Lutrate 3.75 mg Injection

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Lutrate 3.75 mg Injection Specification

Salt Composition
Leuprorelin Acetate (3.75 mg)

Pacakaging (Quantity Per Box)
1 injection vial per box

Origin of Medicine
Synthetic

Drug Type
Injection

Ingredients
Leuprorelin Acetate

Physical Form
Liquid

Function
Treatment of prostate cancer endometriosis and uterine fibroids

Recommended For
Patients with prostate cancer endometriosis and uterine fibroids

Dosage
3.75 mg

Dosage Guidelines
Administered as an injection under the supervision of a healthcare professional typically once every month or as prescribed

Suitable For
Adult patients

Quantity
1 vial

Storage Instructions
Store in a refrigerator at 2-8C. Do not freeze and keep away from light

About Lutrate 3.75 mg Injection

Lutrate 3.75 mg Injection contains Leuprorelin Acetate (3.75 mg) as its active ingredient. This synthetic medicine is stored in a refrigerator at 2-8C, where it should be protected from freezing and light. Each box contains 1 injection vial, suitable for adult patients with prostate cancer, endometriosis, and uterine fibroids. The recommended dosage is 3.75 mg administered monthly under healthcare professional supervision. This liquid form injection is vital for the effective treatment of indicated conditions.

FAQs of Lutrate 3.75 mg Injection:

Q: What is the active ingredient in Lutrate 3.75 mg Injection?

A: The active ingredient in Lutrate 3.75 mg Injection is Leuprorelin Acetate (3.75 mg).

Q: How should Lutrate 3.75 mg Injection be stored?

A: Lutrate 3.75 mg Injection should be stored in a refrigerator at 2-8C, away from freezing and light.

Q: Who is Lutrate 3.75 mg Injection recommended for?

A: Lutrate 3.75 mg Injection is recommended for adult patients with prostate cancer, endometriosis, and uterine fibroids.

Q: What is the dosage and administration guideline for Lutrate 3.75 mg Injection?

A: The dosage for Lutrate 3.75 mg Injection is 3.75 mg and it is typically administered as an injection monthly under healthcare professional supervision.