Audit: QRS - L-Tyrosine for Health & Longevity

Audit conducted on 27/08/2026 13:39 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 84
Failed 0
N/A 9
Pass Rate 100.00%
  • Total = Passed + Failed + N/A
  • Pass Rate = Passed / (Passed + Failed) × 100
  • N/A items are excluded from the pass rate calculation

1. General Rules

# Description Result Comments
1.1 Every claim, magnitude, label, recommendation, and statement in the QRS is literally supported by content in the source ER. 🟢 Every protocol value, gate item, benefit/risk line, biomarker row and cadence statement traces to a literal ER passage (ER lines 319–326, 348–375, 401, 427–451).
1.2 Where the ER uses cautious phrasing (“not formally studied”, “None documented in human trials to date”, “theoretical concern”, “data are limited”), the QRS uses the same phrasing. 🟢 “long-term use is unresolved” (line 437) mirrors ER “unresolved in the long term” (ER line 477); “nothing supports lifelong daily use” (line 533) is ER line 375 verbatim.
1.3 The QRS never strengthens an ER claim (e.g., “not formally studied” → “not required”) or softens one (e.g., “do not use during pregnancy” → “use with caution during pregnancy”). 🟢 Contraindication wording preserves ER strength, e.g. “Pregnancy at any supplemental dose; breastfeeding above dietary intake” (line 584) = ER line 325.
1.4 The QRS does not relabel an ER fact under a different decision category. A “Benefit-Modifying Factor” from ER section is not surfaced as a “Caution”; a “Risk-Modifying Factor” is not surfaced as a “Side Effect”; etc. 🟢 Contraindications gate draws only from the ER “Populations who should avoid” list; Key Interactions gate only from the ER interaction bullets; no Benefit-/Risk-Modifying Factor is surfaced as a gate.
1.5 PubMed IDs, study citations, expert names, clinical trial identifiers (NCT*), and brand names appear in the QRS only if they appear in the source ER for the same fact. 🟢 No PMIDs, study names, expert names, NCT identifiers or brand names appear anywhere in the QRS.
1.6 The QRS does not introduce new attributions. 🟢 No attributions are introduced; the only near-attribution (“Trials recorded shifts under stress”, line 725) is ER line 438 verbatim.

2. Focus, Tone & Audience

# Description Result Comments
2.1 The QRS follows the tone of the ER, which is determined by the ER’s own language, phrasing, and framing. 🟢 Sober, conditional register of the ER is carried through, e.g. “In rested, unstressed people it changes little” (line 435).
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Tiered benefits/risks, quantified targets and dose ranges are expert and data-driven while remaining readable.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 All cells are declarative noun phrases; no imperatives or clinician-voice directives.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 Monitoring targets and cadence are stated as observed practice, not as instructions to a patient.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No “recommend”, “advise”, or “should” appears; content is presented as fact.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronoun appears anywhere in the file (verified).
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Plain language throughout; technical terms are limited to biomarker names that carry no plain-language equivalent.
2.8 Information is presented in a concise and very compact manner 🟢 Every field is a compressed phrase; benefit and risk tiers are semicolon-joined ER headings only.
2.9 It DOES NOT address the reader directly 🟢 Confirmed — no direct address to the reader.
2.10 The target audience is health- and longevity-oriented adults who are risk-aware, proactive, and actively seeking to optimize health or apply the intervention under review. 🟢 Framing assumes a proactive optimiser, e.g. the emphasis that the compound “changes little” absent a stressor.
2.11 The target audience is willing to employ lifestyle and behavioral changes as well as follow protocols that may be inconvenient, costly, or require effort. 🟢 Protocol presents empty-stomach timing, pre-demand dosing and a 10-row monitoring panel without hedging on effort.
2.12 The document is NOT written for the general population, who are unwilling to employ lifestyle and behavioral changes or follow protocols that may be inconvenient, costly, or require effort. 🟢 Content depth (10 biomarkers, 8 contraindications, genotype-free but dose-capped guidance) is beyond general-population material.
2.13 Framing, takeaways, and risk/benefit weighting throughout the document reflect this audience, including where an intervention’s signal for the average person differs from its signal for this audience. 🟢 At-A-Glance leads with the ER’s central point that the effect is conditional — the signal that differs for this audience.
2.14 The document’s own voice frames usage in longevity terms, not “anti-aging” (e.g., “anti-aging clinics”, “anti-aging community”, “anti-aging medicine”). Proper names that contain “anti-aging” (e.g., “American Academy of Anti-Aging Medicine”) are quoted verbatim. 🟢 No “anti-aging” phrasing appears.
2.15 The document’s own voice uses formal clinical and scientific terminology, not colloquial or consumer-grade language (e.g., “oral medication” not “pill(s)”; “injection” not “shot”; “adverse event” not “bad reaction”). Direct quotes from sources are exempt. 🟢 Formal register is used, e.g. “Gastrointestinal upset” (line 630) rather than a colloquial equivalent.

3. Template Integrity

# Description Result Comments
3.1 The following labels and headings on the QRS are fixed and not modified: • Card and section headings: “Protocol”, “Time to effect”, “Benefits”, “Risk & Side Effects”, “Monitoring”, “Qualitative Assessment” • Gate headings: “Contraindications”, “Key Interactions” • Tier labels: “High”, “Medium”, “Low”, “Speculative” • Table column headers in Monitoring: “Marker”, “Target”, “Why” 🟢 “Protocol” (line 445), “Time to effect” (491), “Benefits” (542), “Risk & Side Effects” (616), “Monitoring” (646), “Qualitative Assessment” (796), “Contraindications” (575), “Key Interactions” (590), tier labels and “Marker/Target/Why” (650–652) are all unmodified.
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 All 34 template span names are present; marker_#/qualitative_item_# are expanded to 10 and 6 concrete instances respectively.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 A structural diff against [qrs_template] shows changes confined to variable content and the metadata block; no template chrome altered.

4. Formatting

# Description Result Comments
4.1 When the source ER section is empty, the QRS uses the ER’s own empty-state phrasing verbatim. Typical phrasings are “None documented in human trials to date” and “Not formally studied” N/A No section of the source ER is empty, so no empty-state phrasing applies.
4.2 Where the ER presents a bulleted item as “Label: content”, the QRS uses the ER’s bold label verbatim as the cell or row label. 🟢 ER bold labels are reused verbatim: “Standard practitioner dose”, “Best time of day”, “Age-related adjustment”, “Time to effect”, “Half-life”, “Duration of use”.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 No label is paraphrased, abbreviated or invented.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 No 🟩/🟥/🟨 or any emoji appears; the ER’s “⚠️ Conflicted” markers were correctly stripped from the benefit lines.
4.5 The QRS is designed to render on one A4 page. Any section that has more content in the ER than fits the per-section budget is condensed by the LLM, not extended onto a second page. 🟢 Every section is reduced to headline-level content — benefits and risks are bare ER headings, gate items carry no rationale, and no magnitudes or citations are carried over.

5. Metadata

# Description Result Comments
5.1 The metadata is placed inside a single HTML comment that is the first element after “<!doctype html>” and before any other comment, head, or body content. 🟢 Lines 2–14: the metadata comment is the first element after “<!doctype html>”.
5.2 Inside that HTML comment the YAML block is delimited by a line “—” opening and a line “—” closing. Text before the opening “—” is permitted but is not parsed as YAML. 🟢 Opening “—” at line 3, closing “—” at line 13; the preceding title text is outside the YAML block.
5.3 The metadata is not visible in any rendered view of the QRS and is not surfaced by any other element on the sheet. 🟢 The block sits inside an HTML comment and is not echoed by any visible element.
5.4 All frontmatter values are trimmed: no leading or trailing whitespace, no surrounding quotes unless the value contains a colon, bracket, or leading special character that requires YAML quoting. 🟢 Values are trimmed; only duration: “00:03” is quoted, which the embedded colon requires.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 Line 4: er_filename: l_tyrosine_2026-0827-1055_Opus_ER.md.
5.6 Version of the QRS.md file used to create the document is stated as “qrs_prompt_version: [Version of QRS.md]” 🟢 Line 5: qrs_prompt_version: 26.7.02, matching the QRS.md version badge.
5.7 Creation date and time of the document is stated as “qrs_creation_date: [YYYY-MMDD-HHMM]” (e.g., 2026-0501-1430) 🟢 Line 6: qrs_creation_date: 2026-0827-1332, in YYYY-MMDD-HHMM form.
5.8 The nickname of the AI used to create the document is stated as “qrs_creator_ai_nickname: [qrs_creator_ai_nickname]” 🟢 Line 7: qrs_creator_ai_nickname: Opus.
5.9 The nickname of the AI is just a single word model name without version, etc. (e.g., Opus, Sonnet, Grok, Gemini, ChatGPT) 🟢 “Opus” is a single word with no version or qualifier.
5.10 The full name of the AI used to create the document is stated as “qrs_creator_ai_fullname: [qrs_creator_ai_fullname]” 🟢 Line 8: qrs_creator_ai_fullname: Opus 5.
5.11 The full name of the AI consists of the [qrs_creator_ai_nickname] and the model version number and no additional qualifier (e.g., Opus 4.6, Sonnet 3.2, Grok 4.5, Gemini 3.1, ChatGPT 5.4) 🟢 “Opus 5” is nickname plus version with no trailing qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 Line 9: qrs_filename matches the actual file on disk.
5.13 All frontmatter values are trimmed: no leading or trailing whitespace, no surrounding quotes unless the value contains a colon, bracket, or leading special character that requires YAML quoting. 🟢 Re-verified — all values trimmed and unquoted except where YAML requires quoting.

6. Page Title & Header

# Description Result Comments
6.1 [page_title] is set to the [canonical_topic] of the ER frontmatter followed by “ - Quick Reference Sheet” (e.g., “Intervention - Quick Reference Sheet”). The [canonical_topic] is HTML-entity-encoded as needed (e.g., &amp; for &) 🟢 Line 22: “L-Tyrosine for Health & Longevity - Quick Reference Sheet”, with the ampersand entity-encoded.
6.2 [header_topic] is set to the [canonical_topic] of the ER frontmatter, with HTML entities encoded as needed (e.g., &amp; for &) 🟢 Line 417: “L-Tyrosine for Health & Longevity”, matching the ER canonical_topic.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: 08/27/2026, the MM/DD/YYYY form of qrs_creation_date 2026-0827.
6.4 [header_subline_model] is set to [qrs_creator_ai_fullname] 🟢 Line 425: “Opus 5”.
6.5 No additional header content appears: no badge, version stamp, AKA / alternate names line, source-AI attribution, audit date, or QRS variant marker. 🟢 The header carries only the title and the template subline; no badge, version stamp, alternate-names line, audit date or variant marker.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Lines 434–437 condense the ER Conclusion (ER lines 473–477) into what the compound does, when, and how long it is known to be safe.
7.2 [at_a_glance] is no longer than 60 words 🟢 53 words (counted).
7.3 Every fact in [at_a_glance] is supported by a distinct passage in the ER. 🟢 Each clause maps to a distinct ER Conclusion sentence: amino acid origin (ER 473), no effect at rest (473), four stressors (475), older adults and heat (475), short-course tolerability and unresolved long term (477).
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms or specialist classifications; “low oxygen” and “lost sleep” are used in place of technical equivalents.
7.5 It DOES NOT cite specific trials (names, years, sample sizes, p-values) 🟢 No trial names, years, sample sizes or p-values.
7.6 It DOES NOT cite effect sizes, relative risks, or statistical results 🟢 No effect sizes, relative risks, hazard ratios or confidence intervals.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Lines 577–586 derive from the ER “Populations who should avoid L-Tyrosine” list within Key Interactions & Contraindications (ER 319–326).
8.2 [stop_items] represent the Contraindications from the ER 🟢 All eight ER avoid-populations are represented, one to one.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Each of the eight items is a discrete <li></li> (lines 578–585).
8.4 Items are as concise as possible. No trailing explanations, no elaborations, no mechanistic rationale, no attributions, no citations, no study details. No content after an em-dash, en-dash, or hyphen-dash (e.g., “— dose reduction required”, “— reduced efficacy”) — these trailing clauses are stripped. Just the key fact. 🟢 Mechanistic tails are stripped, e.g. ER “in whom dopamine-raising compounds can precipitate mania or psychosis” is reduced to “Bipolar disorder or a psychotic disorder” (line 582).
8.5 Parenthetical qualifiers from the ER bullet — time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item, kept as concise as possible (shortened or trimmed where needed to fit the one-page budget, but never dropped entirely). 🟢 Decision-relevant qualifiers are kept: “at any stage” (579), “within 14 days of stopping one” (580), “types I, II or III” (583), “Child-Pugh Class B or C” (585).
8.6 When the ER uses ranking notation inside parens (e.g., “>” for severity ordering) that depends on an explanatory phrase to interpret, normalize the items to a plain comma-separated list rather than carrying through the bare symbol. N/A The ER Key Interactions & Contraindications section uses no ranking notation inside parentheses.
8.7 The section is left empty ONLY IF the ER’s Key Interactions & Contraindications section identifies no population, condition, or scenario for which the intervention should be avoided, deferred, or used only under specialist supervision. 🟢 The section is populated, and the ER does identify populations that should avoid the intervention.
8.8 If the section is left empty, an HTML comment inside the [stop_items] span records the ER basis for the absence, naming or quoting the ER text relied on. E.g. N/A The section is not empty (8 contraindications present).

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 Lines 592–607 derive from the ER interaction bullets in Key Interactions & Contraindications (ER 305–315).
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 The levodopa and MAOI bullets are correctly omitted because both already appear in the Contraindications gate; the remaining four ER interactions are all present.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Each of the four items is a discrete <li></li> (lines 593–606).
9.4 Items are as concise as possible. No trailing explanations, no elaborations, no mechanistic rationale, no attributions, no citations, no study details. No content after an em-dash, en-dash, or hyphen-dash (e.g., “— dose reduction required”, “— reduced efficacy”) — these trailing clauses are stripped. Just the key fact. 🟢 Mitigation clauses and mechanism are stripped, e.g. ER “Mitigation: one at a time, never stacked” does not appear.
9.5 Parenthetical qualifiers from the ER bullet — example drug lists, time windows, severity classes, threshold values, clinical staging — ARE preserved as part of the item, kept as concise as possible (shortened or trimmed where needed to fit the one-page budget, but never dropped entirely). 🟢 Named example agents are preserved in parentheses: levothyroxine/liothyronine (593), pseudoephedrine/phenylephrine/methylphenidate/amphetamine salts (595–596), the eight-item supplement list (599–601), and the three redundant-exposure protocols (604–605).
9.6 When the ER uses ranking notation inside parens (e.g., “>” for severity ordering) that depends on an explanatory phrase to interpret, normalize the items to a plain comma-separated list rather than carrying through the bare symbol. N/A The ER Key Interactions & Contraindications section uses no ranking notation inside parentheses.
9.7 The section is left empty ONLY IF the ER’s Key Interactions & Contraindications section identifies no interaction, additive effect, or exposure that changes how the intervention is used. 🟢 The section is populated, and the ER does identify interactions that change how the intervention is used.
9.8 If the section is left empty, an HTML comment inside the [caution_items] span records the ER basis for the absence, naming or quoting the ER text relied on. E.g. N/A The section is not empty (4 key interactions present).

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 Lines 447–488 derive from the ER Therapeutic Protocol section (ER 348, 356, 366).
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Dose, timing and the age-related cap are the three implementation levers the ER treats as decision-relevant; the age cap is reinforced by the ER Medium risk of working-memory loss in older adults.
10.3 If less that three distinct actionable implementation aspects are mentioned in the ER the unused sets are left empty and made invisible, not filled with placeholder text or empty-state phrasing. N/A The ER Therapeutic Protocol section provides well more than three actionable implementation aspects.
10.4 All used [action_#label], [action#value], [action#_sub] items are filled with meaningful content derived from the ER Protocol section. 🟢 All nine action fields carry substantive ER-derived content; none is a placeholder.

11. Time to Effect

# Description Result Comments
11.1 The three sets of [time] items cover the three most important time-to-effect aspects from the ER 🟢 Onset (ER 401), plasma peak and elevation window (ER 358), and duration of use (ER 375) are the ER’s three temporal facts.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Onset leads, matching the High-tier benefit (acute stress cognition, a 30-minute to 3-hour window); peak/duration follow in descending relevance.
11.3 If less that three distinct time-to-effect aspects are mentioned in the ER the unused sets are left empty and made invisible, not filled with placeholder text or empty-state phrasing. N/A The ER provides three distinct time-to-effect aspects; all three sets are used.
11.4 All used [time_#label], [time#value], [time#_sub] items are filled with meaningful content derived from the ER. 🟢 All nine time fields carry substantive ER-derived content.
11.5 If the ER does not provide any information on time to effect, the section is removed completely from the Protocol Panel N/A The ER provides time-to-effect information (Practical Considerations — Time to effect).

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 Lines 544–568 derive from the ER Expected Benefits section.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four span names are present and correctly tiered.
12.3 Items are as concise as possible. No explanations, no elaborations, no effect sizes, no qualifiers, no attributions, no citations, no study details, no mechanistic explanations, etc. Just the key fact. 🟢 Each tier is the ER subheading text alone; no magnitudes, mechanisms, trial names or GRADE notes carried over.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content survives; the ER “⚠️ Conflicted” markers are also removed.
12.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. N/A All four benefit tiers (high, medium, low, speculative) are populated in the ER, so no span needs hiding.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 Lines 618–640 derive from the ER Potential Risks & Side Effects section.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four span names are present and correctly tiered.
13.3 Items are as concise as possible. No explanations, no elaborations, no effect sizes, no qualifiers, no attributions, no citations, no study details, no mechanistic explanations, etc. Just the key fact. 🟢 Each tier is the ER subheading text alone; p-values, hazard ratios and rodent-study detail are omitted.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parenthetical content survives.
13.5 If no items of a specific sub-section (high, medium, low, speculative) are present the respective is set to “display=none”, not filled with “None documented in human trials to date” or similar empty-state phrasing. 🟢 The ER states “No risk reaches High”, and [risks_high] is set to style=”display: none” (line 618) rather than filled with empty-state text.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 Lines 647–791 derive from the ER Monitoring Protocol & Defining Success section.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All ten rows of the ER biomarker table are reproduced in order — TSH, Free T4, Free T3, TPO antibodies, plasma tyrosine, seated blood pressure, fasting glucose, HbA1c, eGFR, ALT — with targets and rationales matching the ER verbatim.
14.3 [monitoring_cadence] is populated with the monitoring cadence/frequency derived from the ER Monitoring section. It is not left with placeholder text or empty. 🟢 Lines 787–789 reproduce the ER cadence sentence (ER 429) in full.

15. Qualitative Assessment

| # | Description | Result | Comments | |—|————-|:——:|———-| | 15.1 | The section is derived from the ER Monitoring section | 🟢 | Lines 798–830 derive from the ER qualitative-marker list in Monitoring Protocol & Defining Success. | | 15.2 | All subjective/qualitative biomarkers from the Monitoring section are listed | 🟢 | All six ER qualitative bullets (ER 446–451) are present, one to one. |

Issues 27/08/2026 13:39

Pass rate 100.00%. No issues found.