BRIUMVI is a 1-HOUR, TWICE PER YEAR* infusion

*Following the starting dose

BRIUMVI is an infusion therapy that is administered by a healthcare provider (such as a doctor or nurse) through a needle placed in a vein in your arm, also known as an intravenous (IV) infusion. Your healthcare provider is there to support you by reviewing the overall treatment process, answering any questions you may have, and monitoring for potential infusion-related reactions. Please allow enough time in your schedule for your infusion treatments.

What to expect on a typical BRIUMVI infusion day

Pre-infusion
30-60 MINUTES
  • Prior to every infusion, your healthcare provider will evaluate your overall health and answer any questions you have about your infusion treatment
  • Pre-infusion medication may be given to you approximately 30 minutes prior to your infusion and can be given orally or intravenously (IV) to help reduce possible infusion-related reactions
During infusion
1-HOUR
  • Once you are comfortably settled in the infusion chair and ready for treatment, your healthcare provider will begin your infusion
  • Infusions (following the starting dose) will typically take 1 hour
Post-infusion
AS DIRECTED
  • Post-infusion monitoring is at your healthcare provider’s discretion and is not required after your third infusion and beyond (unless you have experienced an infusion-related reaction and/or signs of hypersensitivity with your current or prior infusions)
  • For your first 2 infusions, your healthcare provider will observe you for 1 hour after your infusion is completed
95% of all BRIUMVI 1-hour infusions were completed in 1 hour

± 5 minutes

A dosing schedule that provides more time for you and
less time for your infusion

First Infusion: BRIUMVI 150 mg

Also known as your starting dose, your first infusion will last about 4 hours excluding any pre-infusion medication or post-infusion monitoring

Second Infusion: BRIUMVI 450 mg

Will be given 2 weeks after your Day 1 starting dose and will last about 1 hour excluding any pre-infusion medication or post-infusion monitoring

Third Infusion & Beyond: BRIUMVI 450 mg

Will be given every 24 weeks (approximately 6 months) following your Day 1 starting dose.  These infusions will also last about 1 hour. Post-infusion monitoring is at your healthcare provider’s discretion and is not required after your third infusion and beyond (unless you have experienced an infusion-related reaction and/or signs of hypersensitivity with your current or prior infusions)

“My BRIUMVI infusion went really well and it was completed in just 1 hour.”

– Alex K. has taken BRIUMVI

Individual results may vary

See what BRIUMVI Patient Support can offer you
Understand the safety and side effects of BRIUMVI

Have questions?
Call 1-833-BRIUMVI (1-833-274-8684) to speak with a BRIUMVI Patient Support
Case Manager (Mon-Fri, 8 AM to 8 PM ET)
Stay informed on the latest
updates and resources

Indication and Important Safety Information

Indication

BRIUMVI is indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease, in adults.

Who should not receive BRIUMVI?

Do not receive BRIUMVI if you have an active hepatitis B virus (HBV) infection.

Do not receive BRIUMVI if you have had a life-threatening allergic reaction to BRIUMVI. Tell your healthcare provider if you have had an allergic reaction to BRIUMVI or any of its ingredients in the past.

What is the most important information I should know about BRIUMVI?

BRIUMVI can cause serious side effects, including:

Infusion reactions: Infusion reactions are one of the most common side effects of BRIUMVI, which can be serious and may require you to be hospitalized. You will be monitored during your infusion and may be monitored after each infusion of BRIUMVI for signs and symptoms of an infusion reaction. Tell your healthcare provider if you get any of these symptoms:

  • fever
  • chills
  • headache
  • flu-like symptoms
  • fast heartbeat
  • hives
  • itchy skin
  • dizziness

  • feeling faint
  • swelling of tongue or throat
  • trouble breathing
  • wheezing
  • nausea
  • abdominal pain
  • throat irritation
  • redness of the face or skin

 

These infusion reactions can happen over 24 hours after your infusion. It is important that you call your healthcare provider right away if you get any of the signs or symptoms listed above after each infusion. If you get an infusion reaction, your healthcare provider may need to stop or slow down the rate of your infusion.

  • Infection:
    • Infections are a common side effect, and upper respiratory tract infections are one of the most common side effects of BRIUMVI. BRIUMVI increases your risk of getting infections caused by bacteria or viruses that may be life-threatening or cause death. Tell your healthcare provider if you have an infection or have any of the following signs of infection including fever, chills, a cough that does not go away, or painful urination. Your healthcare provider should delay your treatment with BRIUMVI until your infection is gone.
    • Hepatitis B virus (HBV) reactivation: Before starting treatment with BRIUMVI, your healthcare provider will do blood tests to check for hepatitis B viral infection. If you have ever had hepatitis B virus infection, the hepatitis B virus may become active again during or after treatment with BRIUMVI. Hepatitis B virus becoming active again (called reactivation) may cause serious liver problems including liver failure or death. Your healthcare provider will monitor you if you are at risk for hepatitis B virus reactivation during treatment and after you stop receiving BRIUMVI.
    • Weakened immune system: BRIUMVI taken before or after other medicines that weaken the immune system could increase your risk of getting infections.
    • Progressive Multifocal Leukoencephalopathy (PML): PML may happen with BRIUMVI. PML is a rare, serious brain infection caused by a virus that may get worse over days or weeks. PML can result in death or severe disability. Tell your healthcare provider right away if you have any new or worsening neurologic signs or symptoms. These symptoms may include weakness on one side of your body, loss of coordination in arms and legs, vision problems, changes in thinking and memory which may lead to confusion, and personality changes.
  • Low immunoglobulins: BRIUMVI may cause a decrease in some types of antibodies. Your healthcare provider will do blood tests to check your blood immunoglobulin levels.


Before receiving BRIUMVI, tell your healthcare provider about all of your medical conditions, including if you:

  • have or think you have an infection.
  • take or plan to take medicines that affect your immune system. These medicines may increase your risk of getting an infection.
  • have ever had hepatitis B or are a carrier of the hepatitis B virus.
  • have had a recent vaccination or are scheduled to receive any vaccinations.
    • You should receive any required ‘live’ or ‘live-attenuated’ vaccines at least 4 weeks before you start treatment with BRIUMVI. You should not receive ‘live’ or ‘live-attenuated’ vaccines while you are being treated with BRIUMVI and until your healthcare provider tells you that your immune system is no longer weakened.
    • When possible, you should receive any ‘non-live’ vaccines at least 2 weeks before you start treatment with BRIUMVI. If you would like to receive any non-live vaccines while you are being treated with BRIUMVI, talk to your healthcare provider.
    • If you have a baby and you received BRIUMVI during your pregnancy, it is important to tell your baby’s healthcare provider about receiving BRIUMVI so they can decide when your baby should be vaccinated.
  • are pregnant, think that you might be pregnant, or plan to become pregnant.  BRIUMVI may harm your unborn baby. You should use birth control (contraception) during treatment with BRIUMVI and for at least 6 months after your last infusion of BRIUMVI. Talk with your healthcare provider about what birth control method is right for you during this time.
  • are breastfeeding or plan to breastfeed. It is not known if BRIUMVI passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby if you take BRIUMVI.


Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

What are the possible side effects of BRIUMVI?

The most common side effects of BRIUMVI include:

  • Infusion reactions, upper and lower respiratory tract infections, herpes infections, extremity pain, insomnia, and fatigue.


These are not all the possible side effects of BRIUMVI. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects to TG Therapeutics at 1-877-TGTXINC (1-877-848-9462).