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Adverse reactions occurring in at least 2% of the Pagets patients receiving Reclast (single 5 mg intravenous infusion) or risedronate (30 mg oral daily dose for 2 months) over a 6-month study period are listed by system organ class in Table 4

Acknowledgements The authors would like to acknowledge the valuable scientific input and discussions from members of the NEURODIET consortium, which contributed to the development of this review