The FDA has approved a new indication for Phathom Pharmaceuticals’ Voquezna (vonoprazan) oral tablets for the relief of heartburn associated with non-erosive gastroesophageal reflux disease in adults. For all the latest drug news, check out our drug referential resource: https://ow.ly/KJNo50SJqNh. #DrugNews #Pharmacy #Medication #Heartburn
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The FDA has approved Yorvipath (palopegteriparatide) subcutaneous injection for the treatment of hypoparathyroidism in adults. For all the latest drug news, check out our drug referential resource: https://ow.ly/8JhX50T1ysZ. #DrugNews #Medication #Pharmacy
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The US FDA Accepts and Grants Priority Review to the sBLA of Regeneron’s Dupixent for Chronic Rhinosinusitis with Nasal Polyposis (CRSWNP) #regeneron #dupixent #chronicrhinosinusitis #nasalpolyposis #regulatory #usfda #acceptance #priorityreview #sbla #treatment #safety #efficacy
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Pharmacovigilance Consultant and Lead Auditor @ PQE Group | ISO 9001:2015 Quality management system and auditor certified | Active DIA member/PV System compliance monitoring excellence expert
The CDSCO's recent findings, identifying 50 medications including substandard paracetamol, have alarmed the medical community. Paracetamol, a commonly prescribed drug for pain and fever relief, failing to meet quality standards is particularly concerning.A total of 52 samples did not pass the quality tests conducted by the CDSCO and are considered substandard. #CDSCO #PvPI #DrugSafety #Product Quality defect #Pharmacovigilance Please avoid intentional drug misuse and abuse without prescriptions https://lnkd.in/dC_Zcwbn
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In a nutshell: The FDA approved adalimumab-ryvk, the first interchangeable, high-concentration, citrate-free biosimilar to Humira. This is the 10th adalimumab biosimilar approved and the first for Alvotech/Teva. Adalimumab-ryvk is indicated for rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, ulcerative colitis, Crohn's disease, plaque psoriasis, hidradenitis suppurativa, uveitis and panuveitis in adults and some pediatric conditions. It is the third Humira biosimilar granted interchangeability status, but the first for the high-concentration formulation that makes up most Humira prescriptions. The interchangeability allows substitution without clinician involvement. Adalimumab-ryvk will launch soon in the US, but timing and pricing details are not yet available. Other adalimumab biosimilars launched at 5-85% discounts to Humira's price.
FDA OKs 10th Humira Biosimilar, Interchangeability Included: It is the tenth adalimumab biosimilar approved by the regulatory agency. Medscape Medical News
FDA OKs First Interchangeable Humira Biosimilar
medscape.com
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The FDA has approved Aurlumyn (iloprost) injection to treat severe frostbite in adults to reduce the risk of finger or toe amputation. For all the latest drug news, check out our drug referential resource: https://ow.ly/7V4x50QBlUJ #DrugNews #Medication #Pharmacy
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The annual report for the Office of Generic Drugs for 2023 was released by the US FDA's Center for Drug Evaluation and Research (CDER). which talks about how the work of the generic drug program benefits the public by expanding treatment options and enhancing access to medications. #usfda #cder #genericdrugs #annualreport #2023year #publichealth #treatment #medication #regulatoryaffairs #regulation #submission #regorbit #drugs #patientcare #enhancing #access #affordablehealthcare
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Combining medications increases the chance of a dry mouth! 👄 If you or your patients take 3 or more medications the chance of suffering a dry mouth increases by 3 times! Explore the common causes of dry mouth here https://shorturl.at/GF0PC #drymouth #drymouthrelief #mouthcare #pharma #pharmacy #healthcareprofessional
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FREELANCE MEDICAL WRITER✍️ & MEDICAL AFFAIRS 🏆; providing engaging & timely⏳ deliverables through the life-cycle🧬 of your CME initiatives⚕️
FDA ALERT: 📢 Counterfeit Ozempic® (semaglutide) Counterfeiters are parasites! They function as predators and prey. When there are drug shortages, counterfeiters find ways to invade unsuspecting hosts. Counterfeit Ozempic® (semaglutide) injections have entered the market, with thousands of fake injections currently being investigated by the FDA. #Pharmacists must take extra precautions when stocking our shelves with in-demand therapeutics. We must examine our supply sources to ensure we're not inadvertently putting our patients at risk. Please note that packages containing lot number NAR0074 and serial number 430834149057 are counterfeit and should not be used. As healthcare professionals, we must do everything possible to prevent counterfeit activity in our trusted industry. Counterfeiters are predators and parasites, and we must play our part in stopping them. Let's work together to ensure the safety and well-being of our patients. #FDAalert #counterfeitmeds #pharmacists #medicationsafety https://lnkd.in/eTyXskqC
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👋 Check out our recent publication in "Endocrinology, Diabetes and Metabolism" by Wiley.
Excited to share our new publication which shows weekly icodec results in a significant reduction in blood sugar (HbA1c levels) and a superior time in range (time spent within recommended blood sugar range) compared with daily Glargine in both insulin naive and previously insulin-treated patients. Moreover, Icodec was not associated with increased risk of hypoglycemia. Novo Nordisk has received marketing authorisation of Icodec from European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) and an FDA approval of the drug seems very likely as well. Link for the article: https://lnkd.in/dZaMV_ay
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#Lisinopril_Impurities_Instock #VBIOCHEM #pharmaceuticals_impurities #API #Standards #A_Varity_of_Lab_chemicals #ISO17034 #analyticaldevelopment #researchanddevelopment #marketing@vbiochem.com +91 9541263789 #Lisinopril is a medicine to treat high blood pressure (hypertension) and heart failure. It's also prescribed after a heart attack and helps prevent future strokes and heart attacks. It also improves your survival if you're taking it after a recent heart attack or for heart failure
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