Prolia® Postmarketing Active Safety Surveillance Program for Soliciting Adverse Events of Special Interest in the United States (PASP-EMR Program)

First published 16/01/2017

Last updated 22/02/2024

EU PAS number:

EUPAS17198

Study

Finalised

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Documents

Study protocol

Initial protocol

20090601Protocol Amend 2 2016 Fully Redacted

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Updated protocol

20090601Protocol Amend 2 2016-06-23

First published: 22/02/2024

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Study results

Study results

denosumab 20090601 Observational Final Analysis Abstract

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Study report

Other information