Sci Rep 15 , 37913 (2025)
Dose increases are approved by your prescriber, who will check that you are on the right dose for you
From a drug manufacturer perspective, there are still points of uncertainty for biosimilars in the pipeline. To view or add a comment, sign in Caplin Steriles Limited, a Subsidiary Company of Caplin Point Laboratories Ltd, has been granted final approval from the United States Food and Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) Methylprednisolone Acetate Injectable Suspension USP, 40mg/mL & 80mg/mL Single Dose vials, a generic therapeutic equivalent version of the Reference Listed Drug (RLD) DEPO-MEDROL from Pfizer Inc., USA
Large cardiovascular outcome trials have shown these medications provide cardiovascular protection rather than harm, with no identified thrombotic safety concerns from UK or European regulatory bodies
Comparing the clinical utility and diagnostic performance of CSF p-tau181, p-tau217, and p-tau231 assays
If symptoms worsen or are accompanied by chest pain, shortness of breath, severe headache, or confusion, it is crucial to seek emergency care immediately
