Tamoxifen in bodybuilding

Discussion in 'Drugs For Sale' started by Sadist, 31-Aug-2019.

  1. NadejdaS Moderator

    Tamoxifen in bodybuilding


    The bodybuilding supplement Estro Suppress has been found to contain traces of a breast cancer drug, but is the discovery old news? Some may already be familiar with the meme-friendly factoid that entertainer Dwayne “The Rock” Johnson has purportedly undergone liposuction for something called gynecomastia –– a benign enlargement of male breast tissue resulting from metabolic disorder, side-effects from medication, or natural drops in testosterone levels. It follows that, in the bodybuilding community, this unnerving syndrome is relatively common –– so much so that many have traditionally taken to self-medication to keep their pecks in check. Here, unfortunately, is where tamoxifen enters the picture. A high-shelf, prescription-based pharmacological agent, this drug antagonizes the body’s estrogen receptors, lowering the level of the hormone in the body. For women (or men) with estrogen receptor-positive breast cancers, a lower amount of estrogen inhibits the tumor growth. For bodybuilders on a program of shady supplements, it helps offset biological responses that would otherwise result in “moobs.” The use is pervasive and has been going on for about 30 years. For some time, the supplement Esto Suppress has been thrown around in bodybuilding circles as a legal, natural supplement that does more or less the same thing as these pharmacological hormone suppressors. Usually, tamoxifen is sourced from the illicit market.

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    This article will go into some of the details on why Tamoxifen has been recommended for bodybuilders, as well as some side effects that most people fail to. Tamoxifen bodybuilding is used in anabolic steroid cycle as an ancillary drug and also in post anabolic steroid cycle therapy. Combining tamoxifen and bodybuilding can lead to dangers like coagulation abnormalities, elevated blood cholesterol and liver.

    Tamoxifen is a prescription drug used to manage and prevent breast cancer in men and women. Interestingly, the drug has gained popularity in the bodybuilding community. The drug is used in anabolic steroid cycle as an ancillary drug and also in post anabolic steroid cycle therapy. An ancillary drug is a substance consumed to offset the undesired effects of anabolic steroids. Anabolic steroid cycle is the period a bodybuilder uses an anabolic steroid. As a bodybuilder, your main goal is to build lean muscles and at the same time lose weight; this is where Tamoxifen comes in. You may use Tamoxifen as part of your steroid cycle to help you achieve the following: Tamoxifen Citrate is a safe drug to use since it binds to estrogen receptors. Anabolic steroid has aromatization characteristics which may result in breast enlargement (gynecomastia) and an increase in fat deposits. So, you can take this medication together with anabolic steroids. Normally, the dose of the drug is 10 to 40 mg per day. When it comes to the most popular selective estrogen receptor modulator (SERM), which is commonly also known as an anti -estrogen, Nolvadex is one of the most potent and effective choices for those looking to use a SERM while building muscle and improving their overall body strength. While Nolvadex is an estrogen antagonist, it also functions as an agonist, which means that it works in the same way as estrogen does in various parts of the body, while possessing anti estrogenic functions in other parts, such as breast tissue. Nolvadex is one of the oldest and most popular selective estrogen receptor modulators on the market that is still commonly used as a medicine. Nolvadex is often used by those individuals using anabolic steroids, however, it is important to remember that it is not an anabolic steroid itself, which can confuse many people as it is used as part of a steroid cycle. Its official name is Tamoxifen Citrate, and it was created in 1961 by the company known as ICI. This company later changed its name to Astra Zeneca, and Tamoxifen Citrate was manufactured under the brand name of Nolvadex. The initial use of Tamoxifen citrate was as a treatment option for breast cancer, most notably breast cancer that is hormone responsive.

    Tamoxifen in bodybuilding

    Tamoxifen side effects - Forums, What You Need To Know About Tamoxifen In Bodybuilding

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  3. Sep. 2017 - 5 min - Odovzdal-a Doping AnabolicNolvadex Tamoxifen. Doping Anabolic. Loading. #RXRants - Duration. RxMuscle.

    • Nolvadex Tamoxifen - YouTube.
    • What Are the Dangers of Tamoxifen and Bodybuilding?.
    • Tamoxifen - Forums.

    Nolvadex, officially known as Tamoxifen Citrate. Such scenarios are very common in hardcore bodybuilding circles but they are not realistic for most anabolic. Breast cancer drug tamoxifen has been detected in a dietary supplement known as Esto Suppress, according to a letter to the BMJ this week. I've thought about surgery but i really can't afford it right now, so I'm just gonna get some generic nolvadex online. My question is how much.

     
  4. Dimid Moderator

    PO administration: 0.1-0.3 mg q4-6hr; increase by 0.1 mg/day to 0.15-0.75 mg/day if required; do not exceed 2.4 mg/day TD administration: 100-200 mcg/day patch q7Days; initiate 0.1-0.3 mg PO q4-6hr for first 2 days to allow for adequate drug levels Not recommended as routine treatment for hypertension (Beers criteria) Potential for orthostatic hypotension and adverse CNS effects May cause bradycardia Immediate release: Lower initial doses than for nongeriatric adult dosing, as well as gradual adjustments, are recommended Extended release: May require lower initial dose than for nongeriatric adult dosing Skin reactions; patch (15-50%) Dry mouth (40%) Somnolence (19-38%) Headache (19-29%) Fatigue (13-24%) Drowsiness (33%) Dizziness (13-16%) Hypotension, epidural (45%) Postural hypotension, epidural (32%) Anxiety (11%) Epidural clonidine is not recommended for obstetric postpartum or perioperative pain management because the risk of hemodynamic instability (eg, hypotension, bradycardia) may be unacceptable in this population Dilute product with strength of 500 mcg/m L prior to use Epidural: Hemodynamically unstable patients (risk of severe hypotension) Do not discontinue suddenly (risk of rebound hypertension) Patch: May need to remove if severe erythema and/or localized vesicle formation develop at application site or generalized rash; consult physician Severe coronary insufficiency May cause xerostomia Recent MI Cerebrovascular disease Chronic renal failure Raynaud's disease Thromboangiitis obliterans History of depression (may exacerbate depression in cancer patients) May impair ability to perform hazardous tasks Remove patch before MRI (may cause burns) Hypotension may occur; usually responsive to IV fluids and, if necessary, appropriate parenterally administered pressor agents Cardiac conduction abnormalities: Sympatholytic action may worsen sinus node dysfunction and atrioventricular (AV) block, especially if coadministered with other sympatholytic drugs Titrate slowly and monitor vital signs frequently in patients at risk for hypotension, heart block, bradycardia, syncope, cardiovascular disease, vascular disease, cerebrovascular disease or chronic renal failure; measure heart rate and blood pressure prior to initiation of therapy, following dose increases, and periodically while on therapy; avoid concomitant use of drugs with additive effects unless clinically indicated; advise patients to avoid becoming dehydrated or overheated Epidural administration may result in mild respiratory depression (usually with higher than recommended dose) Use with caution in cerebrovascular disease Avoid as first line antihypertensive in the elderly due to high risk for adverse side effects Children may be particularly susceptible to hypertensive episodes when experiencing GI illnesses that lead to vomiting Discontinue oral immediate release formulations within 4 hr of surgery; restart as soon as possible following surgery Due to different pharmacokinetic profiles, oral formulations are not interchangeable with extended release on a mg-mg basis due to different pharmacokinetic profiles Central sympatholytic via stimulation of central alpha receptors; results in reduced sympathetic outflow, causing decreased PVR, HR, BP, and renal vascular resistance; produces presynaptic and postjunctional alpha-2 adrenoreceptor analgesia by preventing pain signal transmission to brain Postsynaptic alpha2-agonist stimulation may regulate subcortical activity in the prefrontal cortex, which may regulate the area of the brain responsible for attention, emotions, and behaviors, and thereby reduces hyperactivity, distractibility, and impulsiveness The above information is provided for general informational and educational purposes only. Individual plans may vary and formulary information changes. Contact the applicable plan provider for the most current information. Transdermal and oral clonidine. - NCBI What is the CPT code for Clonidine Hydrochloride Oral tablet? Clonidin – Wikipedia
     
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