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Febuxostat: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
80 mg
ATC code:

Patient Medication Information: uses, side effects, how to take - Febuxostat

What the medication is used for:

FEBUXOSTAT is used to lower uric acid levels in adult patients with gout. It is used when allopurinol has not worked well enough or when allopurinol is not right for you.

What it does:

FEBUXOSTAT contains febuxostat which is a xanthine oxidase (XO) inhibitor. FEBUXOSTAT works to lower the uric acid in the blood by selectively inhibiting XO involved in uric acid formation. The normal uric acid level should be lower than 360 µmol/L (6.0 mg/dL).

When it should not be used:

Do not take FEBUXOSTAT if you are allergic to febuxostat or any other ingredients in FEBUXOSTAT.

Do not take FEBUXOSTAT if you take:

  • azathioprine
  • mercaptopurine

What the medicinal ingredient is:

Febuxostat as (febuxostat hemihydrate).

What the important nonmedicinal ingredients are: Lactose monohydrate, microcrystalline cellulose, Pregelatinized starch, sodium croscarmellose, colloidal silicon dioxide and magnesium stearate. FEBUXOSTAT tablets are coated with Opadry II green (which contains polyvinyl alcohol, talc, PEG 4000, titanium dioxide, FD&C Yellow No.5 tartrazine aluminium lake, FD&C Blue No.1, and FD&C Blue No.2).

What dosage forms it comes in:

Tablets. Each tablet contains 80 mg febuxostat as (febuxostat hemihydrate).

WARNINGS AND PRECAUTIONS

FEBUXOSTAT treatment should only be started when the acute attack of gout has subsided.

Whenever you start medicines that can lower uric acid levels, like FEBUXOSTAT, gout may flare up. This is due to the body’s efforts to get rid of uric acid crystals from the joints.

However over time, reducing your uric acid level can decrease your gout flares. Your healthcare professional may add other medicines to help prevent or manage flares while taking FEBUXOSTAT.

Heart attacks, strokes and heart- related deaths have been reported. You should not use FEBUXOSTAT if you have heart problems, such as heart failure or have had a stroke or heart attack.

Mild increases in liver function tests were reported in some patients taking FEBUXOSTAT. Your healthcare professional may do blood tests to check your liver function.

Some serious skin and allergic reactions such as rash, skin reddening, pain, swelling or blistering of lips, eyes or mouth, skin peeling and flu-like symptoms have been reported in patients taking FEBUXOSTAT. If you get these symptoms, your doctor may stop your treatment until your skin condition improves. Patients who had previous reactions to allopurinol are at greater risk for these skin conditions.

BEFORE you use FEBUXOSTAT talk to your doctor or pharmacist if you:

  • have taken allopurinol. Tell your doctor what happened to you while you were taking it.
  • have a history of liver or kidney problems.
  • have heart disease, heart problems or had a stroke.
  • are pregnant, breastfeeding or plan to become pregnant, or plan to breast-feed. It is not known if FEBUXOSTAT will harm your unborn baby. It is also unknown if FEBUXOSTAT passes into your breast milk.

  • Have ones of the following hereditary diseases:

    • Galactose intolerance
    • Lapp lactase deficiency
    • Glucose-galactose malabsorption

This is because FEBUXOSTAT contains lactose.

It is not known if FEBUXOSTAT is safe and effective in children under 18 years of age.

INTERACTIONS WITH THIS MEDICATION

Tell your healthcare provider about all the medicines you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. FEBUXOSTAT may affect the way other medicines work, and other medicines may affect how FEBUXOSTAT works.

Know the medicines you take. Keep a list of them and show it to your healthcare provider and pharmacist when you get a new medicine. Serious Warnings and Precautions

A higher number of deaths was seen in a study of gout patients with heart problems who were treated with Febuxostat. This was compared to patients treated with allopurinol.

Your doctor will consider the side effects and benefits of

FEBUXOSTAT before and during your treatment. FEBUXOSTAT should only be used when allopurinol has not worked well enough or when allopurinol is not right for you.

Do not take FEBUXOSTAT if you take:

  • azathioprine
  • mercaptopurine

PROPER USE OF THIS MEDICATION

Usual adult dose:

The recommended dose of FEBUXOSTAT is one 80 mg tablet once daily.

  • Take FEBUXOSTAT exactly as your healthcare

    provider tells you to take it.

  • FEBUXOSTAT can be taken with or without food.

  • FEBUXOSTAT can be taken with antacids.
  • It is important not to stop taking your

    FEBUXOSTAT without first consulting with your healthcare provider even if you have a flare.

  • Your healthcare provider may do certain tests

    while you take FEBUXOSTAT.

Overdose:

Missed Dose: If you miss a dose of FEBUXOSTAT, take your FEBUXOSTAT as soon as you remember. If it is almost time for the next dose, skip the missed dose and go back to the regular dosing schedule.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

The most common side effects of FEBUXOSTAT include:

  • liver problems
  • diarrhea
  • rash
  • nausea
  • dizziness

Tell your healthcare provider if you have any side effect that bothers you or that does not go away.

SERIOUS SIDE EFFECTS, HOW OFTEN THEY
HAPPEN AND WHAT TO DO ABOUT THEM
Talk with yourStop
doctor ortaking
pharmacistdrug and
Symptom / effectOnly ifIn allget
severecasesimmediate
medical
help
Uncommon

Allergic

Reaction: rash, hives, swelling of the face, lips, tongue or throat, Difficulty

swallowing or breathing

√
Serious Skin√
SERIOUS SIDE EFFECTS, HOW OFTEN THEY
HAPPEN AND WHAT TO DO ABOUT THEM
Talk with yourStop
doctor ortaking
pharmacistdrug and
Symptom / effectOnly ifIn allget
severecasesimmediate
medical
help

Reaction

(Stevens-

Johnson

Syndrome,

Toxic Epidermal Necrolysis,

DRESS [drug rash with

eosinophilia and systemic

symptoms]): any combination of red itchy rash with blisters and peeling of the skin and /or of the lips, eyes, mouth, nasal passages or

genitals. It often goes with fever, chills, headache, cough, body

aches or joint pain. You may have less or dark urine, yellow skin or eyes.

Stroke: loss of feeling or

movement on one side of the body, slurring of speech, sudden blurry vision, or severe headache.

√

Heart problems:

chest pain,

shortness of

breath, dizziness, fainting or feeling light-headed, rapid or irregular heart beat.

√

This is not a complete list of side effects. For any unexpected effects while taking FEBUXOSTAT, contact your doctor or pharmacist.

HOW TO STORE IT

FEBUXOSTAT should be protected from light. Store FEBUXOSTAT between 15°C - 30°C.

Keep FEBUXOSTAT and all medicines out of the reach of If you think you have taken too much FEBUXOSTAT, contact your healthcare professional (e.g. doctor), hospital emergency department or the regional Poison Control Centre, immediately even if there are no symptoms.

children.

Reporting Side Effects

You can report any suspected side effects associated with the use of health products to Health Canada by:

  • Visiting the Web page on Adverse Reaction

    Reporting (https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada.html) for information on how to report online, by mail or by fax; or

  • Calling toll-free at 1-866-234-2345.

NOTE: Contact your health professional if you need information about how to manage your side effects. The Canada Vigilance Program does not provide medical advice.

MORE INFORMATION

For more information, please contact your healthcare professionals or pharmacist first, or Sanis Health Inc. at: 1-866-236-4076 or email quality@sanis.com.

The information in this document is current as of the last revision date shown below. For the most current information please contact us directly.

Sanis Health Inc.

1 President's Choice Circle

Brampton, Ontario

L6Y 5S5

Date of Revision: July 21, 2023

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02539837

Revision date stated in the text: July 21, 2023

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Febuxostat

Rx or OTC
Prescription (Rx)?
DIN 02539837
Schedule(s) PRESCRIPTION
Active ingredient(s) Febuxostat (febuxostat hemihydrate) 80 MG
Dosage form(s) Tablet
Route(s) of administration Oral
Drug class (WHO ATC)
  1. M Musculo-skeletal system drugs
    1. M04 Antigout preparations
      1. M04A Antigout preparations
        1. M04AA Preparations inhibiting uric acid production
          1. M04AA03 Febuxostat
Company SANIS HEALTH INC
Current status Marketed
Current status date December 7, 2023

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.