Skip to main content

Branded

  • PhRMA: More than 850 medicines in development for diseases that disproportionately affect women

    WASHINGTON — More than 800 drugs are in development for diseases that affect women, according to a pharmaceutical industry lobbying group.

  • Report: Takeda to acquire Nycomed in $12 billion deal

    NEW YORK — Japan-based Takeda Pharmaceutical may acquire Switzerland’s Nycomed for $12 billion, according to published reports.

    Reuters reported Thursday that Takeda was in talks to buy Nycomed in order to expand its presence in the European market. Most of Takeda’s business is in Asia and the United States.

    Nycomed makes treatments for such diseases as chronic obstructive pulmonary disease, chronic pain, osteoporosis and others.

  • J&J recalls lots of Prezista amid odor reports

    HIGH WYCOMBE, United Kingdom — A subsidiary of Johnson & Johnson is recalling several batches of an HIV drug after reports of a strange odor that may have come from the shipping pallets.

    Janssen-Cilag International said it would recall five lots of Prezista (darunavir) due to consumer reports of a musty or moldy smell coming from them. The odor is believed to result from traces of the chemical TBA, which is used in the construction of the pallets. The recalled lots were found in Canada, the United Kingdom, Ireland, Germany and Austria.

  • Novartis' Diovan HCT wins HCPC’s Compliance Package of the Year award

    RICHMOND, Va. — A blood pressure drug made by Swiss drug maker Novartis has won an award from the Healthcare Compliance Packaging Council.

    Novartis Diovan HCT (valsartan and hydrochlorothiazide) won the HCPC’s Compliance Package of the Year award at the council’s RxAdherence 19th annual symposium for its Shellpak packaging design, made by product packaging manufacturer MeadWestvaco Corp. Anderson Packaging, part of AmerisourceBergen Packaging Group, handles the drug’s fulfillment.

  • UCB’s Cimzia improves rheumatoid arthritis condition among patients in study

    BRUSSELS — Patients with moderate to severe rheumatoid arthritis who respond to 12 weeks of treatment with a drug made by UCB are more likely to show improvement in their condition in the long run, according to results of a study published in the Journal of Rheumatology.

  • Genentech seeks regulatory approval for vemurafenib

    SOUTH SAN FRANCISCO, Calif. — Genentech is seeking approval for a new drug to treat skin cancer, the company said Wednesday.

  • Surgeon general, NCL introduce Script Your Future campaign

    WASHINGTON — The National Consumers League and the U.S. surgeon general are launching a new campaign to educate patients about the risks of not properly taking their medications, the organization said.

  • Bayer's regorafenib granted fast-track review

    WAYNE, N.J. — The Food and Drug Administration will expedite its review of an investigational drug made by Bayer HealthCare Pharmaceuticals for treating tumors of the gastrointestinal tract, the company said Tuesday.

X
This ad will auto-close in 10 seconds