modelS02CA05

Diagram of S02CA05

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:FluocinoloneAcetonideAndAntiinfectives
ATC code:S02CA05
route:otic
compartments:1
dosage:0.25mg
volume of distribution:1L
clearance:0
other parameters in model implementation

Fluocinolone acetonide and antiinfectives (ATC code S02CA05) is a combination topical drug formulation used primarily for the treatment of ear infections, especially otitis externa. It combines the potent synthetic corticosteroid fluocinolone acetonide for anti-inflammatory effects with an antimicrobial agent (such as antibiotics) to address the underlying infection. This combination is prescribed to reduce inflammation, itching, and treat or prevent bacterial growth in the affected area. Fluocinolone acetonide and antiinfectives are generally used in otic (ear) drops and are approved for use in several countries.

Pharmacokinetics

No published pharmacokinetic (PK) models or formal PK parameter studies were found for topical or otic administration of fluocinolone acetonide and antiinfectives in humans of any age or sex. Systemic absorption following otic administration is expected to be minimal based on the corticosteroid's properties and label information.

References

    Parameters

    TypeNameDefaultDescription
    Modelica.Units.SI.Massweight (from PK_1C)75patient weight (kg)
    Modelica.Units.SI.SpecificVolumeVdPerKg (from PK_1C)0.9Volume of distribution (L/kg)
    Modelica.Units.SI.MassFractionF (from PK_1C)0.8bioavailiability (0-1)
    Pharmacolibrary.Types.ClearanceCl (from PK_1C)20clearance
    Modelica.Units.SI.TimeadminTime (from PK_1C)60first administration time (s)
    Modelica.Units.SI.TimeadminDuration (from PK_1C)600administration duration (s)
    Modelica.Units.SI.TimeadminPeriod (from PK_1C)8*60*60period of administration (default 8 hours)(s)
    Pharmacolibrary.Types.MassadminMass (from PK_1C)1000administration mass (mg)
    IntegeradminCount (from PK_1C)8number of dose administered (1)
    Pharmacolibrary.Types.VolumeVd (from PK_1C)VdPerKg*weightVolume of distribution (m3)
    Pharmacolibrary.Types.MassConcentrationCmin (from PK_1C)0.004minimal therapeutic range
    Pharmacolibrary.Types.MassConcentrationCmax (from PK_1C)0.008minimal therapeutic range
    Pharmacolibrary.Types.MassConcentrationCtox_peak (from PK_1C)0.012toxicity peak level
    Pharmacolibrary.Types.MassConcentrationCtox_trough (from PK_1C)0.006toxicity trough level

    Connectors

    TypeNameDefaultDescription
    Types.ConcentrationOutputC_central (from PK_1C)
    Interfaces.ConcentrationPort_bcentralCPort (from PK_1C)

    Components

    TypeNameDefaultDescription
    Pharmacokinetic.NoPerfusedTissueCompartmentcentral (from PK_1C)
    Pharmacokinetic.ClearanceDrivenEliminationelim (from PK_1C)
    Sources.PeriodicDoseperiodicDose (from PK_1C)
    Modelica.Units.SI.Timet1_2 (from PK_1C)elimination half-life

    Revisions

    • 06/2025 Tomas Kulhanek, generated model from data extracted from PUBMED, DrugBank and LLM(GPT4.1)