Although the new FDA green light doesn’t expand the number of people who may be eligible for the drug, since the sleep apnea approval is specifically for people with obesity, it could lead to ...
The FDA green light is for adults with relapsing forms of MS, including relapsing-remitting MS (RRMS), active secondary progressive MS (SPMS) – a more advanced stage that affects patients who ...
The U.S. Food and Drug Administration (FDA) has announced that a subcutaneous version of Bristol Myers Squibb’s (BMY.N) blockbuster cancer treatment, Opdivo, significantly advances cancer ...
In 2022, the U.S. Food and Drug Administration (FDA) proposed a sweeping plan to ban the sale of certain cigarette products ... 20, 2025, remains to be seen. CONNECT with Green Matters ...
Emergent BioSolutions has been given FDA approval to extend the indications for its smallpox vaccine ACAM2000 to include the prevention of mpox, currently deemed a public health emergency by the WHO.
The Food and Drug Administration (FDA) has reaffirmed that Mounjaro and Zepbound are no longer in shortage following a reevaluation of its decision to remove it from the federal drug shortage list ...
The FDA allows compounding pharmacies to sell copies of drugs when the medications are on the agency's shortage list. Now that the FDA has decided tirzepatide is no longer in shortage, companies ...
The FDA is now accepting written or electronic comments, which firms can submit until May 7, when it will begin work on the final version of the guidance. Anay is Green Queen's resident news reporter.
The FDA says women who are taking Veozah may need more frequent blood testing to check for markers of liver problems. In rare cases, the drug may seriously injure the liver, and patients with ...
The FDA guidance caps lead levels for children younger than 2 at 10 parts per billion for fruits, most vegetables, grain and meat mixtures, yogurts, custards and puddings, and single-ingredient meats.