Prospective:Patient Information
GIOTRIF 20mg film-coated tablets
afatinib
Read the entire prospectus carefully before starting to take this medication, as it contains important information for you.
Contents of the prospectus
GIOTRIF is a medication that contains the active ingredient afatinib. It works by blocking the activity of a group of proteins called the ErbB family (including EGFR [Epidermal Growth Factor Receptor or ErbB1], HER2 [ErbB2], ErbB3, and ErbB4). These proteins are involved in the growth and spread of cancer cells and can be affected by changes (mutations) in the genes that produce them. By blocking the activity of these proteins, this medication can inhibit the growth and spread of cancer cells.
This medication is used alone to treat adult patients with a specific type of lung cancer (non-small cell lung cancer):
Do not take GIOTRIF
Warnings and precautions
Consult your doctor or pharmacist before starting to take this medication:
Inform your doctor immediately while taking this medication:
See also section 4 "Possible side effects".
Children and adolescents
GIOTRIF is not recommended for use in children or adolescents. Do not administer this medication to children or adolescents under 18 years of age.
Other medications and GIOTRIF
Inform your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication, including herbal remedies and medications purchased without a prescription.
In particular, the following medications, if taken before GIOTRIF, may increase GIOTRIF levels in the blood and, therefore, the risk of side effects. Therefore, these medications should be taken with as much time as possible between them and the intake of GIOTRIF. This means leaving a gap of at least 6 hours (for medications taken twice a day) or 12 hours (for medications taken once a day) between them and the intake of GIOTRIF:
The following medications may decrease the effectiveness of GIOTRIF:
Ask your doctor if you are unsure when to take these medications.
GIOTRIF may increase blood levels of other medications, including the following:
Inform your doctor before taking these medications with GIOTRIF.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Pregnancy
You should avoid becoming pregnant while taking this medication. If you could become pregnant, you should use adequate contraceptive methods during treatment and for at least 1 month after the last dose of this medication. This is because there may be a risk of harm to the fetus.
If you become pregnant while taking this medication, you should inform your doctor immediately. Your doctor will decide with you whether to continue treatment or not.
You should ask your doctor for advice if you plan to become pregnant after taking the last dose of this medication, as your body may not have completely eliminated this medication.
Breastfeeding
You should not breastfeed your baby while taking this medication, as there may be a risk to the breastfed child.
Driving and using machines
If you notice symptoms related to treatment that affect your vision (e.g., redness and/or irritation of the eye, dry eye, tearing, sensitivity to light) or your ability to concentrate and react, it is recommended that you do not drive or use machines until the side effects have disappeared (see section 4 Possible side effects).
GIOTRIF contains lactose
This medication contains a sugar called lactose. If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.
Follow the administration instructions of this medication indicated by your doctor exactly. In case of doubt, consult your doctor or pharmacist again.
Dosage
The recommended dose is 40 mg once a day.
Your doctor may adjust (increase or decrease) your dose based on how well you tolerate this medication.
When to take GIOTRIF
GIOTRIF should be taken orally. If you have difficulty swallowing the tablet, dissolve it in a glass of still water. Do not use other liquids. Place the tablet in the water without crushing it and stir the water occasionally for about 15 minutes until the tablet has dissolved into very small particles. Drink the liquid immediately. To ensure that you take all of the medication, fill the glass with water again and drink it.
If you are unable to swallow and have a gastric tube, your doctor may suggest that the medication be administered through the tube.
If you take more GIOTRIF than you should
Contact your doctor or pharmacist immediately. You may experience more intense side effects, and your doctor may interrupt treatment and provide supportive treatment.
If you forget to take GIOTRIF
Do not take a double dose (two tablets at once instead of one) to make up for missed doses.
If you interrupt treatment with GIOTRIF
Do not stop taking this medication without consulting your doctor first. It is essential to take this medication every day, as long as your doctor prescribes it. If you do not take this medication as prescribed by your doctor, your cancer may grow again.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, GIOTRIF can cause side effects, although not everyone will experience them.
Inform your doctor immediately if you notice any of the following serious side effects. In some cases, your doctor may need to interrupt treatment and reduce your dose or stop treatment:
Diarrhea that lasts more than 2 days or severe diarrhea can lead to fluid loss (frequent, may affect up to 1 in 10 patients), low potassium levels in the blood (frequent), and worsening of kidney function (frequent). Diarrhea can be treated. As soon as the first symptoms of diarrhea appear, drink plenty of fluids. Inform your doctor immediately and start antidiarrheal treatment as soon as possible. You should have an antidiarrheal medication on hand before starting treatment with GIOTRIF.
It is essential to start treatment for the rash as soon as possible. Inform your doctor as soon as a rash appears. If the treatment for the rash does not work and the rash worsens (e.g., if your skin peels or blisters appear), you should inform your doctor immediately, as your doctor may decide to interrupt your treatment with GIOTRIF. The rash may appear or worsen in areas of the body exposed to the sun. It is recommended to use appropriate clothing and sunscreen as protective measures against the sun.
Eye irritation or inflammation can occur (conjunctivitis/dry eye occurs frequently and keratitis occurs uncommonly). Inform your doctor if you experience sudden onset or worsening of eye symptoms such as pain or redness of the eyes or dry eyes.
If you experience any of these symptoms, inform your doctor as soon as possible.
The following side effects have also been reported:
Very common side effects(may affect more than 1 in 10 patients):
Common side effects(may affect up to 1 in 10 patients):
Uncommon side effects(may affect up to 1 in 100 patients):
Rare side effects(may affect up to 1 in 1,000 patients):
Reporting side effects
If you experience any side effects, consult your doctor or pharmacist, even if they are not listed in this prospectus. You can also report them directly through the national reporting system included in Appendix V. By reporting side effects, you can help provide more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date stated on the carton, pouch, and blister after EXP. The expiration date is the last day of the month indicated.
Store in the original packaging to protect it from moisture and light.
Medications should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of the packaging and any unused medication. This will help protect the environment.
Composition of GIOTRIF
Appearance and Package Contents of the Product
GIOTRIF 30 mg are dark blue, round film-coated tablets. They have the code “T30” engraved on one side and the Boehringer Ingelheim logo on the other.
GIOTRIF film-coated tablets are presented in packs containing 1, 2, or 4 single-dose precut blisters. Each blister contains 7 x 1 film-coated tablets and is packaged in an aluminum bag along with a desiccant that should not be swallowed.
Only certain pack sizes may be marketed.
Marketing Authorization Holder
Boehringer Ingelheim International GmbH
Binger Strasse 173
55216 Ingelheim am Rhein
Germany
Manufacturer
Boehringer Ingelheim Pharma GmbH & Co. KG
Binger Strasse 173
55216 Ingelheim am Rhein
Germany
Boehringer Ingelheim France
100-104 Avenue de France
75013 Paris
France
You can request more information about this medicinal product by contacting the local representative of the marketing authorization holder:
Belgium/Belgique/Belgien Boehringer Ingelheim SComm Tel: +32 2 773 33 11 | Lithuania Boehringer Ingelheim RCV GmbH & Co KG Lithuanian branch Tel: +370 5 2595942 |
Luxembourg/Luxemburg Boehringer Ingelheim SComm Tel: +32 2 773 33 11 | |
Czech Republic Boehringer Ingelheim spol. s r.o. Tel: +420 234 655 111 | Hungary Boehringer Ingelheim RCV GmbH & Co KG Hungarian branch office Tel: +36 1 299 8900 |
Denmark Boehringer Ingelheim Danmark A/S Tel: +45 39 15 88 88 | Malta Boehringer Ingelheim Ireland Ltd. Tel: +353 1 295 9620 |
Germany Boehringer Ingelheim Pharma GmbH & Co. KG Tel: +49 (0) 800 77 90 900 | Netherlands Boehringer Ingelheim B.V. Tel: +31 (0) 800 22 55 889 |
Estonia Boehringer Ingelheim RCV GmbH & Co KG Estonian branch Tel: +372 612 8000 | Norway Boehringer Ingelheim Norway KS Tel: +47 66 76 13 00 |
Greece Boehringer Ingelheim Ελλάς Μονοπρόσωπη Α.Ε. Tel: +30 2 10 89 06 300 | Austria Boehringer Ingelheim RCV GmbH & Co KG Tel: +43 1 80 105-7870 |
Spain Boehringer Ingelheim España, S.A. Tel: +34 93 404 51 00 | Poland Boehringer Ingelheim Sp. z o.o. Tel: +48 22 699 0 699 |
France Boehringer Ingelheim France S.A.S. Tel: +33 3 26 50 45 33 | Portugal Boehringer Ingelheim Portugal, Lda. Tel: +351 21 313 53 00 |
Croatia Boehringer Ingelheim Zagreb d.o.o. Tel: +385 1 2444 600 | Romania Boehringer Ingelheim RCV GmbH & Co KG Bucharest branch Tel: +40 21 302 2800 |
Ireland Boehringer Ingelheim Ireland Ltd. Tel: +353 1 295 9620 | Slovenia Boehringer Ingelheim RCV GmbH & Co KG Ljubljana branch office Tel: +386 1 586 40 00 |
Iceland Vistor hf. Tel: +354 535 7000 | Slovak Republic Boehringer Ingelheim RCV GmbH & Co KG organizational unit Tel: +421 2 5810 1211 |
Italy Boehringer Ingelheim Italia S.p.A. Tel: +39 02 5355 1 | Finland Boehringer Ingelheim Finland Ky Tel: +358 10 3102 800 |
Cyprus Boehringer Ingelheim Ελλάς Μονοπρόσωπη Α.Ε. Tel: +30 2 10 89 06 300 | Sweden Boehringer Ingelheim AB Tel: +46 8 721 21 00 |
Latvia Boehringer Ingelheim RCV GmbH & Co KG Latvian branch Tel: +371 67 240 011 | United Kingdom (Northern Ireland) Boehringer Ingelheim Ireland Ltd. Tel: +353 1 295 9620 |
Date of the 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.