library.onepin.app/fadogia-agrestis Peptide Education Library
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Hormonal Dietary supplementFadogia agrestis (West African Shrub)

Fadogia Agrestis

Fadogia

300-450mg – 400-600 mg Oral 1-2x daily
Testosterone Support (Limited Evidence)Libido BotanicalDietary Supplement (Limited Safety Data)

Fadogia Agrestis is a West African shrub (Rubiaceae family) traditionally used for libido and male vitality. Gained Western prominence after Andrew Huberman cited it as part of his 'Tongkat Ali + Fadogia' stack for testosterone support. Active compounds include alkaloids and saponins.

Quick Start
Route
Oral capsule
Start low
300-450mg Oral
Frequency
1-2x daily
Timing
With food typically

Morning typical.

Start here. Every protocol below is ordered lowest-first. Begin at the smallest effective dose, hold about a week to assess tolerance, and step up only if needed.

Tiered Protocols · lowest first
Conservative start
300-450mg · Oral capsule · 1-2x daily
conservative starter
300-450mg
1-2x daily
Standard
Testosterone Support Cycle
400-600 mg · Oral · Daily
animal study · Yakubu et al. 2005 (Asian J Androl)
Always cycle this supplement (e.g., 3 weeks on, 1 week off) to prevent potential testicular toxicity observed in high-dose animal models. No human trial has been conducted. This dose is extrapolated from animal research and has not been tested for safety or effect in people.
400-600 mg
Daily
01

How it works

Fadogia Agrestis mechanism is incompletely characterized:

Putative LH Stimulation

Rodent studies suggest possible luteinizing hormone elevation, driving testicular T production.

Cytotoxic Concerns

Higher-dose rodent studies show testicular toxicity (reduced sperm count, damaged seminiferous tubules) - mechanism unclear, possibly via alkaloid content.

Saponins

Various saponin compounds may contribute to aphrodisiac and adaptogenic effects.

Insufficient Human Data

No published human RCTs as of this writing. All claims rest on rodent studies plus community/Huberman popularity.

02

What to expect

Early
Days 1–7

Weeks 1-2: subtle effects.

Mid
Weeks 2–4

Weeks 4-8: peak short-cycle effects.

Later
Weeks 4–12

Cycle off; safety data limits long-term continuous use.

03

Evidence

HumanNo published trials
AnimalPresent
In-vitroPresent

Each reference below was re-fetched from its PubMed record, and the quoted sentence was confirmed to appear in that abstract and to support the claim it sits under. Follow any of them to read the source.

Aqueous Fadogia stem extract increased rat blood testosterone, proposed to explain aphrodisiac effects.

The aqueous extract of Fadogia agrestis stem increased the blood testosterone concentrations and this may be the mechanism responsible for its aphrodisiac effects and various masculine behaviors.

Aphrodisiac potentials of the aqueous extract of Fadogia agrestis (Schweinf. Ex Hiern) stem in male albino rats. Asian journal of andrology · 2005 · PMID 16281088

Evidence scope. Animal; proposed mechanism; not LH evidence.

Oral aqueous stem extract adversely altered male-rat testicular-function indices.

The alterations brought about by the aqueous extract of Fadogia agrestis stem are indications of adverse effects on the male rat testicular function and this may adversely affect the functional capacities of the testes.

Effects of oral administration of aqueous extract of Fadogia agrestis (Schweinf. Ex Hiern) stem on some testicular function indices of male rats. Journal of ethnopharmacology · 2008 · PMID 18023305

Evidence scope. Animal; 18-100 mg/kg/day for 28 days; not human safety.

Claims we could not support

No abstract we checked supports these for this molecule at this route. That is not the same as saying they are false — it marks where the evidence is missing.

Dose/route: 300-450 mg oral capsule 1-2x/day. No human trial validated this regimen.

Specific LH, sperm-count, and seminiferous-tubule claims. The checked abstracts did not state these specifics.

Human safety. No human clinical abstract was found.

04

Side effects & safety

Commonly reported

  • Mild GI
  • Possible mild stimulant effect

Less common & notes

  • Theoretical testicular toxicity from rodent data - not directly observed in humans but mechanism cause for caution.
  • Hypertension at high doses.
  • Long-term safety in humans uncharacterized.
  • Discontinue immediately for any testicular symptoms.
05

Pharmacokinetics

Illustrative plasma concentration · 18 h
Half-life

Variable, multi-component

Peak · Tmax
1-3 hours
Elimination

Hours plasma

Bioavailability

Oral moderate

Duration of action

Daily dosing during cycle

Clearance

Hepatic

Storage. Capsule. Cool dry location.

06

Regulatory status

Dietary supplement (US, DSHEA). Limited Western regulatory oversight. Quality varies.

Put it to work

Calculate, log & track

Open Fadogia Agrestis straight into OnePin with your vial and dose pre-filled, then let it handle the syringe math and remind you before the vial runs out.

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Go deeper

The guide & community

The complete Fadogia Agrestis walkthrough, real protocol discussion and coaching live inside the BlessUp community on Skool.

Join the community ↗
Open in app Community

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