Skip to content

Harm-reduction information only — not medical advice. In crisis or experiencing adverse effects, contact a healthcare professional or your local emergency services immediately.

AnabolicDex logo AnabolicDex
Search (no-JS fallback)
SARMs Preclinical (animal) data

Andarine (S4)

S4 · Andarine

3.9 hours
Half-life
12.5–50 mg
Typical dose
Oral, 2×/day
Frequency
6–8 weeks (community protocols)
Cycle length

SARM with notable vision-related side effects; short half-life requiring divided dosing.

Key takeaways

  • Short ~4-hour half-life means reported protocols split dosing twice daily.
  • Human PK data don't exist; the plotter curve is built from canine data.
  • Signature side effect is visual: yellow tint and night-vision problems at higher doses, reported as reversible on stopping.
  • Never advanced to meaningful human trials; unapproved and WADA-prohibited.

Overview

What it is

Andarine (S4) is one of the earliest non-steroidal selective androgen receptor modulators, developed for muscle wasting and osteoporosis. Like other SARMs it aims for anabolic activity in muscle and bone with less androgenic effect on the prostate, but it never advanced to meaningful human trials.

Pharmacokinetics

The half-life is short, roughly 4 hours, which is why reported protocols split dosing twice daily. The PK data behind the plotter come from canine studies, so the human curve is a rough approximation.

Harm reduction

Andarine's signature side effect is visual: a yellow tint and impaired night vision at higher doses, reported as reversible on discontinuation. Testosterone suppression and liver enzyme shifts track with other SARMs. It's unapproved, WADA-prohibited, and human safety data essentially don't exist, so reported protocols are anecdotal and third-party testing plus bloodwork (LH, FSH, total T, ALT/AST) are the minimum safeguards.

Reported dosing protocols

Protocols reported in research literature and clinic/community use — informational context, not a dosing recommendation.

Use case Dose Route Frequency Duration
Physique (community) 25–50 mg split into 2 doses Oral Twice daily 6–8 weeks

Pharmacokinetic summary

Model tier
Advanced (t½ + Cmax + Tmax + F)
Half-life
3.9 hours
Cmax
513.45 ng/mL
Tmax
0.0 days
Bioavailability
50%
Typical dose
12.5–50 mg

Harm reduction

Aromatizes
No
Hepatotoxicity
mild
Injection frequency
Oral, 2×/day

⚠ Known vision side-effect (yellow tint, night blindness) at higher doses.

Frequently asked questions

Why does andarine affect vision?

The exact mechanism isn't established, but users report a yellow tint and difficulty with night vision and light adaptation at higher doses. Reports consistently describe it resolving after discontinuation. It's the distinguishing side effect of S4 versus other SARMs.

Does andarine have human trial data?

Essentially none. Development never reached meaningful human trials, and the PK profile in the plotter comes from canine data. Dosing numbers circulating online are community convention built on animal data and anecdote.

Why twice-daily dosing for andarine?

The roughly 4-hour half-life means a single daily dose produces a sharp peak and near-complete washout within a day. Reported protocols split the daily amount into two doses to keep levels steadier, which the plotter shows directly.

References

Related compounds

Comments

Loading comments…