INREBIC 100 mg HARD CAPSULES

2. What you need to know before you take Inrebic

Do not take Inrebic

• if you are allergic to fedratinib or any of the other ingredients of this medicine (listed in section 6).

• if you are pregnant or think you may be pregnant.

Warnings and precautions

Talk to your doctor or pharmacist before starting to take these capsules and during treatment if you have any of the following signs or symptoms:

A condition that affects the brain called encephalopathy, including Wernicke's encephalopathy

• Confusion, memory loss, or difficulty thinking; loss of balance or problems walking.
• Eye problems such as random eye movement, double vision, blurred vision, and loss of vision.

These may be signs of a brain condition called encephalopathy, including Wernicke's encephalopathy, which can be fatal.

Contact your doctor immediately if you experience any of these signs or symptoms.

Talk to your doctor or pharmacist during treatment

• if you feel very tired, short of breath, pale skin, or a fast heartbeat: these may be signs of a low red blood cell count.
• if you have bleeding or bruising, or bleeding from the gums: these may be signs of a low platelet count.
• if you have frequent infections or recurring infections, which may be a sign of a low white blood cell count.
• if you have nausea, vomiting, or diarrhea.
• if you have or have had kidney problems.
• if you have or have had liver problems.
• if you have or have had pancreas problems.

It has been observed with another type of similar medicine used to treat rheumatoid arthritis: heart problems, blood clots, and cancer. Talk to your doctor or pharmacist before or during treatment if:

• you are over 65 years old. Patients 65 years or older may have a higher risk of heart problems, including heart attack, and some types of cancer.
• you have or have had heart problems.
• you have or have had cancer.
• you are a smoker or have smoked in the past.
• you have had blood clots in the veins of your legs (deep vein thrombosis) or lungs (pulmonary embolism) in the past.

• if you suddenly feel short of breath or have difficulty breathing, chest pain, or pain in the upper back, swelling of the legs or arms, pain or tenderness in the legs, redness or discoloration of the legs or arms, as these may be signs of blood clots in the veins.
• if you notice new growths on the skin or changes in existing ones. Your doctor may recommend that you have regular skin checks while taking Inrebic.

Your doctor will decide if Inrebic is suitable for you.

Blood tests

Before and during treatment, you will have blood tests to check your blood cell counts (red blood cells, white blood cells, and platelets) and liver and pancreas function.

Before treatment, you will have a blood test to check your vitamin B1 levels. Your doctor will also tell you to take a daily dose of 100 mg of vitamin B1 supplement during treatment. Your doctor may also ask for additional blood tests to check your vitamin B1 levels during treatment.

Based on the results of the blood tests, your doctor may adjust the dose or stop treatment.

Children and adolescents

Inrebic should not be used in children or adolescents under 18 years of age because this medicine has not been studied in this age group.

Other medicines and Inrebic

Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, because Inrebic may affect the way some medicines work. Also, some medicines may affect the way Inrebic works.

The following medicines may increase the risk of side effects with Inrebic:

• Ketoconazole, fluconazole (used to treat fungal infections);
• Fluvoxamine (used to treat depression);
• Ritonavir (used to treat HIV/AIDS).

The following medicines may reduce the effectiveness of Inrebic:

• Rifampicin (used to treat tuberculosis (TB) and other infections);
• Phenytoin (used to treat epilepsy and control seizures or convulsions);
• Efavirenz (used to treat HIV/AIDS).

Inrebic may affect other medicines:

• Midazolam (used to help you sleep or relieve anxiety);
• Omeprazole (used to treat stomach problems);
• Metoprolol (used to treat angina or high blood pressure);
• Metformin (used to lower blood sugar levels);
• Also simvastatin, S-mephenytoin, and dextromethorphan.

Your doctor will decide if it is necessary to change the dose.

Also, tell your doctor if you have had surgery recently or are going to have surgery or a procedure, because Inrebic may interact with some anesthetics.

Pregnancy and breastfeeding

If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Do not take Inrebic during pregnancy. If you can become pregnant, you must use an effective contraceptive method while taking these capsules and avoid becoming pregnant for at least one month after the last dose.

Do not breastfeed while taking Inrebic and for at least one month after the last dose, as it is not known if this medicine passes into breast milk.

Driving and using machines

If you feel dizzy, do not drive or use machines until these effects have stopped.

Inrebic contains sodium

This medicine contains less than 23 mg of sodium (1 mmol) per dose; this is essentially “sodium-free”.

3. How to take Inrebic

Take this medicine exactly as your doctor or pharmacist has told you. If you are not sure, ask your doctor or pharmacist again.

The recommended dose is 400 mg (four 100 mg capsules) taken orally once a day.

You will have blood tests before and while taking this medicine to monitor your progress. Your doctor will also tell you to take a daily dose of 100 mg of vitamin B1 supplement during treatment (see section 2, “Blood tests”).

If you experience certain side effects while taking Inrebic (see section 4), your doctor may reduce the dose or pause or stop treatment.

How to take these capsules

• Swallow the capsules whole, preferably with water.
• Do not break, open, or chew the capsules.
• The capsules can be taken with or without food, but it is recommended to take them with food to avoid nausea and vomiting.

You should continue to take Inrebic for as long as your doctor tells you. This is a long-term treatment.

If you take more Inrebic than you should

If you accidentally take too many Inrebic capsules or a higher dose than you should, contact your doctor or pharmacist immediately.

If you forget to take Inrebic

If you miss a dose or vomit after taking a capsule, skip the missed dose and take the next scheduled dose at the usual time the next day. Do not take a double dose to make up for the missed or vomited capsules.

If you stop taking Inrebic

Do not stop taking Inrebic unless your doctor tells you to.

If you have any further questions on the use of this medicine, ask your doctor, pharmacist, or nurse.

4. Possible side effects

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Tell your doctor immediately if you notice any of the following symptoms, which may be signs of a serious brain disease called encephalopathy (including Wernicke's encephalopathy):

• Confusion, memory loss, or difficulty thinking,
• Loss of balance or problems walking,
• Eye problems such as double vision, blurred vision, loss of vision, or random eye movement.

Tell your doctor if you experience any other side effects. These may include:

Very common side effects(may affect more than 1 in 10 people)

• Low red blood cell count, which can cause tiredness, shortness of breath, pale skin, or a fast heartbeat (anemia).
• Low platelet count, which can cause bleeding or bruising (thrombocytopenia).
• Low white blood cell count (neutropenia), sometimes with fever. A low white blood cell count can reduce your ability to fight infections.
• Feeling sick (nausea)and being sick (vomiting).
• Diarrhea.
• Constipation.
• Bleeding.
• Urinary tract infection.
• Headache.
• Muscle spasms.
• Feeling tired (fatigue)or weak (asthenia).
• Changes in blood test results (increased alanine aminotransferase, increased aspartate aminotransferase, increased blood creatinine, increased amylase, and increased lipase). These may be signs of liver, kidney, or pancreas problems.

Common side effects(may affect up to 1 in 10 people)

• Dizziness.
• High blood pressure (hypertension).
• Indigestion (dyspepsia).
• Bone pain.
• Pain in the limbs, hands, or feet (limb pain).
• Weight gain.
• Painful urination.

Reporting of side effects

If you experience side effects, talk to your doctor or pharmacist, even if they are not listed in this leaflet. You can also report side effects directly via the national reporting system listed in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.

5. Storage of Inrebic

Keep this medicine out of the sight and reach of children.

Do not use this medicine after the expiry date which is stated on the carton and bottle after “EXP”. The expiry date refers to the last day of the month shown.

Keep the bottle tightly closed to protect it from moisture.

This medicine does not require any special storage conditions.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.

6. Packaging Contents and Additional Information

Inrebic Contents

• The active ingredient is fedratinib. Each hard capsule contains fedratinib dihydrochloride monohydrate equivalent to 100 mg of fedratinib.

• The other ingredients are:
• • The capsule contents contain silicified microcrystalline cellulose (contains microcrystalline cellulose (E460) and colloidal anhydrous silica (E551)) and sodium stearyl fumarate (see section 2, "Inrebic contains sodium").
  • The capsule shell contains gelatin (E441), titanium dioxide (E171), and red iron oxide (E172).
  • The white printing ink is composed of shellac (E904), titanium dioxide (E171), and propylene glycol (E1520).

Appearance of Inrebic and Packaging Contents

• Inrebic are reddish-brown capsules of 21.4-22.0 mm, with "FEDR" printed on the cap and "100 mg" on the body in white ink.

• The capsules are packaged in a high-density polyethylene (HDPE) bottle with a child-resistant screw cap and a tamper-evident seal. Each bottle contains 120 capsules and is packaged in a cardboard box.

Marketing Authorization Holder

Bristol-Myers Squibb Pharma EEIG

Plaza 254

Blanchardstown Corporate Park 2

Dublin 15, D15 T867

Ireland

Manufacturer

Celgene Distribution B.V.

Orteliuslaan 1000

3528 BD Utrecht

Netherlands

You can request more information about this medication by contacting the local representative of the marketing authorization holder:

Date of Last Revision of this Leaflet:

Other Sources of Information

Detailed information on this medicinal product is available on the European Medicines Agency website: https://www.ema.europa.eu. There are also links to other websites on rare diseases and orphan medicines.

You can access detailed information about this medicinal product by scanning the QR code included in the outer packaging with your smartphone. You can also access this information at the following internet address: www.inrebic-eu-pil.com.