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    Balcolabs STANOZOLOL 5amp 50mg/amp

Balcolabs STANOZOLOL 5amp 50mg/amp


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  • €21.00





Description

In 1962, Stanozolol entered the US market through Winthrop, branded as "Winstrol," and in Europe via Bayer, labeled as "Stromba." As an anabolic androgenic steroid, it acts as an androgen receptor agonist similar to testosterone and DHT. Unlike other steroids, it doesn't undergo 5а-reductase conversion, resulting in a higher anabolic to androgenic activity ratio and a lack of estrogenic effects like gynecomastia or fluid retention. Stanozolol is also devoid of significant progestogenic activity.

Medical Applications:

Stanozolol is utilized to treat various conditions in humans, including anemia and hereditary angioedema, with specific approvals in certain countries. It can induce anabolic effects and weight gain without fluid retention when medically necessary.

Athletic Utilization:

In sports, Stanozolol is highly sought-after due to its ability to enhance strength and weight without typical estrogenic side effects, making it popular among female athletes. It's favored in sports emphasizing strength and explosiveness while minimizing weight gain, owing to its non-aromatizing nature.

Dosage:

Dosage varies depending on the sport and desired outcomes. For power sports and athletics, doses range from 50mg every 3-5 days to 50mg daily for enhanced physical strength and explosiveness. In bodybuilding, doses may be slightly higher, tailored to individual bodybuilder weight and goals.

Combination Therapy:

Stanozolol can be taken alone or in combination with other steroids suited for cutting phases, such as Testosterone propionate, Trenbolone, Drostanolone, and Oxandrolone.

Side Effects and Safety Measures:

Side effects include virilization, hepatotoxicity, and cardiovascular risks due to lowered estrogen levels. Joint dryness and discomfort may occur, especially with a low-fat diet. Proper precautions should be taken to mitigate these risks.

Half-life and Doping Concerns:

Stanozolol has a half-life of approximately 36-48 hours post-administration but remains detectable for up to three months after cessation, rendering it unsuitable for athletes subject to doping tests.

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