Reports of anaphylaxis associated with the use of glatiramer acetate have prompted the Food and Drug Administration (FDA) to add a Boxed Warning to the prescribing information.
From 1996-2024, 82 cases of anaphylaxis associated with glatiramer acetate were reported to the FDA Adverse Event Reporting ...
Opens in a new tab or window The FDA added a boxed warning about rare cases of anaphylaxis associated with the multiple sclerosis (MS) drug glatiramer ... within 1 hour of injection and include ...
For most patients who experienced anaphylaxis with glatiramer acetate use, the symptoms appeared within one hour of injection. All the news that moves the needle in pharma and biotech Exclusive ...