Formulation: An injection, often in a depot (slow-release) form, containing Leuprolide Acetate (22.5 mg).
How it works
It mimics natural GnRH, initially causing a surge in hormones but then suppressing the pituitary gland's release of LH and FSH, leading to significantly reduced testosterone in men and estrogen in women.
Uses
Prostate Cancer: Slows cancer growth by reducing testosterone.
Endometriosis: Reduces painful uterine-like tissue growth by lowering estrogen.
Uterine Fibroids: Shrinks non-cancerous growths by lowering estrogen.
Precocious Puberty: Delays early onset puberty in children.
Important Considerations
Side Effects: Hot flashes, fatigue, decreased libido, mood changes, headache, nausea, dizziness, injection site reactions, potential blood sugar increase, and long-term bone thinning (requiring calcium/Vit D).
Pregnancy: Contraindicated (Category X); effective contraception is crucial for both partners during treatment.
Monitoring: Regular monitoring of blood sugar and bone density is often needed.
Administration: Given as an injection, typically every 3 months.
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LEUPROMAK 22.5INJ delivers leuprolide acetate, a powerful GnRH agonist that works by reducing the production of specific hormones in the body. This makes it a valuable therapeutic option for managing prostate carcinoma, endometriosis, and, in some cases, precocious puberty. Administered intramuscularly under professional supervision, it provides reliable hormone suppression tailored to individual patient needs.
Precise Dosing with Ready-to-Reconstitute Packaging
Each LEUPROMAK vial contains a measured dose of lyophilised powder and an ampoule of sterile solvent, ensuring accurate preparation prior to administration. This format allows healthcare providers to conveniently reconstitute and administer the injection immediately, maintaining maximum potency and safety for every dose.
Trusted Origin and Quality Standards
Manufactured and marketed in India by Maks Drugs Pvt. Ltd., LEUPROMAK 22.5INJ adheres to stringent quality norms. Classified as a Schedule H prescription medication, it is only available through licensed medical channels, ensuring controlled, professional use and robust regulatory compliance.
FAQ's of LEUPROMAK 22.5INJ:
Q: How should LEUPROMAK 22.5INJ be prepared and administered?
A: LEUPROMAK 22.5INJ must be reconstituted with the provided sterile solvent ampoule immediately before use. The fully dissolved solution should be administered as an intramuscular injection by a qualified healthcare professional.
Q: What are the main uses of LEUPROMAK 22.5INJ?
A: LEUPROMAK is primarily recommended for the treatment of prostate cancer, endometriosis, and precocious puberty. Its active ingredient, leuprolide acetate, helps suppress hormone levels involved in these conditions.
Q: When should LEUPROMAK 22.5INJ be used after reconstitution?
A: The reconstituted solution must be used immediately after mixing to ensure effectiveness and reduce the risk of contamination or degradation.
Q: Where should LEUPROMAK 22.5INJ be stored before use?
A: Unopened vials should be stored below 25C and protected from light to preserve the stability of the medication. Do not freeze or expose to direct sunlight.
Q: What are the benefits of using LEUPROMAK 22.5INJ as a hormonal therapy?
A: The main benefit is reliable and sustained suppression of hormones linked to prostate cancer, endometriosis, and precocious puberty, helping to manage symptoms and slow disease progression under medical guidance.
Q: Who is qualified to administer LEUPROMAK 22.5INJ?
A: Only trained healthcare professionals should prepare and inject LEUPROMAK to ensure correct technique and patient safety, as per the prescription.
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