Last updated on November 2019
S-CEI of Nexium in Paediatric Patients
Brief description of study
To capture safety and efficacy when Nexium are administered to pediatric patients in clinical practice after launch
Detailed Study Description
The objective of this investigation is to capture the followings when Nexium capsules or Nexium granules for suspension (single-dose package) are administered to pediatric patients in clinical practice after launch.
- Development of adverse reactions which are unexpected from Precaution for Use
- Development of adverse reactions
- Efficacy
Clinical Study Identifier: NCT03562026