modelCodeineAndOtherNonOpioidAnalgesi

Diagram of CodeineAndOtherNonOpioidAnalgesi

Extends from Pharmacolibrary.Drugs.ATC.N.N02AJ09.

Information

name:CodeineAndOtherNonOpioidAnalgesics
ATC code:N02AJ09
route:oral
n-compartments1

Combination products containing codeine (a mild opioid analgesic and cough suppressant) with non-opioid analgesics are used for the relief of mild to moderate pain unresponsive to non-opioid analgesics alone. These combinations are often found in over-the-counter or prescription formulations for short-term management of pain. Codeine use is approved in certain countries, but its use is restricted or banned in pediatric populations and in some locations due to abuse potential and safety concerns.

Pharmacokinetics

Estimated pharmacokinetic parameters for an adult population based on literature for codeine-containing fixed-dose combination tablets administered orally. Model reflects typical values for codeine with non-opioids in healthy adults. No direct publication reporting full model PK for N02AJ09 combination product.

References

  1. Goelen, N, et al., & Tack, J (2021). Effect of protein composition of enteral formula on gastric content volume during continuous feeding: A randomized controlled cross-over study in healthy adults. Clinical nutrition (Edinburgh, Scotland) 40(5) 2663–2672. DOI:10.1016/j.clnu.2021.03.021 PUBMED:https://pubmed.ncbi.nlm.nih.gov/33933732

  2. Velez de Mendizabal, N, et al., & Carleton, BC (2015). A Compartmental Analysis for Morphine and Its Metabolites in Young Children After a Single Oral Dose. Clinical pharmacokinetics 54(10) 1083–1090. DOI:10.1007/s40262-015-0256-4 PUBMED:https://pubmed.ncbi.nlm.nih.gov/25773480

  3. Coller, JK, et al., & Somogyi, AA (2012). Inhibition of CYP2D6-mediated tramadol O-demethylation in methadone but not buprenorphine maintenance patients. British journal of clinical pharmacology 74(5) 835–841. DOI:10.1111/j.1365-2125.2012.04256.x PUBMED:https://pubmed.ncbi.nlm.nih.gov/22369095

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
Pharmacolibrary.Types.TransferRateka (from PK_1C_enteral)0.016666666666666666first order absorption rate
Modelica.Units.SI.TimeTlag (from PK_1C_enteral)600delay between oral administration and absorption (default 10min)

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 initial generated model