Domain
Pharmacy
NDC codes, dispensing, PBM, RxNorm and formulary management
1,993 pharmacy terms
The enterprise-level master identifier that uniquely links a documented adverse or physiological reaction record across multiple systems, facilities, or data sources within a health system. Used to reconcile duplicate reaction records and maintain a single source of truth in enterprise master patient index environments.
The upper threshold or maximum value associated with a measured clinical parameter at the time of a documented physiological reaction, such as peak heart rate or maximum severity score. Used in clinical data systems to define boundaries for reaction severity assessments and clinical alert configurations.
The medical record number of the patient associated with a documented adverse or physiological reaction. Used as the primary patient identifier to link the reaction event to the correct patient record across clinical documentation, pharmacy safety systems, and allergy management workflows within a healthcare facility.
The middle name or initial of the patient associated with a documented adverse or physiological reaction record. Used in clinical and administrative systems to support accurate patient identity verification and reduce the risk of record mismatches when documenting and retrieving adverse reaction histories.
The lower threshold or minimum value associated with a measured clinical parameter at the time of a documented physiological reaction, such as minimum blood pressure or lowest severity score recorded. Used in clinical data systems to define baseline boundaries for reaction severity assessments and clinical decision support rules.
The mobile phone number associated with a documented adverse or allergic reaction record, used to contact the patient or responsible party regarding the physiological response. Captured in clinical documentation systems to support follow-up care coordination and adverse event reporting.
The unique identifier of the user who last updated a documented physiological reaction record in the clinical system. Used in audit trail tracking to maintain data integrity and accountability for changes to adverse reaction, allergy, or adverse event documentation in EHR systems.
The calendar date on which a physiological reaction record was last updated in the clinical system. Used in audit trail tracking to monitor changes to adverse reaction or allergy documentation, supporting data integrity and regulatory compliance in electronic health record environments.
The timestamp indicating the exact time a physiological reaction record was last updated in the clinical system. Used alongside the modified date in audit trail tracking to provide precise change history for adverse reaction or allergy documentation in electronic health records.
The human-readable display label assigned to a documented physiological reaction, such as an adverse drug reaction or allergic response. Used in clinical documentation and patient records to consistently identify and communicate the nature of the reaction across care settings and healthcare information systems.
Free-text annotation or clinical commentary associated with a documented physiological reaction record. Captures additional clinical context, provider observations, or follow-up instructions related to an adverse drug reaction, allergic response, or other physiological event recorded in the patient's clinical history.
The unique numeric identifier assigned to a documented physiological reaction record within the clinical system. Used to track and reference adverse reactions, allergic responses, or adverse events consistently across electronic health records, clinical data warehouses, and downstream reporting systems.
The calendar date on which a documented physiological reaction first presented or was first observed in the patient. Captured in clinical records to establish the timeline of adverse drug reactions, allergic responses, or other adverse events, supporting clinical decision-making and pharmacovigilance reporting.
The blood oxygen saturation level measured during or in association with a documented physiological reaction event. Recorded as a clinical vital sign indicator to assess the severity of adverse reactions, allergic responses, or anaphylactic events and guide clinical intervention decisions.
The dollar amount paid for treatment or services rendered in connection with a documented physiological reaction event. Used in healthcare claims and billing systems to capture the financial settlement associated with adverse reaction-related encounters, supporting cost analysis and insurance reimbursement workflows.
The date on which payment was processed for treatment or services associated with a documented physiological reaction event. Used in healthcare claims and billing systems to track reimbursement timelines for adverse reaction-related encounters and reconcile financial transactions in revenue cycle management.
The higher-level hierarchical entity or record to which a documented physiological reaction is linked within the clinical data model. Used to establish parent-child relationships in reaction classification structures, supporting grouped reporting of adverse drug reactions and allergic responses in clinical and analytical systems.
A numeric percentage value associated with a documented physiological reaction, representing a calculated ratio such as severity scoring, incidence rate, or body surface area affected. Used in clinical documentation and adverse event reporting to quantify the extent or impact of the reaction on the patient.
The defined time interval or duration over which a documented physiological reaction persisted or was observed. Used in clinical documentation to characterize the temporal course of adverse drug reactions or allergic responses, supporting severity assessment and longitudinal patient safety monitoring.
The primary telephone number associated with a documented physiological reaction record, used to contact the patient or responsible party regarding an adverse drug reaction or allergic event. Captured in clinical systems to support follow-up care coordination and adverse event management workflows.