Audit: QRS - Rhodiola rosea for Health & Longevity

Audit conducted on 15/08/2026 07:54 using AI4L / Opus 5

Iterations

Summary

Items Count
Total 93
Passed 85
Failed 0
N/A 8
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. 🟢 Protocol cells trace to ER lines 382/388/390; time-to-effect cells to ER lines 437/467; benefit and risk items to the ER tier headings; monitoring rows to the ER table at lines 471–478; qualitative items to ER lines 482–487.
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. 🟢 Speculative tiers retain the ER’s hedged framing (“unknown safety beyond twelve weeks”); action_3_sub keeps “not the established default approach” from ER line 388.
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”). 🟢 “Pregnancy and lactation at any stage” stays an absolute contraindication; the longevity claim stays confined to invertebrate work, matching ER line 212.
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 come only from the ER “Populations who should avoid” list; Key Interactions only from the ER interaction bullets; no modifying-factor content is promoted into 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. 🟢 The QRS carries no PMIDs, citations, expert names, NCT identifiers, or brand names at all.
1.6 The QRS does not introduce new attributions. 🟢 No attributions of any kind are present.

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. 🟢 Measured, sceptical register matching the ER, including the sponsorship and adulteration caveats in the At-A-Glance.
2.2 The tone of the QRS is simultaneously expert, accessible, objective, and data-driven, but also empowering and encouraging 🟢 Concrete doses, timings, and monitoring targets give the reader actionable handles without overselling.
2.3 The QRS reads as a trusted, knowledgeable guide rather than a prescriptive doctor 🟢 Content is stated descriptively (“Morning, on an empty stomach…”), not issued as instruction.
2.4 The QRS avoids language that implies medical or clinical advice 🟢 No imperative or prescriptive constructions; marker_4_why mirrors the ER’s own reported-caution wording.
2.5 The QRS “presents information” instead of “providing guidance”, “recommending”, or “advising” 🟢 No “recommended”, “should”, or “we advise” constructions in the document’s own voice.
2.6 The QRS never addresses “the reader” directly — it presents evidence, not guidance 🟢 No second-person pronouns anywhere in the file.
2.7 The QRS is written in plain language, avoiding unnecessary medical jargon 🟢 Technical terms are confined to the decision gates, where drug and enzyme names are load-bearing.
2.8 Information is presented in a concise and very compact manner 🟢 Benefit and risk tiers are semicolon-joined single lines; monitoring rows are trimmed to marker, target, and rationale.
2.9 It DOES NOT address the reader directly 🟢 Confirmed by full-file scan for second-person forms.
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. 🟢 Functional biomarker ranges and a self-tracking qualitative list assume an engaged optimizer.
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. 🟢 Timed saliva cortisol sampling, trough drug levels, and planned break weeks are all retained.
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. 🟢 Cortisol awakening response and narrow-therapeutic-index trough monitoring are far beyond general-population content.
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. 🟢 The At-A-Glance foregrounds that the signal concentrates in depleted or pressured users, and flags product substitution as the dominant practical risk.
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. 🟢 “Longevity” is used in the title and At-A-Glance; “anti-aging” does not appear.
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. 🟢 “Root extract”, “alanine aminotransferase”, “resting heart rate”, “perceived exertion” — all ER-level register.

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” 🟢 All headings verified verbatim at lines 446, 491, 537, 565, 579, 618, 647, 651–653, 780.
3.2 All “…” from the [qrs_template] are present in the the QRS. 🟢 All 38 distinct template variables present; indexed families expanded to 8 markers and 6 qualitative items for a total of 64 spans.
3.3 Spans that are not addressed in a checklist item are left unchanged 🟢 The three website="…" spans and the footer disclaimer are byte-identical to the template.

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 ER section mapped to the QRS is empty; the empty High benefit and risk tiers are governed by items 12.5 and 13.5 instead.
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. 🟢 “Standard daily dose”, “Best time of day”, and “Acute pre-exercise approach” match the ER bold labels at lines 382, 390, and 388 exactly.
4.3 Labels are not paraphrased, abbreviated, or invented. 🟢 Monitoring marker names are ER-verbatim; the three time-to-effect labels use ER terminology from lines 437 and 467.
4.4 The QRS DOES NOT use emoji indicators (no 🟩, 🟥, 🟨, etc.). Color and emphasis are conveyed through CSS and bold labels. 🟢 Full-file scan returns no emoji; the ER’s tier emoji and “⚠️ Conflicted” markers were correctly dropped.
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 condensed against the ER — benefit and risk tiers reduced to heading-level phrases, monitoring targets and cadence trimmed, gate items stripped of rationale.

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, immediately after the doctype at line 1.
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.
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. 🟢 Enclosed in an HTML comment; no metadata value is repeated in the header or body.
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. 🟢 Only duration: "00:02" is quoted, correctly, because it contains a colon.
5.5 The filename of the source ER is stated as “er_filename: [er_filename]” 🟢 Line 4: er_filename: rhodiola_rosea_2026-0815-0452_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 badge version.
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: 2026-0815-0742.
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” — nickname plus version, no qualifier.
5.12 The filename of the document is stated as “qrs_filename: [filename of this document]” 🟢 Line 9 matches the actual filename rhodiola_rosea_2026-0815-0452_Opus_QRS.html.
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 across all eight metadata keys plus git_user and git_issue; no stray whitespace or 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: “Rhodiola rosea for Health & Longevity - Quick Reference Sheet”.
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: “Rhodiola rosea for Health & Longevity”.
6.3 [header_subline_date] is set to [qrs_creation_date reformatted as MM/DD/YYYY] 🟢 Line 421: “08/15/2026”, matching qrs_creation_date 2026-0815.
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. 🟢 Header block (lines 415–428) carries only the template’s title and subline.

7. At-A-Glance Section

# Description Result Comments
7.1 [at_a_glance] is dense, execution-oriented summary of the ER Conclusion section 🟢 Condenses all three ER Conclusion paragraphs (lines 507–511): the fatigue and exercise signal, the invertebrate-only longevity case, and the substitution plus sponsorship discount.
7.2 [at_a_glance] is no longer than 60 words 🟢 55 words.
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; “only from flies, worms, and yeast” is additionally underwritten by ER line 212.
7.4 It DOES NOT use acronyms or technical classifications that require specialist knowledge, uses plain-language terms instead 🟢 No acronyms; “root extract”, “depleted”, “effort that feels easier” are all everyday register.
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 numeric results of any kind.

8. Contraindications

# Description Result Comments
8.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All seven items come from the ER “Populations who should avoid Rhodiola rosea” list at lines 350–356.
8.2 [stop_items] represent the Contraindications from the ER 🟢 Complete 1:1 mapping of all seven ER avoidance populations, plus the MAOI absolute contraindication from ER line 328.
8.3 Individual [stop_items] are formatted as <li></li> 🟢 Lines 568–574, seven discrete <li> elements.
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. 🟢 ER trailing clauses “— no reproductive safety data exist”, “— no trial has enrolled them”, and “, because of the theoretical interaction with anesthetic agents cleared by CYP3A4” are all stripped.
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). 🟢 ”(≥160/100 mmHg)”, “(tacrolimus, cyclosporine)”, “within 14 days”, “under 18”, and “Bipolar I … prior manic or hypomanic episode” all retained.
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 uses no ranking notation in its contraindication list; “≥160/100 mmHg” is a threshold value, not a severity ordering.
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 ER names seven avoidance populations, and the section is correspondingly populated rather than empty.
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.

9. Key Interactions

# Description Result Comments
9.1 The section is derived from the ER Key Interactions & Contraindications section 🟢 All ten items map to the ER interaction bullets at lines 326–346.
9.2 [caution_items] represent the Key Interactions from the ER, excluding any that are already listed as Contraindications 🟢 Ten of the ER’s eleven interaction bullets are carried; the MAOI bullet is correctly excluded because it appears as a contraindication.
9.3 Individual [caution_items] are formatted as <li></li> 🟢 Lines 582–608, ten discrete <li> elements.
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. 🟢 The ER’s “Caution.”/”Monitor.” verdicts, mechanistic sentences, and monitoring instructions are all stripped; the class gloss “— the most common antidepressant class” is removed from the SSRI item.
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). 🟢 Every ER example-drug list is preserved verbatim across all ten items, including the five-item supplement list.
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’s interaction parentheticals contain only plain comma-separated drug names; no ranking notation is used.
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 ER names eleven interactions, and the section is correspondingly populated rather than empty.
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.

10. Protocol

# Description Result Comments
10.1 The section is derived from the ER Protocol section 🟢 All three cells trace to the ER Therapeutic Protocol bullets at lines 382, 388, and 390.
10.2 The three sets of [action] items cover the three most important actionable implementation aspects from the ER Protocol section 🟢 Standard daily dose, best time of day, and the acute pre-exercise approach are the three decision-relevant bullets; the remaining bullets are modifiers or brand-specific regimens.
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 supplies well over three actionable aspects, so all three sets are used.
10.4 All used [action_#label], [action#value], [action#_sub] items are filled with meaningful content derived from the ER Protocol section. 🟢 All nine spans (lines 450–486) carry ER-derived content; none is empty or 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 🟢 Mental fatigue (2–4 weeks), perceived effort (30–60 minutes), and stress/burnout (within 3 days) are the only three time courses the ER quantifies, at lines 437 and 467.
11.2 The sets are picked and ordered by the magnitude of the related benefit 🟢 Order matches the ER Medium-tier benefit order: mental fatigue, endurance/perceived effort, then stress and burnout.
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 Three distinct time-to-effect aspects exist in the ER, so 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 spans (lines 497–528) carry 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 at lines 437 and 467, so the section is correctly retained.

12. Benefits

# Description Result Comments
12.1 The section is derived from the ER Expected Benefits section 🟢 All eleven items correspond to ER benefit headings at lines 158–220.
12.2 Key variables are [benefits_high], [benefits_medium], [benefits_low], [benefits_speculative] 🟢 All four spans present at lines 539, 540, 546, and 553.
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 item is the ER heading reduced to sentence case; all Magnitude lines and “⚠️ Conflicted” markers are dropped.
12.4 Parenthetical content — including effect sizes, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any benefit item.
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. 🟢 Line 539 sets benefits_high to style="display: none" with empty content, matching the ER’s empty High tier at line 154.

13. Risks

# Description Result Comments
13.1 The section is derived from the ER Potential Risks & Side Effects section 🟢 All ten items correspond to ER risk headings at lines 250–306.
13.2 Key variables are [risks_high], [risks_medium], [risks_low], [risks_speculative] 🟢 All four spans present at lines 620, 621, 627, and 635.
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 item is the ER heading reduced to sentence case; all Magnitude lines and the “⚠️ Conflicted” marker on the enzyme-inhibition item are dropped.
13.4 Parenthetical content — including frequencies, severity grades, sample notes, mechanistic hints, and example studies — is stripped, NOT preserved. 🟢 No parentheses appear in any risk item.
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. 🟢 Line 620 sets risks_high to style="display: none" with empty content, matching the ER’s empty High tier at line 246.

14. Monitoring

# Description Result Comments
14.1 The section is derived from the ER Monitoring section 🟢 All rows come from the ER Monitoring Protocol & Defining Success table at lines 471–478.
14.2 All measurable/quantifiable biomarkers from the Monitoring section are listed 🟢 All eight ER biomarkers present: morning salivary cortisol, cortisol awakening response, alanine aminotransferase, fasting glucose, resting heart rate, blood pressure, hs-CRP, and narrow-therapeutic-index drug trough.
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 770–774 reproduce the ER cadence from line 467, including the 6–12 month long-term interval.

15. Qualitative Assessment

# Description Result Comments
15.1 The section is derived from the ER Monitoring section 🟢 All six items come from the ER qualitative marker list at lines 482–487.
15.2 All subjective/qualitative biomarkers from the Monitoring section are listed 🟢 All six ER qualitative markers are present and verbatim, including the planned-break regression check.

Issues 15/08/2026 07:54

Pass rate 100.00%. No issues found.

Issues 15/08/2026 07:48

  1. 1.1 — Default-approach claim over-extended: [action_3_sub] (lines 484-488) says “none of the protocol approaches is the established default”, but the ER (Therapeutic Protocol, line 388) restricts “None of these three is the established default” to the Swedish Herbal Institute, Schwabe, and acute pre-exercise approaches, not to the standard daily dose shown in [action_1].

Fixes 15/08/2026 07:48

  1. 1.1 — Default-approach claim narrowed: [action_3_sub] changed from “none of the protocol approaches is the established default” to “not the established default approach”, matching the ER’s statement that the acute pre-exercise approach is not an established default.