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Adverse Drug Reactions (ADRs) are defined by WHO as harmful and unintended responses to drugs at normal doses, excluding effects from overdose or misuse. They are classified into Type A (predictable) and Type B (unpredictable), with Type A being common and dose-dependent, while Type B is rare and not dose-dependent. Pharmacovigilance is crucial for monitoring and preventing ADRs, involving post-marketing surveillance and data collection to ensure drug safety.

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usaha779

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EN