Treatment of osteoporosis in postmenopausal women and
in men at increased risk of fractures | Treatment of
corticosteroid-induced osteoporosis
▶BY SUBCUTANEOUS INJECTION
▶Adult: 20 micrograms daily for maximum duration of
treatment 24 months (course not to be repeated)
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Bone metastases.
hyperparathyroidism. metabolic bone diseases. Paget’s
disease. pre-existing hypercalcaemia. previous radiation
therapy to the skeleton. skeletal malignancies.
unexplained raised alkaline phosphatase
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Teriparatide
is a biological medicine. Biological medicines must be
prescribed and dispensed by brand name, see Biological
medicines and Biosimilar medicines, under Guidance on
prescribing p. 1.
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NICE decisions
▶Raloxifene and teriparatide for the secondary prevention of
osteoporotic fragility fractures in postmenopausal women
(updated February 2018) NICE TA161
Teriparatide is recommended as an alternative treatment
option for the secondary prevention of osteoporotic
fragility fractures in postmenopausal women:
. who are unable to take alendronate and risedronate, or
have a contra-indication to or are intolerant of
Endocrine system
alendronate and risedronate, or have had an
unsatisfactory response to treatment with alendronate
or risedronate, and
. who are 65 years or older and have a T-score of -4
standard deviations (SD) or below, or a T-score of -3.5
SD or below plus more than two fractures, or who are
aged 55-64 years and have a T-score of -4 SD or below
plus more than two fractures.
Women who are currently receiving treatment, but for
whom treatment would not have been recommended,
should have the option to continue treatment until they
and their NHS clinician consider it appropriate to stop.
www.nice.org.uk/guidance/ta161
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