Popis: |
Background In August 2006, the Netherlands Pharmacovigilance Centre Lareb started with Lareb Intensive Monitoring (LIM). The main objective of LIM is to monitor the safety of new drugs. Patients eligible for participation are identified using the first dispensing signal in the pharmacy. After registration on www.larebmonitor.nl, questionnaires are sent to the patient at specific points in time asking for their experiences with the drug, including Adverse Drug Reactions (ADRs). LIM gives the opportunity to follow drugs more closely than with the current spontaneous reporting system. At the moment, pregabaline and duloxetine are being monitored. |