Lead Sponsor

GlaxoSmithKline

Age

All ages

Sex

FEMALE

Healthy Volunteers

No

•All subjects must satisfy the following criteria at study entry:
•Subjects administered with BONVIVA(ibandronate) injection following the locally approved prescribing information Women diagnosed with postmenopausal osteoporosis. Subjects who the investigator believes that they can and will comply with the requirements of the protocol Subjects with no experience of treatment using ibandronate injection Note: Subjects, who have experience of other bisphosphonates treatment, can be included.
•Subjects who are indicated and administered of ibandronate injection according to the Prescribing Information in normal prescription use

•The following criteria should be checked at the time of study entry.
•According to contraindication on the prescribing information, ibandronate injection should not be administered to the following patients:
•Patients with known hypersensitivity to ibandronate injection or to any of its excipients Uncorrected hypocalcemia Note: Ibandronate injection is not recommended for use in patients who have a serum creatinine above 200 μmol/l (2.3 mg/dl) or who have a creatinine clearance (measured or estimated) below 30 ml/min, because of limited clinical data available from studies including such patients.