(Source: Clinical )Īn unwanted effect caused by the administration of drugs. Canadian lingo trial#Unfavourable changes in health, including abnormal laboratory findings, that occur in trial participants during the clinical trial or within a specified period following the trial. 17)Īn adverse outcome that occurs during or after the use of a drug or other intervention but is not necessarily caused by it. In the case of drugs an adverse effect tends to be seen from the point of view of the drug and an adverse reaction is seen from the point of view of the patient. The term 'adverse effect' applies to all interventions, while 'adverse drug reaction' (ADR) is used only with drugs. The dual role as administrative coordinator does not imply a superior contribution to the leadership of the research program.Īdverse effects ( effet indésirable ou préjudice)Īn adverse event for which the causal relation between the drug/intervention and the event is at least a reasonable possibility. Note: CIHR requires all program leaders to be fully accountable for setting and overseeing the intellectual and strategic direction of the CIHR-funded program of research. In cases when there are multiple program leaders, the administrative coordinator must be from a Canadian academic or research environment at a CIHR eligible institution. The administrative coordinator assumes all responsibility for administrative matters related to the grant including but not limited to submitting the application and coordinating any required reporting. The individual who assumes the role of administrative coordinator for the grant must also be in a role of program leader. AĪdministrative coordinator - program leader ( coordonnateur administratif - directeur de programme) For recommendations on style and usage in English, consult the CIHR English Style Guide. For help with terminology and official titles of CIHR programs and initiatives, consult the CIHR English-French Lexicon.
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