| Product dosage: 20mg | |||
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| Package (num) | Per pill | Price | Buy |
| 60 | $0.72 | $43.15 (0%) | 🛒 Add to cart |
| 90 | $0.67 | $64.72 $60.20 (7%) | 🛒 Add to cart |
| 120 | $0.64 | $86.29 $76.26 (12%) | 🛒 Add to cart |
| 180 | $0.61 | $129.44 $109.37 (16%) | 🛒 Add to cart |
| 270 | $0.59 | $194.16 $159.54 (18%) | 🛒 Add to cart |
| 360 | $0.58
Best per pill | $258.88 $209.71 (19%) | 🛒 Add to cart |
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tamoxifen
Tamoxifen citrate represents one of those fascinating compounds that bridges multiple therapeutic domains - originally developed as a fertility drug in the 1960s, it’s become the cornerstone of hormonal therapy for breast cancer while revealing unexpected benefits in other areas. The molecule’s unique selective estrogen receptor modulator (SERM) properties create this paradoxical effect where it blocks estrogen in breast tissue while acting like estrogen in other tissues. I’ve prescribed it for everything from DCIS to advanced metastatic disease, and the consistency of response still impresses me after twenty-three years in oncology.
Arimidex: Estrogen Suppression for Breast Cancer Treatment - Evidence-Based Review
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. Unlike earlier hormonal therapies like tamoxifen which act as selective estrogen receptor modulators, Arimidex operates upstream at the enzymatic level, providing a more targeted approach to estrogen suppression.
Aromasin: Potent Estrogen Suppression for Breast Cancer - Evidence-Based Review
Aromasin, known generically as exemestane, is a 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 leads to a significant reduction in circulating estrogen levels, effectively starving estrogen-dependent tumor cells. Available in oral tablet form, typically 25 mg, it’s taken once daily, often for extended periods as part of adjuvant therapy or for metastatic disease.
bupron sr
Bupron SR represents one of those interesting cases where the sustained-release mechanism actually makes clinical sense, unlike so many other SR formulations where it’s mostly a marketing gimmick. We initially approached this with skepticism - another sustained-release antidepressant? But the pharmacokinetic profile turned out to be genuinely useful, particularly for patients who struggled with the peak-trough fluctuations of immediate-release bupropion. ## 1. Introduction: What is Bupron SR? Its Role in Modern Medicine
evista
Raloxifene hydrochloride, marketed as Evista, represents one of the more nuanced tools in our endocrine arsenal. I remember first prescribing it back in ‘99 when it got FDA approval—we were all cautiously optimistic about this new selective estrogen receptor modulator (SERM) that promised osteoporosis protection without the uterine risks of tamoxifen. Over two decades and hundreds of patients later, I’ve seen its strengths, limitations, and those unpredictable clinical surprises that never make it into the official monographs.
Femara: Potent Hormone Therapy for Breast Cancer - Evidence-Based Review
Letrozole, marketed under the brand name Femara among others, is an oral non-steroidal aromatase inhibitor that has fundamentally changed the landscape of endocrine therapy for hormone receptor-positive breast cancer in postmenopausal women. It works by selectively inhibiting the aromatase enzyme, which is responsible for the final step in estrogen synthesis—the conversion of androgens like androstenedione and testosterone into estrogens. This mechanism is particularly crucial in postmenopausal women, where ovarian estrogen production has ceased, and estrogen is primarily derived from the conversion of adrenal androgens in peripheral tissues like fat, muscle, and breast tissue itself.
fertomid
Fertomid represents one of those interesting cases where the pharmaceutical mechanism gets repurposed with surprisingly good results in the fertility space. When we first started working with this compound about eight years ago, I was frankly skeptical - another “me-too” product in an already crowded market. But the data kept coming back surprisingly consistent across different patient populations. ## 1. Introduction: What is Fertomid? Its Role in Modern Medicine Fertomid contains clomiphene citrate as its active pharmaceutical ingredient, functioning as a selective estrogen receptor modulator (SERM).
hydroxychloroquine
Hydroxychloroquine sulfate, an antimalarial and immunomodulatory agent derived from quinolone, exists as white crystalline powder with bitter taste, typically formulated as 200mg oral tablets containing equivalent of 155mg base. This disease-modifying antirheumatic drug (DMARD) represents one of medicine’s most fascinating repurposing stories - from its 1955 FDA approval for malaria prophylaxis to becoming cornerstone therapy for autoimmune conditions, though recent controversies have complicated its narrative. Hydroxychloroquine: Immunomodulatory Therapy for Autoimmune Conditions - Evidence-Based Review 1.
isofair
Isofair represents one of those rare convergence points where pharmaceutical-grade manufacturing meets nutritional science in a way that actually delivers reproducible clinical outcomes. We first encountered the raw data during a product review committee meeting back in 2019 - the pharmacokinetic profiles showed something unusual that made several of us skeptical initially. ## 1. Introduction: What is Isofair? Its Role in Modern Medicine Isofair is a high-purity isoflavone complex derived through a proprietary extraction and purification process from red clover (Trifolium pratense).