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Post Cycle Therapy (PCT): A Comprehensive UK Guide to Hormonal Recovery

This article on Post Cycle Therapy (PCT) is provided by the Evolution LAB Team for informational and educational purposes only. The content herein is intended to discuss concepts and practices that are subjects of research and discussion within specific communities. It does not, under any circumstances, endorse, encourage, or condone the use of illegal or controlled substances, nor does it constitute medical or legal advice.

The use of anabolic-androgenic steroids (AAS), Selective Androgen Receptor Modulators (SARMs), and other performance-enhancing compounds carries significant health risks and legal consequences in the United Kingdom. Many substances discussed in the context of PCT are Prescription Only Medicines (POMs) in the UK and should not be used without the guidance and prescription of a qualified UK healthcare professional.

Evolution LAB UK sells compounds strictly for in-vitro laboratory research purposes only. These products are not for human consumption or veterinary use.

Always consult with a qualified UK healthcare professional (e.g., your GP or an endocrinologist) for any health concerns, before making any decisions related to your health, or considering the use of any substance. For legal advice, consult with a qualified legal professional in the UK.

By reading this article, you acknowledge and agree to these terms.

Table of Contents

Introduction to Post Cycle Therapy (PCT)

What is Post Cycle Therapy (PCT)?

Post Cycle Therapy, commonly abbreviated as PCT, refers to a period following the cessation of a cycle of anabolic-androgenic steroids (AAS), Selective Androgen Receptor Modulators (SARMs), or other similar performance-enhancing compounds. The primary purpose of PCT is to help restore the body’s natural (endogenous) hormonal balance, with a particular focus on restarting and recovering natural testosterone production, which is often suppressed or completely shut down by the use of these exogenous anabolic substances. This recovery process is considered by many within fitness and bodybuilding communities to be crucial for maintaining health and preserving muscle gains achieved during a cycle.

Why is PCT Discussed and Considered Important in the UK?

The discussion around Post Cycle Therapy (PCT) in the UK, as elsewhere, stems from the physiological consequences of using substances that disrupt the body’s natural hormone production.

  • The Physiological Need: HPTA Suppression The body’s endocrine system, specifically the Hypothalamic-Pituitary-Testicular Axis (HPTA), is responsible for regulating testosterone production. When exogenous anabolic compounds are introduced, the body senses an excess of hormones. This signals the hypothalamus and pituitary gland to reduce or stop producing their signalling hormones (Gonadotropin-Releasing Hormone (GnRH), Luteinizing Hormone (LH), and Follicle-Stimulating Hormone (FSH)), which in turn causes the testes to significantly decrease or cease natural testosterone production. This state is known as HPTA suppression or shutdown.

    Diagram illustrating the Hypothalamic-Pituitary-Testicular Axis (HPTA) and its role in testosterone production, showing negative feedback from exogenous hormones.

  • Consequences of Unaddressed HPTA Suppression: If HPTA function is not adequately restored post-cycle, individuals may experience a range of undesirable effects due to low testosterone levels and hormonal imbalance, including:

    • Loss of muscle mass gained during the cycle

    • Increased body fat

    • Persistent fatigue and lethargy

    • Decreased libido and sexual dysfunction

    • Mood swings, irritability, and potentially depression

    • Difficulties with concentration and cognitive function

  • Reported Goals of an Effective PCT: Within communities that discuss these practices, the aims of a well-structured PCT are generally reported as:

    • Stimulating and accelerating the recovery of natural testosterone production.

    • Helping to preserve the muscle tissue and strength gains acquired during the cycle.

    • Mitigating the adverse symptoms associated with low endogenous testosterone.

    • Supporting overall physiological and psychological well-being during the transition period post-cycle.

    • Managing oestrogen levels, which can become imbalanced when testosterone production is disrupted.

The prevalence of discussions on PCT within UK-based online forums and fitness circles underscores a user-driven interest in mitigating the potential negative impacts of performance-enhancing substance use, even though the substances themselves are often controlled.

CRUCIAL UK Legal Context for Substances Requiring PCT

Before proceeding, it is essential to understand the legal framework in the United Kingdom concerning substances that typically lead to the need for Post Cycle Therapy.

Anabolic-androgenic steroids (AAS) are classified as Class C controlled substances under the Misuse of Drugs Act 1971. It is illegal to produce, supply, or possess/import AAS with the intent to supply, without a requisite licence. While personal possession is not an offence if for oneself and in a medicinal form, importing them, even for personal use, can carry legal risks depending on the method and quantity.

Selective Androgen Receptor Modulators (SARMs) occupy a more complex legal space. While not explicitly listed under the Misuse of Drugs Act 1971 in the same way as AAS, they are often sold as “research chemicals” and are not approved for human consumption in the UK. Their sale for human use, or as ingredients in unlicensed medicinal products, is illegal.

This article is for informational and educational purposes ONLY. It does not endorse, encourage, or condone the use of illegal or controlled substances. The information on PCT is provided to foster an understanding of practices discussed in relation to the use of such substances, often with a focus on harm reduction.

Evolution LAB UK does not provide medical or legal advice. Always consult a qualified UK healthcare professional (e.g., your GP or an endocrinologist registered with the General Medical Council) for any health concerns or before making any decisions related to your health or the use of any substance. For legal advice, consult with a qualified legal professional in the UK.


Key Compounds Discussed in PCT Protocols

Various pharmaceutical compounds are frequently mentioned in discussions about PCT protocols. It is critical to understand that these are potent medicines, many of which are Prescription Only Medicines (POMs) in the UK, with specific medical indications and potential side effects. Their use outside of medical supervision carries significant risks.

Selective Estrogen Receptor Modulators (SERMs)

Selective Estrogen Receptor Modulators (SERMs) are a class of drugs that bind to oestrogen receptors. Depending on the tissue, they can act as oestrogen agonists (activators) or antagonists (blockers). In the context of PCT, their primary reported role is to act as oestrogen antagonists at the level of the hypothalamus and pituitary gland. By blocking oestrogen’s negative feedback at these sites, SERMs can help stimulate the release of Luteinizing Hormone (LH) and Follicle-Stimulating Hormone (FSH), thereby encouraging the testes to resume endogenous testosterone production.

        • Tamoxifen (e.g., Nolvadex)

    • Mechanism in PCT Context: Tamoxifen citrate is primarily known for its use in breast cancer treatment. In PCT discussions, it is suggested to block oestrogen receptors in the hypothalamus, reducing negative feedback and promoting LH and FSH release, which signals the testes to produce testosterone.

    • Reported Side Effects: Potential side effects can include hot flushes, nausea, fatigue, mood changes, and, less commonly, visual disturbances or an increased risk of certain conditions with long-term use (though PCT use is typically short-term).

    • UK Legal Status & Availability: Tamoxifen is a Prescription Only Medicine (POM) in the UK. It is illegal to supply without a license or possess without a valid prescription from a UK healthcare professional. It is prescribed in the UK for conditions like breast cancer and sometimes off-label for infertility.

        • Clomiphene Citrate (e.g., Clomid)

    • Mechanism in PCT Context: Clomiphene citrate is medically used to treat infertility in women. In PCT discussions, similar to tamoxifen, it is reported to block oestrogen receptors at the hypothalamus and pituitary, thereby increasing LH and FSH production and stimulating testicular testosterone synthesis. Some anecdotal reports suggest it may be more potent in stimulating LH than tamoxifen, but also potentially having more pronounced side effects for some individuals.

    • Reported Side Effects: Common reported side effects include mood swings, emotional volatility, visual disturbances (floaters, blurred vision – which should prompt immediate cessation and medical consultation), headaches, and nausea.

    • UK Legal Status & Availability: Clomiphene citrate is a Prescription Only Medicine (POM) in the UK. Its supply and possession are governed by the same regulations as tamoxifen.

Table: Comparison of Tamoxifen and Clomiphene for PCT (Reported Information)

Aromatase Inhibitors (AIs) – Role In or Alongside PCT

Aromatase Inhibitors (AIs) work by blocking the aromatase enzyme, which is responsible for converting androgens (like testosterone) into oestrogens. Their role in relation to PCT is a subject of debate.

  • Mechanism & Role Discussion: While AIs effectively reduce systemic oestrogen levels, their primary role is often discussed for on-cycle oestrogen management or as a “bridge” into PCT, rather than being a core component for restarting HPTA function during PCT itself. Some argue that maintaining some level of oestrogen is important for health and HPTA recovery, and overly suppressing it with AIs during PCT could be counterproductive or delay recovery. However, if oestrogen levels are excessively high at the start of PCT (rebound), some discussions mention very short-term AI use.

  • Common AIs & Reported Side Effects:

    • Anastrozole (e.g., Arimidex): Potent AI. Potential side effects include joint pain, fatigue, hot flushes, and negative impacts on lipid profiles and bone mineral density with prolonged use.

    • Letrozole (e.g., Femara): A very potent AI, often considered too strong for typical PCT scenarios, potentially crashing oestrogen levels severely. Similar side effects to anastrozole, possibly more pronounced.

    • Exemestane (e.g., Aromasin): A steroidal AI, sometimes favoured for having a slightly different impact on lipids compared to non-steroidal AIs, though it still carries risks.

  • UK Legal Status & Availability: Anastrozole, Letrozole, and Exemestane are all Prescription Only Medicines (POMs) in the UK, primarily used in the treatment of breast cancer.

Expert Note: It is crucial to distinguish the function of AIs (oestrogen reduction) from SERMs (oestrogen receptor modulation for HPTA stimulation). Using AIs incorrectly during PCT could hinder recovery by excessively lowering oestrogen, which also plays roles in male physiology and HPTA function.

Human Chorionic Gonadotropin (HCG)

Human Chorionic Gonadotropin (HCG) is a hormone that mimics Luteinizing Hormone (LH).

  • Mechanism in Relation to Testicular Function: HCG can directly stimulate the Leydig cells in the testes to produce testosterone and maintain testicular size and function.

  • Reported Use: Its use is commonly discussed for during a cycle or in the period immediately leading up to PCT, rather than as a primary HPTA-restarting agent within PCT. The rationale is to prevent severe testicular desensitisation and atrophy during a long cycle, making it easier for the testes to respond to the body’s own LH when PCT begins. Using HCG during PCT can be counterproductive, as it provides an external LH-like signal which can further suppress the pituitary’s own LH production.

  • Reported Side Effects: Potential side effects include gynecomastia (due to increased testosterone aromatising to oestrogen if not managed), headaches, mood changes, and injection site reactions.

  • UK Legal Status & Availability: HCG is a Prescription Only Medicine (POM) in the UK, used legitimately for conditions like infertility and hypogonadism. Sourcing HCG outside of a valid prescription carries legal and health risks.

Other Supplements & “Natural PCT” Considerations

A variety of over-the-counter supplements are often marketed in the UK and elsewhere as “natural PCT” aids or testosterone boosters. These may include ingredients like D-Aspartic Acid, Tribulus Terrestris, Ashwagandha, Fenugreek, Zinc, Magnesium, and Vitamin D.

  • Efficacy for HPTA Restoration: While some of these supplements may have mild benefits for general well-being or potentially support optimal hormone production in individuals who are deficient in certain nutrients (e.g., Zinc, Vitamin D), there is limited robust scientific evidence to suggest they can effectively restore a significantly suppressed HPTA axis in the same way pharmaceutical interventions like SERMs aim to.

  • Role: They might be considered by some as supportive additions after a pharmaceutical PCT or for individuals coming off very mild, short cycles (though even then, their impact on HPTA recovery is debatable and not a substitute for understanding the body’s hormonal state).

  • Importance of Evidence: It is crucial to critically evaluate the marketing claims for such supplements against independent scientific research. Many “T-boosters” lack the potency to address the level of suppression caused by significant AAS/SARM use.

Expertise Note: For significant HPTA suppression, relying solely on “natural” supplements for PCT is generally not considered an effective strategy according to scientific understanding and reported user experiences. They do not address the core issue of restarting pituitary signalling in the same direct manner as SERMs.


Understanding PCT Protocols & Considerations (Descriptive Overview)

Evolution LAB Team Disclaimer: The following information is purely descriptive of discussions and reported practices within communities that use performance-enhancing substances. It is NOT a set of instructions or recommendations. Designing or undertaking any PCT protocol without the guidance of a qualified UK medical professional is extremely risky and not advised. Individual responses vary greatly.

General Principles Discussed for Structuring a PCT

Discussions around PCT protocols often highlight several common principles:

  • Timing of Initiation: A key consideration is when to start PCT after the last administration of anabolic compounds. This is reported to depend heavily on the half-lives of the substances used. For short-ester compounds, PCT might be discussed as starting a few days after the last dose. For long-ester compounds, a waiting period of several weeks is often mentioned to allow the exogenous hormones to clear the system sufficiently, so PCT drugs don’t have to compete with high levels of circulating androgens.

  • Duration: The length of a PCT protocol is variable in discussions, often ranging from 4 to 6 weeks, sometimes longer, depending on the perceived severity of suppression and individual recovery.

  • Compound Selection: The choice of compounds (e.g., Nolvadex vs. Clomid, or sometimes combinations, though this increases complexity and potential side effects) is a frequent topic of debate, with proponents for different approaches based on anecdotal evidence or interpretations of pharmacology.

  • “Tapering” vs. Consistent Dosing: Some discussions involve “front-loading” PCT drugs (higher initial amounts) and then tapering down, while others advocate for a consistent amount throughout. There is no universal consensus in these informal discussions.

Factors Reportedly Influencing PCT Design

The structure and intensity of a PCT, as discussed in user communities, are often tailored based on several factors:

  • Compounds Used in the Cycle: Heavier, more suppressive compounds (e.g., Trenbolone, Nandrolone, high doses of testosterone) or longer stacks are generally reported to necessitate a more robust PCT. Milder compounds or shorter cycles might be discussed with less intensive PCTs, though any exogenous anabolic can cause suppression.

  • Duration of the Cycle: Longer cycles are typically associated with more profound HPTA suppression and thus often discussed with more comprehensive PCT protocols.

  • Individual Physiological Response: It’s widely acknowledged that individuals respond differently to both anabolic compounds and PCT medications. Genetic factors, age, and baseline hormonal health can all play a role.

  • Role of Blood Work (UK Medical Context): Increasingly, responsible discussions, even in user forums, emphasize the importance of blood tests to assess hormonal status. In the UK, obtaining and interpreting comprehensive hormonal blood panels (including Total and Free Testosterone, LH, FSH, Oestradiol, Prolactin, SHBG, etc.) should ideally be done under the guidance of a GP or a private endocrinologist. This allows for an objective assessment of HPTA function before, during (if concerns arise), and after a cycle, and can inform the medical need for intervention if health is compromised. Self-interpreting blood work can be misleading.

What “Successful PCT” Aims to Achieve (Reiteration & Nuance)

Beyond just restarting testosterone production, a PCT, as discussed, aims to facilitate a smoother transition from an “on-cycle” state to a normalized hormonal environment. The reported markers of a “successful” PCT include:

  • Restoration of endogenous testosterone levels to within the individual’s normal, healthy UK reference range.

  • Normalization of LH and FSH levels, indicating pituitary recovery.

  • Effective management of oestrogen levels to avoid symptoms of either high or low oestrogen.

  • Alleviation of low testosterone symptoms (fatigue, low libido, etc.).

  • Maintenance of psychological well-being.

  • Better preservation of lean muscle mass gained.

It’s important to note that even with a PCT protocol based on common discussions, outcomes can vary, and a full return to pre-cycle hormonal function or muscle mass is not always guaranteed.

Potential Risks, Side Effects, and Limitations of PCT

While PCT is discussed as a means to mitigate post-cycle issues, the process and the compounds involved are not without their own risks and limitations.

Risks and Side Effects of PCT Compounds Themselves

As detailed in Part 2, the pharmaceutical drugs commonly mentioned in PCT discussions (SERMs, AIs, HCG) are potent medications with their own potential side effect profiles. These can range from relatively mild (e.g., hot flushes, minor mood changes with SERMs) to more serious (e.g., visual disturbances with Clomid, severe oestrogen suppression with AIs leading to joint issues or negative cardiovascular markers). It is a misconception to view PCT drugs as entirely benign.

Limitations and What PCT Cannot Do

It’s crucial to have realistic expectations about what PCT can and cannot achieve:

  • Not a Guarantee of Full Recovery: PCT does not guarantee a 100% return to baseline HPTA function for every individual, especially after particularly long, heavy, or repeated cycles. Some individuals may experience persistent suppression.

  • Cannot Prevent All Muscle Loss: While a primary goal is to help preserve gains, some loss of muscle mass and strength is often inevitable when exogenous anabolic support is removed. PCT aims to minimize this, not eliminate it entirely.

  • Does Not Reverse All Cycle-Related Health Damage: PCT is focused on hormonal recovery. It cannot undo potential damage caused by AAS/SARMs to other organ systems, such as the cardiovascular system (e.g., adverse lipid changes, cardiac hypertrophy), liver (with oral C17-alpha-alkylated steroids), or kidneys. These require separate health monitoring and management, ideally with a UK healthcare professional.

Risks of Incorrectly Implemented or Inadequate PCT (Based on Reported Information)

Attempting PCT without adequate understanding or using inappropriate protocols, according to discussions, can lead to:

  • Prolonged HPTA Suppression: Resulting in extended periods of low testosterone and its associated negative symptoms.

  • Increased Muscle Catabolism: Greater loss of lean muscle tissue.

  • Persistent Low Libido and Sexual Dysfunction.

  • Negative Mood Changes: Including potential for depression and anxiety.

  • Possible Long-Term Endocrine Issues: In some cases, chronic suppression may lead to secondary hypogonadism requiring long-term medical attention.

Dangers of Sourcing PCT Drugs from Unregulated UK/International Sources

This is a major concern for UK individuals. As most effective PCT drugs are Prescription Only Medicines, obtaining them without a prescription often involves resorting to unregulated or “black market” sources. This carries substantial risks:

  • Counterfeit Products: The product may not be the drug it claims to be.

  • Underdosed or Overdosed Products: Incorrect concentrations can render PCT ineffective or increase side effect risks.

  • Contaminated or Impure Substances: Products may contain harmful bacteria, heavy metals, or other undeclared substances.

  • Incorrectly Labeled Products: Leading to accidental misuse.

  • Lack of Quality Control: No oversight of manufacturing processes.

  • Legal Risks in the UK: Possession of POMs without a valid prescription can carry legal penalties, and importation is also risky.

Infographic listing risks of unregulated Post Cycle Therapy drugs in the UK: counterfeits, contamination, incorrect dosage, legal issues.


Legal Status of PCT Drugs in the UK

Understanding the legal framework for PCT-related drugs in the United Kingdom is crucial for anyone researching this topic.

Prescription Only Medicines (POMs)

The vast majority of pharmaceutical compounds commonly discussed for effective Post Cycle Therapy fall under the category of Prescription Only Medicines (POMs) in the UK. This includes:

  • SERMs: Tamoxifen (Nolvadex), Clomiphene Citrate (Clomid)

  • Aromatase Inhibitors (AIs): Anastrozole (Arimidex), Letrozole (Femara), Exemestane (Aromasin)

  • HCG: Human Chorionic Gonadotropin

What This Means in the UK: According to UK medicines regulations, overseen by the Medicines and Healthcare products Regulatory Agency (MHRA):

  • It is illegal for a retailer to sell or supply a POM to the public except by a registered pharmacy, against a valid prescription issued by an appropriately qualified UK healthcare professional (e.g., a doctor, dentist, or qualified independent prescriber).

  • Possession of a POM without a valid prescription is generally not an offence if it’s for personal use and was legitimately supplied (e.g. from a previous valid prescription). However, obtaining it without a prescription from an illicit source means it was not legitimately supplied.

  • Importing POMs for personal use can be complex. While small quantities for personal use may sometimes be allowed if accompanied by a prescription, importing from non-reputable sources or in larger quantities can lead to seizure by customs and potential legal issues.

These drugs have legitimate medical uses in the UK for specific conditions (e.g., Tamoxifen for breast cancer, Clomiphene and HCG for fertility issues, AIs for breast cancer). However, their use specifically for PCT following non-prescribed AAS/SARM use is an “off-label” application that UK doctors are unlikely to prescribe for directly, given the preceding use of controlled or unapproved substances.

Implications for UK Individuals

The POM status of these drugs has significant implications for individuals in the UK considering PCT:

  • Difficulty in Legitimate Acquisition: It is generally not possible to obtain these medications from a UK doctor or pharmacy specifically for the purpose of PCT after a cycle of illicitly used anabolic substances. Doctors in the UK are bound by strict prescribing guidelines and ethical considerations.

  • Reliance on Unregulated Markets: This often leads individuals to seek these drugs from unregulated (“black market” or “underground lab” – UGL) sources, either domestically or internationally, with all the associated health and legal risks outlined in section 4.4.

  • Legal Risks of Purchase and Possession: Purchasing and possessing POMs obtained without a valid UK prescription is legally precarious and can lead to issues if discovered by UK authorities.

It is vital for UK residents to be aware of these legal realities and the potential consequences.


The Importance of Medical Consultation in the UK

Given the health implications of AAS/SARM use and the complexities of hormonal recovery, seeking advice from qualified UK medical professionals is paramount.

Why See a Doctor (GP or Specialist) in the UK?

Individuals in the UK experiencing health issues or having concerns about their hormonal health, particularly after a cycle of performance-enhancing substances, should consider consulting their General Practitioner (GP) or an endocrinologist (hormone specialist).

  • Proper Diagnosis & Investigation: A UK doctor can arrange for appropriate blood tests to accurately assess hormone levels (testosterone, LH, FSH, oestradiol, etc.) and identify any underlying health problems. The NHS provides reference ranges specific to the UK population.

  • Medically Supervised Treatment (if indicated): If a genuine medical condition, such as clinically diagnosed hypogonadism (low testosterone), is identified, a UK doctor can discuss legitimate and safe treatment options available through the NHS or private healthcare. This would be based on clinical need, not as a “PCT” for recreational drug use.

  • Harm Reduction Advice: Even if direct PCT prescription is unlikely, a doctor can provide harm reduction advice and support for any health issues arising from substance use.

  • Access to NHS Services: Your GP is the gateway to further NHS services, including referrals to specialists like endocrinologists or sexual health clinics if necessary.

Being Honest with UK Healthcare Providers

While it can be daunting, being open and honest with your UK doctor or healthcare provider about any substances used is generally advisable for receiving the best possible care.

  • Informed Medical Advice: Full disclosure allows your doctor to make a more accurate assessment of your health status and provide appropriate advice or treatment, understanding potential drug interactions or underlying causes of symptoms.

  • Patient Confidentiality: Doctors in the UK are bound by strict rules of patient confidentiality. They are there to help with your health, and discussions are typically private unless there’s an immediate serious risk of harm to yourself or others, or if specific legal obligations apply.

  • Focus on Health: Frame the conversation around your health concerns (e.g., “I’ve been feeling X, Y, Z symptoms, and I have used A, B, C substances in the past. I’m concerned about my hormonal health.”).

Seeking professional medical help is a sign of taking responsibility for your health, especially when dealing with the after-effects of potent compounds.


Conclusion & Final Takeaways

Post Cycle Therapy is a complex topic discussed extensively within communities that use performance-enhancing substances like AAS and SARMs. It arises from a genuine physiological need to address the HPTA suppression caused by these exogenous compounds. The goal, as reported, is to help restore natural hormonal balance, preserve gains, and mitigate negative side effects.

However, as this comprehensive UK guide has detailed:

  • The compounds commonly mentioned for PCT are potent pharmaceutical drugs, most of which are Prescription Only Medicines in the UK, carrying their own significant side effect profiles and legal restrictions.

  • Obtaining these drugs without a valid UK prescription involves significant health risks (counterfeits, contamination) and legal risks.

  • There is no one-size-fits-all PCT protocol, and self-administering such protocols based on informal advice carries a high risk of being ineffective or harmful.

  • “Natural” PCT supplements generally lack the scientific backing to effectively restore a significantly suppressed HPTA axis.

This guide is for informational and educational purposes only. It is not an instruction manual, nor does it endorse or encourage any illegal activity or the use of non-prescribed medications.

The Evolution LAB Team strongly advises individuals in the UK to:

  1. Prioritise Health & Safety: Be fully aware of the profound health risks associated with AAS/SARMs and any subsequent attempts at hormonal recovery.

  2. Understand UK Law: Be aware of the legal status of AAS, SARMs, and PCT-related drugs in the United Kingdom.

  3. Seek Professional Medical Advice: If you have any health concerns related to hormone levels, substance use, or post-cycle recovery, consult a qualified UK healthcare professional (GP or endocrinologist). They can provide accurate diagnoses, arrange necessary tests, and discuss safe and legal treatment options if a medical condition is identified.

  4. Beware of Unregulated Sources: Avoid sourcing any pharmaceutical substances from unregulated or illicit channels due to the high risk of fake, contaminated, or incorrectly dosed products.

Evolution LAB UK is committed to providing compounds for legitimate in-vitro laboratory research purposes only. Our products are not designed for human consumption or veterinary use and should not be considered as options for PCT or any other therapeutic use. Responsible research and adherence to UK legal and ethical guidelines are paramount.

References & Further Reading

 
Dunlavey CJ. Introduction to the Hypothalamic-Pituitary-Adrenal Axis: Healthy and Dysregulated Stress Responses, Developmental Stress and Neurodegeneration. J Undergrad Neurosci Educ. 2018;16(2):R59-R60. Published 2018 Jun 15. https://pmc.ncbi.nlm.nih.gov/articles/PMC6057754/
 
Grant, B., Kean, J., Vali, N. et al. The use of post-cycle therapy is associated with reduced withdrawal symptoms from anabolic-androgenic steroid use: a survey of 470 men. Subst Abuse Treat Prev Policy 18, 66 (2023). https://doi.org/10.1186/s13011-023-00573-8
 
Buzdar, A.U., Robertson, J.F.R., Eiermann, W. and Nabholtz, J.-M. (2002), An overview of the pharmacology and pharmacokinetics of the newer generation aromatase inhibitors anastrozole, letrozole, and exemestane. Cancer, 95: 2006-2016. https://doi.org/10.1002/cncr.10908
 
Cole, L.A. New discoveries on the biology and detection of human chorionic gonadotropin. Reprod Biol Endocrinol 7, 8 (2009). https://doi.org/10.1186/1477-7827-7-8
 
Jackson, G., Patel, S. and Khan, S. (2012), Assessing the problem of counterfeit medications in the United Kingdom. International Journal of Clinical Practice, 66: 241-250. https://doi.org/10.1111/j.1742-1241.2011.02826.x
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