- Safety
- Eligard
Drug Interactions
Drug Interactions No pharmacokinetic drug-drug interaction studies were conducted with ELIGARD.
Drug Interactions No pharmacokinetic drug-drug interaction studies were conducted with ELIGARD.
Specific Populations Pregnancy Risk summary Based on findings in animal studies and mechanism of action, ELIGARD® may cause fetal harm when administered to a pregnant woman [see Clinical Pharmacology]. There are no available data in pregnant women to inform the drug-associated risk. Expected horm...
Overdosage In clinical trials in patients with prostate cancer using daily subcutaneous injections of leuprolide acetate and doses as high as 20 mg/day for up to two years caused no adverse effects differing from those observed with the 1 mg/day dose.
Cold Storage & Shipping ELIGARD is shipped refrigerated. Store at 35.6 – 46.4 °F (2 – 8 °C). Once outside the refrigerator this product may be stored in its original packaging at room temperature 15 – 30 °C (59 – 86 °F) for up to eight weeks prior to mixing and administration.
How Supplied ELIGARD® is available in a single-dose kit consisting of a two syringe-mixing system with a sterile safety needle. Order ELIGARD direct via the phone or online through Besse Medical or use one of our preferred GPO partners. ELIGARD® is also available in a single-dose kit of a pre-con...
Room Temperature Storage Eight-week room temperature storage If it’s cold, ELIGARD will be more difficult to mix and may not reconstitute properly. It must be brought to room temperature before mixing. Though ELIGARD is shipped refrigerated, it can be stored for up to eight (8) weeks at room temp...
NDC Numbers and Codes Order ELIGARD direct via the phone or online through Besse Medical or use one of our preferred GPO partners. NDC numbers ELIGARD Pre-connected Syringe System 45 mg (6 month dose)NDC: 62935-461-50 Other codes
Inventory Management TOLMARsync A simple & powerful inventory and patient management solution for your practice, TOLMARsync® is designed to integrate with your practice workflow. Simple & powerful Order, receive, dispense, and track ELIGARD: Easy on-boarding and training Intuitive reporti...
Patient Care Guide Download our Patient Care Guide to provide your patients with up-to-date information regarding prostate cancer, healthy living, and tools for managing treatment.
About Prostate Cancer Prostate cancer statistics in 2017 About 1 in 7 men will be diagnosed with prostate cancer during their lifetime. Prostate cancer can be a serious disease, but most men diagnosed with prostate cancer do not die from it. In fact, more than 2.9 million men in the United States...
ELIGARD®, (leuprolide acetate) for injectable suspension, is indicated for the palliative treatment of advanced prostate cancer.
ELIGARD is contraindicated in patients with hypersensitivity to GnRH, GnRH agonists, or any of the components of ELIGARD. Anaphylactic reactions to synthetic GnRH or GnRH agonists have been reported in the literature. Transient increase in serum levels of testosterone during treatment may result in worsening of symptoms or onset of new signs and symptoms during the first few weeks of treatment, including bone pain, neuropathy, hematuria, bladder outlet obstruction, ureteral obstruction, or spinal cord compression. Monitor patients at risk closely and manage as appropriate.
Hyperglycemia and an increased risk of developing diabetes have been reported in men receiving GnRH agonists. Monitor blood glucose level and manage according to current clinical practice. Increased risk of myocardial infarction, sudden cardiac death and stroke has also been reported with use of GnRH agonists in men. Monitor for cardiovascular disease and manage according to current clinical practice. Androgen deprivation therapy may prolong the QT/QTc interval. Consider risks and benefits. May cause fetal harm. Convulsions have been observed in patients taking leuprolide acetate with or without a history of predisposing factors. Manage convulsions according to current clinical practice.
ELIGARD may impair fertility in males of reproductive potential.
The most common injection site adverse events are transient burning and stinging, pain, bruising, and erythema. The most common systemic adverse events include mild to severe hot flashes/sweats, malaise and fatigue, weakness, myalgia, dizziness, clamminess, testicular atrophy, and gynecomastia. As with other GnRH agonists, other adverse reactions, including decreased bone density and rare cases of pituitary apoplexy have been reported.
See package insert for full prescribing and safety information.
Please see full Prescribing Information for ELIGARD and full Prescribing Information for ELIGARD with Pre-connected Syringe System.