Package Leaflet: Information for the User
Lorviqua 25 mg film-coated tablets
Lorviqua 100 mg film-coated tablets
lorlatinib
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
What is Lorviqua
Lorviqua contains the active substance lorlatinib, a medicine used to treat adults with advanced non-small cell lung cancer (NSCLC). Lorviqua belongs to a group of medicines that inhibit an enzyme called anaplastic lymphoma kinase (ALK). Lorviqua is only given to patients who have an alteration in the ALK gene, see section How Lorviqua worksbelow.
What Lorviqua is used for
Lorviqua is used to treat adults with a type of lung cancer called non-small cell lung cancer (NSCLC). It is used if your lung cancer:
You may be prescribed Lorviqua if:
How Lorviqua works
Lorviqua inhibits a type of enzyme called tyrosine kinase and causes the death of cancer cells in patients with alterations in the ALK gene. Lorviqua is only given to patients whose disease is due to an alteration in the ALK tyrosine kinase gene.
If you have any questions about how Lorviqua works or why you have been prescribed this medicine, ask your doctor.
Do not take Lorviqua
Warnings and precautions
Tell your doctor before you start taking Lorviqua:
If you are not sure, talk to your doctor, pharmacist, or nurse before taking Lorviqua.
Tell your doctor immediately if you notice:
Your doctor may perform additional tests and decide to reduce the dose of Lorviqua or stop treatment if:
For more information, see Possible side effectsin section 4.
Children and adolescents
This medicine is only indicated in adults and should not be given to children or adolescents.
Tests and checks
You will have blood tests before you start treatment and during treatment. These tests are to check the level of cholesterol, triglycerides, and amylase or lipase enzymes in your blood before you start treatment with Lorviqua and regularly during treatment.
Other medicines and Lorviqua
Tell your doctor, pharmacist, or nurse if you are taking, have recently taken, or might take any other medicines, including herbal medicines and medicines obtained without a prescription. This is because Lorviqua may affect the way other medicines work. Also, certain medicines may affect the way Lorviqua works.
Do not take Lorviqua with certain medicines. These are listed in the section Do not take Lorviquaat the beginning of section 2.
In particular, tell your doctor, pharmacist, or nurse if you are taking any of the following medicines:
Taking Lorviqua with food and drinks
Do not drink grapefruit juice or eat grapefruit while you are being treated with Lorviqua, as it may change the amount of Lorviqua in your body.
Pregnancy, breast-feeding, and fertility
Do not become pregnant while you are taking this medicine. If you can become pregnant, you must use highly effective contraception (such as double-barrier contraception like a condom and a diaphragm) during treatment and for at least 5 weeks after stopping treatment. Lorlatinib may reduce the effectiveness of hormonal contraceptives (such as the pill); therefore, hormonal contraceptives cannot be considered highly effective. If the use of hormonal contraceptives is unavoidable, they should be used in combination with a condom.
Talk to your doctor about the contraceptive methods that are suitable for you and your partner.
Do not father a child while you are taking Lorviqua, as this medicine may harm the baby. If there is a possibility that you may father a child while you are taking this medicine, you must use a condom during treatment and for at least 14 weeks after stopping treatment. Talk to your doctor about the contraceptive methods that are suitable for you and your partner.
Do not breast-feed while you are taking this medicine and for 7 days after the last dose. It is not known if Lorviqua can pass into breast milk and may harm your baby.
Lorviqua may affect male fertility. Talk to your doctor about preserving fertility before you start taking Lorviqua.
Driving and using machines
Be careful when driving or using machines while you are taking Lorviqua due to its effects on mental status.
Lorviqua contains lactose
If your doctor has told you that you have an intolerance to some sugars, talk to them before taking this medicine.
Lorviqua contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per 25 mg or 100 mg tablet; this is essentially “sodium-free”.
Always take this medicine exactly as your doctor, pharmacist, or nurse has told you. If you are not sure, talk to your doctor, pharmacist, or nurse.
If you vomit after taking Lorviqua
If you vomit after taking a dose of Lorviqua, do not take an extra dose, just take your next dose at the usual time.
If you take more Lorviqua than you should
If you accidentally take too many tablets, talk to your doctor, pharmacist, or nurse immediately. You may need medical attention.
If you forget to take Lorviqua
The way to proceed if you miss a tablet depends on how much time is left until your next dose.
Then take the next tablet at the usual time.
Do not take a double dose to make up for missed doses.
If you stop taking Lorviqua
It is important to take Lorviqua every day for as long as your doctor tells you to. If you cannot take the medicine as your doctor has prescribed, or if you feel that you no longer need it, talk to your doctor immediately.
If you have any other questions about the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Some side effects may be serious.
Tell your doctor immediately if you notice any of the following side effects(see also section 2 What you need to know before you take Lorviqua). Your doctor may reduce the dose, stop treatment for a short period, or stop it completely:
Other side effects of Lorviqua may include:
Very common:may affect more than 1 in 10 people
Common: may affect up to 1 in 10 people
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist, or nurse, even if it is possible that they are not listed in this leaflet. You can also report side effects directly through 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 blister and the carton after “EXP”. The expiry date is the last day of the month stated.
This medicine does not require any special storage conditions.
Do not use this medicine if you notice that the packaging is damaged or shows signs of deterioration.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
Lorviqua Composition
Lorviqua 25 mg: each film-coated tablet (tablet) contains 25 mg of lorlatinib.
Lorviqua 100 mg: each film-coated tablet (tablet) contains 100 mg of lorlatinib.
Tablet core: microcrystalline cellulose, calcium hydrogen phosphate, sodium starch glycolate, and magnesium stearate.
Film coating: hypromellose, lactose monohydrate, macrogol, triacetin, titanium dioxide (E171), black iron oxide (E172), and red iron oxide (E172).
See Lorviqua contains lactoseand Lorviqua containssodium in section 2.
Product Appearance and Package Contents
Lorviqua 25 mg is presented as pink, round, film-coated tablets with "Pfizer" engraved on one side and "25" and "LLN" on the other.
Lorviqua 25 mg is presented in blisters of 10 tablets, which are available in packs of 90 tablets (9 blisters).
Lorviqua 100 mg is presented as dark pink, oval, film-coated tablets with "Pfizer" engraved on one side and "LLN 100" on the other.
Lorviqua 100 mg is presented in blisters of 10 tablets, which are available in packs of 30 tablets (3 blisters).
Only some pack sizes may be marketed.
Marketing Authorization Holder
Pfizer Europe MA EEIG
Boulevard de la Plaine 17
1050 Brussels
Belgium
Manufacturer
Pfizer Manufacturing Deutschland GmbH
Mooswaldallee 1
79108 Freiburg im Breisgau
Germany
For more information about this medicinal product, please contact the local representative of the marketing authorization holder:
Belgium/Belgique/Belgien Luxembourg/Luxemburg Pfizer NV/SA Tel: +32 (0)2 554 62 11 | Latvia Pfizer Luxembourg SARL, Latvian branch Tel: +371 670 35 775 |
Lithuania Pfizer Luxembourg SARL, Lithuanian branch Tel: +370 5 251 4000 | |
Czech Republic Pfizer, s.r.o. Tel: +420 283 004 111 | Hungary Pfizer Kft. Tel: +36-1-488-37-00 |
Denmark Pfizer ApS Tel: +45 44 20 11 00 | Malta Vivian Corporation Ltd. Tel: +356 21344610 |
Germany PFIZER PHARMA GmbH Tel: +49 (0)30 550055-51000 | Netherlands Pfizer B.V. Tel: +31 (0)800 63 34 636 |
Estonia Pfizer Luxembourg SARL, Estonian branch Tel: +372 666 7500 | Norway Pfizer AS Tel: +47 67 52 61 00 |
Greece Pfizer Hellas A.E. Tel: +30 210 6785800 | Austria Pfizer Corporation Austria Ges.m.b.H. Tel: +43 (0)1 521 15-0 |
Spain Pfizer, S.L. Tel: +34 91 490 99 00 | Poland Pfizer Polska Sp. z o.o. Tel: +48 22 335 61 |
France Pfizer Tel: +33 (0)1 58 07 34 40 | Portugal Laboratórios Pfizer, Lda. Tel: +351 21 423 5500 |
Croatia Pfizer Croatia d.o.o. Tel: +385 1 3908 777 | Romania Pfizer Romania S.R.L. Tel: +40 (0)21 207 28 00 |
Ireland Pfizer Healthcare Ireland Unlimited Company Tel: +1800 633 363 (toll free) Tel: +44 (0)1304 616161 | Slovenia Pfizer Luxembourg SARL, Slovenian branch Pfizer, pharmaceutical consulting branch, Ljubljana Tel: +386 (0)1 52 11 400 |
Iceland Icepharma hf. Tel: +354 540 8000 | Slovak Republic Pfizer Luxembourg SARL, Slovak branch Tel: +421 2 3355 5500 |
Italy Pfizer S.r.l. Tel: +39 06 33 18 21 | Finland Pfizer Oy Tel: +358 (0)9 430 040 |
Cyprus Pfizer Hellas A.E. (Cyprus branch) Tel: +357 22817690 | Sweden Pfizer AB Tel: +46 (0)8 550 520 00 |
Date of Last Revision of this Leaflet:{MM/YYYY}
Other Sources of Information
Detailed information on this medicinal product is available on the European Medicines Agency website: https://www.ema.europa.eu.