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Dimethyl Fumarate (Sandoz) TM

You should seek medical advice in relation to medicines and use only as directed by a healthcare professional. Always read the label. If symptoms persist see your healthcare professional.

Active ingredients: dimethyl fumarate

Brand name

(ARTG)

: DIMETHYL FUMARATE SANDOZ dimethyl fumarate 120 mg modified release capsule blister pack

Download the Consumer Medicine Information Leaflet

Download consumer medicine information leaflet (pdf) from the Therapeutic Goods Administration (TGA) website

What this medicine is used for

(ARTG)

DIMETHYL FUMARATE SANDOZ is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.

How to use this medicine

(ARTG)

This medicine contains one component only.

Component :

  • Capsule, modified release
  • Oral
  • Hard gelatin capsules with white body and light-green cap with overprint on the body 120 mg; size of capsules No. 1

Storage conditions

(ARTG)

  • Store below 25 degrees Celsius
  • Shelf lifetime is 36 Months.

Do I need a prescription ?

(ARTG)

These medicine packs are available from a pharmacist and requires a prescription. It is Schedule 4 : Prescription Only Medicine.

  • 14 pack
  • 56 pack

Is this medicine subsidised ?

(PBS)

This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on December, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.

Pregnant or planning a pregnancy ?

(AHT)

For the active ingredient dimethyl fumarate

You should seek advice from your doctor or pharmacist about taking this medicine. They can help you balance the risks and the benefits of this medicine during pregnancy.

Reporting side effects

You can help ensure medicines are safe by reporting the side effects you experience.

You can report side effects to your doctor, or directly at www.tga.gov.au/reporting-problems

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