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Methylprednisolone News
ASA: Adjuvant Methylprednisolone Role Examined in Acute Ischemic Stroke
WEDNESDAY, Feb. 14, 2024 – For patients with acute ischemic stroke secondary to large-vessel occlusion (LVO) undergoing endovascular thrombectomy, adjuvant low-dose methylprednisolone does not...
Lavage + Steroid No Benefit in Calcific Rotator Cuff Tendinopathy
THURSDAY, Oct. 12, 2023 – For patients with calcific rotator cuff tendinopathy of the shoulder, there is no benefit for ultrasound-guided lavage with a corticosteroid injection or for sham lavage...
EMS Crews May Not Always Follow Guidelines When Dosing Kids: Study
MONDAY, July 10, 2023 – Less than half of all children treated by emergency medical services receive the right amount of medication during out-of-hospital emergencies, a new study found. In some...
FDA Medwatch Alert: Methylprednisolone Sodium Succinate for Injection 40mg, 125mg, and 1g by Sagent Pharmaceuticals: Recall - High Out of Specification Impurity Results
ISSUE: Sagent Pharmaceuticals, Inc. announced the voluntary nationwide recall of ten lots of Methylprednisolone Sodium Succinate for Injection, USP, 40mg, 125mg, and 1g. A detailed listing of...
FDA Medwatch Alert: Epidural Corticosteroid Injection: Drug Safety Communication - Risk of Rare But Serious Neurologic Problems
Including methylprednisolone, hydrocortisone, triamcinolone, betamethasone, and dexamethasone [Posted 04/23/2014] ISSUE: FDA is warning that injection of corticosteroids into the epidural space of...
FDA Medwatch Alert: Olympia Pharmacy Sterile Compounded Products: Recall - Concerns About Sterility Assurance
[Posted 05/30/2013] ISSUE: Lowlite Investments d/b/a Olympia Pharmacy ("Lowlite") notified the public of a voluntary multi-state recall of all sterile drug products compounded by the pharmacy that ...
FDA Medwatch Alert: Main Street Family Pharmacy in Tennessee: FDA Alerts Health Care Providers of Adverse Reactions Associated with Steroid Injections
ISSUE: The U.S. Food and Drug Administration is working closely with the Centers for Disease Control and Prevention and Tennessee Board of Pharmacy to investigate reports of seven adverse events...
FDA Medwatch Alert: Fungal Meningitis Outbreak
[UPDATE 10/24/2012] The updated list of customers (consignees) who were shipped product on or after May 21, 2012 from the New England Compounding Center’s (NECC) Framingham, MA facility is now pos...
FDA Medwatch Alert: Fungal Meningitis Outbreak
FDA provides NECC Customer List [UPDATE 10/22/2012] FDA is making available two lists of customers (consignees) who received products that were shipped on or after May 21, 2012 from New England ...
FDA Medwatch Alert: FDA Statement on Fungal Meningitis Outbreak: Additional Patient Notification Advised
[Update 10/16/2012] On 10/15/12 the health care facility notified CDC that the initial report of two transplant patients has been revised to one patient who received cardioplegia solution from NECC....
FDA Medwatch Alert: New England Compounding Center (NECC) Potentially Contaminated Medication: Fungal Meningitis Outbreak
[UPDATED 10/06/2012] On October 4, 2012, the CDC and FDA recommended that all health care professionals cease use and remove from their pharmaceutical inventory any product produced by the New E...
FDA Medwatch Alert: New England Compounding Center (NECC) Potentially Contaminated Medication: Fungal Meningitis Outbreak
[Posted 10/05/2012] ISSUE: FDA has observed fungal contamination by direct microscopic examination of foreign matter taken from a sealed vial of methylprednisolone acetate collected from New ...
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