Bioavailability after subcutaneous administration: 62%
T1/2: mean 28 days (14-55 days)
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No information is present at this moment.
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No information is present at this moment.
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| Giant cell tumour of bone |
|---|
|
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Dose adjustment is not required in renal impairment.
Monitoring of serum calcium concentration is recommended in severe renal impairment (creatinine clearance less than 30 ml / min) and in dialysis due to the increased risk of hypocalcaemia in these patients.
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The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here
The side effect profile in children (12-18 years) is similar to the side effect profile in adults. Clinically significant hypercalcaemia after treatment discontinuation has been reported in the post-marketing setting in pediatric patients.
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The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here
No information available on specific contra indications in children.
The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here
No information available on specific warnings and precautions in children.
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The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here
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| Bisphosphonates | ||
|---|---|---|
| M05BA04 | ||
| M05BA03 | ||
| M05BA07 | ||
| Other drugs affecting bone structure and mineralization | ||
|---|---|---|
| M05BX05 | ||
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