• FDA Approves First Oral Blood Thinner for Children americanpharmaceuticalreview
    June 23, 2021
    The U.S. FDA approved Pradaxa (dabigatran etexilate) oral pellets to treat children 3 months to less than 12 years old with venous thromboembolism (a condition where blood clots form in the veins) directly after they have been treated with a blood ...
  • FDA Approves Over-the-Counter Nasal Antihistamine americanpharmaceuticalreview
    June 23, 2021
    The U.S. FDA approved a nasal antihistamine for nonprescription use through a process called a partial prescription to nonprescription switch.
  • FDA Authorizes Stem Cell Trials for Parkinson’s americanpharmaceuticalreview
    June 23, 2021
    Hope Biosciences Stem Cell Research Foundation (HBSCRF) has received FDA authorization for a Phase II clinical trial to assess the efficacy and safety of multiple intravenous infusions of allogeneic adipose-derived mesenchymal stem cells in improving ...
  • Mankind Pharma launches Justoza, a Dapagliflozin approved by USFDA expresspharma
    June 23, 2021
    The Active Pharmaceutical Ingredient (API) is procured from the Drug Master File (DMF) facility approved by USFDA, EU GMP and WHO GMP, which ensures the highest global efficacy and safety standards.
  • FDA OKs First Oral Blood Thinning Medication for Children drugs
    June 23, 2021
    The first oral blood thinning medication for children was approved by the U.S. Food and Drug Administration, the agency announced Monday.
  • Memos reveal internal FDA struggle over thorny Alzheimer's drug approval firstwordpharma
    June 23, 2021
    The FDA on Tuesday made public new documents laying bare a struggle within the agency ahead of its controversial decision on June 7 to grant accelerated approval to Biogen and Eisai's Alzheimer's drug Aduhelm (aducanumab) amid heated debate
  • FDA Approves Pradaxa (dabigatran) as First Oral Blood Thinning Medication for Children drugs
    June 22, 2021
    Today, the U.S. Food and Drug Administration approved Pradaxa (dabigatran etexilate) oral pellets to treat children 3 months to less than 12 years old with venous thromboembolism (a condition where blood clots form in the veins) directly
  • FDA Approves First Oral Blood Thinning Medication for Children fda.gov
    June 22, 2021
    Today, the U.S. Food and Drug Administration approved Pradaxa (dabigatran etexilate) oral pellets to treat children 3 months to less than 12 years old with venous thromboembolism directly after they have been treated with a blood thinner
  • Alkem’s St Louis facility gets two observations from US FDA expresspharma
    June 21, 2021
    Alkem Laboratories informed that the US FDA has issued Form 483 with two observations for its manufacturing facility located in St Louis, US. The US FDA had conducted an inspection of the company’s manufacturing facility from 14-18, June 2021.
  • FDA Approves Avapritinib for Advanced Systemic Mastocytosis americanpharmaceuticalreview
    June 18, 2021
    The U.S. FDA approved avapritinib (Ayvakit™, Blueprint Medicines Corp.) for adult patients with advanced systemic mastocytosis (AdvSM), including patients with aggressive systemic mastocytosis (ASM), systemic mastocytosis with an associated ...
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