S-4, S4, GTx-007, acetamidoxolutamide · Evidence-based safety and harm-reduction overview.
| Also known as | S-4, S4, GTx-007, acetamidoxolutamide |
| Category | SARM |
| vision_effect | Distinctive reported yellow tint and night vision disturbance, reversible upon stopping |
| gtx_developer | One of the earliest SARMs from GTx Inc., alongside ostarine |
| partial_agonist | Demonstrates tissue-specific partial agonism, explaining both effects and off-target activity |
| US legal status | Andarine is not approved by the FDA for any use, and it is illegal to market or sell it as a dietary supplement. The FDA has warned that SARMs are associated with serious risks including liver injury, heart attack, and stroke, and products are sold as research chemicals not for human consumption. It is prohibited at all times in sport under the WADA list. |
Andarine (S-4) is an early investigational selective androgen receptor modulator studied for muscle and bone effects. It was an earlier-generation compound and did not advance to approval.
Andarine is a selective nonsteroidal androgen receptor agonist with partial agonist activity in some tissues and full agonism in others. It demonstrates selectivity for muscle androgen receptors but retains activity in the prostate and eye, which likely explains both anabolic and visual adverse effects. The partial agonism profile differed from later SARMs.
Andarine (S-4, GTx-007) was developed by GTx Inc. in the early 2000s as one of the first investigational SARMs. It entered early clinical development for benign prostate hyperplasia and bone health but was abandoned before large trials. The vision disturbance signal and lack of competitive advantage versus later compounds led to discontinuation of development.
Research suggests andarine has anabolic activity on muscle and bone in animal models. Human data are very limited, development did not progress, and a distinctive reported side effect is yellow-tinted or disturbed vision linked to its action on the eye.
In limited preclinical and early human exploration, doses ranged from low milligram amounts upward. No published human dose-response or safety studies exist in peer-reviewed literature. Any contemporary claims of human dosing are speculative and lack scientific support.
This is general research/context information, not medical advice or a recommended protocol.
Andarine is occasionally mentioned in stacking discussions, but its vision effects and lack of human data make combination use especially problematic. Stacking amplifies both hormonal and tissue-specific risks, and the vision disturbance becomes harder to attribute or manage safely with multiple compounds.
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Compare testing optionsAndarine is reported to affect the eye, causing a yellow tint and trouble seeing in dim light; the changes are reported to reverse after stopping, but it signals off-target activity.
We do not provide human dosing guidance. Andarine is unapproved and any use should involve a qualified clinician.
No. Human data are very limited and the compound was not developed further, so its safety profile is poorly defined.
No reliable preventive strategy exists; the vision effects appear to be dose and time-dependent and reversible upon cessation, but they are unpredictable.
Users report vision returns to normal weeks after stopping, but individual timelines vary and this is not guaranteed.
Medical & legal disclaimer. This site is for informational and harm-reduction purposes only. It is not medical advice and is not a substitute for a licensed healthcare professional. The compounds discussed are largely not approved by the FDA for human use and many are sold strictly as research chemicals 'not for human consumption.' Nothing here is an endorsement to purchase, possess, or use any substance. Laws vary by jurisdiction. Always consult a qualified physician and follow the law where you live.
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