Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Jun;85(6):1063-1071.
doi: 10.1111/bcp.13759. Epub 2018 Oct 17.

Side effects of drugs for osteoporosis and metastatic bone disease

Affiliations
Review

Side effects of drugs for osteoporosis and metastatic bone disease

Michael Kriegbaum Skjødt et al. Br J Clin Pharmacol. 2019 Jun.

Abstract

Osteoporosis is a common condition that leads to substantial morbidity and mortality and affects an increasing number of persons worldwide. Several pharmacological therapies that inhibit bone resorption, promote bone formation, or both, are available for the treatment of osteoporosis. The osteoanabolic treatment spectrum was recently expanded by the introduction of a novel bone-forming agent in the United States, and clinical trials indicate that a new class of bone anabolic therapy may become available. Both antiresorptive and bone anabolic therapies are associated with common and rare adverse effects, which are particularly important to address as these drugs are used for long-term treatment in numerous patients with a large proportion being elderly and/or having multimorbidity. In addition, antiresorptive drugs are used to inhibit bone resorption in patients with malignant hypercalcaemia or to prevent skeletal events in cancer patients, and bisphosphonates have been repurposed as a cancer preventive therapy. However, therapeutic doses are generally higher when antiresorptive drugs are used in the oncological setting, which influence the prevalence of adverse effects significantly. This review highlights key issues and controversies regarding adverse effects of currently available and emerging drugs used for osteoporosis and metastatic bone diseases.

Keywords: clinical pharmacology; drug information; drug safety; osteoporosis rheumatology.

PubMed Disclaimer

Conflict of interest statement

B.A. has institutional research contracts with UCB and Novartis with funds paid to the institution. M.K.S. and M.F. have no competing interests to declare.

Figures

Figure 1
Figure 1
Total sale (DDD) of osteoporosis medications in Denmark per year per 1000 persons aged 50 years or older from 1999 to 2016. Bisphosphonates remain the most commonly used osteoporosis medication. Denosumab use has been steadily increasing since its market introduction. As compared to bisphosphonates and denosumab, raloxifene and teriparatide are less frequently used, while strontium is scarcely used. Abaloparatide is not licensed in EuropeSource: www.medstat.dk (an open‐access, online database of all prescribtion‐based and over‐the‐counter sales of medications in Denmark) and Statistics Denmark (www.dst.dk). DDD, defined daily dose.

References

    1. Bliuc D, Nguyen ND, Milch VE, Nguyen TV, Eisman JA, Center JR. Mortality risk associated with low‐trauma osteoporotic fracture and subsequent fracture in men and women. JAMA 2009; 301: 513–521. - PubMed
    1. Johnell O, Kanis JA, Oden A, Johansson H, de Laet C, Delmas P, et al Predictive value of BMD for hip and other fractures. J Bone Miner Res 2005; 20: 1185–1194. - PubMed
    1. Ettinger B, Black DM, Mitlak BH, Knickerbocker RK, Nickelsen T, Genant HK, et al Reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: results from a 3‐year randomized clinical trial. Multiple Outcomes of Raloxifene Evaluation (MORE) investigators. JAMA 1999; 282: 637–645. - PubMed
    1. Murad MH, Drake MT, Mullan RJ, Mauck KF, Stuart LM, Lane MA, et al Clinical review. Comparative effectiveness of drug treatments to prevent fragility fractures: a systematic review and network meta‐analysis. J Clin Endocrinol Metab 2012; 97: 1871–1880. - PubMed
    1. Black DM, Delmas PD, Eastell R, Reid IR, Boonen S, Cauley JA, et al Once‐yearly zoledronic acid for treatment of postmenopausal osteoporosis. N Engl J Med 2007; 356: 1809–1822. - PubMed

Substances