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FBMM-001
metformin
multi-morbid
High glucose variance; low mitochondrial reserve
Variance down; exercise tolerance up
Partial persistence
AMPK activation improves energy handling
metabolic; mitochondrial
mitochondrial efficiency
GI discomfort early
Medium
Low
Positive
Classic resilience mechanism
Under 260 words.
axes+mechanism+durability
FBMM-002
rapamycin
aging
Inflammaging; slow recovery
Inflammatory markers down; recovery faster
Returns baseline
mTOR modulation reduces chronic inflammatory tone
immune; metabolic
inflammaging reduction
Infection susceptibility
Low
Medium
Mixed
Dose sensitive buffering
Under 260 words.
axes+mechanism+durability
FBMM-003
exercise_mimetic
aging
Low stress tolerance; fatigue
Tolerance improves; HRV up
Persists
Mitochondrial biogenesis signal
mitochondrial; autonomic
energy reserve expansion
Transient fatigue
High
Low
Positive
Durable capacity gain
Under 260 words.
axes+mechanism+durability
FBMM-004
SSRI
depression
Autonomic rigidity; sleep fragility
Flexibility improves; sleep stable
Reverts baseline
Neural plasticity increase
neural; autonomic
network plasticity
Emotional blunting
Low
Low
Neutral
Resilience tied to dosing
Under 260 words.
axes+mechanism+durability
FBMM-005
beta_blocker
cardiac
Stress-induced arrhythmia; low tolerance
Arrhythmia suppressed; fatigue
Returns baseline
Autonomic dampening
autonomic
sympathetic suppression
Reduced exercise capacity
Low
Medium
Mixed
Control without buffering
Under 260 words.
axes+mechanism+durability
FBMM-006
senolytic
aging
High senescent burden; slow recovery
Markers down; stress response improves
Partial persistence
Senescent cell clearance
immune; tissue repair
damage load reduction
Transient inflammation
Medium
Medium
Positive
System-level reset effect
Under 260 words.
axes+mechanism+durability

Resilience-Enhancing Pharmacopeia

Index README

Core premise

Some drugs work across diseases because they increase system capacity, not because they hit a target.

This collection defines, measures, and deploys that class of drugs.

Not pathology-first. Resilience-first.

What this pharmacopeia tests

Does a drug broaden the healthy basin

Which fragility axes it buffers

Who should receive it based on systemic vulnerability

These datasets do not ask “Does this drug treat condition X”

They ask “Does this drug make the system harder to break”

The Trinity

  1. Systemic Resilience Gain Profiling

Path ClarusC64/clinical-systemic-resilience-gain-profiling-v0.1

What it establishes

resilience gain under stress

operating range widening

recovery speed after perturbation

durability of benefit

Core output

Is this drug a capacity builder or just symptom control

This is the entry gate.

  1. Fragility Buffering Mechanism Mapping

Path ClarusC64/clinical-fragility-buffering-mechanism-mapping-v0.1

What it explains

which fragility axes are reinforced

how buffering is achieved

what tradeoffs are introduced

Axes include

inflammaging

mitochondrial reserve

autonomic flexibility

stress-response coherence

This separates true resilience from cosmetic calm.

  1. Resilience-First Indication and Patient Matching

Path ClarusC64/clinical-resilience-first-indication-patient-matching-v0.1

What it deploys

patient selection based on fragility profile

off-label use with structural justification

contraindication awareness

This enables prescribing by system need, not diagnosis.

How these sets connect to the wider Clarus ecosystem

These datasets integrate directly with

Fragility Amplification Detection

Basin Constraint Mapping

Therapeutic Niche Synthesis

Polypharmacy Coherence Matrix

Together they form a loop

Measure capacity

Explain buffering

Match patient

Monitor stability

What this enables that did not exist before

A defensible category of resilience-enhancing drugs

Safer off-label use grounded in structure

Early identification of patients at systemic risk

Drug development framed as basin widening, not target pursuit

This is not incremental improvement.

It is a new pharmacological lens.

Intended users

translational medicine teams

aging and longevity programs

complex chronic disease clinics

pharma discovery groups exploring non-target effects

regulators evaluating off-label rationale

Summary

These datasets answer three questions in order

Does the drug increase resilience

How does it do so

Who should receive it

If any one fails the chain breaks

If all three hold a new class of medicine becomes legible.

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