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LONDON (Reuters) - The death toll from Ebola in the three West Africa countries hardest hit by the epidemic has risen to 7,518 out of 19,340 confirmed cases recorded there to date, the World Health Organization said on Monday.

(Reuters) - Data from Achillion Pharmaceuticals Inc's hepatitis C drug trials showed the company could develop a shorter-duration treatment rivaling offerings from Gilead Sciences Inc and Abbvie Inc.

WASHINGTON (Reuters) - Eating fast food may lead to lower student test scores in math, science and reading, a recent study of U.S. school children said.

BEIRUT (Reuters) - The Syrian government has approved the delivery of medicine and surgical supplies to three areas of the country aid workers were previously unable to reach regularly, including opposition-held Aleppo, the World Health Organization said on Monday.

WASHINGTON (Reuters) - Eli Lilly and Co has won approval to buy Novartis AG's animal health unit on condition that it divests its Sentinel line of products for treating heartworm in dogs, the Federal Trade Commission said on Monday.

TORONTO (Reuters) - Tekmira Pharmaceuticals Corp will supply one of its experimental Ebola treatments for clinical studies to be conducted in West Africa by a consortium that includes England's Oxford university, the Canadian company said on Monday.

(Reuters) - The nation's largest pharmacy benefit manager has lined up a cheaper price from AbbVie Inc on its newly approved hepatitis C treatment and, in most cases, will no longer cover Gilead Sciences Inc treatments, Express Scripts said on Monday.

CHICAGO (Reuters) - For months, Vanderbilt University researcher Dr. James Crowe has been desperately seeking access to the blood of U.S. Ebola survivors, hoping to extract the proteins that helped them overcome the deadly virus for use in new, potent drugs.

PHNOM PENH (Reuters) - Cambodian prosecutors said they charged an unlicensed medical practitioner with murder on Monday, alleging he spread HIV among at least 106 villagers in the country's remote northwest.

(Reuters) - The U.S. Food and Drug Administration approved Biocryst Pharmaceuticals Inc's intravenous flu drug, sending the company's shares up nearly 10 percent in premarket trading.

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