Trial Information

Summary: Observational Study to Evaluate Risks of Side Effects, Drug Abuse and Dependence in Patients Who Received Xyrem ® on Prescription

Post-Marketing Non-Interventional Pharmacoepidemiology Study to Evaluate Long-Term Safety, Tolerability and Compliance in Administration of Xyrem ® (Sodium Oxybate) in Regular Clinical Practice

Patients will be followed up for max 18 months. Information on the adverse events and potential misuse or abuse of Xyrem ® will be collected

Inclusion Criteria:
Patient s who received Xyrem® on prescription

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Trial listings updated: March 17, 2008 at 3:01:37 PM