Andarine (S-4)

Andarine (S-4) is one of the earlier non-steroidal SARMs developed by GTx Inc. It is known for a unique and dose-dependent visual side effect: yellow-tinted vision and difficulty adjusting to darkness, caused by binding to androgen receptors in the retina. This side effect is reversible on cessation.

Overview

SARM

Andarine (S-4) is one of the earlier non-steroidal SARMs developed by GTx Inc. It is known for a unique and dose-dependent visual side effect: yellow-tinted vision and difficulty adjusting to darkness, caused by binding to androgen receptors in the retina. This side effect is reversible on cessation.

Effects on Markers

Mild-moderate suppression of testosterone and SHBG, HDL reduction, mild elevation of liver enzymes, dose-dependent reversible yellow-tinted vision and impaired dark adaptation

Compound Guide

Structure: Non-steroidal SARM. Partial androgen receptor agonist with activity in muscle and bone. Shorter half-life than most SARMs requires split dosing.

Dosage:

  • Bodybuilding: 25-50 mg/day for 6-8 weeks
  • Split into 2-3 doses/day due to the short half-life (~4-6 hours)
  • Lower doses (25-35 mg/day) to minimise visual side effects

Administration:

  • Oral. Available as raw powder or liquid suspension (research-chemical grade only; no approved pharmaceutical form).
  • Dosing 2-3 times daily due to short half-life. Avoid high single doses to reduce visual side effect risk.

Key Notes:

  • Unique visual side effect: S-4 binds androgen receptors in the retina, causing a yellow or golden tint to vision (xanthopsia) and difficulty adjusting from bright light to darkness. This is dose-dependent, typically begins within 1-2 weeks, and resolves fully within 1-4 weeks of cessation.
  • Visual side effects are not permanent at typical bodybuilding doses but can be disorienting and may affect night driving safety. Dose reduction or cessation resolves the issue.
  • HPTA suppression is mild to moderate. Testosterone, LH, and FSH should be monitored. A SERM-based PCT is advisable after longer or higher-dose cycles.
  • HDL suppression and mild liver enzyme elevation are consistent with other SARMs in its class.
  • Less studied than ostarine or LGD-4033; published human clinical data is limited. Most available information is from animal studies and anecdotal human reports.
  • Does not aromatise. Estradiol is not directly elevated.
  • WADA prohibited under S1 (anabolic agents). Detection window is not well-characterised.
  • Monitor: testosterone, LH, FSH, HDL, ALT, AST at baseline and post-cycle.

Usage History

Markers to Monitor

Frequently Asked Questions

Quick Reference

Category

SARM

Half-Life

~4-6 hours

Detection Time

Unknown (limited published detection data)

Usage Summary