Product image of Goserrelina Teva (Goserelin) supplied by GNH India

Goserrelina Teva

Active Ingredient:
Goserelin
Origin:
EU

Goserrelina Teva (Goserelin)

Goserrelina Teva is a prescription medication containing the active ingredient goserelin, supplied as an implantable formulation marketed in the European Union. It belongs to the gonadotropin‑releasing hormone (GnRH) agonist class and works by modulating pituitary hormone release. The product is used under medical supervision for hormone‑dependent conditions. It is administered by a subcutaneous implant that releases the drug continuously over several months, providing sustained suppression of sex hormone production.

Manufacturer / TM Owner

Teva Pharma – Produtos Farmacêuticos Lda

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Indications & Clinical Uses

Goserrelina Teva is indicated for several hormone‑sensitive diseases where reduction of testosterone or estrogen levels is desired.

  • Treatment of advanced prostate cancer in men.
  • Management of hormone‑responsive breast cancer in pre‑menopausal women.
  • Therapy for endometriosis to reduce pelvic pain and lesion growth.
  • Reduction of uterine fibroid size and associated bleeding.
  • Adjunctive use in assisted reproduction protocols to control ovarian stimulation.

The medication may be prescribed as part of a multidisciplinary treatment plan and is typically given by a healthcare professional experienced in hormone therapy.

Side Effects

Side‑effect profiles for Goserrelina Teva reflect its hormonal suppression and can vary in frequency and severity.

Common

  • Hot flashes and sweating.
  • Decreased libido or sexual dysfunction.
  • Mood changes such as irritability or depression.
  • Injection‑site reactions including pain, erythema, or swelling.
  • Fatigue or general weakness.

Serious

  • Bone mineral density loss leading to osteoporosis.
  • Cardiovascular events such as hypertension or thromboembolism.
  • Severe allergic reactions (anaphylaxis, angioedema).

Patients should report any new or worsening symptoms to their clinician promptly.

Precautions & Warnings

Before starting Goserrelina Teva, clinicians assess several safety considerations to minimize risks associated with long‑term hormone suppression.

  • Evaluate bone health; consider calcium and vitamin D supplementation.
  • Review cardiovascular risk factors such as hypertension, hyperlipidemia, or smoking.
  • Assess liver and kidney function, especially in patients with chronic disease.
  • Discuss potential impact on fertility and consider sperm or oocyte preservation.
  • Monitor for signs of depression or mood disorders during therapy.
  • Use caution in patients with a history of thromboembolic events.

Avoid Interactions

Goserrelina Teva can alter the metabolism or effectiveness of other medicines; certain combinations should be avoided while others require close monitoring.

Avoid

  • Concurrent use with estrogen‑containing hormone replacement therapy, which may counteract the drug’s effect.
  • Combining with other GnRH agonists or antagonists, leading to excessive hormone suppression.

Use with caution

  • Anticoagulants, because changes in hormone levels can affect clotting risk.
  • Corticosteroids, which may increase bone loss when used together.
  • Chemotherapy agents, requiring timing adjustments to avoid overlapping toxicities.
  • Bisphosphonates or denosumab, to manage potential osteoporosis.

Frequently Asked Questions

Goserrelina Teva is a prescription GnRH agonist that contains the active ingredient goserelin and is supplied as an implantable formulation.

It is a synthetic analogue of GnRH that initially stimulates, then down‑regulates pituitary gonadotropin release, leading to reduced production of sex hormones such as testosterone and estrogen.

The drug is commonly used in the management of advanced prostate cancer in men and hormone‑responsive breast cancer in pre‑menopausal women.

Yes, it is also indicated for endometriosis and uterine fibroids to help control hormone‑driven tissue growth and associated symptoms.

Common side effects include hot flashes, sweating, decreased libido, mood changes, injection‑site reactions, and fatigue.

Serious reactions can include loss of bone mineral density leading to osteoporosis, cardiovascular events such as hypertension, and severe allergic responses like anaphylaxis.

Clinicians should assess bone health, cardiovascular risk, liver and kidney function, fertility considerations, and a history of mood disorders or thromboembolic events.

Patients should avoid concurrent estrogen‑containing hormone therapy and the use of other GnRH agonists or antagonists, as these can diminish effectiveness or cause excess suppression.

Anticoagulants, corticosteroids, chemotherapy agents, and bone‑protective drugs such as bisphosphonates or denosumab should be used with caution and monitored closely.

The pregnancy safety category is not established; the drug is generally contraindicated during pregnancy because it suppresses sex hormone production.

It is delivered via a subcutaneous implant that releases the medication continuously over a period of months, administered by a qualified healthcare professional.

Regular monitoring of bone density, cardiovascular status, hormone levels, and mental health is recommended throughout treatment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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