Glass Box
// what the AI reads
No black box. Every paper and data source behind the pharmacokinetic model is listed here. You see what the math sees — nothing hidden, nothing invented. The source code will be released for independent review.
ANCHORED
The PK model is pinned to published pharmacokinetic parameters — not a drifting LLM. The math cannot silently change between updates.
ON-DEVICE
The model lives on your phone. No cloud. No server. No API calls. Your medication data never leaves your device.
LOCAL
Every dose log and subjective report stays on your phone. We cannot read it. We cannot sell it. It does not exist anywhere else.
TRACEABLE
Every parameter in the Bateman equation traces to a published source below. If it's not in the Glass Box, the model won't use it.
Pharmacokinetic Model Sources
Clinical Framework
10
Bateman, H. — The solution of a system of differential equations in pharmacokinetics
Proc. Cambridge Phil. Soc., 1910
Simulation Parameters Derived From
Sinemet IR: t½ 90 min, Tmax 30-60 min, F=99% — from FDA prescribing label + Nutt & Fellman (1993)
Sinemet CR: t½ 90 min, Tmax 120 min, F=71% — from FDA prescribing label + controlled-release PK studies
Rytary ER: dual-phase absorption (60% fast / 40% slow), Tmax 1h/4h — from Hauser et al. (2013) + FDA label
Food effect: high-protein meals delay Tmax by ~30 min, reduce Cmax — from competitive amino acid transport literature
GLASS_BOX_POLICY: Every parameter in this simulation traces to a published pharmacokinetic source. The Bateman equation is the standard one-compartment oral absorption model used in clinical pharmacology. No proprietary algorithms. No hidden tuning. No synthetic data.
