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A Non-Interventional, Post-Marketing Surveillance (NI-PMS) study whose objectives were to assess the impact of pregabalin on subjects' pain, quality of sleep, and their general wellbeing, as well as the tolerance and safety of pregabalin in subjects with neuropathic pain.
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A non-interventional study of patients diagnosed with neuropathic pain administered pregabalin and followed up for 8 weeks
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691 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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