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(a) A prima facie case of excessive pricing shall be established where the wholesale price of a patented prescription drug in the District is over 30 percent higher than the comparable price in any high income country in which the product is protected by patents or other exclusive marketing rights.

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(b) [If a prima facie case is made, a defense is to show that the] given prescription drug is not excessively priced given demonstrated costs of invention, development and production of the prescription drug, global sales and profits to date, consideration of any government funded research that supported the development of the drug, and the impact of price on access to the prescription drug by residents and the government of the District of Columbia.

Meridia/Reductil (SIBUTRAMINE HCI) is a prescription medication thats used to help people lose weight by acting on the appetite control centers in the brain. Studies have shown that using Meridia helps patients lose weight and maintain weight loss for up to 2 years.

Today, a new treatment cannot be launched into the world without considering its overall cost. Many thousands of postmenopausal women will undoubtedly be convinced by this study to take Femara in order to ward off the possibility of a breast cancer recurrence. They are understandably eager to have any edge at all in the fight against this frightening disease. But the rush to prescribe Femara as a long-term treatment comes at a time when the US and other countries are struggling with the problem of runaway drug costs. Many Americans are already desperately trying to cope with the inflated price of prescription drugs, and are looking to decrease those costs by shopping on the Internet or by buying from Canadian or Mexican pharmacies. Thus, the imperative to take Femara could be a serious economic blow to many older women and their families, who are trying to survive in perilous economic times.

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Researchers reviewed charts of 238 consecutive postmenopausal patients who had osteoporosis or osteopenia and were referred to the Loyola's Osteoporosis and Metabolic Bone Disease Center from 2000 to 2006. (Osteopenia is lower than normal bone mineral density, but not low enough to be classified as osteoporosis.) The patients included 64 women with breast cancer referred from Loyola's Cardinal Bernardin Cancer Center and 174 patients without breast cancer referred from primary care physicians.

Vitamin D deficiency can be treated with prescription doses of vitamin D supplements. Excessive calcium excretion can be treated with a "water pill" that's also used to treat high blood pressure, Camacho said. There are various treatments for parathyroid gland disorder, depending on its cause.

Patient Rosaleen O'Connor, 71, of Elmhurst, Il., learned she had osteoporosis while being treated by Albain for breast cancer. Albain referred O'Connor to Camacho, who prescribed calcium supplements, prescription vitamin D and the osteoporosis drug Boniva. Three years after O'Connor was diagnosed, her Stage 3 cancer is in remission, and she has suffered no bone fractures.

Source: Loyola University Health System Citation: Study identifies causes of bone loss in breast cancer survivors (2008, November 19) retrieved 30 March 2023 from -11-bone-loss-breast-cancer-survivors.html This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only. Explore further

Some 15,000 of an expected 50,000 people are now enrolled in Medicare's prescription drug assistance program for cancer patients and others. Still, a new analysis concludes that beneficiaries will lose coverage and various protections under the newMedicare Act.

Breast cancer will strike 1 in 8 women in her lifetime. But women who face an increased risk of being that one unlucky patient may improve their chances with three prescription medications, according to a new report.

Tamoxifen is usually taken once or twice a day with or without food. Take tamoxifen at around the same time(s) every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain anything you do not understand. Take tamoxifen exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

If you are taking tamoxifen to prevent breast cancer, you will probably take it for five years. If you are taking tamoxifen to treat breast cancer, your doctor will decide how long your treatment will last. Do not stop taking tamoxifen without talking to your doctor.

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• MONTREAL, QC--(Marketwired - June 30, 2016) - Sunshine Biopharma Inc. (OTCQB: SBFM), a pharmaceutical company focused on the research, development and commercialization of drugs for the treatment of various forms of cancer, is pleased to announce that it has signed a Cross Referencing Agreement with a major pharmaceutical company for three additional prescription generic drugs for treatment of Breast Cancer, Prostate Cancer and Enlarged Prostate. Sunshine will market and sell these new pharmaceutical products under its own label.Sunshine's three new generic products together with the previously announced initial generic product are as follows:Anastrozole (brand name Arimidex by AstraZenica) for treatment of Breast Cancer

• Letrozole (brand name Femara by Novartis) for treatment of Breast Cancer

• Bicalutamide (brand name Casodex by AstraZenica) for treatment of Prostate Cancer

• Finasteride (brand name Propecia by Merck) for treatment of BPH (Benign Prostatic Hyperplasia)

• Worldwide sales of the brand name version of these products as reported by the respective owner of the registered trademark are as follows:Arimidex $250M in 2015

• Femara $380M in 2014

• Casodex $267M in 2015

• Propecia $183M in 2015

Sunshine is currently in the process of securing a Drug Identification Number ("DIN") for each of these products from Health Canada. The Company is also working on obtaining a Drug Establishment License ("DEL") from Health Canada. Upon receipt of the DEL and DIN's, Sunshine will be able to accept orders for its own label SBI-Anastrozole, SBI-Letrozole, SBI-Bicalutamide and SBI-Finasteride. Sunshine expects to build a portfolio of "SBI" label Generic Pharmaceuticals over time.Revenues from sales of Generic Products are intended to be used to finance the Company's proprietary drug development program including Adva-27a, the Company's flagship anticancer compound. A Topoisomerase II inhibitor, Adva-27a is a small molecule that has recently been shown to be effective at destroying Multidrug Resistant Breast Cancer cells, Pancreatic Cancer cells, Small-Cell Lung Cancer cells and Uterine Sarcoma cells (Published in ANTICANCER RESEARCH, Volume 32, Pages 4423-4432, October 2012). Sunshine Biopharma is direct owner of all issued and pending worldwide patents pertaining to Adva-27a including U.S. Patent Number 8,236,935.Safe Harbor Forward-Looking StatementsTo the extent that statements in this press release are not strictly historical, including statements as to revenue projections, business strategy, outlook, objectives, future milestones, plans, intentions, goals, future financial conditions, future collaboration agreements, the success of the Company's development, events conditioned on stockholder or other approval, or otherwise as to future events, such statements are forward-looking, and are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. The forward-looking statements contained in this release are subject to certain risks and uncertainties that could cause actual results to differ materially from the statements made.For Additional Information:Sunshine Biopharma Inc.Camille SebaalyCFODirect Line: 514-814-0464camille.sebaaly@sunshinebiopharma.com Email thisFacebookTwitterLinkedInPinterestRedditBack to news 041b061a72