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Clinical Trial Summary

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


Clinical Trial Description

All the patients whom an investigator prescribes the first Gabapentin should be registered consecutively until the number of subjects reaches target number in order to extract patients enrolled into the investigation at random. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00567268
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date August 2007
Completion date May 2014

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