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Participant Information Sheet Study title: for the Treatment of CANVAS associated Chronic CoughLocality:Center for Brain Research Neurogenetic Research Clinic. University of Auckland. Ethics committee
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Gather all necessary information about the drug including its name, dosage, manufacturer, and potential side effects.
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Follow up with patients who have reported side effects to gather more information and assess their severity.
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Update the drug safety documentation regularly to ensure it reflects the most up-to-date information.

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A comprehensive drug safety refers to a detailed assessment and reporting of the safety profile of a drug, including any potential risks or adverse effects.
Manufacturers, sponsors, or distributors of drugs are typically required to file a comprehensive drug safety report.
To fill out a comprehensive drug safety report, one must gather all relevant safety data, analyze it, and submit the report to the appropriate regulatory authorities.
The purpose of a comprehensive drug safety report is to ensure that the safety of a drug is continuously monitored and addressed to minimize potential risks to patients.
Information that must be reported on a comprehensive drug safety includes adverse reactions, side effects, patient outcomes, and any additional safety data.
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