WASHINGTON DC (April 2, 2019) — Today the US Food and Drug Administration announced the issuance of two warning letters to operators of websites that illegally market potentially dangerous, unapproved, and misbranded opioid medications, including tramadol.

WASHINGTON DC (April 2, 2019) — In recent years, we’ve seen a growing interest in the development of therapies and other FDA-regulated consumer products derived from cannabis (Cannabis sativa L.) and its components, including cannabidiol (CBD). This interest spans the range of product categories that the agency regulates.

WASHINGTON DC (April 2, 2019) — Access to affordable insulin can be a matter of life and death for Americans with diabetes. Insulin is a critical hormone that regulates sugar metabolism. The body’s inability to produce sufficient levels of natural insulin can lead to diabetes — both inherited Type 1 and Type 2, typically called adult-onset.

WEST DES MOINES, IOWA (April 2, 2019) — In honor of National Diabetes Awareness Month, Hy-Vee Inc is providing free Hemoglobin A1C screenings throughout its eight-state region during the month of April.

WASHINGTON DC (April 1, 2019) — The US Food and Drug Administration (USFDA) today posted warning letters to four companies who produce homeopathic drug-products for significant violations of current good manufacturing practice (CGMP) regulations, including a letter to King Bio Inc of Asheville, NC.

CHICAGO, ILLINOIS (April 1, 2019) — In defense of significant coverage gains and key patient protection provisions of the Affordable Care Act (ACA), the American Medical Association (AMA) and other leading physician organizations today filed an amicus brief in the case of Texas v United States.

WASHINGTON DC (March 29, 2019) — The US Food and Drug Administration (USDA) today approved Mavenclad (cladribine) tablets to treat relapsing forms of multiple sclerosis (MS) in adults, to include relapsing-remitting disease and active secondary progressive disease. Mavenclad is not recommended for MS patients with clinically-isolated syndrome.

WASHINGTON DC (March 28, 2019) — The US Food and Drug Administration today approved Cimzia (certolizumab pegol) injections for treatment of adults with a certain type of inflammatory arthritis called non-radiographic axial spondyloarthritis (nr-axSpA) with objective signs of inflammation. This is the first time that the FDA has approved a treatment for nr-axSpA.

WASHINGTON DC (March 27, 2019) — Today, the US Food and Drug Administration (FDA) announced important new steps to modernize breast-cancer screening and help empower patients with more information when they are considering important decisions regarding their breast health care.

MUSCATINE, IOWA (March 26, 2019) — Beginning in March 2019, Gilda’s Club Quad Cities launched an 8-Week Mind, Body, Spirit Challenge to help people diagnosed with cancer, including those undergoing treatment and caregivers, to improve quality of life by better managing the stress of diagnosis and treatment.

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