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CMS is extending the registration and bid submission deadlines for the first round of the Medicare Durable Medical Equipment, Prosthetics, Orthotics, and Supplies Competitive Bidding Program.

CMS believes that eliminating the exemption will encourage healthcare providers to move as quickly as possible to e-prescribing using the SCRIPT standard.

HHS secretary Michael Leavitt announced a two-year effort designed to further protect Medicare beneficiaries from fraudulent suppliers of durable medical equipment, prosthetics, and orthotics supplies (DMEPOS).

Responding to CMS' calls for healthcare providers to get and share their NPI numbers, NCPDP has created a special look-up tool that pharmacists can use to search for physician data.

The FDA has issued a public health advisory following a report of a cystic fibrosis patient who died after inhaling premixed liquid colistimethate through a nebulizer.

The Medicare IVIG Access Act of 2007, which seeks adequate reimbursement for intravenous immunoglobulin (IVIG) products and accompanying care for patients with primary immunodeficiency diseases (PIDDs) and other conditions.

To prevent drug traffickers from diverting iodine for the illicit production of methamphetamine, DEA has issued a final rule governing iodine crystals and chemical mixtures containing more than 2.2% iodine.

In the book, And when the police gave us their guns, we knew that this was?no ordinary hurricane, they wrote about their ideas to help stranded patients in New Orleans obtain their medications, including breaking into an area Walgreens pharmacy and volunteering for one of the local hospitals.

Pharmacists should not expect Congressional changes soon in the controversial Medicare Part D drug benefit program but even so, several administrative issues still need to be resolved.

The Food and Drug Administration's "Medication Guide" program, set up nine years ago as a major avenue of informing patients about risks or special issues with certain drugs, has a host of problems, according to pharmacists and other witnesses at a recent hearing.

Most Americans probably never gave tuberculosis (TB) a passing thought until a case of extensively drug-resistant TB (XDR TB) recently made national headlines. An American with XDR TB traveled from the United States to Europe and back in May, potentially exposing hundreds of fellow travelers to the disease. Since then, national public concern about TB has ballooned.

Adults and children six years of age and older who suffer with seasonal and perennial allergic rhinitis will now have another option for relief of their symptoms. Levocetirizine (Xyzal) from UCB Inc. and Sanofi-Aventis has received regulatory approval from the FDA.