Article and paper data contributed by Molecular
spec sheet15 rows
Anavar is a brand name for oxandrolone, a synthetic anabolic-androgenic steroid developed in the early 1960s. A derivative of dihydrotestosterone with an oxygen atom substituted into its steroid ring, it is taken by mouth and is known for a relatively high ratio of anabolic to androgenic activity. It has been used medically to help patients regain weight after trauma, surgery, or severe burns and in other catabolic conditions, and it is also misused for physique and performance enhancement.
- Clean strength gains
- Hard, dry pumps
- Minimal side effects
- Great for cutting
- Preserved muscle in a deficit
- Changes in cholesterol (lower HDL)
- Suppressed natural testosterone
- Liver enzyme elevations
- Acne and oily skin
- Virilizing effects in women (deeper voice, facial hair)
- Mood changes
Overview
Oxandrolone, sold under brand names such as Anavar and Oxandrin, is an orally active anabolic-androgenic steroid. It is structurally unusual among these drugs: it is a derivative of dihydrotestosterone in which one carbon of the steroid A-ring is replaced by an oxygen atom, making it a "2-oxa" steroid, and it carries a 17-alpha-methyl group that lets it survive oral dosing. These features give it strong anabolic activity relative to its androgenic activity [4].
The drug was first described in 1962 by researchers at Searle Laboratories and introduced for medical use in 1964 as Anavar. Production was discontinued for a period and then reintroduced in the mid-1990s under the name Oxandrin. It has been applied to a range of conditions requiring restoration of body weight and lean tissue.
Recognized medical uses include promoting weight gain after surgery, trauma, chronic infection, or prolonged corticosteroid therapy. Oxandrolone is well studied as an aid in the recovery of patients with severe burns; a systematic review of randomized trials reported that it shortened hospital stay and healing time and improved lean body mass without a clear increase in serious harm in that setting [1][3]. In girls with Turner syndrome treated with growth hormone, adding oxandrolone has been found to produce a modest gain in final adult height, at the cost of some virilizing effects such as voice deepening [2].
Because it is comparatively mild and available in oral form, oxandrolone is also used without prescription by athletes and bodybuilders, including women. Possible adverse effects include changes in blood lipids that may raise cardiovascular risk, suppression of natural testosterone, and, with higher or prolonged exposure, liver effects; although often considered less hepatotoxic than many 17-alpha-alkylated steroids, cases of liver injury have been reported.
Oxandrolone is a Schedule III controlled substance in the United States and is similarly scheduled in several other countries; it is banned in competitive sport. Its United States marketing approval was withdrawn in 2023, reflecting the availability of other treatments.
Mechanism
Like other anabolic-androgenic steroids, oxandrolone binds and activates the in muscle and other tissues, where it promotes nitrogen retention and protein synthesis and thereby favors growth of lean body mass and bone density [4]. Its 2-oxa modification and 17-alpha-methyl group shift the balance so that it produces relatively more anabolic than androgenic effect and resists breakdown in the liver, allowing oral use. It is a poor substrate for the aromatase enzyme, so it is not readily converted to , which limits estrogen-related effects such as fluid retention. In catabolic states such as severe burns, this androgen-receptor-mediated anabolic action is thought to counteract the muscle breakdown driven by stress hormones, which underlies its clinical use in recovery [1][3].
receptor fingerprint
agonist
Muscle protein synthesis / nitrogen balanceimproves
Aromatizationdoes not aromatize
Safetyrisks and cautions, not medical advice
Anavar (oxandrolone) is a c17-alpha-alkylated oral steroid, so despite its mild reputation it carries dose-dependent hepatotoxicity and can raise liver enzymes and disturb liver function on prolonged use. Its most consistent documented harm is a sharp, unfavorable shift in lipids; it markedly suppresses HDL and raises LDL, straining cardiovascular health even at modest doses. It suppresses natural testosterone production (less severely than many steroids but enough to warrant recovery support after longer runs), and can cause virilization in women including voice deepening, clitoral enlargement, and hair changes that may be irreversible. Other reported effects include acne, mood changes, and reduced HDL-driven vascular risk. It is contraindicated in pregnancy, liver disease, and prostate or breast cancer.
Interactionsdocumented pairs only, not exhaustive
Oxandrolone (Anavar) potentiates oral anticoagulants such as warfarin, and the labeling directs that anticoagulant doses be reduced and INR monitored closely to avoid bleeding. It can enhance the glucose-lowering effect of insulin and oral antidiabetic agents, so those doses may need adjustment. Oxandrolone is intrinsically hepatotoxic and can cause cholestatic injury and peliosis, so combining it with other hepatotoxic agents raises liver risk. Concurrent adrenocorticosteroids or ACTH can increase fluid retention and edema. This is research information, not medical advice.
Checking a whole stack? Run it through interactions + stacks.
History
Anavar is the original brand name for oxandrolone, a synthetic derivative of dihydrotestosterone first synthesized around 1962 by Raphael Pappo and Christopher J. Jung at Searle Laboratories and introduced for medical use in 1964. Its distinctive 2-oxa A-ring modification was designed to maximize anabolic activity while minimizing androgenic effects, and it was prescribed for involuntary weight loss, burn recovery and bone-density loss. Searle discontinued Anavar in 1989 amid scrutiny of anabolic-steroid abuse by bodybuilders, and the drug nearly vanished from the market. It reappeared in 1995 when Bio-Technology General Corp relaunched oxandrolone under the brand Oxandrin, while the Anavar name lived on in bodybuilding and grey-market circles.
Subjective profileweighing the evidence above
An anabolic steroid, not a supplement, and the mild reputation is only mild by steroid standards. It reliably tanks HDL, suppresses natural testosterone, raises liver enzymes as a 17-alpha-alkylated oral, and can cause irreversible virilization in women. Bloodwork and medical oversight, or not at all.
Resources
Don't even think about it.
Research
- 2008first citedInfluence of muscle mass and physical activity on serum and urinary creatinine and serum cystat…
- 2016meta-analysisThe efficacy and safety of oxandrolone treatment for patients with severe burns: a systematic r…
- 2023most recentAndrogen receptor blockade by flutamide down-regulates renal fibrosis, inflammation, and apopto…
- 1.The efficacy and safety of oxandrolone treatment for patients with severe burns: a systematic review and meta-analysis
- 2.Oxandrolone for growth hormone-treated girls aged up to 18 years with Turner syndrome.
- 3.Burns: an update on current pharmacotherapy
- 4.Pharmacology of anabolic steroids
- 5.A comparative study of the effect of the dose and exposure duration of anabolic androgenic steroids on behavior, cholinergic regulation, and oxidative stress in rats
- 6.Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: A comprehensive review
- 7.Human hydroxysteroid dehydrogenases and pre-receptor regulation: insights into inhibitor design and evaluation
- 8.Influence of muscle mass and physical activity on serum and urinary creatinine and serum cystatin C
- 9.Androgen receptor blockade by flutamide down-regulates renal fibrosis, inflammation, and apoptosis pathways in male rats
- 10.Liver injury from herbal and dietary supplements
10 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
What is Anavar used for?
It is a mild oral anabolic steroid favored for lean strength and cutting phases.
How does Anavar work?
It is an anabolic-androgenic steroid that supports muscle retention and strength with relatively mild androgenic effects.
Is Anavar well-researched?
It has medical origins and is considered milder than many steroids, but non-medical use still carries risks.
What are the main side effects?
It can suppress natural testosterone, affect cholesterol, and put some strain on the liver.
Adverse effects
- Changes in cholesterol (lower HDL)
- Suppressed natural testosterone
- Liver enzyme elevations
- Acne and oily skin
- Virilizing effects in women (deeper voice, facial hair)
- Mood changes