Clomid, is an oral medication most commonly prescribed as a fertility drug. It’s classified as a selective estrogen receptor modulator or SERM, meaning it doesn’t directly alter hormone levels but instead works by blocking estrogen receptor sites. This gives the body the false impression that estrogen levels are low, triggering the pituitary gland to increase luteinizing hormone (LH) and follicle-stimulating hormone (FSH). These hormones then signal the testicles to produce more testosterone. This mechanism can be effective for specific situations, such as secondary hypogonadism caused by pituitary dysfunction or when fertility is the goal. However, Clomid’s ability to artificially stimulate testosterone production comes with significant drawbacks when used outside of these scenarios, especially as a long-term replacement therapy. Men often report a rapid increase in testosterone levels during the early stages of Clomid use. But within months, issues like mood swings, depression, diminished libido, weight gain, and other estradiol-related metabolic problems tend to appear. These side effects occur because while estrogen levels may be sufficient in the bloodstream, Clomid blocks estrogen’s ability to act on its target tissues. The result is a mismatch between hormonal balance and physiological function—similar to having money in the bank but no access to spend it. It can even result in vision issues, including floaters and, in rare cases, farsightedness, have been reported. These effects occur because estradiol also plays a role in the health of the optic nerve and retina. Blocking estrogen receptors in these areas can lead to visual disturbances, particularly with prolonged use or higher doses. Bodybuilders often use it after steroid cycles to reignite the hypothalamic-pituitary-testicular axis (HPTA), restoring natural testosterone production. While effective in this context, reliance on PCT and frequent cycling can eventually damage the pituitary gland.