Vumerity, INN-diroximel fumarate EPAR 2026

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  1. Click ‘Get Form’ to open the Vumerity EPAR document in the editor.
  2. Begin by reviewing the 'Name of the Medicinal Product' section. Ensure that it states 'Vumerity 231 mg gastro-resistant hard capsules' clearly.
  3. Proceed to the 'Qualitative and Quantitative Composition' section. Here, confirm that each capsule contains 231 mg of diroximel fumarate as listed.
  4. In the 'Pharmaceutical Form' section, verify that it describes the product accurately as a gastro-resistant hard capsule.
  5. Move on to 'Clinical Particulars'. This section outlines therapeutic indications and posology. Make sure to note that treatment should be initiated under physician supervision.
  6. Fill out any relevant fields regarding contraindications and special warnings. Highlight important information such as risks associated with PML and lymphopenia.
  7. Review the 'Undesirable Effects' section for any potential side effects that may need attention during treatment.

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Most medicines for treating MS require an injection; however, newer oral medicines, like Vumerity, provide an easier treatment option. Oral options can be more convenient, but they may not be better or worse than other types of MS treatments.
In a statement following the approval, Biogen said weve made the decision to launch Vumerity in the US with the lowest annual WAC price for oral MS disease-modifying therapies at an annualised price of $88,000.
Vumerity has anti-inflammatory and antioxidant properties. It contains the active ingredient diroximel fumarate and comes as a delayed-release oral capsule. Vumerity is not a chemotherapy or immunosuppressant drug.
Vumerity is a medicine used to treat adults with a type of multiple sclerosis (MS) known as relapsing-remitting MS.

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