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Methodology

Sources & Methodology

Last updated: 9 April 2026

This page describes where Milligram's compound data and AI-generated information comes from. Milligram is an informational tracking tool — it does not provide medical advice, diagnosis, or treatment.

1. About Milligram AI

Milligram AI is powered by Google's Gemini large language model. It draws from the app's built-in compound database, published pharmacokinetic research, and manufacturer documentation to answer questions about compounds, dosing, reconstitution, and protocols. Responses are framed as general educational information, not personalised medical advice.

2. Compound Database

The app includes a database of 103 compounds with the following data for each:

This data is derived from published pharmacokinetic studies, manufacturer prescribing information, and established clinical dosing guidelines. Pharmacokinetic calculations (level buildup curves, steady-state projections) use standard one-compartment and two-compartment mathematical models.

3. Reference Categories

Pharmacokinetic Research

Regulatory & Manufacturer Data

Notable Prescribing References

4. AI Methodology

When you ask Milligram AI a question, your message and relevant context (age, sex, goals, active compounds) are sent to Google's Gemini API. Gemini generates a response drawing from its training data, which includes published medical and scientific literature. The app also injects compound-specific data from its built-in database into the AI's context to improve accuracy for dosing, reconstitution, and protocol questions.

Milligram AI does not generate formal per-response citations because the underlying language model synthesises information from its training data rather than retrieving specific papers. The reference links above represent the categories of sources that inform both the compound database and the AI's training knowledge.

5. Pharmacokinetic Model

Level buildup curves and steady-state projections use standard compartmental pharmacokinetic models:

Parameters (half-life, bioavailability, absorption rate, volume of distribution) are population averages derived from published clinical pharmacokinetic studies. Individual responses vary based on body composition, metabolism, injection technique, and other factors.

6. Limitations

7. Contact

Questions about our sources or methodology can be directed to enzoanderson2010@icloud.com.