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2System of adverse drug reactions reporting: What, where, how, and whom to report?
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3Audit to evaluate the completeness of adverse drug reporting in an ADR monitoring centre in Tamilnadu
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4Public-private partnership (3Ps) in ensuring safe use of medicines: An Indian experience
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5An overview of the pharmacovigilance system in India
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6Adverse events following immunisation (AEFI) reports from the Zimbabwe expanded programme on immunisation (ZEPI): an analysis of spontaneous reports in Vigibase® from 1997 to 2017
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7Best Practices for Improving the Quality of Individual Case Safety Reports in Pharmacovigilance
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9Risk of Intussusception with Rotavirus Vaccine
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10Risk of Intussusception with Rotavirus Vaccine
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11An analysis of the trends, characteristics, scope, and performance of the Zimbabwean pharmacovigilance reporting scheme
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