Livarine (Oxandrolone)
Active Substance: Livarine
Description
What Is Livarine (Oxandrolone)
“Livarine” is a trade name used by some underground labs for Oxandrolone, better known as Anavar.
It is a synthetic oral anabolic–androgenic steroid (AAS), derived from dihydrotestosterone (DHT). It is non-aromatizing and was originally developed for medical uses such as promoting weight gain after trauma or surgery and for conditions involving muscle wasting.
Benefits
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LeanMassGain: Promotes moderate but high-quality muscle gains with minimal water retention.
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StrengthIncrease: Enhances strength disproportionately to bodyweight gain (popular in power sports).
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FatLossSupport: Because of its DHT-derived nature and high affinity for androgen receptors in fat cells, it can support fat loss while preserving muscle.
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LowHepatotoxicityRelativeToOtherOrals: It’s 17-alpha-alkylated, so still liver-toxic, but less so than many other oral steroids.
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MinimalAromatization: No conversion to estrogen, so no gynecomastia or water retention from estrogen.
Side Effects
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LiverStrain (though milder than most orals).
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AndrogenicEffects: Acne, oily skin, hair loss in genetically predisposed men.
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CholesterolShift: LDL goes up, HDL drops, increasing cardiovascular risk.
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TestosteroneSuppression: Shuts down natural production despite being considered “mild.”
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VirilizationInWomen: Deepened voice, clitoral enlargement, body hair (even though it’s one of the “milder” options for women).
Pros
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Mildest oral steroid on liver relative to potency.
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Excellent for cutting cycles and recomposition.
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Almost zero estrogenic side effects.
Cons
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Expensive.
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Still suppresses endogenous testosterone.
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Negative impact on lipids is significant.
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Limited mass-building potential compared to stronger injectables.
Dosage And Frequency
Typical male performance dose:
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20–60 mg per day (split into 1–2 doses daily due to short half-life).
Typical female performance dose (very cautious):
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5–15 mg per day (once daily).
Cycle length: usually 6–8 weeks (liver and lipid safety).
Half Life And Detection Time
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Half-life: ~9 hours.
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Detectiontime: Up to 3–4 weeks in standard anti-doping tests (some modern tests may pick up metabolites longer).
Sterogenic ProgestronicP rolactin Effects
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NoProgesteroneActivity: It does not bind progesterone receptors.
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NoProlactinElevation: It does not raise prolactin.
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PurelyAndrogenic/Anabolic without steroidogenic progestational side effects.
Anabolic Androgenic Ratio
Oxandrolone is famously mild on the androgenic side relative to its anabolic potency:
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Anabolic rating: ~322–630
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Androgenic rating: ~24
Ratio = roughly 322:24 to 630:24 (commonly cited ~322:24).
Pharmacological Properties
Half Life
9.8 hours
Active Dose
100%
Detection
2.05 days
Concentration
10 mg/tab
Anabolic/Androgenic Profile
Usage Effectiveness
Activity Profile
Estrogenic
None
Progestanic
None
Water Retention
None
Aromatization
No
Benefits
Dosage Recommendations
Beginner
20-40 mg/week
Intermediate
40-60 mg/week
Advanced
60-100 mg/week
Evidence-based planning resources
Dive deeper into Livarine (Oxandrolone) cycle design, stacking options, and harm-reduction checklists available inside Anabolic Planner.
- Livarine (Oxandrolone) compound database overviewCompare Livarine (Oxandrolone) with other steroid agents in the structured compound index.
- Livarine (Oxandrolone) stack and cycle templatesReview evidence-based cycle outlines, dose progressions, and PCT pairings that incorporate Livarine (Oxandrolone).
- Harm-reduction guide for Livarine (Oxandrolone)Refresh safety monitoring, lab work, and countermeasure strategies tailored for Livarine (Oxandrolone) protocols.
Peer-reviewed reference material
Validate mechanisms, contraindications, and regulatory guidance for Livarine (Oxandrolone) with trusted clinical databases.
- Livarine clinical research on PubMedSearch peer-reviewed human and veterinary studies discussing efficacy, endocrine impact, and contraindications.
- Livarine pharmacology via Drug Information PortalReview mechanisms, synonyms, regulatory status, and toxicology summaries from the U.S. National Library of Medicine.
Side Effects
Common
Severe
Safety Information
Liver Toxicity
Moderate
Kidney Toxicity
Low
Cardiovascular Risk
Moderate
Disclaimer: This information is for educational purposes only. Always consult with a qualified healthcare professional before using any compounds.