Triptorelin
Brand names: Decapeptyl SR, Gonapeptyl
Triptorelin is a gonadotrophin-releasing hormone (GnRH) agonist given as a depot injection, used in hormone-sensitive prostate cancer, endometriosis, uterine fibroids, central precocious puberty, and as part of assisted reproduction. It produces a reversible medical suppression of sex hormone production.
Adult dose
Dose auto-extracted from US FDA prescribing information (openFDA / DailyMed) — cross-check; US labelling may differ from UK — not yet clinician-verified. Always confirm against the product SmPC and your local formulary before prescribing.
Contraindications
- Known hypersensitivity to triptorelin or any other component of the product, or to other GnRH agonists or GnRH
Side effects
- Hot flushes
- Skeletal pain
- Erectile dysfunction / impotence
- Headache
- Oedema in legs / leg pain; testicular atrophy
Interactions
- No drug-drug interaction studies conducted; hepatic microsomal enzymes unlikely to be involved in metabolism
- Hyperprolactinaemic drugs should not be used concomitantly (hyperprolactinaemia reduces pituitary GnRH receptors)
Clinical monograph
How it works
As a GnRH agonist it initially stimulates and then, with continuous administration, downregulates pituitary GnRH receptors, suppressing luteinising hormone and follicle-stimulating hormone release and so reducing testosterone or oestrogen production to castrate or postmenopausal levels.
Prescribing in practice
- In men with prostate cancer the initial testosterone surge can cause a temporary tumour flare, which may worsen bone pain or cause spinal cord compression or urinary obstruction, so anti-androgen cover should be considered, especially with metastatic disease.
- Long-term use reduces bone mineral density, so bone health should be considered with prolonged treatment.
- It must not be used in pregnancy, and prolonged use causes hypo-oestrogenic effects in women that may need addition of add-back therapy.
Monitoring
Monitor the relevant hormonal response (testosterone or oestrogen and, in prostate cancer, PSA), bone mineral density with prolonged use, and clinical disease response.
Counselling the patient
- This is given as a depot injection at regular intervals by a healthcare professional.
- Men may notice a brief worsening of symptoms when starting; report new or worsening bone pain, weakness, or trouble passing urine.
- Hot flushes and reduced libido are common; women may have menopause-like symptoms.
Evidence & guidelines
Efficacy across its hormone-dependent indications is supported by randomised trials and extensive clinical experience with GnRH agonist therapy.
Reference: NICE NG131; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. The structured dose values shown have been reviewed by a clinician. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Diabetic Ketoacidosis (DKA) · JBDS 2013 / Joint British Diabetes Societies; NICE NG17
- Adult Hypoglycaemia (Treated Diabetes) · JBDS-IP (2023): Hospital Management of Hypoglycaemia
- Adrenal Crisis · Society for Endocrinology Emergency Guidance (2024)
- Type 2 Diabetes Management · NICE NG28 2022
- Hyperthyroidism Management · BTA / ETA 2018
- Adrenal Insufficiency · Society of Endocrinology / ESE 2016