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Clinical Trial Summary

The objective of this surveillance is to collect information about 1. adverse drug reaction not expected from the LPD (unknown adverse drug reaction) 2. the incidence of adverse drug reactions in this surveillance 3. factors considered to affect the safety and/or efficacy of this drug.


Clinical Trial Description

The patients should be registered by central registration system. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02501330
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date July 1, 2015
Completion date February 28, 2024

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