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FDA has approved the supplemental New Drug Application for tapentadol extended-release tablets (Nucynta ER, Janssen), an oral analgesic taken twice daily, for the management of neuropathic pain associated with diabetic peripheral neuropathy in adults when a continuous, around-the-clock opioid analgesic is needed for an extended period of time.

At its Pharmacy and Technology Conference, the National Association of Chain Drug Stores presented Doug Long with the prestigious Harold W. Pratt Award.

The National Association of Chain Drug Stores Foundation has announced the inaugural class of their Faculty Scholars Program.

Mallinckrodt, the largest U.S. supplier of opioid pain medications, plans to purchase Xanodyne Pharmaceuticals’ Roxicodone (oxycodone hydrochloride tablets USP) in 5-mg, 15-mg, and 30-mg dosage strengths.

Individuals taking statins are at higher risk of developing cataract at an earlier age than those not taking them, according to a study published in the August issue of Optometry and Vision Science.

Walgreens is expanding its electronic health record program to all of its stores by the summer of 2013.

In a letter to Pennsylvania state lawmakers, the National Community Pharmacists Association urged the leaders to support legislation concerning pharmacy audits.

FDA has approved Watson's lidocaine topical patch 5%, the first generic version of (Endo) for the relief of pain associated with post-herpetic neuralgia.

Growth hormone-releasing hormone shows favorable effects on cognition in older adults and those with mild cognitive impairment, according to a study published in the Archives of Neurology.

Aminoglycoside-loaded bone cement implants, frequently used in orthopedic surgery, may result in systemic effects that raise aminoglycoside serum concentrations and lead to acute kidney injury, according to a study published July 3 in The Annals of Pharmacotherapy.

Vitamin D deficiency in critically ill children may make them more vulnerable to severe illnesses, according to two new studies published ahead of the print September issue of Pediatrics.

FDA has approved buprenorphine and naloxone (Suboxone, Reckitt Benckiser Pharmaceuticals) sublingual film in the 4-mg and 12-mg strengths for the maintenance treatment of dependence on prescription opioid painkillers and heroin.

Teva Pharmaceutical Industries Ltd has launched authorized generics of products indicated for use with diet and exercise to improve blood glucose control in adults with type 2 diabetes.

Certain Rite Aid pharmacies are taking part in a pilot project designed to make patient medication information easier for consumers to understand.

What's different in your drug stores this month or coming very soon?

The FTC has filed an amicus curiae brief on the issue of “pay-for-delay†actions in the U.S. District Court for the District of New Jersey, as part of an antitrust lawsuit between Wyeth and Teva Pharmaceuticals.

FDA approved Mylan Pharmaceutical's 15-mg, 30-mg, and 45-mg pioglitazone hydrochloride tablets, the first generic version of Actos (Takeda), along with diet and exercise to improve blood glucose control in adults with type 2 diabetes.

Seattle-based Bartell Drugs and the Space Needle are set to launch back-to-school promotion.

At the urging of the Texas Legislature, the Texas Department of Public Safety developed the Prescription Access in Texas program, which provides controlled substances dispensing history to authorized healthcare and law enforcement professionals.

Healthcare delivery in the United States has evolved as more patients visit their neighborhood retail clinics for acute and preventive care.

The U.S. Department of Health and Human Services has created partnerships with several pharmacies to help patients learn about new Medicare benefits available under the Affordable Care Act, the healthcare reform legislation that was upheld as constitutional by the Supreme Court in late June.

FDA’s latest “Drug Info Rounds†video for health professionals helps pharmacists understand the agency’s Accelerated Approval Program for drugs when there is an unmet medical need.

It’s important to put processes in place to be sure a patient’s medication list at discharge from the hospital is the same information that is provided to the primary care physician to avoid medication errors, according to a recent study published online July 24 in The Annals of Pharmacotherapy.

FDA has issued a Drug Safety Communication concerning three children who died and one child who experienced a nonfatal but life-threatening case of respiratory depression after taking the pain-reliever codeine following tonsillectomy and/or adenoidectomy.

FDA has approved the influenza vaccine formulation for six manufacturers for the 2012-2013 influenza season.

Systemic corticosteroid monotherapy using prednisone is not effective for patients with acute rhinosinusitis, according to a new study published in the August 7 issue of the Canadian Medical Association Journal.

The use of generic prescription drugs instead of their brand-name counterparts has saved Americans and the nation’s healthcare system $1.07 trillion over 10 years ending in 2011, according to the results of a study commissioned by the Generic Pharmaceutical Association.

Federal legislation is needed to control pharmacies that are re-selling drugs on the gray market, according to Carmen Catizone, the executive director of the National Association of Boards of Pharmacy.