MANILA, Philippines —The Food and Drug Administration (FDA) warned the public against the use of seven "unauthorized" cosmetic products that were laced with mercury. Seven different public ...

FDA Commissioner Marty Makary, M.D., has made his pick for the next director of the FDA’s Center for Drug Evaluation and ...

The FDA granted orphan drug designation to leronlimab for the prevention of GvHD. Due to the lack of patients during the COVID-19 pandemic, the Company suspended its Phase 2 trial for acute GvHD.

Quezon City.  The EcoWaste Coalition and the Consumer Rights to Safe Food (CRSF) appealed to the Food and Drug Administration ...

The Philippines will allow a 42-day interval between doses of Russia's Sputnik V COVID-19 vaccine, the head of its Food and Drug Administration (FDA) said on Wednesday, though still below the 90 ...

The company announced FDA that the U.S. Food and Drug Administration has approved LungFit PH to treat term and near-term neonates with hypoxic respiratory failure, often referred to as persistent ...

MANILA, Philippines — The Food and Drug Administration (FDA) has ordered the recall of several batches of a brand of antibiotics used to treat bacterial infections, including pneumonia ...

Beyond Air has developed its LungFit PH II system to be smaller, lighter and fully transport-ready — while delivering all the breakthrough features of the currently FDA-approved version from the ...

In an effort that will contribute to raising the quality of medicines in the Philippines and surrounding regions, the Laboratory Services Division of the Philippine Food and Drug Administration ...

The FDA has granted accelerated approval to Takeda’s supplemental New Drug Application for Iclusig (ponatinib) plus chemotherapy to treat adults with newly diagnosed Philadelphia chromosome ...

FDA’s approval of YUTREPIA paves the way for prescribers to add a new treatment option for patients with PAH and PH-ILDYUTREPIA is designed to enhance deep-lung delivery with an easy-to-use ...