FEMISTRA ANASTROZOLE TABLETS
FEMISTRA ANASTROZOLE TABLETS

FEMISTRA ANASTROZOLE TABLETS

FEMISTRA ANASTROZOLE TABLETS Specification

  • Indication
  • Breast cancer in postmenopausal women
  • Pacakaging (Quantity Per Box)
  • 1 x 10 tablets per box
  • Salt Composition
  • Anastrozole 1 mg
  • Dosage Form
  • Solid
  • Origin of Medicine
  • Allopathic
  • Drug Type
  • Prescription Medicine
  • Ingredients
  • Anastrozole
  • Physical Form
  • Tablets
  • Function
  • Aromatase inhibitor for breast cancer treatment
  • Recommended For
  • Women with hormone receptor-positive breast cancer, postmenopausal women
  • Dosage
  • 1 mg once daily or as directed by physician
  • Dosage Guidelines
  • Take orally, do not exceed recommended dose
  • Suitable For
  • Adults
  • Quantity
  • 1 strip of 10 tablets
  • Storage Instructions
  • Store in a cool, dry place away from direct sunlight
 

FEMISTRA ANASTROZOLE TABLETS Trade Information

  • Packaging Details
  • PACK OF 50 TABLETS
  • Main Domestic Market
  • All India
 

About FEMISTRA ANASTROZOLE TABLETS

Femistra Tabs

Specifications:-

  • Strength:1 MG
  • Form Of Medicines:Tablets
  • Composition:Anastrozole
  • Brand:FEMISTRA
  • Packaging Size:pack of 5x10 tablets

Note :- FEMISTRA Is A Prescription Drug And Should Be Used Under Proper Medical Guidance And Advice. Do Not Share The Medicine With Others, Since They May Be Suffering From A Problem That Is Not Effectively Treated By This Drug.............



Targeted Treatment for Breast Cancer

Femistra is specifically designed for postmenopausal women diagnosed with hormone receptor-positive breast cancer. Its active ingredient, Anastrozole, efficiently inhibits the aromatase enzyme, reducing estrogen levels in the body, and thus helping to slow or stop tumor progression. This targeted approach delivers significant therapeutic benefit under medical supervision.


Usage and Dosage Guidelines

Each Femistra tablet contains 1 mg of Anastrozole and is administered orally, ideally at the same time each day. Patients must adhere strictly to the prescribed dose, as exceeding or missing doses may reduce treatment effectiveness or increase the risk of side effects. Dosage adjustments should only be made by a healthcare provider, particularly in cases of hepatic or renal impairment.

FAQs of FEMISTRA ANASTROZOLE TABLETS:


Q: How should Femistra Anastrozole Tablets be taken for optimal results?

A: Femistra Anastrozole Tablets should be taken orally once daily at the prescribed dose of 1 mg, preferably at the same time each day. Follow your physicians instructions carefully and do not exceed the recommended dose.

Q: What conditions are Femistra Anastrozole Tablets recommended for?

A: These tablets are indicated for the treatment of hormone receptor-positive breast cancer in postmenopausal women, primarily used as part of an allopathic treatment regimen.

Q: When is Femistra typically prescribed during cancer treatment?

A: Femistra is usually prescribed to postmenopausal women after diagnosis of hormone receptor-positive breast cancer and may be administered during the initial or subsequent phases of therapy based on physician evaluation.

Q: Where should Femistra Anastrozole Tablets be stored to maintain efficacy?

A: Store Femistra tablets in a cool, dry place, away from direct sunlight and moisture. Ensure they are kept out of reach of children.

Q: What benefits does Femistra offer compared to other treatments?

A: Femistra specifically targets estrogen production, aiding in the management of hormone receptor-positive breast cancer. This focused approach may result in better disease control for eligible postmenopausal women.

Q: What side effects should users be aware of while taking Femistra?

A: Common side effects include hot flashes, joint pain, weakness, and sore throat. Report any persistent or severe symptoms to your healthcare provider promptly.

Q: Is a prescription required for purchasing Femistra Anastrozole Tablets?

A: Yes, a valid prescription is mandatory to obtain Femistra Anastrozole Tablets, as determined by healthcare regulations and ensuring appropriate medical supervision.

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