Daily regimen

Dose means the active drug amount. For combination levodopa products, enter the levodopa component only.

Daily Parkinson medication doses
Time Medication Dose (mg) LEDD contribution Curve Remove
Model settings

“Days represented” adds prior-day carryover for longer-half-life preparations. Thresholds are optional and user-defined; they are not validated clinical On/Off or dyskinesia cutoffs.

Modeled exposure over 24 hours

Relative normalized exposure index—not a measured plasma concentration or direct prediction of clinical effect.

Time
Relative exposure
User-defined zoneUnclassified

Use the slider or Left/Right arrow keys for minute-by-minute values. Page Up/Down moves by one hour.

Summary

LEDD is a research comparison measure. The remaining values come from this simplified exposure model and should not guide medication changes.

Save or load a regimen

Exports include a schema version and model version so saved regimens can be interpreted after the model changes.

Medication parameters and sources

LEDD conversion and exposure-curve shape are stored separately. Component curves are normalized so their integrated area matches the declared exposure factor. “Consensus proposal” does not mean clinically validated equivalence for an individual patient.

Medication LEDD formula Exposure model Evidence/source

Not included: the model covers five levodopa preparations (Sinemet, Sinemet CR, Rytary, Crexont, and Inbrija). Other Parkinson medications — levodopa infusions, dopamine agonists, MAO-B inhibitors, COMT inhibitors, and adjuncts — remain outside the graph even when a research LED proposal exists.

Model assumptions and limitations

Exposure shapes. Oral and inhaled doses use a simplified linear rise to a peak followed by exponential elimination. Extended-release products use multiple components. Component areas are normalized to a declared exposure factor.

Important omissions. Absorption lag, protein and meal effects, gastroparesis, renal/hepatic function, endogenous dopamine, drug interactions, rescue-dose context, and person-to-person variability are not modeled. Pharmacokinetics is not pharmacodynamics.

Primary conversion reference. Jost ST et al. Levodopa Dose Equivalency in Parkinson’s Disease: Updated Systematic Review and Proposals. Movement Disorders. 2023.