• FDA again warns drug facility where workers poured acid on quality data

    The FDA sent another warning to an Intas Pharmaceuticals plant in India, where investigators imposed import bans in late 2022 after finding shredded quality control documents doused in acid.
  • Only device for Janssen pulmonary hypertension drug discontinued

    Janssen is recommending physicians withhold prescribing its pulmonary arterial hypertension drug because Philips Respironics is discontinuing the only approved delivery system for the drug.
  • Mark Cuban drug company taps mail-order pharmacy

    Mark Cuban Cost Plus Drug Co. is teaming up with PharmcoRx, a pharmacy services business, to expand its pharmacy affiliate network. 
  • Reading Hospital to open 3rd pharmacy

    West Reading, Pa.-based Reading Hospital is planning to open a full-service retail pharmacy Nov. 29 in Wyomissing, Pa., according to Lehigh Valley Business.
  • Some antiseizure drugs can cause extensive rash, FDA warns

    Antiseizure medications made of levetiracetam and clobazam might cause a rash that can quickly injure organs and hospitalize patients, the FDA said Nov. 28. 
  • Menopausal women turn to Wegovy, Ozempic for weight loss

    A popular class of Type 2 diabetes and weight management drugs is gaining the attention of women going through menopause who want to lose weight, The New York Times reported Nov. 27.
  • FDA approves 1st drug for aggressive, noncancerous tumors

    The FDA approved Ogsiveo (nirogacestat), the first drug indicated for locally aggressive, noncancerous tumors, on Nov. 27. 
  • Cost Plus Drugs partners with digital health company

    Mark Cuban Cost Plus Drug Co. has partnered with digital health company Expion Health in an effort to tackle the rising costs of specialty drugs.
  • MercyOne hospital scoops pharmacy

    Genesis Medical Center-Dewitt, a MercyOne-owned hospital in Iowa, bought a local pharmacy to include in its network, Our Quad Cities reported Nov. 27. 
  • Mounjaro more effective than Ozempic for weight loss: Study

    Eli Lilly's Mounjaro helped patients lose weight more effectively than Novo Nordisk's Ozempic, according to a preprint study that included more than 40,000 patients. 
  • Exela Pharma recalls 400K drugs

    Exela Pharma Sciences, an injectable drug company, is recalling more than 415,000 drug vials in a Class I recall because of a possible presence of silicone, according to the FDA. 
  • Uptake of RSV drugs spikes early

    The fill rate of antibiotics for bacterial infections from respiratory syncytial virus surpassed the previous season's trend, indicating an unusually early RSV season. 
  • Surgeons raise concerns about Ozempic, other GLP-1s

    Surgeons and health system leaders are voicing concerns about the unknown long-term risks of glucagon-like peptide-1 receptor agonists, such as Ozempic, Wegovy and Saxenda. 
  • FDA finalizes tougher rules for consumer drug ads

    The FDA issued a final rule Nov. 21 that will require drugmakers to clearly state side effects and contraindications in direct-to-consumer advertisements. The rule is effective May 20, 2024. 
  • 6 drugs now in shortage

    There's been a slight slowdown in reports of new drug shortages before the winter holiday season, but six medications recently entered the list of ongoing shortages, which include about 300 drugs. 
  • Senators prod Beyfortus drugmaker over shortage

    Seven senators are questioning why Sanofi and AstraZeneca underestimated the demand for Beyfortus, the first pediatric drug approved for respiratory syncytial virus. 
  • Timber Pharmaceuticals files for bankruptcy

    Timber Pharmaceuticals filed for Chapter 11 bankruptcy Nov. 17. 
  • ASHP President Dr. Leigh Briscoe-Dwyer inspires next gen

    Leigh Briscoe-Dwyer, PharmD, is mentoring the next generation of pharmacists as she pulls on her years of experience, according to a Nov. 17 article from Binghamton (N.Y.) University. 
  • FDA approves 1st drug for bloodstream infections

    The FDA approved CorMedix's Defencath Nov. 15, marking it the first and only catheter lock solution for catheter-related bloodstream infections. 
  • FDA eyes efficacy of $900K cancer drug

    An FDA panel is urging Acrotech Biopharma to accelerate research into the efficacy of two blood cancer drugs brought to market via the agency's accelerated approval pathway.

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