The main objective of this PMS study was to monitor and assess the safety of Mobic® intramuscular injection (7.5mg \~ 15mg, q.d.) up to 3 days (in case of need for prolonged treatment, switch to Mobic® capsule therapy was possible) in Korean patients with osteoarthritis and rheumatoid arthritis.
Study Type
OBSERVATIONAL
Enrollment
425
Boehringer Ingelheim Investigational Site
Busan, South Korea
Boehringer Ingelheim Investigational Site
Daegu, South Korea
Boehringer Ingelheim Investigational Site
Daejeon, South Korea
Efficacy assessment by the treating physician
Time frame: up to 3 day
Combined efficacy, safety and tolerability assessment by the treating physician
Time frame: up tp 3 day
Incidence of adverse events
Time frame: up tp 3 day
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Boehringer Ingelheim Investigational Site
Gangwondo, South Korea
Boehringer Ingelheim Investigational Site
Gwangju, South Korea
Boehringer Ingelheim Investigational Site
Gyeongbuk, South Korea
Boehringer Ingelheim Investigational Site
Gyeonggido, South Korea
Boehringer Ingelheim Investigational Site
Gyeongnam, South Korea
Boehringer Ingelheim Investigational Site
Jeonnam, South Korea
Boehringer Ingelheim Investigational Site
Jungbuk, South Korea
...and 1 more locations