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Oncologists will soon be able to offer patients the first 5-HT3 receptor antagonist with an indication for delayed chemotherapy-induced nausea and vomiting (CINV). The FDA recently approved palonosetron (Aloxi, MGI Pharma/Helsinn Healthcare) injection for the prevention of acute nausea and vomiting associated with initial and repeat courses of moderately and highly emetogenic cancer chemotherapy and the prevention of delayed nausea and vomiting associated with initial and repeat courses of moderately emetogenic chemotherapy. Palonosetron will be available to patients within the next several weeks.

Here's how to get more R.Ph.s to use their prescriptive authority, allowed in most states but lagging in practice

The American Foundation for Pharmaceutical Education launched a campaign to help recruit more pharmacists to teaching using grants totaling $12 million to fund fellowships for pharmacy faculty positions.

Men with benign prostatic hyperplasia (BPH) will soon have a therapeutic option that uses a unique drug delivery system. The FDA recently approved alfuzosin (UroXatral, Sanofi-Synthelabo) extended-release tablets for the treatment of the signs and symptoms of BPH. Alfuzosin is not indicated for the treatment of hypertension. The manufacturer expects alfuzosin to be available in pharmacies sometime in the second half of 2003.

Clinicians can now offer their patients with non-Hodgkin?s lymphoma (NHL) therapy that combines targeted radiation with patient-specific dosing. The FDA recently approved tositumomab and iodine I-131 tositumomab (Bexxar, Corixa Corporation/GlaxoSmithKline) for the treatment of patients with CD20-positive, follicular NHL, with and without transformation, whose disease is refractory to rituxamab (Rituxan, Genentech) and has relapsed following chemotherapy. Training can be requested and orders placed by calling (877) 423-9927. Corixa recently began supplying Bexxar to cancer treatment centers.

Provisions under House and Senate versions of prescription drug benefits legislation and their impact on FDA final rules regarding generic drug approvals under the Waxman-Hatch Act.

Provisions under House and Senate versions of prescription drug benefits legislation and their impact on FDA final rules regarding generic drug approvals under the Waxman-Hatch Act.