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Testogel is a testosterone replacement therapy prescribed to treat male hypogonadism, a condition where the body produces insufficient testosterone. This topical gel delivers testosterone through the skin into the bloodstream, helping restore normal hormone levels in men with confirmed testosterone deficiency. Hypogonadism can result from testicular dysfunction, pituitary disorders, or hypothalamic problems, causing symptoms such as reduced libido, fatigue, muscle loss, and mood changes. Diagnosis requires biochemical confirmation through blood tests before treatment begins. Testogel is only prescribed for adult men with medically confirmed testosterone deficiency and must be used under specialist supervision.
Summary: Testogel is a testosterone replacement therapy gel prescribed to treat male hypogonadism, a condition characterised by abnormally low testosterone levels in adult men.
Testogel is a testosterone replacement therapy (TRT) prescribed to treat male hypogonadism, a condition characterised by abnormally low testosterone levels in men. Testosterone is the primary male sex hormone responsible for maintaining numerous physiological functions, including sexual development, muscle mass, bone density, mood regulation, and energy levels.
The gel contains testosterone as its active ingredient and is applied topically to the skin, where it is absorbed into the bloodstream. Testogel is specifically indicated for testosterone replacement in adult males with confirmed hypogonadism, where clinical features and biochemical tests confirm testosterone deficiency. Primary hypogonadism results from testicular dysfunction, whilst secondary hypogonadism occurs when the hypothalamus or pituitary gland fails to signal adequate testosterone production.
Symptoms of low testosterone that may prompt investigation include:
Reduced libido and erectile dysfunction
Persistent fatigue and low energy
Loss of muscle mass and increased body fat
Mood changes, including depression or irritability
Decreased bone density (osteoporosis)
Reduced facial and body hair growth
Diagnosis requires biochemical confirmation through blood tests, typically performed in the morning when testosterone levels are naturally highest. According to NICE Clinical Knowledge Summary guidance, testosterone deficiency should be confirmed with at least two separate early-morning (ideally fasting) testosterone measurements showing levels below the normal reference range. Additional tests including luteinising hormone (LH), follicle-stimulating hormone (FSH), and sometimes prolactin are needed to determine the cause.
Before starting Testogel, reversible causes of low testosterone should be addressed, including obesity, chronic illness, and certain medications like opioids. It's important to note that Testogel is not licensed for use in women or children and should only be used under specialist supervision. Testogel suppresses sperm production and may impair fertility, so it's not suitable for men trying to conceive.
Testogel is prescribed exclusively for adult men with confirmed testosterone deficiency resulting from recognised medical conditions affecting the testes, pituitary gland, or hypothalamus. The decision to initiate testosterone replacement therapy follows thorough clinical and biochemical evaluation by a healthcare professional, often an endocrinologist or specialist in sexual health.
Conditions warranting Testogel prescription include:
Klinefelter syndrome – a genetic condition affecting testicular development
Pituitary disorders – tumours or damage affecting hormone production
Testicular injury or infection – physical trauma or orchitis
Chemotherapy or radiotherapy – treatments affecting gonadal function
Kallmann syndrome – a congenital condition affecting puberty
While some clinicians may consider TRT for age-related testosterone decline, this is not a licensed indication and should only be considered if true hypogonadism is confirmed biochemically and symptoms are significant.
Before prescribing Testogel, clinicians must exclude contraindications and assess individual risk factors. According to the UK Summary of Product Characteristics (SmPC), Testogel is contraindicated in men with:
Prostate cancer or breast cancer (current or suspected)
Hypersensitivity to testosterone or gel excipients
Careful consideration and optimisation are required in men with:
Severe cardiac, hepatic or renal insufficiency
Benign prostatic hyperplasia with urinary obstruction
Polycythaemia (elevated red blood cell count)
Untreated sleep apnoea
Cardiovascular disease
History of thromboembolism
According to NICE guidance, baseline investigations before initiating TRT should include prostate-specific antigen (PSA) testing, full blood count (especially haemoglobin/haematocrit), liver function tests, and consideration of lipid profile based on individual risk. Digital rectal examination may be performed in men over 40 or those with risk factors for prostate disease. LH, FSH and prolactin should be measured if secondary hypogonadism is suspected.
Patients should be informed that TRT reduces fertility by suppressing spermatogenesis. Men wishing to father children should discuss fertility-preserving options and may need referral to specialist andrology services.
Correct application technique is essential to ensure optimal testosterone absorption whilst minimising the risk of accidental transfer to others. Testogel is available in two formulations in the UK: 50 mg/5 g (1%) gel in sachets and 16.2 mg/g gel in a pump dispenser. Application instructions differ slightly between formulations.
Testogel 50 mg/5 g (1%) sachets:
Usual starting dose is 50 mg (one sachet) daily
May be adjusted between 25-100 mg (½-2 sachets) based on response
Apply to clean, dry skin on shoulders, upper arms, or abdomen
Avoid washing the application site for approximately 6 hours
Testogel 16.2 mg/g pump:
Usual starting dose is 40.5 mg (2 pump actuations) daily
May be adjusted between 20.25-81 mg (1-4 actuations) based on response
Apply only to clean, dry skin on shoulders or upper arms (not abdomen)
Avoid washing the application site for at least 2 hours
Prime the pump before first use by pressing 3 times (discard this gel)
Step-by-step application guidance:
Critical safety measures to prevent testosterone transfer:
Cover the application site with clothing once the gel has dried
Avoid skin-to-skin contact with others, especially women and children
Shower or wash the application area before anticipated close physical contact
Wash any area of another person's skin that accidentally contacts the gel
Keep the gel away from children and pregnant women, as testosterone exposure can cause harm
If you miss a dose, apply it as soon as you remember on the same day. If you remember the following day, skip the missed dose and continue with your regular schedule – do not double the dose. Testogel is flammable until dry, so avoid flames, smoking, or sparks near the application site. Store sachets or pumps at room temperature, away from heat and moisture, and keep out of reach of children.
Like all medicines, Testogel can cause side effects, though not everyone experiences them. Understanding potential adverse effects enables early recognition and appropriate management. Most side effects are mild and resolve with continued use or dose adjustment, but some require medical attention.
Common side effects (affecting up to 1 in 10 people) include:
Skin reactions at the application site – redness, itching, or dryness
Acne or oily skin
Mood changes or emotional lability
Headache
Increased red blood cell count (polycythaemia)
Weight gain
Prostate enlargement (benign prostatic hyperplasia)
Less common but significant side effects include:
Gynaecomastia (breast enlargement or tenderness)
Sleep disturbances or worsening sleep apnoea
Fluid retention and peripheral oedema
Changes in libido (increase or decrease)
Elevated blood pressure
Altered liver function tests
Changes in cholesterol levels
Reduced sperm production and fertility
Serious side effects requiring immediate medical attention (call 999 or go to A&E):
Signs of blood clots – sudden chest pain, breathlessness, leg pain or swelling
Prolonged or painful erections (priapism) lasting more than 4 hours
Signs of liver problems – yellowing of skin or eyes, dark urine, severe abdominal pain
Allergic reactions – difficulty breathing, facial swelling, severe rash
Important drug interactions to be aware of:
Testogel may enhance the effect of warfarin (requiring more frequent INR monitoring)
It may reduce insulin requirements in diabetic patients
Combined use with corticosteroids may increase the risk of fluid retention
Regular monitoring is essential throughout Testogel treatment. Follow-up should include testosterone level measurement at 3 months after starting or adjusting the dose, then every 6–12 months. Haemoglobin/haematocrit should be checked at baseline, 3–6 months, then annually. PSA and prostate assessment should be performed according to age and risk factors. More frequent monitoring is needed if abnormalities arise.
Regarding cardiovascular safety, the MHRA advises there is no consistent evidence of increased cardiovascular risk when testosterone is used as indicated for confirmed hypogonadism, but individual cardiovascular risk factors should be discussed and monitored.
Contact your GP if you experience persistent side effects, mood changes, or any concerning symptoms. If you suspect you're experiencing a side effect from Testogel, you can report it through the MHRA Yellow Card Scheme (yellowcard.mhra.gov.uk).
Testogel is not licensed for age-related testosterone decline alone. It should only be prescribed if true hypogonadism is confirmed biochemically through blood tests and symptoms are significant, following thorough clinical evaluation.
Testosterone levels typically begin to rise within days of starting Testogel, but clinical improvements in symptoms such as energy, mood, and libido may take several weeks to months. Testosterone levels are usually measured at 3 months to assess response and adjust dosing if needed.
Yes, testosterone can transfer to others through direct skin-to-skin contact with the application site. To prevent transfer, cover the area with clothing once dry, avoid close contact until showering, and wash any skin that accidentally contacts the gel immediately with soap and water.
The health-related content published on this site is based on credible scientific sources and is periodically reviewed to ensure accuracy and relevance. Although we aim to reflect the most current medical knowledge, the material is meant for general education and awareness only.
The information on this site is not a substitute for professional medical advice. For any health concerns, please speak with a qualified medical professional. By using this information, you acknowledge responsibility for any decisions made and understand we are not liable for any consequences that may result.
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