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Anastrozole tablets

Listing ID #1314546

  • Supply Type Manufacturer, Exporter, Supplier
  • Preferred Buyer Location All over the world

The company is a reputed Supplier and Exporter of Anastrozole Tablets. Anastrozole Tablets are indicated for metastatic breast cancer or as first-line treatment of menopausal women. Our company makes Anastrozole Tablets available in well-sealed packaging. Also, Anastrozole Tablets are offered by us at industry leading prices.
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  • Member Since 12 Years
  • Nature of Business Retailer

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Generic Name Anastrozole
Brand Name Altraz Tablet
Strength Available 1 MG
Packing 14 Tablet
Name of Company Alkem Laboratories Ltd.
Classification Nonsteroidal aromatase inhibitor
Mechanism of Action
  • Potent and selective nonsteroidal inhibitor of aromatase.
  • Inhibits the synthesis of estrogens by inhibiting the conversion of adrenal androgens (andro­stenedione and testosterone) to estrogens (estrone, estrone sulfate, and estradiol). Serum estradiol levels are suppressed by 90% within 14 days, and nearly compietely suppressed after 6 weeks of therapy.
  • No inhibitory effect on adrenal corticosteroid or aldosterone biosynthesis .
Mechanism of Resistance None characterized.
Absorption Excellent bioavailability via the oral route, with 85% of a dose absorbed within 2 hours of ingestion. Absorption is not affected by food.
Distribution Widely distributed throughout the body. About 40% of drug is bound to plasma proteins.
Metabolism NonExtensively metabolized in the liver (up to 85%) by N-dealkylation, hydroxylation, and glucuronidation, to inactive forms. Han-life of drug is about 50 hours. Steady-state levels of drug are achieved after 7 days of a once-daily administration. The major route of elimination is fecal, with renal excretion accounting for only 10% of drug ciearance.
Indications & Usage
  • Metastatic breast cancer - First-line treatment of postmenopausal women with estrogen­receptor positive or estrogen-receptor unknown disease.
  • Metastatic breast cancer - Postmenopausal women with estrogen-receptor positive, advanced disease, and proqression while on tamoxifen therapy.
  • Adjuvant treatment of postmenopausal women with hormone-receptor positive early-stage breast cancer.
Dosage Range Usual dose is 1 mg PO qd for both first-line and second-line therapy
Drung Preparation Available as a 1 mg white, film-eoated tabiet for oral use.
Drung Interaction None known.
Special Considerations
  • No dose adjustments are required for patients with either hepatic or renal dysfunction.
  • Caution patients about the risk of hot fiashes.
  • No need for glucocorticoid and/or mineralocorticoid replacement.
  • Pregnancy category D.
Toxicity
  • Asthenia. Most common toxicity, occurs in 1%-20%.
  • Mild nausea and vomiting. Constipation or diarrhea can also occur.
  • Hot fiushes. Occurs in 10% of patients.
  • Dry, scaling skin rash.
  • Arthralgias occur in 10%-15% of patients involving hands, knees, hips, lower back, and shoulders. Early morning stiffness is usual.
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