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Goserelin

    DEA Class; Rx

    Common Brand Names; Zoladex, Zoladex LA

    • Antineoplastics, GNRH Agonist

    A synthetic gonadotropin-releasing hormone (GnRH) agonist
    Used for the palliative treatment of advanced prostate cancer or breast cancer, for the management of endometriosis, dysfunctional uterine bleeding, and the adjunct medical management of uterine fibroids
    A transient tumor flare may occur during the first few weeks of treatment, which may cause ureteral obstruction and spinal cord compression; monitor patients at risk for these complications

    Indicated for the treatment of breast cancer.

    For the treatment of endometriosis, including pain relief and reduction of endometriotic lesions.
    For use as an endometrial thinning agent prior to endometrial ablation for dysfunctional uterine bleeding.
    For the treatment of prostate cancer.
    For the treatment of uterine leiomyomata (fibroids).

    Hypersensitivity to LHRH, LHRH-agonists, any component of product

    Pregnancy (for endometriosis), lactation, undiagnosed abnormal vaginal bleeding

    • Flushing (46-96%)
    • Vaginitis (5-75%)
    • Hot flashes (62%)
    • Reduced libido (47-61%)
    • Mood swings (60%)
    • Depression (women 54%)
    • Sweating (16-45%)
    • Acne (42%)
    • Diarrhea (40%)
    • Breast atrophy (33%)
    • Headache (women 32-75%)
    • Seborrhea (26%)
    • Tumor flare (23%)
    • Sexual dysfunction (21%)
    • Peripheral edema (21%)
    • Erectile dysfunction (18%)
    • Pain (8-17%)
    • UTI (13%)
    • Nausea (9%)
    • Lethargy (8%)
    • Rash (6%)
    • Chronic obstructive pulmonary disease (5%)
    • Congestive heart failure(5%)
    • Cerebrovascular accident (1-5%)
    • Renal impairment (1-5%)
    • Headache (men 1-5%)
    • Depression (men 1-5%)
    • Immune hypersensitivity reaction (>1%)

    Manifestations of disease may worsen at beginning of therapy

    Increase in cervical resistance may occur; caution is recommended when dilating the cervix for endometrial ablation

    Avoid pregnancy; premenopausal women should use nonhormonal contraception until >12 wk following end of treatment

    Risk of reduced glucose tolerance in men

    Males at risk of ureteral obstruction or spinal compression

    Risk of pituitary apoplexy (rare)

    Ongoing analysis found that men receiving GnRH agonists for prostate cancer were at a small increased risk for diabetes, heart attack, stroke, and sudden death

    Do not exceed 1 year treatment duration with GnRH angonists in women except when treating breast cancer

    Androgen deprivation therapy may prolong the QT interval; consider risks and benefits

    Hypercalcemia has been reported in patients with bone metastases treated with goserelin; monitor and manage appropriately

    Increased risk of myocardial infarction, sudden cardiac death and stroke reported in association with use of GnRH analogs in men; monitor for cardiovascular disease and manage according to current clinical practice

    Hyperglycemia and an increased risk of developing diabetes have been reported in men receiving GnRH analogs. Monitor blood glucose level and manage according to current clinical practice

    Pregnancy must be excluded for use in benign gynecological conditions

    Transient worsening of tumor symptoms may occur during first few weeks of therapy, which may include ureteral obstruction and spinal cord compression; monitor patients at risk for complications of tumor flare

    Injection site injury and vascular injury including pain, hematoma, hemorrhage and hemorrhagic shock, requiring blood transfusions and surgical intervention, reported; use extra care when administering to patients with low BMI and/or to patients receiving full dose anticoagulation

    Pregnancy Category: D (advanced breast cancer); X (endometriosis, endometrial thinning)

    Lactation: excretion in milk unknown; not recommended

    Adults

    Males: 3.6 mg subcutaneously depot every 28 days or one 10.8 mg depot subcutaneously every 3 months.
    Females: 3.6 mg subcutaneously depot every 28 days.

    Geriatric

    Males: 3.6 mg subcutaneously depot every 28 days or one 10.8 mg depot subcutaneously every 3 months.
    Females: 3.6 mg subcutaneously depot every 28 days.

    Adolescents

    Safety and effectiveness have not been established.

    Children

    Safety and effectiveness have not been established.

    Goserelin Acetate

    implant

    • 3.6mg
    • 10.8mg