Berlin: Bayer has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency ...

Aflibercept 8 mg recommended for marketing authorization in EU for third retinal indication: Berlin Monday, December 15, 2025, 13:00 Hrs [IST] The Committee for Medicinal Products ...

The U.S. Food and Drug Administration (FDA) has approved Armlupeg (pegfilgrastim-unne) 6 milligrams per 0.6 milliliter (mg/mL ...

The police said a penalty for drunken driving is Rs.10,000 or six months imprisonment. Driving license will be suspended for ...

The Cyberabad Traffic Police conducted a special weekend drive against drunken driving, during which 407 offenders were apprehended across the Cyberabad commissionerate limits.

Long-term 7-year follow-up data from the Portal extension trial support the port delivery system as an effective strategy to ...

Therapeutic antibodies packaged into microparticles could be injected with a standard syringe, avoiding the need for time-consuming transfusions.

Caffeine offers some real health benefits—but not if you go overboard. Here’s how coffee, energy drinks, and other caffeine ...

Follow TNM’s WhatsApp channel for news updates and story links.A neurosurgeon and two hospital employees are among five ...

Celltrion receives US FDA approval of 300mg strength of Omlyclo, the first and only interchangeable biosimilar to Xolair: Incheon, South Korea Thursday, December 4, 2025, 11:00 Hr ...

Celltrion, Inc. today announced the U.S. Food and Drug Administration (FDA) has approved a new presentation of OMLYCLO® (omalizumab-igec), the first and only biosimilar designated as interchangeable ...

The FDA has approved pegfilgrastim-unne (Armlupeg) for the treatment of patients with nonmyeloid cancers undergoing treatment with myelosuppressive anticancer drugs linked to a significant chance of ...