The first new quarterly report identifies adverse drug effects that are under FDA investigation.
WebMD Health News
20 Drugs the FDA Is Watching
Government Of Canada And Province Of British Columbia Collaborate On Addictions Treatment Programs In Vancouver’s Downtown Eastside
Individuals living in Vancouver’s Downtown Eastside will benefit from two new treatment services thanks to an investment by the Government of Canada. The Honourable Tony Clement, Minister of Health, and the Honourable George Abbott, B.C. Minister of Health Services, today announced an investment of $10 million for two new treatment initiatives aimed at helping people with complex mental health issues and addiction problems to full recovery.
Pharmacy White Paper Consultation On Legislative Changes
In response to the Pharmacy White Paper related consultation on legislative changes published on 27 August, the NPA has called for new money to be made available for future pharmacy services and for a clear timetable to be put in place for a more ordered entry of businesses into the pharmacy market. John Turk, NPA Chief Executive said: “The consultation heralds further reforms of entry into the pharmacy market.
Amgen And Wyeth Statement On The FDA Safety Announcement Regarding Tumor Necrosis Factor (TNF) Blockers
Amgen (NASDAQ: AMGN) and Wyeth Pharmaceuticals, a division of Wyeth (NYSE: WYE), issued a statement in response to the Food and Drug Administration (FDA) safety announcement regarding opportunistic fungal infections in patients treated with Tumor Necrosis Factor (TNF) blockers [marketed as Remicade® (infliximab), Enbrel® (etanercept), Humira® (adalimumab) and Cimzia® (certolizumab pegol)].
Handling, Transfer And Transport Of Waste Consultation - Pharmacy Bodies Comment
The NPA is one of five bodies representing community pharmacy businesses that have submitted a joint response to the second consultation carried out by DEFRA on the Handling, Transfer and Transport of Waste. The consultation seeks views on the measures needed to reduce the incidence of fly-tipping and inappropriate disposal of waste.
Research Suggests That Cigarettes’ Power May Not Be In Nicotine Itself
There may be a very good reason why coffee and cigarettes often seem to go hand in hand. A Kansas State University psychology professor’s research suggests that nicotine’s power may be in how it enhances other experiences. For a smoker who enjoys drinking coffee, the nicotine may make a cup of joe even better. And that may explain why smoking is so hard to quit.
USP’s 2008 Annual Scientific Meeting To Convene Scientific Experts From Around The World
The U.S. Pharmacopeial (USP) Convention’s 2008 Annual Scientific Meeting (ASM) will be held in Kansas City, Mo., September 24 to 26. The meeting is an opportunity to interact with the USP experts responsible for establishing internationally recognized standards for prescription and over-the-counter medicines, food ingredients and dietary supplements. The focus will be on Quality of Manufactured Medicines, Food Ingredients and Dietary Supplements.
An Essential And Comprehensive Report On Biopharmaceuticals In The US And European Markets, By Research And Markets
Research and Markets has announced the addition of the “Biopharmaceuticals in the US and European Markets” report to their offering.
Pain Killers And Stimulants Less Risky Than Cocaine, More Risky Than Marijuana, According To College Freshmen
First year college students believe that occasional nonmedical use of prescription pain killers and stimulants is less risky than cocaine, but more risky than marijuana or consuming five or more alcoholic beverages every weekend, according to a new study published in the September issue of Prevention Science, the peer-reviewed journal of the Society for Prevention Research.
Celator Pharmaceuticals Receives Orphan Drug Designation For Anticancer Agent CPX-351
Celator Pharmaceuticals announced that the U.S. Food & Drug Administration (FDA) has granted orphan drug designation to CPX-351 (Cytarabine:Daunorubicin) Liposome Injection for the treatment of Acute Myeloid Leukemia (AML). Celator is currently preparing to conduct two randomized Phase 2 studies with CPX-351. The first Phase 2 study, in newly diagnosed, elderly patients with AML, is expected to start enrolling patients before the end of 2008.
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Recent Entries
- Circassia Completes Patient Recruitment For Phase II Clinical Trial Of Toleromune(R) Allergy Treatment
- ImQuest Submits Investigational New Product Application To The Food And Drug Administration To Initiate HIV Therapeutic Clinical Trials With IQP-0410
- FDA Issues A Complete Response Letter For Lilly’s Olanzapine LAI For Treatment Of Schizophrenia In Adults
- Kaunitz on Women’s Health: A Safer Approach to Prescribing Menopausal Estrogen
- Sun Pharmaceutical extends tender offer for Taro
- Sun Pharmaceutical receives FDA approvals for 4 generics
- Codexis announces licensing agreement with Teva Pharmaceutical Industries
- GlaxoSmithKline Successfully Completes Tender Offer for Shares of Genelabs Technologies, Inc.
- Codexis, Teva in Licensing Agreement Final
- FDA Safety Changes: Norditropin, Rozerem, Zomig
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