Patient Information: Summary of Product Characteristics
Orkambi 100 mg/125 mg granules in sachet
Orkambi 150 mg/188 mg granules in sachet
lumacaftor/ivacaftor
Read all of this leaflet carefully before your child starts taking this medicine because it contains important information for you.
Contents of the pack
Orkambi contains two active substances: lumacaftor and ivacaftor. It is a medicine used for the long-term treatment of cystic fibrosis (CF) in patients aged 1 year and older who have a specific mutation (called F508del mutation) in the gene for a protein called cystic fibrosis transmembrane conductance regulator (CFTR), which plays an important role in regulating the flow of mucus in the lungs. People with this mutation will produce abnormal CFTR protein. Cells contain two copies of the CFTR gene. Orkambi is used in patients where the F508del mutation affects both copies (homozygous).
Lumacaftor and ivacaftor work together to improve the function of the abnormal CFTR protein.
Lumacaftor increases the amount of CFTR available and ivacaftor helps the abnormal protein to work more normally.
Do not use Orkambi
Warnings and precautions
Talk to your child's doctor or pharmacist before your child starts taking Orkambi.
Orkambi must not be used in patients who do not have two copies of the F508del mutationin the CFTR gene.
Talk to your child's doctor before your child starts taking Orkambi if your child has been told they have liver or kidney disease, as the doctor may need to adjust the dose of Orkambi.
Abnormal results in liver blood tests have been commonly seen in some people taking Orkambi. If your child has any of the following symptoms, which could be signs of liver problems, tell your child's doctor right away:
Your child's doctor should do blood tests to check how your child's liver is working before and while your child is taking Orkambi, especially during the first year.
Respiratory events such as difficulty breathing or shortness of breathor narrowing of the airwayshave been seen in patients when starting treatment with Orkambi, especially in patients with decreased lung function. If your child's lung function is decreased, your child's doctor may keep a close eye on them when starting treatment with Orkambi.
An increase in blood pressurehas been seen in some patients taking Orkambi. Your child's doctor may keep a close eye on your child's blood pressure during treatment with Orkambi.
In some children and adolescents taking Orkambi and ivacaftor alone (one of the ingredients in Orkambi), a lens opacity (cataract) in the eyehas been seen without any effect on vision. Your child's doctor may do some eye examinations before and during treatment with Orkambi.
Orkambi is not recommended in patients who have had an organ transplant.
Children under 1 year of age
It is not known if Orkambi is safe and effective in children under 1 year of age. Therefore, Orkambi must not be used in children under 1 year of age.
Other medicines and Orkambi
Tell your child's doctor or pharmacist if your child is taking, has recently taken or might take any other medicines.
telithromycin, clarithromycin, rifampicin, rifabutin, rifapentine, erythromycin
phenobarbital, carbamazepine, phenytoin
midazolam, triazolam
fluconazole, ketoconazole, itraconazole, posaconazole, voriconazole
ciclosporin, everolimus, sirolimus, tacrolimus
St. John's Wort (Hypericum perforatum)
montelukast, fexofenadine
citalopram, escitalopram, sertraline, bupropion
ibuprofen
digoxin
warfarin, dabigatran
oral, injectable and implantable contraceptives as well as contraceptive patches; may include ethinylestradiol, norethindrone and other progestogens. These should not be considered a reliable method of contraception when taken with Orkambi.
methylprednisolone, prednisone
omeprazole, esomeprazole, lansoprazole
repaglinide
There have been reports of false positive results in urine tests for tetrahydrocannabinol (THC, an active component in cannabis) in patients taking Orkambi. Your child's doctor may request another test to confirm the results.
Driving and using machines
Dizziness has been reported in patients who received ivacaftor, a component of Orkambi, which may affect the ability to drive and use machines.
If your child experiences dizziness while taking Orkambi, it is recommended that your child does not ride a bicycle or do anything that requires full attention until the symptoms go away.
Orkambi contains sodium
This medicine contains less than 23 mg of sodium (1 mmol) per dose; this is essentially “sodium-free”.
Follow the instructions for administration of this medicine exactly as told by your child's doctor. If you are not sure, ask the doctor again.
Your child's doctor will decide the correct dose for your child. Your child should keep using all their other medicines unless the doctor tells them to stop taking any.
Recommended dose
The recommended dose for patients aged 1 year and older is shown in the following table.
Orkambi should be taken in the morning and in the evening (every 12 hours) with fat-containing foods.
There are different strengths of Orkambi depending on the age and weight of the child. Check that your child has been prescribed the correct dose (below).
Age | Weight | Product | Dose | |
Morning | Evening | |||
1 to <2years | 7 kg to <9 kg | Orkambi 75 mg/94 mg granules in sachet | 1 sachet | 1 sachet |
9 kg to <14 kg | Orkambi 100 mg/125 mg granules in sachet | 1 sachet | 1 sachet | |
≥14 kg | Orkambi 150 mg/188 mg granules in sachet | 1 sachet | 1 sachet | |
2 to 5years | <14 kg | Orkambi 100 mg/125 mg granules in sachet | 1 sachet | 1 sachet |
≥14 kg | Orkambi 150 mg/188 mg granules in sachet | 1 sachet | 1 sachet |
If your child has moderate or severe liver problems, the doctor may need to reduce the dose of Orkambi, as your child's liver will not get rid of Orkambi from their body as quickly as in children with normal liver function.
Method of administration
Orkambi is taken by mouth.
Each sachet is for single use only.
You can start giving Orkambi to your child on any day of the week.
Administration of Orkambi granules to your child:
It is important to take Orkambi with fat-containing foodsto get the right levels of the medicine in the body. Meals and snacks recommended in the cystic fibrosis guidelines or meals recommended in standard nutritional guidelines contain the right amounts of fat. Examples of fat-containing foods or snacks are those made with butter or oils or those that contain eggs. Other examples of fat-containing foods are:
If your child takes more Orkambi than they should
Talk to your child's doctor or pharmacist for advice. If possible, show them the medicine and this leaflet. Your child may experience side effects, including those listed in section 4 below.
If you forget to give Orkambi to your child
Give the missed dose with fat-containing foods if it has been less than 6 hours since the time your child was supposed to take the granules. Otherwise, wait until it is time for your child's next dose. Do not give your child a double dose to make up for a missed dose.
If you stop giving Orkambi to your child
Give Orkambi to your child for as long as the doctor has told you to. Do not stop treatment unless the doctor tells you to. You should keep giving the medicine as the doctor has told you, even if your child seems better.
If you have any other questions about the use of this medicine, ask your child's doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them. The side effects reported with Orkambi and ivacaftor taken alone (one of the active substances in Orkambi) are listed below and may occur with Orkambi.
The serious side effectsof Orkambi include increased liver enzymes in the blood, liver damage and worsening of existing severe liver disease. Worsening of liver function can be fatal. These serious side effects are uncommon (may affect up to 1 in 100 people).
Tell your child's doctor right awayif your child experiences:
Other side effects
Very common(may affect more than 1 in 10 people):
Common(may affect up to 1 in 10 people):
Uncommon(may affect up to 1 in 100 people):
*Side effects seen with ivacaftor alone.
Additional side effects in children
The side effects seen in children are similar to those seen in adults and adolescents.
However, increased liver enzymes in the blood are more common in younger children than in adults.
Reporting of side effects
If your child experiences any side effects, talk to your child's doctor or pharmacist, even if it is 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.
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/sachet after EXP. The expiry date refers to the last day of the month shown.
This medicine does not require any special storage conditions.
Medicines should not be disposed of via wastewater or household waste. Ask your child's pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Orkambi Composition
The active ingredients are lumacaftor and ivacaftor.
Orkambi 75 mg/94 mg granules in sachet:
Each sachet contains 75 mg of lumacaftor and 94 mg of ivacaftor.
Orkambi 100 mg/125 mg granules in sachet:
Each sachet contains 100 mg of lumacaftor and 125 mg of ivacaftor.
Orkambi 150 mg/188 mg granules in sachet:
Each sachet contains 150 mg of lumacaftor and 188 mg of ivacaftor.
The other ingredients are: microcrystalline cellulose; sodium croscarmellose; hypromellose acetate succinate; povidone (K30); and sodium lauryl sulfate (see section 2 “Orkambi contains sodium”).
Product Appearance and Package Contents
Orkambi granules are a white to off-white granule.
The granules are supplied in sachets.
Package size of 56 sachets (contains 4 individual blister packs with 14 sachets each)
Marketing Authorization Holder
Vertex Pharmaceuticals (Ireland) Limited
Unit 49, Block 5, Northwood Court, Northwood Crescent,
Dublin 9, D09 T665,
Ireland
Tel.: +353 (0)1 761 7299
Manufacturer
Almac Pharma Services (Ireland) Limited
Finnabair Industrial Estate
Dundalk
Co. Louth
A91 P9KD
Ireland
Almac Pharma Services Limited
Seagoe Industrial Estate
Craigavon
BT63 5UA
United Kingdom
Further information about this medicinal product can be obtained from the local representative of the marketing authorization holder:
Vertex Pharmaceuticals (Ireland) Limited Tel: +353 (0) 1 761 7299 | Spain Vertex Pharmaceuticals Spain, S.L. Tel: + 34 91 7892800 |
Greece Vertex Φαρμακευτικ? Μονοπρ?σωπη Αν?νυμη Εταιρ?α Tel: +30 (211) 2120535 | Italy Vertex Pharmaceuticals (Italy) S.r.l. Tel: +39 0697794000 |
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: http://www.ema.europa.eu. There are also links to other websites on rare diseases and orphan medicines.