| Product dosage: 20mg | |||
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| 60 | $0.72 | $43.18 (0%) | 🛒 Add to cart |
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tamoxifen
Tamoxifen citrate represents one of the most significant advances in endocrine oncology over the past half-century. Initially developed as a failed contraceptive, this selective estrogen receptor modulator (SERM) has fundamentally transformed breast cancer management. I’ve prescribed it to hundreds of patients across my thirty-year oncology practice, watching it evolve from controversial newcomer to established standard of care. ## 1. Introduction: What is Tamoxifen? Its Role in Modern Medicine Tamoxifen belongs to the selective estrogen receptor modulator class, functioning as both an antagonist and partial agonist depending on the target tissue.
arimidex
Anastrozole, marketed under the brand name Arimidex, represents a cornerstone in the endocrine therapy arsenal for hormone receptor-positive breast cancer. As a non-steroidal aromatase inhibitor, it fundamentally alters the hormonal landscape in postmenopausal women by blocking the conversion of androgens to estrogens in peripheral tissues. We’ve moved from blunt instruments like tamoxifen to these more targeted approaches, and the clinical results speak for themselves—though the journey hasn’t been without its complications and learning curves.
Aromasin: Estrogen Suppression for Breast Cancer - Evidence-Based Review
Aromasin, known generically as exemestane, is an oral steroidal aromatase inactivator used primarily in postmenopausal women with hormone receptor-positive early or advanced breast cancer. It functions by irreversibly binding to the aromatase enzyme, which is responsible for converting androgens into estrogens in peripheral tissues. This results in a significant reduction of circulating estrogen levels, which can slow or stop the growth of estrogen-sensitive tumors. The standard dosage is 25 mg once daily, taken orally after a meal to enhance absorption.
casodex
Casodex, known generically as bicalutamide, is a non-steroidal anti-androgen medication primarily used in the management of advanced prostate cancer. It belongs to a class of drugs that competitively inhibit the binding of androgens, like testosterone and dihydrotestosterone (DHT), to their receptors in prostate cancer cells. This action is crucial because prostate cancer growth is often driven by androgens. Casodex is typically administered orally, in tablet form, and is often used in combination with a luteinizing hormone-releasing hormone (LHRH) analog as part of combined androgen blockade (CAB) therapy.
chloroquine
Chloroquine is a 4-aminoquinoline compound that’s been kicking around since the 1930s, originally derived from quinine. Most people think of it as an antimalarial, but its immunomodulatory properties have made it a staple in rheumatology for decades. The chemical structure gives it that unique lysosomotropic character - basically it accumulates in acidic organelles and messes with antigen processing. We’ll get into the nitty-gritty of that mechanism later. I remember my first rotation in infectious diseases back in ‘98 - we had this 62-year-old missionary, Robert, who’d been in Papua New Guinea for six months.
Estrace: Effective Menopausal Symptom Relief and Osteoporosis Prevention - Evidence-Based Review
Estrace is the brand name for estradiol, which is the primary estrogen hormone produced by the ovaries. It’s available as oral tablets, vaginal cream, and vaginal rings, primarily used for managing menopausal symptoms like hot flashes, vaginal dryness, and preventing osteoporosis in postmenopausal women. The oral tablets contain micronized 17β-estradiol, which is chemically identical to the estrogen produced by the human body, making it particularly effective for systemic hormone replacement therapy.
evista
Evista, known generically as raloxifene hydrochloride, is a selective estrogen receptor modulator (SERM) structurally related to tamoxifen but with a distinct pharmacological profile. Initially investigated for breast cancer applications, its unexpected bone-preserving properties shifted development toward osteoporosis management. Available as 60 mg oral tablets, it’s classified as a prescription medication rather than a dietary supplement or medical device, representing one of the few SERMs approved for long-term osteoporosis prevention and treatment in postmenopausal women.
Femara: Potent Aromatase Inhibition for Breast Cancer and Fertility - Evidence-Based Review
Letrozole, marketed under the brand name Femara among others, is an oral non-steroidal aromatase inhibitor (AI) used primarily in the treatment of hormone receptor-positive breast cancer in postmenopausal women. It works by inhibiting the aromatase enzyme, which is responsible for the conversion of androgens to estrogens in peripheral tissues. This significant reduction in circulating estrogen levels deprives estrogen-sensitive breast cancer cells of the hormonal stimulation they need to grow and proliferate.
hydroxychloroquine
Hydroxychloroquine sulfate, an antimalarial and immunomodulatory agent derived from quinine, exists as white to off-white crystalline powder with bitter taste, typically formulated as 200mg film-coated tablets equivalent to 155mg base. This 4-aminoquinoline compound demonstrates unique physicochemical properties including high volume of distribution and extensive tissue binding, particularly to melanin-containing cells. ## 1. Introduction: What is Hydroxychloroquine? Its Role in Modern Medicine Hydroxychloroquine represents a cornerstone in autoimmune disease management since its 1955 FDA approval, though its mechanism remained partially elusive for decades.