Internat Pharmacie (Côte d'Ivoire) study materials
Internat Pharmacie (Côte d'Ivoire) study resources

Internat Pharmacie (Côte d'Ivoire) flashcards

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27 cards. Read the term and the definition here. The deck at the top of this page is optional.

Potency
The amount or concentration associated with a defined response in a specified comparison, distinct from the maximum achievable effect.
Efficacy
The capacity to produce a specified effect under the relevant conditions, distinguished from potency and individual clinical suitability.
Selectivity
The relative preference for a biological target, which can depend on exposure and does not imply absolute specificity.
Clearance
The proportional removal of drug relative to its measured concentration, expressed as a volume per unit time under the relevant model.
Apparent distribution volume
A model quantity relating the amount of drug in the body to concentration, rather than a literal anatomical fluid container.
Bioavailability
The relevant fraction of an administered dose reaching systemic circulation under the stated route, product and comparison assumptions.
Disintegration
The breakup of a dosage form into smaller components, which is distinct from dissolving the active ingredient and absorbing it.
Dissolution
Movement of a substance into solution under specified conditions, influenced by the actual material, environment and dosage-form design.
Modified release
A delivery design altering release characteristics, whose safe manipulation depends on the actual formulation and current product instructions.
Precision
Agreement among repeated measurements under defined conditions, which does not alone establish agreement with an appropriate true or reference value.
Selectivity of an assay
The ability to assess the intended target in the presence of relevant other components under the validated method conditions.
Stability evidence
Data supporting the behavior of a particular product over time under specified conditions, rather than one universal expiry convention.
Preanalytical error
A problem arising before measurement through identification, collection, handling or storage, which can change the reported laboratory result.
Screening result
An initial classification under a defined testing purpose, interpreted with performance and population context rather than automatic final diagnosis.
Decision limit
A threshold used for a defined clinical decision under a particular framework, which need not equal a population reference-interval boundary.
Medication review
A structured assessment of the actual medicine list, indications, benefit, risk and practical use in the context of the patient.
Teach-back
A communication method checking the explanation through the person account of understanding, used to improve clarity rather than assign blame.
Therapeutic objective
The intended patient-relevant benefit used to assess whether a medicine plan is useful, with monitoring for harms and limitations.
Medication reconciliation
Comparison and investigation of medicine information across care transitions to distinguish intended changes from unintended discrepancies.
Near miss
A detected medication-process problem that did not result in the feared harm but can still reveal a useful system weakness.
High-alert medicine
A medicine associated with important harm potential when used incorrectly, requiring controls matched to the actual risk and process.
Absolute risk reduction
The comparator risk minus the intervention risk for a defined outcome and follow-up, interpreted with uncertainty and actual applicability.
Allocation concealment
Protection against knowledge of the next randomized assignment during recruitment, distinct from blinding later assessment or treatment.
Cost perspective
The specified viewpoint defining which resources and outcomes enter an economic comparison, rather than acquisition price alone.
Qualification scope
The actual organizer, level, professional role and assessment purpose of a credential, distinguished from a similar title in another jurisdiction.
Traceability
Records connecting a product, preparation or treatment with its relevant identity and history so appropriate investigation and action remain possible.
Professional authorization
The actual permission for a defined service under current local requirements, which is not conferred by a scientific practice question.