Brand Name Jakavi Common Name ruxolitinib
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How does this medication work? What will it do for me?
Ruxolitinib belongs to the group of medications called antineoplastics, or anti-cancer medications. More specifically, it is a protein kinase inhibitor.
It is used to treat people with an enlarged spleen and other symptoms of myelofibrosis, a rare type of blood cancer. It is also used to control the amount of red blood cells in the blood (hematocrit) in people with the condition polycythemia vera who have not responded to other medications.
How should I use this medication?
The recommended starting dose of ruxolitinib depends on the condition being treated and baseline levels of certain blood cells (e.g., platelets, hemoglobin, neutrophils). Your doctor will adjust your dose based on how you respond to and tolerate this medication. Doses range between 5 mg and 20 mg taken twice daily. The maximum dose of ruxolitinib is 25 mg taken twice daily.
This medication can be taken with or without food. Swallow the tablets whole with a glass of water. Do not break, cut, crush, or chew the tablets. It is important to take this medication around the same time every day.
Many things can affect the dose of medication that a person needs, such as body weight, other medical conditions, and other medications. If your doctor has recommended a dose different from the ones listed here, do not change the way that you are taking the medication without consulting your doctor.
It is important to take this medication exactly as prescribed by your doctor.
If you miss a dose, skip the missed dose and continue with your regular dosing schedule. Do not take a double dose to make up for a missed one. If you are not sure what to do after missing a dose, contact your doctor or pharmacist for advice.
Store this medication in its original package at room temperature and keep it out of the reach of children.
What form(s) does this medication come in?
Each round, white-to-almost-white tablet, with "NVR" debossed on one side and "L5" debossed on the other side, contains 5 mg of ruxolitinib. Nonmedicinal ingredients: hydroxypropylcellulose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, colloidal silicon dioxide, sodium starch glycolate (Type A), and povidone.
Each round, curved, white-to-almost-white tablet with "NVR" debossed on one side and "L10" debossed on the other side contains 10 mg of ruxolitinib. Nonmedicinal ingredients: hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, colloidal silicon dioxide, sodium starch glycolate (Type A), and povidone.
Each ovaloid, curved, white-to-almost-white tablet, with "NVR" debossed on one side and "L15" debossed on the other side, contains 15 mg of ruxolitinib. Nonmedicinal ingredients: hydroxypropylcellulose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, colloidal silicon dioxide, sodium starch glycolate (Type A), and povidone.
Each elongated, curved, white-to-almost-white tablet with "NVR" debossed on one side and "L20"debossed on the other side, contains 20 mg of ruxolitinib. Nonmedicinal ingredients: hydroxypropylcellulose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, colloidal silicon dioxide, sodium starch glycolate (Type A), and povidone.
Who should NOT take this medication?
Do not take this medication if you:
- are allergic to ruxolitinib or any ingredients of the medication
- have a history of an illness called progressive multifocal leukoencephalopathy
What side effects are possible with this medication?
Many medications can cause side effects. A side effect is an unwanted response to a medication when it is taken in normal doses. Side effects can be mild or severe, temporary or permanent.
The side effects listed below are not experienced by everyone who takes this medication. If you are concerned about side effects, discuss the risks and benefits of this medication with your doctor.
Contact your doctor if you experience these side effects and they are severe or bothersome. Your pharmacist may be able to advise you on managing side effects.
- increased blood pressure
- increased cholesterol and triglycerides
- muscle spasms
- passing gas (flatulence)
- ringing in the ears
- weight gain
Although most of the side effects listed below don't happen very often, they could lead to serious problems if you do not seek medical attention.
Check with your doctor as soon as possible if any of the following side effects occur:
- back pain
- high blood pressure
- symptoms of an infection (e.g., fever, chills, cough, difficult or painful urination)
- symptoms of anemia (e.g., unusual tiredness, shortness of breath, pale skin)
- symptoms of heart problems (e.g., low heart beat, chest pain, dizziness, fainting, palpitations)
- symptoms of shingles (e.g., painful skin rash with blisters)
- symptoms of tuberculosis (e.g., chronic cough with blood-tinged sputum, fever, night sweats, weight loss)
- symptoms of a urinary tract infection (e.g., pain when urinating, urinating more often than usual, low back or flank pain)
- unexpected bruising or bleeding (e.g., nose bleeds, blood in urine, black stools, bleeding gums, cuts that won't stop bleeding)
Stop taking the medication and seek immediate medical attention if any of the following occur:
- signs of bleeding in the brain (e.g., sudden altered level of consciousness, persistent headache, numbness, tingling, weakness, or paralysis)
- signs of bleeding in the stomach or intestine (e.g., passing black or bloodstained stools, or vomiting blood)
- signs of progressive multifocal leukoencephalopathy (PML) (e.g., memory loss, vision loss, difficulty thinking or walking)
- signs of a serious allergic reaction (e.g., abdominal cramps, hives, difficulty breathing, nausea and vomiting, or swelling of the face and throat)
Are there any other precautions or warnings for this medication?
Before you begin using a medication, be sure to inform your doctor of any medical conditions or allergies you may have, any medications you are taking, whether you are pregnant or breast-feeding, and any other significant facts about your health. These factors may affect how you should use this medication.
Anemia: Ruxolitinib may cause low levels of red blood cells. If you experience symptoms of reduced red blood cell count (anemia) such as shortness of breath, feeling unusually tired, or pale skin, contact your doctor as soon as possible.
Your doctor will do blood tests regularly to monitor the amounts of specific types of blood cells in your blood.
Bleeding: Ruxolitinib can reduce the number of platelet cells in the blood. Platelets help the blood to clot and if there aren't enough, you may bleed more easily. If you notice signs of unusual bruising or bleeding (e.g., blood in urine, cuts that won't stop bleeding, black stools, bleeding gums), contact your doctor.
Grapefruit juice: Grapefruit juice affects how ruxolitinib is removed from the body. It may cause too much of the medication to build up in the body and cause possibly harmful side effects. People should not drink grapefruit juice or eat grapefruit at anytime while taking this medication for treatment.
Heart rhythm: Ruxolitinib can cause changes to the normal rhythm of the heart, including a decrease in heart rate and an irregular heartbeat.
If you are at risk for heart rhythm problems (e.g., have a slow heart rate, an abnormal heart rhythm, heart failure, or heart disease), discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed.
Infection: Ruxolitinib can reduce the number of cells that fight infection in the body (white blood cells). Tell your doctor immediately if you notice signs of an infection, such as fever or chills, severe diarrhea, shortness of breath, prolonged dizziness, headache, stiff neck, weight loss, or listlessness. Your doctor will do blood tests regularly to monitor the number of specific types of blood cells in your blood.
Kidney function: If you have reduced kidney function or kidney disease, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed.
Lactose intolerance: This medication contains lactose. If you have galactose intolerance (galactosemia, glucose-galactose malabsorption, or Lapp lactase deficiency), you should not take this medication.
Liver function: If you have liver problems, discuss with your doctor how this medication may affect your medical condition, how your medical condition may affect the dosing and effectiveness of this medication, and whether any special monitoring is needed. This medication can affect your liver function. Your doctor may want to regularly test your liver function with blood tests while you are taking this medication. If you experience symptoms of liver problems such as fatigue, feeling unwell, loss of appetite, nausea, yellowing of the skin or whites of the eyes, dark urine, pale stools, abdominal pain or swelling, and itchy skin, contact your doctor immediately.
Progressive multifocal leukoencephalopathy (PML): There have been reports of PML after using ruxolitinib. PML is a rare disorder that causes nerve damage in the brain. If you experience memory loss, vision loss, trouble thinking, or difficulty walking, contact your doctor immediately.
Skin cancer: People taking this mediation have reported certain types of skin cancer. Report any skin changes or sores that do not heal to your doctor.
Pregnancy: This medication should not be used during pregnancy. If you become pregnant while taking this medication, contact your doctor immediately. Men and women taking ruxolitinib should use an effective method of birth control (e.g., birth control pill, condoms) during treatment.
Breast-feeding: It is not known if ruxolitinib passes into breast milk. Women taking ruxolitinib should not breast-feed.
Children: The safety and effectiveness of this medication have not been clearly established for children less than 18 years of age.
What other drugs could interact with this medication?
There may be an interaction between ruxolitinib and any of the following:
- azole antifungals (e.g., ketoconazole, itraconazole, posaconazole, and voriconazole)
- bacillus Calmette-Guérin (BCG)
- beta-adrenergic blockers (e.g., atenolol, metoprolol, propranolol)
- calcium channel blockers (e.g., amlodipine, nifedipine, verapamil, diltiazem)
- grapefruit juice
- HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs; e.g., delavirdine, efavirenz, etravirine, nevirapine)
- HIV protease inhibitors (e.g., atazanavir, indinavir, ritonavir, saquinavir)
- macrolide antibiotics (e.g., clarithromycin, erythromycin)
- St. John's wort
- certain tyrosine kinase inhibitors (e.g., dabrafenib, imatinib, nilotinib)
- stop taking one of the medications,
- change one of the medications to another,
- change how you are taking one or both of the medications, or
- leave everything as is.
All material copyright MediResource Inc. 1996 – 2018. Terms and conditions of use. The contents herein are for informational purposes only. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Source: www.medbroadcast.com/drug/getdrug/Jakavi