julina in clinical practice. A total 100 patients will be recruited and followed 3 years since starting Julina administration.
Study Type
OBSERVATIONAL
Enrollment
148
Patients in daily life treatment receiving Julina for postmenopausal osteoporosis
Unnamed facility
Many Locations, Japan
Incidence of adverse drug reactions and serious adverse events in subject who received Julina
Time frame: After Julina administration, upto 3 years
Incidence of adverse drug reactions in subpopulation with baseline data (such as demographic data, concomitant disease, hysterectomy) and dose of Julina
Time frame: At baseline and after Julina administration, upto 3 years
Effectiveness evaluation assessment by the three rank scales: improvement, not changed, and worse
Time frame: At baseline and at end of Julina treatment, upto 3 years
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