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Syed Sulaiman
Discipline of Clinical Pharmacy, School of Pharmaceutical Sciences, University Sains Malaysia, Penang, Malaysia
Publications
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Review Article
Safety Review of Quinolone and Fluoroquinolone Containing Medicinal Products: Global Regulatory Scenario and Way Forward
Author(s): Muhammad Haseeb Tariq*, Muhammad Junaid Farrukh, Syed Azhar, Syed Sulaiman and Obaidullah
Drugs are introduced into the market for use by the patients after year’s long drug development processes including extensive clinical trials and stringent approval pathway by drug regulatory authority keeping in view safety, efficacy and quality parameters. Drugs are usually approved after successful completion of phase III clinical trial. Post marketing surveillance or phase-IV clinical trials are focused on long term safety studies and may continue for years. Drugs are withdrawn from the market if serious adverse events appeared even after approvals like withdrawal of rofecoxib [1]. .. View more»